Sorbonne Universités AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Médecine Interne et Immunologie Clinique, F-75013, Paris, France; Centre National de Références Maladies Autoimmunes Systémiques Rares, Centre National de Références Maladies Autoinflammatoires et Amylose Inflammatoire, France; Inflammation-Immunopathology-Biotherapy Department (DMU 3iD), France; INSERM 959, Groupe Hospitalier, AP-HP, Paris, France.
Hôpital Lariboisière, Département de Médecine Interne et Immunologie, Clinique, Université, Paris, Cité, France.
J Autoimmun. 2022 Oct;132:102868. doi: 10.1016/j.jaut.2022.102868. Epub 2022 Jul 20.
To determine whether giant cell arteritis and polymyalgia rheumatica (GCA/PMR) represent independent risk factors for worse outcomes in COVID-19.
Observational, national, French, multicenter cohort (NCT04353609) comprising patients aged ≥18 years with confirmed diagnoses of either GCA, PMR or rheumatoid arthritis (RA) having presented COVID-19; those under rituximab were excluded. Primary endpoint was COVID-19 severity in GCA/PMR patients as compared to RA. We also aimed to describe the evolution of GCA/PMR patients following COVID-19. Multinomial logistic regression models were performed, with and without adjustment on pre-specified confounding factors (i.e., age, sex, body mass index, arterial hypertension, diabetes and cardiovascular disease). Unadjusted and adjusted multinomial odds-ratio (OR/aOR) and their 95% confidence intervals (CIs) were calculated as effect size using RA as reference group.
Between April 15, 2020, and August 20, 2021, 674 patients [45 (6.6%) GCA, 47 (7.0%) PMR, 582 (86.4%) RA; 62.8 years, 73.2% female] were included. Compared to RA patients, those with GCA/PMR were older and more frequently presented hypertension, diabetes and cardiovascular disease. Severe COVID-19 and death occurred in 24 (26.1%) and 16 (17.8%) patients with GCA/PMR, respectively. Unadjusted analyses revealed higher odds of severe COVID-19 [OR = 3.32 (95% CI 1.89-5.83; p < 0.001)] and death [OR = 3.20 (95%CI 1.67-6.13; p < 0.001)] for GCA/PMR compared to RA. After model adjustment, these odds were attenuated.
Patients with GCA/PMR were more likely to have severe COVID-19 and higher mortality compared to those with RA. This worse prognosis is mostly due to well known risk factors for the general population rather than vasculitis per se.
确定巨细胞动脉炎和多发性肌痛(GCA/PMR)是否是 COVID-19 预后不良的独立危险因素。
观察性、全国性、法国多中心队列(NCT04353609)纳入了年龄≥18 岁、确诊为 GCA、PMR 或类风湿关节炎(RA)且患有 COVID-19 的患者;排除了接受利妥昔单抗治疗的患者。主要终点是 GCA/PMR 患者与 RA 患者相比 COVID-19 的严重程度。我们还旨在描述 COVID-19 后 GCA/PMR 患者的病情演变。采用多分类逻辑回归模型,并在预先指定的混杂因素(即年龄、性别、体重指数、动脉高血压、糖尿病和心血管疾病)上进行调整。未调整和调整后的多分类优势比(OR/aOR)及其 95%置信区间(CI)采用 RA 作为参考组计算效应大小。
2020 年 4 月 15 日至 2021 年 8 月 20 日期间,共纳入 674 例患者[45 例(6.6%)为 GCA,47 例(7.0%)为 PMR,582 例(86.4%)为 RA;62.8 岁,73.2%为女性]。与 RA 患者相比,GCA/PMR 患者年龄更大,更常出现高血压、糖尿病和心血管疾病。24 例(26.1%)和 16 例(17.8%)GCA/PMR 患者发生严重 COVID-19 和死亡。未调整分析显示,与 RA 相比,GCA/PMR 患者发生严重 COVID-19[OR=3.32(95%CI 1.89-5.83;p<0.001)]和死亡[OR=3.20(95%CI 1.67-6.13;p<0.001)]的可能性更高。在模型调整后,这些比值有所减弱。
与 RA 相比,GCA/PMR 患者更易发生严重 COVID-19 和更高的死亡率。这种较差的预后主要是由于一般人群的已知危险因素,而不是血管炎本身。