PMID- 30482560 OWN - NLM STAT- MEDLINE DCOM- 20191025 LR - 20191025 IS - 1365-229X (Electronic) IS - 0009-9260 (Linking) VI - 74 IP - 1 DP - 2019 Jan TI - Evaluation of FDG PET combined with cardiac MRI for the diagnosis and therapeutic monitoring of cardiac sarcoidosis. PG - 81.e9-81.e18 LID - S0009-9260(18)30552-X [pii] LID - 10.1016/j.crad.2018.09.015 [doi] AB - AIM: To compare combined 2-[(18)F]-fluoro-2-deoxy-d-glucose (FDG)-positron-emission tomography (PET) and cardiac magnetic resonance imaging (CMR) for the diagnosis and therapy monitoring of cardiac sarcoidosis (CS). MATERIALS AND METHODS: Eighty patients with sarcoidosis and a suspicion of CS who underwent PET and CMR were included retrospectively. PET was undertaken after a low-carbohydrate-high-fat diet in all patients using a combined 16-section PET/computed tomography (CT) camera. PET was considered positive (PET+) in cases of focal or multifocal FDG uptake. CMR was considered positive (CMR+) in cases of subepicardial late gadolinium enhancement (LGE). A subgroup of 50 patients (50/80) was monitored during therapy and classified as responders or non-responders. RESULTS: Eighty-two percent of patients with PET+ (9/11) also had CMR+ imaging, with good spatial agreement (kappa=0,79; 95% confidence interval [CI]: 0.65-0.94). Twenty-seven percent (22/80) had residual physiological FDG uptake, with a standardised uptake value (SUV) not significantly different compared to the SUV from pathological uptake (6.4 versus 6 respectively, p=0,92). The clinical response was more frequent in patients with baseline PET+ compared to baseline PET- (80% versus 45%, p=0.07). PET findings improved in all cases under treatment (7/7), whereas LGE improved in only 33% of patients (3/9). CONCLUSION: Due to high risk of false-positive or undetermined findings, PET might be performed as a second-line study in cases of LGE, to assess inflammatory load. In addition, PET seems suitable to predict and assess response under therapy. CI - Copyright (c) 2018. Published by Elsevier Ltd. FAU - Sgard, B AU - Sgard B AD - Department of Nuclear Medicine, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Brillet, P-Y AU - Brillet PY AD - Department of Radiology, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Bouvry, D AU - Bouvry D AD - Department of Pneumology, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Djelbani, S AU - Djelbani S AD - Department of Nuclear Medicine, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Nunes, H AU - Nunes H AD - Department of Pneumology, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Meune, C AU - Meune C AD - Department of Cardiology, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Valeyre, D AU - Valeyre D AD - Department of Pneumology, Hopital Avicenne, Paris 13 University, Bobigny, France. FAU - Soussan, M AU - Soussan M AD - Department of Nuclear Medicine, Hopital Avicenne, Paris 13 University, Bobigny, France. Electronic address: michael.soussan@aphp.fr. LA - eng PT - Journal Article DEP - 20181025 PL - England TA - Clin Radiol JT - Clinical radiology JID - 1306016 RN - 0Z5B2CJX4D (Fluorodeoxyglucose F18) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Cardiomyopathies/*diagnostic imaging/pathology MH - Female MH - Fluorodeoxyglucose F18 MH - Heart/*diagnostic imaging MH - Humans MH - *Magnetic Resonance Imaging/methods MH - Male MH - Middle Aged MH - Myocardium/pathology MH - *Positron-Emission Tomography/methods MH - Sarcoidosis/*diagnostic imaging/pathology MH - Young Adult EDAT- 2018/11/30 06:00 MHDA- 2019/10/28 06:00 CRDT- 2018/11/29 06:00 PHST- 2018/05/26 00:00 [received] PHST- 2018/09/26 00:00 [accepted] PHST- 2018/11/30 06:00 [pubmed] PHST- 2019/10/28 06:00 [medline] PHST- 2018/11/29 06:00 [entrez] AID - S0009-9260(18)30552-X [pii] AID - 10.1016/j.crad.2018.09.015 [doi] PST - ppublish SO - Clin Radiol. 2019 Jan;74(1):81.e9-81.e18. doi: 10.1016/j.crad.2018.09.015. Epub 2018 Oct 25.