Internal Medicine/Rheumatology, University of Michigan Medical School.
VA Ann Arbor Healthcare System, Center for Clinical Management Research, Ann Arbor, MI.
Rheumatology (Oxford). 2022 Apr 11;61(4):1556-1562. doi: 10.1093/rheumatology/keab583.
Over one-third of patients with RA exhibit evidence of fibromyalgianess, which is associated with higher rates of disability and inadequate responsiveness to RA treatment. Patients with RA often remain on glucocorticoids long-term, despite the known risk of dose-dependent morbidity. We undertook this study to examine the relationship between fibromyalgianess and glucocorticoid persistence among RA patients.
We followed participants with active RA on oral prednisone for ∼3 months after initiating a new DMARD. Fibromyalgianess was measured using the Fibromyalgia Survey Questionnaire (FSQ), previously shown to correlate with key FM features often superimposed upon RA. Severity of fibromyalgianess was stratified as follows: FSQ <8 low, FSQ 8-10 moderate and FSQ >10 high/very high. The association between baseline fibromyalgianess and glucocorticoid persistence, defined as prednisone use at 3-month follow-up visit after DMARD initiation, was assessed using multiple logistic regression adjusted for baseline demographics, RA duration, serostatus and inflammatory activity assessed using swollen joint count and CRP.
Of the 97 participants on prednisone at baseline, 65% were still taking prednisone at follow-up. Fifty-seven percent of participants with low baseline fibromyalgianess had persistent glucocorticoid use, compared with 84% of participants with high or very high fibromyalgianess. After adjustment for non-inflammatory factors and inflammatory activity, participants with high/very high baseline fibromyalgianess were more likely to be taking prednisone at follow-up relative to those with low fibromyalgianess [odds ratio 4.99 (95% CI 1.20, 20.73)].
High fibromyalgianess is associated with persistent glucocorticoid use, independent of inflammatory activity.
超过三分之一的类风湿关节炎 (RA) 患者表现出纤维肌痛样特征,这与更高的残疾率和对 RA 治疗的反应不足有关。尽管已知存在剂量依赖性发病率风险,但 RA 患者仍长期使用糖皮质激素。我们进行这项研究是为了检查 RA 患者中纤维肌痛样特征与糖皮质激素持续存在之间的关系。
我们对正在服用口服泼尼松龙的活动期 RA 患者进行了研究,这些患者在开始新的 DMARD 后大约 3 个月。使用先前显示与经常叠加在 RA 上的关键 FM 特征相关的纤维肌痛调查问卷 (FSQ) 来测量纤维肌痛样特征。纤维肌痛样特征的严重程度分层如下:FSQ<8 为低,FSQ8-10 为中,FSQ>10 为高/极高。使用多变量逻辑回归评估基线纤维肌痛样特征与糖皮质激素持续存在之间的关联,定义为在开始 DMARD 后 3 个月的随访时使用泼尼松龙。调整了基线人口统计学、RA 持续时间、血清学状态和使用肿胀关节计数和 CRP 评估的炎症活动。
在基线时服用泼尼松龙的 97 名参与者中,65%的人在随访时仍在服用泼尼松龙。基线纤维肌痛样特征低的参与者中,57%持续使用糖皮质激素,而基线纤维肌痛样特征高/极高的参与者中,84%持续使用糖皮质激素。在调整非炎症因素和炎症活动后,与低纤维肌痛样特征的参与者相比,基线纤维肌痛样特征高/极高的参与者在随访时更有可能服用泼尼松龙[比值比 4.99(95%CI 1.20,20.73)]。
高纤维肌痛样特征与糖皮质激素持续存在相关,与炎症活动无关。