Disability trajectories by progression independent of relapse activity status differ in pediatric, adult and late-onset multiple sclerosis

被引:1
作者
Simone, Marta [1 ]
Lucisano, Giuseppe [2 ,3 ]
Guerra, Tommaso [3 ]
Paolicelli, Damiano [3 ]
Rocca, Maria A. [4 ]
Morra, Vincenzo Brescia [5 ]
Patti, Francesco [6 ]
Annovazzi, Pietro [7 ]
Gasperini, Claudio [8 ]
De Luca, Giovanna [9 ]
Ferraro, Diana [10 ]
Margari, Lucia [1 ]
Granella, Franco [11 ]
Pozzilli, Carlo [12 ]
Romano, Silvia [13 ]
Perini, Paola [14 ]
Bergamaschi, Roberto [15 ]
Coniglio, Maria Gabriella [16 ]
Lus, Giacomo [17 ]
Vianello, Marika [18 ]
Lugaresi, Alessandra [19 ,20 ]
Portaccio, Emilio [21 ]
Filippi, Massimo [4 ]
Amato, Maria Pia [21 ,22 ]
Iaffaldano, Pietro [3 ]
机构
[1] Univ Bari Aldo Moro, Dept Precis & Regenerat Med, Child Neuropsychiat Unit, Jon Area, Bari, Italy
[2] CORESEARCH, Pescara, Italy
[3] Univ Aldo Moro Bari, Dept Translat Biomed & Neurosci DiBraiN, Piazza Giulio Cesare 11, I-70124 Bari, Italy
[4] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Dipartimento Neurol Neurofisiol & Neuroriabilitaz, Milan, Italy
[5] Univ Naples Federico II, Multiple Sclerosis Clin Care & Res Ctr, Dept Neurosci NSRO, Naples, Italy
[6] Univ Catania, Ctr Sclerosi Multipla, Sez Neurosci,GF Ingrassia, Dipartimento Sci Med & Chirurg & Tecnol Avanzate, Catania, Italy
[7] Gallarate Hosp, ASST Valle Olona, Multiple Sclerosis Ctr, Neuroimmunol Unit, Gallarate, Italy
[8] S Camillo Forlanini Hosp, Dept Neurosci, Rome, Italy
[9] Policlin SS Annunziata, Ctr Sclerosi Multipla, Clin Neurol, Chieti, Italy
[10] Azienda Osped Univ Modena, OCB, UO Neurol, Milan, Italy
[11] Univ Parma, Dept Med & Surg, Unit Neurosci, Parma, Italy
[12] S Andrea Hosp, Multiple Sclerosis Ctr, Dept Human Neurosci, Rome, Italy
[13] Sapienza Univ Rome, Ctr Expt Neurol Therapies CENTERS, Dept Neurosci Mental Hlth & Sensory Organs, Rome, Italy
[14] Univ Hosp Padova, Multiple Sclerosis Ctr Veneto Reg CeSMuV, Dept Neurosci, Padua, Italy
[15] IRCCS Mondino Fdn, Pavia, Italy
[16] Hosp ASM Madonna delle Grazie, Ctr Multiple Sclerosis, I-75100 Matera, Italy
[17] Univ Naples 2, Multiple Sclerosis Ctr, Dept Clin & Expt Med, Div Neurol 2, Naples, Italy
[18] Ca Foncello Hosp, Unit Neurol, Treviso, Italy
[19] IRCCS Ist Sci Neurolog Bologna, Bologna, Italy
[20] Univ Bologna, Dipartimento Sci Biomed & Neuromotorie, Bologna, Italy
[21] Univ Florence, Dept NEUROFARBA, Florence, Italy
[22] IRCCS Fdn Don Carlo Gnocchi, Florence, Italy
关键词
PIRA; Disability trajectories; POMS; AOMS; LOMS; AGE;
D O I
10.1007/s00415-024-12638-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background To compare Expanded Disability Status Scale (EDSS) trajectories over time between Multiple Sclerosis (MS) groups with pediatric (POMS), adult (AOMS) and late (LOMS) onset, and between patients with and without progression independent of relapse activity (PIRA). Methods Patients with a first visit within 1 year from onset, >= 5-year follow-up and >= 1 visit every 6 months were selected from the Italian MS Register. Adjusted disability trajectories were assessed by longitudinal models for repeated measures. Comparisons between groups and between patients with and without PIRA in subgroups were performed by evaluating the yearly differences of mean EDSS score changes versus baseline (delta-EDSS). A first CDA event was defined as a 6-months confirmed disability increase from study baseline, measured by EDSS (increase >= 1.5 points with baseline EDSS = 0; >= 1.0 with baseline EDSS score <= 5.0 and >= 0.5 point with baseline EDSS > 5.5).PIRA was defined as a CDA event occurring more than 90 days after and more than 30 days before the onset of a relapse. Results 3777 MS patients (268 POMS, 3282 AOMS, 227 LOMS) were included. The slope of disability trajectories significantly diverged in AOMS vs POMS starting from the second year of follow-up (Year 2: delta2-EDSS 0.18 (0.05; 0.31), p = 0.0054) and then mean delta2-EDSS gradually increased up to 0.23 (0.07; 0.39, p = 0.004) at year 5. Patients with PIRA had significant (p < 0.0001) steeper increase in EDSS scores than those without PIRA in all groups, although in POMS, the disability trajectories began to diverge later and at a lesser extent with delta-EDSS score of 0.48 vs 0.83 in AOMS and 1.57 in LOMS, at 3 years after the first PIRA. Conclusions Age is relevant in determining disability progression in MS. POMS shows a less steep increase in EDSS scores over time than older patients. The effect of PIRA in accelerating EDSS progression is less pronounced in POMS than in AOMS and LOMS.
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收藏
页码:6782 / 6790
页数:9
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