AI Article Synopsis

  • This study investigates the relationship between GLP-1 receptor gene variations (SNPs) and bone mineral density (BMD) in postmenopausal women in Shanghai.
  • Out of eight SNPs analyzed, the A/A genotype of rs2295006 showed a negative correlation with BMD in the lumbar spine and the A allele was linked to lower hip BMD.
  • The findings suggest that the rs2295006 SNP may influence bone health in postmenopausal women, while other SNPs studied did not show a significant effect on BMD.

Article Abstract

Background: Glucagon-like peptide-1 receptor (GLP-1R) agonists are able to inhibit bone resorption to a certain extent and improve bone formation. GLP-1R single nucleotide polymorphism (SNP) is related to its activity, but the relationship between GLP-1R SNP and osteoporosis in postmenopausal women was still unclear. This study was to investigate the association between GLP-1R SNP and bone mineral density (BMD) in postmenopausal women in Shanghai.

Methods: Eight SNPs of GLP-1R were detected (rs3765467, rs1042044, rs2268657, rs6923761, rs2268641, rs2295006, rs4714210 and rs10305420) in 884 postmenopausal women in Shanghai. The correlation between GLP-1R SNP and BMD was further assessed.

Results: The A/A genotype of rs2295006 was negatively related to lumbar vertebrae 1-4 BMD (P<0.05). Allele A was negatively related to hip BMD (P<0.05). There was a negative correlation between haplotype CGAGCCA and lumbar BMD, and a positive correlation between haplotype CGGGCTA and lumbar BMD. The remaining seven GLP-1R SNPs had no relationship with BMD.

Conclusions: The rs2295006 of GLP-1R is related to the BMD of postmenopausal women in Shanghai, China.

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Source
http://dx.doi.org/10.21037/apm-19-396DOI Listing

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