73 results on '"Jiménez ME"'
Search Results
2. Evaluation of DiaSorin Liaison® calprotectin fecal assay adapted for pleural effusion
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de Paz Poves Cristina, Barneo-Caragol Clara, Cillero Sánchez Ana Isabel, Jimenez Mendiguchia Lucía, Quirós Caso Covadonga, Moreno Rodríguez María, López González Francisco J., and Prieto García Mᵃ Belén
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automation ,calprotectin ,chemiluminescence ,pleural fluid ,validation ,Medical technology ,R855-855.5 - Abstract
Calprotectin (CP) is a calcium and zinc binding protein that is widely measured on faecal samples but its determination in other biological fluids might be of interest. The aim of this work was to validate the measurement of CP in pleural fluid by chemiluminescence.
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- 2023
- Full Text
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3. Hernias diafragmáticas traumáticas: revisión de la literatura a propósito de un caso
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De la Puente Azpitarte, V., primary, Regueiro Martín-Albo, C., additional, Sanchez-Migallón Jiménez, ME., additional, and Vallejo Carrasco, M., additional
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- 2017
- Full Text
- View/download PDF
4. Multiple sclerosis in the tropics: genetic association to STR’s loci spanning the HLA and TNF
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Jiménez Me, Jorge Sánchez, Juan José Builes, Mauricio Camargo, Mauricio Arcos-Burgos, Juan-Manuel Anaya, M. Salgar, Dora Rivera, Palacio Lg, and Jiménez I
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Adult ,Male ,Linkage disequilibrium ,Multiple Sclerosis ,Locus (genetics) ,Human leukocyte antigen ,Colombia ,Biology ,HLA-DQ alpha-Chains ,Linkage Disequilibrium ,Genetic determinism ,03 medical and health sciences ,0302 clinical medicine ,Gene Frequency ,HLA-DQ Antigens ,Prevalence ,Humans ,Genetic Predisposition to Disease ,030212 general & internal medicine ,Allele ,Allele frequency ,Genetic association ,Genetics ,Polymorphism, Genetic ,Tumor Necrosis Factor-alpha ,Middle Aged ,Phenotype ,Neurology ,Immunology ,Microsatellite ,Chromosomes, Human, Pair 6 ,Female ,Neurology (clinical) ,030217 neurology & neurosurgery ,Microsatellite Repeats - Abstract
Clear evidence has been presented correlating gene polymorphisms at 6p21.3-21.4 (containing HLA and TNF) and the predisposition to acquire multiple sclerosis (MS). In a previous study, we found that polymorphisms at HLA DQA1 were associated with being or not being predisposed to MS in individuals inhabiting the tropics, where the prevalence of MS is significantly lower than in subtropical areas. Here, we tested the hypothesis that polymorphisms at D6S276, D6S265, D6S273 and D6S291 microsatellite loci are in strong linkage disequilibrium with a major genetic factor predisposing to MS. These microsatellites span the 6p21.3 region with intervals of 5 cM establishing particular landmarks for the HLA and TNF loci. Thirty-five MS patients and 35 controls, age, sex, social, ethnically and geographically matched healthy individuals, were studied. After testing the fit of gene frequencies to the normal distribution and performing the correlation for multiple comparisons, we found significant differences among the case and the control frequencies for the allele 202 belonging to the marker D6S276 (Pc =0.00455) and for the allele 114 belonging to the marker D6S265 (Pc=0.0084). For these two alleles at different loci, we found higher frequencies in the cases than in the controls. A nonsignificant p value was found in testing the existence of linkage disequilibrium among the studied loci in the cases and in the controls. In conclusion, the current study adds evidence to the established association among polymorphisms of genes located at 6p21.3-21.4 and MS. Furthermore, because of the distribution of the tested microsatellite loci, the more probable critical region could be correlated with the TNF neighborhood.
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- 2002
5. Multiple Sclerosis: Association to HLA DQα in a Tropical Population
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C. Espinal, Jaramillo N, Alfredo Villa, Carlos Santiago Uribe, M.A Moreno, Jiménez Me, Jorge Sánchez, Guillermo Palacio, Jiménez I, María Luisa Bravo, Juan José Builes, Mauricio Arcos-Burgos, Ana C. Londoño, and Juan M. Anaya
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Adult ,Male ,musculoskeletal diseases ,Linkage disequilibrium ,Multiple Sclerosis ,endocrine system diseases ,Immunology ,Population ,Human leukocyte antigen ,Colombia ,Major histocompatibility complex ,HLA-DQ alpha-Chains ,Linkage Disequilibrium ,Double-Blind Method ,HLA-DQ Antigens ,Genetics ,medicine ,Humans ,Allele ,skin and connective tissue diseases ,education ,Alleles ,Genetics (clinical) ,Genetic association ,Tropical Climate ,education.field_of_study ,biology ,Multiple sclerosis ,nutritional and metabolic diseases ,Middle Aged ,medicine.disease ,Phenotype ,Case-Control Studies ,biology.protein ,Female - Abstract
Studies performed in subtropical populations have found significant association between the phenotype multiple sclerosis (MS) and the major histocompatibility complex (MHC). We present the results of a case-control study conducted on a tropical population (Antioquia, Colombia) in order to detect a possible association between MS and HLA DQα (HLA DQA1*) alleles. Forty chromosomes belonging to MS patients were compared to two sets of controls (40 and 910 chromosomes, respectively). The HLA DQA1*0101 and DQA1*0102 alleles were found in a significantly higher proportion among the cases than among the controls, whereas the HLA DQA1*0103 allele was found in a significantly lower proportion of the cases. These results suggest that the association of HLA DQA1*0101, DQA1*0102 and DQA1*0103 to the MS phenotype found in Caucasian subtropical populations remains in individuals with MS inhabiting the tropics. This finding could mean that the major genetic component associated to the MHC in subtropical populations is the same in the tropics.
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- 1999
6. Neurocysticercosis in Persons with Epilepsy in Medellin, Colombia
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Victor C. W. Tsang, Jiménez I, Jiménez Me, Jorge Sánchez, Palacio Lg, J. Noh, Margarita Giraldo, Hector H. Garcia, O. Mora, and L. Ahn
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medicine.medical_specialty ,Pediatrics ,business.industry ,Neurocysticercosis ,Helminthiasis ,Cysticercosis ,medicine.disease ,Surgery ,Serology ,medicine.drug_formulation_ingredient ,Epilepsy ,Neurology ,parasitic diseases ,Taenia solium ,medicine ,Etiology ,Seroprevalence ,Neurology (clinical) ,business - Abstract
Summary: Purpose: A prospective series of 643 persons with epilepsy attending a reference neurologic center in Medellin, Colombia, was examined by computed tomography (CT scan) or serology or both with the enzyme-linked immunoelectrotransfer blot assay (EITB) to assess the prevalence of Taenia solium cysticercosis. Methods: All presenting patients were consecutively enrolled in the study. Five hundred forty-six persons underwent cerebral CT scans; 376 of them also had serum EITB performed. Results: Prevalence of neurocys@ercosis by CT scan was 13.92%. Overall prevalence of T. solium antibodies with EITB was 9.82%, but for those with late-onset epilepsy (onset after age 30 years), prevalence increased to 17.5% and 19% for those who originated from outside urban Medellin. Seroprevalence in individuals with mixed lesions (cysts and calcifications) was 88.2% and 64.10% in those with live cysts. Conversely, only 2.72% of persons with CT findings not related to neurocysticercosis had positive EITB tests. Conclusions: Our study shows that an important proportion of individuals with epilepsy have radiologic or serologic evidence of T. solium infection, suggesting that neurocysticercosis is an important etiology for epilepsy in Colombia.
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- 1998
7. Description of a new case of Bohring-Opitz (or Oberklaid-Danks) syndrome
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Aldea-Romero, AE, López-Dueñas, A, Rubio-Jiménez, ME, Hernández-Bejarano, MJ, García-García, A, Martínez-Fernández, ML, Bermejo-Sanchez, Eva, and Martínez-Frías, ML
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Bohring-Opitz ,Oberklaid-Danks - Abstract
Dismorfología y Genética Clínica In 1999, Bohring et al. reported a new syndrome clinically distinguishable from cases with C syndrome or Opitz trigonocephaly. All the patients showed failure to thrive, microcephaly with metopic suture ridging, nevus flammeus over the forehead, thick hair and forehead hirsutism, shallow orbits with prominent eyes, depressed nasal root, anomalous ears, retrognathia, cleft lip and palate, flexion deformities of the upper limbs with radial head dislocation and ulnar deviation of fingers. Patients have severe developmental delay, sucking and swallowing difficulties starting in the prenatal period, as suggested by the usual polyhydramnios. The brain anomalies include hydrocephaly/large ventricles, agenesis/hypoplasia of corpus callosum, Dandy-Walker malformation, myelin abnormalities, and cortical atrophy. Occasional symptoms are a small or closed fontanel at birth, inguinal hernias and cryptorchidism in males, and intestinal malrotation. Most patients die early in childhood because of bradycardia and apnea. Although there is an overlap between C-like syndrome and C syndrome, different manifestations in these patients suggest a different entity. This new syndrome has been called (apart from C-like syndrome) Bohring-Optiz or Oberklaid-Danks syndrome. Recently, it has been associated in some patients to heterozygous de novo nonsense mutations in ASXL1 gene, which is required for maintenance of both activation and silencing of Hox genes, suggesting that the syndrome is genetically Heterogeneous. Here we describe the first case of this syndrome identified in the Spanish Collaborative Study of Congenital Malformations (ECEMC) Registry, and possibly in Spain. Therefore, its minimal frequency has been estimated in 1:2,648,286 newborn infants. No
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- 2011
8. Clinical features of multiple sclerosis in a genetically homogeneous tropical population
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Juan-Manuel Anaya, Carlos Santiago Uribe, Palacio Lg, Jiménez I, Mauricio Arcos-Burgos, Jorge Sánchez, A. Villa, Mauricio Camargo, Ana C. Londoño, and Jiménez Me
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Male ,Pathology ,medicine.medical_specialty ,Asia ,Multiple Sclerosis ,Optic Neuritis ,Population ,Disease ,Colombia ,White People ,Central nervous system disease ,03 medical and health sciences ,Myelopathy ,0302 clinical medicine ,Recurrence ,medicine ,Humans ,Optic neuritis ,030212 general & internal medicine ,education ,Caucasian population ,Tropical Climate ,education.field_of_study ,Movement Disorders ,business.industry ,Incidence ,Multiple sclerosis ,medicine.disease ,Neurology ,Homogeneous ,Immunology ,Female ,Neurology (clinical) ,business ,030217 neurology & neurosurgery - Abstract
Individuals affected with multiple sclerosis (MS) from a genetically homogeneous Caucasian population in Antioquia, a tropical region of Colombia, were evaluated in order to observe the clinical behavior of the disease. The frequency of clinical manifestations in 65 patients with definite MS from Antioquia was compared with those reported from temperate regions. The most common manifestations were optic neuritis and motor symptoms with absence of cerebellar symptoms. This presentation is significantly different from the frequency distribution at onset in series from temperate regions. These differences suggest that environmental factors could modify the clinical expression of MS in this population.
