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

Author:

Zanghì Aurora1ORCID,Galgani Simonetta2,Bellantonio Paolo3,Zaffaroni Mauro4,Borriello Giovanna5,Inglese Matilde6,Romano Silvia7,Conte Antonella8,Patti Francesco9,Trojano Maria10,Avolio Carlo1,D'Amico Emanuele1ORCID,

Affiliation:

1. Department of Medical and Surgical Sciences University of Foggia Foggia Italy

2. Centro Sclerosi Multipla Az. Osp. S. Camillo Forlanini Rome Italy

3. Unit of Neurology IRCCS Neuromed Pozzilli Italy

4. Multiple Sclerosis Center Gallarate Hospital, ASST della Valle Olona Gallarate Italy

5. Ospedale San Pietro fatebenefratelli Rome Italy

6. Centro Per Lo Studio E La Cura Della Sclerosi Multipla E Malattie Demielinizzanti Dipartimento Di Neuroscienze, Riabilitazione, Oftalmologia, Genetica E Scienze Materno−Infantili, Clinica Neurologica−Ospedale Policlinico San Martino (DiNOGMI) Genoa Italy

7. Neurology Unit, NESMOS Department S. Andrea Hospital, Sapienza University of Rome Rome Italy

8. Multiple Sclerosis Center Policlinico Umberto I, Sapienza, University of Rome Rome Italy

9. Department “G.F. Ingrassia” MS Center, University of Catania Catania Italy

10. Department of Basic Medical Sciences, Neuroscience and Sense Organs University of Bari “Aldo Moro” Bari Italy

Abstract

AbstractBackground and purposeThe overall disability in patients with relapsing–remitting multiple sclerosis is likely to be partly rather than entirely attributed to relapse.Materials and methodsThe 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.ResultsA 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.ConclusionsAge and pyramidal phenotype were the strongest determinants of RAW in early disease epochs.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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