Neuroticism polygenic risk score predicts 20-year burden of depressive symptoms for Whites but not Blacks.

S. Assari, A. Javanbakht, Mohammed Saqib, H. Helmi, M. Bazargan, Jennifer A. Smith
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引用次数: 4

Abstract

Background Black-White differences are reported in social, psychological, behavioral, medical, and biological correlates of depression. This study was conducted to compare Black and White older adults for the association between neuroticism polygenic risk score (N-PRS) and chronicity of depressive symptoms over 20 years. Methods Data came from the Health and Retirement Study (HRS), 1990 - 2012, a nationally representative sample of Americans above age 50. Current analysis followed 9,249 individuals (7,924 Whites and 1,325 Blacks) for up to 22 years. Depressive symptoms were measured every two years between 1992 and 2012 using the 8-item Center for Epidemiological Studies-Depression Scale (CES-D-8). The independent variable was N-PRS. The dependent variable was average depressive symptoms between 1992 and 2012. Linear regression was used for data analysis. Results In the pooled sample, higher N-PRS was associated with higher average depressive symptoms over the 20-year follow up period [b=0.01, 95%CI=0.00 to 0.04], net of all covariates. We also found an interaction between race and N-PRS [b=-0.02, 95%CI=-0.03 to 0.00], suggesting a stronger effect of N-PRS on 20-year average depressive symptoms for Whites than Blacks. Based on our race-specific linear regression models, higher N-PRS was associated with higher depressive symptoms from 1992 to 2012 for Whites [b=0.01, 95%CI=0.01 to 0.02] but not Blacks [b=0.00, 95%CI=-0.02 to 0.02]. Conclusion Black and White older adults may differ in the salience of the existing N-PRS for depressive symptoms, which better reflects the burden of depression for Whites than Blacks. This may be because the existing PRSs are derived from mostly or exclusively White samples, limiting their applicability in other race groups. Racial variation in psychosocial, clinical, and biological correlates of depression needs further research.
神经质多基因风险评分预测白人20年抑郁症状负担,而非黑人。
背景据报道,黑人和白人在抑郁症的社会、心理、行为、医学和生物学方面存在差异。这项研究是为了比较黑人和白人老年人20年来神经质多基因风险评分(N-PRS)与抑郁症状的慢性性之间的关系。方法数据来自1990-2012年的健康与退休研究(HRS),这是一个具有全国代表性的50岁以上美国人样本。目前的分析对9249人(7924名白人和1325名黑人)进行了长达22年的跟踪调查。1992年至2012年间,每两年使用流行病学研究中心抑郁量表(CES-D-8)对抑郁症状进行一次测量。自变量为N-PRS。因变量是1992年至2012年间的平均抑郁症状。数据分析采用线性回归。结果在合并样本中,在20年的随访期内,较高的N-PRS与较高的平均抑郁症状相关[b=0.01,95%CI=0.00~0.04],扣除所有协变量。我们还发现种族和N-PRS之间存在相互作用[b=0.02,95%CI=0.03-0.00],这表明N-PRS对白人20年平均抑郁症状的影响比黑人更强。根据我们的种族特异性线性回归模型,从1992年到2012年,白人的N-PRS越高,抑郁症状就越严重[b=0.01,95%CI=0.01-0.02],而黑人则不然[b=0.00,95%CI=0.02-0.02],这比黑人更能反映白人的抑郁负担。这可能是因为现有的PRS大多或完全来自白人样本,限制了它们在其他种族群体中的适用性。抑郁症的社会心理、临床和生物学相关性的种族差异需要进一步研究。
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