Musliner K L, Seifuddin F, Judy J A, Pirooznia M, Goes F S, Zandi P P
Department of Mental Health,Bloomberg School of Public Health,Johns Hopkins University,Baltimore,MD,USA.
Department of Psychiatry and Behavioral Sciences,Johns Hopkins Institute of Medicine,Baltimore,MD,USA.
Psychol Med. 2015 Jun;45(8):1709-20. doi: 10.1017/S0033291714002839. Epub 2014 Dec 9.
Previous studies suggest that the relationship between genetic risk and depression may be moderated by stressful life events (SLEs). The goal of this study was to assess whether SLEs moderate the association between polygenic risk of major depressive disorder (MDD) and depressive symptoms in older adults.
We used logistic and negative binomial regressions to assess the associations between polygenic risk, SLEs and depressive symptoms in a sample of 8761 participants from the Health and Retirement Study. Polygenic scores were derived from the Psychiatric Genomics Consortium genome-wide association study of MDD. SLEs were operationalized as a dichotomous variable indicating whether participants had experienced at least one stressful event during the previous 2 years. Depressive symptoms were measured using an eight-item Center for Epidemiologic Studies Depression Scale subscale and operationalized as both a dichotomous and a count variable.
The odds of reporting four or more depressive symptoms were over twice as high among individuals who experienced at least one SLE (odds ratio 2.19, 95% confidence interval 1.86-2.58). Polygenic scores were significantly associated with depressive symptoms (β = 0.21, p ⩽ 0.0001), although the variance explained was modest (pseudo r 2 = 0.0095). None of the interaction terms for polygenic scores and SLEs was statistically significant.
Polygenic risk and SLEs are robust, independent predictors of depressive symptoms in older adults. Consistent with an additive model, we found no evidence that SLEs moderated the association between common variant polygenic risk and depressive symptoms.
先前的研究表明,遗传风险与抑郁症之间的关系可能会受到生活应激事件(SLEs)的调节。本研究的目的是评估SLEs是否会调节老年人中重度抑郁症(MDD)的多基因风险与抑郁症状之间的关联。
我们使用逻辑回归和负二项回归,在来自健康与退休研究的8761名参与者样本中,评估多基因风险、SLEs与抑郁症状之间的关联。多基因分数来自精神疾病基因组学联盟对MDD的全基因组关联研究。SLEs被操作为一个二分变量,表明参与者在过去2年中是否经历过至少一次应激事件。抑郁症状使用一个包含8个条目的流行病学研究中心抑郁量表子量表进行测量,并操作为二分变量和计数变量。
在经历过至少一次SLE的个体中,报告有四种或更多抑郁症状的几率是其他人的两倍多(优势比2.19,95%置信区间1.86 - 2.58)。多基因分数与抑郁症状显著相关(β = 0.21,p⩽0.0001),尽管所解释的方差较小(伪r² = 0.0095)。多基因分数与SLEs的交互项均无统计学意义。
多基因风险和SLEs是老年人抑郁症状的有力、独立预测因素。与相加模型一致,我们没有发现证据表明SLEs调节了常见变异多基因风险与抑郁症状之间的关联。