Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
J Card Fail. 2021 Jan;27(1):83-91. doi: 10.1016/j.cardfail.2020.08.013. Epub 2020 Sep 2.
Cardiac sarcoidosis (CS) is an increasingly recognized cause of cardiomyopathy; however, data on immunosuppressive strategies are limited. Treatment with tumor necrosis factor (TNF) alpha inhibitors is not well described; moreover, there may be heart failure-related safety concerns.
Retrospective multicenter study of patients with CS treated with TNF alpha inhibitors. Baseline characteristics, treatments, and outcomes were adjudicated.
Thirty-eight patients with CS (mean age 49.9 years, 42% women, 53% African American) were treated with TNF alpha inhibitor (30 infliximab, 8 adalimumab). Prednisone dose decreased from time of TNF alpha inhibitor initiation (21.7 ± 17.5 mg) to 6 months (10.4 ± 6.1 mg, P = .001) and 12 months (7.3 ± 7.3 mg, P = .002) after treatment. On pre-TNF alpha inhibitor treatment positron emission tomography with 18-flourodoxyglucose (FDG-PET), 84% of patients had cardiac FDG uptake. After treatment, there was a significant decrease in number of segments involved (3.5 ± 3.8 to 1.0 ± 2.5, P = .008) and maximum standardized uptake value (3.59 ± 3.70 to 0.57 ± 1.60, P = .0005), with 73% of patients demonstrating complete resolution or improvement of cardiac FDG uptake. The left ventricular ejection fraction remained stable (45.0 ± 16.5% to 47.0 ± 15.0%, P = .10). Four patients required inpatient heart failure treatment, and 8 had infections; 2 required treatment cessation.
TNF alpha inhibitor treatment guided by FDG-PET imaging may minimize corticosteroid use and effectively reduce cardiac inflammation without significant adverse effect on cardiac function. However, infections were common, some of which were serious, and therefore patients require close monitoring for both infection and cardiac symptoms.
心肌结节病(CS)是越来越被认可的心肌病病因之一;然而,关于免疫抑制策略的数据有限。肿瘤坏死因子(TNF)α抑制剂的治疗方法描述得并不完善;此外,可能存在与心力衰竭相关的安全问题。
对接受 TNFα抑制剂治疗的 CS 患者进行回顾性多中心研究。对基线特征、治疗方法和结局进行了裁定。
38 例 CS 患者(平均年龄 49.9 岁,42%为女性,53%为非裔美国人)接受 TNFα抑制剂(30 例英夫利昔单抗,8 例阿达木单抗)治疗。从开始使用 TNFα抑制剂时(21.7±17.5mg)到治疗后 6 个月(10.4±6.1mg,P=0.001)和 12 个月(7.3±7.3mg,P=0.002),泼尼松剂量逐渐减少。在使用 18-氟脱氧葡萄糖(FDG)-正电子发射断层扫描(PET)的 TNFα抑制剂治疗前,84%的患者有心脏 FDG 摄取。治疗后,受累节段数量明显减少(3.5±3.8 至 1.0±2.5,P=0.008),最大标准化摄取值也明显降低(3.59±3.70 至 0.57±1.60,P=0.0005),73%的患者心脏 FDG 摄取完全缓解或改善。左心室射血分数保持稳定(45.0±16.5%至 47.0±15.0%,P=0.10)。4 例患者需要住院心力衰竭治疗,8 例患者发生感染;2 例需要停止治疗。
FDG-PET 成像指导的 TNFα抑制剂治疗可能会减少皮质类固醇的使用,并有效地降低心脏炎症,而不会对心脏功能产生显著的不良影响。然而,感染很常见,其中一些感染很严重,因此患者需要密切监测感染和心脏症状。