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两个常见的CAG/CTG重复序列位点:与情感障碍有关吗?

Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders?

作者信息

Lindblad K, Nylander P O, Zander C, Yuan Q P, Ståhle L, Engström C, Balciuniene J, Pettersson U, Breschel T, McInnis M, Ross C A, Adolfsson R, Schalling M

机构信息

Department of Molecular Medicine, Karolinska Institute, Stockholm, Sweden.

出版信息

Mol Psychiatry. 1998 Sep;3(5):405-10. doi: 10.1038/sj.mp.4000416.

Abstract

An association between bipolar affective disorder and CAG/CTG trinucleotide repeat expansions (TRE) has previously been detected using the repeat expansion detection (RED) method. Here we report that 89% of RED products (CAG/CTG repeats) > 120 nt (n = 202) detected in affective disorder patients as well as unaffected family members and controls correlate with expansions at two repeat loci, ERDA1 on chromosome 17q21.3 and CTG18.1 on 18q21.1. In a set of patients and controls in which we had previously found a significant difference in RED size distribution, the frequency of expansions at the CTG18.1 locus was 13% in bipolar patients (n = 60) and 5% in controls (n = 114) (P < 0.07) with a significantly different size distribution (P < 0.03). A second set of patients were ascertained from 14 affective disorder families showing anticipation. Twelve of the families had members with RED products > 120 nt. The RED product distribution was significantly different (P < 0.0007) between affected (n = 53) and unaffected (n = 123) offspring. Using PCR, a higher frequency (P < 0.04) of CTG18.1 expansions as well as a different (P < 0.02) repeat size distribution was seen between affected and unaffected offspring. In addition, a negative correlation between RED product size and the age-of-onset could be seen in affected offspring (rs = -0.3, P = 0.05, n = 43). This effect was due to an earlier onset in individuals with long CTG18.1 expansions. No difference in ERDA1 expansion frequency was seen either between bipolar patients (35%, n = 60) and matched controls (29%, n = 114), or between affected and unaffected offspring in the families. We conclude that expanded alleles at the CTG18.1 locus confers an odds ratio of 2.6-2.8 and may thus act as a vulnerability factor for affective disorder, while the ERDA1 locus seems unrelated to disease.

摘要

先前使用重复序列扩增检测(RED)方法已检测到双相情感障碍与CAG/CTG三核苷酸重复序列扩增(TRE)之间存在关联。在此我们报告,在情感障碍患者以及未受影响的家庭成员和对照中检测到的89%的RED产物(CAG/CTG重复序列)>120 nt(n = 202)与17q21.3染色体上的ERDA1和18q21.1染色体上的CTG18.1这两个重复序列位点的扩增相关。在一组患者和对照中,我们先前发现RED大小分布存在显著差异,CTG18.1位点的扩增频率在双相情感障碍患者中为13%(n = 60),在对照中为5%(n = 114)(P < 0.07),大小分布有显著差异(P < 0.03)。第二组患者来自14个显示出遗传早现的情感障碍家族。其中12个家族有RED产物>120 nt的成员。在受影响(n = 53)和未受影响(n = 123)的后代中,RED产物分布有显著差异(P < 0.0007)。使用聚合酶链反应(PCR),在受影响和未受影响的后代之间观察到CTG18.1扩增的频率更高(P < 0.04)以及重复序列大小分布不同(P < 0.02)。此外,在受影响的后代中可以看到RED产物大小与发病年龄之间存在负相关(rs = -0.3,P = 0.05,n = 43)。这种效应是由于CTG18.1长重复序列扩增的个体发病更早。在双相情感障碍患者(35%,n = 60)和匹配的对照(29%,n = 114)之间,以及在家族中受影响和未受影响的后代之间,均未观察到ERDA1扩增频率的差异。我们得出结论,CTG18.1位点的扩增等位基因的优势比为2.6 - 2.8,因此可能作为情感障碍的一个易患因素,而ERDA1位点似乎与疾病无关。

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