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- 2001
9. Complex segregation analysis of non-myoclonic idiopathic generalized epilepsy in families ascertained from probands affected with idiopathic epilepsy with tonic-clonic seizures in Antioquia, Colombia
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Mauricio Arcos-Burgos, Jiménez Me, Rodrigo Isaza, Zuluaga L, Mora O, Rafael Blanco, Carlos Santiago Uribe, Jorge Sánchez, and Jiménez I
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Proband ,Genetics ,Male ,Heterozygote ,Models, Genetic ,Locus (genetics) ,Complex segregation analysis ,Biology ,Colombia ,medicine.disease ,Major gene ,Idiopathic generalized epilepsy ,Epilepsy ,medicine ,Epistasis ,Multifactorial Inheritance ,Cluster Analysis ,Humans ,Epilepsy, Generalized ,Female ,Epilepsy, Tonic-Clonic ,Genetics (clinical) ,Alleles ,Genes, Dominant - Abstract
In an attempt to identify the possible role of major genes, multifactorial inheritance, and cohort effects in the susceptibility to idiopathic epilepsy with generalized tonic-clonic seizures of the awakening type (GTCS), complex segregation analysis was performed in 196 nuclear families ascertained through affected probands with idiopathic epilepsy with GTCS belonging to the Paisa community of Antioquia (Colombia). Models postulating no transmission, single major locus (dominant and recessive) only, and multifactorial component only, were rejected. Since the codominant single major locus model could not be rejected and models that assign no major locus to transmission, no polygenic component to transmission, and no transmission of the major effect were rejected, complex segregation analysis suggested that a major autosomal codominant allele together with a multifactorial component (mixed model) best explained clustering of idiopathic epilepsy with GTCS in families of the Paisa community. The deficit of transmission of heterozygotes (0.17) is compatible with the existence of epistasis acting on a major gene whose frequency was estimated to be 0.0211. Its transmission variance accounts for 81% of the susceptibility to idiopathic epilepsy with GTCS. The complementary variance (19%) is due to the polygenic component.
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- 1996
10. Factores de riesgo para recurrencia de convulsiones y pronóstico a corto plazo en cirugía de epilepsia para esclerosis mesial temporal
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Restrepo-Marín Dm, Massaro-Ceballos M, Jiménez-Ramírez I, Mora-López O, Cortés-Silva E, Jaramillo-Betancur H, and Jiménez Me
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Neurology (clinical) ,General Medicine - Abstract
Objetivo. Determinar los factores de riesgo para recurrencia de convulsiones y la clasificacion posquirurgica a corto plazo en pacientes operados por esclerosis mesial temporal (EMT). Sujetos y metodos. Estudio de casos y controles anidado en la cohorte de pacientes con EMT diagnosticados por resonancia magnetica con dos anos de seguimiento posquirurgico; se excluyeron pacientes con EMT bilateral. Se evaluaron caracteristicas clinicas prequirurgicas, foco epileptogenico en videoelectroencefalograma (video-EEG) y variables quirurgicas con respecto a recurrencia de convulsiones en los primeros dos anos tras la intervencion y clasificacion de Engel en el primer y segundo aniversario de la cirugia. Resultados. Entre octubre de 2001 y junio de 2008 se evaluo a 144 pacientes con EMT candidatos a cirugia de epilepsia; hasta junio de 2007, se habia operado a 89 pacientes, un 51,7% con EMT izquierda. El 35,8% de los pacientes presento recurrencia de convulsiones antes del segundo ano tras la intervencion; el factor de riesgo prequirurgico asociado a recurrencia fue foco bitemporal o temporal unico con diseminacion contralateral por video-EEG (odds ratio = 6,32; intervalo de confianza al 95% = 1,64-26,41); y el posquirurgico, la presencia de convulsiones durante el primer mes tras la operacion (p = 0,0004); no se encontro asociacion con recurrencia para genero, convulsiones tonicoclonicas generalizadas prequirurgicas, lado de la EMT ni tiempo de evolucion prequirurgica de la epilepsia. El 66,3 y el 75,8% de los pacientes estaban en Engel I al primer y segundo ano de la cirugia, respectivamente. El 91% de los pacientes intervenidos estaba en buen pronostico posquirurgico a los dos anos. Conclusion. La localizacion del foco epileptogenico por electrofisiologia es un factor determinante en el pronostico posquirurgico a corto plazo en la EMT.
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- 2009
11. Análisis de ligamiento en una familia multigeneracional extendida qye segrega para epilepsia idiopática
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Rivera-Valencia D, Arcos Om, Jiménez-Ramírez I, Palacio Lg, Jorge Sánchez, and Jiménez Me
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Neurology (clinical) ,General Medicine - Abstract
Introduccion. Los analisis de ligamiento permiten identificar loci que confieren susceptibilidad a diversas enfermedades en las que se presume una etiologia genetica mediante la determinacion de la cosegregacion de alelos de marcadores especificos dentro de las familias. Objetivo. Determinar si existe susceptibilidad para desarrollar epilepsia idiopatica generalizada (EIG) en las regiones 8q22.1 -q24.23, 16p13.3 y 21q22.3 en una familia multigeneracional extendida perteneciente a la comunidad Paisa de Antioquia, un aislado genetico localizado en Colombia segregando para EIG y con un fuerte poder para detectar ligamiento. Pacientes y metodos. Se selecciona una familia con multiples individuos afectados de epilepsia idiopatica que consultaron al Instituto Neurologico de Antioquia. El individuo afectado debia tener un diagnostico realizado por neurologo de epilepsia idiopatica no mioclonica o de epilepsia idiopatica parcial. Se realizo videomonitorizacion a todos los pacientes con sospecha de epilepsia idiopatica, con el fin de caracterizar electroencefalograficamente las crisis. Resultados. De los 106 individuos en esta familia incluidos en la genealogia, se genotipificaron 76, de los que 15 se afectan con crisis tonicoclonicas generalizadas y seis se consideraron posiblemente afectados. Los resultados de lod score son significativamente negativos para todos los marcadores con relacion a cada modelo considerado. Conclusiones. Se descarta que los genes localizados en las regiones 8q22.1 -q24.23, 16p13.3 y 21q22.3 sean los responsables de la agregacion familiar de la EIG en esta familia, como lo han sugerido estudios anteriores en otras familias.
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- 2004
12. Análisis de ligamiento a la región 15Q25-15Q22 de una familia multigeneracional extendida segregando epilepsia idiopática
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Rivera-Valencia D, Mauricio Arcos-Burgos, Palacio Lg, Jiménez Me, Jiménez-Ramírez I, and Jorge Sánchez
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Neurology (clinical) ,General Medicine ,Biology ,Humanities ,Lod score - Abstract
Introduccion. Los analisis de ligamiento proveen una poderosa evidencia de la influencia de la herencia en la epilepsia, debido a que determinan la cosegregacion de alelos de marcadores especificos con la epilepsia dentro de las familias. Objetivo. Determinar si existe susceptibilidad para desarrollar epilepsia idiopatica generalizada (EIG) en la region 15q22.1-q25.1 en una familia multigeneracional extendida perteneciente a la comunidad paisa de Antioquia, un aislado genetico localizado en Colombia que segrega para la EIG y con un fuerte poder para detectar ligamiento. Pacientes y metodos. Se selecciono una familia con multiples individuos afectados de epilepsia que consultaron al Instituto Neurologico de Antioquia. El individuo afectado debia tener un diagnostico realizado por neurologo de epilepsia idiopatica no mioclonica o de epilepsia idiopatica parcial. Se realizo videomonitorizacion a todos los pacientes con sospecha de epilepsia idiopatica con el fin de caracterizar electroencefalograficamente las crisis. Resultados. De los 106 individuos de esta familia incluidos en la genealogia, se genotipificaron 76, de cuales 15 estaban afectados con crisis tonicoclonicas generalizadas y seis se consideraron posiblemente afectados. Los resultados de lod score son significativamente negativos para todos los marcadores segun cada modelo considerado. Conclusiones. Se descarta que los genes que codifican para las subunidades a-3, a-5 y b-4 del receptor neuronal nicotinico de la acetilcolina (CHRNA3, CHRNA5 y CHRNB4) localizados en la region 15q, sean los responsables de la agregacion familiar de la EIG en esta familia, como lo han sugerido estudios anteriores en otras familias.
