Rosalind Franklin School of Medicine, Chicago Medical School, North Chicago, IL, USA.
J Clin Densitom. 2011 Jul-Sep;14(3):184-9. doi: 10.1016/j.jocd.2011.05.012.
Rheumatoid arthritis is the only secondary cause of osteoporosis that is considered independent of bone density in the FRAX(®) algorithm. Although input for rheumatoid arthritis in FRAX(®) is a dichotomous variable, intuitively, one would expect that more severe or active disease would be associated with a greater risk for fracture. We reviewed the literature to determine if specific disease parameters or medication use could be used to better characterize fracture risk in individuals with rheumatoid arthritis. Although many studies document a correlation between various parameters of disease activity or severity and decreased bone density, fewer have associated these variables with fracture risk. We reviewed these studies in detail and concluded that disability measures such as HAQ (Health Assessment Questionnaire) and functional class do correlate with clinical fractures but not morphometric vertebral fractures. One large study found a strong correlation with duration of disease and fracture risk but additional studies are needed to confirm this. There was little evidence to correlate other measures of disease such as DAS (disease activity score), VAS (visual analogue scale), acute phase reactants, use of non-glucocorticoid medications and increased fracture risk. We concluded that FRAX(®) calculations may underestimate fracture probability in patients with impaired functional status from rheumatoid arthritis but that this could not be quantified at this time. At this time, other disease measures cannot be used for fracture prediction. However only a few, mostly small studies addressed other disease parameters and further research is needed. Additional questions for future research are suggested.
类风湿关节炎是 FRAX(®)算法中唯一被认为独立于骨密度的继发性骨质疏松症病因。虽然 FRAX(®)中类风湿关节炎的输入是一个二分变量,但直观地说,人们会期望更严重或更活跃的疾病与更高的骨折风险相关。我们回顾了文献,以确定是否可以使用特定的疾病参数或药物使用来更好地描述类风湿关节炎患者的骨折风险。尽管许多研究记录了疾病活动或严重程度的各种参数与骨密度降低之间存在相关性,但很少有研究将这些变量与骨折风险相关联。我们详细审查了这些研究,并得出结论,残疾测量,如 HAQ(健康评估问卷)和功能分级,与临床骨折相关,但与形态计量椎体骨折无关。一项大型研究发现疾病持续时间与骨折风险之间存在很强的相关性,但需要进一步研究来证实这一点。几乎没有证据表明其他疾病指标,如 DAS(疾病活动评分)、VAS(视觉模拟评分)、急性期反应物、非糖皮质激素药物的使用与增加的骨折风险相关。我们得出结论,FRAX(®)计算可能低估了类风湿关节炎导致功能状态受损患者的骨折概率,但目前无法对此进行量化。目前,其他疾病指标不能用于骨折预测。然而,只有少数(大多是小型)研究涉及其他疾病参数,需要进一步研究。建议提出未来研究的其他问题。