A Prospective Study on Autonomic Functions in Idiopathic Inflammatory Myopathies: The AFIIM Study
MM Samim, Ganagarajan Inbaraj, Talakad N Sathyaprabha, Ashita Barthur, Seena Vengalil, Saraswati Nashi, Deepak Menon, Nandan Chandregowda, Dipti Baskar, Vidya Nittur, Priya Treesa Thomas, Atchayaram NaliniAbstract
Background and Objectives:
Dysautonomia in idiopathic inflammatory myopathies (IIM) is an underrecognized and poorly characterized manifestation, despite its potential implications for disease prognosis and clinical management. In this study, we assessed autonomic dysfunction in patients with IIM and investigated its correlation with cardiac imaging biomarkers based on cardiac magnetic resonance imaging (CMRI).
Methods:
The study recruited clinically suspected IIM patients aged 10–60 years and age- and sex-matched healthy controls. Evaluations included myositis disease activity assessment tool (MDAAT), autonomic function testing (AFT), tilt table test (TTT), and CMRI with multiparametric mapping.
Results:
Among 31 diagnosed cases of IIM, 28 patients underwent AFT and TTT. Of these, 12 had dermatomyositis, 7 had overlap myositis, 7 had immune-mediated necrotizing myopathy, and 2 had anti-synthetase syndrome. The mean age of onset was 33±12.92 years, with an average illness duration of 16.63±19.43 months, and a female predominance (F:M = 2.1:1). The patients exhibited a lower median total autonomic power (563.2, interquartile range [IQR] = 209.6–1964.6 vs 1606.5, IQR = 1048.6–2676;
Conclusions:
In this first-of-its-kind study integrating AFT and TTT with CMR to evaluate IIM, patients demonstrated significant autonomic dysfunction, with AFT parameters showing a correlation with CMR findings, thus indicating their potential as a simple predictor of cardiac involvement.