Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.

BACKGROUND: MicroRNAs (miRNAs) are small ribonucleotides regulating gene expression. MicroRNAs are present in the blood in a remarkably stable form and have emerged as potential diagnostic markers in patients with cardiovascular disease. Our study aimed to assess circulating miR-133a levels in MHD p...

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Main Authors: Ping Wen, Dan Song, Hong Ye, Xiaochun Wu, Lei Jiang, Bing Tang, Yang Zhou, Li Fang, Hongdi Cao, Weichun He, Yafang Yang, Chunsun Dai, Junwei Yang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4196728?pdf=render
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spelling doaj-349c528a18aa4b2aad0d0e7f2f829ae72020-11-25T01:34:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01910e10307910.1371/journal.pone.0103079Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.Ping WenDan SongHong YeXiaochun WuLei JiangBing TangYang ZhouLi FangHongdi CaoWeichun HeYafang YangChunsun DaiJunwei YangBACKGROUND: MicroRNAs (miRNAs) are small ribonucleotides regulating gene expression. MicroRNAs are present in the blood in a remarkably stable form and have emerged as potential diagnostic markers in patients with cardiovascular disease. Our study aimed to assess circulating miR-133a levels in MHD patients and the relation of miR-133a to cardiac hypertrophy. METHODS: We profiled miRNAs using RNA isolated from the plasma of participants. The results were validated in 64 MHD patients and 18 healthy controls. RESULTS: Levels of plasma miR-133a decreased in MHD patients with LVH compared with those in healthy controls. Plasma miR-133a concentrations were negatively correlated with LVMI and IVS. After single hemodialytic treatment, plasma miR-133a levels remained unchanged. Cardiac Troponin I and T were not associated with LVMI and IVS. CONCLUSIONS: Our observations supplied the possibility that circulating miR-133a could be a surrogate biomarker of cardiac hypertrophy in MHD patients.http://europepmc.org/articles/PMC4196728?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ping Wen
Dan Song
Hong Ye
Xiaochun Wu
Lei Jiang
Bing Tang
Yang Zhou
Li Fang
Hongdi Cao
Weichun He
Yafang Yang
Chunsun Dai
Junwei Yang
spellingShingle Ping Wen
Dan Song
Hong Ye
Xiaochun Wu
Lei Jiang
Bing Tang
Yang Zhou
Li Fang
Hongdi Cao
Weichun He
Yafang Yang
Chunsun Dai
Junwei Yang
Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
PLoS ONE
author_facet Ping Wen
Dan Song
Hong Ye
Xiaochun Wu
Lei Jiang
Bing Tang
Yang Zhou
Li Fang
Hongdi Cao
Weichun He
Yafang Yang
Chunsun Dai
Junwei Yang
author_sort Ping Wen
title Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
title_short Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
title_full Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
title_fullStr Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
title_full_unstemmed Circulating MiR-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
title_sort circulating mir-133a as a biomarker predicts cardiac hypertrophy in chronic hemodialysis patients.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description BACKGROUND: MicroRNAs (miRNAs) are small ribonucleotides regulating gene expression. MicroRNAs are present in the blood in a remarkably stable form and have emerged as potential diagnostic markers in patients with cardiovascular disease. Our study aimed to assess circulating miR-133a levels in MHD patients and the relation of miR-133a to cardiac hypertrophy. METHODS: We profiled miRNAs using RNA isolated from the plasma of participants. The results were validated in 64 MHD patients and 18 healthy controls. RESULTS: Levels of plasma miR-133a decreased in MHD patients with LVH compared with those in healthy controls. Plasma miR-133a concentrations were negatively correlated with LVMI and IVS. After single hemodialytic treatment, plasma miR-133a levels remained unchanged. Cardiac Troponin I and T were not associated with LVMI and IVS. CONCLUSIONS: Our observations supplied the possibility that circulating miR-133a could be a surrogate biomarker of cardiac hypertrophy in MHD patients.
url http://europepmc.org/articles/PMC4196728?pdf=render
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