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

被引:52
作者
Lindblad, K
Nylander, PO
Zander, C
Yuan, QP
Stahle, L
Engstrom, C
Balciuniene, J
Pettersson, U
Breschel, T
McInnis, M
Ross, CA
Adolfsson, R
Schalling, M
机构
[1] Karolinska Hosp & Inst, Dept Mol Med, Neurogenet Unit, S-17176 Stockholm, Sweden
[2] Umea Univ, Dept Psychiat, S-90185 Umea, Sweden
[3] Karolinska Inst, Dept Clin Pharmacol, S-14186 Huddinge, Sweden
[4] Huddinge Hosp, S-14186 Huddinge, Sweden
[5] Uppsala Univ, Dept Med Genet, S-75123 Uppsala, Sweden
[6] Johns Hopkins Univ Hosp, Dept Psychiat & Behav Sci, Baltimore, MD 21287 USA
[7] Johns Hopkins Univ Hosp, Dept Neurosci, Baltimore, MD 21287 USA
关键词
bipolar affective disorder; unipolar affective disorder; depression; trinucleotide repeat expansion; repeat expansion detection; anticipation; ERDA1; CTG18.1; SEF2-1B;
D O I
10.1038/sj.mp.4000416
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (r(s) = -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.
引用
收藏
页码:405 / 410
页数:6
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