35 results on '"Hassan, Mohammed H"'
Search Results
2. Macrophage Migration Inhibitory Factor and Gene Polymorphism (rs755622G>C) in Unstable Vitiligo Patients.
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Ibrahim, Hassan M., Hassan, Mohammed H., El-Taieb, Moustafa A., Nada, Essam, Abdel-Hamid, Soheir, Younis, Ali, Ali, Mahmoud, and Hegazy, Eisa M.
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MACROPHAGE migration inhibitory factor , *RESTRICTION fragment length polymorphisms , *GENETIC polymorphisms , *VITILIGO , *SINGLE nucleotide polymorphisms - Abstract
Vitiligo pathogenesis is related to the macrophage migration inhibitory factor (MIF) protein. This study aimed to assess the lesional MIF levels and gene polymorphisms (rs755622G>C) in patients with vitiligo. To assess the consequences of combining narrow-band ultraviolet B with oral minipulse prednisolone as opposed to a combination with oral methotrexate on MIF levels in vitiligo patients, 50 unstable vitiligo patients and 50 controls were randomly chosen for comparison. MIF levels in skin homogenates and MIF (rs755622G>C) single nucleotide polymorphisms were assessed using the ELISA and the polymerase chain reaction restriction fragment length polymorphism (RFLP-PCR) techniques. We found significantly higher lesional MIF levels, a higher frequency of both (GC) and (CC) genotypes, and a significantly more frequent mutant allele (C) in patients than in controls. In addition, there was a significantly lower frequency of the allele (C) among patients who exhibited moderate to marked therapeutic improvement than among those who showed minimal to mild improvement. In conclusion, tissue MIF and gene polymorphisms were associated with vitiligo. In addition, oral corticosteroids, narrow-band ultraviolet B, methotrexate-targeted tissue MIF, and gene polymorphisms can improve unstable vitiligo. [ABSTRACT FROM AUTHOR]
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- 2023
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3. Predicting the Severity of Alfalfa Root rot Disease Under Salinity Conditions.
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Arafat, Khaled Hussein, Hassan, Mohammed H. A., and Mahmoud, Omar H. H.
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ROOT rots , *SALINITY , *ALFALFA , *ELECTRIC conductivity - Abstract
Alfalfa roots are infected with several fungal pathogens under salinity conditions. The effect of two salts of NaCl and CaCO3 at three concentrations was studied in vitro. Mycelial growth and disease severity (DS%) were estimated to determine the relationship between (DS%) and water salinity. The highest effect on mycelial growth was detected at the electrical conductivity (ECW value) of 18.75 ds/m2 which ranged from 8.80 and 9.44% with NaCl and CaCO3, respectively. Furthermore, Exserohilum sp. was the most affected by water salinity. With the different levels of water salinity, the DS% of alfalfa root rot increased gradually with the increased water salinity level. The highest level of water salinity with NaCl and CaCO3 ECW value at 18.75 ds/m2 ranged (42.76 and 43.53% severity for NaCl) and (44.04 and 44.42% severity for CaCO3, respectively). Moreover, with water salinity NaCl and CaCO3, Fusarium sp. was the highest (DS%) with NaCl. Alfalfa root rot prediction model based on information gathered from the interaction of pathogen, water salinity, disease severity, and root and shoot length. It was found the relation between DS% with fungi, salt type, salt concentration, root and shoot length in the multiple regression model (r² =88.83%). [ABSTRACT FROM AUTHOR]
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- 2023
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4. Antitoxic Effects of Curcumin against Obesity-Induced Multi-Organs' Biochemical and Histopathological Abnormalities in an Animal Model.
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Hassan, Mohammed H., Awadalla, Eatemad A., Abd El-Kader, Abd El-Kader M., Seifeldin, Esraa A., Mahmoud, Marwa Ahmed, Muddathir, Abdel Rahim Mahmoud, and Abdelsadik, Ahmed
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OBESITY complications , *BLOOD sugar analysis , *REDUCING diets , *EXPERIMENTAL design , *TRIGLYCERIDES , *BIOMARKERS , *ANIMAL experimentation , *CURCUMIN , *ANTIOXIDANTS , *APOPTOSIS , *RATS , *INSULIN , *OXIDATIVE stress , *CELLULAR signal transduction , *POLYMERASE chain reaction , *INFLAMMATORY mediators , *ANTITOXINS , *ANTIOBESITY agents , *ANIMALS , *PHARMACODYNAMICS - Abstract
Background. Obesity is a significant public health problem that is characterized by an increase in oxidative stress and enhanced inflammatory responses associated with immune cell invasion of adipose tissues. This study assessed several biochemical abnormalities, apoptosis, oxidative stress status, and associated histological changes in the liver, duodenum, and heart brought on by high-fat diet-induced obesity in rats. It also assessed the mechanistic benefits of curcumin in reversing these inflammatory, metabolic, and histological impairments. Methods. Rats were assigned into three groups each including ten rats: the control group (CD), the high-fat diet group (HFD), and the high-fat diet + curcumin (HFDC) group. Serum glucose, insulin, and triglycerides (TAGs) were observed. In addition, apoptosis (indicated by hepatic DNA fragmentation) and oxidative stress status (indicated by hepatic MPO, GSH, and SOD) were assessed. Histopathological examinations included the GIT (liver and duodenum) and heart in addition to quantitative real-time polymerase chain reaction (qRT-PCR) assays of the adipose tissue genetic expressions for inflammatory signaling pathways (TLR4, IL-6, and TNF-α). Results. The overall findings showed that the HFD group exhibited significantly higher levels of glucose, TAGs, and insulin than the control group (P < 0.01). The histological abnormalities of the studied organs in the HFD group were paralleled by these biochemical abnormalities, which were strongly associated with increased apoptosis, increased oxidative stress, and increased expression of the inflammatory signaling markers. There were significant improvements in the HFDC group in terms of biochemical, inflammatory, and histological investigations. Conclusions. This study's findings concluded that obesity is significantly associated with biochemical and microscopic alterations in many organs. Curcumin exerted potent antitoxic, antioxidant, tissue-protective, and antiobesity effects. Curcumin is recommended to be added to various dietary regimens to prevent or delay the organs' dysfunction among obese people. [ABSTRACT FROM AUTHOR]
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- 2022
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5. KIM-1 and GADDI-153 gene expression in paracetamol-induced acute kidney injury: effects of N-acetylcysteine, N-acetylmethionine, and N-acetylglucosamine.
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Mohamed, Nahed A., Hassan, Mohammed H., Saleem, Tahia H., Mohamed, Sotohy A., El-Zeftawy, Marwa, Ahmed, Eman A., Mostafa, Nashwa A. M., Hetta, Helal F., Hasan, Al Shaimaa, and Abdallah, Ahmed Alamir Mahmoud
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- 2022
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6. Vitamin D Receptor Gene Polymorphisms and Risk of Knee Osteoarthritis: Possible Correlations with TNF-α, Macrophage Migration Inhibitory Factor, and 25-Hydroxycholecalciferol Status.
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Hassan, Mohammed H., Elsadek, Amer Alkot Mostafa, Mahmoud, Marwa Ahmed, and Elsadek, Bakheet E. M.
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MACROPHAGE migration inhibitory factor , *VITAMIN D receptors , *KNEE , *TUMOR necrosis factors , *KNEE osteoarthritis , *CALCIFEDIOL , *GENETIC polymorphisms - Abstract
Osteoarthritis (OA) etiology and pathogenesis not yet fully understood. We studied the role of vitamin D receptor single-nucleotide polymorphisms (VDR-SNPs), vitamin D3, serum and synovial macrophage migration inhibitory factor (MIF), and tumor necrosis factor-α (TNF-α) in the development and progression of knee OA (KOA). This study included 205 Egyptian subjects (105 patients with KOA and 100 unrelated, healthy matched subjects selected as controls). The patient group was divided into three groups according to KOA severity (mild, moderate, and severe), with 35 patients in each group. The polymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) technique was used for the ApaI and TaqI SNPs. Vitamin D, serum and synovial TNF-α, and MIF assays were performed using ELISA kits. There were significantly lower serum levels of 25-hydroxycholecalciferol with significant increasing TNF-α and MIF levels in relation to disease severity among the cases (all: p˂0.05).Wild homozygous and heterozygous mutant genotypes (GG+GT) and G allele of ApaI demonstrated risk for KOA development, with odds ratio OR = 6.313 (95% confidence interval (CI) 2.074–19.210) and OR = 1.532 (95%CI 1.013–2.317), respectively. Homozygous mutant CC genotype and C allele of TaqI could be considered a risk factor associated with KOA development, with OR = 2.667 (95%CI 1.270–5.601) and OR = 0.737 (95%CI 0.496–1.095), respectively. VDR-SNPs, vitamin D3, TNF-α, and MIF could play an essential role in the pathogenesis and progression of KOA with mechanistic associations. [ABSTRACT FROM AUTHOR]
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- 2022
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7. NLRP3 inflammasome pathway involved in the pathogenesis of metabolic associated fatty liver disease.
