TY - JOUR
T1 - Japanese antibacterial drug management for cardiac Sarcoidosis (J‐ACNES)
T2 - A multicenter, open‐label, randomized controlled study
AU - Ishibashi, Kohei
AU - Eishi, Yoshinobu
AU - Tahara, Nobuhiro
AU - Asakura, Masanori
AU - Sakamoto, Naka
AU - Nakamura, Kazufumi
AU - Takaya, Yoichi
AU - Nakamura, Tomohisa
AU - Yazaki, Yoshikazu
AU - Yamaguchi, Tetsuo
AU - Asakura, Koko
AU - Anzai, Toshihisa
AU - Noguchi, Teruo
AU - Yasuda, Satoshi
AU - Terasaki, Fumio
AU - Hamasaki, Toshimitsu
AU - Kusano, Kengo
N1 - Funding Information:
The J‐ACNES trial is supported by Daiichi Sankyo Company and Grant‐in‐Aid for Scientific Research (18k080920019).
Publisher Copyright:
© 2018 The Authors.
PY - 2018/10
Y1 - 2018/10
N2 - 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.
AB - 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.
KW - Antibacterial drug
KW - Cardiac sarcoidosis
KW - Corticosteroid therapy
KW - Propionibacterium acnes
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U2 - 10.1002/joa3.12084
DO - 10.1002/joa3.12084
M3 - Article
AN - SCOPUS:85052828856
SN - 1880-4276
VL - 34
SP - 520
EP - 526
JO - Journal of Arrhythmia
JF - Journal of Arrhythmia
IS - 5
ER -