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Prognostic Role of Circulating LTBP-2 in Patients With Dilated Cardiomyopathy: A Novel Biomarker Reflecting Extracellular Matrix LTBP-2 Accumulation

医学 扩张型心肌病 生物标志物 活检 内科学 心力衰竭 细胞外基质 心脏病学 危险系数 射血分数 心肌病 病理 胃肠病学 置信区间 生物化学 化学 细胞生物学 生物
作者
Kazuto Nishiura,Tetsuro Yokokawa,Tomofumi Misaka,Shohei Ichimura,Yusuke Tomita,Shunsuke Miura,Takeshi Shimizu,Takamasa Sato,Takashi Kaneshiro,Masayoshi Oikawa,Atsushi Kobayashi,Akiomi Yoshihisa,Yasuchika Takeishi
出处
期刊:Canadian Journal of Cardiology [Elsevier]
卷期号:39 (10): 1436-1445 被引量:3
标识
DOI:10.1016/j.cjca.2023.05.015
摘要

Dilated cardiomyopathy (DCM) is a life-threatening disease related to heart failure. Extracellular matrix proteins have an important role in the pathogenesis of DCM. Latent transforming growth factor beta-binding protein 2 (LTBP-2), a type of extracellular matrix protein, has not been investigated in DCM.First, we compared plasma LTBP-2 levels in 131 patients with DCM who underwent endomyocardial biopsy and 44 controls who were matched for age and sex and had no cardiac abnormalities. Next, we performed immunohistochemistry for LTBP-2 on endomyocardial biopsy specimens and followed the DCM patients for ventricular assist device (VAD) implantation, cardiac death, and all-cause death.Patients with DCM had elevated plasma LTBP-2 levels compared with controls (P < 0.001). Plasma LTBP-2 levels were positively correlated with LTBP-2-positive fraction in the myocardium from the biopsy specimen. When patients with DCM were divided into 2 groups according to LTBP-2 levels, Kaplan-Meier analysis demonstrated that patients with high plasma LTBP-2 were associated with increased incidences of cardiac death/VAD and all-cause death/VAD. In addition, patients with high myocardial LTBP-2-positive fractions were associated with increased incidences of these adverse outcomes. Multivariable Cox proportional hazard analysis showed that plasma LTBP-2 and myocardial LTBP-2-positive fraction were independently associated with adverse outcomes.Circulating LTBP-2 can serve as a biomarker to predict adverse outcomes, reflecting extracellular matrix LTBP-2 accumulation in the myocardium in DCM.
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