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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression
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Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression

机译:瘦蛋白基因多态性与主要抑郁症患者锂增强期间的体重增加有关

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摘要

Weight gain is a common adverse effect of lithium augmentation. Previous studies indicate an impact of genetic variants at the leptin gene on weight gain as a consequence of psychopharmacological treatment. The primary aim of our study was to identify variants at the leptin locus that might predict lithium-induced weight gain. The secondary aim was to investigate if these variants modulate leptin levels. In 180 patients with acute major depressive disorder, body mass index was measured before and after 4 weeks of lithium augmentation, in a subsample also after 4 and/or 7 months. In a subsample of 89 patients, leptin serum concentrations were measured before and during lithium augmentation. We used linear mixed model analyzes to investigate the effects of 2 polymorphisms at the leptin locus (rs4731426 and rs7799039, employing the respective proxy SNPs rs2278815 and rs10487506) on changes in body mass index and leptin levels. For both polymorphisms, which are in high linkage disequilibrium, body mass index was significantly lower in homozygous A-allele carriers than in carriers of other genotypes at baseline. Over the follow-up period, body mass index increased less in homozygous A-allele carriers of rs4731426 than in carriers of other genotypes. This was not the case for rs7799039. Neither polymorphism modulated leptin protein expression. Our study strongly supports the hypothesis that genetic variability at the leptin locus is involved in lithium augmentation-associated weight gain in major depressive disorder. Furthermore, Genotype-Tissue Expression data provide strong evidence that rs4731426 influences the expression of leptin messenger ribonucleic acid in fibroblasts. (c) 2018 Published by Elsevier B.V.
机译:体重增加是锂增强的常见不良影响。以前的研究表明遗传变异在瘦蛋白基因对体重增加的影响,因精神医药治疗而产生的重量增益。我们的研究的主要目的是鉴定可能预测锂诱导的体重增加的瘦蛋白基因座的变体。二次目的是研究这些变体调节瘦素水平。在180名急性抑郁症患者中,在锂增强之前和之后测量体重指数,在4周和7个月后,在锂增强。在89名患者的子样本中,锂延长前和在锂增强之前和期间测量瘦蛋白血清浓度。我们使用了线性混合模型分析来研究瘦蛋白基因座(RS4731426和RS7799039的2种多态性的影响,采用各个代理SNPS RS2278815和RS10487506)对体重指数和瘦素水平的变化。对于在高连杆不平衡中的多态性,纯合的a - 等位基因载体中体重指数显着低于基线的其他基因型的载体。在随访期间,体重指数在RS4731426的纯合A-等位基因载体中比在其他基因型的载体中增加。 RS7799039并非如此。既不是多态性调节瘦素蛋白表达。我们的研究强烈支持假设瘦素基因座的遗传变异性参与了主要抑郁症的锂增强相关的重量增益。此外,基因型 - 组织表达数据提供了强的证据,即RS4731426影响瘦素信使核糖核酸在成纤维细胞中的表达。 (c)2018由elsevier b.v发布。

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