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. 2023 Sep;30(9):2736-2744.
doi: 10.1111/ene.15910. Epub 2023 Jun 29.

Relapse-associated worsening in a real-life multiple sclerosis cohort: the role of age and pyramidal phenotype

Aurora Zanghì  1 , Simonetta Galgani  2 , Paolo Bellantonio  3 , Mauro Zaffaroni  4 , Giovanna Borriello  5 , Matilde Inglese  6 , Silvia Romano  7 , Antonella Conte  8 , Francesco Patti  9 , Maria Trojano  10 , Carlo Avolio  1 , Emanuele D'Amico  1 ; Italian MS Registry
Affiliations

Relapse-associated worsening in a real-life multiple sclerosis cohort: the role of age and pyramidal phenotype

Aurora Zanghì et al. Eur J Neurol. 2023 Sep.

Abstract

Background and purpose: The overall disability in patients with relapsing-remitting multiple sclerosis is likely to be partly rather than entirely attributed to relapse.

Materials and methods: The aim was to investigate the determinants of recovery from first relapse and relapse-associated worsening (RAW) in relapsing-remitting multiple sclerosis patients from the Italian MS Registry during a 5-year epoch from the beginning of first-line disease-modifying therapy. To determine recovery, the functional system (FS) score was used to calculate the difference between the score on the date of maximum improvement and the score before the onset of relapse. Incomplete recovery was defined as a combination of partial (1 point in one FS) and poor recovery (2 points in one FS or 1 point in two FSs or any other higher combination). RAW was indicated by a confirmed disability accumulation measured by the Expanded Disability Status Scale score confirmed 6 months after the first relapse.

Results: A total of 767 patients had at least one relapse within 5 years of therapy. Of these patients, 57.8% experienced incomplete recovery. Age (odds ratio [OR] 1.02, 95% confidence interval [CI] 1.01-1.04; p = 0.007) and pyramidal phenotype were associated with incomplete recovery (OR = 2.1, 95% CI 1.41-3.14; p < 0.001). RAW was recorded in 179 (23.3%) patients. Age (OR = 1.02, 95% CI 1.01-1.04; p = 0.029) and pyramidal phenotype (OR = 1.84, 95% CI 1.18-2.88; p = 0.007) were the strongest predictors in the multivariable model.

Conclusions: Age and pyramidal phenotype were the strongest determinants of RAW in early disease epochs.

Keywords: clinical neurology; multiple sclerosis.

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