Autonomic impairment in amyotrophic lateral sclerosisBaltadzhieva, Rositsa; Gurevich, Tanya; Korczyn, Amos DCurrent Opinion in Neurology: October 2005 - Volume 18 - Issue 5 - p 487–493 doi: 10.1097/01.wco.0000183114.76056.0e Special commentary Abstract Author Information Purpose of review Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by progressive loss of motor neurones, but it is increasingly recognized to be a more disseminated disease. The autonomic nervous system may also be involved. Here we review the literature with specific emphasis on autonomic functions in ALS. Recent studies Ample evidence exists for subclinical dysfunction of cardiovascular, sudomotor, gastrointestinal, salivary and lacrimal regulation, even in early ALS cases. Autonomic disturbances may lead to circulatory collapse or sudden death in respirator dependent patients. Several studies suggest the existence of sympathetic hyperactivity in ALS. We discuss some possible pathophysiological mechanisms of the subtle abnormalities and some clinical and treatment implications. Summary The wide range of autonomic involvement, together with results suggesting cognitive and extrapyramidal dysfunction, supports the view that ALS is a multisystem degenerative disease. Neurology Department, Tel-Aviv Medical Center and the Sieratzki Chair of Neurology, Tel-Aviv University, Ramat-Aviv, Israel Correspondence to Professor Amos D. Korczyn, Sieratzki Chair of Neurology, Tel-Aviv University Medical School, Ramat-Aviv 69978, Israel Tel: +972 3 6974229; fax: +972 3 6409113; e-mail: firstname.lastname@example.org © 2005 Lippincott Williams & Wilkins, Inc.