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高血压患者中基质金属蛋白酶及其抑制剂的血浆水平:系统评价和荟萃分析。

Plasma levels of matrix metalloproteinases and their inhibitors in hypertension: a systematic review and meta-analysis.

机构信息

Department of Clinical Medicine, University of Insubria, Varese, Italy.

出版信息

J Hypertens. 2012 Jan;30(1):3-16. doi: 10.1097/HJH.0b013e32834d249a.

Abstract

BACKGROUND

Hypertension is a major cause of cardiovascular remodeling. In the cardiovascular system, the remodeling of the extracellular matrix is controlled by the matrix metalloproteinases (MMPs) and the tissue inhibitors of MMPs (TIMPs). The aim of this meta-analysis is to elucidate the behavior of plasma MMP and TIMP levels in hypertension and their relationship to cardiovascular remodeling.

METHODS

MEDLINE and EMBASE databases were searched up to July 2011. Studies were considered eligible if they provided values of plasma MMPs and TIMPs in hypertensive patients. Given the high variability of the plasma biomarker values among studies, the standardized mean difference (SMD) was calculated.

RESULTS

Ten studies provided plasma MMP-9; the SMD between 778 hypertensive patients and 669 controls was 1.95 units (P < 0.05). Thirteen studies provided plasma TIMP-1; the SMD between 851 hypertensive patients and 646 normotensive individuals was 1.92 units (P < 0.01). Three studies investigated whether plasma TIMP-1 predicted left ventricular (LV) remodeling; the SMD between 92 hypertensive patients with and 88 hypertensive patients without LV hypertrophy was 5.81 units (P < 0.05). As for diastolic heart failure (HF), five studies provided data for plasma MMP-2; the SMD between 321 hypertensive patients with and 334 hypertensive patients without HF was 2.36 units (P < 0.01). The heterogeneity among studies was high.

CONCLUSIONS

These results suggest that MMP-2, MMP-9 and TIMP-1 may have a role as biomarkers of cardiovascular remodeling in hypertension. If these results are confirmed in prospective clinical studies, they could provide new tools to stratify cardiovascular risk in hypertensive patients.

摘要

背景

高血压是心血管重构的主要原因。在心血管系统中,细胞外基质的重构受基质金属蛋白酶(MMPs)和基质金属蛋白酶抑制剂(TIMPs)的控制。本荟萃分析旨在阐明高血压患者血浆 MMP 和 TIMP 水平的变化及其与心血管重构的关系。

方法

检索 MEDLINE 和 EMBASE 数据库,截止到 2011 年 7 月。如果研究提供了高血压患者血浆 MMPs 和 TIMPs 的数值,则认为其符合入选标准。由于研究间血浆生物标志物数值的变异性较大,因此计算了标准化均数差(SMD)。

结果

10 项研究提供了 MMP-9 血浆值;778 例高血压患者和 669 例对照者之间的 SMD 为 1.95 个单位(P<0.05)。13 项研究提供了 TIMP-1 血浆值;851 例高血压患者和 646 例血压正常者之间的 SMD 为 1.92 个单位(P<0.01)。有 3 项研究探讨了 TIMP-1 是否可预测左心室重构;92 例有左心室肥厚的高血压患者和 88 例无左心室肥厚的高血压患者之间的 SMD 为 5.81 个单位(P<0.05)。对于舒张性心力衰竭(HF),5 项研究提供了 MMP-2 血浆值数据;321 例有 HF 的高血压患者和 334 例无 HF 的高血压患者之间的 SMD 为 2.36 个单位(P<0.01)。研究间的异质性很高。

结论

这些结果表明 MMP-2、MMP-9 和 TIMP-1 可能作为高血压患者心血管重构的生物标志物发挥作用。如果这些结果在前瞻性临床研究中得到证实,它们可能为高血压患者的心血管风险分层提供新的工具。

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