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循环 miR-133a 和 miR-423-5p 不能作为心肌梗死后左心室重构的生物标志物。

Circulating miR-133a and miR-423-5p fail as biomarkers for left ventricular remodeling after myocardial infarction.

机构信息

Inserm, U744, University Lille Nord de France, Lille, France; Institut Pasteur de Lille, Lille, France; Centre Hospitalier Régional et Universitaire de Lille, Lille, France; Faculté de Médecine de Lille, Lille, France.

出版信息

Int J Cardiol. 2013 Oct 3;168(3):1837-40. doi: 10.1016/j.ijcard.2012.12.074. Epub 2013 Jan 22.

Abstract

BACKGROUND

Recent studies have suggested that the microRNAs miR-133a and miR-423-5p may serve as useful biomarkers in patients with left ventricular (LV) heart failure or with LV remodeling after myocardial infarction (MI). These results were however obtained in small series of patients and control subjects were used as reference groups. Whether these microRNAs may be indicators of the degree of LV remodeling after MI is unknown.

METHODS

246 patients with a first anterior Q-wave MI were included. Serial echocardiographic studies were performed at hospital discharge, 3 months, and 1 year after MI and analyzed at a core laboratory. We investigated the temporal profile (baseline, 1, 3 and 12 months) of circulating miR-133a and miR-423-5p and their relations with cardiac biomarkers (B-type natriuretic peptide, C-reactive protein, and cardiac troponin I) and LV remodeling during the 1 year follow-up.

RESULTS

There were time-dependent changes in the levels of circulating miR-133a and miR-423-5p with significant increase of miR-133a at 12 months compared to 3 months and significant increase of miR-423-5p at 1, 3, and 12 months compared to baseline. However, miR-133a and miR-423-5p were not associated with indices of LV function and LV remodeling serially assessed during a 1 year period after an acute anterior MI, nor with B-type natriuretic peptide.

CONCLUSIONS

Circulating levels of miR-133a and miR-423-5p are not useful biomarkers of LV remodeling after MI.

摘要

背景

最近的研究表明,微小 RNA miR-133a 和 miR-423-5p 可能作为左心室(LV)心力衰竭或心肌梗死后 LV 重构患者的有用生物标志物。然而,这些结果是在小系列患者中获得的,并且将对照受试者用作参考组。这些微小 RNA 是否可以指示心肌梗死后 LV 重构的程度尚不清楚。

方法

纳入 246 例首次前壁 Q 波心肌梗死患者。在心肌梗死后出院时、3 个月和 1 年进行连续超声心动图研究,并在核心实验室进行分析。我们研究了循环 miR-133a 和 miR-423-5p 的时间分布(基线、1、3 和 12 个月)及其与心脏生物标志物(B 型利钠肽、C 反应蛋白和心肌肌钙蛋白 I)和 1 年随访期间 LV 重构的关系。

结果

循环 miR-133a 和 miR-423-5p 水平随时间呈依赖性变化,与 3 个月相比,12 个月时 miR-133a 水平显著升高,与基线相比,1、3 和 12 个月时 miR-423-5p 水平显著升高。然而,miR-133a 和 miR-423-5p 与急性前壁心肌梗死后 1 年内连续评估的 LV 功能和 LV 重构指数均无相关性,也与 B 型利钠肽无关。

结论

循环 miR-133a 和 miR-423-5p 水平不适用于心肌梗死后 LV 重构的生物标志物。

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