Association between inflammatory-related disease burden and frailty: Results from the Women's Health and Aging Studies (WHAS) I and II
Abstract
Frailty is associated with a pro-inflammatory state, which has been characterized by elevated levels of systemic inflammatory biomarkers, but has not been related to the number of co-existing chronic diseases associated with inflammation. We sought to determine the extent to which a higher number of inflammatory-related diseases is associated with frailty and to identify the most common disease patterns associated with being frail in older adults. We performed binomial regression analyses to assess whether a higher count of inflammatory-related diseases increases the probability of frailty using data from the WHAS I and II, companion cohorts composed of 70–79-year-old community-dwelling older women in Baltimore, Maryland (n
=
620). An increase of one inflammatory-related disease was associated log-linearly with frailty (Prevalence Ratio (PR)
=
2.28, 95% Confidence Interval (CI)
=
1.81–2.87). After adjusting for age, race, education, and smoking status, the probability of frailty remained significant (PR
=
1.97, 95%CI
=
1.52–2.55). In the frail population, chronic kidney disease (CKD) and depressive symptoms (Prevalence
=
22.9%, 95%CI
=
14.2–34.8%); CVD and depressive symptoms (21.7%, 95%CI
=
13.2–33.5%); CKD and anemia (18.7%, 95%CI
=
11.1–29.7%); cardiovascular disease (CVD), CKD, and pulmonary disease (10.7%, 95%CI
=
5.2–21.0%); CKD, anemia, and depressive symptoms (8.7%, 95%CI
=
3.9–18.2%); and CVD, anemia, pulmonary disease, and depressive symptoms (5.0%, 95%CI
=
1.6–14.4%) were among the most frequent disease combinations. Their prevalence percentages were significantly higher in the frail versus non-frail women. A higher inflammatory-related disease count, perhaps reflecting a greater pro-inflammatory burden, increases the likelihood of frailty. Shared mechanisms among specific disease combinations may further contribute to this risk.
Keywords: Comorbidity, Inflammation, Frailty
PII: S0167-4943(11)00130-0
doi:10.1016/j.archger.2011.05.020
© 2011 Elsevier Ireland Ltd. All rights reserved.