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- 2004
13. Prevalencia de miastenia grave en Antioquia, Colombia
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Jiménez Me, Franco Af, Arcos-Burgos Om, Palacio Lg, Carlos Santiago Uribe, and Jorge Sánchez
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Weakness ,Pediatrics ,medicine.medical_specialty ,business.industry ,Incidence (epidemiology) ,Neuromuscular transmission ,General Medicine ,medicine.disease ,Epidemiological indicators ,Myasthenia gravis ,Surgery ,medicine ,Neurology (clinical) ,Skeletal muscle fatigue ,medicine.symptom ,business - Abstract
Introduction. Myasthenia gravis (MG), considered the commonest of all the illnesses that affect neuromuscular transmission, is a disorder in which the autoimmune system attacks the post-synaptic acetylcholine-receptor proteins in the end plate terminal; it is characterised by weakness and skeletal muscle fatigue, with no anomalies in reflexes, sensitivity or coordination. Epidemiological indicators, such as incidence and prevalence, are not known in Colombia. Aims. To determine the prevalence of MG among the inhabitants of Antioquia, through the use of the capture-recapture method. Patients and methods. The capture-recapture method was used for two sources, the Instituto NeurolOgico de Antioquia and the Hospital Universitario San Vicente de Pa´ul, which are the most important institutions for the diagnosis of neurological diseases in Antioquia. MG prevalence was calculated using the following formula: p=n/N×10 5 . We examined the datafrom the period between 1 July 1995 and 30 June 2000 with the aim of identifying subjects who fitted the profile of MG sufferers. Results. General MG prevalence in Antioquia was 27.7 cases per million inhabitants (CI 95%= 23.2-32.2). The male/female ratio was 1:3.77. Conclusions. The estimated prevalence of MG is lower than that reported in United States and other temperate regions, where it varies between 60 and 150 cases per million. The prevalence ofMG is low in Antioquia, as in other tropical areas.
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- 2002
14. Aspectos genético-moleculares de la susceptibilidad a desarrollar epilepsia idiopática
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Palacio Lg, Mauricio Arcos-Burgos, Mora O, Jiménez I, Jorge Sánchez, and Jiménez Me
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Genetics ,Locus (genetics) ,General Medicine ,Biology ,medicine.disease ,Clinical onset ,Phenotype ,Variable Expression ,Epilepsy ,Genetic linkage ,Etiology ,medicine ,Neurology (clinical) ,Gene - Abstract
INTRODUCTION There are more than 40 clinical types of epilepsy classified according to aetiology and/or mode of clinical onset. The term idiopathic epilepsy is reserved for cases with convulsions but no detectable structural lesions of the brain or neurological anomalies. DEVELOPMENT AND CONCLUSIONS In spite of many studies confirming the importance of genetic factors in the occurrence of idiopathic epilepsy, these appear to be complex and probably involve a locus of variable expression or several loci with similar phenotype expression (epistaxis). Also, environmental factors have variable effects. In recent years the principal genes involved in susceptibility to develop epilepsy have been mapped. In this way one mitochondrial and three autosomic genes have been cloned as responsible for the development of certain forms of this disorder. Also several studies of genetic linkage have given evidence, sometimes inconsistent, regarding the influence of another five loci in the susceptibility to develop epilepsy (6p21.2, 6q23-25, 8q24, 8p, 10q). On occasions the same locus has been linked with different forms of epilepsy, and on other occasions one form of epilepsy has been shown to be linked to several loci.
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- 2000
15. Prevalencia de la esclerosis múltiple en Colombia
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Jiménez Me, León F, Arcos-Burgos Om, Uribe B, Jiménez I, Volcy M, Pareja J, Pradilla G, Palacio Lg, Carlos Javier Flores Aguirre, A. Villa, Carlos Santiago Uribe, and Jorge Sánchez
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education.field_of_study ,Latin Americans ,business.industry ,Multiple sclerosis ,Population ,General Medicine ,medicine.disease ,Etiology ,Medicine ,Prevalence studies ,Neurology (clinical) ,business ,education ,Demography - Abstract
INTRODUCTION Multiple sclerosis (MS) is the commonest demyelinating condition of the nervous system. It is characterized by numerous demyelinating areas or plaques of demyelination which are found dispersed throughout the nervous system. It has been shown that MS is less frequent in tropical regions than in subtropical regions. In Latin America particularly, there are some studies which show this phenomenon. However, in Colombia no studies of prevalence of MS have been done. OBJECTIVE To determine the prevalence of multiple sclerosis in five provinces of Colombia (Antioquia, Caldas, Santander, Risaralda and Bolivar). PATIENTS AND METHODS The capture-recapture method was used for two sources to determine the number of cases defined on the criteria of Poser et al seen between July 1995 and June 2000. RESULTS The prevalence (cases of MS per 100,000 inhabitants) varied between 1.48 in Antioquia (95% CI 1.12; 1.78) and 4.98 in Risaralda (95% CI 3.52; 6.43). Seventy two percent were women. The regions included in this study represented 25% of the population of Colombia. CONCLUSIONS There is a low prevalence of MS which is as expected in tropical areas. Persons with MS in these regions may be very useful in the study of other factors involved in the aetiology of MS (genetic). The capture-recapture method is an excellent tool for carrying out prevalence studies since it is cheap and requires little time.
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- 2000
16. Esclerosis múltiple: aproximación epidemiológico-genética en habitantes de Antioquia, Colombia. Desequilibrio de ligamiento al HLA Dqa
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Mauricio Arcos-Burgos, Carlos Santiago Uribe, Jiménez I, Jorge Sánchez, Juan-Manuel Anaya, Palacio Lg, Jaramillo N, Espinal C, Ana C. Londoño, Gabriel Bedoya, Villa La, Bravo Ml, and Jiménez Me
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Genetics ,Linkage disequilibrium ,education.field_of_study ,Population ,Locus (genetics) ,General Medicine ,Human leukocyte antigen ,Biology ,Genotype ,HLA-DQ ,Neurology (clinical) ,Allele ,education ,Allele frequency - Abstract
INTRODUCTION AND OBJECTIVE Discrimination and quantification of the environmental and genetic components involved in developing multiple sclerosis (MS) have not been made. In order to discriminate these components we have ascertained affected individuals by MS belonging to the Paisa community from Antioquia, Colombia, a state localized in the tropical area of South America, to detect eventual linkage disequilibrium to HLA, locus DQ alpha, which could demonstrate the relevance of the genetic component. DEVELOPMENT A contingence analysis among case-control HLA DQ alpha genotype distributions, by using Monte Carlo resampling method to solve small number sample, showed that there are significant differences between the two groups. We observe that HLA DQ alpha 1.1, 1.2 allele frequencies were higher in the cases than in the controls. Also, there was significant HLA DQ alpha 3 allele lower frequency (p < 0.05) in the cases than in the controls. CONCLUSIONS Similar results have been described in other Caucasian populations living in non tropical areas. Before results could indicate that the Caucasoid populations genetic component implied in the susceptibility to MS have remained in Paisa community, whether the environmental component, being meaningful to develop MS.
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- 2000
17. Sistema de evaluación multidimensional de la conducta. Escala para padres de niños de 6 a 11 años, versión Colombiana
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Claudia Valencia, Jiménez I, David Pineda, Jiménez Me, Restrepo Ma, Holguín Ja, Vallejo Le, Silvia Mejia, Velásquez Jf, Arango Jc, Mora O, Randy W. Kamphaus, M. Arcos, M. Garcia, Francisco Lopera, Palacio Lg, Bartolino Ne, Margarita Giraldo, Lina María Rendón López, Mark Raymond Adams, Puerta Ic, and Antonio G. García
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Aggression ,Behavioral assessment ,General Medicine ,Parent ratings ,Developmental psychology ,Attention Problems ,Cronbach's alpha ,Scale (social sciences) ,medicine ,Neurology (clinical) ,Analysis of variance ,medicine.symptom ,Psychology ,Socioeconomic status ,Clinical psychology - Abstract
INTRODUCTION Behavioral Assessment System for Children (BASC) has demonstrated to be useful in the diagnosis of Attention Deficit Disorder (ADD). PATIENTS AND METHODS A randomized sample of 120 children, 6 to 11-year-old, participants from the school of the city of Medellin, Colombia, was selected. The sample was stratified by sex and two socioeconomic status (SES). Parents were asked to answer the BASC Parent Rating Scale (PRS) 6-11, authorized Spanish version. RESULTS Cronbach's alpha coefficient was 0.85 for the clinical scale (9 items). It was 0.75 for the Adaptive Scale (3 items). A scale designed with 4 items to assess ADD (hyperactivity, attention problems, aggression, and conduct problems) showed an alpha coefficient of 0.82. Male children scored significantly higher than female (ANOVA, p < 0.05) in hyperactivity, conduct problems, and atypicality. Children from low SES scored significantly higher than children of high SES on the most of clinical measures (p < 0.05) and lower on the three adaptive measures. Cluster analysis selecting six clusters found a prevalence of 61.6% for normal male children. In the total sample there were a 4% at risk of DDA type II (inattentive) and 14% at risk of DDA type I (combined). CONCLUSIONS BASC PRS (6-11) showed reliability and validity to assessing the behavior in Spanish speaking Colombian children.
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- 1999
18. Anticipación genética en epilepsia idiopática
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Jiménez Me, Carlos Santiago Uribe, Mauricio Arcos-Burgos, Palacio Lg, López-Gartner G, Zuluaga L, Jiménez I, Mora O, and Jorge Sánchez
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Pediatrics ,medicine.medical_specialty ,Wilcoxon signed-rank test ,business.industry ,Pedigree chart ,General Medicine ,medicine.disease ,medicine.disease_cause ,Epilepsy ,Variable number tandem repeat ,Anticipation (genetics) ,Heredity ,medicine ,Genetic Anticipation ,Neurology (clinical) ,business ,Intergenerational differences - Abstract
INTRODUCTION In extended and multigenerational pedigrees, the idiopathic epilepsy phenotype shows an extreme variability. OBJECTIVE The range of idiopathic epilepsy onset age in multigenerational pedigrees was studied in order to determine if genetic anticipation play a role in the heredity of Idiopathic Epilepsies. PATIENTS AND METHODS We compare the seizures onset age among relative-pairs of (parents-children, grandfathers-grandsons and nephew uncles). The mean onset age was compared using the Wilcoxon sign-rank paired-sample non-parametrical test to determine whether or not significant differences over > 0 exist, which refutes the null hypothesis of not anticipation. 84 pairs of relatives were taken from 72 extended multigenerational pedigrees. RESULTS The onset age of idiopathic epilepsy of the pairs showed a difference significantly > 0, which confirm the existence of intergenerational differences. This difference has a tendency to decrease in age which each successive generation. This difference occur in all relative pairs and therefore contradicts the ascertainment bias described by Penrose. CONCLUSIONS The results outline the existence of unstable mutations (those produced by a nucleotidic variable number of tandem repeats) as a probable explanation of the susceptibility to develop some forms of idiopathic epilepsy.
