Does depression increase the risk of cardiovascular events and all-cause mortality in adults with type 2 diabetes at high risk for cardiovascular events?
In adults with type 2 diabetes at high cardiovascular risk, depression is associated with a significantly increased risk of all-cause mortality, though not significantly with the primary composite cardiovascular outcome.
OBJECTIVE: Depression affects up to 20-25% of adults with type 2 diabetes and may increase all-cause mortality, but few well-designed studies have examined the effects of depression on the full range of cardiovascular disease outcomes in type 2 diabetes. RESEARCH DESIGN AND METHODS: A total of 2,053 participants in the ACCORD (Action to Control Cardiovascular Risk in Diabetes) Health-Related Quality of Life substudy completed the Patient Health Questionnaire (PHQ)-9 measure of depression symptoms at baseline and 12, 36, and 48 months. Cox proportional hazards regression models were used to estimate hazard ratios (HRs) (95% CI) for the time-varying impact of depression on protocol-defined clinical outcomes with and without adjustment for demographic, trial-related, clinical, and behavioral variables. RESULTS: In fully adjusted models, depression was not significantly related to the ACCORD primary composite outcome (cardiovascular death, nonfatal heart attack, or stroke) (HR 1.53 95% CI 0.85-2.73) or to the ACCORD microvascular composite outcome (0.93 0.53-1.62), but all-cause mortality was significantly increased both in those with PHQ-assessed probable major depression (2.24 1.24-4.06) and PHQ score of ≥ 10 (1.84 1.17-2.89). The effect of depression on all-cause mortality was not related to previous cardiovascular events or to assignment to intensive or standard glycemia control. Probable major depression (by PHQ-9) had a borderline impact on the ACCORD macrovascular end point (1.42 0.99-2.04). CONCLUSIONS: Depression increases the risk of all-cause mortality and may increase the risk of macrovascular events among adults with type 2 diabetes at high risk for cardiovascular events.
Sullivan et al. (Thu,) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: