TY - JOUR
T1 - The familial aggregation of rheumatoid arthritis and its relationship to the hla-dr4 association
AU - Junco, Deborah J.Del
AU - Luthra, Harvinder S.
AU - Annegers, John F.
AU - Worthington, John W.
AU - Kurland, Leonard T.
N1 - Funding Information:
This research was supported in part by grants from the Mayo Foundation and by Grant AM 30582 from the National Institutes of Health.
PY - 1984/5
Y1 - 1984/5
N2 - del Junco, D. J., H. S. Luthra, J. F. Annegers (U. of Texas Health Science Center at Houston, School of Public Health, Houston, TX 77025), J. W. Wor-thington and L. T. Kurland. The familial aggregation of rheumatoid arthritis and its relationship to the HLA-DR4 association. Am J Epidemiol 1984; 119: 813-29.This investigation of the familial aggregation of rheumatoid arthritis in Rochester, Minnesota, was prompted by the considerable variability in previous reports and the need to interpret findings in light of the recently established human lymphocyte antigen (HLA)-DR4 association. The historical cohort methodology was applied to determine the incidence of adult-onset rheumatoid arthritis in 1631 biologic relatives of 78 probands compared with the Rochester population incidence. The ratio of the age- and sex-adjusted rates in first-degree relatives compared with the general population was 1.7 (95% confidence interval 1.0-2.9). The increase was concentrated in the 16- to 40-year-old age group, suggesting some disease heterogeneity. However, the level of familial risk was not significantly affected by the proband's sex, seropositivity, age, or parental disease status. Integrating these findings with prior research in which case ascertainment was complete led to the conclusion that familial aggregation of rheumatoid arthritis is weak. The apparent discrepancy between weak familial aggregation and the known strong HLA-DR4 association with rheumatoid arthritis was resolved by examining the mathematical relationship between the measures of association in the two different types of studies. Results show that to be consistent with weak familial clustering, any putative susceptibility gene must have very low penetrance, and/or there must be a large residual of sporadic cases.
AB - del Junco, D. J., H. S. Luthra, J. F. Annegers (U. of Texas Health Science Center at Houston, School of Public Health, Houston, TX 77025), J. W. Wor-thington and L. T. Kurland. The familial aggregation of rheumatoid arthritis and its relationship to the HLA-DR4 association. Am J Epidemiol 1984; 119: 813-29.This investigation of the familial aggregation of rheumatoid arthritis in Rochester, Minnesota, was prompted by the considerable variability in previous reports and the need to interpret findings in light of the recently established human lymphocyte antigen (HLA)-DR4 association. The historical cohort methodology was applied to determine the incidence of adult-onset rheumatoid arthritis in 1631 biologic relatives of 78 probands compared with the Rochester population incidence. The ratio of the age- and sex-adjusted rates in first-degree relatives compared with the general population was 1.7 (95% confidence interval 1.0-2.9). The increase was concentrated in the 16- to 40-year-old age group, suggesting some disease heterogeneity. However, the level of familial risk was not significantly affected by the proband's sex, seropositivity, age, or parental disease status. Integrating these findings with prior research in which case ascertainment was complete led to the conclusion that familial aggregation of rheumatoid arthritis is weak. The apparent discrepancy between weak familial aggregation and the known strong HLA-DR4 association with rheumatoid arthritis was resolved by examining the mathematical relationship between the measures of association in the two different types of studies. Results show that to be consistent with weak familial clustering, any putative susceptibility gene must have very low penetrance, and/or there must be a large residual of sporadic cases.
KW - Arthritis, rheumatoid
KW - Epidemiologic methods
KW - Genetics
KW - HLA antigens
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U2 - 10.1093/oxfordjournals.aje.a113802
DO - 10.1093/oxfordjournals.aje.a113802
M3 - Article
C2 - 6609637
AN - SCOPUS:0021363322
SN - 0002-9262
VL - 119
SP - 813
EP - 829
JO - American Journal of Epidemiology
JF - American Journal of Epidemiology
IS - 5
ER -