Barbour Kamil E, Murphy Louise B, Helmick Charles G, Hootman Jennifer M, Renner Jordan B, Jordan Joanne M
Centers for Disease Control and Prevention, Atlanta, Georgia.
University of North Carolina, Chapel Hill.
Arthritis Care Res (Hoboken). 2017 Dec;69(12):1863-1870. doi: 10.1002/acr.23211. Epub 2017 Nov 2.
To address knowledge gaps regarding the relationship between bone mineral density (BMD) and incident hip or knee osteoarthritis (OA); specifically, lack of information regarding hip OA or symptomatic outcomes.
Using data (n = 1,474) from the Johnston County Osteoarthritis Project's first (1999-2004) and second (2005-2010) followup of participants ages ≥45 years, we examined the association between total hip BMD and both hip and knee OA. Total hip BMD was measured using dual x-ray absorptiometry, and participants were classified into sex-specific quartiles (low, intermediate low, intermediate high, and high). Radiographic OA (ROA) was defined as development of Kellgren/Lawrence grade ≥2. Symptomatic ROA (sROA) was defined as onset of both ROA and symptoms. Weibull regression modeling was used to estimate hazard ratios (HRs) and 95% confidence intervals (95% CIs).
Median followup time was 6.5 years (range 4.0-10.2 years). In multivariate models, and compared with participants with low BMD, those with intermediate high and high BMD were less likely to develop hip sROA (HR 0.52 [95% CI 0.31-0.86] and 0.56 [95% CI 0.31-0.86], respectively; P = 0.024 for trend); high BMD was not associated (HR 0.69 [95% CI 0.45-1.06]) with risk of hip ROA. Compared with participants with low BMD, those with intermediate low and intermediate high total hip BMD were more likely to develop knee sROA (HR 2.15 [95% CI 1.40-3.30] and 1.65 [95% CI 1.02-2.67], respectively; P = 0.325 for trend); similar associations were seen with knee ROA.
Our findings suggest that higher BMD may reduce the risk of hip sROA, while intermediate levels may increase the risk of both knee sROA and ROA.
解决关于骨密度(BMD)与髋部或膝部骨关节炎(OA)发病之间关系的知识空白;具体而言,是缺乏关于髋部OA或症状性结局的信息。
利用约翰斯顿县骨关节炎项目对年龄≥45岁参与者的首次(1999 - 2004年)和第二次(2005 - 2010年)随访数据(n = 1474),我们研究了全髋部BMD与髋部和膝部OA之间的关联。使用双能X线吸收法测量全髋部BMD,并将参与者按性别分为四分位数(低、中低、中高和高)。放射学OA(ROA)定义为Kellgren/Lawrence分级≥2级的发展情况。症状性ROA(sROA)定义为ROA和症状的出现。使用威布尔回归模型估计风险比(HRs)和95%置信区间(95% CIs)。
中位随访时间为6.5年(范围4.0 - 10.2年)。在多变量模型中,与BMD低的参与者相比,BMD中高和高的参与者发生髋部sROA的可能性较小(HR分别为0.52 [95% CI 0.31 - 0.86]和0.56 [95% CI 0.31 - 0.86];趋势P = 0.024);高BMD与髋部ROA风险无关(HR 0.69 [95% CI 0.45 - 1.06])。与BMD低的参与者相比,全髋部BMD中低和中高的参与者发生膝部sROA的可能性更大(HR分别为2.15 [95% CI 1.40 - 3.30]和1.65 [95% CI 1.02 - 2.67];趋势P = 0.325);膝部ROA也有类似关联。
我们的研究结果表明,较高的BMD可能降低髋部sROA的风险,而中等水平可能增加膝部sROA和ROA的风险。