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Osman, Heba Ahmed, Abuhamdah, Sawsan M. A., Hassan, Mohammed H., Hashim, Abdelkader Ahmed, Ahmed, Abdelazeem E., Elsayed, Sameh Salaheldin, El-Sawy, Samer A., Gaber, Mostafa A., and Abdelhady, Marwa
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FATTY liver , *NLRP3 protein , *HEPATIC fibrosis , *INFLAMMASOMES , *PYRIN (Protein) , *INTERLEUKIN receptors - Abstract
The prevalence of Metabolic-associated fatty liver disease (MAFLD) has been steadily increasing worldwide, paralleling the global epidemic of obesity and diabetes. It is estimated that approximately one-quarter of the global population is affected by MAFLD. Despite its high prevalence, MAFLD often goes undiagnosed due to the lack of specific symptoms in its early stages. However, as the disease progresses, it can lead to more severe liver-related complications such as fibrosis, cirrhosis, and hepatocellular carcinoma. Therefore, we aimed to investigate the expression levels of the nucleotide-binding oligomerization domain, leucine-rich repeat (LRR)—containing proteins (NLR) family pyrin domain-containing protein 3 [NLRP3] inflammasome pathway components, NLRP3 and interleukin 1β (IL-1β) genes in patients with MAFLD with various degrees of steatosis and fibrosis. Participants were classified into two equal groups; MAFLD group: consisted of 120 patients with different degrees of hepatic fibrosis and steatosis based on fibro scan results. The non-MAFLD group was comprised of 107 participants. Molecular analysis of pyrin domain-containing protein 3 and IL-1β relative gene expressions was performed in the blood of all participants, using Real-time quantitative polymerase chain reaction (RT-qPCR). Patients with post-MAFLD hepatic fibrosis had significantly higher relative gene expression levels of IL-1β and NLRP3; with IL-1β > 1.1 had AUC of 0.919, sensitivity of 88.33, specificity of 96.26, PPV of 96.4, and NPV of 88 and 92.3 accuracy (p value < 0.001). NLRP3 > 1.33 had a sensitivity of 97.5, specificity of 99.07, PPV of 99.2, NPV of 97.2, and 98.3 accuracy with an AUC of 0.991 (p value < 0.001) as predictors of post-MAFLD hepatic fibrosis.. A significant increase in the mean relative gene expression levels of both IL-1β and NLRP3 found in patients with early fibrosis (F0-F1-2); 31.97 ± 11.8 and 6.76 ± 2.18, respectively; compared with patients with advanced hepatic fibrosis stages (F2-F3); 2.62 ± 3.71 and 4.27 ± 2.99 (p < 0.001 each). The present study provides novel evidence for the possible involvement of IL-1β and NLRP3 inflammasome in metabolic-associated fatty liver disease pathogenesis and could be valid markers for the early detection of post-MAFLD hepatic fibrosis. [ABSTRACT FROM AUTHOR]
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- 2024
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8. Combined metformin and insulin therapy improves neurocognitive dysfunction in type 2 diabetic rat model via anti-inflammatory and antioxidant mechanisms.
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Salem, Heba Rady, Hanna, Gergess S., Hassan, Mohammed H., El-kotb, Safaa, Rashad, Samar, Yassien, Rania Ibrahim, Selim, Mahmoud, and Amer, Ghada Samir
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LABORATORY rats , *NF-kappa B , *OXIDANT status , *TYPE 2 diabetes , *GLYCEMIC control , *INSULIN - Abstract
Introduction: Improper glycemic control is associated with diabetic cognitive dysfunction. Several studies have confirmed the neuroprotective effects of metformin and insulin. This study aimed to investigate the effects of metformin and/or insulin therapy on neurocognitive functions in a type 2 diabetes mellitus (T2DM) rat model. Methods: Fifty adult male Wistar rats were used in this study and had free access to water and a normal chow diet. After an acclimatization period, 10 rats were kept on a normal chow diet and considered as the control group. T2DM was induced in the other 40 rats by a high-fat diet and low-dose streptozotocin method. Then, diabetic rats were randomly allocated into 4 equal groups: Non-treated diabetic group; Metformin-treated diabetic group (treated with metformin 250 mg/kg/day for 6 weeks); Insulin-treated diabetic group (treated with NPH insulin 40 U/kg for 6 weeks); and Metformin and insulin-treated diabetic group. Neurocognitive functions were assessed by footprint assay, Y-maze, open field test, and Morris water maze. Glycaemic profile, serum levels of amyloid A, interleukin-18, and nuclear factor-kappa B were analyzed. Brain malondialdehyde and total antioxidant capacity were measured. A histopathological examination of the frontal lobe was performed. Results: Treatment with metformin and/or insulin significantly improved the impaired neurocognitive dysfunction, brain oxidative stress, changes in biochemical parameters, and the associated histopathological changes in the frontal cortex of diabetic rats. The combined therapy showed a better effect than either monotherapy alone. Conclusion: Metformin and insulin therapy may be valuable for the prevention of neurocognitive dysfunction in T2DM. [ABSTRACT FROM AUTHOR]
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- 2024
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9. Plexin B2 tissue expression and related gene polymorphisms in psoriasis and their relation to NB-UVB and Acitretin therapy.
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Hegazy, Eisa Mohamed, Taieb, Moustafa A. El, Hassan, Mohammed H., Ibrahim, Ahmed K., El-Din, Ebtehal A., and Ibrahim, Hassan M.
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Psoriasis is a chronic, immune-mediated, hyperproliferative skin disease. Etiopathogenesis of psoriasis is not well understood. Plexin B2 was found to have effects on CD100-mediated T-cell morphology and expressed in the immune system. It may play a role in the pathogenesis of psoriasis. To assess the tissue level of plexin-B2 and plexin B2 related gene polymorphism which is signal regulatory protein gamma (SIRPγ-rs71212732) in psoriatic patients before and after NB-UVB, acitretin therapy alone or in combination and to detect correlation between level of tissue plexin B2 and disease severity and improvement. This single blinded randomized controlled trial was carried on 50 psoriatic patients and 50 healthy controls. Psoriasis Area and Severity Index score (PASI) was used to evaluate the disease severity. Tissue plexin-b2 level was measured using ELISA and SIRPγ-rs71212732 (T\C) was assessed using TaqMan™ assays and real-time PCR. A significant lower tissue plexin-B2 level was observed in control group (2.9 ± 0.6 pg/g) than cases (25.8 ± 2.8, pg/g) (p < 0.001). Also, a significantly higher tissue plexin-B2 level was observed in sever psoriasis (32.7 ± 3.8 pg/ml) in than moderate psoriasis (13.6 ± 2.1 pg/ml, p = 0.001). Tissue plexin B2 was positively correlated with diseases severity. Significantly higher (TC& TT) genotypes and mutant (C) allele among patients compared to the controls, p < 0.001 for all. Tissue plexin-b2 level was high in psoriasis vulgaris with positive correlation with disease severity and decreased after treatment. This may indicate a role of plexin-b2 in psoriasis vulgaris pathogenesis. [ABSTRACT FROM AUTHOR]
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- 2024
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10. Circulating and local nuclear expression of survivin and fibulin-3 genes in discriminating benign from malignant respiratory diseases: correlation analysis.
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Hassan, Mohammed H., Abuhamdah, Sawsan, Abdel-Bary, Mohamed, Wahman, Mohammed, Abd-Elhamid, Tarek Hamdy, Beshay, Morris, Mosallam, Karam, and Elsadek, Bakheet E. M.
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RESPIRATORY diseases , *GENES , *STATISTICAL correlation , *WESTERN immunoblotting , *LUNG diseases - Abstract
Survivin is an inhibitor of apoptosis as well as a promoter of cell proliferation. Fibulin-3 is a matrix glycoprotein that displays potential for tumor suppression or propagation. The present study aimed to validate the expression levels of survivin and fibulin-3 in benign and malignant respiratory diseases. This case-control study included 219 patients categorized into five groups. Group A included 63 patients with lung cancer, group B included 63 patients with various benign lung diseases, group D included 45 patients with malignant pleural mesothelioma (MPM), and group E included 48 patients with various benign pleural diseases. Group C included 60 healthy individuals (control group). Serum survivin and fibulin-3 levels were measured by ELISA, whereas their nuclear expressions in the lung and pleura were assessed via Western blot analysis. The results showed significantly higher survivin serum levels and significantly lower fibulin-3 levels in group A compared with in group B and controls (P<0.001). There were significantly higher serum levels of survivin and fibulin-3 in group D compared with in group E and controls (P<0.001), consistent with observed nuclear survivin and fibulin-3 expression levels. Fibulin-3 was determined to have higher value than survivin in discriminating lung cancer from MPM (P<0.05). Survivin and fibulin-3 could be useful diagnostic markers for lung and pleural cancers, and fibulin-3 expression was particularly useful in differentiating lung cancer from MPM. [ABSTRACT FROM AUTHOR]
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- 2021
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11. 25-Hydroxy cholecalciferol, anti-Müllerian hormone, and thyroid profiles among infertile men.
