4.6 Article

Role of environmental confounding in the association between FKBP5 and first-episode psychosis

期刊

FRONTIERS IN PSYCHIATRY
卷 5, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2014.00084

关键词

FKBP5; psychosis; confounding factors; cannabis; childhood adversity; gene-environment; GWAS; missing heritability

资金

  1. United Kingdom National Institute of Health Research Biomedical Research Centre for Mental Health, South London and Maudsley NHS Foundation Trust
  2. Institute of Psychiatry at King's College London
  3. Psychiatry Research Trust
  4. Maudsley Charitable research fund
  5. Medical Research Council UK [G1002366]
  6. MRC [G108/603, G0901885, G1002366] Funding Source: UKRI
  7. Academy of Medical Sciences (AMS) [AMS-SGCL5-Mondelli] Funding Source: researchfish
  8. Alzheimers Research UK [ART-PhD2009-3] Funding Source: researchfish
  9. Medical Research Council [G1002366, G108/603, MR/J002739/1, G0901885] Funding Source: researchfish
  10. National Institute for Health Research [CL-2008-17-005, NF-SI-0510-10129, CL-2012-17-004] Funding Source: researchfish

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Background:Failure to account for the etiological diversity that typically occurs in psychiatric cohorts may increase the potential for confounding as a proportion of genetic variance will be specific to exposures that have varying distributions in cases. This study investigated whether minimizing the potential for such confounding strengthened the evidence for a genetic candidate currently unsupported at the genome-wide level. Methods:Two hundred and ninety-one first-episode psychosis cases from South London, UK and 218 unaffected controls were evaluated for a functional polymorphism at the rs1360780 locus in FKBP5. The relationship between FKBP5 and psychosis was modeled using logistic regression. Cannabis use (Cannabis Experiences Questionnaire) and parental separation (Childhood Experience of Care and Abuse Questionnaire) were included as confounders in the analysis. Results:Association at rs1360780 was not detected until the effects of the two environmental factors had been adjusted for in the model (OR = 2.81, 95% CI 1.23-6.43, p = 0.02). A statistical interaction between rs1360780 and parental separation was confirmed by stratified tests (OR = 2.8, p = 0.02 vs. OR = 0.89, p = 0.80). The genetic main effect was directionally consistent with findings in other (stress-related) clinical phenotypes. Moreover, the variation in effect magnitude was explained by the level of power associated with different cannabis constructs used in the model (r = 0.95). Conclusion: Our results suggest that the extent to which genetic variants in FKBP5 can influence susceptibility to psychosis may depend on other etiological factors. This finding requires further validation in large independent cohorts. Potentially this work could have translational implications; the ability to discriminate between genetic etiologies based on a case-by-case understanding of previous environmental exposures would confer an important clinical advantage that would benefit the delivery of personalizable treatment strategies.

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