Changing epidemiology of motor neurone disease in Scotland

Objectives Scotland benefits from an integrated national healthcare team for motor neurone disease (MND) and a tradition of rich clinical data capture using the Scottish MND Register (launched in 1989; one of the first national registers). The Scottish register was re-launched in 2015 as C linical A...

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Veröffentlicht in:Journal of neurology 2019-04, Vol.266 (4), p.817-825
Hauptverfasser: Leighton, Danielle J., Newton, Judith, Stephenson, Laura J., Colville, Shuna, Davenport, Richard, Gorrie, George, Morrison, Ian, Swingler, Robert, Chandran, Siddharthan, Pal, Suvankar
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container_end_page 825
container_issue 4
container_start_page 817
container_title Journal of neurology
container_volume 266
creator Leighton, Danielle J.
Newton, Judith
Stephenson, Laura J.
Colville, Shuna
Davenport, Richard
Gorrie, George
Morrison, Ian
Swingler, Robert
Chandran, Siddharthan
Pal, Suvankar
description Objectives Scotland benefits from an integrated national healthcare team for motor neurone disease (MND) and a tradition of rich clinical data capture using the Scottish MND Register (launched in 1989; one of the first national registers). The Scottish register was re-launched in 2015 as C linical A udit R esearch and E valuation of MND (CARE-MND), an electronic platform for prospective, population-based research. We aimed to determine if incidence of MND is changing over time. Methods Capture–recapture methods determined the incidence of MND in 2015–2016. Incidence rates for 2015–2016 and 1989–1998 were direct age and sex standardised to allow time-period comparison. Phenotypic characteristics and socioeconomic status of the cohort are described. Results Coverage of the CARE-MND platform was 99%. Crude incidence in the 2015–2017 period was 3.83/100,000 person-years (95% CI 3.53–4.14). Direct age-standardised incidence in 2015 was 3.42/100,000 (95% CI 2.99–3.91); in 2016, it was 2.89/100,000 (95% CI 2.50–3.34). The 1989–1998 direct standardised annual incidence estimate was 2.32/100,000 (95% CI 2.26–2.37). 2015–2016 standardised incidence was 66.9% higher than Northern European estimates. Socioeconomic status was not associated with MND. Conclusions Our data show a changing landscape of MND in Scotland, with a rise in incidence by 36.0% over a 25-year period. This is likely attributable to ascertainment in the context of improved neurological services in Scotland. Our data suggest that CARE-MND is a reliable national resource and findings can be extrapolated to the other Northern European populations.
doi_str_mv 10.1007/s00415-019-09190-7
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The Scottish register was re-launched in 2015 as C linical A udit R esearch and E valuation of MND (CARE-MND), an electronic platform for prospective, population-based research. We aimed to determine if incidence of MND is changing over time. Methods Capture–recapture methods determined the incidence of MND in 2015–2016. Incidence rates for 2015–2016 and 1989–1998 were direct age and sex standardised to allow time-period comparison. Phenotypic characteristics and socioeconomic status of the cohort are described. Results Coverage of the CARE-MND platform was 99%. Crude incidence in the 2015–2017 period was 3.83/100,000 person-years (95% CI 3.53–4.14). Direct age-standardised incidence in 2015 was 3.42/100,000 (95% CI 2.99–3.91); in 2016, it was 2.89/100,000 (95% CI 2.50–3.34). The 1989–1998 direct standardised annual incidence estimate was 2.32/100,000 (95% CI 2.26–2.37). 2015–2016 standardised incidence was 66.9% higher than Northern European estimates. Socioeconomic status was not associated with MND. Conclusions Our data show a changing landscape of MND in Scotland, with a rise in incidence by 36.0% over a 25-year period. This is likely attributable to ascertainment in the context of improved neurological services in Scotland. Our data suggest that CARE-MND is a reliable national resource and findings can be extrapolated to the other Northern European populations.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-019-09190-7</identifier><identifier>PMID: 30805795</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Adult ; Age ; Aged ; Aged, 80 and over ; Amyotrophic lateral sclerosis ; Capture-recapture studies ; Female ; Humans ; Incidence ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Motor Neuron Disease - epidemiology ; Motor neurone disease ; Neurology ; Neuroradiology ; Neurosciences ; Original Communication ; Prevalence ; Prospective Studies ; Registries ; Scotland - epidemiology ; Socioeconomic factors ; Time Factors ; Young Adult</subject><ispartof>Journal of neurology, 2019-04, Vol.266 (4), p.817-825</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2019</rights><rights>Journal of Neurology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-cb4d6f9823193768e123cf0d0e83515c4f26c23da99350ad070edccab915df833</citedby><cites>FETCH-LOGICAL-c386t-cb4d6f9823193768e123cf0d0e83515c4f26c23da99350ad070edccab915df833</cites><orcidid>0000-0003-2015-7198</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-019-09190-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-019-09190-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30805795$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leighton, Danielle J.