12 results on '"Amy Brown"'
Search Results
2. Deep phenotyping of socio-emotional skills in children with typical development, neurodevelopmental disorders, and mental health conditions: Evidence from the PEERS.
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Vicki Anderson, Simone Darling, Stephen Hearps, David Darby, Julian Dooley, Skye McDonald, Lyn Turkstra, Amy Brown, Mardee Greenham, Louise Crossley, George Charalambous, and Miriam H Beauchamp
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Medicine ,Science - Abstract
ObjectiveSocio-emotional skills, including social competence and social cognition, form the basis for robust relationships and wellbeing. Despite their importance, these skills are poorly defined and measured, particularly in children with developmental vulnerabilities. As a consequence, targets for effective management and treatment remain unclear. We aimed to i) phenotype social competence and social cognition in typically developing children (TDC) and in children with neurodevelopmental or mental health disorders (clinical groups) and ii) establish the relationships between these child-direct measures and parent ratings of social competence and behavior.MethodUsing a multi-site, cross-sectional study design, we recruited 513 TDC and 136 children with neurodevelopmental (autism spectrum disorder [ASD], attention deficit hyperactivity disorder [ADHD]) or mental health (Anxiety Disorder [ANX]) diagnoses (age range 5-15 years). We administered the Paediatric Evaluation of Emotions, Relationships and Socialisation (PEERS) to children, and parents completed standardised questionnaires rating children's socio-emotional function.ResultsStandardised parent questionnaires revealed a global pattern of everyday socio-emotional impairment that was common to all clinical groups, while PEERS identified disorder-specific socio-cognitive profiles for children with ASD, ADHD and ANX. Compared to TDCs, children with ASD demonstrated global socio-cognitive impairment. Children with ADHD were impulsive, demonstrating difficulties managing speed accuracy trade-offs. Children with ANX exhibited slowed social decision-making, but otherwise intact skills.ConclusionsStandardized parent questionnaires of child socio-emotional function reveal differences between children with typical and atypical development, but do not yield disorder-specific, socio-emotional profiles. In contrast, findings from the PEERS objective assessment suggest that that ASD, ADHD and ANX are associated with distinct socio-cognitive phenotypes, to more accurately guide and target management and treatment of impaired social competence.
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- 2023
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3. A realist review of health passports for Autistic adults.
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Rebecca Ellis, Kathryn Williams, Amy Brown, Eleanor Healer, and Aimee Grant
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Medicine ,Science - Abstract
BackgroundAutism is a normal part of cognitive diversity, resulting in communication and sensory processing differences, which can become disabling in a neurotypical world. Autistic people have an increased likelihood of physical and mental co-occurring conditions and die earlier than neurotypical peers. Inaccessible healthcare may contribute to this. Autism Health Passports (AHPs) are paper-based or digital tools which can be used to describe healthcare accessibility needs; they are recommended in UK clinical guidance. However, questions remained as to the theoretical underpinnings and effectiveness of AHPs.MethodsWe undertook a systematic literature search identifying studies focused on AHPs for adults (aged over 16 years) from five databases. Included literature was subjected to realist evaluation. Data were extracted using a standardised form, developed by the research team, which considered research design, study quality for realist review and the Context, Mechanisms and Outcomes (CMOs) associated with each AHP tool.Findings162 unique records were identified, and 13 items were included in the review. Only one item was considered high quality. Contextual factors focused on the inaccessibility of healthcare to Autistic patients and staff lack of confidence and training in supporting Autistic needs. Interventions were heterogeneous, with most sources reporting few details as to how they had been developed. The most frequently included contents were communication preferences. Mechanisms were often not stated or were inferred by the reviewers and lacked specificity. Outcomes were included in four studies and were primarily focused on AHP uptake, rather than Outcomes which measured impact.ConclusionThere is insufficient evidence to conclude that AHPs reduce the health inequalities experienced by Autistic people. Using an AHP tool alone in a healthcare Context that does not meet Autistic needs, without the inclusion of the local Autistic community developing the tool, and a wider intervention to reduce known barriers to health inequality, may mean that AHPs do not trigger any Mechanisms, and thus cannot affect Outcomes.
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- 2023
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4. Does a mother's childbirth experience influence her perceptions of her baby's behaviour? A qualitative interview study.
