One in four people may develop symptomatic hip osteoarthritis in his or her lifetime

被引:240
作者
Murphy, L. B. [1 ]
Helmick, C. G. [1 ]
Schwartz, T. A. [2 ]
Renner, J. B. [3 ,4 ]
Tudor, G. [5 ]
Koch, G. G. [2 ]
Dragomir, A. D. [6 ]
Kalsbeek, W. D. [2 ]
Luta, G. [7 ]
Jordan, J. M. [8 ]
机构
[1] Ctr Dis Control & Prevent, Div Adult & Community Hlth, Arthrit Program, Atlanta, GA 30341 USA
[2] Univ N Carolina, Dept Biostat, Gillings Sch Global Publ Hlth, Chapel Hill, NC USA
[3] Univ N Carolina, Dept Radiol, Chapel Hill, NC USA
[4] Univ N Carolina, Dept Allied Hlth Sci, Chapel Hill, NC USA
[5] Husson Univ, Bangor, ME USA
[6] Georgetown Univ, Lombardi Comprehens Canc Ctr, Washington, DC USA
[7] Georgetown Univ, Dept Biostat Bioinformat & Biomath, Washington, DC USA
[8] Univ N Carolina, Thurston Arthrit Res Ctr, Chapel Hill, NC USA
关键词
osteoarthritis; hip osteoarthritis; surveillance; lifetime risk; population-based study; NATIONAL DEATH INDEX; BODY-MASS INDEX; KNEE OSTEOARTHRITIS; RISK-FACTORS; PROSPECTIVE COHORT; AFRICAN-AMERICANS; UNITED-STATES; REPLACEMENT; PREVALENCE; POPULATION;
D O I
10.1016/j.joca.2010.08.005
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: To estimate the lifetime risk of symptomatic hip osteoarthritis (OA). Design: We analyzed data from the Johnston County Osteoarthritis Project [a longitudinal population-based study of OA in North Carolina, United States (n = 3068)]. The weighted baseline sample comprised 18% blacks and 54% women, and the mean age was 63 years (range = 45-93). Symptomatic hip OA was defined as a Kellgren-Lawrence (K-L) radiographic score of >= 2 (anterior posterior pelvis X-rays) and pain, aching or stiffness on most days, or groin pain, in the same hip. Lifetime risk, defined as the proportion who developed symptomatic hip OA in at least one hip by age 85, among people who live to age 85, was modeled using logistic regression with repeated measures (through generalized estimating equations). Results: Lifetime risk of symptomatic hip OA was 25.3% [95% confidence interval (Cl) = 21.3-29.3]. Lifetime risk was similar by sex, race, highest educational attainment, and hip injury history. We studied lifetime risk by body mass index (BMI) in three forms: at age 18; at baseline and follow-up; and at age 18, baseline and follow-up and found no differences in estimates. Conclusion: The burden of symptomatic hip OA is substantial with one in four people developing this condition by age 85. The similar race-specific estimates suggest that racial disparities in total hip replacements are not attributable to differences in disease occurrence. Despite increasing evidence that obesity predicts an increased risk of both hip OA and joint replacement, we found no association between BMI and lifetime risk. Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International.
引用
收藏
页码:1372 / 1379
页数:8
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