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Japanese Antibacterial Drug Management for Cardiac Sarcoidosis (J‐ ACNES ): A multicenter, open‐label, randomized, controlled study
Author(s) -
Ishibashi Kohei,
Eishi Yoshinobu,
Tahara Nobuhiro,
Asakura Masanori,
Sakamoto Naka,
Nakamura Kazufumi,
Takaya Yoichi,
Nakamura Tomohisa,
Yazaki Yoshikazu,
Yamaguchi Tetsuo,
Asakura Koko,
Anzai Toshihisa,
Noguchi Teruo,
Yasuda Satoshi,
Terasaki Fumio,
Hamasaki Toshimitsu,
Kusano Kengo
Publication year - 2018
Publication title -
journal of arrhythmia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.463
H-Index - 21
eISSN - 1883-2148
pISSN - 1880-4276
DOI - 10.1002/joa3.12084
Subject(s) - medicine , propionibacterium acnes , sarcoidosis , clinical endpoint , randomized controlled trial , adverse effect , corticosteroid , clinical trial , dermatology , acne
Background Cardiac sarcoidosis ( CS ) is a noncaseating granulomatous disease of unknown etiology. Lifelong immunosuppressive therapy, most frequently using corticosteroids, is a standard therapy to control hypersensitivity of immune reactions and prevent inflammation. However, it sometimes causes various systemic adverse effects and requires dose escalation. Thus, additional therapy may be required for the treatment of this disease. Recently, Propionibacterium acnes ( P. acnes ) was reported as one of the etiologic agents of CS , indicating that antibacterial drugs ( ABD ) may be effective for the treatment of CS . The objective of this study was to investigate the effect of ABD treatment, in addition to standard corticosteroid therapy, in patients with CS . Methods The Japanese Antibacterial Drug Management for Cardiac Sarcoidosis (J‐ ACNES ) trial was designed as a prospective, multicenter, randomized, open‐label, controlled clinical trial. The patients will be randomized to receive either standard corticosteroid therapy plus ABD therapy ( ABD group) or standard corticosteroid therapy (standard group). The primary endpoint is change in the total standardized uptake value at 6 months vs baseline using fluorine‐18 fluorodeoxyglucose positron emission tomography and computed tomography. Secondary endpoints include efficacy, prognosis, and safety. Results The results of this study are currently under investigation. Conclusion The J‐ ACNES trial will be the first prospective study assessing the clinical benefit and safety of ABD therapy, in addition to corticosteroid treatment, in patients with CS . Our findings may improve treatment of patients with CS , as additional ABD therapy reduces recurrence of inflammation and elucidates the mechanism of sarcoidosis.

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