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- 1999
19. Uso de una escala multidimensional para padres de niños de 6 a 11 años en el diagnóstico de deficiencia atencional con hiperactividad
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David Pineda, Puerta Ic, Jiménez Me, Mora O, Jiménez I, Silvia Mejia, Palacio Lg, M. Garcia, Randy W. Kamphaus, Francisco Lopera, and Arango Jc
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Contingency table ,education.field_of_study ,Percentile ,business.industry ,Population ,General Medicine ,Linear discriminant analysis ,Discriminant function analysis ,Medicine ,Neurology (clinical) ,Analysis of variance ,business ,education ,Socioeconomic status ,Categorical variable ,Clinical psychology - Abstract
Summary. Introduction. The BASC is a multidimensional approach to evaluate the child behavior and it has been validated on the diagnosis of ADD/+H in North American children. Objective. Validating BASC-PRS 6-11 on the diagnosis of ADD/+H. Patients and methods. We selected 25 male DSM IV-ADD/+H (combined type), 6 to 11-years-old children, and 25 age, gender, and socioeconomic status matched controls. Mean ages of both groups 8.16 (1.5), schooling of controls 2.64 (1.4), and cases 2.6 (1.9). Results. On the Clinical Scale ADD/+H children had significant (Anova p< 0.01) higher scores in hyperactivity, conduct problems, and attention problems. On the Adaptive Scale only significant differences on social skills and leadership were found, with lower score in the ADD/+H group. A crosstab analysis between group code and each rating variable transformed into categorical (0 and 1) variable, cut-off point= 85 percentile, found that the case children's parents qualified as clinically in higher risk the variables attention problems (OR= 24.4; 95% CI= 4.5-130), conduct problems (OR= 9.0; 95% CI= 1.7-46.9) and hyperactivity (OR= 6.8; 95% CI= 1.6-28.5) (p< 0.01). A discriminant analysis selected attention problems as discriminant function (p< 0.0001). Classification capability 84% for each group. Conclusion. Our results proved the validity of the BASC-PRS 6-11 questionnaire for the screening diagnosis of ADD/+H children in a Spanish speaking population (REV NEUROL 1999; 28: 952-9).
- Published
- 1999
20. Modo de herencia de epilepsia idiopática generalizada no mioclónica en familias pesquisadas a través de probandos afectados de epilepsia idiopática con crisis tonicoclónicas del despertar en Antioquia, Colombia
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Jiménez Me, Jorge Sánchez, Carlos Santiago Uribe, R. Isaza, Jiménez I, Zuluaga L, O. Mora, Muñoz A, Palacio Lg, and Mauricio Arcos-Burgos
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Genetics ,Proband ,medicine.medical_specialty ,business.industry ,Locus (genetics) ,General Medicine ,Complex segregation analysis ,medicine.disease ,Major gene ,Epilepsy ,medicine ,Myoclonic epilepsy ,Epistasis ,Multifactorial Inheritance ,Neurology (clinical) ,business ,Psychiatry - Abstract
In attempt to identify the possible role of mayor genes, multifactorial inheritance, and cohort effects in the susceptibility to idiopathic epilepsy with generalized tonic clonic seizures of the awakening type (GTCS), complex segregation analysis was performed in 196 nuclear families ascertained through affected with probands with idiopathic epilepsy with GTCS belonging to the Paisa community of Antioquia (Colombia). Models postulating no transmission, single mayor locus (dominant and recessive) only, and multifactorial component only, were rejected. The models postulating no polygenic component to transmission, and no transmission of the major effect were also rejected. Thus far, complex segregation analysis suggested that a major autosomal codominant allele together with a multifactorial component (mixed model) best explains clustering of idiopathic epilepsy with GTCS in families of the Paisa community. The deficit of transmission of heterozygotes (0.17) is compatible with the existence of epistasis acting on a major gene whose frequency was estimated to be 0.0211. Its transmission variance accounts for 81% of the susceptibility to idiopathic epilepsy with GTCS. The complementary variance (19%) is due to polygenic component.
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- 1999
21. Discriminación de factores genéticos en el déficit de atención
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Jiménez Me, Mauricio Arcos-Burgos, P. Villegas, Francisco Lopera, Puerta Ic, Jiménez I, David Pineda, and Palacio Lg
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Genetics ,education.field_of_study ,Population ,General Medicine ,Complex segregation analysis ,Heritability ,Biology ,medicine.disease ,Penetrance ,Major gene ,medicine ,Attention deficit hyperactivity disorder ,Neurology (clinical) ,education ,Allele frequency ,Nuclear family - Abstract
INTRODUCTION AND OBJECTIVE In order to elucidate the genetic and environmental components involved in the susceptibility to develop attention deficit hyperactivity disorder (ADHD), a complex segregation analysis on nuclear families (n = 53) ascertained from affected probands belonging to Medellin, in the Antioquian State, Colombia, was performed. METHODS AND RESULTS Models of cohort effect (non-inheritance), multifactorial, recessive major gene, non-major gene component and non-transmission of major gene were rejected. Contrarily, dominant and codominant major gene models and non-multifactorial component could not be rejected. Thus, the better model fitting the data was that of the major gene (dominant/codominant). This major gene explains more than 99.99% of the ADHD phenotypic variance (value of heritability in the mixed model equal to 0.007%), which permit to assume a low aport of the environmental component to the phenotype ADHD. Gene frequency of the major gene was 3% in the general population of Antioquia and its penetrance was closed to 30%. CONCLUSION Some cautions and aspects related to the bias of the interview and diagnosis of the parents are discussed.
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- 1999
22. Contraste del modelo multifactorial como mecanismo hereditario de epilepsia idiopática generalizada no mioclónica y de eilepsia idiopática parcial
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Jiménez I, R. Isaza, Jiménez Me, Mora O, Zuluaga L, A. Villa, Palacio Lg, Rafael Blanco, Carlos Santiago Uribe, López-Gardner, Mauricio Arcos-Burgos, and Jorge Sánchez
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Genetics ,Future studies ,business.industry ,Locus (genetics) ,General Medicine ,Disease ,medicine.disease_cause ,medicine.disease ,symbols.namesake ,Epilepsy ,Heredity ,Mendelian inheritance ,symbols ,medicine ,Neurology (clinical) ,Threshold model ,Age of onset ,business - Abstract
Objective and methods An experimental study about the predictions from the multifactorial threshold model created by Falconer is presented, assuming that this model may explain the genetic mechanisms underlying the family aggregation of idiopathic epilepsies. Results We failed to confirm the following predictions from the falconer model: decreased prevalence of disease in relatives, proportional to decreased family links, and the order of birth effect. An heredity greater than 100% was calculated which is concordant with the presence of at least a locus with a major gen affect. Conclusion Our results reject the multifactorial threshold effect and suggest the presence of a major gen or Mendelian effect. An analysis of complex segregation is suggested for future studies.
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- 1998
23. 1-17-14 Prevalence of neurocysticercosis in individuals affected with epilepsy in Antioquia, Colombia
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Jiménez Me, Victor C. W. Tsang, I. Canasteros, J. Pilcher, Margarita Giraldo, Jiménez I, G. Palacio, Jorge Sánchez, and Mauricio Arcos-Burgos
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Pediatrics ,medicine.medical_specialty ,Epilepsy ,Neurology ,business.industry ,Neurocysticercosis ,medicine ,Neurology (clinical) ,medicine.disease ,business - Published
- 1997
24. 1-17-15 Idiopathic epilepsy: Is the syndromatic classification able to discriminate genetic heterogeneity? Results from complex segregation analysis applied to some types of generalized and partial idiopathic epilepsies
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Carlos Santiago Uribe, Jiménez Me, R. Isaza, Jiménez I, Mora O, Zuluaga L, Mauricio Arcos-Burgos, G. Palacio, Jorge Sánchez, A. Villa, and G. López
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Pathology ,medicine.medical_specialty ,Epilepsy ,Neurology ,Genetic heterogeneity ,Evolutionary biology ,medicine ,Neurology (clinical) ,Complex segregation analysis ,Biology ,medicine.disease - Published
- 1997
25. Multiple sclerosis in the tropics: genetic association to STR's loci spanning the HLA and TNF.
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Palacio, LG, Rivera, D, Builes, JJ, Jiménez, ME, Salgar, M, Anaya, JM, Jiménez, I, Camargo, M, Arcos-Burgos, M, and Sánchez, JL
- Subjects
GENETICS of multiple sclerosis ,MICROSATELLITE repeats ,GENETIC polymorphisms - Abstract
Clear evidence has been presented correlating gene polymorphisms at 6p21.3 - 21.4 (containing HLA and TNF) and the predisposition to acquire multiple sclerosis (MS). In a previous study, we found that polymorphisms at HLA DQA1 were associated with being or not being predisposed to MS in individuals inhabiting the tropics, where the prevalence of MS is significantly lower than in subtropical areas. Here, we tested the hypothesis that polymorphisms at D6S276, D6S265, D6S273 and D6S291 microsatellite loci are in strong linkage disequilibrium with a major genetic factor predisposing to MS. These microsatellites span the 6p21.3 region with intervals of 5 cM establishing particular landmarks for the HLA and TNF loci. Thirty-five MS patients and 35 controls, age, sex, social, ethnically and geographically matched healthy individuals, were studied. After testing the fit of gene frequencies to the normal distribution and performing the correlation for multiple comparisons, we found significant differences among the case and the control frequencies for the allele 202 belonging to the marker D6S276 (Pc = 0.00455) and for the allele 114 belonging to the marker D6S265 (Pc = 0.0084). For these two alleles at different loci, we found higher frequencies in the cases than in the controls. A nonsignificant p value was found in testing the existence of linkage disequilibrium among the studied loci in the cases and in the controls. In conclusion, the current study adds evidence to the established association among polymorphisms of genes located at 6p21.3 - 21.4 and MS. Furthermore, because of the distribution of the tested microsatellite loci, the more probable critical region could be correlated with the TNF neighborhood. [ABSTRACT FROM AUTHOR]
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- 2002
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26. Determination of the postural disorders in students from the Stomatology Clinics of the Benemerita Autonomous University of Puebla, Mexico.
