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Cognitive and patient-reported outcomes in adults with pediatric-onset multiple sclerosis.
Baruch, Natalie F; O'Donnell, Ellen H; Glanz, Bonnie I; Benedict, Ralph H B; Musallam, Alexander J; Healy, Brian C; Rintell, David; Chitnis, Tanuja.
Afiliación
  • Baruch NF; Partners Multiple Sclerosis Center, Brigham and Women's Hospital, USA.
  • O'Donnell EH; Department of Psychiatry, Massachusetts General Hospital, USA.
  • Glanz BI; Partners Multiple Sclerosis Center, Brigham and Women's Hospital, USA.
  • Benedict RH; Department of Neurology, University at Buffalo, State University of New York, USA.
  • Musallam AJ; Partners Multiple Sclerosis Center, Brigham and Women's Hospital, USA.
  • Healy BC; Partners Multiple Sclerosis Center, Brigham and Women's Hospital, USA/ Biostatistics Center, Massachusetts General Hospital, USA.
  • Rintell D; Partners Multiple Sclerosis Center, Brigham and Women's Hospital, USA.
  • Chitnis T; Partners Multiple Sclerosis Center, Brigham and Women's Hospital, USA tchitnis@partners.org.
Mult Scler ; 22(3): 354-61, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26041802
ABSTRACT

BACKGROUND:

Little is known about long-term cognitive and patient-reported outcomes of pediatric-onset multiple sclerosis (POMS).

OBJECTIVE:

The objective of this paper is to compare cognitive and patient-reported outcomes in adults with POMS vs. adult-onset MS (AOMS).

METHODS:

We compared standardized patient-reported measures MSQOL54, MFIS, CES-D and SDMT in adult patients with MS onset prior to and after age 18, using data gathered in the Comprehensive Longitudinal Investigations in MS at Brigham and Women's Hospital (CLIMB) study.

RESULTS:

Fifty-one POMS and 550 AOMS patients were compared. SDMT scores were significantly lower in POMS after adjusting for age (-7.57 (-11.72, -3.43; p < 0.001), but not after adjusting for disease duration. Estimated group difference demonstrated lower normative z scores in POMS vs. AOMS in unadjusted analysis (-0.74 (95% CI -1.18, -0.30; p = 0.0009) and after adjusting for disease duration (-0.60; 95%CI -1.05, -0.15; p = 0.0097). Findings were unchanged in a subset of POMS diagnosed prior to age 18. In unadjusted and adjusted analyses, no significant differences were observed in health-related quality-of-life, fatigue, depression or social support between POMS and AOMS.

CONCLUSIONS:

Younger age of onset was associated with more impairment in information-processing speed in adults with POMS compared to AOMS, and remained significant when controlling for disease duration in age-normed analysis. The two groups were similar in terms of patient-reported outcomes, suggesting similar qualitative experiences of MS.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cognición / Esclerosis Múltiple Tipo de estudio: Qualitative_research Límite: Adult / Child / Female / Humans / Male Idioma: En Revista: Mult Scler Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cognición / Esclerosis Múltiple Tipo de estudio: Qualitative_research Límite: Adult / Child / Female / Humans / Male Idioma: En Revista: Mult Scler Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos