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Clinical significance of matrix metalloproteinases activity in acute myocardial infarction.

机译:急性心肌梗死中基质金属蛋白酶活性的临床意义。

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Matrix metalloproteinases (MMP) degrade myocardial fibrillar collagen in acute myocardial infarction (MI) patients. Their activity is tightly controlled in normal myocardium by a family of closely related tissue inhibitors known as TIMP. An imbalance in their activity might contribute to post-MI remodeling. Plasma levels of MMP-1, TIMP-1 and MMP-1/TIMP-1 complex were measured, using relevant ELISA kits, in 24 (22 males-2 females), acute MI patients with a mean age 59 +/- 14 years. Blood samples were taken on admission (0h),and 3h, 6h, 9h, 18h, 24h, 36h, 48h, 3(rd), 4(th), 5(th), 7(th), 15 (th), 30 (th) days after MI. All patients underwent coronary arteriography with ventriculography for estimation of left ventricular ejection fraction (LVEF) and extent of coronary artery diseases, and echocardiographic study for measuring end-diastolic diameter (EDD). Ten patients with an LVEF < 45%, an EDD > 47.5mm, and heart failure symptoms were included in group A and compared against 12 patients with an LVEF > 45% an EDD < 47.5mm in group B.Mean plasma concentrations of MMP-1 were higher by 21% in group A (1.3 +/- 0.2 ng/mL) compared to group B (1 +/- 0.1 ng/mL) over the total study period. TIMP-1 plasma concentrations showed very little difference between the 2 groups, (704 +/- 213 ng/mL versus 691 +/- 165 ng/mL, (6%)) Finally, plasma concentrations of MMP-1/TIMP-1 complex were lower by -36% in group A with a mean value of 2.7 +/- 0.6 ng/mL versus 3.7 +/- 0.5 ng/mL in group B. Mean values for the differences were significant at time points 0, 6, 18, 24 and 48 hours for MMP-1 (p < 0.036), and on 48h and the 4(th) day for MMP-1/TIMP-1 complex (p < 0.031). Moreover, a good correlation was found between plasma concentrations of creatine kinase (CK) and MMP-1 at 18h (r = 0.422, p = 0.041) and on the 4(th) day (r = 0.67, p = 0.046), and TIMP-1 on the 4(th) day (r = 0.67, p = 0.047). Additionally, mean values for LVEF were 35.8 +/- 8.8% in group A versus 51.2 +/- 1.8% (p = 0.00014) in group B. Also, the EDD in-group A was 52.1 +/- 6.9 mm versus 42.9 +/- 3.2 mm in group B (p = 0.00013). In acute MI patients, increased MMP-1, with no change in TIMP-1, is associated with left ventricular dysfunction and dilatation, suggesting that increased collagenolytic activity contributes to loss of LV function.
机译:基质金属蛋白酶(MMP)在急性心肌梗死(MI)患者中降解心肌纤维胶原。在正常心肌中,它们的活性受到一系列密切相关的组织抑制剂TIMP的严格控制。他们活动的不平衡可能会导致心梗后重塑。使用相关的ELISA试剂盒,对24名平均年龄59 +/- 14岁的急性心肌梗死患者(22位男性至2位女性)中的MMP-1,TIMP-1和MMP-1 / TIMP-1复合物的血浆水平进行了测量。在入院(0h),3h,6h,9h,18h,24h,36h,48h,3(rd),4(th),5(th),7(th),15(th)时取血样MI后30(th)天。所有患者均接受冠状动脉造影和心室造影,以评估左心室射血分数(LVEF)和冠状动脉疾病的程度,并进行超声心动图检查以测量舒张末期直径(EDD)。 A组包括10例LVEF <45%,EDD> 47.5mm,心力衰竭症状的患者,而B组则与12例LVEF> 45%EDD <47.5mm的患者进行了比较。在整个研究期间,A组(1.3 +/- 0.2 ng / mL)的1个比B组(1 +/- 0.1 ng / mL)的高21%。 TIMP-1血浆浓度在两组之间几乎没有差异(704 +/- 213 ng / mL与691 +/- 165 ng / mL,(6%))最后,MMP-1 / TIMP-1的血浆浓度A组的复合物浓度降低-36%,平均值为2.7 +/- 0.6 ng / mL,而B组的平均值为3.7 +/- 0.5 ng / mL。差异的平均值在时间点0、6时显着MMP-1为18、24和48小时(p <0.036),MMP-1 / TIMP-1复合物在48h和第4天(p <0.031)。此外,在18h(r = 0.422,p = 0.041)和第4天(r = 0.67,p = 0.046)时,发现肌酸激酶(CK)和MMP-1的血浆浓度之间存在良好的相关性,并且第4天的TIMP-1(r = 0.67,p = 0.047)。此外,A组的LVEF平均值为35.8 +/- 8.8%,B组的平均值为51.2 +/- 1.8%(p = 0.00014)。此外,A组的EDD为52.1 +/- 6.9 mm,而42.9 + B组为3.2毫米(p = 0.00013)。在急性心肌梗死患者中,MMP-1升高而TIMP-1不变,与左心室功能障碍和扩张有关,提示胶原蛋白水解活性增加导致左室功能丧失。

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