Key result
P. acnes appears in ~63% of cardiac sarcoidosis granulomas but not in other cardiomyopathies.
Why the study?
Histopathologic diagnosis of cardiac sarcoidosis is limited, and detection of Propionibacterium acnes in myocardial tissues may aid diagnosis and differentiation from other cardiomyopathies.
Can immunohistochemical detection of P. acnes in myocardial tissues differentiate cardiac sarcoidosis from myocarditis and other cardiomyopathies?
Observational (n=80)
Yes
Can immunohistochemical detection of P. acnes in myocardial tissues differentiate cardiac sarcoidosis from myocarditis and other cardiomyopathies?
Immunohistochemical detection of P. acnes in myocardial biopsy samples may be a highly specific marker for differentiating cardiac sarcoidosis from myocarditis and other cardiomyopathies.
Answers are grounded in this paper and cite their sources.
May support IHC detection of P. acnes for differentiating cardiac sarcoidosis on biopsy; leaves open prospective validation before clinical use.
BACKGROUND: Although rare, cardiac sarcoidosis (CS) is potentially fatal. Early diagnosis and intervention are essential, but histopathologic diagnosis is limited. We aimed to detect Propionibacterium acnes, a commonly implicated etiologic agent of sarcoidosis, in myocardial tissues obtained from CS patients. METHODS AND RESULTS: We examined formalin-fixed paraffin-embedded myocardial tissues obtained by surgery or autopsy and endomyocardial biopsy from patients with CS (n = 26; CS-group), myocarditis (n = 15; M-group), or other cardiomyopathies (n = 39; CM-group) using immunohistochemistry (IHC) with a P. acnes-specific monoclonal antibody. We found granulomas in 16 (62%) CS-group samples. Massive (≥14 inflammatory cells) and minimal (<14 inflammatory cells) inflammatory foci, respectively, were detected in 16 (62%) and 11 (42%) of the CS-group samples, 10 (67%) and 10 (67%) of the M-group samples, and 1 (3%) and 18 (46%) of the CM-group samples. P. acnes-positive reactivity in granulomas, massive inflammatory foci, and minimal inflammatory foci were detected in 10 (63%), 10 (63%), and 8 (73%) of the CS-group samples, respectively, and in none of the M-group and CM-group samples. CONCLUSIONS: Frequent identification of P. acnes in sarcoid granulomas of originally aseptic myocardial tissues suggests that this indigenous bacterium causes granuloma in many CS patients. IHC detection of P. acnes in massive or minimal inflammatory foci of myocardial biopsy samples without granulomas may be useful for differentiating sarcoidosis from myocarditis or other cardiomyopathies.
No takes yet. Share an insight, caveat, or question.
Asakawa et al. (2017) conducted an observational in Cardiac sarcoidosis, myocarditis, and other cardiomyopathies (n=80). Propionibacterium acnes presence vs. Myocarditis or other cardiomyopathies was evaluated on P. acnes-positive reactivity in massive inflammatory foci (p=0.003). Propionibacterium acnes was frequently identified in granulomas (63%), massive inflammatory foci (63%), and minimal inflammatory foci (73%) of myocardial tissues from cardiac sarcoidosis patients, but not in myocarditis or other cardiomyopathies.
Synapse has enriched 10 related papers. Consider them for comparative context: