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Natural history of multiple sclerosis: a unifying concept
Abstract
Multiple sclerosis can follow very different patterns of evolution and variable rates of disability accumulation. This raises the issue whether it represents one or several distinct diseases. We assessed demographic and clinical characteristics in 1844 patients with multiple sclerosis that we categorized according to the classification of Lublin and Reingold (1996) into 1066 (58%) relapsing-remitting, 496 (27%) secondary progressive, 109 (6%) progressive relapsing and 173 (9%) primary progressive cases of multiple sclerosis. Relapsing-remitting and secondary progressive cases shared similar age at disease onset (median = 28.7 versus 29.5 years; P = 0.21), initial symptoms of the relapsing-remitting phase, degree of recovery from the first neurological episode, and time from the first to the second episode. By contrast, disease duration was twice as long in secondary progressive than in relapsing-remitting cases (mean +/- SD = 17.6 +/- 9.6 versus 8.7 +/- 8.6 years; P < 0.001). Progressive relapsing and primary progressive cases were essentially similar in their clinical characteristics. In patients experiencing a progressive course, median age at onset of progressive phase was similar in secondary progressive cases and in cases who were progressive from onset (39.1 versus 40.1 years; P = 0.47). The proportion of cases with superimposed relapses during progression was approximately 40% in both categories. Finally, the 1562 patients with an exacerbating-remitting initial course and the 282 patients with a progressive initial course of the disease were essentially similar with respect to the time course of disability accumulation from assignment to a given disability score, and the age at assignment of disability landmarks. These observational data suggest that the clinical phenotype and course of multiple sclerosis are age dependent. Relapsing-remitting disease can be regarded as multiple sclerosis in which insufficient time has elapsed for the conversion to secondary progression; secondary progressive forms as relapsing-remitting multiple sclerosis that has 'grown older'; and progressive from onset cases as multiple sclerosis 'amputated' from the usual preceding relapsing-remitting phase. Times to reach disability milestones, and ages at which these landmarks are reached, follow a predefined schedule not obviously influenced by relapses, whenever they may occur, or by the initial course of the disease, whatever its phenotype. This leads to a unifying concept of the disease in which primary and secondary progression might be regarded as essentially similar. From the clinical and statistical positions, multiple sclerosis might be considered as one disease with different clinical phenotypes rather than an entity encompassing several distinct diseases-the position of complexity rather than true heterogeneity.
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Cites
Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)
Kurtzke, J. F. (1983) · Neurology · doi:10.1212/wnl.33.11.1444 · Cited by 15,011
The natural history of multiple sclerosis
Confavreux, C., & Compston, A. (2006) · McAlpine's Multiple Sclerosis · doi:10.1016/b978-0-443-07271-0.50006-9 · Cited by 166
Self-citation
Research works printed but not linked: 50
- Amato MP, Ponziani G. A prospective study on the prognosis of multiple sclerosis. Neurol Sci2000; 21 (Suppl): 831–8. · DOI
- Andersson PB, Waubant E, Gee L, Goodkin DE. Multiple sclerosis that is progressive from the time of onset. Clinical characteristics and progression of disability. Arch Neurol1999; 56: 1138–42. · doi:10.1001/archneur.56.9.1138
- Arnold DL. Magnetic resonance spectroscopy: imaging axonal damage in MS. J Neuroimmunol1999; 98: 2–6. · DOI
- Brex PA, Jenkins R, Fox NC, Crum WR, O'Riordan JL, Plant GT, et al. Detection of ventricular enlargement in patients at the earliest clinical stage of MS. Neurology2000; 54: 1689–91. · DOI · Paper page
- Broman T, Andersen O, Bergmann L. Clinical studies on multiple sclerosis. I. Presentation of an incidence material from Gothenburg. Acta Neurol Scand1981; 63: 6–33. · DOI
- Ciccarelli O, Werring DJ, Wheeler-Kingshott CAM, Barker GJ, Parker GJ, Thompson AJ, et al. Investigation of MS normal-appearing brain using diffusion tensor MRI with clinical correlations. Neurology2001; 56: 926–33. · DOI · Paper page
