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Linkage and Association Analyses of Type 2 Diabetes/Impaired Glucose Metabolism and Adiponectin Serum Levels in Japanese Americans From Hawaii

机译:来自夏威夷的日裔美国人的2型糖尿病/受损糖代谢和脂联素血清水平的关联和关联分析

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摘要

Type 2 diabetes is a common disorder associated with obesity. Lower plasma levels of adiponectin were associated with type 2 diabetes. Candidate regions on chromosomes 1 (~70 cM) and 14 (~30 cM) were evaluated for replication of suggestive linkage results for type 2 diabetes/impaired glucose homeostasis in an independent sample of Japanese Americans. Replication of independent linkage evidence for serum levels of adiponectin on chromosome 14 was also evaluated. We investigated 529 subjects from 175 sibships who were originally part of the Honolulu Heart Program. Analyses included nonparametric linkage and association using SAGE (Statistical Analysis for Genetic Epidemiology) and FBAT (family-based test of association) programs and Monte Carlo simulation of Fisher’s exact test in SAS. For type 2 diabetes/impaired glucose metabolism, nominal linkage evidence (P < 0.02) followed-up by genotypic association (P = 0.016) was found with marker D14S297 at 31.8 cM; linkage analyses using only diabetes phenotype were also nominally significant at this marker (P < 0.02). Nominal evidence for genotypic association to adiponectin serum level phenotype (P = 0.04) was found with the marker D14S1032 at 23.2 cM. The present study was limited by relatively small sample size. Nevertheless, these results corroborate earlier studies, suggesting that further research is warranted in the candidate region ~30 cM on chromosome 14.
机译:2型糖尿病是与肥胖相关的常见疾病。血浆脂联素水平降低与2型糖尿病有关。在一个独立的日裔美国人样本中,评估了1号染色体(〜70 cM)和14号染色体(〜30 cM)的候选区域对于2型糖尿病/受损葡萄糖稳态的暗示性连锁结果的复制。还评估了14号染色体上脂联素血清水平的独立连锁证据的复制。我们调查了来自175名同胞的529名受试者,这些受试者最初是檀香山心脏计划的一部分。分析包括使用SAGE(遗传流行病学统计分析)和FBAT(基于家庭的关联测试)程序的非参数链接和关联,以及在SAS中进行Fisher精确测试的Monte Carlo模拟。对于2型糖尿病/糖代谢受损,在31.8 cM处发现标记物D14S297的标称连锁证据(P <0.02)和基因型关联(P = 0.016)。仅使用糖尿病表型的连锁分析在该标记上也具有名义上的显着性(P <0.02)。基因标记与脂联素血清水平表型(P = 0.04)的基因型关联的标称证据是在23.2 cM下用标记D14S1032发现的。本研究受到相对较小的样本量的限制。然而,这些结果证实了较早的研究,表明有必要在14号染色体上约30 cM的候选区域进行进一步的研究。

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