Transition to secondary progression in relapsing-onset multiple sclerosis: Definitions and risk factors

Author:

Iaffaldano Pietro1ORCID,Lucisano Giuseppe2,Patti Francesco3ORCID,Brescia Morra Vincenzo4,De Luca Giovanna5,Lugaresi Alessandra6,Zaffaroni Mauro7,Inglese Matilde8,Salemi Giuseppe9,Cocco Eleonora10ORCID,Conte Antonella11,Ferraro Diana12,Galgani Simonetta13,Bergamaschi Roberto14,Pozzilli Carlo15,Salvetti Marco16,Lus Giacomo17,Rovaris Marco18ORCID,Maniscalco Giorgia Teresa19ORCID,Logullo Francesco Ottavio20,Paolicelli Damiano1,Achille Mariaclara1,Marrazzo Giuseppina21,Lovato Valeria21,Comi Giancarlo22,Filippi Massimo22ORCID,Amato Maria Pia23,Trojano Maria1ORCID,

Affiliation:

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

2. Department of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari “Aldo Moro,” Bari, Italy/Center for Outcomes Research and Clinical Epidemiology, Pescara, Italy

3. Dipartimento di Scienze Mediche e Chirurgiche e Tecnologie Avanzate, GF Ingrassia, Sez. Neuroscienze, Centro Sclerosi Multipla, Università di Catania, Catania, Italy

4. Multiple Sclerosis Clinical Care and Research Center, Department of Neuroscience (NSRO), Federico II University, Naples, Italy

5. Centro Sclerosi Multipla, Clinica Neurologica, Policlinico SS Annunziata, Università G. D’Annunzio, Chieti, Italy

6. IRCCS Istituto delle Scienze Neurologiche di Bologna, Riabilitazione Sclerosi Multipla, Bologna, Italy/Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy

7. Multiple Sclerosis Center, S.Antonio Abate Hospital, Gallarate, Italy

8. Dipartimento Di Neuroscienze, Riabilitazione, Oftalmologia, Genetica E Scienze Materno—Infantili (DINOGMI), Genova, Italy/Ospedale Policlinico San Martino, IRCCS, Genova, Italy

9. Department of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, Palermo, Italy

10. Department Medical Science and Public health, University of Cagliari/ Centro Sclerosi Multipla, ATS Sardegna, Cagliari, Italy

11. Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy/IRCCS Istituto Neurologico Mediterraneo (INM) Neuromed, Pozzilli, Italy

12. Department of Neurosciences, Neurology Unit, University of Modena and Reggio Emilia, Nuovo Ospedale Civile S. Agostino/Estense, Modena, Italy

13. Centro Sclerosi Multipla—Azienda Ospedaliera S. Camillo Forlanini, Rome, Italy

14. IRCCS Mondino Foundation, Pavia, Italy

15. Multiple Sclerosis Center, S.Andrea Hospital, Dept. of Human Neuroscience, Sapienza University, Rome, Italy

16. IRCCS Istituto Neurologico Mediterraneo (INM) Neuromed, Pozzilli, Italy/CENTERS Centro Neurologico Terapie Sperimentali—Sapienza University, S.Andrea Hospital, Rome, Italy

17. Multiple Sclerosis Center, II Division of Neurology, Department of Clinical and Experimental Medicine, Second University of Naples, Caserta, Italy

18. Multiple Sclerosis Center, IRCCS Fondazione don Carlo Gnocchi ONLUS, Milan, Italy

19. Centro regionale SM Ospedale A. Cardarelli, Napoli, Italy

20. UOC Neurologia Macerata Area Vasta 3, Asur Marche, Macerata, Italy

21. Roche SpA, Monza, Italy

22. Department of Neurology, Vita-Salute San Raffaele University, San Raffaele Scientific Institute, Milan, Italy

23. Department of Neurofarba, University of Florence, Florence, Italy/IRCCS Fondazione Don Carlo Gnocchi, Florence, Italy

Abstract

Background: No uniform criteria for a sensitive identification of the transition from relapsing–remitting multiple sclerosis (MS) to secondary-progressive multiple sclerosis (SPMS) are available. Objective: To compare risk factors of SPMS using two definitions: one based on the neurologist judgment (ND) and an objective data-driven algorithm (DDA). Methods: Relapsing-onset MS patients ( n = 19,318) were extracted from the Italian MS Registry. Risk factors for SPMS and for reaching irreversible Expanded Disability Status Scale (EDSS) 6.0, after SP transition, were estimated using multivariable Cox regression models. Results: SPMS identified by the DDA ( n = 2343, 12.1%) were older, more disabled and with a faster progression to severe disability ( p < 0.0001), than those identified by the ND ( n = 3868, 20.0%). In both groups, the most consistent risk factors ( p < 0.05) for SPMS were a multifocal onset, an age at onset >40 years, higher baseline EDSS score and a higher number of relapses; the most consistent protective factor was the disease-modifying therapy (DMT) exposure. DMT exposure during SP did not impact the risk of reaching irreversible EDSS 6.0. Conclusion: A DDA definition of SPMS identifies more aggressive progressive patients. DMT exposure reduces the risk of SPMS conversion, but it does not prevent the disability accumulation after the SP transition.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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