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The novel myokine irisin: clinical implications and potential role as a biomarker for sarcopenia in postmenopausal women

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  • معلومة اضافية
    • Contributors:
      Hye-Sun Park; Hyun Chang Kim; Dongdong Zhang; Hyungseon Yeom; Sung-Kil Lim; Kim, Hyeon Chang
    • بيانات النشر:
      Humana Press
    • الموضوع:
      2019
    • نبذة مختصرة :
      Purpose: To clarify the association of circulating irisin with muscle, liver and bone, and to evaluate irisin as a biomarker for sarcopenia in postmenopausal women. Methods: Quadriceps cross-sectional area (QcCSA), bone mineral density (BMD), liver attenuation (measured in Hounsfield units (HU)) were assessed using quantitative computed tomography in 153 postmenopausal women, mean age of 72.20 ± 5.96 years. Muscle strength and physical performance were evaluated by handgrip test and short physical performance battery, respectively. Serum irisin was measured by an enzyme-linked immunosorbent assay kit. In addition, 147 young women were recruited as a reference group to define cut-off values for sarcopenia. Results: Circulating irisin was positively correlated with QcCSA/body weight (BW) and liver HU even after adjusting for multiple covariates, and the serum level was significantly lower in the sarcopenia group (QcCSA/BW<-2SD of the mean values for young women) than in the presarcopenia (-2SD≤QcCSA/BW<-1SD) or control groups (1SD≤QcCSA/BW<2SD). Logistic regression models showed that the relationship between circulating irisin and prevalence of sarcopenia remained significant after adjusting for confounding factors (per 1.0 ng/mL decrease of irisin, odds-ratio = 1.95, 95% confidence interval 1.33-2.87, p-value = 0.001). Conclusions: In postmenopausal women, serum irisin may be used as a biomarker for sarcopenia, and we showed the potential for the development of irisin-based early screening and staging tool for sarcopenia. ; restriction
    • ISSN:
      1355-008X
      1559-0100
    • Relation:
      ENDOCRINE; J00768; OAK-2022-02307; https://ir.ymlib.yonsei.ac.kr/handle/22282913/188979; https://link.springer.com/article/10.1007/s12020-018-1814-y; T999201986; ENDOCRINE, Vol.64(2) : 341-348, 2019-05
    • الرقم المعرف:
      10.1007/s12020-018-1814-y
    • الدخول الالكتروني :
      https://ir.ymlib.yonsei.ac.kr/handle/22282913/188979
      https://doi.org/10.1007/s12020-018-1814-y
      https://link.springer.com/article/10.1007/s12020-018-1814-y
    • Rights:
      CC BY-NC-ND 2.0 KR
    • الرقم المعرف:
      edsbas.341D5BEA