Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene

✍ Scribed by Middle, Fiona; Jones, Ian; McCandless, Fiona; Barrett, Tim; Khanim, Farhat; Owen, Michael J.; Lendon, Corinne; Craddock, Nick

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 11 KB
• Volume: 96
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/(sici)1096-8628(20000403)96:2<154::aid-ajmg5>3.0.co;2-f

✦ Synopsis

A number of linkage studies provide evidence consistent with the existence of a bipolar susceptibility gene on chromosome 4p16. The gene for Wolfram syndrome, a rare recessive neurodegenerative disorder, lies in this region and has recently been cloned. Psychiatric disturbances including psychosis, mood disorder, and suicide have been reported at increased frequency in Wolfram patients and in heterozygous carriers of a Wolfram mutation. In the current investigation we have undertaken a casecontrol association study using a single nucleotide polymorphism (causing an amino acid change) in exon 8 of the Wolfram gene in a UK Caucasian sample of 312 Diagnostic and Statistical Manual of Mental Disorders (fourth edition; DSM IV) bipolar I probands and 301 comparison individuals. We found no evidence that variation at this polymorphism influences susceptibility to bipolar disorder. It remains possible that variation at other sites within or near the Wolfram gene plays important roles in determining susceptibility to affective illness.