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Carmen Power, Claire Williams, and Amy Brown
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Medicine ,Science - Abstract
BackgroundChildbirth has become increasingly medicalised, which may impact on the mother's birth experience and her newborn infant's physiology and behaviour. Although associations have been found between a mother's subjective birth experience and her baby's temperament, there is limited qualitative evidence around how and why this may occur.ObjectivesThis qualitative study aimed to explore mothers' childbirth and postnatal experiences, perceptions of their baby's early behavioural style, and whether they saw these as related.MethodsA qualitative semi-structured interview schedule collected rich in-depth data. Twenty-two healthy mothers over 18 years of age and with healthy infants aged 0-12 months born at term, were recruited from Southwest regions of England and Wales. Thematic analysis was performed on the data.ResultsMothers experienced childbirth as a momentous physical and psychological process. However, they did not necessarily perceive the birth as affecting their baby's early behaviour or temperament. While some mothers drew a direct relationship, such as linking a straightforward birth to a calm infant, others did not make an explicit connection, especially those who experienced a challenging birth and postnatal period. Nevertheless, mothers who had a difficult or medicalised birth sometimes reported unsettled infant behaviour. It is possible that mothers who feel anxious or depressed after a challenging birth, or those without a good support network, may simply perceive their infant as more unsettled. Equally, mothers who have been well-supported and experienced an easier birth could be more likely to perceive their baby as easier to care for.ConclusionsChildbirth is a physical and psychological event that may affect mother-infant wellbeing and influence maternal perceptions of early infant temperament. The present findings add to prior evidence, reinforcing the importance of providing good physical and emotional support during and after childbirth to encourage positive mother-infant outcomes.
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- 2023
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5. The systemic inflammatory response and clinicopathological characteristics in patients admitted to hospital with COVID-19 infection: Comparison of 2 consecutive cohorts.
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Donogh Maguire, Conor Richards, Marylynne Woods, Ross Dolan, Jesse Wilson Veitch, Wei M J Sim, Olivia E H Kemmett, David C Milton, Sophie L W Randall, Ly D Bui, Nicola Goldmann, Amy Brown, Eilidh Gillen, Allan Cameron, Barry Laird, Dinesh Talwar, Ian M Godber, John Wadsworth, Anthony Catchpole, Alan Davidson, and Donald C McMillan
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Medicine ,Science - Abstract
BackgroundIn order to manage the COVID-19 systemic inflammatory response, it is important to identify clinicopathological characteristics across multiple cohorts.MethodsThe aim of the present study was to compare the 4C mortality score, other measures of the systemic inflammatory response and clinicopathological characteristics in two consecutive cohorts of patients on admission with COVID-19. Electronic patient records for 2 consecutive cohorts of patients admitted to two urban teaching hospitals with COVID-19 during two 7-week periods of the COVID-19 pandemic in Glasgow, U.K. (cohort 1: 17/3/2020-1/5/2020) and (cohort 2: 18/5/2020-6/7/2020) were examined for routine clinical, laboratory and clinical outcome data.ResultsCompared with cohort 1, cohort 2 were older (p70 (p150mg/L (p3) (OR 11.3, 95% C.I. 2.3-96.7, pConclusionIn addition to the 4C mortality score, frailty score and a low albumin were strongly independently associated with 30-day mortality in two consecutive cohorts of patients admitted to hospital with COVID-19.Trial registrationclinicaltrials.gov: NCT04484545.
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- 2021
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6. Lysophosphatidic acid receptor mRNA levels in heart and white adipose tissue are associated with obesity in mice and humans.
