Abstract
Objective: A recent case-control study has suggested that modest enlargements of a highly polymorphic CAG repeat in exon 1 of the gene encoding potassium channel hKCa3 may be associated with bipolar disorder (BPD). We have examined this hypothesis by genotyping this locus in a family-based association study.
Method. One hundred and twenty-eight parent-offspring trios of British Caucasian origin were examined where the proband was diagnosed with the American Psychiatric Association's Diagnostic and Statistical Manual (DSM)-IV BPD I (n - 123) or II (n = 5). An improved assay was used, with redesigned polymerase chain reaction (PCR) primers. permitting quicker and higher resolution genotyping. The resultant genotypes a ere analysed using the extended transmission/disequilibrium test (ETDT).
Results: The experimental data did not provide evidence for the preferential transmission of large alleles to bipolar cases (chi (2) = 11.12, df = 10, p = 0.349).
Conclusions: Our data provide no support for the hypothesis that variation at the hKCa3 ene contributes to susceptibility: to BPD.
Original language | English |
---|---|
Pages (from-to) | 328-331 |
Number of pages | 4 |
Journal | Bipolar Disorders |
Volume | 2 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1 Dec 2000 |
Keywords
- bipolar disorder
- polymorphic CAG repeat
- human potassium channel gene
- hKCa3