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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2185795738</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2185795738</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-cb4d6f9823193768e123cf0d0e83515c4f26c23da99350ad070edccab915df833</originalsourceid><addsrcrecordid>eNp9kLtOwzAUhi0EoqXwAgwoErPhOCdObDZUcZMqMQCz5dpOSNXYxU4G3p6UFtiYzvDfdD5CzhlcMYDqOgEUjFNgkoJkEmh1QKaswJyygstDMgUsgHLkxYScpLQCADEKx2SCIIBXkk_Jzfxd-6b1TeY2rXVdG9ah-cxCnXWhDzHzbojBu8y2yenkstZnLyb0a-3tKTmq9Tq5s_2dkbf7u9f5I108PzzNbxfUoCh7apaFLWspcmQSq1I4lqOpwYITyBk3RZ2XJkerpUQO2kIFzhqjl5JxWwvEGbnc9W5i-Bhc6tUqDNGPkypnYvtGhWJ05TuXiSGl6Gq1iW2n46dioLa41A6XGnGpb1yqGkMX--ph2Tn7G_nhMxpwZ0ij5BsX_7b_qf0C34F0Zw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2185795738</pqid></control><display><type>article</type><title>Changing epidemiology of motor neurone disease in Scotland</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Leighton, Danielle J. ; Newton, Judith ; Stephenson, Laura J. ; Colville, Shuna ; Davenport, Richard ; Gorrie, George ; Morrison, Ian ; Swingler, Robert ; Chandran, Siddharthan ; Pal, Suvankar</creator><creatorcontrib>Leighton, Danielle J. ; Newton, Judith ; Stephenson, Laura J. ; Colville, Shuna ; Davenport, Richard ; Gorrie, George ; Morrison, Ian ; Swingler, Robert ; Chandran, Siddharthan ; Pal, Suvankar ; CARE-MND Consortium ; on behalf of the CARE-MND Consortium</creatorcontrib><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.</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 & 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. Our data suggest that CARE-MND is a reliable national resource and findings can be extrapolated to the other Northern European populations.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Capture-recapture studies</subject><subject>Female</subject><subject>Humans</subject><subject>Incidence</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Motor Neuron Disease - epidemiology</subject><subject>Motor neurone disease</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Prevalence</subject><subject>Prospective Studies</subject><subject>Registries</subject><subject>Scotland - epidemiology</subject><subject>Socioeconomic factors</subject><subject>Time Factors</subject><subject>Young Adult</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kLtOwzAUhi0EoqXwAgwoErPhOCdObDZUcZMqMQCz5dpOSNXYxU4G3p6UFtiYzvDfdD5CzhlcMYDqOgEUjFNgkoJkEmh1QKaswJyygstDMgUsgHLkxYScpLQCADEKx2SCIIBXkk_Jzfxd-6b1TeY2rXVdG9ah-cxCnXWhDzHzbojBu8y2yenkstZnLyb0a-3tKTmq9Tq5s_2dkbf7u9f5I108PzzNbxfUoCh7apaFLWspcmQSq1I4lqOpwYITyBk3RZ2XJkerpUQO2kIFzhqjl5JxWwvEGbnc9W5i-Bhc6tUqDNGPkypnYvtGhWJ05TuXiSGl6Gq1iW2n46dioLa41A6XGnGpb1yqGkMX--ph2Tn7G_nhMxpwZ0ij5BsX_7b_qf0C34F0Zw</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Leighton, Danielle J.</creator><creator>Newton, Judith</creator><creator>Stephenson, Laura J.</creator><creator>Colville, Shuna</creator><creator>Davenport, Richard</creator><creator>Gorrie, George</creator><creator>Morrison, Ian</creator><creator>Swingler, Robert</creator><creator>Chandran, Siddharthan</creator><creator>Pal, Suvankar</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0003-2015-7198</orcidid></search><sort><creationdate>20190401</creationdate><title>Changing epidemiology of motor neurone disease in Scotland</title><author>Leighton, Danielle J. ; Newton, Judith ; Stephenson, Laura J. ; Colville, Shuna ; Davenport, Richard ; Gorrie, George ; Morrison, Ian ; Swingler, Robert ; Chandran, Siddharthan ; Pal, Suvankar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-cb4d6f9823193768e123cf0d0e83515c4f26c23da99350ad070edccab915df833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Amyotrophic lateral sclerosis</topic><topic>Capture-recapture studies</topic><topic>Female</topic><topic>Humans</topic><topic>Incidence</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Motor Neuron Disease - epidemiology</topic><topic>Motor neurone disease</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Original Communication</topic><topic>Prevalence</topic><topic>Prospective Studies</topic><topic>Registries</topic><topic>Scotland - epidemiology</topic><topic>Socioeconomic factors</topic><topic>Time Factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leighton, Danielle J.</au><au>Newton, Judith</au><au>Stephenson, Laura J.</au><au>Colville, Shuna</au><au>Davenport, Richard</au><au>Gorrie, George</au><au>Morrison, Ian</au><au>Swingler, Robert</au><au>Chandran, Siddharthan</au><au>Pal, Suvankar</au><aucorp>CARE-MND Consortium</aucorp><aucorp>on behalf of the CARE-MND Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changing epidemiology of motor neurone disease in Scotland</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>266</volume><issue>4</issue><spage>817</spage><epage>825</epage><pages>817-825</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>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.</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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