Key result
Having both aortic valve sclerosis and mitral annulus calcification was associated with a significantly higher risk of all-cause mortality compared to no affected valves (HR 9.3; 95% CI 3.9-17.4; P<0.001).
Why the study?
Does the presence of aortic valve sclerosis and mitral annulus calcification predict all-cause and cardiovascular mortality in patients with type 2 diabetes?
Cohort (n=902)
Does the presence of aortic valve sclerosis and mitral annulus calcification predict all-cause and cardiovascular mortality in patients with type 2 diabetes?
Answers are grounded in this paper and cite their sources.
Aortic valve sclerosis and mitral annulus calcification are independently associated with a significantly increased risk of all-cause and cardiovascular mortality in type 2 diabetic patients.
OBJECTIVE: To examine the association of aortic valve sclerosis (AVS) and mitral annulus calcification (MAC) with all-cause and cardiovascular mortality in type 2 diabetic individuals. RESEARCH DESIGN AND METHODS: We retrospectively analyzed the data from 902 type 2 diabetic outpatients, who had undergone a transthoracic echocardiography for clinical reasons during the years 1992-2007. AVS and MAC were diagnosed by echocardiography, and a heart valve calcium (HVC) score was calculated by summing up the AVS and MAC variables. The study outcomes were all-cause and cardiovascular mortality. RESULTS: At baseline, 477 (52.9%) patients had no heart valves affected (HVC-0), 304 (33.7%) had one valve affected (HVC-1), and 121 (13.4%) had both valves affected (HVC-2). During a mean follow-up of 9 years, 137 (15.2%) patients died, 78 of them from cardiovascular causes. Compared with patients with HVC-0, those with HVC-2 had the highest risk of all-cause and cardiovascular mortality, whereas those with HVC-1 had an intermediate risk (P < 0.0001 by the log-rank test). After adjustment for sex, age, BMI, systolic blood pressure, diabetes duration, A1C, LDL cholesterol, estimated glomerular filtration rate, smoking, history of myocardial infarction, and use of antihypertensive and lipid-lowering drugs, the hazard ratio of all-cause mortality was 2.3 (95% CI 1.1-4.9; P < 0.01) for patients with HVC-1 and 9.3 (3.9-17.4; P < 0.001) for those with HVC-2. Similar results were found for cardiovascular mortality. CONCLUSIONS: Our findings indicate that AVS and MAC, singly or in combination, are independently associated with all-cause and cardiovascular mortality in type 2 diabetic patients.
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Rossi et al. (2012) conducted a cohort in Type 2 diabetes (n=902). Aortic valve sclerosis (AVS) and mitral annulus calcification (MAC) vs. No heart valves affected (HVC-0) was evaluated on All-cause mortality (HR 9.3, 95% CI 3.9-17.4, p=< 0.001). Having both aortic valve sclerosis and mitral annulus calcification was associated with a significantly higher risk of all-cause mortality compared to no affected valves (HR 9.3; 95% CI 3.9-17.4; P<0.001).
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