Table 4.
Association of Epigenetic Age Acceleration With Multimorbidity Count and Multimorbidity Score Among All Women Eligible to Survive to Age 90 (N = 1 951)
Multimorbidity Count | Multimorbidity Score | |||
---|---|---|---|---|
RR (95% CI)* | p | RR (95% CI)* | p | |
AgeAccelHorvath | 0.99 (0.96–1.02) | .651 | 1.01 (0.98–1.04) | .448 |
AgeAccelHannum | 0.97 (0.94–1.01) | .105 | 0.98 (0.95–1.02) | .360 |
AgeAccelPheno | 1.04 (1.00–1.07) | .040 | 1.07 (1.04–1.10) | <.001* |
AgeAccelGrim | 1.00 (0.97–1.04) | .917 | 0.98 (0.95–1.01) | .252 |
Notes: All models were adjusted for the following baseline covariates: blood cell composition (CD8T, CD4T, NK, Bcell, Mono, Gran), age, race/ethnicity, education, walking frequency, BMI, alcohol consumption, pack-years smoking, broken hip, emphysema, arthritis, depression, urinary incontinency, and visual/auditory sensory impairment; and RAND physical functioning score. There were 1 022 women who survived to age 90 and 929 women who died before age 90. All models included an offset for age to account for differing lengths of follow-up. RR = relative risk; CI = confidence interval; SD = standard deviation; BMI = body mass index.
*Results are presented for one standard deviation increase in DNAmAge measure: AgeAccelHorvath (SD = 5.1 years), AgeAccelHannum (SD = 5.3 years), AgeAccelPheno (SD = 7.0 years), and AgeAccelGrim (SD = 3.9 years).
*p < .05.