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ADIPOQ polymorphisms are associated with insulin resistance in Japanese women

机译:ADIPOQ多态性与日本女性的胰岛素抵抗有关

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摘要

Visceral fat accumulation contributes to the development of insulin resistance, leading to metabolic syndrome. Adiponectin provides a link between visceral fat accumulation and insulin resistance. In addition to environmental factors, genetic factors play important roles in visceral fat accumulation and circulating adiponectin levels. Genome-wide association studies (GWASs) have identified genetic variations in the adiponectin, C1Q and collagen domain containing (ADIPOQ) gene that are associated with adiponectin levels. In this study, we investigated whether ADIPOQ single nucleotide polymorphisms (SNPs) were associated with visceral fat accumulation and insulin resistance. We measured the visceral fat area (VFA) by computed tomography (CT) and examined the presence of the insulin resistance-related phenotype (fasting plasma glucose, fasting insulin, and homeostasis model assessment-insulin resistance [HOMA-IR]) in a set of Japanese individuals (731 men and 864 women) who were genotyped for seven ADIPOQ SNPs reported by recent GWASs (namely, rs6810075, rs10937273, rs1648707, rs864265, rs182052, rs17366568, and rs6773957). SNPs associated with the phenotype (P < 0.05) were then evaluated by association analysis using a second set of the study participants (383 men and 510 women). None of the SNPs was associated with body mass index (BMI) or VFA in men or women. However, the adiponectin-decreasing alleles of rs10937273 and rs1648707 were significantly associated with HOMA-IR (P = 0.0030 and P = 0.00074, respectively) in women, independently of BMI. These SNPs were significantly associated with decreased adiponectin levels in women. Our results suggested that rs10937273 and rs1648707 may affect insulin sensitivity by regulating adiponectin production by adipose tissue in women.
机译:内脏脂肪积聚有助于胰岛素抵抗的发展,导致代谢综合征。脂联素提供内脏脂肪蓄积与胰岛素抵抗之间的联系。除环境因素外,遗传因素在内脏脂肪积累和循环脂联素水平中也起着重要作用。全基因组关联研究(GWAS)已确定与脂联素水平相关的脂联素,C1Q和含胶原结构域(ADIPOQ)基因的遗传变异。在这项研究中,我们调查了ADIPOQ单核苷酸多态性(SNPs)是否与内脏脂肪蓄积和胰岛素抵抗相关。我们通过计算机断层扫描(CT)测量了内脏脂肪区(VFA),并检查了一组胰岛素抵抗相关表型(空腹血糖,空腹胰岛素和体内稳态模型评估-胰岛素抵抗[HOMA-IR])的存在对最近GWAS报告的七个ADIPOQ SNP进行基因分型的日本个体(731名男性和864名女性)(即rs6810075,rs10937273,rs1648707,rs864265,rs182052,rs17366568和rs6773957)。然后使用第二组研究参与者(383名男性和510名女性)通过关联分析评估与该表型相关的SNP(P <0.05)。男性和女性均未与体重指数(BMI)或VFA相关。但是,女性的rs10937273和rs1648707的脂联素降低等位基因与HOMA-IR显着相关(分别为P = 0.0030和P = 0.00074),而与BMI无关。这些SNPs与女性脂联素水平降低显着相关。我们的结果表明,rs10937273和rs1648707可能通过调节女性脂肪组织产生的脂联素来影响胰岛素敏感性。

著录项

  • 来源
    《Endocrine journal》 |2015年第6期|513-521|共9页
  • 作者单位

    Pharmacogenomics, Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan;

    Pharmacogenomics, Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan;

    Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8574, Japan;

    Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8574, Japan;

    Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8574, Japan;

    Department of Gastroenterology and Metabolism, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-8551, Japan;

    Department of Gastroenterology and Metabolism, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-8551, Japan;

    Laboratory for Mathematics, National Defense Medical College, Tokorozawa 359-8513, Japan;

    Health Science University, Yamanashi 401-0380, Japan;

    Department of Hygiene, Faculty of Medicine, Kagawa University, Kagawa 761-0793, Japan;

    Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita 565-0871, Japan;

    Otemae Hospital, Osaka 540-0008, Japan;

    Department of Medicine and Clinical Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan;

    Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine, Yokohama 236-0004, Japan;

    Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine, Yokohama 236-0004, Japan;

    Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine, Yokohama 236-0004, Japan;

    Department of Metabolism and Atherosclerosis, Graduate School of Medicine, Osaka University, Suita 565-0871, Japan;

    Tokyo Postal Services Agency Hospital, Tokyo 102-8798, Japan;

    Itami City Hospital, Itami 664-8540, Japan;

    Division of Endocrinology, Diabetes and Metabolism, Hematology, Rheumatology Graduate School of Medicine, University of the Ryukyus, Okinawa 903-0215, Japan;

    Research Center for Innovative Cancer Therapy, Kurume University, Kurume 830-0011, Japan;

    Department of Gastroenterology and Metabolism, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-8551, Japan;

    Department of Practical Nursing Science, Faculty of Medicine, Oita University, Oita 879-5593, Japan;

    Division of Endocrinology and Metabolism, Department of Medicine, Kurume University, Kurume 830-0011, Japan;

    Department of Internal Medicine (I), Osaka Medical College, Takatsuki 569-8686, Japan;

    Director of Diabetes and Lifestyle Disease Center, Fukujuji Hospital, Tokyo 204-8522, Japan;

    Department of Internal Medicine 1, Faculty of Medicine, Oita University, Oita 879-5593, Japan;

    Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8574, Japan;

    Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita 565-0871, Japan;

    Pharmacogenomics, Kyoto University Graduate School of Medicine, Yoshida-Konoecho, Sakyo-ku, Kyoto 606-8501, Japan;

  • 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
  • 中图分类
  • 关键词

    ADIPOQ; Single nucleotide polymorphism; Visceral adipose tissue; Insulin resistance; Adiponectin;

    机译:ADIPOQ;单核苷酸多态性内脏脂肪组织;胰岛素抵抗;脂联素;

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