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精神分裂症中DRD1、DRD2、DRD3、DRD4、DAT、COMT基因多态性的家系关联研究

[Family based association study of DRD1, DRD2, DRD3, DRD4, DAT, COMT gene polymorphism in schizophrenia].

作者信息

Paweł Kapelski, Hauser Joanna, Skibińska Maria, Szczepankiewicz Aleksandra, Dmitrzak-Weglarz Monika, Gorzkowska Karolina, Pawlak Joanna, Czerski Piotr M

机构信息

Zakład Genetyki w Psychiatrii Katedry Psychiatrii UM w Poznaniu.

出版信息

Psychiatr Pol. 2010 May-Jun;44(3):405-13.

Abstract

AIM

The aim of the study was to estimate of the transmission of six candidate genes alleles (according to the dopaminergic hypothesis of schizophrenia) by parents to their children with schizophrenia. The genes under investigation were the following: DRD1 (polymorphism -48A/G), DRD2 (polymorphism -141C ins/del), DRD3 (polymorphism Ser9Gly), DRD4 (polymorphism -521C/T), DAT (polymorphism VNTR w 3'-UTR), COMT (polymorphism Val108(158)Met). Method. There were 116 families in the group under investigation (the ill person and his/her both parents). The patients and their parents were examined using SCID (Structured Clinical Interview for DSM-IV Axis I Disorders). No mental disturbances were found with all the patients' parents. The DNA was extracted from the peripheral blood leukocytes by the salting out method. Polymorphisms were studied by the PCR method (PCR-RFLP method for: DRDI, DRD2, DRD3, DRD4, COMT and PCR-VNTR method for: DAT). The statistical analysis of the frequency of transmission of alleles was carried out by the TDT (Transmission Disequilibrium Test) method. To analyse the transmission disequilibrium of alleles under examination, the Haploview v. 3.2. programme was used.

RESULTS

According to the results obtained, no connection between analysed polymorphism of genes: DRD2 (-141C ins/del), DRD3 (Ser9Gly), DRD4 (-521C/T), DAT (VNTR), COMT (Val108(158)Met) and schizophrenia was stated. In the case of polymorphism -48A/G of gene DRD1, a trend was observed towards a more frequent transmission of allele A of gene DRD1 by parents to their children with schizophrenia (p = 0.091).

CONCLUSIONS

This trend should be interpreted very carefully. There is also the possibility that other variant of gene in linkage disequilibrium with -48A/G polymorphism was responsible for the trend observed in this study.

摘要

目的

本研究旨在评估(根据精神分裂症的多巴胺能假说)六种候选基因的等位基因由父母向其患有精神分裂症的子女的传递情况。所研究的基因如下:DRD1(多态性-48A/G)、DRD2(多态性-141C插入/缺失)、DRD3(多态性Ser9Gly)、DRD4(多态性-521C/T)、DAT(多态性VNTR位于3'-UTR)、COMT(多态性Val108(158)Met)。方法。被研究组中有116个家庭(患病者及其父母双方)。使用SCID(DSM-IV轴I障碍结构化临床访谈)对患者及其父母进行检查。所有患者的父母均未发现精神障碍。通过盐析法从外周血白细胞中提取DNA。通过PCR方法研究多态性(DRD1、DRD2、DRD3、DRD4、COMT采用PCR-RFLP方法,DAT采用PCR-VNTR方法)。通过TDT(传递不平衡检验)方法对等位基因传递频率进行统计分析。为分析所检测等位基因的传递不平衡情况,使用了Haploview v. 3.2程序。

结果

根据所得结果,未发现所分析的基因多态性:DRD2(-141C插入/缺失)、DRD3(Ser9Gly)、DRD4(-521C/T)、DAT(VNTR)、COMT(Val108(158)Met)与精神分裂症之间存在关联。对于基因DRD1的多态性-48A/G,观察到一种趋势,即患有精神分裂症的子女的父母向其传递DRD1基因的A等位基因的频率更高(p = 0.091)。

结论

对这一趋势的解读应非常谨慎。也有可能是与-48A/G多态性处于连锁不平衡状态的该基因的其他变体导致了本研究中观察到的这一趋势。

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