AI Article Synopsis

  • The study investigates the link between a polymorphism in the MMP-8 gene and the risk of Rotator Cuff Tears (RCT), focusing on how a specific allele may lead to higher collagen degradation.
  • DNA samples from 128 patients (64 with RCT and 64 as controls) were analyzed using PCR, revealing that the T/T genotype was more common in those with RCT.
  • Findings suggest that the MMP-8 g.-799 C>T SNP is a potential risk factor for RCT, highlighting the need for further research to explore prevention and treatment options.

Article Abstract

Objectives: Rotator Cuff Tear (RCT) is a multifactorial disease, but an important one is the increased collagen degradation that would lead to a higher chance of tear. MMP-8 is a protein that degrades type I collagen, and it is known that MMP-8 has a polymorphism in which a T allele in the gene promoter region increases its transcription activity. This study aims to investigate the association between MMP-8 polymorphism g.-799 C>T (rs11225394) and RCT.

Methods: To do that, we collected DNA samples from buccal epithelial cells of 128 patients (separated into RCT group and control group in a proportion 1:1) and genotyped the DNA using PCR. The statistical analyses were done using the ARLEQUIN Version 2.0, and the data normality was tested with the Shapiro-Wilk test.

Results: The results showed a significantly higher frequency of T/T genotype in the test group (29% in the control group and 39% in the test group, p=0.0417), and that would represent a risk factor for increased collagen degradation.

Conclusion: The MMP-8 g.-799 C>T (rs11225394) SNP was associated with RCT. With the description of a new risk factor, future research can be done to analyze how to prevent RCT or develop new treatment strategies since the disease's failure index is currently high.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585477PMC
http://dx.doi.org/10.22038/ABJS.2023.55108.2743DOI Listing

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