Familial Risks and Heritability of Rheumatoid Arthritis: Role of Rheumatoid Factor/Anti–Citrullinated Protein Antibody Status, Number and Type of Affected Relatives, Sex, and Age

• Published in: Arthritis & rheumatology (Hoboken, N.J.) Vol. 65; no. 11; pp. 2773 - 2782
• Main Authors: Frisell, Thomas, Holmqvist, Marie, Källberg, Henrik, Klareskog, Lars, Alfredsson, Lars, Askling, Johan
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.11.2013
• Subjects: Adult; Age Distribution; Age of Onset; Aged; Arthritis, Rheumatoid - epidemiology; Arthritis, Rheumatoid - genetics; Arthritis, Rheumatoid - immunology; Case-Control Studies; Drug therapy; Family; Female; Genetic Predisposition to Disease - epidemiology; Genetic Predisposition to Disease - genetics; Humans; Male; Middle Aged; Peptides, Cyclic - blood; Peptides, Cyclic - genetics; Peptides, Cyclic - immunology; Registries - statistics & numerical data; Rheumatoid arthritis; Rheumatoid Factor - blood; Rheumatoid Factor - genetics; Rheumatoid Factor - immunology; Risk Factors; Sex Distribution; Sweden - epidemiology; Sweden
• ISSN: 0004-3591; 2326-5191; 1529-0131; 1529-0131; 2326-5205
• DOI: 10.1002/art.38097

Objective To estimate familial aggregation of rheumatoid arthritis (RA) in 3 large population‐representative samples and to test if familial aggregation is affected by rheumatoid factor (RF)/anti–citrullinated protein antibody (ACPA) status, type of relative, sex, and age at onset of RA. Methods A register‐based nested case–control study was performed in the Swedish total population. Data on patients with RA were ascertained through the nationwide Swedish Patient Register (n = 88,639), the clinical Swedish Rheumatology Quality Register (n = 11,519), and the Epidemiological Investigation of Rheumatoid Arthritis case–control study (n = 2,871). Data on first‐ and second‐degree relatives were obtained through the Swedish Multigeneration Register. Familial risks were calculated using conditional logistic regression. Results Consistent across data sources, the familial odds ratio for RA was ∼3 in first‐degree relatives of RA patients and 2 in second‐degree relatives. Familial risks were similar among siblings, parents, and offspring. Familial aggregation was not modified by sex, but was higher in RA patients with early‐onset disease and in RF/ACPA‐positive RA patients. The observed familial risks were consistent with a heritability of ∼50% for ACPA‐positive RA and ∼20% for ACPA‐negative RA. Conclusion The pattern of risks suggests that familial factors influence RA in men and women equally and that these factors are of less importance for late‐onset RA. Familial factors are more important for seropositive RA, but there is significant familial overlap between seropositive RA and seronegative RA. Even if the familial risk is assumed to be completely due to genetics, the observed risks suggest that heritability of RA is lower than previously reported, in particular for ACPA‐negative RA.