The effect of interferon (IFN) beta-1a (44 and 22 mg subcutaneously [sc] three times weekly [tiw]) on cognition in mildly disabled patients with relapsing–remitting multiple sclerosis (McDonald criteria; Expanded Disability Status Scale 4.0) was assessed by validated neuropsychological testing at baseline and at regular intervals for up to 2 years in this ongoing open-label, 3-year study. Year-2 data were available for 356 patients (22 mg, n¼175; 44 mg, n¼181). The proportion of patients with impaired cognitive function was stable during the study: 21.4% at baseline and 21.6% at 2 years. At 2 years, the proportion of patients with 3 impaired cognitive tests was significantly lower in the 44 mg treatment group (17.0%) compared with the 22 mg group (26.5%; p¼0.034), although there was already a trend towards a higher proportion of patients with cognitive impairment in the 22 mg group at baseline. Factors associated with impairment in three cognitive tests after 2 years were age (odds ratio [OR]: 1.05; 95% confidence interval [CI]: 1.00–1.09), verbal intelligence quotient (OR: 0.95; 95% CI: 0.92–0.98), and having three impaired cognitive tests at baseline (OR: 11.60; 95% CI: 5.94–22.64). These interim results show that IFN beta-1a sc tiw may have beneficial effects on cognitive function as early as 2 years after treatment initiation, but the final 3-year data of the study are required to confirm these results.

Subcutaneous interferon beta-1a has a positive effect on cognitive performance in mildly disabled patients with relapsing- remitting multiple sclerosis: 2-year results from the COGIMUS study

LUGARESI, Alessandra
2009-01-01

Abstract

The effect of interferon (IFN) beta-1a (44 and 22 mg subcutaneously [sc] three times weekly [tiw]) on cognition in mildly disabled patients with relapsing–remitting multiple sclerosis (McDonald criteria; Expanded Disability Status Scale 4.0) was assessed by validated neuropsychological testing at baseline and at regular intervals for up to 2 years in this ongoing open-label, 3-year study. Year-2 data were available for 356 patients (22 mg, n¼175; 44 mg, n¼181). The proportion of patients with impaired cognitive function was stable during the study: 21.4% at baseline and 21.6% at 2 years. At 2 years, the proportion of patients with 3 impaired cognitive tests was significantly lower in the 44 mg treatment group (17.0%) compared with the 22 mg group (26.5%; p¼0.034), although there was already a trend towards a higher proportion of patients with cognitive impairment in the 22 mg group at baseline. Factors associated with impairment in three cognitive tests after 2 years were age (odds ratio [OR]: 1.05; 95% confidence interval [CI]: 1.00–1.09), verbal intelligence quotient (OR: 0.95; 95% CI: 0.92–0.98), and having three impaired cognitive tests at baseline (OR: 11.60; 95% CI: 5.94–22.64). These interim results show that IFN beta-1a sc tiw may have beneficial effects on cognitive function as early as 2 years after treatment initiation, but the final 3-year data of the study are required to confirm these results.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/157512
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 12
  • ???jsp.display-item.citation.isi??? ND
social impact