Posted by: Thixia | January 14, 2009

Pediatric Onset MS Patients have More Relapses

Relapses More Frequent in Patients Diagnosed With Paediatric-Onset MS




      CHICAGO — January 12, 2009 — Patients who develop multiple sclerosis (MS) before age 18 appear to experience more relapses of symptoms than those diagnosed with the disease as adults, according to a study published in the January issue of Archives of Neurology.




      Mark P. Gorman, MD, Brigham and Women’s Hospital and Massachusetts General Hospital, Boston, Massachusetts, and colleagues studied 110 patients diagnosed with relapsing-remitting MS in adulthood (average age at diagnosis, 34.4) and 21 with paediatric-onset MS (average age at diagnosis, 15.4).




      Study participants who developed their first symptoms in July 2001 or later, were monitored with semi-annual neurological examinations and were followed for 12 months or longer (an average of 3.67 years for paediatric-onset patients and 3.98 years for adult-onset).




      Patients who developed the disease in childhood had, on average, a higher yearly rate of relapses than those who were diagnosed as adults (1.13 vs 0.4 relapses per year). “These findings persisted in multivariate regression models when controlling for sex, race, and proportion of disease spent undergoing disease-modifying treatment and when age at onset was treated as a continuous variable,” the authors wrote.




      “In general, the disease course of MS has been divided into a relapsing-remitting phase, during which inflammatory mechanisms predominate, and a secondary progressive phase, during which neurodegenerative mechanisms predominate,” they continued.




      “Acute relapses are the clinical hallmark of the inflammatory phase of MS. The higher relapse rate in the paediatric-onset group in our study may therefore suggest that patients with paediatric-onset MS are coming to medical attention closer to the true biological onset of their disorder than patients with adult onset during a more inflammatory phase, as has been previously suggested.”


      If patients with paediatric-onset diseases do indeed have more relapses despite their disease progressing more slowly, “this discrepancy may suggest greater plasticity, less neurodegeneration and potentially more repair and remyelination in the younger nervous system. Further study of the biological basis for this discrepancy may yield insight into the apparent disconnect between relapses and long-term disability progression.”






      SOURCE: Archives of Neurology





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