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Hassan, Mohammed H., Ibrahim, Hassan M., and El-Taieb, Moustafa A.
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ANTI-Mullerian hormone , *MALE infertility , *CHOLECALCIFEROL , *THYROID gland - Abstract
Background and Aim: We examined the relationship among vit.D3, AMH, FT3, FT4, and TSH, in addition to the serum levels of reproductive hormones (FSH, LH, prolactin, and free testosterone), in oligoasthenoteratozoospermia and azoospermia patients in a cohort of infertile men from Egypt to establish a clinical marker/cause-effect relationship.Methods: This cross-sectional cohort study was carried out on 301 men (105 males with oligoasthenoteratozoospermia and 96 males with azoospermia), in addition to 100 controls. Measurements of serum vit.D3, AMH, FT3, FT4, and TSH levels, in addition to reproductive hormone assays, were performed on all included subjects, using ELISA kits.Results: Overall, results showed significantly lower serum levels of vit.D3 in infertile men than in the controls, with a greater decrease observed in men with azoospermia than in oligoasthenoteratozoospermia patients, (p < .05 for all). Significantly higher serum TSH and FSH levels and significantly lower serum free testosterone levels were observed in males with azoospermia than in males with oligoasthenoteratozoospermia and the controls (p < .05 for both). There were no significant differences between the studied groups in terms of AMH, FT3 or FT4 levels. LH levels were negatively correlated with TSH levels and positively correlated with AMH levels among men with oligoasthenoteratozoospermia, while among men with azoospermia, LH levels were positively correlated with vit.D3 levels (p < .05 for all).Conclusion: Decreased Vit.D3 could play a role in male infertility, in addition to abnormal thyroid function, which needs further investigation. [ABSTRACT FROM AUTHOR]- Published
- 2020
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12. Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years.
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Sadek, Abdelrahim A, Hassan, Mohammed H, and Mohammed, Nesreen A
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NEUROPSYCHOLOGICAL tests , *NEUROPSYCHOLOGY , *PHENYLKETONURIA , *CHILD psychiatry , *INTELLIGENCE levels , *AUTISM , *ELECTROENCEPHALOGRAPHY - Abstract
Background: Phenylketonuria (PKU) is considered to be a rare inborn error of metabolism but one of the commonest causes of mental retardation if untreated.Objectives: The present study was done to characterize the clinical patterns of PKU and analyze various neuropsychiatric outcomes in PKU children in Sohag Province, Egypt.Patients and methods: A prospective cohort study was conducted on 113 PKU patients, diagnosed during the period from 2012 to 2017, at the Pediatric Neurology Clinic of Sohag University Hospital, Upper Egypt. One hundred and ten cases were diagnosed based on clinical suspicion combined with laboratory confirmation by measuring their plasma phenylalanine levels using amino acid analyzer, while 3 cases were detected during neonatal screening. With the exception of the 3 cases detected during neonatal screening, all patients were clinically diagnosed and treated late. Psychometric evaluations of PKU patients were done using intelligence quotient (IQ, Stanford–Binet V), Childhood Autism Rating Scale, and Children's Attention and Adjustment Survey. Dietetic management was applied. The results of neuroimaging (computed tomography or magnetic resonance imaging of the brain) and electroencephalography were included when available.Results: The overall results showed that 15.9% had hyperphenylalaninemia, 35.4% had mild to moderate PKU, and classic PKU was diagnosed in 48.7%. Global developmental delay (54.9%) and delayed language (29.2%) were the most frequent presentations. Moderately impaired or delayed overall IQ was present in 77%. While, 83.2% had moderately impaired or delayed verbal IQ, autism was diagnosed in 50.4%. Super average and average probability of attention-deficit hyperactivity disorder was diagnosed in 88.5%. Abnormal neuroimaging (white matter abnormalities and brain atrophy) was the most important significant predictor for poor language and motor developmental outcome (P<0.05).Conclusion: PKU children had variable neuropsychological outcomes, mainly attention-deficit hyperactivity disorder and impaired verbal IQ, both of which were not related to the initial phenylalanine levels or to duration of dietary therapy, but were significantly related to early dietary intervention. [ABSTRACT FROM AUTHOR]
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- 2018
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13. Myocardial injury induced by scorpion sting envenoming and evidence of oxidative stress in Egyptian children.
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Ahmed, Ahmed El-Abd, Hassan, Mohammed H., Rashwan, Nagwan I., Sayed, Mohammed M., and Meki, Abdel-Raheim M.A.
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MYOCARDIAL infarction , *SCORPION venom , *TROPONIN , *OXIDATIVE stress , *CHILDREN - Abstract
Abstract In the present study, 45 children in Upper Egypt (less than 16 years old) were admitted to the Pediatric Intensive Care Unit for scorpion envenomation (SE). They were compared with 30 apparently healthy children of matching age and sex as controls. Out of the studied victims, 35 children (78%) showed signs of severe envenomation, while 10 victims (22%) showed signs of mild envenomation. The case fatality was 33%. The serum levels of cardiac markers, cardiac troponin T (cTnT) and I (cTnI), as well as the enzymatic activities of creatine kinase-MB (CPK-MB) and lactate dehydrogenase (LDH) were determined for both victims and controls. In addition, the serum levels of oxidative stress markers, nitric oxide (NO), malondialdehyde (MDA), superoxide dismutase (SOD), reduced glutathione (GSH) and zinc (Zn) were measured. Electrocardiography and echocardiography were done. All the envenomed victims showed significantly higher mean values of cTnT, cTnI, CPK-MB and LDH than control group. These cardiac markers were elevated in severe cases and in non survivors in comparison with mild cases and survivors respectively. Furthermore, the serum levels of NO and MDA were significantly higher while the serum levels of SOD, GSH and Zn were significantly lower in all envenomed victims than the controls (p < 0.05 for all). There were no significant differences in the serum levels of oxidative stress markers among severe and mild cases or between survivors and non survivors victims. There were no significant correlations between the serum levels of cardiac markers and the oxidative stress markers in envenomed victims. In conclusions, oxidative stress occurs in scorpion envenomed children, but does not determine prognosis. Cardiac markers, but not the oxidative stress, remain the most important determining factor for the severity and the outcome of SE. Highlights • Oxidative stress occurs in scorpion envenomed children. • Cardiac markers are essential determining factor for envenomation severity and the outcome. • Oxidative stress not correlated to cardiac markers in scorpion envenomed children. • Oxidative stress not related to the envenomation severity and the outcome. [ABSTRACT FROM AUTHOR]
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- 2018
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14. Validity of B-Type Natriuretic Peptide, Growth Differentiation Factor 15, and High-Sensitivity Troponin I Levels in Ischemic Heart Failure.
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Ismail II, Hossameldin M. and Hassan, Mohammed H.
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GROWTH differentiation factors , *TROPONIN I , *HEART failure , *BRAIN natriuretic factor , *PEPTIDES - Published
- 2022
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15. Biochemical assessments of thyroid profile, serum 25-hydroxycholecalciferol and cluster of differentiation 5 expression levels among children with autism.
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Desoky, Tarek, Hassan, Mohammed H., Fayed, Hanan M., and Sakhr, Hala M.
