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perilipin基因多态性是青少年肥胖发生的危险因素?一项病例对照研究。

Perilipin polymorphisms are risk factors for the development of obesity in adolescents? A case-control study.

作者信息

Tokgöz Yavuz, Işık Ishak Abdurrahman, Akbari Soheil, Kume Tuncay, Sayın Oya, Erdal Esra, Arslan Nur

机构信息

Department of Pediatric Gastroenterology, Hepatology and Nutrition, Dokuz Eylul University Faculty of Medicine, 35330, Inciraltı-Izmir, Turkey.

Department of Medical Biology, Dokuz Eylul University, Faculty of Medicine, Izmir, Turkey.

出版信息

Lipids Health Dis. 2017 Mar 9;16(1):52. doi: 10.1186/s12944-017-0440-7.

Abstract

BACKGROUND

The variations in perilipin gene (PLIN) were previously associated with obesity. We examined the association of polymorphisms at the PLIN locus in adolescents with obesity and their connection with serum adipokines.

METHODS

A total of 308 children (206 obese, 66.8% and 102 healthy control, 33.2%) between the ages of 10-18 years were included into the study. PLIN gene analysis [PLIN 1, PLIN 4, PLIN 6, PLIN 5'UTR-1234 C > G and PLIN 10171 A/T] were studied by Real Time-PCR. Serum leptin, adiponectin, resistin and ghrelin levels were studied by ELISA method in both groups and their link with perilipin polymorphisms were analyzed.

RESULTS

Serum leptin level was found significantly high in obese adolescents. Other adipokine levels were similar in both groups. The incidence of PLIN 1, PLIN 4, PLIN 5'UTR-1234 C > G and PLIN 10171 A/T minor and major alleles was similar in both groups. PLIN 6 T/T allele was determined significantly high in obese adolescents compared to that of control group. No correlation was detected between perilipin polymorphism and serum levels of adipokines.

CONCLUSION

The PLIN 6 polymorphism of the perilipin gene may influence the risk of the obesity during adolescence.

TRIAL REGISTRATION

Retrospectively registered.

摘要

背景

此前研究发现脂联素基因(PLIN)的变异与肥胖有关。我们研究了青少年肥胖患者中PLIN基因座多态性的关联及其与血清脂肪因子的关系。

方法

本研究共纳入308名10至18岁的儿童(206名肥胖儿童,占66.8%;102名健康对照儿童,占33.2%)。通过实时定量聚合酶链反应(Real Time-PCR)对PLIN基因[PLIN 1、PLIN 4、PLIN 6、PLIN 5'非翻译区-1234 C>G和PLIN 10171 A/T]进行分析。采用酶联免疫吸附测定法(ELISA)检测两组儿童血清瘦素、脂联素、抵抗素和胃饥饿素水平,并分析其与脂联素基因多态性的关系。

结果

肥胖青少年的血清瘦素水平显著升高。两组的其他脂肪因子水平相似。两组中PLIN 1、PLIN 4、PLIN 5'非翻译区-1234 C>G和PLIN 10171 A/T等位基因的次要和主要等位基因发生率相似。与对照组相比,肥胖青少年中PLIN 6 T/T等位基因的比例显著升高。未检测到脂联素基因多态性与血清脂肪因子水平之间的相关性。

结论

脂联素基因的PLIN 6多态性可能影响青少年肥胖的风险。

试验注册

回顾性注册。

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