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瘦素和肿瘤坏死因子-α基因多态性对中国2型糖尿病患者罗格列酮反应的影响。

Impact of genetic polymorphisms of leptin and TNF-alpha on rosiglitazone response in Chinese patients with type 2 diabetes.

作者信息

Liu Hai-Ling, Lin Yang-Gen, Wu Jing, Sun Hong, Gong Zhi-Cheng, Hu Ping-Cheng, Yin Ji-Ye, Zhang Wei, Wang Dan, Zhou Hong-Hao, Liu Zhao-Qian

机构信息

Institute of Clinical Pharmacology, Key Laboratory of Pharmacogenetics in Hunan Province, Central South University, Changsha, Hunan 410078, People's Republic of China.

出版信息

Eur J Clin Pharmacol. 2008 Jul;64(7):663-71. doi: 10.1007/s00228-008-0483-9. Epub 2008 Apr 26.

Abstract

BACKGROUND

Leptin and tumor necrosis factor-alpha (TNF-alpha) play important role in homeostasis and insulin resistance in the treatment of Type 2 diabetes (T2DM). The aims of the present study were to investigate the association between leptin G-2548A and TNF-alpha G-308A polymorphisms and rosiglitazone response in T2DM patients.

MATERIALS

245 patients with T2D and 122 health volunteers were enrolled to identify leptin G-2548A and TNF-alpha G-308A genotypes by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. Forty-two T2D patients with different leptin G-2548A and TNF-alpha G-308A genotypes received orally rosiglitazone as a single-agent therapy (4 mg day(-1) p.o.) for 12 weeks. Serum triglyceride (TG), fasting plasma glucose (FPG), postprandial plasma glucose (PPG), fasting serum insulin (FINs), glycated hemoglobin (HbAlc), postprandial serum insulin (PINS), homeostasis model assessment for insulin resistance (HOMA-IR), low-density lipoprotein-cholesterol (LDL-c), and high-density lipoprotein-cholesterol (HDL-c) were determined before and after rosiglitazone treatment.

RESULTS

A significant association between the variation of G-2548A allele with body mass index (BMI), serum leptin levels and FPG was observed in T2DM patients. Moreover, patients with G allele of leptin G-2548A had lower BMI and serum leptin concertration as well as bigger FPG than that in AA genotypes (P < 0.05). Moreover, we found an enhanced rosiglitazone effect in patients with AA genotype of leptin G-2548A on FINS and PINS compared with GG+GA genotype (P < 0.05). Finally, our results showed an attenuated rosiglitazone effect in patients with GA+AA genotype of TNF-alpha G-308A on FINS compared with GG genotype (P < 0.05).

CONCLUSIONS

These data suggest there were not significantly differences in the frequencies of leptin G-2548A and TNF-alpha G-308A between patients with T2DM and health control. TNF-alpha G-308A polymorphism might be associated with the therapeutic efficacy of rosiglitazone in T2DM patients.

摘要

背景

瘦素和肿瘤坏死因子-α(TNF-α)在2型糖尿病(T2DM)治疗中的体内平衡和胰岛素抵抗方面发挥重要作用。本研究旨在探讨T2DM患者中瘦素G-2548A和TNF-α G-308A基因多态性与罗格列酮反应之间的关联。

材料

招募245例T2DM患者和122名健康志愿者,通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析鉴定瘦素G-2548A和TNF-α G-308A基因型。42例具有不同瘦素G-2548A和TNF-α G-308A基因型的T2DM患者接受罗格列酮单药口服治疗(4mg·d⁻¹口服),疗程12周。在罗格列酮治疗前后测定血清甘油三酯(TG)、空腹血糖(FPG)、餐后血糖(PPG)、空腹血清胰岛素(FINs)、糖化血红蛋白(HbAlc)、餐后血清胰岛素(PINS)、胰岛素抵抗稳态模型评估(HOMA-IR)、低密度脂蛋白胆固醇(LDL-c)和高密度脂蛋白胆固醇(HDL-c)。

结果

在T2DM患者中观察到G-2548A等位基因变异与体重指数(BMI)、血清瘦素水平和FPG之间存在显著关联。此外,瘦素G-2548A的G等位基因患者的BMI和血清瘦素浓度较低,FPG高于AA基因型患者(P<0.05)。此外,我们发现与GG+GA基因型相比,瘦素G-2548A的AA基因型患者对罗格列酮在FINS和PINS方面的疗效增强(P<0.05)。最后,我们的结果显示,与GG基因型相比,TNF-α G-308A的GA+AA基因型患者对罗格列酮在FINS方面的疗效减弱(P<0.05)。

结论

这些数据表明,T2DM患者与健康对照者之间瘦素G-2548A和TNF-α G-308A的频率没有显著差异。TNF-α G-308A多态性可能与罗格列酮在T2DM患者中的治疗效果相关。

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