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脂蛋白A rs10455872多态性与儿童肥胖及肥胖相关结局的关联

Association of Lipoprotein A rs10455872 Polymorphism with Childhood Obesity and Obesity-Related Outcomes.

作者信息

Haksayar Ayşen, Donma Mustafa Metin, Batar Bahadır, Tepe Buse, Topçu Birol, Donma Orkide

机构信息

Department of Child Health and Diseases, Faculty of Medicine, Tekirdağ Namık Kemal University, 59030 Tekirdağ, Türkiye.

Department of Medical Biology, Faculty of Medicine, Tekirdağ Namık Kemal University, 59030 Tekirdağ, Türkiye.

出版信息

Diagnostics (Basel). 2025 Jul 18;15(14):1809. doi: 10.3390/diagnostics15141809.


DOI:10.3390/diagnostics15141809
PMID:40722558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12293871/
Abstract

Obesity is associated with cardiovascular disease worldwide. An increased lipoprotein A (LpA) level is an independent risk factor for cardiovascular disease in children. Genetic polymorphisms of the gene may play an important role in susceptibility to obesity. The aim of this study was to investigate the association of rs10455872 polymorphism with the risk and clinical phenotypes of childhood obesity. This study included 103 children with obesity and 77 healthy controls. Genotyping of the rs10455872 polymorphism was performed using real-time PCR. The genotype distributions of the rs10455872 polymorphism did not differ significantly between children with obesity and healthy children ( = 0.563). A marked difference in insulin levels was observed between children with obesity carrying the AG (16.90 IU/mL) and AA (25.57 IU/mL) genotypes. A marked difference was also observed in CRP levels between children with obesity with the AG (2.31 mg/L) and AA (4.25 mg/L) genotypes. After correcting for multiple comparisons using the false discovery rate (FDR), significant differences were found between AG and AA genotypes in vitamin B12 (adjusted = 0.024). Serum iron showed a borderline association (adjusted = 0.072). A statistically significant correlation was found between the metabolic syndrome index and body fat ratio among children with obesity with the AA genotype ( = 0.028). Although limited by the small number of children with obesity with the AG genotype, some differences were noted between the AG and AA genotypes. These exploratory findings require further investigation in adequately powered studies. In children with obesity with the AA genotype, the metabolic syndrome index increases as the body fat ratio increases.

摘要

在全球范围内,肥胖与心血管疾病相关。脂蛋白A(LpA)水平升高是儿童心血管疾病的独立危险因素。该基因的遗传多态性可能在肥胖易感性中起重要作用。本研究的目的是调查rs10455872多态性与儿童肥胖风险及临床表型的关联。本研究纳入了103名肥胖儿童和77名健康对照。采用实时荧光定量PCR对rs10455872多态性进行基因分型。肥胖儿童与健康儿童之间rs10455872多态性的基因型分布无显著差异(P = 0.563)。携带AG(16.90 IU/mL)和AA(25.57 IU/mL)基因型的肥胖儿童之间,胰岛素水平存在显著差异。携带AG(2.31 mg/L)和AA(4.25 mg/L)基因型的肥胖儿童之间,CRP水平也存在显著差异。使用错误发现率(FDR)校正多重比较后,发现AG和AA基因型在维生素B12方面存在显著差异(校正P = 0.024)。血清铁显示出临界关联(校正P = 0.072)。在AA基因型的肥胖儿童中,代谢综合征指数与体脂率之间存在统计学显著相关性(P = 0.028)。尽管受AG基因型肥胖儿童数量较少的限制,但AG和AA基因型之间仍存在一些差异。这些探索性发现需要在样本量充足的研究中进一步调查。在AA基因型的肥胖儿童中,代谢综合征指数随着体脂率的增加而升高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/7e6ad1e293ed/diagnostics-15-01809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/1e6cc6713089/diagnostics-15-01809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/98ee87eb14a7/diagnostics-15-01809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/7e6ad1e293ed/diagnostics-15-01809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/1e6cc6713089/diagnostics-15-01809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/98ee87eb14a7/diagnostics-15-01809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df29/12293871/7e6ad1e293ed/diagnostics-15-01809-g003.jpg

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本文引用的文献

[1]
Peroxisome Proliferator-Activated Receptor Gamma Regulates Interleukin-6-Induced Lipoprotein (a) Gene Expression in Human HepG2 Cells.

J Cardiovasc Pharmacol. 2024-12-1

[2]
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.

Eur Heart J. 2023-6-1

[3]
Lipoprotein(a) beyond the kringle IV repeat polymorphism: The complexity of genetic variation in the LPA gene.

Atherosclerosis. 2022-5

[4]
Prader-Willi Syndrome: Possibilities of Weight Gain Prevention and Treatment.

Nutrients. 2022-5-6

[5]
Immune Response and Lipid Metabolism Gene Polymorphisms Are Associated with the Risk of Obesity in Middle-Aged and Elderly Patients.

J Pers Med. 2022-2-8

[6]
Genotypes and Haplotypes Are Associated with Lipoprotein(a) Levels but Not Arterial Wall Properties in Stable Post-Coronary Event Patients with Very High Lipoprotein(a) Levels.

J Cardiovasc Dev Dis. 2021-12-13

[7]
Monogenic human obesity syndromes.

Handb Clin Neurol. 2021

[8]
Cis-epistasis at the LPA locus and risk of cardiovascular diseases.

Cardiovasc Res. 2022-3-16

[9]
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

Nat Commun. 2018-7-4

[10]
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms.

J Lipid Res. 2017-9

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