How to Cite this Article: Pereira ACP, McQuillin A, Puri V, Anjorin A, Bass N, Kandaswamy R, Lawrence J, Curtis D, Sklar P, Purcell SM, Gurling HMD. 2011. Genetic Association and Sequencing of the Insulin-Like Growth Factor 1 Gene in Bipolar Affective Disorder. Am J Med Genet Part B 156:177–187.
Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder†
Article first published online: 13 JAN 2011
Copyright © 2011 Wiley-Liss, Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Volume 156, Issue 2, pages 177–187, March 2011
How to Cite
Pereira, A. C. P., McQuillin, A., Puri, V., Anjorin, A., Bass, N., Kandaswamy, R., Lawrence, J., Curtis, D., Sklar, P., Purcell, S. M. and Gurling, H. M.D. (2011), Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder. Am. J. Med. Genet., 156: 177–187. doi: 10.1002/ajmg.b.31153
- Issue published online: 8 FEB 2011
- Article first published online: 13 JAN 2011
- Manuscript Accepted: 9 NOV 2010
- Manuscript Received: 3 FEB 2010
- UK Medical Research Council. Grant Numbers: G9623693N, G0500791
- Stanley Foundation and The Stanley Center for Psychiatric Research
- Fundacao Para a Ciencia e Tecnologia (FCT)
- insulin-like growth factor 1;
- bipolar disorder;
- association studies;
- chromosome 12
Insulin-like growth factor 1 (IGF1) has been shown to have an important role in brain development and function. Studies of IGF1 administration in rodents have shown that it has an anxiolytic and antidepressant effect. A genome-wide association study (GWAS) of the first University College London (UCL) cohort of 506 bipolar affective disorder subjects and 510 controls was carried out. The exons and flanking regions of IGF1 were resequenced, any new polymorphisms found were genotyped in an enlarged UCL sample of 937 cases and 941 controls. GWAS data gave good evidence of allelic and haplotypic association between multiple IGF1 SNP's and bipolar disorder (BD). New polymorphisms were found by resequencing IGF1 region. Data from GWAS and the new markers showed that twelve out of 43 SNPs showed association with BD with the four most significant SNPs having values of 3.7 × 10−5, 8.4 × 10−4, 2.6 × 10−4, and 2.5 × 10−4. A 5′ promoter microsatellite polymorphism previously correlated with plasma lipoprotein concentration was also associated with BD (P = 0.013). Haplotypic association confirmed association with BD with significance values similar to the single marker SNP values. The marker rs12426318 has also been found to be associated with BD in a second sample. A test of gene wide significance with permutation testing for all markers genotyped at IGF1 was also significant. These data implicate IGF1 as a candidate gene to cause genetic susceptibility to BD. © 2011 Wiley-Liss, Inc.