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Amy Brown, Intekhab Hossain, Lester J Perez, Carine Nzirorera, Kathleen Tozer, Kenneth D'Souza, Purvi C Trivedi, Christie Aguiar, Alexandra M Yip, Jennifer Shea, Keith R Brunt, Jean-Francois Legare, Ansar Hassan, Thomas Pulinilkunnil, and Petra C Kienesberger
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Medicine ,Science - Abstract
Lysophosphatidic acid (LPA) receptor signaling has been implicated in cardiovascular and obesity-related metabolic disease. However, the distribution and regulation of LPA receptors in the myocardium and adipose tissue remain unclear.This study aimed to characterize the mRNA expression of LPA receptors (LPA1-6) in the murine and human myocardium and adipose tissue, and its regulation in response to obesity.LPA receptor mRNA levels were determined by qPCR in i) heart ventricles, isolated cardiomyocytes, and perigonadal adipose tissue from chow or high fat-high sucrose (HFHS)-fed male C57BL/6 mice, ii) 3T3-L1 adipocytes and HL-1 cardiomyocytes under conditions mimicking gluco/lipotoxicity, and iii) human atrial and subcutaneous adipose tissue from non-obese, pre-obese, and obese cardiac surgery patients.LPA1-6 were expressed in myocardium and white adipose tissue from mice and humans, except for LPA3, which was undetectable in murine adipocytes and human adipose tissue. Obesity was associated with increased LPA4, LPA5 and/or LPA6 levels in mice ventricles and cardiomyocytes, HL-1 cells exposed to high palmitate, and human atrial tissue. LPA4 and LPA5 mRNA levels in human atrial tissue correlated with measures of obesity. LPA5 mRNA levels were increased in HFHS-fed mice and insulin resistant adipocytes, yet were reduced in adipose tissue from obese patients. LPA4, LPA5, and LPA6 mRNA levels in human adipose tissue were negatively associated with measures of obesity and cardiac surgery outcomes. This study suggests that obesity leads to marked changes in LPA receptor expression in the murine and human heart and white adipose tissue that may alter LPA receptor signaling during obesity.
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- 2017
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7. Breastfeeding duration and early parenting behaviour: the importance of an infant-led, responsive style.
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Amy Brown and Bronia Arnott
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Medicine ,Science - Abstract
BackgroundPopular parenting literature promotes different approaches to caring for infants, based around variations in the use of parent-led routines and promoting infant independence. However, there is little empirical evidence of how these early behaviours affect wider parenting choices such as infant feeding. Breastfeeding often requires an infant-led approach, feeding on demand and allowing the infant to regulate intake whilst conversely formula feeding is open to greater caregiver manipulation. The infant-led style associated with breastfeeding may therefore be at odds with philosophies that encourage strict use of routine and independence. The aim of this study was to explore the association between early parenting behaviours and breastfeeding duration.MethodsFive hundred and eight mothers with an infant aged 0-12 months completed a questionnaire examining breastfeeding duration, attitudes and behaviours surrounding early parenting (e.g. anxiety, use of routine, involvement, nurturance and discipline). Participants were attendees at baby groups or participants of online parenting forums based in the UK.ResultsFormula use at birth or short breastfeeding duration were significantly associated with low levels of nurturance, high levels of reported anxiety and increased maternal use of Parent-led routines. Conversely an infant-led approach characterised by responding to and following infant cues was associated with longer breastfeeding duration.DiscussionMaternal desire to follow a structured parenting approach which purports use of Parent-led routines and early demands for infant independence may have a negative impact upon breastfeeding duration. Increased maternal anxiety may further influence this relationship. The findings have important implications for Health Professionals supporting new mothers during pregnancy and the postpartum period.
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- 2014
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8. Breastfeeding is associated with a maternal feeding style low in control from birth.
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Amy Brown and Michelle Lee
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Medicine ,Science - Abstract
BackgroundThe influence of maternal child-feeding style upon child weight and eating style for children over the age of twelve months is well established. However there is little empirical evidence examining maternal child-feeding style during milk feeding despite evidence that mothers who breastfeed exert lower levels of control over later diet. The aim of this paper was to examine variation in maternal child-feeding style during the first six months postpartum and to explore associations with mode of milk feeding and infant weight.MethodsThe Child Feeding Questionnaire (CFQ) is frequently used to measure maternal child-feeding style in preschool children. 390 mothers with an infant aged 0-6 months completed an adapted version of the CFQ to measure maternal child-feeding style during milk feeding. Participants reported breastfeeding duration, infant weight and perceived size.ResultsPrinciple components analysis of questionnaire items produced six factors; encouraging feeding, feeding to a routine, limiting intake, concern for weight, monitoring and perceived responsibility. Breastfeeding was associated with lower levels of control compared to formula feeding. Infant birth weight was significantly inversely associated with concern for weight, monitoring and encouraging feeding.DiscussionFormula feeding is associated with greater maternal control of child-feeding from birth whilst a lower birth weight is linked to concerns for infant weight and pressure to eat. As early maternal child-feeding relationships may impact negatively upon longer term child weight and eating style, identifying variations in maternal feeding style and understanding the factors that influence this is pertinent.
