The "S" Allele of the Serotonin Transporter Is Not Associated with Major Depression or Alcohol Use Disorders in a Veteran Sample.

Jack R Cornelius, Gretchen L Haas, Gerald Goldstein, Barbara Hanusa, Jon D Walker, Lauren J Fox, Dennis Daley, Antoine Douaihy, Gloria Klima, James Ferrell
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Abstract

The results of some studies suggest that the serotonin transporter-linked polymorphic region (5-HTTLPR) short (S) allele, relative to the long (L) allele, is associated with risk for Major Depressive Disorder (MDD) and for Alcohol Use Disorder (AUD), and thus serves as biomarker for those disorders, while results from other studies do not support that conclusion. Persons with an S allele demonstrate a 2- to 2.5 fold decrease in serotonin transcription rate compared to the L-allele, which may increase their risk for MDD. Differences in study populations may help explain the differences in findings between those meta-analyses. To date, there have been no published reports which have addressed the possible association between the S allele and MDD among military veterans. This manuscript describes a first study to assess the possible association of the S allele with MDD or with AUD among a study population of veterans in treatment for a substance use disorder. We hypothesized that the S allele would be associated with MDD in our study sample. Subjects signing informed consent were 101 Veterans recruited from VA behavioral health and substance use treatment clinics in the VA Pittsburgh Healthcare System, and 91 of those subjects were genotyped for 5-HTTLPR polymorphisms. The study sample from whom genetic material was collected included 82 males and 9 females, of whom 53 were white, 38 were black, and one was "other". Fifty-four members of the study sample (59%) met DSM-IV criteria for an MDD on the SCID. Forty-five of the subjects demonstrated one or two S alleles, while 46 did not do so. The presence of the S allele of the serotonin transporter was not found to be significantly associated with the diagnosis of major depressive disorder or with alcohol use disorders in our sample. Those findings, in combination with other recent negative findings from other researchers involving non-veterans, raise questions regarding the clinical utility of utilizing genetics tests involving the assessment of the alleles of the serotonin transporter as a possible biomarker for MDD or for AUD.

在退伍军人样本中,血清素转运体的“S”等位基因与重度抑郁症或酒精使用障碍无关。
一些研究结果表明,相对于长(L)等位基因,5-HTTLPR短(S)等位基因与重度抑郁症(MDD)和酒精使用障碍(AUD)的风险相关,因此可以作为这些疾病的生物标志物,而其他研究的结果并不支持这一结论。携带S等位基因的人血清素转录率比携带l等位基因的人低2- 2.5倍,这可能会增加他们患重度抑郁症的风险。研究人群的差异可能有助于解释这些荟萃分析结果之间的差异。到目前为止,还没有发表过关于退伍军人中S等位基因与抑郁症之间可能存在联系的报告。这篇论文描述了第一项研究,评估了在治疗药物使用障碍的退伍军人研究人群中,S等位基因与重度抑郁症或澳元的可能关联。在我们的研究样本中,我们假设S等位基因与重度抑郁症有关。签署知情同意书的受试者是101名退伍军人,他们来自退伍军人行为健康和物质使用治疗诊所,其中91名受试者进行了5-HTTLPR多态性基因分型。收集遗传物质的研究样本包括82名男性和9名女性,其中53名白人,38名黑人,1名“其他”。研究样本中的54名成员(59%)符合DSM-IV在SCID上的重度抑郁症标准。45名受试者表现出一个或两个S等位基因,46名没有。在我们的样本中,血清素转运体S等位基因的存在与重度抑郁症或酒精使用障碍的诊断没有显著关联。这些发现,结合其他研究人员最近对非退伍军人的其他负面发现,提出了关于利用遗传学测试的临床应用的问题,包括评估5 -羟色胺转运体的等位基因,作为MDD或AUD的可能生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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