Growth differentiation factor 15 can distinguish between hypertrophic cardiomyopathy and hypertensive hearts
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  • 作者:Shinsuke Hanatani (1)
    Yasuhiro Izumiya (1)
    Seiji Takashio (1)
    Sunao Kojima (1)
    Megumi Yamamuro (1)
    Satoshi Araki (1)
    Taku Rokutanda (1)
    Kenichi Tsujita (1)
    Eiichiro Yamamoto (1)
    Tomoko Tanaka (1)
    Shinji Tayama (1)
    Koichi Kaikita (1)
    Seiji Hokimoto (1)
    Seigo Sugiyama (1)
    Hisao Ogawa (1)
  • 关键词:Biomarker ; Cytokine ; Hypertension ; Heart failure
  • 刊名:Heart and Vessels
  • 出版年:2014
  • 出版时间:March 2014
  • 年:2014
  • 卷:29
  • 期:2
  • 页码:231-237
  • 全文大小:340 KB
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  • 作者单位:Shinsuke Hanatani (1)
    Yasuhiro Izumiya (1)
    Seiji Takashio (1)
    Sunao Kojima (1)
    Megumi Yamamuro (1)
    Satoshi Araki (1)
    Taku Rokutanda (1)
    Kenichi Tsujita (1)
    Eiichiro Yamamoto (1)
    Tomoko Tanaka (1)
    Shinji Tayama (1)
    Koichi Kaikita (1)
    Seiji Hokimoto (1)
    Seigo Sugiyama (1)
    Hisao Ogawa (1)

    1. Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Chuo-ku, Kumamoto, 860-8556, Japan
  • ISSN:1615-2573
文摘
To distinguish hypertrophic cardiomyopathy (HCM) from hypertensive left ventricular hypertrophy (H-LVH) based on a morphological examination is often challenging. Growth differentiation factor 15 (GDF-15) is a novel diagnostic and prognostic biomarker for several cardiovascular diseases. In patients with LVH, GDF-15 promises to be a useful biomarker to distinguish between HCM and H-LVH. We evaluated 93 patients with H-LVH, 28 with HCM, and 28 disease control individuals. Serum GDF-15 concentrations were measured with an enzyme-linked immunosorbent assay. Circulating GDF-15 levels were significantly higher in patients with H-LVH than with HCM (P?=?0.003). On the other hand, values for plasma B-type natriuretic peptide (BNP) levels were significantly lower in patients with H-LVH than with HCM (P = 0.004). Serum GDF-15 and plasma BNP levels positively correlated in patients with H-LVH but not with HCM. Multivariate logistic regression analysis revealed GDF-15 (odds ratio 12.06, confidence interval 1.85-8.77, P < 0.01) as an independent predictor of H-LVH among patients with LVH. In receiver-operating characteristic analysis, GDF-15 achieved an area under the curve of 0.70 for the identification of H-LVH. We found that GDF-15 might be a useful biomarker for discriminating HCM from H-LVH. Understanding serum GDF-15 values may have clinical utility for patients with LVH because the therapeutic strategies for treating HCM and H-LVH differ.
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