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哥斯达黎加精神分裂症患者血清素转运体启动子基因多态性(5-HTTLPR)与抑郁症的关联。

Association of serotonin transporter promoter gene polymorphism (5-HTTLPR) with depression in Costa Rican schizophrenic patients.

作者信息

Contreras Javier, Hernández Sandra, Quezada Paulina, Dassori Albana, Walss-Bass Consuelo, Escamilla Michael, Raventos Henriette

机构信息

Psychiatric Genetics Research Center, Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, USA.

出版信息

J Neurogenet. 2010 Jul;24(2):83-9. doi: 10.3109/01677060903583994.

Abstract

Depression and suicidal behavior are frequently observed in patients with schizophrenia. The serotonin transporter protein regulates serotonergic signaling at synapses and is encoded by a single gene (SLC6A4; Locus Link ID: 6532), located at 17q11.1-q12 with two polymorphic variants (the short and the long allele). The short allele of serotonin transporter gene has been associated with depression and suicidality in individuals who suffered negative life events and with depression in individuals with chronic psychosis.. Subjects were recruited from a genetic study of schizophrenia conducted in Costa Rica. The authors replicated their previous research, using a more narrow phenotype (only schizophrenic subjects) and a more ethnically homogenous sample (only Costa Rican schizophrenic individuals who were not included in the previous study). The authors hypothesized that subjects with at least one copy of the serotonin transporter promoter gene polymorphism (5-HTTLPR) "s" allele would have a greater history of lifetime depression and suicidability rate than those who had an "l/l" genotype. The authors analyzed 155 subjects with a DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition) diagnosis of schizophrenia (73% male, age at interview 38.3, SD = 11.23). The genotype distribution was "ss" 58 (37%), "sl" 69 (45%), and "ll" 28 (18%). In the secondary analysis, the authors explored association of the "s" allele with lifetime history of suicide behavior in 173 subjects (18 more subjects than primary analysis because schizophrenic individuals were included regardless of history of depression). The authors found that subjects carrying at least one short allele had a significant increased lifetime risk for depressive syndromes (chi(2) = 5.4, df = 1, P = 0.02; odds ratio [OR] = 2.7, 95% confidence interval [CI] = 1.15-6.3). No association was found for suicidal behavior in the same sample (chi(2) = 0.928, P = 0.629). In conclusion, the genotype at the 5-HTTLPR promoter polymorphic locus increases the risk of developing major depression but not suicidal behavior during the course of the schizophrenia in these patients. Due to the small sample size, these results should be followed by definitive replication.

摘要

抑郁症和自杀行为在精神分裂症患者中很常见。血清素转运蛋白调节突触处的血清素信号传导,由位于17q11.1-q12的单个基因(SLC6A4;基因座链接ID:6532)编码,该基因有两个多态性变体(短等位基因和长等位基因)。血清素转运蛋白基因的短等位基因与经历过负面生活事件的个体的抑郁症和自杀倾向以及慢性精神病患者的抑郁症有关。研究对象来自在哥斯达黎加进行的一项精神分裂症基因研究。作者重复了他们之前的研究,采用了更狭义的表型(仅精神分裂症患者)和种族更同质的样本(仅之前研究未纳入的哥斯达黎加精神分裂症患者)。作者假设,携带至少一份血清素转运蛋白启动子基因多态性(5-HTTLPR)“s”等位基因的受试者比那些具有“l/l”基因型的受试者有更高的终生抑郁症病史和自杀倾向率。作者分析了155名符合《精神疾病诊断与统计手册》第四版(DSM-IV)精神分裂症诊断标准的受试者(73%为男性,访谈时年龄38.3岁,标准差=11.23)。基因型分布为“ss”58例(37%),“sl”69例(45%),“ll”28例(18%)。在二次分析中,作者探讨了173名受试者(比初次分析多18名受试者,因为纳入了无论有无抑郁症病史的精神分裂症患者)中“s”等位基因与自杀行为终生史的关联。作者发现,携带至少一个短等位基因的受试者患抑郁综合征的终生风险显著增加(卡方=5.4,自由度=1,P=0.02;优势比[OR]=2.7,95%置信区间[CI]=1.15-6.3)。在同一样本中未发现与自杀行为的关联(卡方=0.928,P=0.629)。总之,5-HTTLPR启动子多态性位点的基因型增加了这些患者在精神分裂症病程中发生重度抑郁症的风险,但未增加自杀行为的风险。由于样本量小,这些结果应随后进行确定性重复研究。

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