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Left ventricular long-axis function in myasthenia gravis
Authors:Jone Furlund Owe  Einar Skulstad Davidsen  Geir Egil Eide  Eva Gerdts  Nils Erik Gilhus
Affiliation:(1) Dept. of Neurology, Haukeland University Hospital, 5021 Bergen, Norway;(2) Dept. of Clinical Medicine Section for Neurology, University of Bergen, Bergen, Norway;(3) Dept. of Heart Disease, Haukeland University Hospital, Bergen, Norway;(4) Centre for Clinical Research, Haukeland University Hospital, Bergen, Norway;(5) Dept. of Public Health and Primary Health Care, University of Bergen, Bergen, Norway;(6) Institute of Medicine, University of Bergen, Bergen, Norway
Abstract:Abstract   Myasthenia gravis (MG) primarily affects skeletal muscles, but influence on cardiac function has been suggested. The aim of this study was to assess left ventricular long-axis function in MG patients compared to healthy controls, and to examine whether any MG-related heart involvement was influenced by the acetylcholine-esterase inhibitor pyridostigmine. We found that early diastolic atrioventricular-plane velocity and tissue Doppler peak systolic strain was lower in MG patients than in controls before pyridostigmine. The differences disappeared following administration of pyridostigmine. Also, tissue velocities at systole and early diastole tended to be lower in patients before pyridostigmine. In multivariate analyses adjusting for between-group differences in blood pressure, MG was no longer associated with lower longaxis function. Conventional echocardiographic measures of left ventricular diastolic and systolic function did not differ between groups. In conclusion, this study, using modern tissue Doppler imaging as well as conventional echocardiography, could not demonstrate definite MG-related cardiac involvement in a group of MG patients without known cardiac disease, but indicates that pyridostigmine-responsive MG-related alterations in cardiac muscle function exist in MG patients.
Keywords:  KeywordHeading"  > myasthenia gravis  heart function  tissue Doppler imaging  autoimmunity
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