Subclinical left ventricular diastolic dysfunction and incident type 2 diabetes risk: the Korean Genome and Epidemiology Study
- Authors
- Park, Juri; Kim, Jin-Seok; Kim, Seong Hwan; Kim, Sunwon; Lim, Sang Yup; Lim, Hong-Euy; Cho, Goo-Yeong; Sung, Ki-Chul; Kim, Jang-Young; Baik, Inkyung; Koh, Kwang Kon; Lee, Jung Bok; Lee, Seung Ku; Shin, Chol
- Issue Date
- 14-Mar-2017
- Publisher
- BIOMED CENTRAL LTD
- Keywords
- Left ventricle; Diastolic dysfunction; Tissue Doppler echocardiography; Type 2 diabetes; Cohort
- Citation
- CARDIOVASCULAR DIABETOLOGY, v.16
- Journal Title
- CARDIOVASCULAR DIABETOLOGY
- Volume
- 16
- URI
- https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/6316
- DOI
- 10.1186/s12933-017-0519-5
- ISSN
- 1475-2840
- Abstract
- Background: Subclinical left ventricular (LV) diastolic dysfunction in type 2 diabetes (T2D) is a common finding and represents an early sign of diabetic cardiomyopathy. However, the relationship between LV diastolic dysfunction and the incident T2D has not been previously studied. Methods: A total of 1817 non-diabetic participants (mean age, 54 years; 48% men) from the Korean Genome and Epidemiology Study who were free of cardiovascular disease were studied. LV structure and function were assessed by conventional echocardiography and tissue Doppler imaging. Subclinical LV diastolic dysfunction was defined using age-specific cutoff limits for early diastolic (Em) velocity, mitral E/Em ratio, and left atrial volume index. Results: During the 6-year follow-up period, 273 participants (15%) developed T2D. Participants with incident T2D had greater LV mass index (86.7 +/- 16.4 vs. 91.2 +/- 17.0 g/m(2)), worse diastolic function, reflected by lower Em velocity (7.67 +/- 1.80 vs. 7.47 +/- 1.70) and higher E/Em ratio (9.19 +/- 2.55 vs. 10.23 +/- 3.00), and higher prevalence of LV diastolic dysfunction (34.6 vs. 54.2%), compared with those who did not develop T2D (all P < 0.001). In a multivariate logistic regression model, lower Em velocity (odd ratio [OR], 0.867; 95% confidence interval [CI] 0.786-0.957) and the presence of LV diastolic dysfunction (OR, 1.617; 95% CI 1.191-2.196) were associated with the development of T2D, after adjusting for potential confounding factors. Conclusions: In a community-based cohort, the presence of subclinical LV diastolic dysfunction was a predictor of the progression to T2D. These data suggest that the echocardiographic assessment of LV diastolic function may be helpful in identifying non-diabetic subjects at risk of incident T2D.
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