Objective: To investigate the association between serum matrix metalloproteinase-3(MMP-3) concentrations and the promoter 5A/6A polymorphism in patients with coronary heart disease (CHD).
Methods: The study enrolled 137 CHD patients and 106 control subjects without CHD. The diagnosis of both groups were confirmed by coronary artery angiography. One hundred and thirty-seven CHD patients were divided into acute myocardial infarction (AMI)group, unstable angina pectoris (UAP) group and stable angina (SA) group according to World Health Organization criteria. Serum concentration of MMP-3 was measured by enzyme linked immunoadsorbent assay (ELISA). MMP-3 promoter gene containing the 5A/6A polymorphism was amplified by polymerase chain reaction (PCR). PCR products were digested by Tth111 I and then were separated by electrophoresis on agarose gel.
Results: The distribution of MMP-3 genotype was not significantly different between CHD patients and controls, so was it between AMI patients and controls. Serum MMP-3 level was significantly higher in AMI group than controls, UAP group and SA group (56.815+/-38.932)microg/L, (39.149+/-24.155)microg/L, (41.640+/-29.180)microg/L, (33.336+/-20.755)microg/L; P<0.01, P<0.05, P<0.01). Serum MMP-3 levels were not significantly different among genotypes and among controls, UAP and SA groups. No significantly differences in serum MMP-3 levels were found among patients with different numbers of coronary arteries that were involved in CHD.
Conclusion: No marked association could be found between 5A/6A polymorphism in MMP-3 gene and risk of CHD and AMI. Higher serum level of MMP-3 is strong associated with AMI, while not with number of coronary arteries that are involved in CHD. These data suggest that MMP-3 is a useful marker for AMI, and it might play an important role in the induction of disruption of atherosclerosis plaque.
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J Med Biochem
September 2024
Jinan Stomatological Hospital, Department of Periodontics and Oral Mucosa, Jinan, China.
Background: This study aimed to explore the correlation between the Matrix Metalloproteinase-3 (MMP-3) 1171 5A/6A gene polymorphism and susceptibility to Chronic Periodontitis (CP).
Methods: Following the PRISMA guidelines, a systematic search was conducted across four electronic databases (PubMed, Embase, Web of Science, and Cochrane Library) without any time or language limitations. The selection criteria included case-control studies examining the association between the MMP-3 gene polymorphism and CP.
Clin Exp Dent Res
December 2024
Dental Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Objectives: Peri-implantitis (PI) is the most common biological issue surrounding dental implants. According to current knowledge, the aforementioned complication is not equally distributed across different populations, and gene polymorphisms might be one contributing factor. The current study aimed to examine the association between gene polymorphisms of matrix metalloproteinase- (MMP-) 1, -2, -3, -7, and -13 with PI in an Iranian demographic.
View Article and Find Full Text PDFActa Trop
December 2024
Gastroenterology Department, Hospital das Clínicas/EBSERH - Federal University of Pernambuco - UFPE, Recife, Brazil.
Medicine (Baltimore)
December 2023
Department of Obstetrics and Gynecology, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Suzhou, China.
The current investigation aims to explore the relationship between matrix metalloproteinase-3 (MMP-3) gene polymorphism and ovarian cancer (OC) risk. Two hundred forty pathologically confirmed OC patients and 390 healthy controls participated in the present investigation. Polymerase chain reaction-restriction fragment length polymorphism was applied to investigate the present polymorphism.
View Article and Find Full Text PDFJ Med Biochem
October 2023
Beijing Hospital of Integrated Chinese & Western Medicine, Department of Clinical Laboratory, Beijing China.
Background: Conclusions on susceptibility of MMP3-1612 5A/6A to morbid risk of coronary artery disease (CAD) are controversial. This meta-analysis aims to obtain the accurate relationship between them.
Methods: Relevant literatures on susceptibility of MMP3-1612 5A/6A to morbid risk of CAD published before July 2019 were searched in PubMed, Web of Science, Cochrane Library, CNKI, VIP and Wanfang.
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