The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity

Background: Single nucleotide polymorphisms (SNPs) in the low-density lipoprotein receptor-related protein 5 (LRP5) and the low-density lipoprotein receptor-related protein 5 (LRP6) genes have been implicated in the pathogenesis of type 2 diabetes mellitus (T2DM) and obesity (OB). This study aimed t...

Full description

Saved in:
Bibliographic Details
Main Authors: Jun Li, Ya Li, Yunqiu Lu, Siyuan Li, Yecheng Zhu, Chuanbing Sun, Partab Rai, Xuehai Jia
Format: Article
Language:English
Published: SAGE Publishing 2025-01-01
Series:Clinical Medicine Insights: Endocrinology and Diabetes
Online Access:https://doi.org/10.1177/11795514241307180
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832544687176548352
author Jun Li
Ya Li
Yunqiu Lu
Siyuan Li
Yecheng Zhu
Chuanbing Sun
Partab Rai
Xuehai Jia
author_facet Jun Li
Ya Li
Yunqiu Lu
Siyuan Li
Yecheng Zhu
Chuanbing Sun
Partab Rai
Xuehai Jia
author_sort Jun Li
collection DOAJ
description Background: Single nucleotide polymorphisms (SNPs) in the low-density lipoprotein receptor-related protein 5 (LRP5) and the low-density lipoprotein receptor-related protein 5 (LRP6) genes have been implicated in the pathogenesis of type 2 diabetes mellitus (T2DM) and obesity (OB). This study aimed to evaluate the polymorphisms in LRP5 and LRP6 genes in postmenopausal patients with T2DM and OB. Methods: Participants were categorized into the Non-T2DM group (n = 53) and the T2DM group (n = 89) based on glycemic levels. Baseline data and biochemical indices were collected, Bone mineral density (BMD) was measured using dual-energy X-ray absorptiometry, and SNPs at the LRP5 and LRP6 loci were assessed by time-of-flight mass spectrometry. Results: 1. There was a statistical difference in the distribution of genotypes (CC/CT) at locus rs4988331 (χ2 = 67.940, P  = .000) and in the distribution of alleles (C/T) between the T2DM and non-T2DM groups (χ2 = 50.506, P  = .000). Additionally, there were significant differences in the allele (G/A) at locus rs11054704, and both allele (G/T) and genotype (GG/GT) distributions at locus rs1181334 between the OB group and the normal weight group ( P  < .05). 2. OB was identified as a risk factor for T2DM in individuals with the wild-type at locus rs1181334, and the interaction between wild-type and mutant was significant ( P  < .05). 3. Multifactorial logistic regression analysis revealed that BMD (OR 3.755; 95% CI, 1.215-11.608) and triglyceride-glucose (TyG) index (OR 2.855; 95% CI, 1.361-5.986) were risk factors for T2DM in postmenopausal women, whereas alkaline phosphatase (ALP; OR 0.970; 95% CI, 0.945-0.995) and rs4988331 mutation (OR 0.018; 95% CI, 0.006-0.060) were protective factors. Conclusion: Mutations at the LRP5-rs4988331 locus, as well as the LRP6-rs11054704 and rs1181334 loci, may be associated with the development of T2DM and OB in postmenopausal women.
format Article
id doaj-art-6732f20ef0ce4e9c82c2d0e7865dd1f4
institution Kabale University
issn 1179-5514
language English
publishDate 2025-01-01
publisher SAGE Publishing
record_format Article
series Clinical Medicine Insights: Endocrinology and Diabetes
spelling doaj-art-6732f20ef0ce4e9c82c2d0e7865dd1f42025-02-03T10:03:22ZengSAGE PublishingClinical Medicine Insights: Endocrinology and Diabetes1179-55142025-01-011810.1177/11795514241307180The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and ObesityJun Li0Ya Li1Yunqiu Lu2Siyuan Li3Yecheng Zhu4Chuanbing Sun5Partab Rai6Xuehai Jia7Department of Endocrinology and Metabolism, The First Affiliated Hospital, Shihezi University, Shihezi, Xinjiang, ChinaDepartment of Endocrinology and Metabolism, The First Affiliated Hospital, Shihezi University, Shihezi, Xinjiang, ChinaMedical School of Shihezi University, Shihezi, ChinaMedical School of Shihezi University, Shihezi, ChinaDepartment of Endocrinology and Metabolism, The First Affiliated Hospital, Shihezi University, Shihezi, Xinjiang, ChinaDepartment of Endocrinology and Metabolism, The First