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Huixtlaca-Rojo CC, Santiago-Álvarez N, Espinosa-De Santillana, Rebollo-Vázquez, and Hernández-Jiménez ME
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- 2009
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27. Sistema de indicadores de la calidad del aire para puertos marítimos colombianos
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Jiménez Mejía José Fernando and Pulgarín Calle David Esteban
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Puertos marítimos ,calidad del aire ,Indicadores ambientales ,Geography. Anthropology. Recreation ,Environmental sciences ,GE1-350 - Abstract
La calidad del aire en las zonas aledañas a los puertos requiere un monitoreo permanente y cualificado de un conjunto de variables que sirven para calificar los riesgos asociados a las diversas actividades que allí se realizan. La normativa ambiental vigente en Colombia establece topes admisibles para los contaminantes atmosféricos, los cuales se consideran valores de referencia para definir, junto con las variables mencionadas, unos indicadores ambientales adecuados. Este artículo presenta la propuesta entregada, en diciembre de 2009, al Ministerio de Ambiente, Vivienda y Desarrollo Territorial, para la implementación de un Sistema de Vigilancia de la calidad del aire en puertos marítimos y sus áreas de influencia. La propuesta hace parte de un estudio más amplio de seguimiento ambiental permanente en varias áreas portuarias marítimas de Colombia.
- Published
- 2011
28. CYP1A1 gene polymorphisms increase lung cancer risk in a high-incidence region of Spain: a case control study
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San Jose Carmen, Cabanillas Agustin, Benitez Julio, Carrillo Juan, Jimenez Mercedes, and Gervasini Guillermo
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Abstract Background A rural region in south-west Spain has one of the highest lung cancer incidence rates of the country, as revealed by a previous epidemiological 10-year follow-up study. The present work was undertaken to ascertain the role of CYP1A1 gene polymorphisms and their interaction with tobacco smoking in the development of the disease in this location. Methods One-hundred-and-three cases of lung cancer and 265 controls participated in the study. The participants were screened for the presence of four CYP1A1 polymorphisms, namely MspI, Ile462Val, T3205C, and Thr461Asn. Lung cancer risk was estimated as odds ratios (OR) and 95% confidence intervals (CI) using unconditional logistic regression models adjusting for age, sex, and smoking. Results The distribution of the variant CYP1A1 alleles was different from that described for other Caucasian populations, with CYP1A1*2A showing an uncommonly high frequency (p < 0.01). The CYP1A1*2B allele (carrying MspI and Ile462Val mutations) was strongly associated with high lung cancer risk (OR = 4.59, CI:1.4-12.6, p p p = 0.04). Moreover, the Thr461Asn polymorphism was found to be associated with SCLC in a Caucasian population for the first time to our knowledge (OR = 8.33, CI: 1.3-15.2, p = 0.04). Conclusion The results suggest that CYP1A1 polymorphisms contribute to increase lung cancer susceptibility in an area with an uncommon high incidence rate.
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- 2010
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29. Isolation and Characterization of an Antioxidant Aryl Polyene Pigment from Antarctic Bacterium Lysobacter sp. A03.
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Pailliè-Jiménez ME, Stincone P, Pereira JQ, Santagapita PR, Rodrigues E, and Brandelli A
- Abstract
Lysobacter is known as a bacterial genus with biotechnological potential, producing an array of enzymes, antimicrobial metabolites, and bioactive antioxidant compounds, including aryl polyene (APE) pigments that have been described as protecting substances against photooxidative damage and lipid peroxidation. In this study, the pigment extracted from keratinolytic Lysobacter sp. A03 isolated from Antarctic environment was characterized. The results of KOH test, UV-vis spectroscopy, CIELAB color system,
1 H-NMR, and FTIR-ATR spectroscopy suggest the pigment is a yellow xanthomonadin-like pigment. The in vitro antioxidant activity of the pigment was confirmed by the scavenging of ABTS and DPPH radicals. In silico analysis of the genome through antiSMASH software was also performed and the secondary metabolite gene clusters for APE and resorcinol synthesis were identified, suggesting that proteins responsible for the pigment biosynthesis are encoded in Lysobacter A03 genome., (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)- Published
- 2024
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30. Demographics aspects of brain and spine metastatic melanoma. Retrospective analysis in a single third-level center.
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Vega-Moreno DA, Kuramitsu S, Kaoru E, Yasukazu K, García-González U, Ibarra-de la Torre A, Hernández-Hernández L, Vicuña-González RM, and González-Jiménez ME
- Abstract
Background: Melanoma metastases to the CNS rank third in frequency, just after lung and breast metastases. There is controversy regarding the factors predisposing to developing CNS metastases in patients with cutaneous melanoma and their survival with conventional treatments., Methods: We carried out a retrospective analysis in a third-level hospital in Mexico to determine epidemiological aspects of melanoma metastases to the central nervous system, factors related to its appearance, clinical presentation, and survival in three treatment groups: surgery, radiotherapy, and conservative management., Results: We found that the nodular variant has the most significant association with CNS metastases. In addition, the superficial spreading variant has the highest risk of presenting a more substantial number of lesions, up to seven for each case and predominantly in the infratentorial space. On the other hand, we found more remarkable survival in patients treated only with surgery than those treated with radiotherapy or conservatively., Conclusions: This study lays the foundations for future prospective survival analysis of the different current treatment modalities for metastatic melanoma in the brain and spine. It also highlights the clinical risk factors for metastatic brain and spine tumors of melanoma., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2024 The Authors.)
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- 2024
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31. Discovering the fish fauna of a lagoon from the southeast of the Yucatan Peninsula, Mexico, using DNA barcodes.
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Uh-Navarrete AE, Valdez-Moreno M, Callejas-Jiménez ME, and Vásquez-Yeomans L
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- Humans, Animals, Mexico, Fishes, Larva, DNA, Ecosystem, DNA Barcoding, Taxonomic
- Abstract
Background: Aquatic ecosystems in the tropics are typically environments with a high species richness of fishes. These systems are also among the most vulnerable in the world, threatening the overall biodiversity of tropical regions. As a first step, it is important to enumerate the species in any ecosystem to promote its conservation. This study aims to inventory the ichthyofauna in the Chile Verde Lagoon, Quintana Roo, on the Yucatan Peninsula, a system fortunately well protected in Mexico, based on faunal surveys backed up with mtDNA barcodes., Methods: We collected larvae, juveniles, and adults of fishes in the lagoon with a variety of sampling gear targeting various life stages. Species were identified using both morphology and DNA barcodes. The abundance of species and ichthyoplankton biomass (wet weight, suction technique) were calculated from 43 samples., Results: We collected 197 adult and juvenile fishes and 3,722 larvae, of which 306 specimens were DNA-sequenced with a success rate of 96.7%. We identified 13 families, 24 genera, and 27 species in our inventory. The species number was estimated to comprise 75% of the potential total richness using the Chao 1 richness estimator. Clupeids and gobiids accounted for 87.9% of the total abundance of fishes, and, together with cyprinodontids, also accounted for the highest ichthyoplankton biomass., Conclusion: Adult and juvenile fishes were identified by morphology and meristic values, however larvae required DNA barcoding to identify species. The high biomass and abundance of larvae of clupeids, gobiids and cyprinodontids suggests that the Chile Verde Lagoon may be important for reproduction of these species in the region. Microgobius microlepis , a marine goby species, is reported for the first time in an inland oligohaline system. This study provides a basis for future environmental assessment and biomonitoring of the Chile Verde Lagoon in the Yucatan Peninsula of Mexico., Competing Interests: The authors declare there are no competing interests., (©2023 Uh-Navarrete et al.)
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- 2023
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32. Development and Evaluation of Zinc and Iron Nanoparticles Functionalized with Plant Growth-Promoting Rhizobacteria (PGPR) and Microalgae for Their Application as Bio-Nanofertilizers.
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Guardiola-Márquez CE, López-Mena ER, Segura-Jiménez ME, Gutierrez-Marmolejo I, Flores-Matzumiya MA, Mora-Godínez S, Hernández-Brenes C, and Jacobo-Velázquez DA
- Abstract
Micronutrient deficiencies are widespread and growing global concerns. Nanoscale nutrients present higher absorption rates and improved nutrient availability and nutrient use efficiency. Co-application of nanofertilizers (NFs) with biological agents or organic compounds increases NF biocompatibility, stability, and efficacy. This study aimed to develop and evaluate zinc and iron bio-nanofertilizers formulated with plant growth-promoting rhizobacteria (PGPR) and microalgae. Nanoparticles (NPs) were synthesized with the co-precipitation method and functionalized with Pseudomonas species and Spirulina platensis preparation. NPs were characterized and evaluated on seed germination, soil microbial growth, and early plant response under seedbed conditions. NPs corresponded to zinc oxide (ZnO; 77 nm) and maghemite (γ-Fe
2 O3 ; 68 nm). Functionalized nanoparticles showed larger sizes, around 145-233 nm. The seedling vigor index of tomato and maize was significantly increased (32.9-46.1%) by bacteria-functionalized ZnO- and γ-Fe2 O3 -NPs at 75 ppm. NFs at 250 and 75 ppm significantly increased bacterial growth. NFs also improved early plant growth by increasing plant height (14-44%), leaf diameter (22-47%), and fresh weight (46-119%) in broccoli and radish, which were mainly influenced by bacteria capped ZnO- and γ-Fe2 O3 -NPs at 250 ppm. Beneficial effects on plant growth can be attributed to the synergistic interaction of the biological components and the zinc and iron NPs in the bio-nanofertilizers.- Published
- 2023
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33. Phenotypic and genotypic characterization of Colombian clinical isolates of Sporothrix spp.
