Janet M Wojcicki, David Rehkopf, Elissa Epel, Philip Rosenthal
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引用次数: 12
摘要
白细胞端粒长度较短是对与炎症相关的慢性疾病的反应,如糖尿病和冠状动脉疾病。1999年至2002年国家健康与营养调查(NHANES)的数据被用于探索白细胞端粒长度与假定的NAFLD之间的关系,如血清谷丙转氨酶(ALT)水平升高、肥胖或腹部肥胖。使用逻辑回归模型来评估端粒长度与NAFLD推定标记物之间的关系,并对可能的混杂因素进行调整。在NHANES中调整后的模型中,ALT水平升高、腹部肥胖或肥胖与端粒长度没有关系(or 1.13, 95% CI 0.48-2.65;OR 1.17, 95% CI 0.52-2.62)。与假定的NAFLD相比,墨西哥裔美国男性的端粒长度更短(OR 0.07, 95% CI 0.006-0.79),使用不同的NAFLD指标(OR 0.012, 95% CI 0.0006-0.24)。墨西哥裔NAFLD患者的端粒长度比其他人群短。纵向研究对于评估端粒长度作为评估墨西哥NALFD发病机制的潜在预测因子的作用是必要的。
Shorter Leukocyte Telomere Length in Relation to Presumed Nonalcoholic Fatty Liver Disease in Mexican-American Men in NHANES 1999-2002.
Leukocyte telomere length is shorter in response to chronic disease processes associated with inflammation such as diabetes mellitus and coronary artery disease. Data from the National Health and Nutrition Examination Survey (NHANES) from 1999 to 2002 was used to explore the relationship between leukocyte telomere length and presumed NAFLD, as indicated by elevated serum alanine aminotransferase (ALT) levels, obesity, or abdominal obesity. Logistic regression models were used to evaluate the relationship between telomere length and presumed markers of NAFLD adjusting for possible confounders. There was no relationship between elevated ALT levels, abdominal obesity, or obesity and telomere length in adjusted models in NHANES (OR 1.13, 95% CI 0.48-2.65; OR 1.17, 95% CI 0.52-2.62, resp.). Mexican-American men had shorter telomere length in relation to presumed NAFLD (OR 0.07, 95% CI 0.006-0.79) and using different indicators of NAFLD (OR 0.012, 95% CI 0.0006-0.24). Mexican origin with presumed NAFLD had shorter telomere length than men in other population groups. Longitudinal studies are necessary to evaluate the role of telomere length as a potential predictor to assess pathogenesis of NALFD in Mexicans.
期刊介绍:
International Journal of Hepatology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to the medical, surgical, pathological, biochemical, and physiological aspects of hepatology, as well as the management of disorders affecting the liver, gallbladder, biliary tree, and pancreas.