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Common Variants of IL6, LEPR, and PBEF1 Are Associated With Obesity in Indian Children

机译:IL6,LEPR和PBEF1的常见变异与印度儿童肥胖相关

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The increasing prevalence of obesity in urban Indian children is indicative of an impending crisis of metabolic disorders. Although perturbations in the secretion of adipokines and inflammatory molecules in childhood obesity are well documented, the contribution of common variants of genes encoding them is not well investigated. We assessed the association of 125 common variants from 21 genes, encoding adipocytokines and inflammatory markers in 1,325 urban Indian children (862 normal weight [NW group] and 463 overweight/obese [OW/OB group]) and replicated top loci in 1,843 Indian children (1,399 NW children and 444 OW/OB children). Variants of four genes (PBEF1 [rs3801266] [P = 4.5 × 10~(-4)], IL6 [rs2069845] [P = 8.7 × 10~(-4)], LEPR [rsll37100] [P = 1.8 × 10~(-3)], and IL6R [rs7514452] [P = 2.1 × 10~(-3)]) were top signals in the discovery sample. Associations of rs2069845, rsl 137100, and rs3801266 were replicated (P = 7.9 × 10~(-4), 8.3 × 10~(-3), and 0.036, respectively) and corroborated in meta-analysis (P = 2.3 × 10~(-6), 3.9 × 10~(-5), and 4.3 × 10~(-4), respectively) that remained significant after multiple testing corrections. These variants also were associated with quantitative measures of adiposity (weight, BM, and waist and hip circumferences). Allele dosage analysis of rs2069845, rsl 137100, and rs3801266 revealed that children with five to six risk alleles had an approximately four times increased risk of obesity than children with less than two risk alleles (P = 1.2 x 10~7). In conclusion, our results demonstrate the association of the common variants of IL6, LEPR, and PBEF1 with obesity in Indian children.
机译:肥胖在印度城市儿童中的患病率上升表明即将发生新陈代谢疾病的危机。尽管儿童肥胖症中脂肪因子和炎性分子分泌的扰动已得到充分记录,但尚未对编码它们的基因的常见变体做出贡献。我们评估了1,325名印度城市儿童(862名正常体重[NW组]和463名超重/肥胖[OW / OB组])中来自21个基因的125种常见变异的关联,这些基因编码脂肪细胞因子和炎性标志物,并在1,843名印度儿童中复制了最高位点(1399名西北儿童和444名OW / OB儿童)。四个基因的变异(PBEF1 [rs3801266] [P = 4.5×10〜(-4)],IL6 [rs2069845] [P = 8.7×10〜(-4)],LEPR [rsll37100] [P = 1.8×10〜 (-3)]和IL6R [rs7514452] [P = 2.1×10〜(-3)])是发现样本中的最高信号。复制了rs2069845,rsl 137100和rs3801266的关联(分别为P = 7.9×10〜(-4),8.3×10〜(-3)和0.036)并在荟萃分析中得到了证实(P = 2.3×10〜 (-6),3.9×10〜(-5)和4.3×10〜(-4))在多次测试校正后仍然显着。这些变体还与肥胖的定量测量(体重,体重,腰围和臀围)有关。 rs2069845,rsl 137100和rs3801266的等位基因剂量分析显示,患病风险为5至6个等位基因的儿童患肥胖症的风险比患病风险少于两个等位基因的儿童高约4倍(P = 1.2 x 10〜7)。总之,我们的结果证明了IL6,LEPR和PBEF1的常见变异与印度儿童肥胖相关。

著录项

  • 来源
    《Diabetes》 |2012年第3期|p.626-631|共6页
  • 作者单位

    Genomics and Molecular Medicine Unit, Council of Scientific and Industrial Research, Institute of Genomics and Integrative Biology, Delhi, India;

    Genomics and Molecular Medicine Unit, Council of Scientific and Industrial Research, Institute of Genomics and Integrative Biology, Delhi, India;

    Genomics and Molecular Medicine Unit, Council of Scientific and Industrial Research, Institute of Genomics and Integrative Biology, Delhi, India;

    Genomics and Molecular Medicine Unit, Council of Scientific and Industrial Research, Institute of Genomics and Integrative Biology, Delhi, India;

    Human Genetics Unit, Indian Statistical Institute, Kolkata, India;

    Department of Endocrinology and Thyroid Research, Institute of Nu-clear Medicine and Allied Sciences, Delhi, India;

    Department of Endocrinology, All India Institute of Medical Sciences, New Delhi, India;

    Genomics and Molecular Medicine Unit, Council of Scientific and Industrial Research, Institute of Genomics and Integrative Biology, Delhi, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:46:29

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