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沙特人群中患有和未患有2型糖尿病的肥胖个体中该基因单核苷酸变异的情况。

Involvement of Single Nucleotide Variants in the Gene Among Obesity Individuals with and without Type 2 Diabetes Mellitus in the Saudi Population.

作者信息

Alageel Arwa A, Ali Khan Imran

机构信息

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia.

Medical Genomic Research Department, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.

出版信息

Diabetes Metab Syndr Obes. 2024 Sep 29;17:3603-3617. doi: 10.2147/DMSO.S473843. eCollection 2024.

DOI:10.2147/DMSO.S473843
PMID:39363894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11448462/
Abstract

PURPOSE

Aging is characterized by the gradual physiological changes and alterations that accumulate over time in the human body. The combination of obesity and ageing can lead to an increased risk of serious health issues or death. Single nucleotide variants (SNVs) in the gene were commonly studied, including that in type 2 diabetes mellitus (T2DM).

AIM

The aim of this study is to examine the possible effect of SNVs in on the obese population in Saudi Arabia using middle-aged participants with and without T2DM.

METHODS

This study consists of 100 controls and 100 obesity patients, in which 50 had T2DM and the remaining 50 were obese without T2DM. Genotyping was performed with PCR, and Sanger sequencing analysis was used to validate the molecular association.

RESULTS

In this study, rs1207568 (p = 0.001-0.003) and rs9527025 (p = 0.001-0.00004) SNVs were associated with obesity cases. However, none of the genotypes or allele frequencies showed a positive association with the rs564481 SNV (p = 0.344-0.881). The multiple linear regression model showed that waist and hip were associated (p = 0.01-0.02). ANOVA analysis showed age (p = 0.04), hip (p = 0.002), SBP, and TC (p = 0.02) were associated. Finally, SNV (rs1207568 and rs95270250) and obesity (p < 0.001) associations were confirmed through gene multifactor dimensionality reduction analysis with gene-gene interaction, dendrogram, and graphical depletion method.

CONCLUSION

This study concludes that rs1207568 and rs9527025 SNVs are associated with obesity in the Saudi population. Additional genetical statistics showed significant association between dependent and independent variables. SNVs in play a role in the Saudi population's susceptibility to obesity.

摘要

目的

衰老的特征是人体随着时间推移逐渐积累的生理变化和改变。肥胖与衰老相结合会增加严重健康问题或死亡的风险。人们普遍研究该基因中的单核苷酸变异(SNV),包括2型糖尿病(T2DM)中的变异。

目的

本研究的目的是利用患有和未患有T2DM的中年参与者,研究SNV对沙特阿拉伯肥胖人群的可能影响。

方法

本研究包括100名对照者和100名肥胖患者,其中50名患有T2DM,其余50名肥胖但未患T2DM。采用聚合酶链反应(PCR)进行基因分型,并使用桑格测序分析来验证分子关联。

结果

在本研究中,rs1207568(p = 0.001 - 0.003)和rs9527025(p = 0.001 - 0.00004)SNV与肥胖病例相关。然而,没有一种基因型或等位基因频率与rs564481 SNV呈正相关(p = 0.344 - 0.881)。多元线性回归模型显示腰围和臀围相关(p = 0.01 - 0.02)。方差分析显示年龄(p = 0.04)、臀围(p = 0.002)、收缩压和总胆固醇(p = 0.02)相关。最后,通过基因多因素降维分析以及基因 - 基因相互作用、树形图和图形耗尽法,证实了SNV(rs1207568和rs95270250)与肥胖(p < 0.001)之间的关联。

结论

本研究得出结论,rs1207568和rs9527025 SNV与沙特人群的肥胖相关。额外的遗传统计学显示了因变量和自变量之间的显著关联。该基因中的SNV在沙特人群对肥胖的易感性中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc61/11448462/f13bfa7b3b37/DMSO-17-3603-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc61/11448462/fd0f8018c251/DMSO-17-3603-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc61/11448462/f13bfa7b3b37/DMSO-17-3603-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc61/11448462/fd0f8018c251/DMSO-17-3603-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc61/11448462/f13bfa7b3b37/DMSO-17-3603-g0002.jpg

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本文引用的文献

1
Obesogens: a unifying theory for the global rise in obesity.肥胖诱导物:肥胖全球化的统一理论。
Int J Obes (Lond). 2024 Apr;48(4):449-460. doi: 10.1038/s41366-024-01460-3. Epub 2024 Jan 11.
2
Anti-Obesity Medications and Investigational Agents: An Obesity Medicine Association (OMA) Clinical Practice Statement (CPS) 2022.抗肥胖药物与研究性药物:肥胖医学协会(OMA)2022年临床实践声明(CPS)
Obes Pillars. 2022 Apr 15;2:100018. doi: 10.1016/j.obpill.2022.100018. eCollection 2022 Jun.
3
Progression to Obesity: Variations in Patterns of Metabolic Fluxes, Fat Accumulation, and Gastrointestinal Responses.
肥胖的进展:代谢通量模式、脂肪堆积和胃肠道反应的变化
Metabolites. 2023 Sep 15;13(9):1016. doi: 10.3390/metabo13091016.
4
Causes of obesity: a review.肥胖的原因:综述。
Clin Med (Lond). 2023 Jul;23(4):284-291. doi: 10.7861/clinmed.2023-0168.
5
Chronic inflammation and the hallmarks of aging.慢性炎症与衰老的特征。
Mol Metab. 2023 Aug;74:101755. doi: 10.1016/j.molmet.2023.101755. Epub 2023 Jun 15.
6
Editorial: Obesity and nutrition in the most remote parts of Africa.社论:非洲最偏远地区的肥胖与营养问题
Front Public Health. 2023 May 25;11:1197367. doi: 10.3389/fpubh.2023.1197367. eCollection 2023.
7
Obesity prevalence, physical activity, and dietary practices among adults in Saudi Arabia.沙特阿拉伯成年人的肥胖流行率、身体活动和饮食行为。
Front Public Health. 2023 Mar 28;11:1124051. doi: 10.3389/fpubh.2023.1124051. eCollection 2023.
8
Pharmacotherapy of obesity: an update on the available medications and drugs under investigation.肥胖症的药物治疗:现有药物及正在研究的药物的最新情况
EClinicalMedicine. 2023 Mar 20;58:101882. doi: 10.1016/j.eclinm.2023.101882. eCollection 2023 Apr.
9
Aging and aging-related diseases: from molecular mechanisms to interventions and treatments.衰老和与衰老相关的疾病:从分子机制到干预和治疗。
Signal Transduct Target Ther. 2022 Dec 16;7(1):391. doi: 10.1038/s41392-022-01251-0.
10
Investigation of Klotho G395A and C1818T Polymorphisms and Their Association with Serum Glucose Level and Risk of Type 2 Diabetes Mellitus.Klotho G395A 和 C1818T 多态性及其与血清葡萄糖水平和 2 型糖尿病发病风险的关系研究。
Genes (Basel). 2022 Aug 26;13(9):1532. doi: 10.3390/genes13091532.