Rising prevalence of multiple sclerosis worldwide: Insights from the Atlas of MS, third edition

High-quality epidemiologic data worldwide are needed to improve our understanding of disease risk, support health policy to meet the diverse needs of people with multiple sclerosis (MS) and support advocacy efforts. The Atlas of MS is an open-source global compendium of data regarding the epidemiolo...

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Vydáno v:	Multiple sclerosis Ročník 26; číslo 14; s. 1816
Hlavní autoři:	Walton, Clare, King, Rachel, Rechtman, Lindsay, Kaye, Wendy, Leray, Emmanuelle, Marrie, Ruth Ann, Robertson, Neil, La Rocca, Nicholas, Uitdehaag, Bernard, van der Mei, Ingrid, Wallin, Mitchell, Helme, Anne, Angood Napier, Ceri, Rijke, Nick, Baneke, Peer
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	England 01.12.2020
Témata:	Child Female Humans Incidence Male Multiple Sclerosis - epidemiology Prevalence epidemiology Multiple sclerosis
ISSN:	1477-0970, 1477-0970
On-line přístup:	Zjistit podrobnosti o přístupu
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Abstract	High-quality epidemiologic data worldwide are needed to improve our understanding of disease risk, support health policy to meet the diverse needs of people with multiple sclerosis (MS) and support advocacy efforts. The Atlas of MS is an open-source global compendium of data regarding the epidemiology of MS and the availability of resources for people with MS reported at country, regional and global levels. Country representatives reported epidemiologic data and their sources via survey between September 2019 and March 2020, covering prevalence and incidence in males, females and children, and age and MS type at diagnosis. Regional analyses and comparisons with 2013 data were conducted. A total of 2.8 million people are estimated to live with MS worldwide (35.9 per 100,000 population). MS prevalence has increased in every world region since 2013 but gaps in prevalence estimates persist. The pooled incidence rate across 75 reporting countries is 2.1 per 100,000 persons/year, and the mean age of diagnosis is 32 years. Females are twice as likely to live with MS as males. The global prevalence of MS has risen since 2013, but good surveillance data is not universal. Action is needed by multiple stakeholders to close knowledge gaps.
AbstractList	High-quality epidemiologic data worldwide are needed to improve our understanding of disease risk, support health policy to meet the diverse needs of people with multiple sclerosis (MS) and support advocacy efforts.BACKGROUNDHigh-quality epidemiologic data worldwide are needed to improve our understanding of disease risk, support health policy to meet the diverse needs of people with multiple sclerosis (MS) and support advocacy efforts.The Atlas of MS is an open-source global compendium of data regarding the epidemiology of MS and the availability of resources for people with MS reported at country, regional and global levels.OBJECTIVESThe Atlas of MS is an open-source global compendium of data regarding the epidemiology of MS and the availability of resources for people with MS reported at country, regional and global levels.Country representatives reported epidemiologic data and their sources via survey between September 2019 and March 2020, covering prevalence and incidence in males, females and children, and age and MS type at diagnosis. Regional analyses and comparisons with 2013 data were conducted.METHODSCountry representatives reported epidemiologic data and their sources via survey between September 2019 and March 2020, covering prevalence and incidence in males, females and children, and age and MS type at diagnosis. Regional analyses and comparisons with 2013 data were conducted.A total of 2.8 million people are estimated to live with MS worldwide (35.9 per 100,000 population). MS prevalence has increased in every world region since 2013 but gaps in prevalence estimates persist. The pooled incidence rate across 75 reporting countries is 2.1 per 100,000 persons/year, and the mean age of diagnosis is 32 years. Females are twice as likely to live with MS as males.RESULTSA total of 2.8 million people are estimated to live with MS worldwide (35.9 per 100,000 population). MS prevalence has increased in every world region since 2013 but gaps in prevalence estimates persist. The pooled incidence rate across 75 reporting countries is 2.1 per 100,000 persons/year, and the mean age of diagnosis is 32 years. Females are twice as likely to live with MS as males.The global prevalence of MS has risen since 2013, but good surveillance data is not universal. Action is needed by multiple stakeholders to close knowledge gaps.CONCLUSIONSThe global prevalence of MS has risen since 2013, but good surveillance data is not universal. Action is needed by multiple stakeholders to close knowledge gaps. High-quality epidemiologic data worldwide are needed to improve our understanding of disease risk, support health policy to meet the diverse needs of people with multiple sclerosis (MS) and support advocacy efforts. The Atlas of MS is an open-source global compendium of data regarding the epidemiology of MS and the availability of resources for people with MS reported at country, regional and global levels. Country representatives reported epidemiologic data and their sources via survey between September 2019 and March 2020, covering prevalence and incidence in males, females and children, and age and MS type at diagnosis. Regional analyses and comparisons with 2013 data were conducted. A total of 2.8 million people are estimated to live with MS worldwide (35.9 per 100,000 population). MS prevalence has increased in every world region since 2013 but gaps in prevalence estimates persist. The pooled incidence rate across 75 reporting countries is 2.1 per 100,000 persons/year, and the mean age of diagnosis is 32 years. Females are twice as likely to live with MS as males. The global prevalence of MS has risen since 2013, but good surveillance data is not universal. Action is needed by multiple stakeholders to close knowledge gaps.