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CHILDHOOD Autism Rating Scale , *DIAGNOSIS of autism in children , *HYDROXYCHOLECALCIFEROLS , *THYROTROPIN , *GLYCOPROTEIN hormones - Abstract
Background: The exact pathogenesis of autism is still unknown. Both thyroid hormones and 25(OH)D are important for brain development, in addition to CD5; all have immunomodulatory actions by which their dysregulation may have a potential role in autism pathogenesis. Objectives: The objectives of this study were to assess the thyroid profile, serum 25(OH)D levels and CD5 expression levels among autistic patients and to find out the correlations between the measured biomarkers with each other on one side and with the disease severity on the other side. Patients and methods: This cross-sectional case-control study has been conducted on 60 children with autism and 40 controls, recruited from Qena Governorate, Upper Egypt. Childhood Autism Rating Scale (CARS) score was used to assess the included patients. Biochemical assays of thyroid function in the form of free triiodothyronine (FT3), free tetraiodothyronine (FT4), thyroid-stimulating hormone (TSH) and 25(OH)D were done using commercially available enzyme-linked immunosorbent assay (ELISA) kits, while CD5 expression levels were measured using flow cytometry (FCM) analysis for all the included patients and controls. Results: The overall measurement results show significant higher mean serum TSH levels, mean CD5 expression levels with significant lower mean serum 25(OH)D levels among autistic children when compared with the control group (p,0.05 for all). Significant negative correlations between CD5 with FT3, FT4 and 25(OH)D were observed. CARS score showed significant negative correlations with both FT3 and 25(OH)D, while it was positively correlated with CD5 in a significant manner (p,0.05 for all). Conclusion: Elevated CD5 expression and decreased 25(OH)D stores could play a potential role in the pathogenesis of autism via their immune-modulator actions. High TSH serum levels among autistic children, although within the physiological range, reflect the presence of thyroid dysfunction among such children, which needs further assessment. [ABSTRACT FROM AUTHOR]
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- 2017
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16. Dynamic Model of Linear Induction Motor Considering the End Effects.
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Hairik, Haroutuon A. and Hassan, Mohammed H.
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INDUCTION motors , *DYNAMO (Computer program language) , *MATHEMATICAL models , *ELECTROMAGNETIC fields , *MAGNETIZATION , *ELECTRIC circuits , *SPEED , *LOAD factor design , *SIMULATION methods & models - Abstract
In this paper the dynamic behavior of linear induction motor is described by a mathematical model taking into account the end effects and the core losses. The need for such a model rises due to the complexity of linear induction motors electromagnetic field theory. The end affects by introducing speed dependent scale factor to the magnetizing inductance and series resistance in the d-axis equivalent circuit. Simulation results are presented to show the validity of the model during both no-load and sudden load change intervals. This model can also be used directly in simulation researches for linear induction motor vector control drive systems. [ABSTRACT FROM AUTHOR]
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- 2009
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17. International treatment outcomes of neonates on extracorporeal membrane oxygenation (ECMO) with persistent pulmonary hypertension of the newborn (PPHN): a systematic review.
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Alhumaid, Saad, Alnaim, Abdulrahman A., Al Ghamdi, Mohammed A., Alahmari, Abdulaziz A., Alabdulqader, Muneera, Al HajjiMohammed, Sarah Mahmoud, Alalwan, Qasim M., Al Dossary, Nourah, Alghazal, Header A., Al Hassan, Mohammed H., Almaani, Khadeeja Mirza, Alhassan, Fatimah Hejji, Almuhanna, Mohammed S., Alshakhes, Aqeel S., BuMozah, Ahmed Salman, Al‑Alawi, Ahmed S., Almousa, Fawzi M., Alalawi, Hassan S., Al matared, Saleh Mana, and Alanazi, Farhan Abdullah
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PERSISTENT fetal circulation syndrome , *RESPIRATORY distress syndrome , *ETIOLOGY of diseases , *EXTRACORPOREAL membrane oxygenation , *PATENT ductus arteriosus , *MECONIUM aspiration syndrome - Abstract
Background: PPHN is a common cause of neonatal respiratory failure and is still a serious condition and associated with high mortality. Objectives: To compare the demographic variables, clinical characteristics, and treatment outcomes in neonates with PHHN who underwent ECMO and survived compared to neonates with PHHN who underwent ECMO and died. Methods: We adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guideline and searched ProQuest, Medline, Embase, PubMed, CINAHL, Wiley online library, Scopus and Nature for studies on the development of PPHN in neonates who underwent ECMO, published from January 1, 2010 to May 31, 2023, with English language restriction. Results: Of the 5689 papers that were identified, 134 articles were included in the systematic review. Studies involving 1814 neonates with PPHN who were placed on ECMO were analyzed (1218 survived and 594 died). Neonates in the PPHN group who died had lower proportion of normal spontaneous vaginal delivery (6.4% vs 1.8%; p value > 0.05) and lower Apgar scores at 1 min and 5 min [i.e., low Apgar score: 1.5% vs 0.5%, moderately abnormal Apgar score: 10.3% vs 1.2% and reassuring Apgar score: 4% vs 2.3%; p value = 0.039] compared to those who survived. Neonates who had PPHN and died had higher proportion of medical comorbidities such as omphalocele (0.7% vs 4.7%), systemic hypotension (1% vs 2.5%), infection with Herpes simplex virus (0.4% vs 2.2%) or Bordetella pertussis (0.7% vs 2%); p = 0.042. Neonates with PPHN in the death group were more likely to present due to congenital diaphragmatic hernia (25.5% vs 47.3%), neonatal respiratory distress syndrome (4.2% vs 13.5%), meconium aspiration syndrome (8% vs 12.1%), pneumonia (1.6% vs 8.4%), sepsis (1.5% vs 8.2%) and alveolar capillary dysplasia with misalignment of pulmonary veins (0.1% vs 4.4%); p = 0.019. Neonates with PPHN who died needed a longer median time of mechanical ventilation (15 days, IQR 10 to 27 vs. 10 days, IQR 7 to 28; p = 0.024) and ECMO use (9.2 days, IQR 3.9 to 13.5 vs. 6 days, IQR 3 to 12.5; p = 0.033), and a shorter median duration of hospital stay (23 days, IQR 12.5 to 46 vs. 58.5 days, IQR 28.2 to 60.7; p = 0.000) compared to the neonates with PPHN who survived. ECMO-related complications such as chylothorax (1% vs 2.7%), intracranial bleeding (1.2% vs 1.7%) and catheter-related infections (0% vs 0.3%) were more frequent in the group of neonates with PPHN who died (p = 0.031). Conclusion: ECMO in the neonates with PPHN who failed supportive cardiorespiratory care and conventional therapies has been successfully utilized with a neonatal survival rate of 67.1%. Mortality in neonates with PPHN who underwent ECMO was highest in cases born via the caesarean delivery mode or neonates who had lower Apgar scores at birth. Fatality rate in neonates with PPHN who underwent ECMO was the highest in patients with higher rate of specific medical comorbidities (omphalocele, systemic hypotension and infection with Herpes simplex virus or Bordetella pertussis) or cases who had PPHN due to higher rate of specific etiologies (congenital diaphragmatic hernia, neonatal respiratory distress syndrome and meconium aspiration syndrome). Neonates with PPHN who died may need a longer time of mechanical ventilation and ECMO use and a shorter duration of hospital stay; and may experience higher frequency of ECMO-related complications (chylothorax, intracranial bleeding and catheter-related infections) in comparison with the neonates with PPHN who survived. [ABSTRACT FROM AUTHOR]
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- 2024
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18. A Review on Microcellular Injection Moulding.
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Ding, Yifei, Hassan, Mohammed H., Bakker, Otto, Hinduja, Srichand, and Bártolo, Paulo
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INJECTION molding , *DISCONTINUOUS precipitation , *SUPERCRITICAL fluids , *SOFTWARE development tools , *MICROBUBBLES - Abstract
Microcellular injection moulding (MuCell®) is a polymer processing technology that uses a supercritical fluid inert gas, CO2 or N2, to produce light-weight products. Due to environmental pressures and the requirement of light-weight parts with good mechanical properties, this technology recently gained significant attention. However, poor surface appearance and limited mechanical properties still prevent the wide applications of this technique. This paper reviews the microcellular injection moulding process, main characteristics of the process, bubble nucleation and growth, and major recent developments in the field. Strategies to improve both the surface quality and mechanical properties are discussed in detail as well as the relationships between processing parameters, morphology, and surface and mechanical properties. Modelling approaches to simulate microcellular injection moulding and the mathematical models behind Moldex 3D and Moldflow, the two most commonly used software tools by industry and academia, are reviewed, and the main limitations are highlighted. Finally, future research perspectives to further develop this technology are also discussed. [ABSTRACT FROM AUTHOR]
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- 2021
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19. Clinical reappraisal of the composite international diagnostic interview version 3.3 in Qatar's National Mental Health Study.
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Khaled, Salma M., Amro, Iman, Abdelkader, Menatalla, Al Bahari, Dalia, Al Shawwaf, Mahmoud, Alabdulla, Majid, Alhassan, Ahmed, Ali, Amal, Aly, Sheeren, Amin, Asmaa, Chiu, Wai Tat, Currie, James, El Fakki, Hana, First, Michael B., Hassan, Mohammed H. O., Hijawi, Zainab, Mohammed, Rumaisa, Nofal, Marwa, Salman, Salma, and Sampson, Nancy A.
