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UCP-3基因rs1626521与人类肥胖及胃功能的关联

Association of UCP-3 rs1626521 with obesity and stomach functions in humans.

作者信息

Acosta Andres, Camilleri Michael, Shin Andrea, Vazquez-Roque Maria I, Iturrino Johanna, Lanza Ian R, Nair K Sreekumaran, Burton Duane, O'Neill Jessica, Eckert Deborah, Carlson Paula, Vella Adrian, Zinsmeister Alan R

机构信息

Clinical Enteric Neuroscience Translational and Epidemiological Research (C.E.N.T.E.R.), Division of Gastroenterology and Hepatology, Department of Medicine, College of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Obesity (Silver Spring). 2015 Apr;23(4):898-906. doi: 10.1002/oby.21039. Epub 2015 Mar 7.

Abstract

OBJECTIVE

To examine the association of gene variants of uncoupling proteins (UCP)-2 and -3 with obesity and gastrointestinal (GI) traits.

METHODS

In 255 overweight or obese adults, the associations of gene variants in UCP-2 (-3474, rs659366) and UCP-3 (rs1626521, rs2075577, rs15763) with body weight (BW) and GI traits were studied. Gene variants were genotyped by TaqMan® assay. The associations of genotypes with BW and GI traits (gastric emptying, gastric volume, satiety by buffet meal, satiation by nutrient drink test and GI hormones) were assessed using ANOVA corrected for false detection rate (FDR).

RESULTS

A novel UCP-3 gene variant, rs1626521, was identified; it was associated with BW (P = 0.039), waist circumference (P = 0.035), and significantly higher postprandial gastric volume (P = 0.003) and calories ingested at buffet meal (P = 0.006, both significant with FDR). In a subgroup of 11 participants, rs1626521 was also associated with reduced mitochondrial bioenergetics efficiency in skeletal muscle (P = 0.051). In an in vitro study in HEK293 cells, rs1626521 reduced UCP-3 protein expression (P = 0.049). Associations detected between other genotypes and GI traits were nonsignificant with FDR.

CONCLUSIONS

A newly identified functional variant (rs1626521) in UCP-3 affects postprandial gastric functions and satiety and may contribute to weight gain and alter human mitochondrial function.

摘要

目的

研究解偶联蛋白(UCP)-2和-3的基因变异与肥胖及胃肠道(GI)特征之间的关联。

方法

在255名超重或肥胖成年人中,研究UCP-2(-3474,rs659366)和UCP-3(rs1626521、rs2075577、rs15763)基因变异与体重(BW)及GI特征的关联。通过TaqMan®分析对基因变异进行基因分型。使用校正了错误发现率(FDR)的方差分析评估基因型与BW及GI特征(胃排空、胃容积、自助餐饱腹感、营养饮料测试饱腹感及GI激素)之间的关联。

结果

鉴定出一种新的UCP-3基因变异rs1626521;它与BW(P = 0.039)、腰围(P = 0.035)相关,且与餐后胃容积显著升高(P = 0.003)及自助餐摄入热量(P = 0.006,两者经FDR校正后均显著)相关。在11名参与者的亚组中,rs1626521还与骨骼肌线粒体生物能量效率降低相关(P = 0.051)。在HEK293细胞的体外研究中,rs1626521降低了UCP-3蛋白表达(P = 0.049)。经FDR校正后,其他基因型与GI特征之间的关联无统计学意义。

结论

新鉴定出的UCP-3功能性变异(rs1626521)影响餐后胃功能和饱腹感,可能导致体重增加并改变人类线粒体功能。

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