Familial aggregation of osteoarthritis: Data from the Baltimore longitudinal study on aging

Objective To evaluate the familial aggregation of osteoarthritis (OA) in a cohort of healthy volunteers drawn from a community setting. Methods Hand radiographs obtained between 1978 and 1991 and bilateral standing knee radiographs obtained between 1984 and 1991 were read for changes of OA, using Ke...

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Veröffentlicht in:Arthritis and rheumatism 1998-07, Vol.41 (7), p.1227-1232
Hauptverfasser: Hirsch, Rosemarie, Lethbridge‐Cejku, Margaret, Hanson, Robert, Scott, William W., Reichle, Ralph, Plato, Chris C., Tobin, Jordan D., Hochberg, Marc C.
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Sprache:eng
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Zusammenfassung:Objective To evaluate the familial aggregation of osteoarthritis (OA) in a cohort of healthy volunteers drawn from a community setting. Methods Hand radiographs obtained between 1978 and 1991 and bilateral standing knee radiographs obtained between 1984 and 1991 were read for changes of OA, using Kellgren‐Lawrence (K‐L) scales. The hand sites were distal interphalangeal (DIP) joints, proximal interphalangeal (PIP) joints, and first carpometacarpal (CMC1) joints. For each joint group, the presence of OA in at least 1 joint in a joint group, the number of affected digits in each joint group, and the sum of the K‐L grade across all joints were analyzed. Polyarticular OA was recorded if there were OA findings in 2 of 3 hand joint groups plus 1 or both knees. Data from 167 families with hand radiographs, 157 families with knee radiographs, and 148 families with both hand and knee radiographs were analyzed for sib‐sib correlations. Results After adjustment for age, sex, and body mass index, clinically relevant sib‐sib common correlations were found for OA of the DIP, PIP, and CMC1 joints, for OA at 2 or 3 hand sites, and for polyarticular OA (r = 0.33‐0.81) when OA was defined according to the number of affected joints or as the sum of the K‐L grade across all joints. Conclusion These results from a cohort of volunteers drawn from a community setting and ascertained without regard to OA status demonstrate familial aggregation of OA and contribute to the evidence for heritability of OA.
ISSN:0004-3591
1529-0131
DOI:10.1002/1529-0131(199807)41:7<1227::AID-ART13>3.0.CO;2-N