Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 MSA: Progression, Hypoxia Response 1. Progression and prognosis in multiple system atrophy: An analysis of 230 Japanese patients H Watanabe, Y Saito, S Terao, T Ando, T Kachi, E Mukai, I Aiba, Y Abe, A Tamakoshi, M Doyu, M Hirayam, G Sobue Brain 2002;125:1070-1083 The interval from symptom onset to combined motor and autonomic dysfunction is predictive of functional deterioration and survival in MSA, according to this study. Consensus criteria were used to identify 230 patients with MSA, of whom 131 were male. Mean age of onset was 55.4 years. Cerebellar symptoms (MSA-C) predominated in 155 patients, while parkinsonian symptoms (MSA-P) were most prominent in 75. The median time from symptom onset to multi-system involvement was 2 years. Median survival time was 9.0 years (range 2-17 years). Time to assisted walking, wheelchair requirement, bed confinement, and death were proportional to time between symptom onset and multisystem involvement. Patients in whom multisystem involvement occurred within one year of symptom onset proceeded to each of these milestones 2-3 times as fast as those for whom multisystem involvement occurred after 3 years or more. 2. Impaired chemosensitivity to hypoxia is a marker of multiple system atrophy T Suda, H Onodera, S Okabe, Y Kikuchi, Y Itoyama Ann Neurol 2002;52:367-371 Impaired ventilatory response to hypoxia can help predict whether patients with idiopathic late-onset cerebellar ataxia will progress to MSA-C, according to this study. Hypoxia ventilatory response (change in respiratory rate versus change in blood O2) was measured in 9 controls, 6 patients with MSA, 13 with ILOCA, 31 with Parkinson's disease, and 7 with SCA-3. HVR was 0.51 in controls, 0.09 in MSA patients, 0.47 in ILOCA patients (range 0-1.4), 0.16 in PD patients, and 0.59 in SCA-3 patients. Of 7 ILOCA patients whose HVR values were less than 0.3, 6 progressed to MSA-C within 3 years. No ILOCA patients with values above this did. Copyright 2002 WE MOVE Editor: (rrobinson@...) - Your E-MOVE news subscription is provided free of charge, courtesy of WE MOVE. PRIVATE DONATIONS ARE NEEDED TO SUPPORT WE MOVE's VALUABLE, FREE SERVICES LIKE THIS ELECTRONIC NEWS SERVICE. Donate online at http://www.wemove.org, or send your tax-deductible contribution to WE MOVE, 204 West 84th Street New York, NY 10024. TEL 800-437-MOV2 or 212- 875-8312. Thank you so much! - This document may be freely redistributed by email only in its unedited form. We encourage you to share it with your colleagues. Visit http://www.wemove.org/emove for E-MOVE archives and information on subscribing to E-MOVE. To unsubscribe, visit http://www.wemove.org/emove/unsubscribe.asp. - WE MOVE 204 West 84th Street New York, NY 10024 TEL 800-437-MOV2 TEL FAX Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2002 Report Share Posted October 25, 2002 MSA: Progression, Hypoxia Response 1. Progression and prognosis in multiple system atrophy: An analysis of 230 Japanese patients H Watanabe, Y Saito, S Terao, T Ando, T Kachi, E Mukai, I Aiba, Y Abe, A Tamakoshi, M Doyu, M Hirayam, G Sobue Brain 2002;125:1070-1083 The interval from symptom onset to combined motor and autonomic dysfunction is predictive of functional deterioration and survival in MSA, according to this study. Consensus criteria were used to identify 230 patients with MSA, of whom 131 were male. Mean age of onset was 55.4 years. Cerebellar symptoms (MSA-C) predominated in 155 patients, while parkinsonian symptoms (MSA-P) were most prominent in 75. The median time from symptom onset to multi-system involvement was 2 years. Median survival time was 9.0 years (range 2-17 years). Time to assisted walking, wheelchair requirement, bed confinement, and death were proportional to time between symptom onset and multisystem involvement. Patients in whom multisystem involvement occurred within one year of symptom onset proceeded to each of these milestones 2-3 times as fast as those for whom multisystem involvement occurred after 3 years or more. 2. Impaired chemosensitivity to hypoxia is a marker of multiple system atrophy T Suda, H Onodera, S Okabe, Y Kikuchi, Y Itoyama Ann Neurol 2002;52:367-371 Impaired ventilatory response to hypoxia can help predict whether patients with idiopathic late-onset cerebellar ataxia will progress to MSA-C, according to this study. Hypoxia ventilatory response (change in respiratory rate versus change in blood O2) was measured in 9 controls, 6 patients with MSA, 13 with ILOCA, 31 with Parkinson's disease, and 7 with SCA-3. HVR was 0.51 in controls, 0.09 in MSA patients, 0.47 in ILOCA patients (range 0-1.4), 0.16 in PD patients, and 0.59 in SCA-3 patients. Of 7 ILOCA patients whose HVR values were less than 0.3, 6 progressed to MSA-C within 3 years. No ILOCA patients with values above this did. Copyright 2002 WE MOVE Editor: (rrobinson@...) - Your E-MOVE news subscription is provided free of charge, courtesy of WE MOVE. PRIVATE DONATIONS ARE NEEDED TO SUPPORT WE MOVE's VALUABLE, FREE SERVICES LIKE THIS ELECTRONIC NEWS SERVICE. Donate online at http://www.wemove.org, or send your tax-deductible contribution to WE MOVE, 204 West 84th Street New York, NY 10024. TEL 800-437-MOV2 or 212- 875-8312. Thank you so much! - This document may be freely redistributed by email only in its unedited form. We encourage you to share it with your colleagues. Visit http://www.wemove.org/emove for E-MOVE archives and information on subscribing to E-MOVE. To unsubscribe, visit http://www.wemove.org/emove/unsubscribe.asp. - WE MOVE 204 West 84th Street New York, NY 10024 TEL 800-437-MOV2 TEL FAX Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.