Interstitial Lung Diseases Center of Excellence, Department of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.
Department of Clinical Pharmacy, St Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands.
J Nucl Cardiol. 2023 Aug;30(4):1543-1553. doi: 10.1007/s12350-022-03171-6. Epub 2023 Jan 14.
Side effects limit the long-term use of glucocorticoids in cardiac sarcoidosis (CS), and methotrexate has gained attention as steroid sparing agent although the supporting evidence is poor. This study compared prednisone monotherapy, methotrexate monotherapy or a combination of both, in the reduction of myocardial Fluorine-18 fluorodeoxyglucose (FDG) uptake and clinical stabilization of CS patients.
In this retrospective cohort study, 61 newly diagnosed and treatment naïve CS patients commenced treatment with prednisone (N = 21), methotrexate (N = 30) or prednisone and methotrexate (N = 10) between January 2010 and December 2017. Primary outcome was metabolic response on FDG PET/CT and secondary outcomes were treatment patterns, major adverse cardiovascular events, left ventricular ejection fraction, biomarkers and side effects. At a median treatment duration of 6.2 [5.7-7.2] months, 71.4% of patients were FDG PET/CT responders, and the overall myocardial maximum standardized uptake value decreased from 6.9 [5.0-10.1] to 3.4 [2.1-4.7] (P < 0.001), with no significant differences between treatment groups. During 24 months of follow-up, 7 patients (33.3%; prednisone), 6 patients (20.0%; methotrexate) and 1 patient (10.0%; combination group) experienced at least one major adverse cardiovascular event (P = 0.292). Left ventricular ejection fraction was preserved in all treatment groups.
Significant suppression of cardiac FDG uptake occurred in CS patients after 6 months of prednisone, methotrexate or combination therapy. There were no significant differences in clinical outcomes during follow-up. These results warrant further investigation of methotrexate treatment in CS patients.
在心脏结节病(CS)中,副作用限制了糖皮质激素的长期使用,甲氨蝶呤作为一种类固醇节约剂引起了关注,尽管支持证据不足。本研究比较了泼尼松单药治疗、甲氨蝶呤单药治疗或两者联合治疗,以减少氟-18 氟代脱氧葡萄糖(FDG)摄取和 CS 患者的临床稳定。
在这项回顾性队列研究中,61 例新诊断且未经治疗的 CS 患者于 2010 年 1 月至 2017 年 12 月期间开始接受泼尼松(N=21)、甲氨蝶呤(N=30)或泼尼松和甲氨蝶呤(N=10)治疗。主要结局是 FDG PET/CT 的代谢反应,次要结局是治疗模式、主要不良心血管事件、左心室射血分数、生物标志物和副作用。在中位治疗时间为 6.2[5.7-7.2]个月时,71.4%的患者为 FDG PET/CT 应答者,总体心肌最大标准化摄取值从 6.9[5.0-10.1]降至 3.4[2.1-4.7](P<0.001),各组间无显著差异。在 24 个月的随访期间,7 名患者(33.3%;泼尼松)、6 名患者(20.0%;甲氨蝶呤)和 1 名患者(10.0%;联合组)发生了至少一次主要不良心血管事件(P=0.292)。所有治疗组的左心室射血分数均得到保留。
在 CS 患者接受泼尼松、甲氨蝶呤或联合治疗 6 个月后,心脏 FDG 摄取明显受到抑制。在随访期间,临床结局无显著差异。这些结果表明,在 CS 患者中进一步研究甲氨蝶呤治疗是合理的。