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- 2013
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9. The systemic inflammatory response and clinicopathological characteristics in patients admitted to hospital with COVID-19 infection: Comparison of 2 consecutive cohorts
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Ian M Godber, Donogh Maguire, John Wadsworth, Donald C. McMillan, Anthony Catchpole, Allan Cameron, Nicola Goldmann, Dinesh Talwar, Alan Davidson, David C. Milton, Ly D. Bui, Conor Richards, Jesse Wilson Veitch, Ross D. Dolan, Wei M. J. Sim, Sophie L. W. Randall, Marylynne Woods, Barry Laird, Olivia E. H. Kemmett, Amy Brown, and Eilidh Gillen
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Male ,Viral Diseases ,Multivariate analysis ,Neutrophils ,Biochemistry ,White Blood Cells ,Medical Conditions ,0302 clinical medicine ,Animal Cells ,Medicine and Health Sciences ,Medicine ,Lymphocytes ,Hospital Mortality ,030212 general & internal medicine ,Immune Response ,Aged, 80 and over ,Multidisciplinary ,Frailty ,Age Factors ,Middle Aged ,C-Reactive Proteins ,Systemic Inflammatory Response Syndrome ,Hospitalization ,Infectious Diseases ,030220 oncology & carcinogenesis ,Cohort ,Female ,Cellular Types ,Outcome data ,Research Article ,Low albumin ,medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,Immune Cells ,Inflammatory response ,Science ,Immunology ,03 medical and health sciences ,Signs and Symptoms ,Sex Factors ,Albumins ,Sepsis ,Internal medicine ,Humans ,In patient ,Trial registration ,Aged ,Inflammation ,Blood Cells ,SARS-CoV-2 ,business.industry ,Biology and Life Sciences ,Proteins ,COVID-19 ,Covid 19 ,Cell Biology ,medicine.disease ,Systemic inflammatory response syndrome ,Geriatrics ,Clinical Medicine ,Low serum albumin ,business - Abstract
BackgroundIn order to manage the COVID-19 systemic inflammatory response, it is important to identify clinicopathological characteristics across multiple cohorts.MethodsElectronic patient records for 2 consecutive cohorts of patients admitted to two urban teaching hospitals with COVID-19 during two 7-week periods of the COVID-19 pandemic in Glasgow, U.K. (cohort 1: 17th March 2020 – 1st May 2020) and (cohort 2: 18th May 2020 – 6th July 2020) were examined for routine clinical, laboratory and clinical outcome data.ResultsCompared with cohort 1, cohort 2 were older (pConclusionIn addition to the 4C mortality score, frailty score and a low albumin were strongly independently associated with 30-day mortality in two consecutive cohorts of patients admitted to hospital with COVID-19.Article summaryIn two consecutive cohorts of patients with COVID-19 infection admitted to two urban teaching hospitals in Glasgow, UK, there were variations in a number of clinicopathological characteristics despite similar mortality (23 and 22%).In these two cohorts, in a multivariate analysis that included the 4C mortality score, clinical frailty score >3, low serum albumin concentration (145 mmol/L) remained independently associated with 30-day mortality.