- Confavreux C, Aimard G, Devic M. Course and prognosis of multiple sclerosis assessed by the computerized data processing of 349 patients. Brain1980; 103: 281–300. · DOI · Paper page
- Confavreux C, Compston DAS, Hommes OR, McDonald WI, Thompson AJ. EDMUS, a European Database for Multiple Sclerosis. J Neurol Neurosurg Psychiatry1992; 55: 671–6. · DOI · Paper page
- Confavreux C, Vukusic S. Natural History of Multiple Sclerosis: implications for counseling and therapy. Curr Opin Neurol2002; 15: 257–66. · DOI
- Confavreux C, Vukusic S. Age at disability milestones in multiple sclerosis. Brain2006; 129: 595–605. First published January 16, 2006, doi:10.1093/brain/awh714. · DOI · Paper page
- Confavreux C, Vukusic S, Adeleine P. Early clinical predictors and progression of irreversible disability in multiple sclerosis: an amnesic process. Brain2003; 126: 770–82. · DOI · Paper page
- Confavreux C, Vukusic S, Moreau T, Adeleine P. Relapses and progression of disability in multiple sclerosis. N Engl J Med2000; 343: 1430–8. · DOI · Paper page
- Cottrell DA, Kremenchutzky M, Rice GPA, Koopman WJ, Hader W, Baskerville J, et al. The natural history of multiple sclerosis: a geographically based study. 5. The clinical features and natural history of primary progressive multiple sclerosis. Brain1999; 122:625–39. · DOI · Paper page
- Eriksson M, Andersen O, Runmarker B. Long-term follow-up of patients with clinically isolated syndromes, relapsing-remitting and secondary progressive multiple sclerosis. Mult Scler2003; 9: 260–74. · DOI · Paper page
- Evangelou N, Esiri MM, Smith S, Palace J, Matthews PM. Quantitative pathological evidence for axonal loss in normal appearing white matter in multiple sclerosis. Ann Neurol2000; 47: 391–5. · doi:10.1002/1531-8249(200003)47:3<391::aid-ana20>3.0.co;2-j
- Filippi M, Campi A, Martinelli V, Pereira C, Scotti G, Comi G. Transitional progressive multiple sclerosis: MRI and MTI findings. Acta Neurol Scand1995; 92: 178–82. · doi:10.1111/j.1600-0404.1995.tb01036.x
- Filippi M, Bozzali M, Rovaris M, Gonen O, Kesavadas C, Ghezzi A, et al. Evidence for widespread axonal damage at the earliest clinical stage of multiple sclerosis. Brain2003; 126: 433–7. · DOI · Paper page
- Filippi M, Rovaris M, Inglese M, Barkhof F, De Stefano N, Smith S, et al. Interferon beta-1a for brain tissue loss in patients at presentation with syndromes suggestive of multiple sclerosis: a randomized, double-blind, placebo-controlled trial. Lancet2004; 364: 1489–96. · DOI · Paper page
- Fox NC, Jenkins R, Lary SM, Stevenson VL, Losseff NA, Crum WR, et al. Progressive cerebral atrophy in MS: a serial study using registered, volumetric MRI. Neurology2000; 54: 807–12. · DOI · Paper page
- Fu L, Matthews PM, De Stefano N, Worsley KJ, Narayanan S, Francis GS, et al. Imaging axonal damage of normal-appearing white matter in multiple sclerosis. Brain1998; 121: 103–13. · DOI · Paper page
- Gayou A, Brochet B, Dousset V. Transitional progressive multiple sclerosis: a clinical and imaging study. J Neurol Neurosurg Psychiatry1997; 63: 396–8. · DOI
- Ingle GT, Stevenson VL, Miller DH and Thompson AJ. Primary progressive multiple sclerosis: a 5-year clinical and MR study. Brain2003; 126: 2528–36. · DOI
- Kremenchutzky M, Cottrell D, Rice G, Hader W, Baskerville J, Koopman W, et al. The natural history of multiple sclerosis: a geographically based study. 7. Progressive-relapsing and relapsing-progressive multiple sclerosis: a re-evaluation. Brain1999; 122: 1941–9. · DOI
- Kurtzke JF. On the evaluation of disability in multiple sclerosis. Neurology1961; 11: 686–94. · DOI · Paper page
- Losseff NA, Wang L, Lai HM, Yoo DS, Gawne-Cain ML, McDonald WI, et al. Progressive cerebral atrophy in multiple sclerosis. A serial MRI study. Brain1996; 119: 2009–19. · DOI · Paper page
- Losseff NA, Webb SL, O'Riordan JI, Page R, Wang L, Barker GJ, et al. Spinal cord atrophy and disability in multiple sclerosis. A new reproducible and sensitive MRI method with potential to monitor disease progression. Brain1996; 119: 701–8. · DOI · Paper page
- Lublin FD, Reingold SC. Defining the clinical course of multiple sclerosis: results of an international survey. Neurology1996; 46: 907–11. · DOI · Paper page
- Lucchinetti C, Brück W, Parisi J, Scheithauer B, Rodriguez M, Lassmann H. Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination. Ann Neurol2000; 47: 707–17. · DOI
- McAlpine D, Compston ND. Some aspects of the natural history of disseminated sclerosis: incidence, course and prognosis; factors affecting onset and course. Q J Med1952; 21: 135–67.