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MENTAL health surveys , *MENTAL health , *POST-traumatic stress disorder , *OBSESSIVE-compulsive disorder , *PANIC disorders - Abstract
Objectives: Lifetime DSM‐5 diagnoses generated by the lay‐administered Composite International Diagnostic Interview for DSM‐5 (CIDI) in the World Mental Health Qatar (WMHQ) study were compared to diagnoses based on blinded clinician‐administered reappraisal interviews. Methods: Telephone follow‐up interviews used the non‐patient edition of the Structured Clinician Interview for DSM‐5 (SCID) oversampling respondents who screened positive for five diagnoses in the CIDI: major depressive episode, mania/hypomania, panic disorder, generalized anxiety disorder, and obsessive‐compulsive disorder. Concordance was also examined for a diagnoses of post‐traumatic stress disorder based on a short‐form versus full version of the PTSD Checklist for DSM‐5 (PCL‐5). Results: Initial CIDI prevalence estimates differed significantly from the SCID for most diagnoses (χ12 ${\chi }_{1}^{2}$ = 6.6–31.4, p = 0.010 < 0.001), but recalibration reduced most of these differences and led to consistent increases in individual‐level concordance (AU‐ROC) from 0.53–0.76 to 0.67–0.81. Recalibration of the short‐form PCL‐5 removed an initially significant difference in PTSD prevalence with the full PCL‐5 (from χ12 ${\chi }_{1}^{2}$ = 610.5, p < 0.001 to χ12 ${\chi }_{1}^{2}$ = 2.5, p = 0.110) while also increasing AU‐ROC from 0.76 to 0.81. Conclusions: Recalibration resulted in valid diagnoses of common mental disorders in the Qatar National Mental Health Survey, but with inflated prevalence estimates for some disorders that need to be considered when interpreting results. [ABSTRACT FROM AUTHOR]
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- 2024
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20. Therapeutic efficacy of macrolides in management of patients with mild COVID-19.
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Rashad, Alaa, Nafady, Asmaa, Hassan, Mohammed H., Mansour, Haggagy, Taya, Usama, Bazeed, Shamardan Ezzeldin S., Aref, Zaki F., Sayed, Mennatallah Ali Abdelrhman, Nafady-Hego, Hanaa, and Abdelmaksoud, Aida A.
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MACROLIDE antibiotics , *COVID-19 treatment , *DRUG efficacy , *REVERSE transcriptase polymerase chain reaction , *CONTROL groups - Abstract
Evidence on the efficacy of adding macrolides (azithromycin or clarithromycin) to the treatment regimen for COVID-19 is limited. We testify whether adding azithromycin or clarithromycin to a standard of care regimen was superior to standard of supportive care alone in patients with mild COVID-19.This randomized trial included three groups of patients with COVID-19. The azithromycin group included, 107 patients who received azithromycin 500 mg/24 h for 7 days, the clarithromycin group included 99 patients who received clarithromycin 500 /12 h for 7 days, and the control group included 99 patients who received standard care only. All three groups received only symptomatic treatment for control of fever and cough.Clinical and biochemical evaluations of the study participants including assessment of the symptoms duration, real-time reverse transcription-polymerase chain reaction (rRT-PCR), C-reactive protein (CRP), serum ferritin, D-dimer, complete blood count (CBC), in addition to non-contrast chest computed tomography (CT), were performed. The overall results revealed significant early improvement of symptoms (fever, dyspnea and cough) in patients treated with either azithromycin or clarithromycin compared to control group, also there was significant early conversion of SARS-CoV-2 PCR to negative in patients treated with either azithromycin or clarithromycin compared to control group (p < 0.05 for all).There was no significant difference in time to improvement of fever, cough, dyspnea, anosmia, gastrointestinal tract "GIT" symptoms and time to PCR negative conversion between patients treated with azithromycin compared to patients treated with clarithromycin (p > 0.05 for all). Follow up chest CT done after 2 weeks of start of treatment showed significant improvement in patients treated with either azithromycin or clarithromycin compared to control group (p < 0.05 for all).Adding Clarithromycin or azithromycin to the therapeutic protocols for COVID-19 could be beneficial for early control of fever and early PCR negative conversion in Mild COVID-19. Trial registration: (NCT04622891) www.ClinicalTrials.gov retrospectively registered (November 10, 2020). [ABSTRACT FROM AUTHOR]
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- 2021
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21. Could Grapefruit Ameliorate the Oxidative Stress, Biochemical and Histopathological Alterations Induced by Prolonged Metronidazole Therapy in the Liver and Kidney of Male Rats?
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FOUAD, SAMER S., AWADALLA, EATEMAD A., HASSAN, MOHAMMED H., FAHMY, MAHA ABDELBAKY AHMED, ABDEL-KAHAAR, EMAAD, and ALI, RANA A.
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METRONIDAZOLE , *OXIDATIVE stress , *ANTIOXIDANTS , *HISTOPATHOLOGY , *COLORIMETRY - Abstract
We aimed to compare antioxidant versus interaction properties of grapefruit (GP) in reversal of prolonged metronidazole (MTZ)- induced hepatic and renal alterations at both biochemical and histopathological levels. A total 60 male albino Wister rats were included and were divided randomly into 4 groups (n=15 each). The first group (control) received 1% DMSO, the second group (GP) received grapefruit juice, the third group (MTZ) received MTZ and the last group (MTZ+ GP) received MTZ combined with grapefruit juice for 60 days. Biochemical analysis of serum liver enzymes (ALP, AST and ALT), urea and creatinine using colorimetric methods were performed. For both colorimetric assays of oxidative stress markers and for histopathological analyses, tissue samples including the liver and kidneys were used. Significantly higher serum liver enzymes in MTZ group and MTZ+GP groups compared to control and GP groups with higher levels in MTZ+GP, p0.05.Significantly higher serum levels of urea and creatinine among MTZ+GP group compared to other groups. Significantly higher oxidative stress index of liver and kidney tissue homogenates in both MTZ group and MTZ+GP groups compared to control and GP groups with higher levels in MTZ+GP, with significantly lower values in GP group compared to other groups, p0.05. Regressive histological changes in the liver and kidneys of MTZ have shown these effects and more significant in MTZ+GP group, with histological similarities between control and GP groups. Although GP has potent antioxidant effect but its interaction properties deteriorate MTZ- induced adverse liver and kidney changes at both biochemical and histological levels. [ABSTRACT FROM AUTHOR]
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- 2021
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22. The deleterious effects of sofosbuvir and ribavirin (antiviral drugs against hepatitis C virus) on different body systems in male albino rats regarding reproductive, hematological, biochemical, hepatic, and renal profiles and histopathological changes.
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Ali, Rana A., Awadalla, Eatemad A., Amin, Yahia A., Fouad, Samer S., Ahmed, Maha Abd-El Baki, Hassan, Mohammed H., Abdel-Kahaar, Emaad, and Abdel-Aziz, Rehab H.
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RIBAVIRIN , *HEPATITIS C virus , *ANTIVIRAL agents , *CHRONIC hepatitis C , *NEUTROPHILS , *IRON deficiency anemia , *SEMEN , *HISTOPATHOLOGY ,SOFOSBUVIR - Abstract
Sofosbuvir is one of the crucial drugs used in the treatment of chronic hepatitis C virus (HCV) in adults and children with compensated liver disease, including cirrhosis. It may be used alone or with other drugs. Ribavirin is an antiviral medication used to treat HCV infection. It is not effective when used alone and must be used in combination with other medications, such as sofosbuvir. This study pertains to a comprehensive assessment of the deleterious effects of sofosbuvir (an antiviral drug against chronic HCV) or sofosbuvir combined with ribavirin (an antiviral drug against RNA and DNA viruses) on several biological activities of the body, including hematological, hormonal, biochemical, histological, and immunohistochemical examinations during a long-standing period on male healthy rats. In addition, fertility assessments were performed, including sperm collections and semen parameter investigations. This study was conducted on 21 male rats divided into three equal groups. Group I (control group) received distilled water; group II (sofosbuvir group) received sofosbuvir (4 mg/kg); and group III (sofosbuvir + ribavirin) received sofosbuvir (4 mg/kg) plus ribavirin (30 ml/kg). All groups received the specific drug for six months. Blood and tissue samples were collected for hematological, hormonal, biochemical, histological, and immunohistochemical examinations. In addition, sperm collection and assessments of semen parameters were performed. Results revealed that sofosbuvir causes a highly significant decrease in the mean of most hematological, immunological, hormonal, and biochemical parameters, except for a few numbers of parameters such as neutrophils, monocytes, basophils, cortisol, GOT, and lipase, which exhibit a significant increase. The same occurred in the sofosbuvir + ribavirin group, but at much higher levels, as most hematological, immunological, hormonal, and biochemical parameters exhibit a highly significant decrease except for monocytes, triglyceride, and lipase, which exhibit a significant increase. When compared to the sofosbuvir group alone, the sofosbuvir + ribavirin group demonstrated a highly significant decline in the mean of most hematological, immunological, hormonal, and biochemical parameters except lymphocytes and triglycerides, which exhibit a substantial increase. For the reproductive parameters, both groups exhibit a significant decrease in the total sperm motility percentage. Finally, it can be concluded that sofosbuvir causes acute pancreatitis and combined immunodeficiency. Ribavirin is associated with hormonal deficiency, which indicates the occurrence of hypopituitarism. Moreover, sofosbuvir and ribavirin synergistically affect myelosuppression and cause iron-deficiency anemia. However, sofosbuvir, or its combination with ribavirin, is associated with a reduced risk of hepatocellular carcinoma. Besides, adding ribavirin to be combined with sofosbuvir improved the immunodeficiency caused by sofosbuvir; this confirms that using ribavirin with sofosbuvir reduces the side effects of both alone. [ABSTRACT FROM AUTHOR]
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- 2024
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23. Metabolic profile of oxidative stress and trace elements in febrile seizures among children.
