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原发性高血压患者基质金属蛋白酶-9和金属蛋白酶组织抑制因子-1水平。与左心室质量及降压治疗的关系。

Matrix metalloproteinase-9 and tissue inhibitor metalloproteinase-1 levels in essential hypertension. Relationship to left ventricular mass and anti-hypertensive therapy.

作者信息

Li-Saw-Hee F L, Edmunds E, Blann A D, Beevers D G, Lip G Y

机构信息

Haemostasis Thrombosis and Vascular Biology Unit, University Department of Medicine, City Hospital, B18 7QH, Birmingham, UK.

出版信息

Int J Cardiol. 2000 Aug;75(1):43-7. doi: 10.1016/s0167-5273(00)00274-6.

Abstract

To test the hypothesis that the activity of enzymes degrading the extracellular matrix in hypertensive patients are abnormal, and that the treatment of hypertension will normalise these abnormalities, we measured the serum levels of metalloproteinase MMP-9, and its inhibitor, tissue metalloproteinase inhibitor (TIMP-1). Thirty-two patients with untreated hypertension (BP 168/96) had significantly lower levels of both MMP-9 and TIMP-1 when compared to 24 matched normotensive controls (BP 123/80) (P<0.001). There was no significant correlation between MMP-9 and TIMP-1 levels (P>0.2). In the patients, there were no significant correlations observed between left ventricular mass, Doppler V(E)/V(A) ratio (an index of diastolic function), blood pressure, left ventricular mass index and either MMP-9 or TIMP-1 levels (all P=NS). Levels of MMP-9 and TIMP-1 were not significantly altered after 2 months of antihypertensive treatment of 29 patients despite mean blood pressure falling from 170/96 to 143/85 mmHg (P<0.001). Correspondingly, there were also no significant alterations in indices of diastolic function and left ventricular mass. Our study suggests that the proteolytic activities of MMP-9 and TIMP-l are depressed in hypertensive patients and were not significantly affected by short-term antihypertensive treatment. The relationship between collagen metabolism in hypertensive subjects, especially in those with cardiac hypertrophy, and the effects of treatment needs to be further explored in larger trials over a longer period of time.

摘要

为验证高血压患者中降解细胞外基质的酶活性异常,且高血压治疗可使这些异常恢复正常这一假说,我们测定了金属蛋白酶MMP-9及其抑制剂组织金属蛋白酶抑制剂(TIMP-1)的血清水平。与24名匹配的血压正常对照者(血压123/80)相比,32名未经治疗的高血压患者(血压168/96)的MMP-9和TIMP-1水平均显著降低(P<0.001)。MMP-9与TIMP-1水平之间无显著相关性(P>0.2)。在患者中,左心室质量、多普勒V(E)/V(A)比值(舒张功能指标)、血压、左心室质量指数与MMP-9或TIMP-1水平之间均未观察到显著相关性(所有P=无显著性差异)。29名患者接受2个月的抗高血压治疗后,尽管平均血压从170/96降至143/85 mmHg(P<0.001),但MMP-9和TIMP-1水平并未显著改变。相应地,舒张功能指标和左心室质量也无显著变化。我们的研究表明,高血压患者中MMP-9和TIMP-1的蛋白水解活性降低,且不受短期抗高血压治疗的显著影响。高血压患者尤其是心脏肥大患者的胶原代谢与治疗效果之间的关系,需要在更大规模、更长时间的试验中进一步探索。

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