The affected sib method. IV. Sib trios - PubMed (original) (raw)
The affected sib method. IV. Sib trios
H Payami et al. Ann Hum Genet. 1985 Oct.
Abstract
The classical sib pair method uses the expected and observed HLA (human leukocyte antigen) haplotype sharing distribution in sib pairs, who are affected with an HLA associated disease, to make inferences about the inheritance of the disease. In this paper we present the expected HLA haplotype sharing distributions in affected sib trios, and sib pairs, from families with three or more affected sibs. The underlying model for both distributions, as for the classical sib pair method, is that disease predisposition is determined by a single allele at an HLA-linked locus. The sib trio tests of hypotheses (additive and recessive), and disease parameter estimates (additive, recessive and intermediate), can be compared with those obtained from the classical sib pair analysis. In addition, the sib trio data allow parameter estimation for a general disease model to be made, if the data fall within the bounds of the expectation. This study forms the basis of later investigations which show that haplotype sharing of affected sib trios for two susceptibility alleles (negative complementation) model, which appears appropriate for insulin dependent diabetes mellitus (IDDM), moves outside the bound of the single susceptibility expectations outlined here, whereas haplotype sharing values for sib pairs are bound by the single susceptibility allele expectations. Available Caucasian IDDM data have been analysed. The results support genetic heterogeneity of IDDM.
Similar articles
- Analysis of genetic interrelationship among HLA-associated diseases.
Payami H, Khan MH, Grennan DM, Sanders PA, Dyer PA, Thomson G. Payami H, et al. Am J Hum Genet. 1987 Sep;41(3):331-49. Am J Hum Genet. 1987. PMID: 3631074 Free PMC article. - The affected sib method. V. Testing the assumptions.
Louis EJ, Payami H, Thomson G. Louis EJ, et al. Ann Hum Genet. 1987 Jan;51(1):75-92. doi: 10.1111/j.1469-1809.1987.tb00867.x. Ann Hum Genet. 1987. PMID: 3314668 - Investigation of the mode of inheritance of the HLA associated diseases by the method of antigen genotype frequencies among diseased individuals.
Thomson G. Thomson G. Tissue Antigens. 1983 Feb;21(2):81-104. doi: 10.1111/j.1399-0039.1983.tb00377.x. Tissue Antigens. 1983. PMID: 6405504 Review.
Cited by
- Assessing the role of HLA-linked and unlinked determinants of disease.
Risch N. Risch N. Am J Hum Genet. 1987 Jan;40(1):1-14. Am J Hum Genet. 1987. PMID: 3468804 Free PMC article. - Analysis of genetic interrelationship among HLA-associated diseases.
Payami H, Khan MH, Grennan DM, Sanders PA, Dyer PA, Thomson G. Payami H, et al. Am J Hum Genet. 1987 Sep;41(3):331-49. Am J Hum Genet. 1987. PMID: 3631074 Free PMC article. - Asymptotic properties of affected-sib-pair linkage analysis.
Holmans P. Holmans P. Am J Hum Genet. 1993 Feb;52(2):362-74. Am J Hum Genet. 1993. PMID: 8430697 Free PMC article. - Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus.
Thomson G, Robinson WP, Kuhner MK, Joe S, MacDonald MJ, Gottschall JL, Barbosa J, Rich SS, Bertrams J, Baur MP, et al. Thomson G, et al. Am J Hum Genet. 1988 Dec;43(6):799-816. Am J Hum Genet. 1988. PMID: 3057885 Free PMC article. Review. - High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11q.
Hyer RN, Julier C, Buckley JD, Trucco M, Rotter J, Spielman R, Barnett A, Bain S, Boitard C, Deschamps I, et al. Hyer RN, et al. Am J Hum Genet. 1991 Feb;48(2):243-57. Am J Hum Genet. 1991. PMID: 1990836 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials