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Sex Difference in the Association Between Metabolic Syndrome and Left Ventricular Diastolic Dysfunction
- Sex Difference in the Association Between Metabolic Syndrome and Left Ventricular Diastolic Dysfunction
- Kim, Hack-Lyoung; Kim, Myung-A; Oh, Sohee; Kim, Mina; Park, Seong Mi; Yoon, Hyun Ju; Shin, Mi Seung; Hong, Kyung-Soon; Shin, Gil Ja; Shim, Wan-Joo
- Ewha Authors
- SCOPUS Author ID
- Issue Date
- Journal Title
- METABOLIC SYNDROME AND RELATED DISORDERS
- 1540-4196; 1557-8518
- vol. 14, no. 10, pp. 507 - 512
- coronary artery disease; diastolic function; metabolic syndrome; sex
- MARY ANN LIEBERT, INC
- SCIE; SCOPUS
- Background: Sex-related differences in the influence of metabolic syndrome (MetS) on various cardiovascular diseases have been suggested. The aim of this study was to investigate the effect of sex on the association between MetS and left ventricular (LV) diastolic dysfunction in patients with suspected coronary artery disease (CAD). Methods: Two hundred ten patients (105 men and age-matched 105 women; mean age: 56.510.9 years) undergoing elective coronary angiography for the evaluation of CAD were studied. MetS was defined according to the International Diabetes Federation criteria. LV diastolic function was assessed using transthoracic echocardiography. Results: The incidence of MetS was 23.8% in men and 14.3% in women (P=0.079). The incidence of LV diastolic dysfunction was significantly different by MetS in women, but not in men. In multiple linear regression analyses, the number of MetS components was independently associated with septal e velocity, E/e, and left atrial (LA) diameter in women (P<0.05 for each). In men, the number of MetS components was associated with only LA size in this analysis. As the number of components of MetS increased, septal e velocity decreased proportionally in women (P<0.001), but not in men (P=0.117). Conclusions: Among middle-aged and elderly Korean patients at high risk of CAD, the impact of MetS on LV diastolic dysfunction was more pronounced in women than in men. This suggests the important role of sex hormonal effects in the development of LV diastolic dysfunction in relation to MetS in this population.
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