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- 2021
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10. Colonization of the cervicovaginal space with Gardnerella vaginalis leads to local inflammation and cervical remodeling in pregnant mice
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Snehal S. Shetye, Guillermo Barila, Lauren Anton, Michal A. Elovitz, Carrie E. Barnum, Louis J. Soslowsky, Amy Brown, and Luz-Jeannette Sierra
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0301 basic medicine ,Amniotic fluid ,Maternal Health ,Uterus ,lcsh:Medicine ,Artificial Gene Amplification and Extension ,Cervix Uteri ,medicine.disease_cause ,Pathology and Laboratory Medicine ,Biochemistry ,Polymerase Chain Reaction ,Cervix ,Mice ,0302 clinical medicine ,Pregnancy ,Medicine and Health Sciences ,Gardnerella vaginalis ,lcsh:Science ,Immune Response ,030219 obstetrics & reproductive medicine ,Multidisciplinary ,Obstetrics and Gynecology ,Animal Models ,Vaginosis, Bacterial ,3. Good health ,Biomechanical Phenomena ,medicine.anatomical_structure ,Real-time polymerase chain reaction ,Experimental Organism Systems ,Vagina ,Cytokines ,Female ,Bacterial vaginosis ,Anatomy ,Genital Anatomy ,Research Article ,Immunology ,Mouse Models ,Enzyme-Linked Immunosorbent Assay ,Research and Analysis Methods ,Preterm Birth ,Real-Time Polymerase Chain Reaction ,Andrology ,03 medical and health sciences ,Model Organisms ,Signs and Symptoms ,Diagnostic Medicine ,Placenta ,medicine ,Animals ,Molecular Biology Techniques ,Molecular Biology ,Inflammation ,Fetus ,business.industry ,lcsh:R ,Reproductive System ,Biology and Life Sciences ,Proteins ,medicine.disease ,Pregnancy Complications ,030104 developmental biology ,Birth ,Women's Health ,lcsh:Q ,business ,Collagens - Abstract
The role of the cervicovaginal (CV) microbiome in regulating cervical function during pregnancy is poorly understood. Gardnerella vaginalis (G. vaginalis) is the most common bacteria associated with the diagnosis of bacterial vaginosis (BV). While BV has been associated with preterm birth (PTB), clinical trials targeting BV do not decrease PTB rates. It remains unknown if G. vaginalis is capable of triggering molecular, biomechanical and cellular events that could lead to PTB. The objective of this study was to determine if cervicovaginal colonization with G. vaginalis, in pregnant mice, induced cervical remodeling and modified cervical function. CD-1 timed-pregnant mice received a 5X108 CFU/mL intravaginal inoculation of G. vaginalis or control on embryonic day 12 (E12) and E13. On E15, the mice were sacrificed and cervicovaginal fluid (CVF), amniotic fluid (AF), cervix, uterus, placentas and fetal membranes (FM) were collected. Genomic DNA was isolated from the CVF, placenta, uterus and FM and QPCR was performed to confirm colonization. IL-6 was measured in the CVF and AF and soluble e-cadherin (seCAD) was assessed in the CVF by ELISA. RNA was extracted from the cervices to evaluate IL-10, IL-8, IL-1β, TNF-α, Tff-1, SPINK-5, HAS-1 and LOX expression via QPCR. Mucicarmine and trichrome staining was used to assess cervical mucin and collagen. Biomechanical properties of the cervix were studied using quasi-static tensile load-to-failure biomechanical tests. G. vaginalis successfully colonized the CV space. This colonization induced immune responses (increased IL-6 levels in CVF and AF, increased mRNA expression of cervical cytokines), altered the epithelial barrier (increased seCAD in the CVF), induced cervical remodeling (increased mucin production, altered collagen) and altered cervical biomechanical properties (a decrease in biomechanical modulus and an increase in maximum strain). The ability of G. vaginalis to induce these molecular, immune, cellular and biomechanical changes suggests that this bacterium may play a pathogenic role in premature cervical remodeling leading to PTB.
