https://doi.org/10.55788/64a7cf9e
Dr Chao Zhu (Monash University, Australia) and colleagues studied the risk factors associated with persistence or improvement after PIRA, as well as the effects of PIRA persistence on long-term outcomes in MS [1]. PIRA can be a sign of early SPMS, but PIRA events may regress over time. A cohort study was set up using data from 4,713 patients with relapsing-remitting MS, who were enrolled in the MSBase registry between April 1995 and January 2024. One of the inclusion criteria was a minimum of 1 PIRA event, defined as 6-month confirmed disability progression (CDP) without relapse. The primary outcome was time to 6-month confirmed improvement after PIRA.
After a median follow-up of 6.8 years, the primary endpoint was met by almost a third of the investigated patients (n=1,507; 32%). When matched with patients with persistent PIRA (n=3,206) in a multivariate analysis, improvement after PIRA was significantly associated with younger age (HR 0.98; 95% CI 0.98–0.99; P<0.0001), lower EDSS at baseline (HR 0.74; 95% CI 0.69–0.78; P<0.0001), and high-efficacy disease-modifying treatment use at baseline (HR 1.22; 95% CI 1.08–1.38; P<0.0015).
Investigated patients with persistent PIRA were at a substantially higher risk of reaching EDSS 6 and SPMS, compared with non-persistent PIRA: the HR was 5.19 (95% CI 4.05–6.67; P<0.0001) for reaching EDSS 6, and 3.51 (95% CI 2.42–5.08; P<0.0001) for reaching SPMS.
- Zhu C, et al. Risk factors associated with persistent progression independent of relapse activity (PIRA), and the association of persistent PIRA with disability progression in multiple sclerosis. Abstract O055, ECTRIMS 2024, 18–20 September, Copenhagen, Denmark.
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Table of Contents: ECTRIMS 2024
Featured articles
Diagnosis, Biomarkers, and Phenotypes
Revised McDonald criteria allow earlier and more precise MS diagnosis
Approaches to RIS and MS converge
AI versus clinicians: who diagnoses MS faster and better?
Blood markers predict MS progression
Gut microbiota modulate inflammation and cortical damage
Risk factors and importance of persistent PIRA
Vitamin D supplementation in progressive MS should be medically supervised
Treatment: Strategies
Encouraging real-world results of AHSCT to treat aggressive MS
CAR T-cell therapy in MS: in its infancy but highly anticipated
B cell-tailored dosing of ocrelizumab shows good results
First-line moderate-efficacy DMTs show similar efficacy
Treatment: Trials
Tolebrutinib slows disability worsening in relapsing MS
Frexalimab shows favourable safety and efficacy in OLE
Good safety of ozanimod over up to 8 years of treatment
Tolebrutinib slows disability in non-relapsing SPMS
High-dose simvastatin does not slow disability progression in SPMS
Comorbidity Risks and Pregnancy
High genetic burden for depression associated with MS disease activity
More comorbidity is associated with worse clinical outcomes in MS
Transfer of ocrelizumab into breastmilk is negligible
NMOSD/MOGAD
Ineffective response to EBV in MS not seen in similar diseases
Comparative effectiveness and safety of DMTs in NMOSD
Age, time, and treatment determine relapse risk in MOGAD
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