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The serotonin transporter gene and depression.血清素转运体基因与抑郁症。
Depress Anxiety. 2012 Nov;29(11):915-7. doi: 10.1002/da.22009. Epub 2012 Oct 26.
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Early menarcheal age and risk for later depressive symptomatology: the role of childhood depressive symptoms.初潮年龄与后期抑郁症状的关系:儿童抑郁症状的作用。
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Stress, coping, and depression: testing a new hypothesis in a prospectively studied general population sample of U.S.-born Whites and Blacks.压力、应对方式和抑郁:在美国出生的白人和黑人的前瞻性一般人群样本中检验一个新假设。
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The serotonin transporter promoter variant (5-HTTLPR), stress, and depression meta-analysis revisited: evidence of genetic moderation.血清素转运体启动子变体(5-HTTLPR)、压力与抑郁的元分析再探讨:基因调节的证据
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Race and unhealthy behaviors: chronic stress, the HPA axis, and physical and mental health disparities over the life course.种族与不良行为:慢性压力、HPA 轴与生命历程中的身心健康差异。
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非裔美国女性和欧裔美国女性患重度抑郁症的遗传和环境风险。

Genetic and environmental risk for major depression in African-American and European-American women.

作者信息

Duncan Alexis E, Munn-Chernoff Melissa A, Hudson Darrell L, Eschenbacher Michaela A, Agrawal Arpana, Grant Julia D, Nelson Elliot C, Waldron Mary, Glowinski Anne L, Sartor Carolyn E, Bucholz Kathleen K, Madden Pamela A F, Heath Andrew C

机构信息

George Warren Brown School of Social Work,Washington University,St. Louis,MO,USA.

Midwest Alcoholism Research Center,Washington University School of Medicine,St. Louis,MO,USA.

出版信息

Twin Res Hum Genet. 2014 Aug;17(4):244-53. doi: 10.1017/thg.2014.28. Epub 2014 Jun 9.

DOI:10.1017/thg.2014.28
PMID:24910290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4222066/
Abstract

It is unknown whether there are racial differences in the heritability of major depressive disorder (MDD) because most psychiatric genetic studies have been conducted in samples comprised largely of white non-Hispanics. To examine potential differences between African-American (AA) and European-American (EA) young adult women in (1) Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) MDD prevalence, symptomatology, and risk factors, and (2) genetic and/or environmental liability to MDD, we analyzed data from a large population-representative sample of twins ascertained from birth records (n = 550 AA and n = 3226 EA female twins) aged 18-28 years at the time of MDD assessment by semi-structured psychiatric interview. AA women were more likely to have MDD risk factors; however, there were no significant differences in lifetime MDD prevalence between AA and EA women after adjusting for covariates (odds ratio = 0.88, 95% confidence interval [CI]: 0.67-1.15). Most MDD risk factors identified among AA women were also associated with MDD at similar magnitudes among EA women. Although the MDD heritability point estimate was higher among AA women than EA women in a model with paths estimated separately by race (56%, 95% CI: 29-78% vs. 41%, 95% CI: 29-52%), the best fitting model was one in which additive genetic and non-shared environmental paths for AA and EA women were constrained to be equal (A = 43%, 33-53% and E = 57%, 47-67%). In spite of a marked elevation in the prevalence of environmental risk exposures related to MDD among AA women, there were no significant differences in lifetime prevalence or heritability of MDD between AA and EA young women.

摘要

目前尚不清楚重度抑郁症(MDD)的遗传力是否存在种族差异,因为大多数精神科遗传学研究都是在主要由非西班牙裔白人组成的样本中进行的。为了研究非裔美国(AA)和欧裔美国(EA)年轻成年女性在以下方面的潜在差异:(1)《精神疾病诊断与统计手册》第4版(DSM-IV)中MDD的患病率、症状学和风险因素;(2)MDD的遗传和/或环境易感性,我们分析了一个具有广泛代表性的双胞胎大样本数据,这些双胞胎通过出生记录确定(n = 550名AA女性双胞胎和n = 3226名EA女性双胞胎),在通过半结构化精神科访谈进行MDD评估时年龄为18 - 28岁。AA女性更有可能具有MDD风险因素;然而,在调整协变量后,AA和EA女性的终生MDD患病率没有显著差异(优势比 = 0.88,95%置信区间[CI]:0.67 - 1.15)。在AA女性中确定的大多数MDD风险因素在EA女性中也与MDD有相似程度的关联。尽管在一个按种族分别估计路径的模型中,AA女性的MDD遗传力点估计值高于EA女性(56%,95% CI:29 - 78%对41%,95% CI:29 - 52%),但最佳拟合模型是将AA和EA女性的加性遗传和非共享环境路径约束为相等的模型(A = 43%,33 - 53%;E = 57%,47 - 67%)。尽管与MDD相关的环境风险暴露在AA女性中的患病率显著升高,但AA和EA年轻女性在MDD的终生患病率或遗传力方面没有显著差异。