Scholarlink

Background <p>Endometriosis (EM) is defined as gynecological chronic inflammation and the presence of active foci of uterine mucous membrane outside the uterine cavity. Susceptibility to endometriosis is influenced by single nucleotide polymorphisms (SNPs) in intronic or intergenic regions. This study aimed to analyze the frequencies of genotypes and alleles of LEP G2548A (rs7799039) of the LEP gene and LEPR Q223R (rs1137101) of the LEPR gene to investigate their contributions to the pathogenesis of endometriosis.</p> Methods <p>Peripheral blood samples of 178 endometriosis patients and 160 healthy donors were isolated from peripheral blood leukocytes. Polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) techniques were used. A novel Bioinformatics analysis was undertaken to anticipate the potential roles of these polymorphisms.</p> Results <p>The <i>LEP</i> rs7799039 AA genotype and mutant allele (A) were frequent in EM women as compared to healthy subjects (OR = 2.35, <i>p</i> = 0.024; OR = 1.35, <i>p</i> = 0.048, respectively). The <i>LEPR</i> rs1137101 mutant GG genotype mutant allele (G) was related to an increased risk of endometriosis (OR=3.22, <i>p</i> = 0.003; OR=1.45, <i>p</i> = 0.022, respectively). The combination of mutant AA and GG genotypes of <i>LEP</i> and <i>LEPR</i> SNPs showed an extremely adverse effect on disease susceptibility and more than ten times more susceptibility to EM. In addition, carriers of the mutant allele for <i>LEP</i> rs7799039 and <i>LEPR</i> rs1137101 polymorphism were more frequent in the moderate/severe (stage III and IV) group of the disease. The LEP G2548A (rs7799039) gene polymorphism may lead to varying allelic expression, as indicated by an in-silico research. Furthermore, bioinformatics analysis indicated that the LEPR Q223R (rs1137101) SNP will significantly alter its secondary structure and physicochemical properties.</p> Conclusion <p>Our research indicates that the LEP G2548A (rs7799039) and LEPR Q223R (rs1137101) polymorphisms may play a role in the pathophysiology of endometriosis. Considering the proven association between leptin signaling and endometriosis, these SNPs may function as potential indicators of disease risk.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Leptin G2548 A and Leptin Receptor Q223R Gene Polymorphisms are Associated with an Increased Risk of Endometriosis

  • 期刊论文

  • 发表日期：

    2025年5月19日

查看全文
  • E. Kiyani-Afzali,
  • F. Forghani,
  • D. Jahantigh,
  • S. Ghazaey-Zidanloo,
  • M. Rezaei,
  • M. Taheri

摘要

Background

Endometriosis (EM) is defined as gynecological chronic inflammation and the presence of active foci of uterine mucous membrane outside the uterine cavity. Susceptibility to endometriosis is influenced by single nucleotide polymorphisms (SNPs) in intronic or intergenic regions. This study aimed to analyze the frequencies of genotypes and alleles of LEP G2548A (rs7799039) of the LEP gene and LEPR Q223R (rs1137101) of the LEPR gene to investigate their contributions to the pathogenesis of endometriosis.

Methods

Peripheral blood samples of 178 endometriosis patients and 160 healthy donors were isolated from peripheral blood leukocytes. Polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) techniques were used. A novel Bioinformatics analysis was undertaken to anticipate the potential roles of these polymorphisms.

Results

The LEP rs7799039 AA genotype and mutant allele (A) were frequent in EM women as compared to healthy subjects (OR = 2.35, p = 0.024; OR = 1.35, p = 0.048, respectively). The LEPR rs1137101 mutant GG genotype mutant allele (G) was related to an increased risk of endometriosis (OR=3.22, p = 0.003; OR=1.45, p = 0.022, respectively). The combination of mutant AA and GG genotypes of LEP and LEPR SNPs showed an extremely adverse effect on disease susceptibility and more than ten times more susceptibility to EM. In addition, carriers of the mutant allele for LEP rs7799039 and LEPR rs1137101 polymorphism were more frequent in the moderate/severe (stage III and IV) group of the disease. The LEP G2548A (rs7799039) gene polymorphism may lead to varying allelic expression, as indicated by an in-silico research. Furthermore, bioinformatics analysis indicated that the LEPR Q223R (rs1137101) SNP will significantly alter its secondary structure and physicochemical properties.

Conclusion

Our research indicates that the LEP G2548A (rs7799039) and LEPR Q223R (rs1137101) polymorphisms may play a role in the pathophysiology of endometriosis. Considering the proven association between leptin signaling and endometriosis, these SNPs may function as potential indicators of disease risk.