Highlights: What are the main findings? A lower baroreflex sensitivity in the MG group was associated with worse clinical disease outcomes and reduced pulmonary function. Age, forced vital capacity, and total lung capacity could predict the heart rate response during deep breathing. What is the implication of the main finding? There is a significant relationship between reduced pulmonary ventilation function or respiratory mechanics and cardiovascular autonomic parameters in MG patients. Future studies should prioritize investigating how respiratory and autonomic function testing interact, alongside exploring the impact of pulmonary rehabilitation. This study aimed to investigate the relationship between pulmonary function and cardiac autonomic function parameters in clinically stable myasthenia gravis (MG) patients. A total of 22 MG patients and 22 healthy controls (HCs) were evaluated. Pulmonary function test parameters, heart rate variability (HRV), baroreflex sensitivity (BRS), and cardiovascular autonomic function test parameters (the Valsalva ratio, expiration/inspiration (E/I) ratio) were assessed. Compared with the HCs, the patients demonstrated a similar diffusion capacity for carbon monoxide (DLCO); a lower forced vital capacity (FVC%pred); a lower forced expiratory volume in 1 s (FEV1%pred); lower BRS and HRV, including high-frequency and total power spectral density; and a higher percentage of abnormal cardiovagal function test results (p < 0.05). A lower BRS in the patient group was associated with worse clinical disease outcomes and reduced pulmonary function (DLCO%pred, R = 0.59; TLC%pred, R = 0.48). Age, forced vital capacity, and total lung capacity predicted the E/I ratio (R2 values ranging from 0.48 to 0.49). Our study demonstrated a significant relationship between a reduced pulmonary ventilation function and respiratory mechanics with cardiovascular autonomic parameters, including the E/I ratio, BRS, and HRV measures at rest, as shown in the MG group. Future studies should focus on the interplay between respiratory and autonomic function testing, as well as pulmonary rehabilitation, to mitigate cardiovascular risk in these patients.
CITATION STYLE
Zawadka-Kunikowska, M., Rzepiński, Ł., Cieślicka, M., Fanslau, J., Klawe, J. J., & Tafil-Klawe, M. (2023). Correlation between Cardiovascular Autonomic and Pulmonary Ventilation Functions in Myasthenia Gravis Patients. Advances in Respiratory Medicine, 91(6), 546–559. https://doi.org/10.3390/arm91060040
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