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肿瘤坏死因子-α(TNF-α)-308 G>A多态性与氯氮平治疗期间体重纵向变化的遗传关联。

Genetic association between TNF-alpha -308 G>A polymorphism and longitudinal weight change during clozapine treatment.

作者信息

Wang Ying-Chieh, Bai Ya-Mei, Chen Jen-Yeu, Lin Chao-Cheng, Lai I-Ching, Liou Ying-Jay

机构信息

Department of Psychiatry, Yuli Veterans Hospital, Yuli, Hualien, Taiwan, ROC.

出版信息

Hum Psychopharmacol. 2010 Jun-Jul;25(4):303-9. doi: 10.1002/hup.1122.

Abstract

OBJECTIVE

The aim of the study was to investigate the association between genetic variation in the tumor necrosis factor-alpha (TNF-alpha) gene and longitudinal weight change during long-term clozapine treatment.

METHODS

Fifty-five patients with refractory schizophrenia treated with clozapine for 8 years were recruited. Gender, age, treatment response to clozapine in the first 14 months, baseline BMI, clozapine dose, concomitant use of mood stabilizers and other antipsychotics, and -308 G > A polymorphism in the human TNF-alpha gene were analyzed using generalized estimating equations.

RESULTS

In addition to having a lower baseline BMI (p = 0.0013) and a longer treatment time (p = 0.050), the -308 GG carriers gained significantly more weight than the -308 A allele carriers (p = 0.0084) during 8 years of clozapine treatment, after controlling for other non-genetic factors.

CONCLUSIONS

The -308 G > A genetic variant of the TNF-alpha gene is associated with longitudinal weight change during clozapine treatment. Follow-up duration is an important factor to consider when performing pharmacogenetic study of clozapine-induced weight gain.

摘要

目的

本研究旨在探讨肿瘤坏死因子-α(TNF-α)基因的遗传变异与长期使用氯氮平治疗期间体重的纵向变化之间的关联。

方法

招募了55例接受氯氮平治疗8年的难治性精神分裂症患者。使用广义估计方程分析性别、年龄、前14个月对氯氮平的治疗反应、基线体重指数(BMI)、氯氮平剂量、是否同时使用心境稳定剂和其他抗精神病药物以及人类TNF-α基因中的-308 G>A多态性。

结果

在控制其他非遗传因素后,-308 GG携带者除了基线BMI较低(p = 0.0013)和治疗时间较长(p = 0.050)外,在8年的氯氮平治疗期间体重增加明显多于-308 A等位基因携带者(p = 0.0084)。

结论

TNF-α基因的-308 G>A基因变异与氯氮平治疗期间体重的纵向变化有关。在进行氯氮平所致体重增加的药物遗传学研究时,随访时间是一个需要考虑的重要因素。

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