Affiliated Hospital, Shihezi University, Shihezi, Xinjiang, ChinaOcaf Hospital, Karachi, PakistanWest China Hospital of Sichuan University, Chengdu, Sichuan, ChinaBackground: Single nucleotide polymorphisms (SNPs) in the low-density lipoprotein receptor-related protein 5 (LRP5) and the low-density lipoprotein receptor-related protein 5 (LRP6) genes have been implicated in the pathogenesis of type 2 diabetes mellitus (T2DM) and obesity (OB). This study aimed to evaluate the polymorphisms in LRP5 and LRP6 genes in postmenopausal patients with T2DM and OB. Methods: Participants were categorized into the Non-T2DM group (n = 53) and the T2DM group (n = 89) based on glycemic levels. Baseline data and biochemical indices were collected, Bone mineral density (BMD) was measured using dual-energy X-ray absorptiometry, and SNPs at the LRP5 and LRP6 loci were assessed by time-of-flight mass spectrometry. Results: 1. There was a statistical difference in the distribution of genotypes (CC/CT) at locus rs4988331 (χ2 = 67.940, P  = .000) and in the distribution of alleles (C/T) between the T2DM and non-T2DM groups (χ2 = 50.506, P  = .000). Additionally, there were significant differences in the allele (G/A) at locus rs11054704, and both allele (G/T) and genotype (GG/GT) distributions at locus rs1181334 between the OB group and the normal weight group ( P  < .05). 2. OB was identified as a risk factor for T2DM in individuals with the wild-type at locus rs1181334, and the interaction between wild-type and mutant was significant ( P  < .05). 3. Multifactorial logistic regression analysis revealed that BMD (OR 3.755; 95% CI, 1.215-11.608) and triglyceride-glucose (TyG) index (OR 2.855; 95% CI, 1.361-5.986) were risk factors for T2DM in postmenopausal women, whereas alkaline phosphatase (ALP; OR 0.970; 95% CI, 0.945-0.995) and rs4988331 mutation (OR 0.018; 95% CI, 0.006-0.060) were protective factors. Conclusion: Mutations at the LRP5-rs4988331 locus, as well as the LRP6-rs11054704 and rs1181334 loci, may be associated with the development of T2DM and OB in postmenopausal women.https://doi.org/10.1177/11795514241307180
spellingShingle Jun Li
Ya Li
Yunqiu Lu
Siyuan Li
Yecheng Zhu
Chuanbing Sun
Partab Rai
Xuehai Jia
The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity
Clinical Medicine Insights: Endocrinology and Diabetes
title The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity
title_full The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity
title_fullStr The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity
title_full_unstemmed The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity
title_short The Relationship Between LRP-5 and LRP-6 Gene Mutations and Postmenopausal Type 2 Diabetes and Obesity
title_sort relationship between lrp 5 and lrp 6 gene mutations and postmenopausal type 2 diabetes and obesity
url https://doi.org/10.1177/11795514241307180
work_keys_str_mv AT junli therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT yali therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT yunqiulu therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT siyuanli therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT yechengzhu therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT chuanbingsun therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT partabrai therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT xuehaijia therelationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT junli relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT yali relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT yunqiulu relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT siyuanli relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT yechengzhu relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT chuanbingsun relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT partabrai relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity
AT xuehaijia relationshipbetweenlrp5andlrp6genemutationsandpostmenopausaltype2diabetesandobesity