Wei Xiaojie, Cai Fangfang, Zhou Siyao, Zhang Jinjing, Xu Kewei, Shen Guanghui, Sun Huankun, Yang Fan, Hong Liuzhi, Zou Yang, Chen Yu-Hsin, Liu Yanlong, Chen Li, Wang Fan, Wang Wei
Affiliated Cixi Hospital, Wenzhou Medical University, Ningbo, China.
School of Mental Health, Wenzhou Medical University, Wenzhou, China.
Front Psychiatry. 2022 Sep 29;13:1012850. doi: 10.3389/fpsyt.2022.1012850. eCollection 2022.
Previous studies suggest that alcohol dependence is associated with depression, however, the effect of alcohol dependence varies from individual to individual, which may be due to different genetic backgrounds. The interactions between alcohol dependence and different gene polymorphisms may finally shape the onset of depression. Neuropeptide Y (NPY), which can maintain homeostasis from high-stress stimulation, may protect individuals from the onset of depression. Here, we explored whether the NPY > has an association with depression in individuals with alcohol dependence during the period of alcohol dependence withdrawal.
A total of 455 males with alcohol dependence were recruited. The scale of Michigan Alcoholism Screening Test (MAST) and Self-Depression Scale (SDS) were respectively used to analyze the condition of alcohol dependence and depression. Genomic DNA was extracted from each blood sample and NPY polymorphisms were genotyped. The interaction between NPY > and alcohol dependence on depression was first analyzed. Then, region of significance analysis was used to confirm which model provided the best fit for the interaction (diathesis-stress or differential susceptibility). Finally, by using internal replication analyses, the accuracy and robustness of the interaction results were improved.
Alcohol dependence was positively correlated with depression. CC homozygotes of NPY > exhibited less depression when exposed to low alcohol dependence, but more depression when exposed to high alcohol dependence. Individuals with the T allele showed the opposite result.
NPY > might be correlated with susceptibility for depression in males during alcohol dependence withdrawal. The findings support the differential susceptibility model.
先前的研究表明酒精依赖与抑郁症有关,然而,酒精依赖的影响因人而异,这可能是由于不同的基因背景所致。酒精依赖与不同基因多态性之间的相互作用最终可能影响抑郁症的发病。神经肽Y(NPY)能够维持机体在高应激刺激下的内稳态,可能保护个体免受抑郁症的侵袭。在此,我们探讨了在酒精依赖戒断期,NPY是否与酒精依赖个体的抑郁症有关。
共招募了455名男性酒精依赖者。分别使用密歇根酒精ism筛查测试(MAST)量表和自评抑郁量表(SDS)分析酒精依赖和抑郁状况。从每份血样中提取基因组DNA,并对NPY多态性进行基因分型。首先分析NPY与酒精依赖对抑郁的相互作用。然后,使用显著性区域分析来确定哪种模型最适合这种相互作用(素质应激或差异易感性)。最后,通过内部重复分析,提高了相互作用结果的准确性和稳健性。
酒精依赖与抑郁症呈正相关。NPY的CC纯合子在低酒精依赖时抑郁程度较轻,但在高酒精依赖时抑郁程度较重。携带T等位基因的个体结果相反。
在酒精依赖戒断期,NPY可能与男性抑郁症易感性有关。这些发现支持差异易感性模型。