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Álvarez-Acevedo LC, Zuleta-González MC, Gómez-Guzmán ÓM, Rúa-Giraldo ÁL, Hernández-Ruiz O, McEwen-Ochoa JG, Urán-Jiménez ME, Arango-Arteaga M, Zancopé-Oliveira RM, Evangelista de Oliveira MM, and Jiménez-Alzate MDP
- Subjects
- Colombia, Genotype, Phenotype, Antifungal Agents, Culture Media, Sporothrix genetics
- Abstract
Introduction: For over a century, Sporothrix schenckii was considered the sole species responsible for sporotrichosis. In 2007, scientific community confirmed the disease could be caused by various Sporothrix species. These species differed in their virulence factors and their antifungal sensitivity., Objective: This study aims to characterize 42 Colombian clinical isolates of Sporothrix spp. phenotypically and genotypically., Material and Methods: Forty-two clinical isolates were characterized using phenotypic methods. It involved various culture media to determine their growth range at different temperatures and to assess the type and distribution of pigment and colony texture. Microscopic morphology was evaluated through microcultures, as well as the conidia diameter, type of sporulation, and morphology. Additionally, the assimilation of carbohydrates was selected as a physiological trait for species identification. Genotyping of 40 isolates was performed through partial amplification of the calmodulin gene, followed by sequence analysis., Results: Molecular studies enabled the identification of 32 isolates of S. schenckii and 8 isolates of S. globosa. The combination of phenotypic and genotypic methods eased these species characterizations and the recognition keys development based on parameters such as growth diameter at 25 and 30 ºC, colony texture (membranous or velvety) on potato dextrose agar, and microscopic morphology with predominance of pigmented triangular, elongated oval globose, or subglobose conidia., Conclusions: Confirmation of the phenotypic characteristics and molecular analysis is crucial for identifying Sporothrix species and determining adequate treatment. This study represents the first phenotypical and genotypical characterization of clinical isolates of Sporothrix spp. reported in Colombia.
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- 2023
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34. Pseudoepitheliomatous hyperplasia: Squamous cell carcinoma versus oral paracoccidioidomycosis, a case from a dermatological perspective
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Osorio-Cock LM, Jaramillo-Pulgarín SC, Ferrín-Bastidas AP, Molina-Colorado DY, Gómez-Guzmán ÓM, Zuluaga A, McEwen-Ochoa JG, Urán-Jiménez ME, and Jiménez-Alzate MDP
- Subjects
- Humans, Hyperplasia, Skin, Cell Differentiation, Paracoccidioidomycosis diagnosis, Carcinoma, Squamous Cell diagnosis
- Abstract
Paracoccidioidomycosis is a systemic mycosis endemic in Latin America. The most frequent form involves a chronic compromise of the lungs, skin, and mucosa. The patient started with a single oral lesion that lasted for several years. The absence of other symptoms pointed out a possible malignant neoplasm, specifically a squamous cell carcinoma. Differentiation between both diagnoses –fungal infection and carcinoma– depends on the results of the direct examination, the histopathological study, and the initial and subsequent cultures. However, in this case, those findings were not conclusive. The coexistence of both diagnoses is frequent and increases the diagnostic challenge. After several consultations and tests, direct examination, immunodiffusion and real-time PCR findings the multifocal chronic paracoccidioidomycosis diagnosis was confirmed. This case warns about a systematical absence of clinical suspicion of endemic mycoses before the appereance of mucocutaneous lesions, which can be produced by fungi like Paracoccidioides spp, and the importance of considering those mycoses among the differential diagnoses.
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- 2023
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35. [Patient with cervical spinal cord injury and benign paroxysmal positional vertigo treated with particle repositioning maneuvers].
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Peñaloza-Polo P, Santandreu-Jiménez ME, Bárbara-Bataller E, and Méndez-Suárez JL
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- Humans, Aged, Benign Paroxysmal Positional Vertigo therapy, Benign Paroxysmal Positional Vertigo diagnosis, Patient Positioning, Semicircular Canals, Cervical Cord, Spinal Cord Injuries complications
- Abstract
Benign paroxysmal positional vertigo (BPPV) is characterized by short, sudden episodes of vertigo when the head moves in specific positions. The treatment is particle repositioning maneuvers. BPPV usually is underdiagnosed, unreported and therefore not adequately treated. We present the case of a patient with spinal cord injury and BPPV. A 72-year-old patient who suffered a C5 fracture with spinal cord injury C5 AIS C that required surgical fixation. In the spinal cord injury unit BPPV of the left lateral semicircular canal was documented and treated using specific repositioning maneuvers, the patient progressively improved and was able to complete the rehabilitation treatment. The spinal cord injury unit with access to vestibular rehabilitation units can carry out the diagnosis and specific treatment of BPPV, minimizing the risks for the patient., (Copyright © 2023 Sociedad Española de Rehabilitación y Medicina Física. Publicado por Elsevier España, S.L.U. All rights reserved.)
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- 2023
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36. A randomized, double-blind study on the efficacy of oral domperidone versus placebo for reducing SARS-CoV-2 viral load in mild-to-moderate COVID-19 patients in primary health care.
- Author
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Rabanal Basalo A, Navarro Pablos M, Viejo Pinero N, Vila Méndez ML, Molina Barcena V, Montilla Bernabé A, Villanueva Morán MDP, Blanco Gallego AM, Guirao Sánchez C, Juárez Antón S, Fernández Rodríguez Á, Revuelta Puigdollers ML, Sarriá Sánchez MT, Martín Alegre C, Martínez Álvarez MÁ, Mestre de Juan M, Mielgo Salvador R, Gijón Seco MT, Saníger Herrera JM, Rodríguez Jiménez ME, Navas de la Peña B, Santa Cruz Hernández J, Abad Esteban AM, Díaz Martín R, García Pérez L, Herrero Vanrell P, Arias de Saavedra Criado MI, Vaquero Vinent A, López Gómez V, Montegrifo Rentero VM, Simón Miguel L, Campo Martos I, Ortiz Zamorano S, Izquierdo Zamarriego MJ, Vázquez Carrión I, López Valero RM, Gil C, Martínez A, and Soler López B
- Subjects
- Humans, SARS-CoV-2, Domperidone therapeutic use, Double-Blind Method, Viral Load, Treatment Outcome, Antiviral Agents therapeutic use, Primary Health Care, COVID-19
- Abstract
Introduction: The clinical effect of domperidone against COVID-19 has been investigated in a double-blind phase III clinical trial (EudraCT number 2021-001228-17). Domperidone has shown in vitro antiviral activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and potential immudolatory properties through the stimulation of prolactin secretion., Patients and Methods: The efficacy of oral domperidone plus standard of care (SOC; n = 87) versus placebo plus SOC ( n = 86) was evaluated in a 28-day randomized double-blind multicentre study in primary health care centres. A total of 173 outpatients with mild-to-moderate COVID-19 were included. Three daily doses of 10 mg (30 mg/day) of domperidone or placebo were administered for 7 days. Reduction of viral load on day 4 was the primary efficay endpoint. It was estimated in saliva samples by reverse transcription-quantitative polymerase chain reaction (RT-qPCR), as the cycle thresholds detected ORF1ab, N Protein and S Protein genes., Results: A significant reduction in the viral load was observed ( p < 0.001) from baseline to days 4, 7 and 14 of the three genes studied with non-significant differences between domperidone and placebo groups. Twenty-three patients (13.3%) experienced adverse events, 14 patients in the domperidone group (16.1%) and 9 patients in the placebo group (10.5%). No patients needed to be hospitalized., Conclusion: Results do not prove the use of domperidone as antiviral in patients with COVID-19.
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- 2023
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37. Fighting Obesity-Related Micronutrient Deficiencies through Biofortification of Agri-Food Crops with Sustainable Fertilization Practices.
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Guardiola-Márquez CE, Santos-Ramírez MT, Segura-Jiménez ME, Figueroa-Montes ML, and Jacobo-Velázquez DA
- Abstract
Obesity is a critical medical condition worldwide that is increasingly involved with nutritional derangements associated with micronutrient deficiencies, including iron, zinc, calcium, magnesium, selenium, and vitamins A, C, D, and E. Nutritional deficiencies in obesity are mainly caused by poor-quality diets, higher nutrient requirements, alterations in micronutrient metabolism, and invasive obesity treatments. The current conventional agricultural system is designed for intensive food production, focusing on food quantity rather than food quality, consuming excessive agricultural inputs, and producing nutrient-deficient foods, thus generating severe health and environmental problems; agricultural food products may worsen obesity-related malnutrition. Therefore, modern agriculture is adopting new biofortification technologies to combat micronutrient deficiencies and improve agricultural productivity and sustainability. Biofertilization and nanofertilization practices are increasingly used due to their efficiency, safety, and reduced environmental impact. Biofertilizers are preparations of PGP-microorganisms that promote plant growth by influencing plant metabolism and improving the nutrient uptake, and nanofertilizers consist of synthesized nanoparticles with unique physicochemical properties that are capable of increasing plant nutrition and enriching agricultural products. This review presents the current micronutrient deficiencies associated with obesity, the modern unsustainable agri-food system contributing to obesity progression, and the development of bio- and nanofertilizers capable of biofortifying agri-food crops with micronutrients commonly deficient in patients with obesity.
- Published
- 2022
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38. HelperFriend, a Serious Game for Promoting Healthy Lifestyle Behaviors in Children: Design and Pilot Study.
