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性别和肥胖对椎间盘退变中变体和瘦素水平关联的影响。

Effects of Sex and Obesity on Variant and Leptin Level Associations in Intervertebral Disc Degeneration.

机构信息

Division of Neurosurgery, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan.

School of Medicine, Buddhist Tzu Chi University, Hualien 97004, Taiwan.

出版信息

Int J Mol Sci. 2022 Oct 14;23(20):12275. doi: 10.3390/ijms232012275.

DOI:10.3390/ijms232012275
PMID:36293132
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9603873/
Abstract

Intervertebral disc degeneration (IVDD), for which obesity and genetics are known risk factors, is a chronic process that alters the structure and function of the intervertebral discs (IVD). Circulating leptin is positively correlated with body weight and is often measured to elucidate the pathogenesis of IVD degeneration. In this study, we examined the associations of LEP single nucleotide polymorphisms (SNPs) genetic and environmental effects with IVDD. A total of 303 Taiwanese patients with IVDD (mean age, 58.6 ± 12.7 years) undergoing cervical discectomy for neck pain or lumbar discectomy for back pain were enrolled. Commercially available enzyme-linked immunosorbent assay (ELISA) kits measured the circulating plasma leptin levels. TaqMan SNP genotyping assays genotyped the LEP SNPs rs2167270 and rs7799039. Leptin levels were significantly increased in obese individuals (p < 0.001) and non-obese or obese women (p < 0.001). In the dominant model, recoded minor alleles of rs2167270 and rs7799039 were associated with higher leptin levels in all individuals (p = 0.011, p = 0.012). Further, the association between these LEP SNPs and leptin levels was significant only in obese women (p = 0.025 and p = 0.008, respectively). There was an interaction effect between sex and obesity, particularly among obese women (interaction p = 0.04 and 0.02, respectively). Our findings demonstrate that these SNPs have sex-specific associations with BMI in IVDD patients, and that obesity and sex, particularly among obese women, may modify the LEP transcription effect.

摘要

椎间盘退变(IVDD)是一种慢性过程,会改变椎间盘(IVD)的结构和功能,已知肥胖和遗传是其危险因素。循环瘦素与体重呈正相关,常被用来阐明 IVDD 的发病机制。在这项研究中,我们研究了 LEP 单核苷酸多态性(SNP)的遗传和环境效应与 IVDD 的关联。共纳入 303 名因颈痛行颈椎间盘切除术或腰痛行腰椎间盘切除术的 IVDD 台湾患者(平均年龄 58.6±12.7 岁)。采用商业酶联免疫吸附测定(ELISA)试剂盒测量循环血浆瘦素水平。采用 TaqMan SNP 基因分型检测技术对 LEP SNPs rs2167270 和 rs7799039 进行基因分型。肥胖个体(p<0.001)和非肥胖或肥胖女性(p<0.001)的瘦素水平显著升高。在显性模型中,rs2167270 和 rs7799039 的次要等位基因编码与所有个体的高瘦素水平相关(p=0.011,p=0.012)。此外,这些 LEP SNPs 与瘦素水平的相关性仅在肥胖女性中具有统计学意义(分别为 p=0.025 和 p=0.008)。性别和肥胖之间存在交互作用,尤其是在肥胖女性中(交互作用 p=0.04 和 0.02)。我们的研究结果表明,这些 SNP 与 IVDD 患者的 BMI 具有性别特异性关联,肥胖和性别,特别是肥胖女性,可能会调节 LEP 的转录效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abfb/9603873/4762714b46e9/ijms-23-12275-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abfb/9603873/4762714b46e9/ijms-23-12275-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abfb/9603873/4762714b46e9/ijms-23-12275-g001.jpg

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