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  Vol. 63 No. 11, November 2006 TABLE OF CONTENTS
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Natural History of Human T-Lymphotropic Virus 1–Associated Myelopathy

A 14-Year Follow-up Study

Stéphane Olindo, MD; Philippe Cabre, MD; Agnes Lézin, PhD; Harold Merle, MD; Martine Saint-Vil, MD; Aissatou Signate, MD; Mickael Bonnan, MD; Aurelie Chalon, PhD; Lionel Magnani, MD; Raymond Cesaire, MD, PhD; Didier Smadja, MD

Arch Neurol. 2006;63:1560-1566.

Background  The progression of neurological disability in human T-lymphotropic virus 1 (HTLV-1)–associated myelopathy/tropical spastic paraparesis (HAM/TSP) remains undefined.

Objectives  To determine the time course of disability scores and to identify predictors of outcome among patients with HAM/TSP.

Design  Clinical 14-year follow-up study.

Setting  University hospital.

Patients  One hundred twenty-three patients with HAM/TSP.

Main Outcome Measures  We determined time from onset to the following 4 Kurtzke Disability Status Scale (DSS) end points: scores of 6 (unilateral aid required), 6.5 (bilateral aid required), 8 (wheelchair confinement), and 10 (death related to the disease). Times to reach selected DSS scores were estimated using the Kaplan-Meier method. Univariate and multivariate analyses identified variables related to the rate of progression to DSS 8. The HTLV-1 proviral loads were also assessed.

Results  The disability of the cohort progressed throughout the follow-up period. The median times from onset to DSS 6, 6.5, and 8 were 6, 13, and 21 years, respectively. The median time from DSS 6 to DSS 8 was 8 years; DSS 10 was reached by one fourth of the patients within 20 years. Age at onset of 50 years or older and high HTLV-1 proviral load were associated with a shorter time to DSS 8 (P = .01 and P = .02, respectively). A shorter time to DSS 6 significantly adversely affected the time to progression from DSS 6 to DSS 8.

Conclusions  Human T-lymphotropic virus 1–associated myelopathy/tropical spastic paraparesis is a rapidly disabling disease. Monitoring for HTLV-1 proviral load is recommended in future therapeutic trials.


Author Affiliations: Departments of Neurology (Drs Olindo, Cabre, Saint-Vil, Signate, Bonnan, and Smadja), Viro-Immunology (Drs Lézin, Chalon, and Cesaire), Ophthalmology (Dr Merle), and Statistics (Dr Magnani), University Hospital of Fort de France, Fort de France, Martinique.


RELATED LETTERS

Other Important Aspects of Human T-Lymphotropic Virus 1–Associated Myelopathy
Marco A. Lima, Ana C. Leite, Marcus T. Silva, and Abelardo Q. Araújo
Arch Neurol. 2007;64(7):1059.
EXTRACT | FULL TEXT  

Other Important Aspects of Human T-Lymphotropic Virus 1–Associated Myelopathy—Reply
Stéphane Olindo, Agnès Lézin, and Didier Smadja
Arch Neurol. 2007;64(7):1059-1060.
EXTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Other Important Aspects of Human T-Lymphotropic Virus 1-Associated Myelopathy
Lima et al.
Arch Neurol 2007;64:1059-1059.
FULL TEXT  

Other Important Aspects of Human T-Lymphotropic Virus 1-Associated Myelopathy--Reply
Olindo et al.
Arch Neurol 2007;64:1059-1060.
FULL TEXT  





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