Benign prognosis in idiopathic hyper-CK-emia
Publication date
2000-04
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Abstract
We report on the long-term follow-up in 31 patients with idiopathic hyper-CK-emia. At referral, all patients underwent a neurological interview and examination. Ancillary investigations included an open muscle biopsy and electromyography (EMG) in almost all, and other ancillary tests in some patients. After a follow-up period of 7.2 (mean; range 4-18) years, 74% of the patients had a final evaluation. The most common complaints at referral were fatigue and myalgia. EMG and muscle biopsy demonstrated minor, non- diagnostic abnormalities in 30 and 71% of patients, respectively. At follow- up, the pattern and the number of complaints had not changed substantially. One patient developed a sensory polyneuropathy. Neurological abnormalities were absent in all other patients. In conclusion, long-term follow-up of patients with idiopathic hyper-CK-emia does not reveal clinical deterioration. It seems justifiable to refrain from routine long-term follow- up in these patients. (C) 2000 John Wiley and Sons, Inc.
Keywords
Creatine kinase, Exercise, Follow-up, Idiopathic hyper-CK- emia, Myopathy, Physiology, Clinical Neurology, Cellular and Molecular Neuroscience, Physiology (medical)
Citation
Reijneveld, J C, Notermans, N C, Linssen, W H J P & Wokke, J H J 2000, 'Benign prognosis in idiopathic hyper-CK-emia', Muscle and Nerve, vol. 23, no. 4, pp. 575-579. https://doi.org/10.1002/(SICI)1097-4598(200004)23:4<575::AID-MUS17>3.0.CO;2-5