Leptin receptor polymorphism increases the risk of painful symptoms in Brazilian women with endometriosis.

IF 1.4
Jéssica Vilarinho Cardoso, Daniel Escorsim Machado, Fernanda Nunes de Almeida, Plínio Tostes Berardo, Rui Medeiros, Jamila Alessandra Perini
{"title":"Leptin receptor polymorphism increases the risk of painful symptoms in Brazilian women with endometriosis.","authors":"Jéssica Vilarinho Cardoso, Daniel Escorsim Machado, Fernanda Nunes de Almeida, Plínio Tostes Berardo, Rui Medeiros, Jamila Alessandra Perini","doi":"10.61622/rbgo/2025rbgo43","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Endometriosis pain is associated with inflammatory cytokines, such as leptin (LEP), through activation with its receptor (LEPR), and its expression can be influenced by the presence of genetic polymorphisms. Therefore, this study aims to evaluate the role of the <i>LEP</i> rs7799039 and <i>LEPR</i> rs1137100 polymorphisms in the painful symptoms of endometriosis in Brazilian women.</p><p><strong>Methods: </strong>A retrospective study was carried out in two Brazilian public hospitals with 237 cases of endometriosis, divided into two comparison groups according to the painful symptoms associated with the disease (absence or presence of severe and disabling symptoms). Genetic analysis was performed by real-time PCR technique, and association analyses were estimated using odds ratio (OR) and 95% confidence interval (CI), using a non-conditional logistic regression model.</p><p><strong>Results: </strong>Endometriosis cases showed a high prevalence of painful symptoms: 82% dysmenorrhea, 67% dyspareunia, 53% chronic pelvic pain, and 52% cyclical intestinal and 25% urinary complaints. Regarding genetic analyses, cases had 32.7% of the A allele and 11.4% of the AA genotype for the <i>LEP</i> rs7799039 G>A SNP, and 17.5% of the G allele and 2.5% for of GG genotype for the <i>LEPR</i> rs1137100 A>G SNP. There is a significant association of the <i>LEPR</i> rs1137100 polymorphism with chronic pelvic pain (OR=1.75; CI 95%=1.05-2.89) and dyspareunia (OR=1.78; CI 95%=1.01-3.12) in women with endometriosis.</p><p><strong>Conclusion: </strong>Our findings suggest that the <i>LEPR</i> rs1137100 polymorphism is associated with increased endometriosis-related gynecological pain and may be a potential target for molecular diagnosis of the disease and development of individualized treatment strategies.</p>","PeriodicalId":74699,"journal":{"name":"Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia","volume":"47 ","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12266861/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.61622/rbgo/2025rbgo43","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Endometriosis pain is associated with inflammatory cytokines, such as leptin (LEP), through activation with its receptor (LEPR), and its expression can be influenced by the presence of genetic polymorphisms. Therefore, this study aims to evaluate the role of the LEP rs7799039 and LEPR rs1137100 polymorphisms in the painful symptoms of endometriosis in Brazilian women.

Methods: A retrospective study was carried out in two Brazilian public hospitals with 237 cases of endometriosis, divided into two comparison groups according to the painful symptoms associated with the disease (absence or presence of severe and disabling symptoms). Genetic analysis was performed by real-time PCR technique, and association analyses were estimated using odds ratio (OR) and 95% confidence interval (CI), using a non-conditional logistic regression model.

Results: Endometriosis cases showed a high prevalence of painful symptoms: 82% dysmenorrhea, 67% dyspareunia, 53% chronic pelvic pain, and 52% cyclical intestinal and 25% urinary complaints. Regarding genetic analyses, cases had 32.7% of the A allele and 11.4% of the AA genotype for the LEP rs7799039 G>A SNP, and 17.5% of the G allele and 2.5% for of GG genotype for the LEPR rs1137100 A>G SNP. There is a significant association of the LEPR rs1137100 polymorphism with chronic pelvic pain (OR=1.75; CI 95%=1.05-2.89) and dyspareunia (OR=1.78; CI 95%=1.01-3.12) in women with endometriosis.

Conclusion: Our findings suggest that the LEPR rs1137100 polymorphism is associated with increased endometriosis-related gynecological pain and may be a potential target for molecular diagnosis of the disease and development of individualized treatment strategies.

Abstract Image

Abstract Image

瘦素受体多态性增加巴西子宫内膜异位症妇女疼痛症状的风险。
目的:子宫内膜异位症疼痛与炎性细胞因子,如瘦素(LEP),通过激活其受体(LEPR)相关,其表达可受遗传多态性的影响。因此,本研究旨在评估LEP rs7799039和LEPR rs1137100多态性在巴西女性子宫内膜异位症疼痛症状中的作用。方法:对巴西两家公立医院237例子宫内膜异位症患者进行回顾性研究,根据与疾病相关的疼痛症状(有无严重和致残症状)分为两组。采用实时PCR技术进行遗传分析,采用非条件logistic回归模型,采用比值比(OR)和95%置信区间(CI)估计关联分析。结果:子宫内膜异位症患者疼痛症状发生率高:痛经82%,性交困难67%,慢性盆腔疼痛53%,周期性肠道和泌尿系统疾病52%。在遗传分析方面,LEP rs7799039 G>A SNP有32.7%的A等位基因和11.4%的AA基因型,LEPR rs1137100 A>G SNP有17.5%的G等位基因和2.5%的GG基因型。LEPR rs1137100多态性与慢性盆腔疼痛有显著相关性(OR=1.75;CI 95%=1.05-2.89)和性交困难(OR=1.78;CI 95%=1.01-3.12)。结论:我们的研究结果表明,LEPR rs1137100多态性与子宫内膜异位症相关的妇科疼痛增加有关,可能是该病分子诊断和个性化治疗策略制定的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信