ORCID Profile
0000-0001-9768-0513
Current Organisation
San Diego State University
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Publisher: Public Library of Science (PLoS)
Date: 20-12-2018
Publisher: Springer Science and Business Media LLC
Date: 04-10-2023
Publisher: F1000 Research Ltd
Date: 14-02-2018
DOI: 10.12688/WELLCOMEOPENRES.13893.1
Abstract: Background: Stressful life events (SLEs) and neuroticism are risk factors for major depressive disorder (MDD). However, SLEs and neuroticism are heritable and genetic risk for SLEs is correlated with risk for MDD. We sought to investigate the genetic and environmental contributions to SLEs in a family-based s le, and quantify genetic overlap with MDD and neuroticism. Methods: A subset of Generation Scotland: the Scottish Family Health Study (GS), consisting of 9618 in iduals with information on MDD, past 6 month SLEs, neuroticism and genome-wide genotype data was used in the present study. We estimated the heritability of SLEs using GCTA software. The environmental contribution to SLEs was assessed by modelling familial, couple and sibling components. Using polygenic risk scores (PRS) and LD score regression (LDSC) we analysed the genetic overlap between MDD, neuroticism and SLEs. Results: Past 6-month life events were positively correlated with lifetime MDD status (β=0.21, r 2 =1.1%, p=2.5 x 10 -25 ) and neuroticism (β =0.13, r 2 =1.9%, p=1.04 x 10 -37 ) at the phenotypic level. Common SNPs explained 8% of the phenotypic variance in personal life events (those directly affecting the in idual) (S.E.=0.03, p= 9 x 10 -4 ). A significant effect of couple environment was detected accounting for 13% (S.E.=0.03, p=0.016) of the phenotypic variation in SLEs. PRS analyses found that reporting more SLEs was associated with a higher polygenic risk for MDD (β =0.05, r 2 =0.3%, p=3 x 10 -5 ), but not a higher polygenic risk for neuroticism. LDSC showed a significant genetic correlation between SLEs and both MDD (r G =0.33, S.E.=0.08 ) and neuroticism (r G =0.15, S.E.=0.07). Conclusions: These findings suggest that SLEs should not be regarded solely as environmental risk factors for MDD as they are partially heritable and this heritability is shared with risk for MDD and neuroticism. Further work is needed to determine the causal direction and source of these associations.
Publisher: Informa UK Limited
Date: 10-2016
Publisher: Frontiers Media SA
Date: 28-01-2020
Publisher: Springer Science and Business Media LLC
Date: 16-11-2021
DOI: 10.1038/S41467-021-26783-X
Abstract: Previous genome-wide association studies revealed multiple common variants involved in eczema but the role of rare variants remains to be elucidated. Here, we investigate the role of rare variants in eczema susceptibility. We meta-analyze 21 study populations including 20,016 eczema cases and 380,433 controls. Rare variants are imputed with high accuracy using large population-based reference panels. We identify rare exonic variants in DUSP1 , NOTCH4 , and SLC9A4 to be associated with eczema. In DUSP1 and NOTCH4 missense variants are predicted to impact conserved functional domains. In addition, five novel common variants at SATB1-AS1 / KCNH8 , TRIB1 / LINC00861 , ZBTB1 , TBX21 / OSBPL7 , and CSF2RB are discovered. While genes prioritized based on rare variants are significantly up-regulated in the skin, common variants point to immune cell function. Over 20% of the single nucleotide variant-based heritability is attributable to rare and low-frequency variants. The identified rare/low-frequency variants located in functional protein domains point to promising targets for novel therapeutic approaches to eczema.
Publisher: Springer Science and Business Media LLC
Date: 18-01-2019
DOI: 10.1038/S41398-018-0356-7
Abstract: Depression has well-established influences from genetic and environmental risk factors. This has led to the diathesis-stress theory, which assumes a multiplicative gene-by-environment interaction (GxE) effect on risk. Recently, Colodro-Conde et al . empirically tested this theory, using the polygenic risk score for major depressive disorder (PRS, genes) and stressful life events (SLE, environment) effects on depressive symptoms, identifying significant GxE effects with an additive contribution to liability. We have tested the diathesis-stress theory on an independent s le of 4919 in iduals. We identified nominally significant positive GxE effects in the full cohort ( R 2 = 0.08%, p = 0.049) and in women ( R 2 = 0.19%, p = 0.017), but not in men ( R 2 = 0.15%, p = 0.07). GxE effects were nominally significant, but only in women, when SLE were split into those in which the respondent plays an active or passive role ( R 2 = 0.15%, p = 0.038 R 2 = 0.16%, p = 0.033, respectively). High PRS increased the risk of depression in participants reporting high numbers of SLE ( p = 2.86 × 10 −4 ). However, in those participants who reported no recent SLE, a higher PRS appeared to increase the risk of depressive symptoms in men ( β = 0.082, p = 0.016) but had a protective effect in women ( β = −0.061, p = 0.037). This difference was nominally significant ( p = 0.017). Our study reinforces the evidence of additional risk in the aetiology of depression due to GxE effects. However, larger s le sizes are required to robustly validate these findings.
Location: United States of America
No related grants have been discovered for Aleix Arnau Soler.