Shifting paradigms in multiple sclerosis: from disease-specific, through population-specific toward patient-specific

被引:7
作者
Golan, Daniel [1 ,2 ,3 ]
Staun-Ram, Elsebeth [3 ]
Miller, Ariel [1 ,2 ,3 ]
机构
[1] Lady Davis Carmel Med Ctr, Div Neuroimmunol, Haifa, Israel
[2] Lady Davis Carmel Med Ctr, Multiple Sclerosis Ctr, Haifa, Israel
[3] Technion Israel Inst Technol, Ruth & Bruce Rappaport Fac Med, Haifa, Israel
关键词
biomarkers; multiple sclerosis; digital sensor; personalized medicine; population epigenetics; quality of life; INTERFERON-BETA THERAPY; CEREBROSPINAL-FLUID CXCL13; N-ACETYLASPARTATE; PROGRESSIVE FORMS; CSF NEUROFILAMENT; CHANGING FACE; L-SELECTIN; PML RISK; IFN-BETA; BIOMARKERS;
D O I
10.1097/WCO.0000000000000324
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of review In recent years we notice paradigm shifts in the understanding of multiple sclerosis (MS), leading to important transition in the patients' management. This review discusses some of the recent findings and developments underlying the conceptual changes being translated from 'treating the disease' to 'treating the patient' with MS (PwMS). Recent findings Applying advanced technologies combined with cross-disciplinary efforts in the fields of neuropathology, neuroimmunology, neurobiology, and neuroimaging, together with clinical neurology provided support for the notion that MS is not a single disease but rather a spectrum. Predictive markers of disease subtypes, disease activity and response to therapy are being developed; some already applied to practice, allowing informed management. In parallel, population-specific issues, some genetic-driven, others caused by environmental (sun-exposure, life-style, etc.), gender-related (hormones) and epigenetic factors, are being elucidated. Additionally, patient empowerment-based approaches, including integration of patient-reported outcome measures (PRO) as well as tools to enhance patients' adherence to medications, are being developed, some already provided as part of emerging mobile-health technologies. Summary Developments in the MS field, elucidating disease subtypes and interpopulation diversities, together with integration of patient-centered approaches, allow transition toward precision medicine in MS clinical trials and patient care.
引用
收藏
页码:354 / 361
页数:8
相关论文
共 85 条
[1]   Trabid epigenetically drives expression of IL-12 and IL-23 [J].
Afonina, Inna S. ;
Beyaert, Rudi .
NATURE IMMUNOLOGY, 2016, 17 (03) :227-228
[2]   Multiple sclerosis frequency in Israel's diverse populations [J].
Alter, M ;
Kahana, E ;
Zilber, N ;
Miller, A .
NEUROLOGY, 2006, 66 (07) :1061-1066
[3]   Glial fibrillary acidic protein: a potential biomarker for progression in multiple sclerosis [J].
Axelsson, M. ;
Malmestrom, C. ;
Nilsson, S. ;
Haghighi, S. ;
Rosengren, L. ;
Lycke, J. .
JOURNAL OF NEUROLOGY, 2011, 258 (05) :882-888
[4]   The burden of multiple sclerosis variants in continental Italians and Sardinians [J].
Barizzone, Nadia ;
Zara, Ilenia ;
Sorosina, Melissa ;
Lupoli, Sara ;
Porcu, Eleonora ;
Pitzalis, Maristella ;
Zoledziewska, Magdalena ;
Esposito, Federica ;
Leone, Maurizio ;
Mulas, Antonella ;
Cocco, Eleonora ;
Ferrigno, Paola ;
Guerini, Franca R. ;
Brambilla, Paola ;
Farina, Gabriele ;
Murru, Raffaele ;
Deidda, Francesca ;
Sanna, Sonia ;
Loi, Alessia ;
Barlassina, Cristina ;
Vecchio, Domizia ;
Zauli, Andrea ;
Clarelli, Ferdinando ;
Braga, Daniele ;
Poddie, Fausto ;
Cantello, Roberto ;
Martinelli, Vittorio ;
Comi, Giancarlo ;
Frau, Jessica ;
Lorefice, Lorena ;
Pugliatti, Maura ;
Rosati, Giulio ;
Melis, Maurizio ;
Marrosu, Maria G. ;
Cusi, Daniele ;
Cucca, Francesco ;
Boneschi, Filippo Martinelli ;
Sanna, Serena ;
D'Alfonso, Sandra .
MULTIPLE SCLEROSIS JOURNAL, 2015, 21 (11) :1385-1395
[5]   Association between soluble L-selectin and anti-JCV antibodies in natalizumab-treated relapsing-remitting MS patients [J].
Basnyat, Pabitra ;
Hagman, Sanna ;
Kolasa, Marcin ;
Koivisto, Keijo ;
Verkkoniemi-Ahola, Auli ;
Airas, Laura ;
Elovaara, Irina .
MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2015, 4 (04) :334-338
[6]   Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel [J].
Benedek, G. ;
Paperna, T. ;
Avidan, N. ;
Lejbkowicz, I. ;
Oksenberg, J. R. ;
Wang, J. ;
Brautbar, C. ;
Israel, S. ;
Miller, A. .
GENES AND IMMUNITY, 2010, 11 (05) :423-431
[7]   Prevalence of multiple sclerosis among immigrants in Norway [J].
Berg-Hansen, Pal ;
Moen, Stine M. ;
Sandvik, Leiv ;
Harbo, Hanne F. ;
Bakken, Inger J. ;
Stoltenberg, Camilla ;
Celius, Elisabeth G. .
MULTIPLE SCLEROSIS JOURNAL, 2015, 21 (06) :695-702
[8]   Biological monitoring of IFN-β therapy in Multiple Sclerosis [J].
Bertolotto, A. ;
Granieri, L. ;
Marnetto, F. ;
Valentino, P. ;
Sala, A. ;
Capobianco, M. ;
Malucchi, S. ;
Di Sapio, A. ;
Malentacchi, M. ;
Matta, M. ;
Caldano, M. .
CYTOKINE & GROWTH FACTOR REVIEWS, 2015, 26 (02) :241-248
[9]   Risk of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy [J].
Bloomgren, Gary ;
Richman, Sandra ;
Hotermans, Christophe ;
Subramanyam, Meena ;
Goelz, Susan ;
Natarajan, Amy ;
Lee, Sophia ;
Plavina, Tatiana ;
Scanlon, James V. ;
Sandrock, Alfred ;
Bozic, Carmen .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (20) :1870-1880
[10]   The Chemokine CXCL13 Is a Prognostic Marker in Clinically Isolated Syndrome (CIS) [J].
Brettschneider, Johannes ;
Czerwoniak, Anne ;
Senel, Makbule ;
Fang, Lubin ;
Kassubek, Jan ;
Pinkhardt, Elmar ;
Lauda, Florian ;
Kapfer, Tamara ;
Jesse, Sarah ;
Lehmensiek, Vera ;
Ludolph, Albert C. ;
Otto, Markus ;
Tumani, Hayrettin .
PLOS ONE, 2010, 5 (08)