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Fetuin-A as a predicator of sarcopenic left ventricular dysfunction.

Abstract
Sarcopenia is an aging condition involving low muscle mass and function. Fetuin-A (FetA) appears to be a factor for body composition remodeling. We hypothesized that age increases FetA levels and deteriorates the myocardial function by affecting diastolic function, especially in people with sarcopenia. We enrolled 541 asymptomatic elderly (≥ 65 years) patients. Compared with non-sarcopenic population, FetA levels were significantly elevated in the ninety-two (17%) patients (79 ± 6 years; male: 34.7%) diagnosed with sarcopenia (621.1 ± 140.7 vs. 697.3 ± 179.6 μg/ml, < 0.001). Sarcopenic left ventricular dysfunction (S-LVD) was defined by the coexistence of sarcopenia and systolic impairment (LVEF < 50%) and 23 (4.3%) of them met the criteria. Patients with S-LVD showed relatively reduced systolic heart function, higher end-diastolic pressure and a higher FetA level (all p < 0.001) than did those with sarcopenia but without LV dysfunction (S-NLVD). Conversely, in the group without sarcopenia, FetA levels were similar regardless of systolic function. Multivariable logistic regression showed that older age, impaired diastolic function, and higher FetA levels were significantly associated with S-LVD. In conclusion, we found that FetA was significantly higher in elderly patients with sarcopenia, which was associated with impaired diastolic and systolic functions.
AuthorsWei-Ting Chang, Wei-Chuan Tsai, Chih-Hsing Wu, Yen-Wei Lee, Yun-Lin Tai, Yi-Heng Li, Liang-Miin Tsai, Jyh-Hong Chen, Ping-Yen Liu
JournalScientific reports (Sci Rep) Vol. 5 Pg. 12078 (Jul 10 2015) ISSN: 2045-2322 [Electronic] England
PMID26159840 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • AHSG protein, human
  • alpha-2-HS-Glycoprotein
Topics
  • Aged
  • Body Composition (physiology)
  • Diastole (physiology)
  • Female
  • Heart Failure (metabolism, pathology)
  • Humans
  • Male
  • Sarcopenia (metabolism)
  • Systole (physiology)
  • Ventricular Dysfunction, Left (metabolism, pathology)
  • alpha-2-HS-Glycoprotein (metabolism)

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