A 5-unit increase in the CES-D depression score over time was associated with a 25% increased risk of all-cause mortality (RR 1.25; 95% CI 1.15-1.36) and an 18% increased risk of stroke or MI.
RCT (n=4,367)
double-blind
randomized
Yes
Effect estimate: RR 1.25 (95% CI 1.15 to 1.36)
OBJECTIVE: To determine the relationship between increasing depressive symptoms and cardiovascular events or mortality. DESIGN: Cohort analytic study of data from randomized placebo-controlled double-blind clinical trial of antihypertensive therapy. Depressive symptoms were assessed semi-annually with the Center for Epidemiological Studies-Depression (CES-D) scale during an average follow-up of 4.5 years. SETTING: Ambulatory patients in 16 clinical centers of the Systolic Hypertension in the Elderly Program. PATIENTS: Generally healthy men and women aged 60 years or older randomized to active antihypertensive drug therapy or placebo who were 70% white and 53% women and had follow-up CES-D scores and no outcome events during the first 6 months (N=4367). MAIN OUTCOME MEASURES: All-cause mortality, fatal or nonfatal stroke, or myocardial infarction. RESULTS: Baseline depressive symptoms were not related to subsequent events; however, an increase in depression was prognostic. Cox proportional hazards regression analyses with the CES-D scale as a time-dependent variable, controlling for multiple covariates, indicated a 25% increased risk of death per 5-unit increase in the CES-D score (relative risk RR, 1.25;95% confidence interval CI, 1.15 to 1.36). The RR for stroke or myocardial infarction was 1.18(95%CI,1.08 to 1.30). Increase in CES-D score was an independent predictor in both placebo and active drug groups, and it was strongest as a risk factor for stroke among women (RR,1.29;95%CI,1.07 to 1.34). CONCLUSIONS: Among elderly persons, a significant and substantial excess risk of death and stroke or myocardial infarction was associated with an increase in depressive symptoms over time, which may be a marker for subsequent major disease events and warrants the attention of physicians to such mood changes. However, further studies of casual pathways are needed before wide-spread screening for depression in clinical practice is to be recommended.
Sylvia Wassertheil‐Smoller (Mon,) conducted a rct in Systolic hypertension (n=4,367). Increase in depressive symptoms was evaluated on All-cause mortality (RR 1.25, 95% CI 1.15 to 1.36). A 5-unit increase in the CES-D depression score over time was associated with a 25% increased risk of all-cause mortality (RR 1.25; 95% CI 1.15-1.36) and an 18% increased risk of stroke or MI.