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Genetic validation study of protein tyrosine phosphatase receptor type D (PTPRD) gene variants and risk for antipsychotic-induced weight gain

机译:蛋白酪氨酸磷酸酶受体型D(PTPRD)基因变异性和抗精神病诱导体重增加风险的遗传验证研究

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Schizophrenia is a severe, debilitating disorder with a lifetime prevalence of 1% irrespective of gender or ethnicity and is typically treated with antipsychotic drugs. Antipsychotic-induced weight gain (AIWG) is a leading factor of patient non-compliance and has previously been shown to increase the risk of type 2 diabetes, metabolic syndrome, and cardiovascular events. The current study intends to replicate findings from a recent genome-wide association study in Han-Chinese patients implicating two gene variants (rs10977144 and rs10977154) of the protein tyrosine phosphatase receptor type D (PTPRD) in antipsychotic-induced weight gain (AIWG). We investigated a sample of European and African American ancestry (n=201) and calculated percentage of weight change using linear regression corrected for type of antipsychotics, duration of treatment and principal components from ancestry checks. As secondary goal, we investigated additional gene variants of PTPRD previously not associated with AIWG. We found no association with rs10977144 and rs10977154. However, we found nominally significant results between PTPRD and AIWG with rs73398242 in Europeans (BETA=-0.267, p=0.002) and rs13294608 in African Americans (BETA=0.423, p=0.003). According to Haploreg, both SNPs are histone marks for enhancers and promoters across various brain regions including the cingulate gyrus and dorsolateral prefrontal cortex. In summary, our results tentatively suggest that PTPRD might be associated with AIWG although different SNPS might be involved in different ethnic groups.
机译:精神分裂症是一种严重的,衰弱的紊乱,而且无论性别或种族如何,寿命患病率为1%,通常用抗精神病药物治疗。抗精神病药诱导的体重增加(AIWG)是患者不合规的主要因素,并已被证明是增加2型糖尿病,代谢综合征和心血管事件的风险。目前的研究旨在复制来自汉族 - 中文患者最近的基因组 - 型患者基因组患者的发现,这意味着抗精神病药诱导的体重增加(AIWG)中的蛋白酪氨酸磷酸酶受体类型D(PTPRD)的两个基因变体(Rs1097144和RS1097154)。我们调查了欧洲和非洲裔美国血统(n = 201)的样本,并使用线性回归校正的抗精神病患者类型,治疗持续时间和祖先检查的主要成分的计算百分比。作为二级目标,我们研究了以前与AIWG无关的PTPR的另外的基因变体。我们发现与RS10977144和RS10977154没有关联。然而,我们在非洲裔美国人(Beta = -0.267,P = 0.002)和13294608中,PTPRD和AIWG之间的名义上在PTPRD和AIWG之间找到了名义上的显着结果(Beta = -0.267,P = 0.002)和13294608(β= 0.423,P = 0.003)。根据HAPLOREG的说法,SNP都是各种脑区域的增强剂和启动子的组蛋白标记,包括铰接旋转和背侧前额外皮层。总之,我们的结果暂定表明,尽管不同的SNP可能涉及不同的族裔,但PTPR可能与AIWG相关联。

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