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Espinosa-Curiel IE, Pozas-Bogarin EE, Hernández-Arvizu M, Navarro-Jiménez ME, Delgado-Pérez EE, Martínez-Miranda J, and Pérez-Espinosa H
- Abstract
Background: The use of health games is a promising strategy for educating and promoting healthy lifestyle behaviors among children., Objective: We aimed to describe the design and development of a serious game, called HelperFriend, and evaluate its feasibility, acceptability, and preliminary effects in children in a pilot study. HelperFriend is a vicarious experiential video game designed to promote 3 lifestyle behaviors among young children: physical activity, healthy eating, and socioemotional wellness., Methods: Participants aged 8 to 11 years were recruited from an elementary school and randomized to receive a healthy lifestyle behavior educational talk (control) or play six 30-minute sessions with HelperFriend (intervention). Assessments were conducted at baseline (T0) and after the intervention (ie, 4 weeks) (T1). The primary outcome was gain in knowledge. The secondary outcomes were intention to conduct healthy behaviors, dietary intake, and player satisfaction., Results: Knowledge scores of intervention group participants increased from T0 to T1 for physical activity (t
14 =2.01, P=.03), healthy eating (t14 =3.14, P=.003), and socioemotional wellness (t14 =2.75, P=.008). In addition, from T0 to T1, the intervention group improved their intention to perform physical activity (t14 =2.82, P=.006), healthy eating (t14 =3.44, P=.002), and socioemotional wellness (t14 =2.65, P=.009); and there was a reduction in their intake of 13 unhealthy foods. HelperFriend was well received by intervention group., Conclusions: HelperFriend appears to be feasible and acceptable for young children. In addition, this game seems to be a viable tool to help improve the knowledge, the intention to conduct healthy behaviors, and the dietary intake of children; however, a well-powered randomized controlled trial is needed to prove the efficacy of HelperFriend., (©Ismael Edrein Espinosa-Curiel, Edgar Efrén Pozas-Bogarin, Maryleidi Hernández-Arvizu, Maria Elena Navarro-Jiménez, Edwin Emeth Delgado-Pérez, Juan Martínez-Miranda, Humberto Pérez-Espinosa. Originally published in JMIR Serious Games (https://games.jmir.org), 06.05.2022.)- Published
- 2022
- Full Text
- View/download PDF
39. Critical role of acute hypoxemia on the cognitive impairment after severe COVID-19 pneumonia: a multivariate causality model analysis.
- Author
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García-Grimshaw M, Chirino-Pérez A, Flores-Silva FD, Valdés-Ferrer SI, Vargas-Martínez MLÁ, Jiménez-Ávila AI, Chávez-Martínez OA, Ramos-Galicia EM, Marché-Fernández OA, Ramírez-Carrillo MF, Grajeda-González SL, Ramírez-Jiménez ME, Chávez-Manzanera EA, Tusié-Luna MT, Ochoa-Guzmán A, Cantú-Brito C, Fernandez-Ruiz J, and Chiquete E
- Subjects
- Adolescent, Female, Humans, Hypoxia etiology, Male, Middle Aged, Prospective Studies, Respiration, Artificial, SARS-CoV-2, COVID-19 complications, Cognitive Dysfunction etiology
- Abstract
Background: A high proportion of coronavirus disease 2019 (COVID-19) survivors may develop long-term cognitive impairment. We aimed to develop a multivariate causal model exposing the links between COVID-19-associated biomarkers, illness-related variables, and their effects on cognitive performance., Methods: In this prospective study, we assess the potential drivers for the development of cognitive impairment in patients with severe COVID-19 pneumonia aged ≥ 18 years at 6-month follow-up after hospital discharge, using the Montreal Cognitive Assessment (MoCA). Patients with pre-existing cognitive impairment were excluded. Laboratory results at hospital admission were clustered by principal component analysis (PCA) and included in a path analysis model evaluating the causal relationship between age, comorbidities, hypoxemia, invasive mechanical ventilation (IMV) requirement, in-hospital delirium, and cognitive performance., Results: We studied 92 patients: 54 (58.7%) men and 38 (41.3%) women, with median age of 50 years (interquartile range 42-55), among whom 50 (54.4%) tested positive for cognitive impairment at 6-month follow-up. Path analysis revealed a direct link between the thrombo-inflammatory component of PCA (C-reactive protein, fibrinogen, and neutrophils) and hypoxemia severity at hospital admission. Our model showed that low PaO
2 /FiO2 ratio values, unlike the thrombo-inflammatory component, had a direct effect on cognitive performance, independent from age, in-hospital delirium, and invasive mechanical ventilation., Conclusion: In this study, biomarkers of thrombo-inflammation in COVID-19 and low PaO2 /FiO2 had a negative effect on cognitive performance 6 months after hospital discharge. These results highlight the critical role of hypoxemia as a driver for impaired cognition in the mid-term., (© 2021. Fondazione Società Italiana di Neurologia.)- Published
- 2022
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40. Case of anterolateral migration of herniated cervical disc fragment mimicking a spinal meningioma.
- Author
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Vega-Moreno DA, González-Jiménez ME, Reyes-Rodríguez VA, Ibarra-de la Torre A, Santellán-Hernández JO, Betancourt-Quiroz C, López-Valdés JC, Moral-Naranjo AA, and García-González U
- Abstract
Background: Before the introduction of high-resolution MR, few disc fragments were misdiagnosed as meningiomas., Case Description: A 63-year-old female presented with a 6-month history of mild to moderate pain in the left arm, weakness 4/5 in the left arm C5-C6 distribution, and a loss of the left biceps reflex response. Although the MR study was read as showing a C5-C6 level probable spinal meningioma, this proved to be a sequestrated disc fragment at surgery., Conclusion: Rarely, cervical disc herniations may be misdiagnosed on MR studies as spinal meningiomas., Competing Interests: There are no conflicts of interest., (Copyright: © 2021 Surgical Neurology International.)
- Published
- 2021
- Full Text
- View/download PDF
41. Potential Tamoxifen Repurposing to Combat Infections by Multidrug-Resistant Gram-Negative Bacilli.
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Miró-Canturri A, Ayerbe-Algaba R, Del Toro R, Mejías ME, Pachón J, and Smani Y
- Abstract
The development of new strategic therapies for multidrug-resistant bacteria, like the use of non-antimicrobial approaches and/or drugs repurposed to be used as monotherapies or in combination with clinically relevant antibiotics, has become urgent. A therapeutic alternative for infections by multidrug-resistant Gram-negative bacilli (MDR-GNB) is immune system modulation to improve the infection clearance. We showed that immunocompetent mice pretreated with tamoxifen at 80 mg/kg/d for three days and infected with Acinetobacter baumannii , Pseudomonas aeruginosa , or Escherichia coli in peritoneal sepsis models showed reduced release of the monocyte chemotactic protein-1 (MCP-1) and its signaling pathway interleukin-18 (IL-18), and phosphorylated extracellular signal-regulated kinase 1/2 (ERK1/2). This reduction of MCP-1 induced the reduction of migration of inflammatory monocytes and neutrophils from the bone marrow to the blood. Indeed, pretreatment with tamoxifen in murine peritoneal sepsis models reduced the bacterial load in tissues and blood, and increased mice survival from 0% to 60-100%. Together, these data show that tamoxifen presents therapeutic efficacy against MDR A. baumannii , P. aeruginosa , and E. coli in experimental models of infection and may be a new candidate to be repurposed as a treatment for GNB infections.
- Published
- 2021
- Full Text
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42. School and Community Involvement of Adolescents With Chronic Health Conditions.
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Noonan K, Reichman NE, Corman H, and Jiménez ME
- Subjects
- Adolescent, Cohort Studies, Community Participation, Humans, Students, Schools, Sports
- Abstract
Purpose: To investigate associations between chronic health conditions and participation in school and community activities at age 15 years., Methods: Secondary analysis of data from an urban U.S. birth cohort study was conducted to investigate associations between chronic health conditions and participation in specific types of school and community activities. Logistic regression was used to adjust for potentially confounding factors., Results: Over one third of the teens had a chronic health condition. Having a chronic developmental or behavioral health condition (vs. no chronic developmental or behavioral health condition) was associated with lower odds of participation in sports (odds ratio [OR], .714; 95% confidence interval [CI], .577-.883), volunteer activities (OR, .751; 95% CI, 0.611-.924), and any activities (OR, .690; 95% CI, .516-.921), after adjusting for potential confounders. The associations for having a chronic physical health condition were less consistent., Conclusions: Chronic developmental or behavioral conditions of teens are negatively associated with school and community participation, particularly sports and volunteering, both of which can substantially enhance their development. Schools can play a role in promoting participation by offering activities designed for students with disabilities that may also include typical students or by referring families to such activities in the community. Clinicians can play a role by educating families about the benefits of extracurricular activities, providing information about laws and regulations requiring schools and other organizations to provide accommodations, and linking families to activities and programs in their community., (Copyright © 2020 Society for Adolescent Health and Medicine. Published by Elsevier Inc. All rights reserved.)
- Published
- 2020
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43. Dam implications on salt-water intrusion and land use within a tropical estuarine environment of the Gulf of Mexico.
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Alcérreca-Huerta JC, Callejas-Jiménez ME, Carrillo L, and Castillo MM
- Abstract
Estuaries are highly productive ecosystems, defined by salt-freshwater exchanges that are significantly altered by changes upstream and in adjacent coastal areas. Tropical estuaries are characterized by the periodic advance and retreat of saline intrusion, depending on seasonality, episodic river flows and flooding events. Salt-water intrusion due to the estuarine dynamics might be affected by dam systems, which could modify the hydrological regime of the estuary in relation to other stressors, such as land use changes. For this purpose, field measurements of salinity, temperature, river-discharge and flow velocities were conducted over a year to analyze the current hydrological regime in the upper estuary of the Grijalva River in the southern Gulf of Mexico, part of the Biosphere Reserve "Pantanos de Centla", one of the most biodiverse areas in the world. Analysis of land use and vegetation cover was performed. Historical implications of the hydrological performance of the four-dam system (1957 to 2014) are presented, together with the upstream-induced changes (i.e. discharge and seasonal water volumes variations): before, between and after the full operation of the dam system. A general loss of seasonality in the river discharge was identified (1974-1987), when critical mean annual water discharges were registered (Q
mean from 263.56 to 126.49 m3 /s). Chronological changes in the estuary and in the surrounding area due to the introduction of large extensions of cultivated grassland (~1020 km2 ), reduction in mangrove cover (~223 km2 ) and tular (~1340 km2 ) were noticed. These modifications mostly occurred before conservation strategies were implemented, such as the designation of the Biosphere Reserve (1992). This study contributes to a better understanding of the response of estuarine systems to anthropic perturbations and the development of long-term management plans that could take into account climate change and the increase of hydropower development., (Copyright © 2018 Elsevier B.V. All rights reserved.)- Published
- 2019
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44. Infant Health and Future Childhood Adversity.
