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作 者:林东平[1] 仰礼真[1] 潘晓骅[2] 姜博仁[1] 郭郁郁[1] 朱惠[1] 雷涛[3] 陆颖理[1]
机构地区:[1]上海交通大学医学院附属第九人民医院内分泌科, 200011 [2]上海交通大学医学院附属第九人民医院检验科(, 200011 [3]上海同济大学附属同济医院内分泌科
出 处:《中华内分泌代谢杂志》2011年第5期418-419,共2页Chinese Journal of Endocrinology and Metabolism
摘 要:用荧光法检测正常组、糖尿病HbA1c〈7.0%组和HbA1c〉7.0%组的低密度脂蛋白(LDL)糖化值分别为(17.7±2.31)、(34.29±5.73)和(48.79±7.82)Glycogroups/LDL,用酶联免疫受体法检测上述3组LDL与人内皮细胞LDL受体的特异结合活性分别为(37.65±5.20)、(27.36±4.34)和(15.07±2.23)ng/mg细胞蛋白,2组糖尿病的LDL糖化值均高于对照组(P〈0.01),HbA1c〉7.O%组高于HbA1c〈7.0%组(P〈0.01),而LDL与其受体结合的结果相反。[ Summary] The levels of low-density lipoprotein (LDL) glycation from control group, diabetic HbA1c 〈 7.0% , and HbA1c〉7.0% groups were ( 17.7±2.31 ) , (34.29±5.73) , and (48.79±7.82) Glycogroups/LDL by fluorimetry. The LDL binding to its receptor in three groups were (37.65±5.20) , (27.36±4.34), and ( 15.07± 2.23 )ng/mg cell protein measured by enzyme-linked immunoreceptor assay. The glycated levels in two diabetic groups were higher than that in control group, and higher in HbA1c〉7.0% group than in HbAlc〈7.0% group ( all P〈 0. 01 ). The results of LDL binding capacity to its receptor were just the opposite.
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