Low relative muscle mass and left ventricular diastolic dysfunction in middle-aged adults

Byung Joon Ko, Yoosoo Chang, Jeong Gyu Kang, Jimin Kim, Hyun Suk Jung, Kyung Eun Yun, Chan Won Kim, Hocheol Shin, Seungho Ryu

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Objectives: The association between low skeletal muscle mass and left ventricular diastolic dysfunction (LVDD), a predictor of future heart failure, is largely unexplored. We investigated the relationship between relative muscle mass and LVDD. Methods: We conducted a cross-sectional study in 67,106 Koreans who underwent an echocardiography as part of a comprehensive health examination between January 2012 and December 2014. Skeletal muscle mass index (SMI) [SMI (%) = total skeletal muscle mass (kg) / body weight (kg) × 100] was estimated using a bioelectrical impedance analyzer. The presence of LVDD was determined using echocardiographic findings. Results: In 67,106 participants, 19,232 subjects (28.7%) and 1553 subjects (2.3%) had LVDD and left ventricular (LV) hypertrophy, respectively. SMI was positively associated with E/A ratio and septal E′, whereas E/E′ ratio and LV mass index were negatively associated with SMI. Lower SMI was associated with increased presence of LVDD. In a multivariable-adjusted model controlling for potential confounders including physical activity, insulin resistance, and LV mass, the odds ratios for LVDD in SMI quartiles 1, 2, and 3 compared with quartile 4 were 2.11 (1.97–2.25), 1.79 (1.68–1.90), and 1.45 (1.36–1.55), respectively (P for trend < 0.001). Conclusions: In a large sample of young and middle-aged Korean adults, low relative muscle mass was independently associated with increased risk of LVDD, indicating an independent role of skeletal muscle mass in the pathogenesis of LVDD.

Original languageEnglish
Pages (from-to)118-123
Number of pages6
JournalInternational Journal of Cardiology
Volume255
DOIs
StatePublished - 15 Mar 2018

Keywords

  • Left ventricular dysfunction
  • Left ventricular hypertrophy
  • Sarcopenia
  • Skeletal muscle

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