Frontiers in Psychiatry (Jul 2023)

The interaction between the major vault protein rs4788186 polymorphism, alcohol dependence, and depression among male Chinese problem drinkers

  • Yuyu Wu,
  • Yuyu Wu,
  • Ke Zhao,
  • Yingjie Chen,
  • Liujun Wu,
  • Liujun Wu,
  • Liujun Wu,
  • Liujun Wu,
  • Feng Qiu,
  • Yuying Yuan,
  • Guanghui Shen,
  • Guanghui Shen,
  • Kexin Wang,
  • Kexin Wang,
  • Yimin Kang,
  • Yongsheng Jiang,
  • Wei Wang,
  • Wei Wang,
  • Li Chen,
  • Li Chen,
  • Yanlong Liu,
  • Yanlong Liu,
  • Xuebo Pan,
  • Fan Wang,
  • Longteng Xie

DOI
https://doi.org/10.3389/fpsyt.2023.1111712
Journal volume & issue
Vol. 14

Abstract

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ObjectiveAlcohol use disorder (AUD) is the second most prevalent mental disorder and might be related to depression. Major vault protein (MVP) is a cytoplasmic protein related to vesicle transport. The present study aimed to investigate the interaction between a genetic variant (MVP rs4788186) and depression in adult male Han Chinese with AUD during withdrawal.MethodsAll participants (N = 435) were diagnosed with AUD. Alcohol dependence level was measured using the Michigan Alcoholism Screening Test, and depression was measured using the self-rating depression scale. Genomic DNA was extracted from peripheral blood and genotyped.ResultsHierarchical regression analysis identified an interaction between MVP rs4788186 and alcohol dependence level for depression (β = −0.17, p < 0.05). Then, a region of significance test was performed to interpret the interaction effect. Re-parameterized regression models revealed that the interaction between MVP rs4788186 and alcohol problem severity fit the strong differential susceptibility model (R2 = 0.08, p < 0.001), suggesting that the AA homozygotes would be more likely subjects with the G allele to experience major depression symptoms.ConclusionCarriers of the AA homozygote of MVP rs4788186 may be more susceptible to severe alcohol problems and higher levels of depression during withdrawal.

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