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Reichman NE, Corman H, Noonan K, and Jiménez ME
- Subjects
- Caregivers, Child Health, Child of Impaired Parents psychology, Child, Preschool, Disabled Persons, Female, Humans, Male, Socioeconomic Factors, Substance-Related Disorders epidemiology, Substance-Related Disorders psychology, United States epidemiology, Adverse Childhood Experiences, Child Abuse psychology, Child of Impaired Parents statistics & numerical data, Divorce statistics & numerical data, Domestic Violence statistics & numerical data, Exposure to Violence statistics & numerical data, Family Characteristics, Infant Health
- Abstract
Objective To investigate the extent to which disabling infant health conditions are associated with adverse childhood experiences at age 5. Methods We conducted a secondary analysis of data from the Fragile Families and Child Wellbeing Study, a national urban birth cohort. We estimated logistic regression models of associations between the presence of a disabling infant health condition and the child's ACE exposures at age 5, controlling for factors that preceded the child's birth, including the mother's sociodemographic characteristics, physical health, mental illness, and substance abuse and the parents' criminal justice system involvement and domestic violence or sexual abuse. ACEs included 4 categories of child maltreatment (physical, sexual, psychological abuse, neglect) and 5 categories of household dysfunction (father absence, substance use, mental illness, caregiver treated violently, incarceration). Results 3.3% of the children were characterized as having a disabling health condition that was likely present at birth. Logistic regression estimates indicate that having a disabling infant health condition was associated with 83% higher odds of the child experiencing 2 or more ACEs (AOR 1.83, CI 1.14-2.94) and 73% higher odds of the child experiencing 3 or more ACEs (AOR 1.73, CI 1.07-2.77) at age 5. Conclusions for Practice The finding of strong links between disabling infant health conditions and ACEs at age 5 suggests that child health and ACEs play intertwining and mutually reinforcing roles during the early lifecourse and highlights the critical importance of investing in systems that simultaneously promote optimal child development and address childhood adversity.
- Published
- 2018
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45. Depletion of Neutrophils Exacerbates the Early Inflammatory Immune Response in Lungs of Mice Infected with Paracoccidioides brasiliensis.
- Author
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Pino-Tamayo PA, Puerta-Arias JD, Lopera D, Urán-Jiménez ME, and González Á
- Subjects
- Animals, Antibodies, Monoclonal pharmacology, Chemokines metabolism, Cytokines metabolism, Inflammation immunology, Lung immunology, Lung microbiology, Lung Diseases immunology, Male, Mice, Mice, Inbred BALB C abnormalities, Neutrophils drug effects, Paracoccidioidomycosis immunology, Paracoccidioidomycosis metabolism, Inflammation metabolism, Lung metabolism, Lung Diseases metabolism, Neutrophils metabolism, Paracoccidioides immunology, Paracoccidioides pathogenicity
- Abstract
Neutrophils predominate during the acute phase of the Paracoccidioides brasiliensis infection. Herein, we determined the role of the neutrophil during the early stages of experimental pulmonary paracoccidioidomycosis using a monoclonal antibody (mAb) specific for neutrophils. Male BALB/c mice were inoculated intranasally with 1.5 × 10(6) or 2 × 10(6) P. brasiliensis yeast cells. The mAb was administered 24 h before infection, followed by doses every 48 h until mice were sacrificed. Survival time was evaluated and mice were sacrificed at 48 h and 96 h after inoculation to assess cellularity, fungal load, cytokine/chemokine levels, and histopathological analysis. Neutrophils from mAb-treated mice were efficiently depleted (99.04%). Eighty percent of the mice treated with the mAb and infected with 1.5 × 10(6) yeast cells died during the first two weeks after infection. When mice were treated and infected with 2 × 10(6) yeast cells, 100% of them succumbed by the first week after infection. During the acute inflammatory response significant increases in numbers of eosinophils, fungal load and levels of proinflammatory cytokines/chemokines were observed in the mAb-treated mice. We also confirmed that neutrophils are an important source of IFN-γ and IL-17. These results indicate that neutrophils are essential for protection as well as being important for regulating the early inflammatory immune response in experimental pulmonary paracoccidioidomycosis.
- Published
- 2016
- Full Text
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46. Estimation of Symmetric Channels for Discrete Cosine Transform Type-I Multicarrier Systems: A Compressed Sensing Approach.
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Domínguez-Jiménez ME, Luengo D, and Sansigre-Vidal G
- Abstract
The problem of channel estimation for multicarrier communications is addressed. We focus on systems employing the Discrete Cosine Transform Type-I (DCT1) even at both the transmitter and the receiver, presenting an algorithm which achieves an accurate estimation of symmetric channel filters using only a small number of training symbols. The solution is obtained by using either matrix inversion or compressed sensing algorithms. We provide the theoretical results which guarantee the validity of the proposed technique for the DCT1. Numerical simulations illustrate the good behaviour of the proposed algorithm.
- Published
- 2015
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47. [Conceptual proposal for an operational model of integrated care in public health services for children].
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Pérez Cuevas R, Nakamura López MÁ, Pascasio Martínez ZL, Mancilla Gallegos NV, Montesinos Álvarez ME, Rodríguez Ramos SL, Gómez Pérez JA, Pérez López MLÁ, and López Jiménez ME
- Published
- 2014
- Full Text
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48. [Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) in an imbalance patient].
- Author
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Benítez del Rosario JJ, Santandreu Jiménez ME, and Lousa Gayoso M
- Subjects
- Female, Humans, Middle Aged, Syndrome, Cerebellar Ataxia diagnosis, Postural Balance, Reflex, Abnormal, Sensation Disorders diagnosis, Vestibular Diseases diagnosis
- Published
- 2014
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49. [Chemical characterization and quantification of fructooligosaccharides, phenolic compounds and antiradical activity of Andean roots and tubers grown in Northwest of Argentina].
- Author
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Jiménez ME and Sammán N
- Subjects
- Argentina, Carbohydrates analysis, Carbohydrates chemistry, Dietary Fiber analysis, Food Analysis, Free Radical Scavengers analysis, Free Radical Scavengers chemistry, Oligosaccharides chemistry, Phenols chemistry, Reference Values, Nutritive Value, Oligosaccharides analysis, Phenols analysis, Plant Roots chemistry, Plant Tubers chemistry
- Abstract
There is great interest in consuming foods that can provide the nutrients for a good nutrition and other health beneficial compounds. The aim of this work was to determine the chemical composition of native foods of the Andean region and to quantify some functional com-ponents. Proximal composition, vitamin C, total phenolic compounds, antiradical activity (DPPH) in peel and pulp, dietary fiber soluble and insoluble, fructooligosaccharides (FOS), total and resistant starch (in tubers and raw roots, boiled and boiled and stored) of 6 varieties of Oca (Oxalis tuberosa), 4 clones of manioc (Manihot esculenta Crantz) and yacon (Smallanthus sonchifolius were determined. The results showed greater amount of bioactive compounds and antiradical activity in the skin of these products. The highest content was found in the oca peel. In all cases, the content of insoluble fiber was greater than the soluble. The manioc had higher total starch than Andean roots and tubers. The boiling process decreased the resistant starch content of ocas and maniocs, but when these are stored for 48 h at 5 ° C, the resistant starch content increased. The FOS content of the ocas was similar for all varieties (7%). The main component of yacon carbohydrates were FOS (8.89%). The maniocs did not contain FOS. It can be concluded that the roots and tubers studied, in addition to provide nutrients, contain functional compounds that confer additional helpful value for preventing no communicable diseases.
- Published
- 2014
50. Suppression of guanylyl cyclase (beta1 subunit) expression impairs neurite outgrowth and synapse maturation in cultured cerebellar granule cells.
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López-Jiménez ME, Bartolomé-Martín D, Sánchez-Prieto J, and Torres M
- Subjects
- Animals, Apoptosis, Cells, Cultured, Cerebellum enzymology, Fluorescent Dyes pharmacology, GAP-43 Protein metabolism, Gene Knockdown Techniques, Guanylate Cyclase genetics, Pyridinium Compounds pharmacology, Quaternary Ammonium Compounds pharmacology, RNA, Small Interfering metabolism, Rats, Receptors, Cytoplasmic and Nuclear genetics, Soluble Guanylyl Cyclase, Synapsins metabolism, Cerebellum cytology, Guanylate Cyclase metabolism, Neurites physiology, Receptors, Cytoplasmic and Nuclear metabolism, Synapses physiology
- Abstract
The increased expression of different soluble guanylyl cyclase (sGC) subunits during development is consistent with these proteins participating in the formation and establishment of interneuronal contacts. Functional sGC is generated by the dimerization of an alpha-subunit (sGCalpha1/2) with the beta1-subunit (sGCbeta1), and both depletion of the sGCbeta1 subunit and inhibiting sGC activity impair neurite outgrowth. Similarly, impairing sGC activity diminishes the amount of growth-associated protein (GAP-43) and synapsin I, two proteins that participate in axon elongation and synaptogenesis, suggesting a role for sGC in these processes. Indeed, fewer synapses form when sGC is inhibited, as witnessed by FM1-43 imaging and synapsin I immunostaining, and the majority of synapses that do form remain functionally immature. These findings highlight the importance of sGC in the regulation of neurite outgrowth and synapse formation, and in the functional maturation of cerebellar granule cells in vitro.
- Published
- 2009
- Full Text
- View/download PDF
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