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对巴西双相情感障碍和精神分裂症患者血清素转运体基因(5-HTT)启动子区域内一种新型功能多态性的分析。

Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophrenia.

作者信息

Mendes de Oliveira J R, Otto P A, Vallada H, Lauriano V, Elkis H, Lafer B, Vasquez L, Gentil V, Passos-Bueno M R, Zatz M

机构信息

Departamento de Biologia, Instituto de Biociências, Universidade de São Paulo, Brazil.

出版信息

Am J Med Genet. 1998 May 8;81(3):225-7. doi: 10.1002/(sici)1096-8628(19980508)81:3<225::aid-ajmg4>3.0.co;2-v.

Abstract

It has been suggested that the serotonin transporter (5-hydroxytryptamine-transporter or 5-HTT) may be involved in the pathogenesis of affective disorders. Recently, Collier et al. (1996) found that the frequency of the low-activity short variant (s) of the 5-HTT-linked polymorphic region (5-HTTLPR) was higher among patients with affective disorders than in normal controls. However, since the observed level of significance was not high, they suggest that these findings should be replicated in independent samples. We have analyzed 86 unrelated patients (47 with bipolar disorder and 39 with schizophrenia) and 98 normal controls from the Brazilian population for the 5-HTTLPR. Statistical analysis revealed that the genotypes (LL, Ls, ss) as well as the estimated allele frequencies (L,s) did not differ significantly among the three studied groups or between bipolar and normal controls. In addition, although not statistically significant, the genotype ss in our sample was less frequent among our bipolar patients than in our normal controls (12.8% versus 16.3%) which is the opposite of what was found by Collier et al. (24% versus 18%) in the European study. Although it will be important to extend the present analysis in a larger sample, our preliminary results suggest that the 5-HTTLPR does not seem to play a major role in the genetics of bipolar and schizophrenic disorders at least in this group of Brazilian psychiatric patients.

摘要

有人提出,血清素转运体(5-羟色胺转运体或5-HTT)可能与情感障碍的发病机制有关。最近,科利尔等人(1996年)发现,5-HTT连锁多态性区域(5-HTTLPR)低活性短变体(s)在情感障碍患者中的出现频率高于正常对照组。然而,由于观察到的显著性水平不高,他们建议这些发现应在独立样本中得到重复验证。我们对来自巴西人群的86名无亲缘关系的患者(47名双相情感障碍患者和39名精神分裂症患者)以及98名正常对照进行了5-HTTLPR分析。统计分析显示,在三个研究组之间或双相情感障碍患者与正常对照之间,基因型(LL、Ls、ss)以及估计的等位基因频率(L、s)没有显著差异。此外,虽然无统计学意义,但我们样本中双相情感障碍患者的ss基因型频率低于正常对照(12.8%对16.3%),这与科利尔等人在欧洲研究中的发现相反(24%对18%)。尽管扩大当前分析样本很重要,但我们的初步结果表明,至少在这组巴西精神病患者中,5-HTTLPR似乎在双相情感障碍和精神分裂症的遗传学中不发挥主要作用。

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