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HLA antigens and acute rheumatic fever: Evidence for a recessive susceptibility gene linked to HLA
Author(s) -
Hafez M.,
Chakravarti A.,
ElShennawy F.,
ElMorsi Z.,
ElSallab S. H.,
AlTonbar Y.,
Rao D. C.
Publication year - 1985
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.1370020305
Subject(s) - proband , human leukocyte antigen , genetics , linkage disequilibrium , biology , immunology , concordance , haplotype , etiology , genetic predisposition , multiplex polymerase chain reaction , genetic linkage , rheumatic fever , antigen , gene , allele , medicine , polymerase chain reaction , mutation
From 60 probands with acute rheumatic fever (ARF), 19 multiplex families segregating for ARF were ascertained. The parents and rheumatic and normal sibs of the probands in these 19 families were also studied. HLA typing using the microlymphocytotoxic assay was then performed on the 60 unrelated probands, the multiplex families, and 234 unrelated controls using 23 antigens from the HLA‐A and ‐B loci. The controls lacked a past history of ARF and were from the same geographic locality. Calculations of relative risk demonstrate an increase of HLA‐B5 antigen in the 60 patients, but the result might not be significant from the point of view of multiple comparisons. Nevertheless, affected sib pairs from the multiplex families show 93% concordance for both or one HLA haplotype. A formal linkage analysis demonstrates that a recessive etiology is most likely (lod score of 3.3) with approximately 68% of cases being due to a gene closely linked to HLA and in linkage disequilibrium with HLA‐B5. The remaining 32% of cases are due to other familial factors such as polygenic inheritance or common environmental factors. The results confirm a strong genetic predisposition to ARF and its heterogeneous nature in families.