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Genomewide scan for gout in taiwanese aborigines reveals linkage to chromosome 4q25.


ABSTRACT: Gout is a disorder of uric-acid metabolism. The Pacific Austronesian population, including Taiwanese aborigines, has a remarkably high prevalence of hyperuricemia and gout, which suggests a founder effect across the Pacific region. We report here a genomewide linkage study of 21 multiplex pedigrees with gout from an aboriginal tribe in Taiwan. From observations of familial clustering, early onset of gout, and clinically severe manifestations, we hypothesized that a major gene plays a role in this trait. Using 382 random polymorphic markers spread across 22 autosomes, we demonstrated a highly significant linkage for gout at marker D4S2623 on chromosome 4q25 (P=.0002 by nonparametric linkage [the NPL(all) statistic]; empirical P=.0006; LOD=4.3, P=4.4x10-6 by logistic regression). When alcohol consumption was included as a covariate in the model, the LOD score increased to 5.66 (P=1.3x10-6). Quantitative traits, including serum uric acid and creatinine, also showed a moderate linkage to this region. To our knowledge, this is the first genome-scan report to identify a genetic locus harboring a gout-susceptibility gene.

SUBMITTER: Cheng LS 

PROVIDER: S-EPMC1182028 | biostudies-literature | 2004 Sep

REPOSITORIES: biostudies-literature

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Genomewide scan for gout in taiwanese aborigines reveals linkage to chromosome 4q25.

Cheng Li Shu-Chuan LS   Chiang Shang-Lun SL   Tu Hung-Pin HP   Chang Shun-Jen SJ   Wang Tsu-Nai TN   Ko Allen Min-Jen AM   Chakraborty Ranajit R   Ko Ying-Chin YC  

American journal of human genetics 20040713 3


Gout is a disorder of uric-acid metabolism. The Pacific Austronesian population, including Taiwanese aborigines, has a remarkably high prevalence of hyperuricemia and gout, which suggests a founder effect across the Pacific region. We report here a genomewide linkage study of 21 multiplex pedigrees with gout from an aboriginal tribe in Taiwan. From observations of familial clustering, early onset of gout, and clinically severe manifestations, we hypothesized that a major gene plays a role in thi  ...[more]

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