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PMID: 10402510 Published · ppublish English Journal Article

Lithium responsive bipolar disorder, unilineality, and chromosome 18: A linkage study.

American journal of medical genetics ·Vol. 88 ·No. 4 ·1999-08-20 ·Pages 411-5

Turecki G, Grof P, Cavazzoni P, Duffy A, Grof E, Martin R, Joober R, Rouleau GA, Alda M

Abstract

Over the last three years several studies have investigated the hypothesis of linkage between bipolar disorder and markers on chromosome 18. Although independent groups have reported positive results, it is still not clear how these should be interpreted, as linkage spans a considerably large segment of the chromosome. In this study we have investigated linkage with chromosome 18 markers in 19 families of lithium-responsive bipolar patients, as a way to select a more homogeneous population. In addition, we have investigated whether there is evidence of a parent-of-origin effect as suggested by previous studies. Eleven markers spanning the whole chromosome were typed and linkage analysis was carried out using parametric and nonparametric methods. Analysis of the whole sample provided nonsignificant linkage results. However, when the sample included only unilineal families, and was further stratified according to parental origin, two chromosomal regions provided modestly positive lod scores. Maximum lod scores of 1.04 (P = 0.001) at D18S53 and 0.87 (P = 0.045) at D18S61 were observed for maternal and paternal pedigrees, respectively. Nonparametric analysis yielded similar results. In conclusion, our results are congruent with previous reports that suggest an advantage of unilineal pedigrees in linkage analysis of bipolar disorder and cannot rule out a parent-of-origin effect in this genomic region.

MeSH Terms
Adolescent Adult Age of Onset Bipolar Disorder/drug therapy,genetics Chromosomes, Human, Pair 18 Fathers Female Genetic Linkage Genetic Markers Humans Lithium/therapeutic use Lod Score Male Models, Statistical Mothers
Chemicals
Genetic Markers Lithium
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Turecki G
Centre for Research in Neuroscience, The Montreal General Hospital, McGill University, Montreal, Canada. gustavo@bagel.epi.mcgill.ca
Grof P
Cavazzoni P
Duffy A
Grof E
Martin R
Joober R
Rouleau G A
Alda M
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1999-08-20
Pages
411-5
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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