Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Institute for Genomic Medicine, Columbia University, 701 West 168th Street, New York, NY, 10032, USA.
Clin Epigenetics. 2021 Feb 25;13(1):42. doi: 10.1186/s13148-021-01028-2.
Cardiovascular health (CVH) has been defined by the American Heart Association (AHA) as the presence of the "Life's Simple 7" ideal lifestyle and clinical factors. CVH is known to predict longevity and freedom from cardiovascular disease, the leading cause of death for women in the United States. DNA methylation markers of aging have been aggregated into a composite epigenetic age score, which is associated with cardiovascular morbidity and mortality. However, it is unknown whether poor CVH is associated with acceleration of aging as measured by DNA methylation markers in epigenetic age.
We performed a cross-sectional analysis of racially/ethnically diverse post-menopausal women enrolled in the Women's Health Initiative cohort recruited between 1993 and 1998. Epigenetic age acceleration (EAA) was calculated using DNA methylation data on a subset of participants and the published Horvath and Hannum methods for intrinsic and extrinsic EAA. CVH was calculated using the AHA measures of CVH contributing to a 7-point score. We examined the association between CVH score and EAA using linear regression modeling adjusting for self-reported race/ethnicity and education. Among the 2,170 participants analyzed, 50% were white and mean age was 64 (7 SD) years. Higher or more favorable CVH scores were associated with lower extrinsic EAA (~ 6 months younger age per 1 point higher CVH score, p < 0.0001), and lower intrinsic EAA (3 months younger age per 1 point higher CVH score, p < 0.028).
These cross-sectional observations suggest a possible mechanism by which ideal CVH is associated with greater longevity.
心血管健康 (CVH) 已被美国心脏协会 (AHA) 定义为存在“生命的七大简单要素”理想生活方式和临床因素。CVH 已知可预测长寿和免于心血管疾病,这是美国女性的主要死因。衰老的 DNA 甲基化标志物已被汇总为一个综合表观遗传年龄评分,与心血管发病率和死亡率相关。然而,尚不清楚较差的 CVH 是否与 DNA 甲基化标志物所衡量的表观遗传年龄加速衰老有关。
我们对 1993 年至 1998 年间参加妇女健康倡议队列的、种族/民族多样化的绝经后女性进行了横断面分析。使用部分参与者的 DNA 甲基化数据和已发表的 Horvath 和 Hannum 内在和外在表观遗传年龄加速 (EAA) 方法计算表观遗传年龄加速 (EAA)。使用 AHA 对 CVH 的测量来计算 CVH,这些测量有助于计算 7 分制的 CVH 评分。我们使用线性回归模型,在调整了自我报告的种族/民族和教育背景后,研究了 CVH 评分与 EAA 之间的关联。在分析的 2170 名参与者中,50%为白人,平均年龄为 64(7 标准差)岁。更高或更有利的 CVH 评分与外在 EAA 降低相关(CVH 评分每增加 1 分,EAA 降低约 6 个月,p<0.0001),与内在 EAA 降低相关(CVH 评分每增加 1 分,EAA 降低 3 个月,p<0.028)。
这些横断面观察结果表明,理想的 CVH 与长寿相关的一种可能机制。