- McDonnell GV, Hawkins SA. Primary progressive multiple sclerosis:a distinct syndrome? Mult scler1996; 2: 137–41. · DOI
- McDonnel GV, Hawkins SA. Clinical study of primary progressive multiple sclerosis in Northern Ireland, UK. J Neurol Neurosurg Psychiatry1998; 64: 451–4. · DOI
- Minderhoud JM, Van der Hoeven JH, Prange AJA. Course and prognosis of chronic progressive multiple sclerosis. Results of an epidemiological study. Acta Neurol Scand1988; 78: 10–5. · DOI
- Myhr KM, Riise T, Vedeler C, Nortvedt MW, Gronning R, Midgard R, et al. Disability and prognosis in multiple sclerosis: demographic and clinical variables important for the ability to walk and awarding of disability pension. Multiple Sclerosis2001; 7: 59–65. · DOI
- Patzold U, Pocklington PR. Course of multiple sclerosis. First results of a prospective study carried out of 102 MS patients from 1976–1980. Acta Neurol Scand1982; 65: 248–66. · DOI
- Poser S. Multiple sclerosis. An analysis of 812 cases by means of electronic data processing. Berlin: Springer-Verlag; 1978.
- Poser CM, Paty DW, Scheinberg L, McDonald WI, Davis FA, Ebers GC, et al. New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann Neurol1983; 13: 227–31. · DOI · Paper page
- Robertson NP, Clayton D, Fraser M, Deans J, Compston DA. Clinical concordance in sibling pairs with multiple sclerosis. Neurology1996; 47: 347–52. · DOI
- Rudick RA, Fischer E, Lee JC, Simon J, Jacobs L. Use of the brain parenchymal fraction to measure whole brain atrophy in relapsing-remitting MS. Multiple Sclerosis Collaborative Research Group. Neurology1999; 53: 1698–704. · DOI · Paper page
- Runmarker B, Andersen O. Prognostic factors in a multiple sclerosis incidence cohort with twenty-five years of follow-up. Brain1993; 116: 117–34. · DOI · Paper page
- Schumacher GA, Beebe G, Kibler RF, Kurland LT, Kurtzke JF, McDowell F, et al. Problems of experimental trials of therapy in MS: report by the panel on the evaluation of experimental trials of therapy in MS. Ann N Y Acad Sci1965; 122: 552–68. · DOI · Paper page
- Stevenson VL, Miller DH, Rovaris M, Barkhof F, Brochet B, Dousset V, et al. Primary and transitional progressive MS. A clinical and MRI cross-sectional study. Neurology1999; 52: 839–45. · DOI · Paper page
- Stevenson VL, Miller DH, Leary SM, Rovaris M, Barkhof F, Brochet B, et al. One year follow-up study of primary and transitional progressive multiple sclerosis. J Neurol Neurosurg Psychiatry2000; 68: 713–8. · DOI
- Thompson AJ, Kermode AG, Wicks D, MacManus DG, Kendall BE, Kingsley DP, et al. Major differences in the dynamics of primary and secondary progressive multiple sclerosis. Ann Neurol1991; 29: 53–62. · DOI · Paper page
- Thompson AJ, Polman CH, Miller DH, McDonald WI, Brochet B, Filippi M, et al. Primary progressive multiple sclerosis. Brain1997; 120: 1085–96. · DOI · Paper page
- Tortorella C, Viti B, Bozzali M, Sormani MP, Rizzo G, Gilardi MF, et al. A magnetization transfer histogram study of normal-appearing brain tissue in MS. Neurology2000; 54: 186–93. · DOI · Paper page
- Traboulsee A, Dehmeshki J, Brex PA, Dalton CM, Chard D, Barker GJ, et al. Normal-appearing brain tissue MTR histograms in clinically isolated syndromes suggestive of MS. Neurology2002; 59: 126–8. · DOI
- Vukusic S, Confavreux C. Prognostic factors for progression of disability in the secondary progressive phase of multiple sclerosis. J Neurol Sci2003; 206: 135–7. · DOI
- Weinshenker BG. Progressive forms of MS: classification streamlined or consensus overtuned? Lancet2000; 355: 162–3. · DOI
- Weinshenker BG, Bulman D, Carriere W, Baskerville J, Ebers GC. A comparison of sporadic and familial multiple sclerosis. Neurology1990; 40: 1354–8. · DOI
- Youl BD, Turano G, Miller DH, Towell AD, MacManus DG, Moore SG, et al. The pathophysiology of acute optic neuritis. An association of gadolinium leakage with clinical and electrophysiological deficits. Brain1991; 114: 2437–50. · DOI · Paper page
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“2020;383(6):546–557 [PubMed: 32757523] 28.”
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Metadata
- Authors
- Confavreux, C., & Vukusic, S.
- Venue
- Brain
- Publisher
- Oxford University Press (OUP)
- Published
- 2006-01-16
- Volume
- 129
- Issue
- 3
- Pages
- 606-616
- ISSN
- 0006-8950 (ISSN-L)
- 1460-2156
- OpenAlex
- W2148563799
- Cited by
- 905
- References
- 2
- FWCI
- 21.24
- Type
- journal article
- Language
- en
- Open access
- closed
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