</creatorcontrib><creatorcontrib>Newton, Judith</creatorcontrib><creatorcontrib>Stephenson, Laura J.</creatorcontrib><creatorcontrib>Colville, Shuna</creatorcontrib><creatorcontrib>Davenport, Richard</creatorcontrib><creatorcontrib>Gorrie, George</creatorcontrib><creatorcontrib>Morrison, Ian</creatorcontrib><creatorcontrib>Swingler, Robert</creatorcontrib><creatorcontrib>Chandran, Siddharthan</creatorcontrib><creatorcontrib>Pal, Suvankar</creatorcontrib><creatorcontrib>CARE-MND Consortium</creatorcontrib><creatorcontrib>on behalf of the CARE-MND Consortium</creatorcontrib><title>Changing epidemiology of motor neurone disease in Scotland</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Objectives Scotland benefits from an integrated national healthcare team for motor neurone disease (MND) and a tradition of rich clinical data capture using the Scottish MND Register (launched in 1989; one of the first national registers). The Scottish register was re-launched in 2015 as C linical A udit R esearch and E valuation of MND (CARE-MND), an electronic platform for prospective, population-based research. We aimed to determine if incidence of MND is changing over time. Methods Capture–recapture methods determined the incidence of MND in 2015–2016. Incidence rates for 2015–2016 and 1989–1998 were direct age and sex standardised to allow time-period comparison. Phenotypic characteristics and socioeconomic status of the cohort are described. Results Coverage of the CARE-MND platform was 99%. Crude incidence in the 2015–2017 period was 3.83/100,000 person-years (95% CI 3.53–4.14). Direct age-standardised incidence in 2015 was 3.42/100,000 (95% CI 2.99–3.91); in 2016, it was 2.89/100,000 (95% CI 2.50–3.34). The 1989–1998 direct standardised annual incidence estimate was 2.32/100,000 (95% CI 2.26–2.37). 2015–2016 standardised incidence was 66.9% higher than Northern European estimates. Socioeconomic status was not associated with MND. Conclusions Our data show a changing landscape of MND in Scotland, with a rise in incidence by 36.0% over a 25-year period. This is likely attributable to ascertainment in the context of improved neurological services in Scotland. 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one of the first national registers). The Scottish register was re-launched in 2015 as C linical A udit R esearch and E valuation of MND (CARE-MND), an electronic platform for prospective, population-based research. We aimed to determine if incidence of MND is changing over time. Methods Capture–recapture methods determined the incidence of MND in 2015–2016. Incidence rates for 2015–2016 and 1989–1998 were direct age and sex standardised to allow time-period comparison. Phenotypic characteristics and socioeconomic status of the cohort are described. Results Coverage of the CARE-MND platform was 99%. Crude incidence in the 2015–2017 period was 3.83/100,000 person-years (95% CI 3.53–4.14). Direct age-standardised incidence in 2015 was 3.42/100,000 (95% CI 2.99–3.91); in 2016, it was 2.89/100,000 (95% CI 2.50–3.34). The 1989–1998 direct standardised annual incidence estimate was 2.32/100,000 (95% CI 2.26–2.37). 2015–2016 standardised incidence was 66.9% higher than Northern European estimates. Socioeconomic status was not associated with MND. Conclusions Our data show a changing landscape of MND in Scotland, with a rise in incidence by 36.0% over a 25-year period. This is likely attributable to ascertainment in the context of improved neurological services in Scotland. Our data suggest that CARE-MND is a reliable national resource and findings can be extrapolated to the other Northern European populations.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30805795</pmid><doi>10.1007/s00415-019-09190-7</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2015-7198</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Age
Aged
Aged, 80 and over
Amyotrophic lateral sclerosis
Capture-recapture studies
Female
Humans
Incidence
Male
Medicine
Medicine & Public Health
Middle Aged
Motor Neuron Disease - epidemiology
Motor neurone disease
Neurology
Neuroradiology
Neurosciences
Original Communication
Prevalence
Prospective Studies
Registries
Scotland - epidemiology
Socioeconomic factors
Time Factors
Young Adult
title Changing epidemiology of motor neurone disease in Scotland
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