Author	Uitdehaag, Bernard Rijke, Nick Robertson, Neil Marrie, Ruth Ann Rechtman, Lindsay van der Mei, Ingrid Helme, Anne La Rocca, Nicholas Leray, Emmanuelle Walton, Clare Wallin, Mitchell Kaye, Wendy Baneke, Peer King, Rachel Angood Napier, Ceri
Author_xml	– sequence: 1 givenname: Clare orcidid: 0000-0002-8128-6439 surname: Walton fullname: Walton, Clare organization: Multiple Sclerosis International Federation, London, UK – sequence: 2 givenname: Rachel surname: King fullname: King, Rachel organization: Multiple Sclerosis International Federation, London, UK – sequence: 3 givenname: Lindsay surname: Rechtman fullname: Rechtman, Lindsay organization: McKing Consulting Corporation, Atlanta, GA, USA – sequence: 4 givenname: Wendy surname: Kaye fullname: Kaye, Wendy organization: McKing Consulting Corporation, Atlanta, GA, USA – sequence: 5 givenname: Emmanuelle surname: Leray fullname: Leray, Emmanuelle organization: EA 7449 REPERES, Epidemiology, Ecole des Hautes Etudes en Sante Publique, Rennes, France – sequence: 6 givenname: Ruth Ann orcidid: 0000-0002-1855-5595 surname: Marrie fullname: Marrie, Ruth Ann organization: Internal Medicine, University of Manitoba, Winnipeg, MB, Canada – sequence: 7 givenname: Neil surname: Robertson fullname: Robertson, Neil organization: Institute of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff, UK – sequence: 8 givenname: Nicholas surname: La Rocca fullname: La Rocca, Nicholas organization: National MS Society, West Bath, ME, USA – sequence: 9 givenname: Bernard surname: Uitdehaag fullname: Uitdehaag, Bernard organization: Neurology, Amsterdam UMC-Locatie VUMC, Amsterdam, Netherlands – sequence: 10 givenname: Ingrid surname: van der Mei fullname: van der Mei, Ingrid organization: Menzies Research Institute, University of Tasmania, Hobart, TAS, Australia – sequence: 11 givenname: Mitchell surname: Wallin fullname: Wallin, Mitchell organization: Department of Neurology, George Washington University, Washington, DC, USA – sequence: 12 givenname: Anne surname: Helme fullname: Helme, Anne organization: Multiple Sclerosis International Federation, London, UK – sequence: 13 givenname: Ceri surname: Angood Napier fullname: Angood Napier, Ceri organization: Multiple Sclerosis International Federation, London, UK – sequence: 14 givenname: Nick surname: Rijke fullname: Rijke, Nick organization: Multiple Sclerosis International Federation, London, UK – sequence: 15 givenname: Peer surname: Baneke fullname: Baneke, Peer organization: Multiple Sclerosis International Federation, London, UK
BackLink	https://www.ncbi.nlm.nih.gov/pubmed/33174475$$D View this record in MEDLINE/PubMed
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References	33174499 - Mult Scler. 2020 Dec;26(14):1807-1808. doi: 10.1177/1352458520968811.
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SubjectTerms	Child Female Humans Incidence Male Multiple Sclerosis - epidemiology Prevalence
Title	Rising prevalence of multiple sclerosis worldwide: Insights from the Atlas of MS, third edition
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