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El-Masry, Hosny M. A., Sadek, Abdelrahim A., Hassan, Mohammed H., Ameen, Hesham H., and Ahmed, Hosny A.
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FEBRILE seizures , *PHYSIOLOGICAL effects of trace elements , *OXIDATIVE stress , *ANTIOXIDANTS , *VALPROIC acid , *PATIENTS , *PHYSIOLOGY - Abstract
Febrile seizures (FS) are frequent convulsive disorders, occurring in infants and young children. The present study aims to assess and compare the serum levels of oxidative stress markers and some essential trace minerals in FS with normal or abnormal EEG and evaluate the effect of antioxidant therapy on the clinical outcome. This study has been carried out on 80 children with FS (40 with simple FS and 40 with complex FS) and 40 febrile children without seizures. Clinical and EEG findings were recorded for the included patients. Biochemical assays of serum nitric oxide (NO), malondialdehyde (MDA), superoxide dismutase (SOD), copper (Cu), zinc (Zn) and selenium (Se), using colorimetric methods, were measured in the studied groups. The overall results showed an increased values of NO, MDA and Cu with decreased values of SOD, Zn and Se in patients with FS (simple and complex) in comparison with febrile children without seizures (p < 0.05 for all). Additionally, NO and MDA was increased in complex FS patients with EEG abnormalities in comparison with complex FS with normal EEG findings (p < 0.05); NO and MDA were also significantly decreased after valproate therapy in complex FS patients (p < 0.05 for all). In conclusions, oxidative stress, decreased Zn and Se with increased Cu may play a role in FS. Valproate improves the oxidative stress status in complex FS. [ABSTRACT FROM AUTHOR]
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- 2018
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24. Comparative Protective Effects of N-Acetylcysteine, N-Acetyl Methionine, and N-Acetyl Glucosamine against Paracetamol and Phenacetin Therapeutic Doses–Induced Hepatotoxicity in Rats.
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Saleem, Tahia H., Abo El-Maali, Nagwa, Hassan, Mohammed H., Mohamed, Nahed A., Mostafa, Nashwa A. M., Abdel-Kahaar, Emaad, and Tammam, Azza S.
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ACETYLCYSTEINE , *GLUCOSAMINE , *ACETAMINOPHEN , *PHENACETIN , *ANTIPYRETICS , *HEPATOTOXICOLOGY , *THERAPEUTICS - Abstract
Background and Aims. Both paracetamol (PA) and phenacetin (PH) are analgesic and antipyretic agents. Part of phenacetin therapeutic activity is attributed to its metabolism into paracetamol. Paracetamol causes direct hepatic oxidative stress damage. The present study aimed to investigate the possible damaging effects of both PA and PH, when used in therapeutic doses, on rat liver and to compare the antioxidant and hepatoprotective effects of N-acetylcysteine (NAC), N-acetyl-methionine (NAM), and N-acetylglucosamine (NAG) against PA- or PH-induced hepatic damage. Methods. 90 male Wistar albino rats (120-140 gm) were undertaken, categorized randomly into 9 groups of 10 rats each, and administered by gavage for 2 weeks with DMSO 1% (controls), PA, PA+NAC, PA+NAM, PA+NAG, PH, PH+NAC, PH+NAM, and PH+NAG. Biochemical assays of malondialdehyde (MDA), nitric oxide (NO), reduced glutathione (GSH), total thiols, and alpha-fetoprotein (AFP) in liver homogenates and serum assays of ALT, AST, 8-hydroxy guanine (8-OH-Gua), and AFP were done. Also histopathological examinations of liver tissues in various groups were done. Results. PA and PH cause significant increase in hepatic levels of MDA, NO, and AFP and serum ALT, AST, and 8-OH-Gua levels, with significant decrease in hepatic GSH and total thiols. NAG and NAC significantly improve the PA- and PH-induced hepatic and blood, biochemical, and histopathological disturbances, respectively. Conclusions. Both PA and PH induce oxidative stress in rat liver within their therapeutic doses. NAG and NAC in pharmacological doses can antagonize the oxidative damaging effect of both PA and PH. [ABSTRACT FROM AUTHOR]
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- 2018
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25. Thyroid Function among Children with Iron Deficiency Anaemia: Pre and Post Iron Replacement Therapy.
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EL-MASRY, HOSNY MA, HAMED, AMIRA MM., HASSAN, MOHAMMED H., FAYED, HANAN M., and ABDELZAHER, MH.
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THYROID gland function tests , *IRON deficiency anemia prevention , *HYPOCHROMIC anemia - Abstract
Introduction: Metabolism of thyroid hormones and iron is quite interdependent. Data indicates that Iron Deficiency (ID) could impair thyroid metabolism. Aim: To investigate the possible occurrence of thyroid dysfunction among children with isolated Iron Deficiency Anaemia (IDA) of various severities, and test if the oral iron replacement therapy alone can reverse the associated thyroid function disturbances, if present or additional therapies are required. Materials and Methods: This prospective study was carried out on 60 children selected from the attendants to the outpatient paediatric clinics of Al-Azhar University, Assiut and Qena university hospitals, Egypt, in addition to 60 controls. Complete blood count, thyroid profile, ferritin, iron, Total Iron Binding Capacity (TIBC), Transferrin Saturation% (TFS%), unsaturated iron binding capacity and Urinary Iodine Excretion (UIE) were assessed in the studied groups at baseline, then haemoglobin level and thyroid profile repeated among the studied patients after three months of oral iron supplementation therapy. Thyroid profile and ferritin were measured using commercially available Enzyme Linked Immunosorbent Assay (ELISA) kits; while, iron, TIBC and UIE were measured using colorimetric methods. Results: Significant higher serum Thyroid Stimulating Hormone (TSH) levels with significant lower serum levels of Free Triiodothyronine (FT3) and Free Thyroxine (FT4) among patients versus controls (p<0.001 for all). Significant positive correlation between serum iron and FT3 (r=0.284, p<0.05) with significant negative correlations between TSH versus both serum iron (r=-0.635, p<0.001) and ferritin (r=-0.342, p<0.01). Significant decrease in the serum levels of TSH, with significant increase in the serum levels of FT3 and FT4 (p<0.001 for all) to euthyroid status following oral iron replacement therapy. Conclusion: Subclinical or primary hypothyroidism can occur among children suffering from moderate to severe IDA, which is reversible following oral iron replacement therapy only, without need to add thyroid replacement therapy. [ABSTRACT FROM AUTHOR]
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- 2018
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26. Genetic profile of MIF single nucleotide polymorphism (rs755622 G>C) in hepatocellular carcinoma among Egyptian patients.
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Osman, Heba Ahmed, El-Sayed, Marwa, Tag-Adeen, Mohammed, Sabra, Ahlam, El-Sawy, Samer A., Mahmoud, Marwa Ahmed, Elwahab, Saeda Mohamed Abd, Wahman, Mohammed, and Hassan, Mohammed H.
