Genome Scan for Familial Abdominal Aortic Aneurysm Using Sex and Family History as Covariates Suggests Genetic Heterogeneity and Identifies Linkage to Chromosome 19q13
| Autor: | Magdalena Skunca, Sarah G. Buxbaum, Natzi Sakalihasan, Olivier D. Defawe, Gerard Tromp, Raymond Limet, Jane M. Olson, Claudette Arthur, Alain Verloes, Hidenori Shibamura, Gerard Pals, Clarissa van Vlijmen-van Keulen, Alan G. Lossing, Marjorie Burnett, Gerald L. MacKean, Taijiro Sueda, Toru Ogata, Helena Kuivaniemi, Doreen M. Dudek |
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| Rok vydání: | 2004 |
| Předmět: | |
| Zdroj: | Circulation. 109:2103-2108 |
| ISSN: | 1524-4539 0009-7322 |
| DOI: | 10.1161/01.cir.0000127857.77161.a1 |
| Popis: | Background— Abdominal aortic aneurysm (AAA) is a relatively common disease, with 1% to 2% of the population harboring aneurysms. Genetic risk factors are likely to contribute to the development of AAAs, although no such risk factors have been identified. Methods and Results— We performed a whole-genome scan of AAA using affected-relative-pair (ARP) linkage analysis that includes covariates to allow for genetic heterogeneity. We found strong evidence of linkage (logarithm of odds [LOD] score=4.64) to a region near marker D19S433 at 51.88 centimorgans (cM) on chromosome 19 with 36 families (75 ARPs) when including sex and the number of affected first-degree relatives of the proband (N aff ) as covariates. We then genotyped 83 additional families for the same markers and typed additional markers for all families and obtained a LOD score of 4.75 ( P =0.00014) with sex, N aff , and their interaction as covariates near marker D19S416 (58.69 cM). We also identified a region on chromosome 4 with a LOD score of 3.73 ( P =0.0012) near marker D4S1644 using the same covariate model as for chromosome 19. Conclusions— Our results provide evidence for genetic heterogeneity and the presence of susceptibility loci for AAA on chromosomes 19q13 and 4q31. |
| Databáze: | OpenAIRE |
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