Key result
Higher myocardial T2 values are linked to worsening diastolic function in idiopathic inflammatory myopathy.
Why the study?
To investigate associations between left ventricular diastolic dysfunction and myocardial tissue characteristics in idiopathic inflammatory myopathy using multi-parameter CMR.
Are myocardial tissue characteristics assessed by multi-parameter CMR associated with LV diastolic dysfunction in patients with idiopathic inflammatory myopathy?
Cross-Sectional (n=119)
Are myocardial tissue characteristics assessed by multi-parameter CMR associated with LV diastolic dysfunction in patients with idiopathic inflammatory myopathy?
Effect estimate: β = -0.245
p-value: p=0.042
In patients with idiopathic inflammatory myopathy, LV diastolic dysfunction is closely linked to myocardial tissue characteristics on CMR, particularly in those with concurrent active myocarditis and necrosis/fibrosis.
May link active myocardial inflammation to diastolic dysfunction in IIM; leaves open whether CMR phenotyping informs prognosis or therapy.
OBJECTIVES: This study aimed to investigate associations between left ventricular (LV) diastolic dysfunction and myocardial tissue characteristics in idiopathic inflammatory myopathy (IIM) using multi-parameter cardiac magnetic resonance. METHODS: A total of 82 IIM patients [56 late gadolinium enhancement (LGE)-negative, 26 LGE-positive] and 37 controls were included. Patients were stratified: group 1 (active myocardial inflammation + necrosis/fibrosis: elevated T2, native T1 values + LGE-positive, n = 24), group 2 (active myocardial inflammation only: elevated T2, native T1 values, LGE-negative, n = 35) and group 3 (chronic myocardial fibrosis: normal T2, elevated native T1 value/LGE-positive, n = 12). LV volume-time indices, LV/left atrial (LA) strain, and myocardial tissue parameters [T1/T2 mapping values, extracellular volume (ECV)] were analysed via linear regression. RESULTS: IIM patients showed prolonged time-to-peak filling rate and reduced peak filling rate (PFR) vs controls (P < 0.05), with group 1 having the lowest PFR. Group 1 exhibited significantly impaired LV/LA strain, elevated T2/native T1 value and higher ECV compared with Groups 2 and 3 (all P < 0.05). Multivariable analysis revealed inverse correlations between PFR and T2 value (β = -0.245, P = 0.042), while LV global circumferential and longitudinal peak strains positively correlated with T2 value (β = 0.288 and 0.276, respectively; P < 0.05). Group 1 demonstrated the most severe diastolic dysfunction (P < 0.05 vs other groups). CONCLUSION: LV diastolic dysfunction in IIM is closely linked to myocardial tissue characteristics, particularly in patients with concurrent active myocarditis and necrosis/fibrosis. Both active myocarditis and chronic myocardial fibrosis contribute to diastolic impairment.
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Wang et al. (2025) conducted a cross-sectional in Idiopathic inflammatory myopathy (n=119). Myocardial tissue characteristics (active myocardial inflammation and fibrosis) vs. Controls and patients without active inflammation/fibrosis was evaluated on Peak filling rate (PFR) correlation with T2 value (β = -0.245, p=0.042). In patients with idiopathic inflammatory myopathy, myocardial T2 value was inversely correlated with peak filling rate (β = -0.245, P = 0.042), linking active myocarditis to diastolic impairment.
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