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功能性基质金属蛋白酶(MMP)-9 遗传变异可改变血液透析对循环 MMP-9 水平的影响。

Functional matrix metalloproteinase (MMP)-9 genetic variants modify the effects of hemodialysis on circulating MMP-9 levels.

机构信息

Department of Pharmacology, Faculty of Medical Sciences, State University of Campinas, Campinas, Brazil.

出版信息

Clin Chim Acta. 2012 Dec 24;414:46-51. doi: 10.1016/j.cca.2012.08.014. Epub 2012 Aug 21.

Abstract

BACKGROUND

Altered levels of matrix metalloproteinases (MMPs) and their inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), are involved in cardiovascular alterations associated with end stage kidney disease (ESKD). Genetic polymorphisms in MMP-9 gene affect MMP-9 levels. We examined how MMP-9 polymorphisms and haplotypes affect the changes in plasma MMP-9 and TIMP-1 levels found in patients with ESKD undergoing hemodialysis.

METHODS

We studied 94 ESKD patients undergoing hemodialysis for at least 3 months. MMP-9 and TIMP-1 were measured by ELISA in plasma from blood samples collected before and after a session of hemodialysis. Genotypes for three MMP-9 polymorphisms (C(-1562)T, rs3918242; -90 (CA)(14-24), rs2234681; and Q279R, rs17576) were determined by Taqman® Allele Discrimination Assay and real-time polymerase chain reaction. Haplotype frequencies were determined with the software program PHASE 2.1.

RESULTS

Hemodialysis increased MMP-9 and TIMP-1 levels (P<0.05). Genotypes had no effects on baseline MMP-9 and TIMP-1 levels (P>0.05). Hemodialysis increased MMP-9 and TIMP-1 levels in subjects with the CC (but not CT or TT) genotype for the C(-1562)T polymorphism (P<0.05), and increased MMP-9 levels in subjects with the QQ (but not QR or RR) genotype for the Q279R polymorphism (P<0.05), whereas the CA(n)(14-24) polymorphism had no major effects. While MMP-9 haplotypes had no effects on baseline MMP-9 levels (P>0.05), hemodialysis increased MMP-9 levels and MMP-9/TIMP-1 ratios in subjects carrying the CLQ haplotype (P=0.0012 and P=0.0045, respectively).

CONCLUSION

ESKD patients with the QQ genotype for the Q279R polymorphism or with the CLQ haplotype are exposed to more severe increases in MMP-9 levels after hemodialysis. Such patients may benefit from the use of MMP inhibitors.

摘要

背景

基质金属蛋白酶(MMPs)及其抑制剂组织金属蛋白酶抑制剂(TIMPs)的水平改变与终末期肾病(ESKD)相关的心血管改变有关。MMP-9 基因的遗传多态性影响 MMP-9 水平。我们研究了 MMP-9 多态性和单倍型如何影响接受血液透析的 ESKD 患者中发现的血浆 MMP-9 和 TIMP-1 水平的变化。

方法

我们研究了 94 名接受血液透析至少 3 个月的 ESKD 患者。使用 ELISA 从血液透析治疗前后采集的血液样本中测量 MMP-9 和 TIMP-1。通过 Taqman®等位基因鉴别测定和实时聚合酶链反应确定三个 MMP-9 多态性(C(-1562)T,rs3918242;-90(CA)(14-24),rs2234681;和 Q279R,rs17576)的基因型。使用软件程序 PHASE 2.1 确定单倍型频率。

结果

血液透析增加了 MMP-9 和 TIMP-1 水平(P<0.05)。基因型对基线 MMP-9 和 TIMP-1 水平没有影响(P>0.05)。C(-1562)T 多态性的 CC(而非 CT 或 TT)基因型的受试者血液透析增加了 MMP-9 和 TIMP-1 水平(P<0.05),而 Q279R 多态性的 QQ(而非 QR 或 RR)基因型的受试者 MMP-9 水平增加(P<0.05),而 CA(n)(14-24)多态性没有主要影响。虽然 MMP-9 单倍型对基线 MMP-9 水平没有影响(P>0.05),但携带 CLQ 单倍型的受试者血液透析后 MMP-9 水平和 MMP-9/TIMP-1 比值增加(P=0.0012 和 P=0.0045)。

结论

接受血液透析的 Q279R 多态性 QQ 基因型或 CLQ 单倍型的 ESKD 患者在血液透析后 MMP-9 水平升高更为严重。这些患者可能受益于 MMP 抑制剂的使用。

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