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- 2018
11. Exposure to intrauterine inflammation alters metabolomic profiles in the amniotic fluid, fetal and neonatal brain in the mouse
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Natalia M. Tulina, Amy Brown, Michael S. Hester, Michal A. Elovitz, and Guillermo Barila
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0301 basic medicine ,Amniotic fluid ,Physiology ,lcsh:Medicine ,Pathology and Laboratory Medicine ,Biochemistry ,Mice ,Pregnancy ,Medicine and Health Sciences ,Metabolites ,Medicine ,Brain Damage ,lcsh:Science ,Immune Response ,Multidisciplinary ,Obstetrics ,Brain ,3. Good health ,Body Fluids ,Neurology ,Purine Metabolism ,Female ,Metabolic Pathways ,medicine.symptom ,Anatomy ,Research Article ,medicine.medical_specialty ,Offspring ,Traumatic brain injury ,Immunology ,Inflammation ,03 medical and health sciences ,Signs and Symptoms ,Diagnostic Medicine ,Metabolome ,Xenobiotic Metabolism ,Metabolomics ,Animals ,Fetus ,business.industry ,Uterus ,lcsh:R ,Biology and Life Sciences ,medicine.disease ,Amniotic Fluid ,Amino Acid Metabolism ,030104 developmental biology ,Metabolism ,Animals, Newborn ,lcsh:Q ,business ,Drug metabolism - Abstract
Introduction Exposure to prenatal inflammation is associated with diverse adverse neurobehavioral outcomes in exposed offspring. The mechanism by which inflammation negatively impacts the developing brain is poorly understood. Metabolomic profiling provides an opportunity to identify specific metabolites, and novel pathways, which may reveal mechanisms by which exposure to intrauterine inflammation promotes fetal and neonatal brain injury. Therefore, we investigated whether exposure to intrauterine inflammation altered the metabolome of the amniotic fluid, fetal and neonatal brain. Additionally, we explored whether changes in the metabolomic profile from exposure to prenatal inflammation occurs in a sex-specific manner in the neonatal brain. Methods CD-1, timed pregnant mice received an intrauterine injection of lipopolysaccharide (50 μg/dam) or saline on embryonic day 15. Six and 48 hours later mice were sacrificed and amniotic fluid, and fetal brains were collected (n = 8/group). Postnatal brains were collected on day of life 1 (n = 6/group/sex). Global biochemical profiles were determined using ultra performance liquid chromatography/tandem mass spectrometry (Metabolon Inc.). Statistical analyses were performed by comparing samples from lipopolysaccharide and saline treated animals at each time point. For the P1 brains, analyses were stratified by sex. Results/conclusions Exposure to intrauterine inflammation induced unique, temporally regulated changes in the metabolic profiles of amniotic fluid, fetal brain and postnatal brain. Six hours after exposure to intrauterine inflammation, the amniotic fluid and the fetal brain metabolomes were dramatically altered with significant enhancements of amino acid and purine metabolites. The amniotic fluid had enhanced levels of several members of the (hypo) xanthine pathway and this compound was validated as a potential biomarker. By 48 hours, the number of altered biochemicals in both the fetal brain and the amniotic fluid had declined, yet unique profiles existed. Neonatal pups exposed to intrauterine inflammation have significant alterations in their lipid metabolites, in particular, fatty acids. These sex-specific metabolic changes within the newborn brain offer an explanation regarding the sexual dimorphism of certain psychiatric and neurobehavioral disorders associated with exposure to prenatal inflammation.
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- 2017
12. Differential Methylation of Genes Associated with Cell Adhesion in Preeclamptic Placentas
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Lauren Anton, Michal A. Elovitz, Marisa S. Bartolomei, and Amy Brown
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Male ,Embryology ,Placenta ,Maternal Health ,Gene Expression ,Biochemistry ,Pre-Eclampsia ,Pregnancy ,Gene expression ,Medicine and Health Sciences ,Oligonucleotide Array Sequence Analysis ,Regulation of gene expression ,DNA methylation ,Multidisciplinary ,Methylation ,Trophoblasts ,medicine.anatomical_structure ,Medicine ,Female ,Epigenetics ,Anatomy ,DNA modification ,Research Article ,Adult ,Science ,Biology ,Preeclampsia ,Andrology ,Cell Adhesion ,Genetics ,medicine ,Humans ,RNA, Messenger ,Biology and life sciences ,Gene Expression Profiling ,Reproductive System ,Trophoblast ,Sequence Analysis, DNA ,DNA ,Cell Biology ,medicine.disease ,Molecular biology ,Pregnancy Complications ,Pregnancy Trimester, First ,Case-Control Studies ,Women's Health ,Blastocysts ,Developmental Biology - Abstract
Preeclampsia (PE), a hypertensive disorder of pregnancy, is hypothesized to be associated with, if not mechanistically related to abnormal placental function. However, the exact mechanisms regulating the pathogenesis of PE remain unclear. While many studies have investigated changes in gene expression in the PE placenta, the role of epigenetics in PE associated placental dysfunction remains unclear. Using the genome-wide Illumina Infinium Methylation 450 BeadChip array, we analyzed gene-specific alterations in DNA methylation in placental biopsies collected from normal pregnant women delivering at term (n = 14), with term PE (≥37 weeks; n = 19) or with preterm PE (5% methylation difference). Functional annotation of the differentially methylated genes in preterm PE placentas revealed a 32 gene cluster in the cadherin and cell adhesion functional groups (Benjamini p
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- 2014
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