First fracture in rheumatoid arthritis: analysis by fracture site, gender, age, and comorbidities.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Owen Taylor-Williams, Helen Keen, David B Preen, Johannes Nossent, Charles A Inderjeeth
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引用次数: 0

Abstract

Rheumatoid arthritis (RA) is a potentially devastating disorder associated with increased risk of fractures, but current studies do not completely evaluate the RA fracture risk profile. This study estimates fracture incidence by site of fracture and makes comparisons between RA and controls using the key variables gender, age, and comorbidities.

Background: Rheumatoid arthritis RA is a potentially devastating osteoimmunological disorder, predisposing to osteoporosis (OP), fragility fracture (FF), and major osteoporotic fractures (MOF). As few studies incorporate statistical matching, comorbidity and non-MOF sites, we compared the incidence of first FF, MOF, and non-MOF in RA patients with a matched control cohort adjusting for comorbidities.

Methods: This longitudinal cohort study uses routinely collected administrative data from the West Australian Rheumatic Disease Epidemiological Registry (WARDER) between 1980 and 2015. RA patients, as defined using International Classification of Disease (ICD) codes, were compared to hospitalised patients free of rheumatic disease. Case-control matching adjusted for age, gender, and comorbidities (Charlson Comorbidity Index). Incidence rates (IR) per 1000 person years (PY) with 95% confidence intervals (CI) were compared by incidence rate ratios (IRR).

Findings: In RA patients from 2000 to 2010, the first fracture IR was 18.3 (15.7-21.2) for an IRR of 1.32 (1.10-1.60). Upper limb, lower limb, and axial IR were 5.56 (95% CI 4.18-7.26), 10.60 (95% CI 8.66-12.87), and 2.47 (95% CI 2.58-3.68) with IRR of 1.18 (95% CI 0.84-1.65), 1.44 (95% CI 1.19-1.86), and 1.01 (95% CI 0.61-1.63) respectively. The first fracture IR increased 6 years before first RA hospital record (RR 1.58, CI 1.05-2.39).

Conclusions: After age, gender, and comorbidity adjustment, RA is associated with a 32% higher incidence of first fracture, increased MOF, and a fracture incidence that is already increased before a first recorded RA diagnosis. This suggests a need for early attention to prevention of all fractures in RA patients.

类风湿性关节炎首次骨折:按骨折部位、性别、年龄和合并症分析。
类风湿性关节炎(RA)是一种潜在的破坏性疾病,与骨折风险增加有关,但目前的研究并未完全评估RA的骨折风险概况。本研究按骨折部位估算骨折发生率,并利用性别、年龄和合并症等关键变量对类风湿关节炎患者和对照组进行比较:背景:类风湿性关节炎 RA 是一种潜在的破坏性骨免疫疾病,易导致骨质疏松症(OP)、脆性骨折(FF)和重大骨质疏松性骨折(MOF)。由于很少有研究将统计匹配、合并症和非骨质疏松性骨折部位纳入其中,因此我们将 RA 患者的首次脆性骨折、骨质疏松性骨折和非骨质疏松性骨折的发生率与调整合并症的匹配对照队列进行了比较:这项纵向队列研究使用了西澳大利亚风湿病流行病学登记处(WARDER)在1980年至2015年间定期收集的管理数据。根据国际疾病分类(ICD)代码定义的RA患者与无风湿病的住院患者进行了比较。病例对照匹配调整了年龄、性别和合并症(夏尔森合并症指数)。通过发病率比(IRR)比较了每千人年(PY)的发病率(IR)和95%置信区间(CI):在2000年至2010年的RA患者中,首次骨折IR为18.3(15.7-21.2),IRR为1.32(1.10-1.60)。上肢、下肢和轴向IR分别为5.56(95% CI 4.18-7.26)、10.60(95% CI 8.66-12.87)和2.47(95% CI 2.58-3.68),IRR分别为1.18(95% CI 0.84-1.65)、1.44(95% CI 1.19-1.86)和1.01(95% CI 0.61-1.63)。首次骨折IR在首次RA住院记录前6年增加(RR 1.58,CI 1.05-2.39):在对年龄、性别和合并症进行调整后,RA 与首次骨折发生率增加 32%、MOF 增加以及在首次有 RA 诊断记录之前骨折发生率已经增加有关。这表明,有必要尽早注意预防RA患者的所有骨折。
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来源期刊
Osteoporosis International
Osteoporosis International 医学-内分泌学与代谢
CiteScore
8.10
自引率
10.00%
发文量
224
审稿时长
3 months
期刊介绍: An international multi-disciplinary journal which is a joint initiative between the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA, Osteoporosis International provides a forum for the communication and exchange of current ideas concerning the diagnosis, prevention, treatment and management of osteoporosis and other metabolic bone diseases. It publishes: original papers - reporting progress and results in all areas of osteoporosis and its related fields; review articles - reflecting the present state of knowledge in special areas of summarizing limited themes in which discussion has led to clearly defined conclusions; educational articles - giving information on the progress of a topic of particular interest; case reports - of uncommon or interesting presentations of the condition. While focusing on clinical research, the Journal will also accept submissions on more basic aspects of research, where they are considered by the editors to be relevant to the human disease spectrum.
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