Table 2:

Sex- and age-adjusted association between interleukin-6 levels at baseline and over the 5-year exposure period and aging phenotypes at 10-year follow-up *

Variable Successful aging
n = 721
Fatal or nonfatal CVD event
n = 321
Non-CVD death
n = 147
No. of patients OR (95% CI) No. of patients OR (95% CI) No. of patients OR (95% CI)
Interleukin-6 level at baseline
 Low (ref) 257 1.00 49 1.00 19 1.00
 Intermediate 344 0.64 (0.53–0.78) 158 1.47 (1.04–2.06) 58 1.39 (0.81–2.36)
 High 120 0.36 (0.28–0.46) 114 1.97 (1.37–2.82) 70 3.06 (1.80–5.18)
No. of times interleukin-6 level was high over 5-yr exposure period §
 0 (ref) 526 1.00 164 1.00 67 1.00
 1 145 0.58 (0.47–0.72) 98 1.47 (1.12–1.93) 41 1.48 (0.99–2.21)
 2 50 0.42 (0.31–0.58) 59 1.54 (1.30–2.35) 39 2.75 (1.80–4.20)
  • Note: CI = confidence interval, CVD = cardiovascular disease, OR = odds ratio, ref = reference group.

  • * Age- and sex-adjusted logistic regression assessed associations of inflammation with 3 outcomes: successful aging (v. normal aging, CVD event and non-CVD death phenotypes combined), total n = 3044; fatal or nonfatal CVD event (v. successful and normal aging phenotypes combined), total n = 2897 (excludes 147 participants who had a non-CVD death); and non-CVD death (v. successful and normal aging phenotypes combined), total n = 2723 (excludes 321 participants who had CVD event).

  • Free of major chronic disease and with optimal physical, mental and cognitive functioning.

  • Low = ≤ 1.0 ng/L, intermediate = 1.1–2.0 ng/L, high = > 2.0 ng/L.

  • § Interleukin-6 was measured twice (5 yr before baseline and at baseline); 0 = neither measurement was high, 1 = either measurement was high, 2 = both measurements were high.