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HEPATOCELLULAR carcinoma , *SINGLE nucleotide polymorphisms , *CANCER genetics , *CANCER invasiveness , *PUBLIC health - Abstract
Aim of the study: To evaluate the role of MIF gene polymorphism rs755622 G>C in occurrence and progression of hepatocellular carcinoma (HCC) among a cohort of Egyptian patients. Material and methods: This case-control study was conducted on 50 patients with HCC after chronic viral hepatitis and 50 healthy volunteers, recruited between July 2021 and January 2022. All patients with HCC were evaluated for severity of liver disease using a Child-Pugh score, and TNM and BCLC scoring systems. MIF 173 G>C (rs755622) single nucleotide polymorphism was performed for all participants by polymerase chain reaction using restriction fragment length polymorphism technique (RFLP-PCR). Results: Overall results showed significantly higher frequencies of GG (wild homozygous genotype) and mutant heterozygous genotype GC and G allele (OR = 6.303, 95% CI: 3.374-11.775) among patients with HCC compared to the control group (p = 0.001) for all. Also, significantly higher frequency of genotype GG was detected among patients with advanced Child scores (B and C) (p = 0.039) and TNM stages (III and IV) (p = 0.013). There was significantly higher frequency of the G allele among patients with multiple hepatic focal lesions compared to those with a single focal lesion (p = 0.01). Conclusions: An obvious role of MIF (rs755622) gene polymorphism could have an important role in susceptibility and progression of HCC among patients with chronic viral hepatitis induced liver cirrhosis. [ABSTRACT FROM AUTHOR]
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- 2023
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27. Clinico-Radiological Correlation in 26 Egyptian Children with Glutaric Acidemia Type 1.
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Sadek, Abdelrahim A., Aladawy, Mohammed A., Magdy, Rofaida M., Mansour, Tarek M. M., Othman, Amr A., Hawary, Bahaa, Ibrahim, Mohamed F., Hassan, Mohammed H., and Abdelkreem, Elsayed
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MAGNETIC resonance imaging , *BRAIN abnormalities , *ACIDOSIS , *GENETIC disorders , *EPILEPSY , *GLOBUS pallidus - Abstract
Background Glutaric acidemia type 1 (GA1) is an inherited neurometabolic disease with significant morbidity. However, neuro-radiological correlation is not completely understood. Objective The study aimed to characterize the neuroimaging findings and their association with neurological phenotype in GA1 children. Methods Twenty-six Egyptian children (median age = 12 months) diagnosed with GA1 underwent clinical evaluation and brain magnetic resonance imaging (MRI). We objectively assessed the severity of neurological phenotype at the time of MRI using movement disorder (MD) and morbidity scores. Evaluation of brain MRI abnormalities followed a systematic and region-specific scoring approach. Brain MRI findings and scores were correlated with MD and morbidity scores, disease onset, and presence of seizures. Results Fifteen (57.7%) cases had insidious onset, eight (30.8%) manifested acute onset, whereas three (11.5%) were asymptomatic. Ten (38.5%) cases had seizures, five of which had no acute encephalopathic crisis. Putamen and caudate abnormalities (found in all acute onset, 93.3 and 73.3% of insidious onset, and one of three asymptomatic cases) were significantly related to MD (p = 0.007 and 0.013) and morbidity (p = 0.005 and 0.003) scores. Globus pallidus abnormalities (50% of acute onset, 46.7% of insidious onset, and one of three of asymptomatic cases) were significantly associated with morbidity score (p = 0.023). Other MRI brain abnormalities as well as gray and white matter score showed no significant association with neurological phenotype. Younger age at onset, acute onset, and seizures were significantly associated with worse neurological manifestations. Conclusion Patients with GA1 manifest characteristic and region-specific brain MRI abnormalities, but only striatal affection appears to correlate with neurological phenotype. [ABSTRACT FROM AUTHOR]
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- 2021
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28. Diabetic ketoacidosis in patients with SARS-CoV-2: a systematic review and meta-analysis.
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Alhumaid, Saad, Al Mutair, Abbas, Al Alawi, Zainab, Rabaan, Ali A., Alomari, Mohammed A., Al Salman, Sadiq A., Al-Alawi, Ahmed S., Al Hassan, Mohammed H., Alhamad, Hesham, Al-kamees, Mustafa A., Almousa, Fawzi M., Mufti, Hani N., Alwesabai, Ali M., Dhama, Kuldeep, Al-Tawfiq, Jaffar A., and Al-Omari, Awad
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DIABETIC acidosis , *SARS-CoV-2 , *COVID-19 , *TYPE 2 diabetes , *PEOPLE with diabetes , *ADULTS , *KETOACIDOSIS - Abstract
Background: One possible reason for increased mortality due to SARS-CoV-2 in patients with diabetes is from the complication of diabetic ketoacidosis (DKA). Objectives: To re-evaluate the association of SARS-CoV-2 and development of DKA and analyse the demographic and biochemical parameters and the clinical outcomes in COVID-19 patients with DKA. Design: A systematic review and meta-analysis. Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement was followed. Methods: Electronic databases (Proquest, Medline, Embase, Pubmed, CINAHL, Wiley online library, Scopus and Nature) were searched from 1 December 2019 to 30 June 2021 in the English language using the following keywords alone or in combination: COVID-19 OR SARS-CoV-2 AND diabetic ketoacidosis OR DKA OR ketosis OR ketonemia OR hyperglycaemic emergency OR hyperglycaemic crisis. We included studies in adults and children of all ages in all healthcare settings. Binary logistic regression model was used to explore the effect of various demographic and biochemical parameters variables on patient's final treatment outcome (survival or death). Results: Of the 484 papers that were identified, 68 articles were included in the systematic review and meta-analysis (54 case report, 10 case series, and 4 cohort studies). Studies involving 639 DKA patients with confirmed SARS-CoV-2 [46 (7.2%) were children and 334 (52.3%) were adults] were analyzed. The median or mean patient age ranged from < 1 years to 66 years across studies. Most of the patients (n = 309, 48.3%) had pre-existing type 2 diabetes mellitus. The majority of the patients were male (n = 373, 58.4%) and belonged to Hispanic (n = 156, 24.4%) and black (n = 98, 15.3%) ethnicity. The median random blood glucose level, HbA1c, pH, bicarbonate, and anion gap in all included patients at presentation were 507 mg/dl [IQR 399–638 mg/dl], 11.4% [IQR 9.9–13.5%], 7.16 [IQR 7.00–7.22], 10 mmol/l [IQR 6.9–13 mmol/l], and 24.5 mEq/l [18–29.2 mEq/l]; respectively. Mortality rate was [63/243, 25.9%], with a majority of death in patients of Hispanic ethnicity (n = 17, 27%; p = 0.001). The odd ratios of death were significantly high in patients with pre-existing diabetes mellitus type 2 [OR 5.24, 95% CI 2.07–15.19; p = 0.001], old age (≥ 60 years) [OR 3.29, 95% CI 1.38–7.91; p = 0.007], and male gender [OR 2.61, 95% CI 1.37–5.17; p = 0.004] compared to those who survived. Conclusion: DKA is not uncommon in SARS-CoV-2 patients with diabetes mellitus and results in a mortality rate of 25.9%. Mortality key determinants in DKA patients with SARS-CoV-2 infection are individuals with pre-existing diabetes mellitus type 2, older age [≥ 60 years old], male gender, BMI ≥ 30, blood glucose level > 1000 mg/dl, and anion gap ≥ 30 mEq/l. [ABSTRACT FROM AUTHOR]
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- 2021
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29. The child Who Presents with Recurrent Infections.
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Bellanti, Joseph A., Wallerstedt, Dawn B., and Hassan, Mohammed H.
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INFECTION , *ETIOLOGY of diseases , *CHILDREN , *IMMUNODEFICIENCY , *PATIENTS - Abstract
The child presenting with recurrent infections is a frequent clinical situation in which the physician has to determine if the patient requires immune-logical evaluation, For the clinical differentiation between a primary immunodeficiency and other causes of recurrent infection, it is of foremost importance to consider factors conditioning host environment relationship and the clinical history of the patient. Important factors to consider are frequency of infections, age of onset, sites of infection and types of infecting organisms. This review discusses such factors and the relevance of physical examination and laboratory evaluation on the disclosure of primary immunodeficiency. [ABSTRACT FROM AUTHOR]
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- 2002
30. Relations between vitamin D3, total and specific IgE for house dust mites in atopic dermatitis patients.
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Ibrahim, Hassan M., El-Taieb, Moustafa A., Hassan, Mohammed H., Mohamed, Abd Allah E., Kotop, Ebtihal A., Abd-ellah, Osama H., and Hegazy, Eisa M.
