Treiber Julia Mareen, Wolter Jan Sebastian, Backhaus Sören J, Siefert Erika Platt, Rieth Andreas, Kriechbaum Steffen D, Klemm Philipp, Tarner Ingo, Mueller-Ladner Ulf, Sossalla Samuel, Rolf Andreas
Department for Cardiology, Kerckhoff Clinic, Bad Nauheim, Germany
German Center for Cardiovascular Research, Bad Nauheim, Germany.
BMJ Open. 2025 Aug 25;15(8):e098540. doi: 10.1136/bmjopen-2024-098540.
OBJECTIVE: To evaluate changes in cardiac magnetic resonance (CMR) tissue characteristics in patients with active cardiac sarcoidosis (CS) confirmed by positron emission tomography (PET)-CT undergoing immunomodulatory therapy (IMT), and to explore their potential use for inflammation monitoring. DESIGN: Retrospective observational cohort study. SETTING: Tertiary care referral centre in Germany. PARTICIPANTS: From a cohort of 47 patients with CS, 24 patients with PET-confirmed active myocardial inflammation and complete baseline and follow-up CMR imaging after ≥6 months of IMT were included. PRIMARY AND SECONDARY ENDPOINTS: Primary outcome: Changes in CMR-derived tissue characteristics (T1, T2 mapping, late gadolinium enhancement (LGE) mass). SECONDARY OUTCOMES: Changes in functional (ejection fraction (EF) and global longitudinal strain (GLS)) and morphological parameters (end-diastolic/systolic volume indices (EDVi/ESVi)). RESULTS: Patients with PET-confirmed active CS show increased global T1 and T2 compared with healthy volunteers. Over the course of IMT, significant reductions in global T2 (median (IQR): 39 (38-41) ms vs 37 (36-39) ms; p=0.002), LGE-region T2 (43 (40-46) ms vs 41 (38-42) ms; p=0.003), and relative LGE mass (23% (17-38) vs 15% (8-32); p=0.006) were observed. No significant differences were found in EF (p=0.78), GLS (p=0.49), EDVi (p=0.56), ESVi (p=0.28) or native T1 values (p=0.23). CONCLUSION: In patients with PET-confirmed active CS undergoing IMT, serial CMR demonstrated measurable changes in T2 mapping and LGE parameters, suggesting a potential role for CMR tissue characterisation in monitoring myocardial inflammation. However, due to the observational design and absence of a control group, causal treatment effects cannot be confirmed. Further prospective studies are needed to validate the utility of CMR for treatment monitoring in CS.
目的:评估经正电子发射断层扫描(PET)-CT确诊为活动性心脏结节病(CS)并接受免疫调节治疗(IMT)的患者心脏磁共振(CMR)组织特征的变化,并探讨其在炎症监测中的潜在用途。 设计:回顾性观察队列研究。 地点:德国的三级医疗转诊中心。 参与者:在47例CS患者队列中,纳入24例经PET确诊有活动性心肌炎症且在IMT≥6个月后有完整基线和随访CMR成像的患者。 主要和次要终点:主要结局:CMR衍生的组织特征(T1、T2映射、延迟钆增强(LGE)质量)的变化。 次要结局:功能(射血分数(EF)和整体纵向应变(GLS))和形态学参数(舒张末期/收缩末期容积指数(EDVi/ESVi))的变化。 结果:与健康志愿者相比,经PET确诊的活动性CS患者的整体T1和T2升高。在IMT过程中,观察到整体T2(中位数(四分位间距):39(38 - 41)ms对37(36 - 39)ms;p = 0.002)、LGE区域T2(43(40 - 46)ms对41(38 - 42)ms;p = 0.003)和相对LGE质量(23%(17 - 38)对15%(8 - 32);p = 0.006)显著降低。在EF(p = 0.78)、GLS(p = 0.49)、EDVi(p = 0.56)、ESVi(p = 0.28)或固有T1值(p = 0.23)方面未发现显著差异。 结论:在接受IMT的经PET确诊的活动性CS患者中,系列CMR显示T2映射和LGE参数有可测量的变化,提示CMR组织特征在监测心肌炎症方面有潜在作用。然而,由于观察性设计且缺乏对照组,无法确认因果治疗效果。需要进一步的前瞻性研究来验证CMR在CS治疗监测中的效用。
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