Assari Shervin, Javanbakht Arash, Saqib Mohammed, Helmi Hamid, Bazargan Mohsen, Smith Jennifer A
Department of Family Medicine, Charles R Drew University of Medicine and Science, Los Angeles, CA, USA.
Department of Psychiatry and Behavioral Neuroscience, Wayne State University, Detroit, MI, USA.
J Med Res Innov. 2020;4(1). doi: 10.32892/jmri.183. Epub 2019 Aug 26.
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.
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.
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].
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.
抑郁症的社会、心理、行为、医学和生物学相关因素存在黑人和白人差异。本研究旨在比较黑人和白人老年人的神经质多基因风险评分(N-PRS)与20年期间抑郁症状慢性化之间的关联。
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。当前分析对9249名个体(7924名白人,1325名黑人)进行了长达22年的跟踪。在1992年至2012年期间,每两年使用8项流行病学研究中心抑郁量表(CES-D-8)测量一次抑郁症状。自变量是N-PRS。因变量是1992年至2012年期间的平均抑郁症状。使用线性回归进行数据分析。
在合并样本中,排除所有协变量后,较高的N-PRS与20年随访期内较高的平均抑郁症状相关[b = 0.01,95%CI = 0.00至0.04]。我们还发现种族与N-PRS之间存在交互作用[b = -0.02,95%CI = -0.03至0.00],表明N-PRS对白人20年平均抑郁症状的影响比对黑人更强。根据我们的种族特异性线性回归模型,较高的N-PRS与1992年至2012年期间白人较高的抑郁症状相关[b = 0.01,95%CI = 0.01至0.02],但与黑人无关[b = 0.00,95%CI = -0.02至0.02]。
黑人和白人老年人在现有N-PRS对抑郁症状的显著性方面可能存在差异,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、临床和生物学相关因素的种族差异需要进一步研究。