来自基因间研究的非裔美国母亲DNA甲基化年龄加速、抑郁症状和心脏代谢特征之间的关系。

IF 3.2 Q2 GENETICS & HEREDITY
Epigenetics Insights Pub Date : 2022-06-28 eCollection Date: 2022-01-01 DOI:10.1177/25168657221109781
Nicole Beaulieu Perez, Allison A Vorderstrasse, Gary Yu, Gail D'Eramo Melkus, Fay Wright, Stephen D Ginsberg, Cindy A Crusto, Yan V Sun, Jacquelyn Y Taylor
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引用次数: 0

摘要

背景:非裔美国妇女(AAW)同时患有心脏代谢(CM)疾病和抑郁症状的风险很高。CM患者同时出现抑郁症状的比率高于普通人群,加速衰老可能解释了这一点。在这项二次分析中,我们研究了年龄加速之间的关系;抑郁症状;以及AAW队列中的CM特征(高血压、糖尿病[DM]和肥胖)。方法:使用来自InterGEN队列(n=227)的基因组和临床数据。年龄加速是基于DNA甲基化(DNAm)年龄估计的Horvath方法。因此,DNAm年龄加速(DNAm-AA)被定义为DNAm年龄对时间年龄的线性回归的残差。Spearman相关性、线性和逻辑回归检验了DNAm AA、抑郁症状和CM特征之间的相关性。结果:DNAm-AA与抑郁症状总分无相关性。DNAm-AA与包括自我厌恶/自我憎恨在内的特定症状相关(-0.13,95%CI-0.26,-0.01);决策困难(-0.15,95%CI-0.28,-0.02);和对身体健康的担忧(0.15,95%CI 0.02,0.28),但在多次比较校正后没有统计学意义。调整潜在混杂因素后,DNAm AA与肥胖(0.08,95%CI 1.02,1.16)、高血压(0.08,95%CI 1.01,1.17)和糖尿病(0.20,95%CI 1.09,1.40)相关。结论:年龄加速和抑郁症状之间的关联可能非常微妙,并取决于研究设计背景。年龄加速以外的因素可能解释抑郁症状和CM特征之间的联系。具有CM特征的AAW可能会增加加速衰老的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Associations Between DNA Methylation Age Acceleration, Depressive Symptoms, and Cardiometabolic Traits in African American Mothers From the InterGEN Study.

Associations Between DNA Methylation Age Acceleration, Depressive Symptoms, and Cardiometabolic Traits in African American Mothers From the InterGEN Study.

Associations Between DNA Methylation Age Acceleration, Depressive Symptoms, and Cardiometabolic Traits in African American Mothers From the InterGEN Study.

Associations Between DNA Methylation Age Acceleration, Depressive Symptoms, and Cardiometabolic Traits in African American Mothers From the InterGEN Study.

Background: African American women (AAW) have a high risk of both cardiometabolic (CM) illness and depressive symptoms. Depressive symptoms co-occur in individuals with CM illness at higher rates than the general population, and accelerated aging may explain this. In this secondary analysis, we examined associations between age acceleration; depressive symptoms; and CM traits (hypertension, diabetes mellitus [DM], and obesity) in a cohort of AAW.

Methods: Genomic and clinical data from the InterGEN cohort (n = 227) were used. Age acceleration was based on the Horvath method of DNA methylation (DNAm) age estimation. Accordingly, DNAm age acceleration (DNAm AA) was defined as the residuals from a linear regression of DNAm age on chronological age. Spearman's correlations, linear and logistic regression examined associations between DNAm AA, depressive symptoms, and CM traits.

Results: DNAm AA did not associate with total depressive symptom scores. DNAm AA correlated with specific symptoms including self-disgust/self-hate (-0.13, 95% CI -0.26, -0.01); difficulty with making decisions (-0.15, 95% CI -0.28, -0.02); and worry over physical health (0.15, 95% CI 0.02, 0.28), but were not statistically significant after multiple comparison correction. DNAm AA associated with obesity (0.08, 95% CI 1.02, 1.16), hypertension (0.08, 95% CI 1.01, 1.17), and DM (0.20, 95% CI 1.09, 1.40), after adjustment for potential confounders.

Conclusions: Associations between age acceleration and depressive symptoms may be highly nuanced and dependent on study design contexts. Factors other than age acceleration may explain the connection between depressive symptoms and CM traits. AAW with CM traits may be at increased risk of accelerated aging.

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Epigenetics Insights
Epigenetics Insights GENETICS & HEREDITY-
CiteScore
5.10
自引率
0.00%
发文量
10
审稿时长
8 weeks
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