Arthritis Section, VA Puget Sound Health Care System, Seattle, WA, USA; Division of Rheumatology, Department of Medicine, University of Washington Department of Medicine, Seattle, WA, USA.
Arthritis Section, VA Puget Sound Health Care System, Seattle, WA, USA; Division of Rheumatology, Department of Medicine, University of Washington Department of Medicine, Seattle, WA, USA.
Semin Arthritis Rheum. 2022 Apr;53:151972. doi: 10.1016/j.semarthrit.2022.151972. Epub 2022 Jan 31.
Prior studies have found conflicting results when evaluating the association between rheumatoid arthritis (RA) disease activity and bone mineral density (BMD). Whether or not cumulative RA disease activity is associated with BMD remains unanswered.
Data were from the University of California San Francisco RA Cohort from years 2006-2018. Those with BMD measures and at least two study visits prior to BMD measure were included in the study. The association between low cumulative disease activity, as measured by DAS28ESR, with the primary outcome of femoral neck BMD was assessed using multivariable linear regression. Sensitivity analyses were performed substituting CDAI for the disease activity measure as well as total hip and lumbar spine BMD as outcomes.
161 participants with RA were studied. The cohort was 62.4 ± 10.2 years old and 88% female. Hispanic/Latino (N = 73, 45%) and Asian (N = 59, 37%) were the most common racial/ethnic groups in our cohort. Mean RA duration was 10.5 ± 7.3 years and 83% were ACPA positive. Low disease activity was independently associated with higher femoral neck BMD compared to the moderate/high disease activity group (β= 0.071 [95%CI: 0.021 to 0.122], p = 0.020). The relationship between low cumulative disease activity was similar when CDAI and other BMD sites were substituted in the multivariable models.
Low cumulative disease activity as measured by DAS28ESR was associated with higher femoral neck BMD, independent of traditional osteoporosis risk factors (e.g., age, sex, BMI) in a unique RA cohort. Results were similar when evaluating cumulative low CDAI and other BMD sites.
先前的研究在评估类风湿关节炎(RA)疾病活动与骨密度(BMD)之间的关系时得出了相互矛盾的结果。累积性 RA 疾病活动是否与 BMD 相关仍未得到解答。
数据来自于 2006 年至 2018 年期间的加利福尼亚大学旧金山 RA 队列。将至少有两次研究访视且在 BMD 测量之前有 BMD 测量值的患者纳入研究。使用多变量线性回归评估通过 DAS28ESR 测量的低累积疾病活动与股骨颈 BMD 主要结局之间的关系。进行敏感性分析,用 CDAI 替代疾病活动测量值,并将总髋部和腰椎 BMD 作为结局。
研究纳入了 161 名 RA 患者。该队列的平均年龄为 62.4±10.2 岁,88%为女性。西班牙裔/拉丁裔(N=73,45%)和亚裔(N=59,37%)是队列中最常见的种族/民族群体。RA 病程的平均时间为 10.5±7.3 年,83%的患者 ACPA 阳性。与中/高度疾病活动组相比,低疾病活动与股骨颈 BMD 较高独立相关(β=0.071[95%CI:0.021 至 0.122],p=0.020)。当在多变量模型中替代 CDAI 和其他 BMD 部位时,低累积疾病活动之间的关系相似。
在一个独特的 RA 队列中,用 DAS28ESR 测量的低累积疾病活动与股骨颈 BMD 较高相关,独立于传统的骨质疏松风险因素(如年龄、性别、BMI)。当评估累积性低 CDAI 和其他 BMD 部位时,结果相似。