Polyglutamine coding genes in bipolar disorder: lack of association with selected candidate loci

• Published in: Journal of affective disorders Vol. 58; no. 1; pp. 63 - 68
• Main Authors: Turecki, G, Alda, M, Grof, P, Joober, R, Lafrenière, R, Cavazzoni, P, Duffy, A, Grof, E, Ahrens, B, Berghöfer, A, Müller-Oerlinghausen, B, Dvoráková, M, Libigerová, E, Vojtechovský, M, Zvolský, P, Nilsson, A, Prochazka, H, Licht, R.W, Rasmussen, N.A, Schou, M, Vestergaard, P, Holzinger, A, Schumann, C, Thau, K, Rouleau, G.A
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-04-2000
• Subjects: Adult; Aged; Alleles; Antimanic Agents - therapeutic use; Association studies; Bipolar disorder; Bipolar Disorder - diagnosis; Bipolar Disorder - drug therapy; Bipolar Disorder - genetics; Chromosome Mapping; Female; Genetic Testing; Humans; Lithium Carbonate - therapeutic use; Lithium response; Male; Middle Aged; Peptides - genetics; Trinucleotide repeats; Trinucleotide Repeats - genetics; Trinucleotide repeats; Association studies; Bipolar disorder; Lithium response
• ISSN: 0165-0327; 1573-2517
• DOI: 10.1016/S0165-0327(99)00074-9

Background: Several studies have suggested that expanded trinucleotide repeats, particularly CAG, may have a role in the etiology of BD. Results obtained with the repeat expansion detection technique (RED) have indicated that bipolar patients have an excess of expanded CAG repeats. However, it is not clear which loci account for this difference.
Methods: Using lithium-responsive bipolar patients in order to reduce heterogeneity, we investigated five loci that are expressed in the brain and contain translated CAG repeats. A sample of 138 cases and 108 controls was studied. Genotypes were coded quantitatively or qualitatively and repeat distributions were compared.
Results: No difference was found in allele distribution between cases and controls for any of the loci studied. In one locus — L10378 — patients had a tendency to present shorter alleles (28.1 versus 27.9 repeats;
t=2.55, df=205,
P=0.011), however, this difference disappeared after correction for multiple testing.
Limitations: The study has limitations common to most candidate gene association studies, that is, limited number of loci investigated and limited power to detect loci that account for a small proportion of the total genetic variability.
Conclusions: Our results suggest that the loci investigated have no major role in the genetic predisposition to bipolar disorder.