Morandi Anita, Pinelli Leonardo, Petrone Antonio, Vatin Vincent, Buzzetti Raffaella, Froguel Philippe, Meyre David
1Department of Mother and Child, Biology-Genetics, Section of Pediatrics, University of Verona, Verona, Italy.
Obesity (Silver Spring). 2009 Jan;17(1):202-6. doi: 10.1038/oby.2008.470. Epub 2008 Oct 23.
Ectonucleotide Pyrophosphatase Phosphodiesterase 1 (ENPP1) downregulates insulin signaling by inhibiting the insulin receptor's tyrosine-kinase. K121Q and other ENPP1 single-nucleotide polymorphisms (SNPs), IVS20delT-11 and A/G+1044TGA, have been previously associated with obesity in French children, and the risk haplotype QdelTG has also been associated with this condition in both French and German children. Our aim was to perform a case-control replication study in order to assess the possible association of childhood obesity and overweight with the above-mentioned ENPP1 SNPs, and with the QdelTG haplotype, in the Italian population. A total of 865 healthy Italian children were studied: 453 normal-weight, 243 overweight and 169 obese subjects. Genotyping was performed by Taq-Man or Light-Cycler Technology. The Q variant of K121Q showed a negative association with overweight-obesity under both additive (odds ratio (OR) = 0.74, 95% confidence interval (CI) = 0.57-0.97, P = 0.030) and recessive (OR = 0.32, 95% CI = 0.10-0.97, P = 0.035) modes of inheritance. The Z-score of BMI showed a significant decreasing trend from children K/K homozygous to K/Q heterozygous, and to Q/Q homozygous (0.45 vs. 0.28 vs. -0.19; P = 0.009), according to the additive model. The two other SNPs and the QdelTG haplotype did not exhibit any association with overweight/obesity. This is the first child-based study showing a protective role of the 121Q variant of ENPP1 against overweight/obesity.
胞外核苷酸焦磷酸酶磷酸二酯酶1(ENPP1)通过抑制胰岛素受体的酪氨酸激酶来下调胰岛素信号传导。K121Q及其他ENPP1单核苷酸多态性(SNP),即IVS20delT-11和A/G+1044TGA,先前已被证实与法国儿童的肥胖有关,并且风险单倍型QdelTG在法国和德国儿童中也与这种情况相关。我们的目的是进行一项病例对照重复研究,以评估意大利人群中儿童肥胖和超重与上述ENPP1 SNP以及QdelTG单倍型之间的可能关联。总共对865名健康的意大利儿童进行了研究:453名体重正常、243名超重和169名肥胖受试者。采用Taq-Man或Light-Cycler技术进行基因分型。在加性(优势比(OR)=0.74,95%置信区间(CI)=0.57-0.97,P=0.030)和隐性(OR=0.32,95%CI=0.10-0.97,P=0.035)遗传模式下,K121Q的Q变体与超重-肥胖呈负相关。根据加性模型,体重指数(BMI)的Z评分从K/K纯合子儿童到K/Q杂合子儿童,再到Q/Q纯合子儿童呈现出显著下降趋势(0.45对0.28对-0.19;P=0.009)。另外两个SNP和QdelTG单倍型与超重/肥胖无任何关联。这是第一项基于儿童的研究,表明ENPP1的121Q变体对超重/肥胖具有保护作用。