Hloch Karel, Doseděl Martin, Duintjer Tebbens Jurjen, Žaloudková Lenka, Medková Helena, Vlček Jiří, Soukup Tomáš, Pávek Petr
Department of Social & Clinical Pharmacy, Faculty of Pharmacy in Hradec Kralove, Charles University, Prague, Czechia.
Department of Biophysics & Physical Chemistry, Faculty of Pharmacy in Hradec Kralove, Charles University, Prague, Czechia.
Front Pharmacol. 2021 Nov 5;12:703279. doi: 10.3389/fphar.2021.703279. eCollection 2021.
Cardiovascular diseases (CVDs) lead to higher morbidity and mortality in rheumatoid arthritis; thus, we aimed to determine whether patients who had discontinued methotrexate treatment before the study enrollment (group MTX 0) were at a higher risk of CVD than patients treated with methotrexate at the time of the data collection (group MTX 1). A retrospective, prospective, observational, cross-sectional study was conducted. A total of 125 patients were enrolled in the study. Patients from the MTX 0 group ( = 35) were not treated with methotrexate for 7.54 (SD ± 4.21) years in average. Medical documentation as well as information taken in patient examinations during regular rheumatologist visits was used to obtain the required data. The composite of any CVD occurred less frequently in patients in the MTX 1 group than in the MTX 0 group (18.8 vs. 40.0%, OR 0.35, 95% CI, 0.15 to 0.83; = 0.017) with a non-significant trend after adjustment for other treatments, which differed between study groups at the baseline ( = 0.054). Significant difference was found for the reduction of myocardial infarction in the MTX 1 group compared to the MTX 0 group (3.5 vs. 14.3%, OR 0.22, 95% CI, 0.05 to 0.97; = 0.046). There were 4 deaths (4.7%) in the MTX 1 group as compared with 7 (20.0%) in the MTX 0 group (OR 0.20, 95% CI, 0.05 to 0.73; = 0.015). Our results demonstrate that patients who discontinued methotrexate treatment are at a significantly higher risk of CVD and all-cause mortality. Based on our findings, we recommend stricter control of CVD in cases of methotrexate discontinuation.
心血管疾病(CVDs)在类风湿关节炎中导致更高的发病率和死亡率;因此,我们旨在确定在研究入组前停用甲氨蝶呤治疗的患者(MTX 0组)是否比在数据收集时接受甲氨蝶呤治疗的患者(MTX 1组)患CVD的风险更高。进行了一项回顾性、前瞻性、观察性横断面研究。共有125名患者纳入研究。MTX 0组(n = 35)的患者平均7.54(标准差±4.21)年未接受甲氨蝶呤治疗。利用医疗记录以及在风湿病专家定期门诊时患者检查中获取的信息来获得所需数据。MTX 1组患者中任何CVD的综合发生率低于MTX 0组(18.8%对40.0%,OR 0.35,95%CI,0.15至0.83;P = 0.017),在对其他治疗进行调整后有非显著趋势,而这些治疗在研究组基线时存在差异(P = 0.054)。与MTX 0组相比,MTX 1组心肌梗死的减少有显著差异(3.5%对14.3%,OR 0.22,95%CI,0.05至0.97;P = 0.046)。MTX 1组有4例死亡(4.7%),而MTX 0组有7例(20.0%)(OR 0.20,95%CI,0.05至0.73;P = 0.015)。我们的结果表明,停用甲氨蝶呤治疗的患者患CVD和全因死亡率的风险显著更高。基于我们的研究结果,我们建议在甲氨蝶呤停药的情况下更严格地控制CVD。