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The genetic susceptibility to insulin-dependent diabetes mellitus: combined segregation and linkage analysis.
Genet Epidemiol. 1985; 2(1):1-15.GE

Abstract

We report a combined segregation and linkage analysis of a Danish sample of 216 insulin-dependent diabetes mellitus (IDDM) nuclear families: of these 216, twenty multiplex families were haplotyped regarding HLA-DR and -B markers. The analysis was conducted using the computer program COMBIN, which includes a modifier to absorb family resemblance that is additional to the effect of the major locus that is assumed linked to a marker locus, eg, within the HLA region. The initial analysis could clearly reject a dominant major locus but could not discriminate between other models with or without modifier. However, after adding supplementary information on population associations between HLA and IDDM together with the identity-by-descent (IBD) distribution to the analysis, a final model was identified. This invokes an additive major locus, linked to HLA with recombination not significantly different from 0, a disease gene frequency of 0.217, plus a dominant modifier. From this model it can be predicted that about 0.15% of the general population is at 100% risk of IDDM, about 5% is at intermediate risk (approximately 10%), while the remaining population has a risk of 0. The model predicts recurrence risks compatible with empirically estimated values. Particularly strong, positive haplotype associations were found for the DR3,B8, DR3,B18, and DR4,B15 haplotypes, but detailed analyses showed that neither these particular haplotypes nor the DR3 and DR4 haplotypes in general could entirely explain the HLA-associated susceptibility. The DR2 haplotypes showed a strong negative association. The results are discussed in the light of available data on the epidemiology of IDDM in order to provide a framework for further epidemiological studies.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

3863777

Citation

Green, A, et al. "The Genetic Susceptibility to Insulin-dependent Diabetes Mellitus: Combined Segregation and Linkage Analysis." Genetic Epidemiology, vol. 2, no. 1, 1985, pp. 1-15.
Green A, Svejgaard A, Platz P, et al. The genetic susceptibility to insulin-dependent diabetes mellitus: combined segregation and linkage analysis. Genet Epidemiol. 1985;2(1):1-15.
Green, A., Svejgaard, A., Platz, P., Ryder, L. P., Jakobsen, B. K., Morton, N. E., & MacLean, C. J. (1985). The genetic susceptibility to insulin-dependent diabetes mellitus: combined segregation and linkage analysis. Genetic Epidemiology, 2(1), 1-15.
Green A, et al. The Genetic Susceptibility to Insulin-dependent Diabetes Mellitus: Combined Segregation and Linkage Analysis. Genet Epidemiol. 1985;2(1):1-15. PubMed PMID: 3863777.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The genetic susceptibility to insulin-dependent diabetes mellitus: combined segregation and linkage analysis. AU - Green,A, AU - Svejgaard,A, AU - Platz,P, AU - Ryder,L P, AU - Jakobsen,B K, AU - Morton,N E, AU - MacLean,C J, PY - 1985/1/1/pubmed PY - 1985/1/1/medline PY - 1985/1/1/entrez SP - 1 EP - 15 JF - Genetic epidemiology JO - Genet Epidemiol VL - 2 IS - 1 N2 - We report a combined segregation and linkage analysis of a Danish sample of 216 insulin-dependent diabetes mellitus (IDDM) nuclear families: of these 216, twenty multiplex families were haplotyped regarding HLA-DR and -B markers. The analysis was conducted using the computer program COMBIN, which includes a modifier to absorb family resemblance that is additional to the effect of the major locus that is assumed linked to a marker locus, eg, within the HLA region. The initial analysis could clearly reject a dominant major locus but could not discriminate between other models with or without modifier. However, after adding supplementary information on population associations between HLA and IDDM together with the identity-by-descent (IBD) distribution to the analysis, a final model was identified. This invokes an additive major locus, linked to HLA with recombination not significantly different from 0, a disease gene frequency of 0.217, plus a dominant modifier. From this model it can be predicted that about 0.15% of the general population is at 100% risk of IDDM, about 5% is at intermediate risk (approximately 10%), while the remaining population has a risk of 0. The model predicts recurrence risks compatible with empirically estimated values. Particularly strong, positive haplotype associations were found for the DR3,B8, DR3,B18, and DR4,B15 haplotypes, but detailed analyses showed that neither these particular haplotypes nor the DR3 and DR4 haplotypes in general could entirely explain the HLA-associated susceptibility. The DR2 haplotypes showed a strong negative association. The results are discussed in the light of available data on the epidemiology of IDDM in order to provide a framework for further epidemiological studies. SN - 0741-0395 UR - https://www.unboundmedicine.com/medline/citation/3863777/The_genetic_susceptibility_to_insulin_dependent_diabetes_mellitus:_combined_segregation_and_linkage_analysis_ L2 - https://doi.org/10.1002/gepi.1370020102 DB - PRIME DP - Unbound Medicine ER -