Tareev Clinic of Internal Diseases, Sechenov First Moscow State Medical University of the Ministry of Health Care of the Russian Federation (Sechenov University), Moscow, Russia.
Russian Gerontological Research and Clinical Center, Moscow, Russia.
Dokl Biochem Biophys. 2024 Aug;517(1):250-258. doi: 10.1134/S1607672924700984. Epub 2024 Jul 13.
The aim of the study was to evaluate the clinical manifestations and survival of patients with giant cell arteritis (GCA).
. A retrospective study included 166 patients with newly diagnosed GCA. Clinical, laboratory, and instrumental data and three sets of classification criteria were used to confirm the diagnosis: the American College of Rheumatology (ACR) 1990, the revised ACR criteria of 2016 and/or the new ACR and European Alliance of Rheumatologic Associations (EULAR) 2022 criteria. Some of the patients underwent instrumental investigations: temporal artery ultrasound Doppler (n = 61), contrast-enhanced computed tomography (n = 5), CT angiography (n = 6), magnetic resonance imaging (n = 4), MR angiography (n = 3), and 18F-FDG PET/CT (n = 47). Overall and recurrence-free survival rates were analyzed using survival tables and Kaplan-Meier method.
. The most frequent first manifestations of GCA were headache (81.8%), weakness (64%), fever (63.8%), and symptoms of rheumatic polymyalgia (56.6%). Changes in temporal arteries in color duplex scanning were detected in 44 out of 61 patients. GCs therapy was performed in all patients who agreed to be treated (n = 158), methotrexate was used in 49 out of 158 patients, leflunomide in 9 patients. In 45 (28.5%) out of 158 patients, a stable remission was achieved as a result of GC monotherapy; in 120 (75.9%) patients, long-term maintenance therapy with GCs was required to prevent exacerbations, including 71 (44.9%) patients in combination with methotrexate or other immunosuppressive drugs. The follow-up period of patients with a history of relapses was 21.0 (8.0-54.0) months. Relapses developed in 73 (46.2%) patients. The overall one-year survival rate was 97.1% [95% CI 94.3; 99.9], and the five-year survival rate of patients was 94.6% [95% CI 90.2; 99.0]. The one-year relapse-free survival rate was 86.4% [95% CI 80.5; 92.3], and the five-year relapse-free survival rate was 52.4% [95% CI 42.0; 62.8]. Twelve (7.2%) of 166 patients died. The cause of death was myocardial infarction in two patients, stroke in two patients, and breast cancer in one patient; in the remaining seven cases, the cause of death was not determined.
: Given the high frequency of disease exacerbation, patients with GCA require long-term follow-up, especially during the first year after diagnosis.
评估巨细胞动脉炎(GCA)患者的临床表现和生存情况。
采用回顾性研究方法,纳入 166 例新诊断的 GCA 患者。使用三种分类标准来确认诊断:美国风湿病学会(ACR)1990 年标准、2016 年修订的 ACR 标准和/或新的 ACR 和欧洲风湿病联盟(EULAR)2022 年标准。部分患者进行了仪器检查:颞动脉超声多普勒(n=61)、对比增强计算机断层扫描(n=5)、CT 血管造影(n=6)、磁共振成像(n=4)、MR 血管造影(n=3)和 18F-FDG PET/CT(n=47)。使用生存表和 Kaplan-Meier 方法分析总生存率和无复发生存率。
GCA 最常见的首发症状是头痛(81.8%)、乏力(64%)、发热(63.8%)和风湿性多肌痛症状(56.6%)。61 例患者中有 44 例在彩色双功能超声检查中发现颞动脉改变。所有同意治疗的患者(n=158)均接受了 GCs 治疗,其中 49 例患者接受了甲氨蝶呤治疗,9 例患者接受了来氟米特治疗。45 例(28.5%)患者经 GCs 单药治疗后达到稳定缓解;120 例(75.9%)患者需要长期维持 GCs 治疗以预防病情恶化,其中 71 例(44.9%)患者联合使用甲氨蝶呤或其他免疫抑制剂。有复发史的患者随访时间为 21.0(8.0-54.0)个月。73 例(46.2%)患者出现复发。总体一年生存率为 97.1%[95%可信区间(CI)94.3%至 99.9%],五年生存率为 94.6%[95%CI 90.2%至 99.0%]。一年无复发生存率为 86.4%[95%CI 80.5%至 92.3%],五年无复发生存率为 52.4%[95%CI 42.0%至 62.8%]。166 例患者中有 12 例(7.2%)死亡。死亡原因包括两名患者心肌梗死、两名患者卒中、一名患者乳腺癌;其余 7 例患者的死亡原因未确定。
鉴于疾病恶化的高频率,GCA 患者需要长期随访,尤其是在诊断后第一年。