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肥胖与患有代谢疾病的青少年中高密度脂蛋白亚类分布的改变有关。

Obesity is associated with an altered HDL subspecies profile among adolescents with metabolic disease.

作者信息

Davidson W Sean, Heink Anna, Sexmith Hannah, Dolan Lawrence M, Gordon Scott M, Otvos James D, Melchior John T, Elder Deborah A, Khoury Jane, Geh Esmond, Shah Amy S

机构信息

Center for Lipid and Arteriosclerosis Science, Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45237-0507.

Department of Pediatrics, Cincinnati Childrenʼns Hospital Research Foundation, Cincinnati, OH 45229-3039.

出版信息

J Lipid Res. 2017 Sep;58(9):1916-1923. doi: 10.1194/jlr.M078667. Epub 2017 Jul 25.

Abstract

We aimed to determine the risk factors associated with the depletion of large HDL particles and enrichment of small HDL particles observed in adolescents with T2D. Four groups of adolescents were recruited: ) lean insulin-sensitive (L-IS), normal BMI and no insulin resistance; ) lean insulin-resistant (L-IR), normal BMI but insulin resistance (fasting insulin levels ≥ 25 mU/ml and homeostatic model assessment of insulin resistance ≥ 6); ) obese insulin-sensitive (O-IS), BMI ≥ 95th percentile and no insulin resistance; and ) obese insulin-resistant (O-IR), BMI ≥ 95th percentile and insulin resistance. Plasma was separated by using gel-filtration chromatography to assess the HDL subspecies profile and compared with that of obese adolescents with T2D (O-T2D). Large HDL subspecies were significantly lower across groups from L-IS > L-IR > O-IS > O-IR > O-T2D ( < 0.0001); small HDL particles were higher from L-IS to O-T2D ( < 0.0001); and medium-sized particles did not differ across groups. The contributions of obesity, insulin resistance, and diabetes to HDL subspecies profile were between 23% and 28%, 1% and 10%, and 4% and 9%, respectively. Obesity is the major risk factor associated with the altered HDL subspecies profile previously reported in adolescents with T2D, with smaller contributions from insulin resistance and diabetes.

摘要

我们旨在确定与2型糖尿病青少年中观察到的大高密度脂蛋白(HDL)颗粒减少和小HDL颗粒富集相关的风险因素。招募了四组青少年:(1)瘦型胰岛素敏感(L-IS)组,体重指数(BMI)正常且无胰岛素抵抗;(2)瘦型胰岛素抵抗(L-IR)组,BMI正常但存在胰岛素抵抗(空腹胰岛素水平≥25 mU/ml且胰岛素抵抗稳态模型评估≥6);(3)肥胖胰岛素敏感(O-IS)组,BMI≥第95百分位数且无胰岛素抵抗;以及(4)肥胖胰岛素抵抗(O-IR)组,BMI≥第95百分位数且存在胰岛素抵抗。通过凝胶过滤色谱法分离血浆以评估HDL亚类谱,并与患有2型糖尿病的肥胖青少年(O-T2D)的谱进行比较。大HDL亚类在各分组中显著降低,顺序为L-IS > L-IR > O-IS > O-IR > O-T2D(P < 0.0001);小HDL颗粒从L-IS到O-T2D逐渐升高(P < 0.0001);中等大小颗粒在各分组之间无差异。肥胖、胰岛素抵抗和糖尿病对HDL亚类谱的贡献分别在23%至28%、1%至10%和4%至9%之间。肥胖是与先前报道的2型糖尿病青少年中HDL亚类谱改变相关的主要风险因素,胰岛素抵抗和糖尿病的贡献较小。

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