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CHOLECALCIFEROL , *ATOPIC dermatitis , *HOUSE dust mites , *DERMATOPHAGOIDES , *IMMUNOGLOBULIN E - Abstract
Atopic dermatitis (AD) is a chronic recurrent inflammatory skin disease. There are a lot of evidences on the importance of vitamin D and house dust mite (HDM) allergens in the etiology and course of AD. The objectives of this study are to evaluate the relation between vitamin D3 level and house dust mites (HDM) Dermatophagoidspecies sensitization in pathogenesis of atopic dermatitis. Cross-sectional design study was conducted on 50 atopic dermatitis patients. Blood analysis were done to determine level of vitamin D3, total IgE by fluorescent immunoassay & specific IgE for HDM (d1, d2) & other inhalant allergens by ELISA test. There was significant high negative correlation with the specific IgE for HDM (r = −0. 62, p < 0.001) and vitamin D3. & there was non-significant minimal negative correlation with the specific IgE and other inhalant allergens (r = − 0.10, p > 0.05). There was a statistically significant relation between level of vitamin D3 and atopic dermatitis severity and sensitization to HDM and other allergens. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
31. Lesional and circulating levels of interleukin‐17 and 25‐hydroxycholecalciferol in active acne vulgaris: Correlation to disease severity.
- Author
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Abd‐Elmaged, Wafaa M., Nada, Essam A., Ahmed, Heba T. I., Hassan, Mohammed H., Elsadek, Bakheet E. M., Abdelrahim, Eman A., Ahmed, Nagwa S., and Toghan, Rana
- Subjects
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ACNE , *INTERLEUKIN-17 , *VITAMIN deficiency , *ORTHOSTATIC hypotension , *CHOLECALCIFEROL , *WESTERN immunoblotting - Abstract
Summary: Objectives: The immunological aspects of inflammatory acne are still incompletely understood, so this study aimed to investigate the possible role of IL‐17 and 25 hydroxycholecalciferol (25(OH)D3) in the disease pathogenesis and progression. Materials and Methods: Across‐sectional study has been conducted on 135 patients with active acne vulgaris of various severities and 150 matched controls. ELISA assays of serum and tissue levels of IL‐17 and 25(OH)D3, also immunohistochemical and Western blotting demonstration of the expression patterns of lesional IL‐17 in comparison with control group, were performed. Results: The mean serum levels of IL‐17 were 544.2 pg/mL ± 477.4 SD and 42.2 pg/mL ± 8.1 SD for acne patients and controls, respectively, with significantly higher levels among the patient group (P < 0.05). Higher IL‐17 expression levels in active acne lesions when compared with its level in healthy skin of the controls. The mean serum levels of 25(OH)D3 among patients and controls were 33.3 ng/mL ± 9.7 SD and 51.7 ng/mL ± 2.7 SD, respectively, with significantly lower levels among the patient group (P < 0.05). There were significantly negative correlations between IL‐17 and 25(OH)D3 levels (P < 0.001 for both). Conclusions: Deficiency of vitamin D3 accompanied with higher IL‐17 in an inverse pattern may have a possible role in active acne vulgaris. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
32. Clinical and biochemical study of d-serine metabolism among schizophrenia patients.
- Author
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El-Tallawy, Hamdy N., Saleem, Tahia H., El-Ebidi, Abdallah M. A. A., Hassan, Mohammed H., Gabra, Romany H., Farghaly, Wafaa M. A., El-Maali, Nagwa Abo, and Sherkawy, Hoda S.
- Subjects
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SCHIZOPHRENIA treatment , *SERINE , *METHYL aspartate receptors , *BRAIN physiology , *ENZYME-linked immunosorbent assay , *THERAPEUTICS - Abstract
Background: Schizophrenia is a typical N-methyl-d-aspartate receptor (NMDA-R) hypofunction disorder. Decreased d-serine (d-Ser) levels in the periphery occur in schizophrenia and may reflect decreased availability of d-Ser to activate NMDA-R in the brain. Objective: The objective of this study was to investigate the role of d-Ser metabolism in the pathogenesis of schizophrenia via biochemical assays and correlates, the serum level of d-Ser, d-serine racemase (SR) (responsible for its formation from l-serine [l-Ser]) and d-amino acid oxidase (DAAO) (responsible for its catabolism), among different clinical types of schizophrenia patients. Patients and methods: This cross-sectional case-control study was carried out on 100 patients and 50 controls. They were recruited from the outpatients' psychiatric unit of the Neuropsychiatric Department of Assiut University Hospital, Upper Egypt. The type of schizophrenia was determined according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV), while the severity of schizophrenia was determined according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). Serum d-Ser levels were estimated using high-performance liquid chromatography (HPLC), while serum SR and DAAO were measured using commercially available enzyme-linked immunosorbent assay kits. Results: There were significantly lower mean serum levels of d-Ser and SR and significantly higher mean serum levels of DAAO (P-value, 0.01 for each) among schizophrenia patients when compared with the control group. Paranoid schizophrenia had the highest frequency, with a significantly lower serum levels of d-Ser and SR in the residual type and significantly higher serum levels of DAAO in undifferentiated and catatonic types. Combined receiveroperating characteristic curve for serum d-Ser, SR and DAAO indicated that the best serum level cutoff points at which schizophrenia manifestations started to appear were ≤61.4 mg/L for d-Ser, ≤5.5 pg/mL for SR and .35.6 pg/mL for DAAO. Conclusion: The present study confirms that disturbed d-Ser metabolism could be implicated in the pathogenesis of schizophrenia. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
33. Survivin as a Novel Biomarker in the Pathogenesis of Acne Vulgaris and Its Correlation to Insulin-Like Growth Factor-I.
- Author
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Assaf, Hanan A., Abdel-Maged, Wafaa M., Elsadek, Bakheet E. M., Hassan, Mohammed H., Adly, Mohamed A., and Ali, Soher A.
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SURVIVIN (Protein) , *ACNE , *SOMATOMEDIN C , *BIOMARKERS , *STATISTICAL correlation , *DIAGNOSIS - Abstract
Survivin, a member of the inhibitor of apoptosis protein family, has an important role in cell cycle regulation. Insulin-like growth factor-I (IGF-I) is a polypeptide hormone with wide range of biologic effects including stimulation of lipogenesis in sebaceous glands. Their overexpression in some fibrotic disorders suggests a possible implication of both IGF-I and survivin in the pathogenesis of acne and/or acne scars. The current study aimed to assess and correlate serum levels of IGF-I and survivin in patients with active acne vulgaris and postinflammatory acne scars and to evaluate their lesional expressions in comparison to healthy controls. Serum IGF-I and survivin were estimated using commercially available ELISA kits and their tissues expressions were investigated using Western blotting. Our findings suggest that IGF-I and survivin could play potential roles in the pathogenesis of active acne vulgaris and more importantly in postinflammatory acne scars with significant positive correlation coefficient between serum levels of IGF-I and survivin which support IGF-I-/PI3K-/AKT-mediated downregulation of nuclear expression of FoxO transcription factors resulting in enhanced survivin expression. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
34. Assessments of Amino Acids, Ammonia and Oxidative Stress Among Cohort of Egyptian Autistic Children: Correlations with Electroencephalogram and Disease Severity [Corrigendum].
- Author
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Saleem, Tahia H, Shehata, Ghaydaa Ahmed, Toghan, Rana, Sakhr, Hala M, Bakri, Ali Helmi, Desoky, Tarek, Hamdan, Fatma Rabea A, Mohamed, Nesma Foaud, and Hassan, Mohammed H
- Subjects
- *
AUTISTIC children , *OXIDATIVE stress , *AMINO acids , *ELECTROENCEPHALOGRAPHY , *AMMONIA - Published
- 2020
- Full Text
- View/download PDF
35. Prevalence of Lactose Intolerance in Primary School Children in Qena Governorate, Egypt.
- Author
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Abuhamdah, Sawsan M. A., Oriquat, Ghaleb A., Saleem, Tahia H., and Hassan, Mohammed H.
- Subjects
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CARBOHYDRATE intolerance , *LACTOSE intolerance , *DAIRY products industry , *MILKING , *DAIRY products - Abstract
Most people are born with the ability to digest lactose. Approximately 75% of the general population loses this ability, to some extent, going into adulthood (adult hypolactasia), while others retain such ability. The aim of the present study was to determine the prevalence of lactose intolerance, and its correlation with gastrointestinal symptoms, in primary school children aged 6-12 years in Qena Governorate, Egypt. A cross-sectional study was carried out on 300 school children with clinical suspicion of lactose intolerance. Biological and clinical data were obtained from children's parents or guardians. The history of diarrheal attacks especially following ingestion of milk or dairy products, as well as the incidence of diabetes in the children or family history of such diseases was also obtained. The children were instructed to maintain a low fiber diet without lactose for 48 hours prior to the day of examination. After 12 hours of fasting lactose tolerance test was carried out. The data obtained revealed that 74% of the participants in the study were intolerant to lactose. However, only 56.8% of lactose-intolerant children had positive clinical history of abdominal pain, abdominal distension or diarrheal attacks following ingestion of milk or dairy products. The prevalence of lactose intolerance in the studied cohort increased with age. Such genetically determined intolerance was 58% at 6-7 years of age and increased to 90% by the age of 11-12. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
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