Department of Rheumatology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
Department of Rheumatology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
Joint Bone Spine. 2022 Nov;89(6):105432. doi: 10.1016/j.jbspin.2022.105432. Epub 2022 Jun 28.
Fatigue is a prominent and disabling symptom in patients with rheumatoid arthritis (RA), that is only partially explained by inflammation and responds poorly to DMARD-therapy. We hypothesized that inflammation explains fatigue to a larger extent in the phase of clinically suspect arthralgia (CSA), when persistent clinical arthritis is still absent and fatigue has not yet become chronic. We therefore studied the course of fatigue in CSA during progression to RA and the association with inflammation at CSA-onset and at RA-diagnosis.
600 consecutive CSA-patients were followed for RA-development. Additionally, 710 early RA-patients were studied at diagnosis. Fatigue was assessed every study visit and expressed on a 0-100 scale. Inflammation was measured with the DAS44-CRP, with and without including subclinical inflammation. The course of fatigue over time was studied with linear mixed models. Associations between fatigue and inflammation were studied with linear regression. Analyses were stratified by ACPA-status.
In 88 CSA-patients who developed RA, pre-arthritis fatigue-levels increased gradually with 7 points/year, towards 48 (95%CI=41-55) at RA-development (P=ns). Fatigue decreased in CSA-patients who did not develop RA (4 points/year, P<0.001). At CSA-onset, inflammation was associated with fatigue (β=18, meaning 18 points more fatigue per point increase DAS-score, P<0.01). This association was stronger than at RA-diagnosis (β=5, P<0.001). Fatigue-levels were lower in ACPA-positive pre-RA, but its association with inflammation was stronger compared to ACPA-negative pre-RA.
Fatigue increased gradually during progression from arthralgia to clinical arthritis, and fatigue was better explained by inflammation in CSA than in RA. This implies a 'phase-dependent relation' between inflammation and fatigue.
疲劳是类风湿关节炎(RA)患者的一种突出且致残的症状,其仅部分由炎症解释,且对 DMARD 治疗反应不佳。我们假设,在持续存在临床关节炎之前且疲劳尚未变为慢性的临床可疑关节炎(CSA)阶段,炎症对疲劳的解释程度更大。因此,我们研究了 CSA 进展为 RA 过程中的疲劳变化以及与 CSA 发病时和 RA 诊断时炎症的关系。
对 600 例连续的 CSA 患者进行 RA 进展的随访。此外,对 710 例早期 RA 患者进行了诊断时的研究。每一次研究访问时都评估疲劳,并在 0-100 刻度上表示。使用 DAS44-CRP 测量炎症,包括和不包括亚临床炎症。使用线性混合模型研究疲劳随时间的变化过程。使用线性回归研究疲劳与炎症之间的关系。分析按 ACPA 状态分层。
在 88 例发展为 RA 的 CSA 患者中,关节炎前的疲劳水平逐渐增加,每年增加 7 分,在 RA 进展时达到 48(95%CI=41-55)(P=ns)。未发展为 RA 的 CSA 患者的疲劳减少(每年减少 4 分,P<0.001)。在 CSA 发病时,炎症与疲劳相关(β=18,意味着 DAS 评分每增加 1 分,疲劳增加 18 分,P<0.01)。这种相关性比在 RA 诊断时更强(β=5,P<0.001)。在 RA 前的 ACPA 阳性患者中,疲劳水平较低,但与 ACPA 阴性患者相比,其与炎症的相关性更强。
从关节炎到临床关节炎的进展过程中,疲劳逐渐增加,且 CSA 中的炎症对疲劳的解释优于 RA。这意味着炎症与疲劳之间存在“阶段相关关系”。