Key result
Somatic depressive symptoms linked to ~8% higher mortality and MACE in suspected myocardial ischemia.
Why the study?
Previous research suggested somatic depression symptoms may contribute to IHD risk factors and MACE in women, but whether somatic versus cognitive symptoms differentially predict biomedical risk and adverse outcomes required further study.
Do somatic symptoms of depression predict metabolic syndrome and cardiac events better than cognitive symptoms in women with suspected myocardial ischemia?
Cohort (n=1,000)
Yes
Do somatic symptoms of depression predict metabolic syndrome and cardiac events better than cognitive symptoms in women with suspected myocardial ischemia?
Hazard Ratio: 1.08 (95% CI 1.01–1.15)
p-value: p=<0.05
Somatic symptoms of depression, but not cognitive symptoms, are independently associated with metabolic syndrome and predict all-cause mortality and MACE in women with suspected myocardial ischemia.
May support somatic symptom assessment for prognosis in women with suspected ischemia; leaves open causal mechanisms and intervention effects.
Background: Ischemic heart disease (IHD) risk in women includes biomedical, behavioral, and psychosocial contributors. The purpose of this study was to build upon previous research suggesting that in women, somatic symptoms (SS) of depression may be important to the development of IHD risk factors and major adverse cardiovascular events (MACE). Based on previous findings, we hypothesized that: (1) SS would be associated with robust biomedical predictors of heart disease and functional capacity, while cognitive symptoms (CS) of depression would not, and (2) SS would independently predict adverse health outcomes while CS would not. Methods: We examined the relationships between symptoms of depression (SS/CS), metabolic syndrome (MetS), inflammatory markers (IM), coronary artery disease (CAD) severity, and functional capacity in two independent cohorts of women with suspected IHD. In the Women's Ischemia Syndrome Evaluation (WISE), we also examined these variables as predictors of all-cause mortality (ACM) + MACE over a median 9.3-year follow-up. The WISE sample included 641 women with suspected ischemia with or without obstructive CAD. The WISE-Coronary Vascular Dysfunction (WISE-CVD) sample consisted of 359 women with suspected ischemia and no obstructive CAD. All study measures were collected uniformly at baseline. Depressive symptoms were measured via the Beck Depression Inventory. MetS was assessed according to Adult Treatment Panel III (ATP-III) criteria. Results: < 0.05, respectively), while CS was not. Within WISE, using Cox Proportional Hazard Regression, SS (Hazard ratio [HR] = 1.08, 95% confidence interval [CI] = 1.01-1.15; HR = 1.07, 95% CI = 1.00-1.13) and MetS (HR = 1.89, 95% CI = 1.16-3.08; HR = 1.74, 95% CI=1.07-2.84) were independent predictors of ACM + MACE after controlling for demographics, IM, and CAD severity, while CS was not. Conclusions: In two independent samples of women undergoing coronary angiography due to suspected ischemia, SS but not CS of depression were associated with MetS, and both SS and MetS independently predicted ACM and MACE. These results add to previous studies suggesting that SS of depression may warrant specific attention in women with elevated cardiovascular disease (CVD) risk. Future research evaluating the biobehavioral basis of the relationship between depression, MetS, and CVD is needed.
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Virzi et al. (2022) conducted a cohort in Suspected myocardial ischemia (n=1,000). Somatic symptoms of depression vs. Cognitive symptoms of depression was evaluated on All-cause mortality and major adverse cardiovascular events (ACM + MACE) (HR 1.08, 95% CI 1.01-1.15, p=<0.05). Somatic symptoms of depression independently predicted all-cause mortality and major adverse cardiovascular events (HR 1.08) in women with suspected myocardial ischemia, whereas cognitive symptoms did not.
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