Why the study?
Patients with SLE typically develop myocardial fibrosis, but no studies had investigated the clinical significance of the presence, location, and degree of fibrosis.
Does the presence, location, and degree of late gadolinium enhancement predict major adverse cardiac events and myocardial dysfunction in patients with systemic lupus erythematosus?
Does the presence, location, and degree of late gadolinium enhancement predict major adverse cardiac events and myocardial dysfunction in patients with systemic lupus erythematosus?
The presence, location, and severity of late gadolinium enhancement on cardiac MRI independently predict major adverse cardiac events and correlate with myocardial dysfunction in patients with systemic lupus erythematosus.
May support CMR fibrosis assessment in SLE for risk stratification; leaves open prognostic value of location and degree.
Patients with systemic lupus erythematosus (SLE) typically develop myocardial fibrosis. No studies have investigated the clinical significance of the presence, location, and degree of fibrosis in SLE patients. Seventy-four SLE patients were included. Thirty-seven non-autoimmune disease patients and thirty-seven healthy individuals were included as controls. Myocardial fibrosis was evaluated at cardiac magnetic resonance via a qualitative and quantitative assessment of late gadolinium enhancement (LGE). Myocardial function was measured via speckle-tracking echocardiography. All patients were followed up for the occurrence of major adverse cardiac events (MACE). The presence, locations, and degrees of LGE disturbed regional and global myocardial function. The presence of LGE, left ventricular free-wall LGE (LVFW LGE), and severe LGE were all independent predictors of MACE in SLE patients [LGE presence HR: 3.746 (1.434–9.79), p = 0.007; LVFW LGE HR: 2.395 (1.023–5.606), p = 0.044; severe LGE HR: 3.739 (1.241–11.266), p = 0.019]. LGE combined with SLE-related organ damage identified patients at high risk of MACE (p < 0.001). In conclusion, the presence, degree, and location of LGE were associated with myocardial dysfunction. The presence, location, and degree of LGE had the potential to independently predict poor prognosis and improve risk stratification in SLE patients.
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Feng et al. (2023) studied this question.
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