Inserm U, UMR, institut Pasteur de Lille, université de Lille, France.
Diabetes Metab. 2009 Sep;35(4):287-92. doi: 10.1016/j.diabet.2008.12.005. Epub 2009 May 15.
Although the ANGPTL6 (angiopoietin-like 6) gene product is now known to be involved in the regulation of fat mass and insulin sensitivity in mice, its physiological functions in humans have yet to be determined.
Subjects from the population-based French MONICA Study (n=3402) were genotyped for single nucleotide polymorphisms (SNPs) in ANGPTL6, and associations with anthropometric or biochemical phenotypes were looked for.
On evaluating the frequency of 17 ANGPTL6 SNPs in 100 randomly selected subjects on the basis of linkage disequilibrium mapping, four SNPs (rs6511435, rs8112063, rs11671983 and rs15723) were found to cover more than 95% of the known ANGPTL6 genetic variability. Subjects from the entire MONICA Study were then genotyped for these four SNPs. No significant association was detected for rs11671983 and rs15723. In contrast, the G allele of rs8112063 was associated with lower plasma glucose levels (P=0.009). Also, obese subjects carrying the G allele of rs6511435 had higher plasma insulin levels than AA subjects (P=0.0055). Moreover, the G allele of rs6511435 tended to be associated with a 20% higher risk of the metabolic syndrome (P=0.034). However, when false discovery rate testing (40 tests) was applied, these associations were no longer statistically significant.
These findings constitute the first study in humans of ANGPTL6 genetic variability. Although there was no evidence that polymorphisms in ANGPTL6 might be significantly associated with the metabolic syndrome-related phenotypes, a weak association of these polymorphisms with these parameters cannot be excluded. Further association studies are needed to arrive at any definite conclusions.
虽然现在已知 ANGPTL6(血管生成素样蛋白 6)基因产物参与调节小鼠的脂肪量和胰岛素敏感性,但它在人类中的生理功能尚未确定。
从基于人群的法国 MONICA 研究(n=3402)中选择受试者,对 ANGPTL6 的单核苷酸多态性(SNP)进行基因分型,并寻找与人体测量或生化表型的关联。
在根据连锁不平衡图谱对 100 名随机选择的受试者进行的 17 个 ANGPTL6 SNP 频率评估中,发现 4 个 SNP(rs6511435、rs8112063、rs11671983 和 rs15723)可覆盖超过 95%的已知 ANGPTL6 遗传变异性。然后对整个 MONICA 研究的受试者进行这 4 个 SNP 的基因分型。rs11671983 和 rs15723 未检测到显著关联。相比之下,rs8112063 的 G 等位基因与较低的血浆葡萄糖水平相关(P=0.009)。此外,携带 rs6511435 的 G 等位基因的肥胖受试者的血浆胰岛素水平高于 AA 受试者(P=0.0055)。此外,rs6511435 的 G 等位基因与代谢综合征的风险增加 20%相关(P=0.034)。然而,当应用虚假发现率检验(40 次检验)时,这些关联不再具有统计学意义。
这些发现构成了人类 ANGPTL6 遗传变异性的首次研究。尽管没有证据表明 ANGPTL6 多态性可能与代谢综合征相关表型显著相关,但不能排除这些多态性与这些参数之间存在微弱关联。需要进一步的关联研究才能得出任何明确的结论。