Key result
Myocardial 18 FDG-avidity was associated with an increased unadjusted risk of a heart failure composite outcome (HR 1.69; 95% CI 1.04-2.75), but this was not significant after multivariable adjustment.
Why the study?
The prognostic implications of myocardial 18 FDG-avidity in patients with and without genetic cardiomyopathy, and the effects of immunosuppression in the latter, remain uncertain.
Does immunosuppression improve heart failure or arrhythmia outcomes in 18FDG-avid cardiomyopathy patients without clear cardiac sarcoidosis, and does 18FDG-avidity predict adverse outcomes?
Cohort (n=372)
Yes
Does immunosuppression improve heart failure or arrhythmia outcomes in 18FDG-avid cardiomyopathy patients without clear cardiac sarcoidosis, and does 18FDG-avidity predict adverse outcomes?
Myocardial 18FDG-avidity without clear sarcoidosis is not an independent predictor of adverse outcomes in genetic or idiopathic cardiomyopathies, and immunosuppression does not appear to modify the disease course in these patients.
18FDG-avidity should not yet guide immunosuppression in non-sarcoid cardiomyopathies; leaves open its independent prognostic value after multivariable adjustment.
BACKGROUND: Myocardial 18 fluorodeoxyglucose ( 18 FDG)-avidity is frequently seen in patients with genetic cardiomyopathy, as well as a growing “idiopathic 18 FDG-avidity” group of genotype-negative patients who do not clearly have cardiac sarcoidosis. The prognostic implications of 18 FDG-avidity in patients with and without genetic cardiomyopathy, and the effects of immunosuppression in the latter, remain uncertain. METHODS: This multicenter, retrospective study included all patients who were referred for both 18 FDG-PET and cardiomyopathy genetic testing. Patients with acute myocarditis, biopsy-proven sarcoidosis, or extracardiac 18 FDG-avidity were excluded. We investigated heart failure (HF) composite (left ventricular assist device, heart transplant, HF hospitalization, or death) and arrhythmia composite (sustained ventricular arrhythmias [ventricular tachycardia/VF], atrioventricular block, or death) outcomes using survival analysis, including Cox proportional hazards modeling and inverse probability of treatment weighting. RESULTS: Among 372 patients, 142 (38%) were 18 FDG-avid. The prevalence of genetic cardiomyopathy among 18 FDG-avid patients (12%) was similar to that of 18 FDG-negative patients (18%; P =0.11). Unadjusted, 18 FDG-avidity was associated with an increased risk of HF composite (hazard ratio, 1.69 [95% CI, 1.04–2.75]; P =0.034) and arrhythmia composite (hazard ratio, 1.63 [95% CI, 1.1–2.4]; P =0.014) outcomes compared with 18 FDG-negative patients. However, these associations were not statistically significant after multivariable adjustment, nor were there significant differences in 18 FDG-associated risks in patients with genetic cardiomyopathy versus genotype-negative patients. After inverse probability of treatment weighting, immunosuppression of 18 FDG-avid patients (n=49) was not associated with a reduction in HF or arrhythmia composite outcomes compared with those who were not immunosuppressed (n=93). CONCLUSIONS: Myocardial-only 18 FDG-avidity is not significantly associated with HF or arrhythmia risk in patients who do not clearly have cardiac sarcoidosis (including those with genetic cardiomyopathy). Immunosuppression therapy does not seem to modify the disease course, suggesting that not all myocardial 18 FDG uptake reflects clinically significant inflammation.
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Tabaghi et al. (2026) conducted a cohort in Idiopathic and Genetic Cardiomyopathies (n=372). Myocardial 18 FDG-avidity vs. 18 FDG-negative was evaluated on Heart failure (HF) composite (left ventricular assist device, heart transplant, HF hospitalization, or death) (HR 1.69, 95% CI 1.04-2.75, p=0.034). Myocardial 18 FDG-avidity was associated with an increased unadjusted risk of a heart failure composite outcome (HR 1.69; 95% CI 1.04-2.75), but this was not significant after multivariable adjustment.
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