CBLL1 is hypomethylated and correlates with cortical thickness in transgender men before gender affirming hormone treatment DOI Creative Commons
Rosa Fernández, Leire Zubiaurre‐Elorza,

Andrea Santisteban

et al.

Scientific Reports, Journal Year: 2023, Volume and Issue: 13(1)

Published: Dec. 7, 2023

Abstract Gender identity refers to the consciousness of being a man, woman or other condition. Although it is generally congruent with sex assigned at birth, for some people not. If incongruity distressing, defined as gender dysphoria (GD). Here, we measured whole-genome DNA methylation by Illumina © Infinium Human Methylation 850k array and reported its correlation cortical thickness (CTh) in 22 transgender men (TM) experiencing GD versus 25 cisgender (CM) 28 women (CW). With respect analysis, TM vs. CW showed significant differences 35 CpGs, while 2155 CpGs were found when CM compared. CBLL1 DLG1 genes that correlated global left hemisphere CTh. Both hypomethylated compared groups. Early onset positive between several regions frontal (left caudal middle frontal), temporal (right inferior temporal, fusiform) parietal cortices supramarginal right paracentral). This first study relating CTh persons supports neurodevelopmental hypothesis identity.

Language: Английский

The Role of Hydrogen Sulfide (H2S) in Epigenetic Regulation of Neurodegenerative Diseases: A Systematic Review DOI Open Access

Bombonica Gabriela Dogaru,

Constantin Munteanu

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(16), P. 12555 - 12555

Published: Aug. 8, 2023

This review explores the emerging role of hydrogen sulfide (H

Language: Английский

Citations

21

DNA methylation as a possible causal mechanism linking childhood adversity and health: Results from two-sample mendelian randomization study DOI
Isabel K. Schuurmans, Erin C. Dunn, Alexandre A. Lussier

et al.

American Journal of Epidemiology, Journal Year: 2024, Volume and Issue: 193(11), P. 1541 - 1552

Published: May 17, 2024

Abstract Childhood adversity is an important risk factor for adverse health across the life course. Epigenetic modifications, such as DNA methylation (DNAm), are a hypothesized mechanism linking to disease susceptibility. Yet, few studies have determined whether adversity-related DNAm alterations causally related future outcomes or if their developmental timing plays role in these relationships. Here, we used 2-sample mendelian randomization obtain stronger causal inferences about association between adversity-associated loci development (ie, birth, childhood, adolescence, and young adulthood) 24 mental, physical, behavioral outcomes. We identified particularly strong associations attention-deficit/hyperactivity disorder, depression, obsessive-compulsive suicide attempts, asthma, coronary artery disease, chronic kidney disease. More of were birth childhood DNAm, whereas adolescent adulthood more closely linked mental health. also had primarily risk-suppressing relationships with outcomes, suggesting that might reflect compensatory buffering mechanisms against rather than acting solely indicator risk. Together, our results suggest both physical impacts differences emerging earlier development.

Language: Английский

Citations

5

Exposure to Endocrine Disruptors in Early life and Neuroimaging Findings in Childhood and Adolescence: a Scoping Review DOI Creative Commons
Kim N. Cajachagua‐Torres, Hugo G. Quezada‐Pinedo, Tong Wu

et al.

Current Environmental Health Reports, Journal Year: 2024, Volume and Issue: 11(3), P. 416 - 442

Published: July 30, 2024

PURPOSE OF REVIEW: Evidence suggests neurotoxicity of endocrine disrupting chemicals (EDCs) during sensitive periods development. We present an overview pediatric population neuroimaging studies that examined brain influences EDC exposure prenatal period and childhood. RECENT FINDINGS: found 46 used magnetic resonance imaging (MRI) to examine EDCs. These showed associations phthalates, organophosphate pesticides (OPs), polyaromatic hydrocarbons persistent organic pollutants with global regional structural alterations. Few suggested alteration in functional MRI associated OP exposure. However, on other groups EDCs, such as bisphenols, those childhood were less conclusive. findings underscore the potential profound lasting effects development, emphasizing need for better regulation strategies reduce mitigate impacts. More are needed influence postnatal imaging.

Language: Английский

Citations

5

Glucocorticoid Receptor Gene (NR3C1) Methylation Childhood Maltreatment Multilevel Reward Responsiveness and Depressive and Anxiety Symptoms: A Neuroimaging Epigenetic Study DOI Creative Commons

Yajing Xu,

Shan Yang, Cong Cao

et al.

NeuroImage, Journal Year: 2025, Volume and Issue: 306, P. 121003 - 121003

Published: Jan. 7, 2025

Although epigenomic and environment interactions (Epigenome × Environment; Epi E) might constitute a novel mechanism underlying reward processing direct evidence is still scarce. We conducted the first longitudinal study to investigate extent which DNA methylation of stress-related gene-NR3C1-interacts with childhood maltreatment in association young adult responsiveness (RR) downstream risk depressive (anhedonia dimension particular) anxiety symptoms. A total 192 Chinese university students aged 18∼25 (M NR3C1-1F significantly interacted on RewP but not delta theta components or self-reported RR. The severity exposure number were negatively associated among individuals heightened positively blunted demonstrating "goodness-of-fit" interaction. This interaction was specifically linked anhedonia scores current findings provide preliminary for an E highlight cross-level analyses electrophysiological signals advance knowledge biological foundation stress-induced function relevant However caution should be paid generalizability these high-risk clinical samples given high-functioning characteristic present sample.

Language: Английский

Citations

0

Epigenetic age across development in children and adolescents with ADHD DOI Creative Commons
Jo Wrigglesworth, Peter Fransquet, Peter Ryabinin

et al.

Psychiatry Research, Journal Year: 2025, Volume and Issue: 345, P. 116373 - 116373

Published: Jan. 20, 2025

Language: Английский

Citations

0

Biospecimens in the HEALthy Brain and Child Development Study (HBCD) Study: Rationale and Protocol DOI Creative Commons
Elinor L. Sullivan, Ryan Bogdan, Ludmila N. Bakhireva

et al.

Developmental Cognitive Neuroscience, Journal Year: 2024, Volume and Issue: 70, P. 101451 - 101451

Published: Sept. 18, 2024

Language: Английский

Citations

3

Elevated plasma B12and betaine levels in women with anorexia nervosa: possible role in illness pathophysiology and epigenetic regulation DOI Open Access
Howard Steiger,

Kevin F. Casey,

Jessica Burdo

et al.

Journal of Psychiatry and Neuroscience, Journal Year: 2025, Volume and Issue: 50(2), P. E85 - E91

Published: March 4, 2025

Phenomenology in anorexia nervosa (AN) appears to be subject epigenetic regulation via DNA methylation. The micronutrients B12 and betaine contribute directly methylation have been shown abnormally elevated blood samples from people with AN. We measured plasma levels, as well leukocyte among women active AN (AN-active group), those 1-year remission (AN-remitted who had never experienced an eating disorder (NED group). compared the groups on micronutrient levels strength of association between included 64 AN-active group, 49 AN-remitted NED group. Relative (B12: mean 339.6 [standard deviation (SD) 224.3] μmol/L; betaine: 33.74 [SD 17.10] μmol/L), participants showed high 571.0 505.2] 43.73 22.50] μmol/L); alone 588.2 379.9] 33.50 19.20] μmol/L). There were also group-based differences site-specific at genes regulating insulin function, glucose metabolism, cell regulation, neurotransmitter function. These associations generally stronger without ED than either or remitted extent which nutrient provide a meaningful proxy cellular processes affecting is uncertain sample size limits stability results. only biological females this investigation. Elevated resemble elevations reported autoimmune, neoplastic, other disorders. Such imply that may misrepresent nutritional status Observed certain gene regions ambiguous importance, but indicate influence mechanisms coincidence separate independently affect

Language: Английский

Citations

0

The Nature of Intelligence DOI

Barco J. You

Lecture notes in networks and systems, Journal Year: 2025, Volume and Issue: unknown, P. 793 - 817

Published: Jan. 1, 2025

Language: Английский

Citations

0

Implications of Hydrogen Sulfide in Epigenetic Controlling in Neurodegenerative Diseases: A Narrative Review DOI Open Access
Kulvinder Kochar Kaur

Clinical Pathology & Research Journal, Journal Year: 2024, Volume and Issue: 8(1), P. 1 - 13

Published: Jan. 1, 2024

Previously we had have reviewed various neurodegenerative diseases (NDD), inclusive of Alzheimer’s disease (AD), Parkinson’s (PD), as well Huntington’s (HD), role hydrogen sulfide (H2 S), in treatment different cancers breast cancer, glioma, hepatocellular carcinoma along with epigenetics Diabetic Kidney Disease (DKD), pregnancy. There by the objective this review is provision an exhaustive outline present research controlling epigenetic events correlated NDD. Here conducted a narrative utilizing search engine pubmed, google scholar; web science; embase; Cochrane library MeSH terms like (NDD); ; H2 S disease; sulfide; Epigenetics; DNA methylation; Histone post-translational modifications; protein acetylation; methylation from 2000 till 2023 December date. Emerging proof has initiated unravelling facets which impacts topography followed propagation NDD AD, PD), HD. possesses capacity modulating crucial machinery for instance methylation, histone modifications noncoding RNAs influencing gene expression cellular working germane to neuronal survival, neuroinflammation, synaptic plasticity. Thus it constructed how works form imperative actor amongst close-knit network possessing probability opening innovative therapeutic arena. Although considerable work done, still lot lacunae exist on exact molecular modes plausible repercussions H2S quantities/its downstream targets. Finally isolation future directions having using

Language: Английский

Citations

1

DNA methylation at birth and lateral ventricular volume in childhood: a neuroimaging epigenetics study DOI Creative Commons
Mannan Luo, Esther Walton, Alexander Neumann

et al.

Journal of Child Psychology and Psychiatry, Journal Year: 2023, Volume and Issue: 65(1), P. 77 - 90

Published: July 19, 2023

Background Lateral ventricular volume (LVV) enlargement has been repeatedly linked to schizophrenia; yet, what biological factors shape LVV during early development remain unclear. DNA methylation (DNAm), an essential process for neurodevelopment that is altered in schizophrenia, a key molecular system of interest. Methods In this study, we conducted the first epigenome‐wide association study neonatal DNAm cord blood with childhood (measured using T1‐weighted brain scans at 10 years), based on data from large population‐based birth cohort, Generation R Study ( N = 840). Employing both probe‐level and profile score (MPS) approaches, further examined whether epigenetic modifications identified are: (a) also observed cross‐sectionally peripheral age years (Generation R, 370) (b) prospectively associated measured young adulthood all‐male sample Avon Longitudinal Parents Children (ALSPAC, 114). Results At birth, levels four CpGs (annotated potassium channel tetramerization domain containing 3, KCTD3 ; SHH signaling ciliogenesis regulator, SDCCAG8 glutaredoxin, GLRX ) after genome‐wide correction; these genes have implicated psychiatric traits including schizophrenia. An MPS capturing broader – but not individual top hits showed significant cross‐sectional associations within ALSPAC. Conclusions This finds suggestive evidence associates different life stages, albeit small effect sizes. The prediction independent male adult underscores stability reproducibility as potential marker LVV. Future studies larger samples comparable time points across are needed elucidate how clinically relevant structure risk neuropsychiatric disorders, explain birth.

Language: Английский

Citations

3