Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study
Summary Background Dementia occurs in at least 10% of patients within 1 year after stroke. However, the risk of dementia after spontaneous intracerebral haemorrhage that accounts for about 15% of all strokes has not been investigated in prospective studies. We aimed to determine the incidence of dem...
Gespeichert in:
Veröffentlicht in: | Lancet neurology 2016-07, Vol.15 (8), p.820-829 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 829 |
---|---|
container_issue | 8 |
container_start_page | 820 |
container_title | Lancet neurology |
container_volume | 15 |
creator | Moulin, Solène, MD Labreuche, Julien, Bst Bombois, Stéphanie, PhD Rossi, Costanza, PhD Boulouis, Gregoire, MD Hénon, Hilde, PhD Duhamel, Alain, Prof Leys, Didier, Prof Cordonnier, Charlotte, Prof |
description | Summary Background Dementia occurs in at least 10% of patients within 1 year after stroke. However, the risk of dementia after spontaneous intracerebral haemorrhage that accounts for about 15% of all strokes has not been investigated in prospective studies. We aimed to determine the incidence of dementia and risk factors after an intracerebral haemorrhage. Methods We did a prospective observational cohort study in patients with spontaneous intracerebral haemorrhage from the Prognosis of Intracerebral Haemorrhage (PITCH) cohort who were admitted to Lille University Hospital, Lille, France. We included patients aged 18 years and older with parenchymal haemorrhage on the first CT scan. Exclusion criteria were pure intraventricular haemorrhage; intracerebral haemorrhage resulting from intracranial vascular malformation, intracranial venous thrombosis, head trauma, or tumour; haemorrhagic transformation within an infarct; and referral from other hospitals. Median follow-up was 6 years. We studied risk factors (clinical and neuroradiological [MRI] biomarkers) of new-onset dementia as per a prespecified subgroup analysis, according to intracerebral haemorrhage location. Dementia diagnosis was based on the National Institute on Aging-Alzheimer's Association criteria for all-cause dementia. We did multivariable analyses using competing risk analyses, with death during follow-up as a competing event. Findings From the 560 patients with spontaneous intracerebral haemorrhage enrolled in the PITCH cohort between Nov 3, 2004 and March 29, 2009, we included 218 patients (median age 67·5 years) without pre-existing dementia who were alive at 6 months follow-up. 63 patients developed new-onset dementia leading to an incidence rate of 14·2% (95% CI 10·0–19·3) at 1 year after intracerebral haemorrhage, and incidence reached 28·3% (22·4–34·5) at 4 years. The incidence of new-onset dementia was more than two times higher in patients with lobar intracerebral haemorrhage (incidence at 1 year 23·4%, 14·6–33·3) than for patients with non-lobar intracerebral haemorrhage (incidence at 1 year 9·2%, 5·1–14·7). Disseminated superficial siderosis (subhazard ratio [SHR] 7·45, 95% CI 4·27–12·99), cortical atrophy score (SHR per 1-point increase 2·61, 1·70–4·01), a higher number of cerebral microbleeds (SHR for >5 cerebral microbleeds 2·33, 1·38–3·94), and older age (SHR per 10-year increase 1·34, 1·00–1·79) were risk factors of new-onset dementia. Interpretation There is a substantial ris |
doi_str_mv | 10.1016/S1474-4422(16)00130-7 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1808622192</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1474442216001307</els_id><sourcerecordid>1808622192</sourcerecordid><originalsourceid>FETCH-LOGICAL-c533t-3f633706b963958d5fcc560a515b2f25f4bbb65b204b32ca53fcfa7719455c5e3</originalsourceid><addsrcrecordid>eNqFkctuFDEQRS0EIg_4BJAlNsmig9_uZgGKAgSkSCwga8vtLjNO-jGx3ZHm7-OZHoKUTVYuW6euq-5F6B0lZ5RQ9fE3FVpUQjB2QtUpIZSTSr9Ah_tnJV8-1owdoKOUbghhVNT0NTpgmnLOeH2Irr_CAGMOFseQbrH1GSJO62nMdoRpTjiMOVoHEdpoe7yyMEwxruxf-IQtXscprcHlcA_YTaspZpzy3G3eoFfe9gne7s9jdP3925-LH9XVr8ufF-dXlZOc54p7xbkmqm0Ub2TdSe-cVMRKKlvmmfSibVtVaiJazpyV3DtvtaaNkNJJ4MfoZNEtg9zNkLIZQnLQ98vwhtakVozRhj2P6kZLQSklBf3wBL2Z5jiWRRaKKKZ0oeRCuWJCiuDNOobBxo2hxGwjMruIzNZ_U267iMy27_1efW4H6B67_mVSgC8LAMW5-wDRJBdgdNCFWLw23RSe_eLzEwXXhzE429_CBtL_bUxihiwiWw2qdgqaPwBQT7RH</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1797506267</pqid></control><display><type>article</type><title>Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Moulin, Solène, MD ; Labreuche, Julien, Bst ; Bombois, Stéphanie, PhD ; Rossi, Costanza, PhD ; Boulouis, Gregoire, MD ; Hénon, Hilde, PhD ; Duhamel, Alain, Prof ; Leys, Didier, Prof ; Cordonnier, Charlotte, Prof</creator><creatorcontrib>Moulin, Solène, MD ; Labreuche, Julien, Bst ; Bombois, Stéphanie, PhD ; Rossi, Costanza, PhD ; Boulouis, Gregoire, MD ; Hénon, Hilde, PhD ; Duhamel, Alain, Prof ; Leys, Didier, Prof ; Cordonnier, Charlotte, Prof</creatorcontrib><description>Summary Background Dementia occurs in at least 10% of patients within 1 year after stroke. However, the risk of dementia after spontaneous intracerebral haemorrhage that accounts for about 15% of all strokes has not been investigated in prospective studies. We aimed to determine the incidence of dementia and risk factors after an intracerebral haemorrhage. Methods We did a prospective observational cohort study in patients with spontaneous intracerebral haemorrhage from the Prognosis of Intracerebral Haemorrhage (PITCH) cohort who were admitted to Lille University Hospital, Lille, France. We included patients aged 18 years and older with parenchymal haemorrhage on the first CT scan. Exclusion criteria were pure intraventricular haemorrhage; intracerebral haemorrhage resulting from intracranial vascular malformation, intracranial venous thrombosis, head trauma, or tumour; haemorrhagic transformation within an infarct; and referral from other hospitals. Median follow-up was 6 years. We studied risk factors (clinical and neuroradiological [MRI] biomarkers) of new-onset dementia as per a prespecified subgroup analysis, according to intracerebral haemorrhage location. Dementia diagnosis was based on the National Institute on Aging-Alzheimer's Association criteria for all-cause dementia. We did multivariable analyses using competing risk analyses, with death during follow-up as a competing event. Findings From the 560 patients with spontaneous intracerebral haemorrhage enrolled in the PITCH cohort between Nov 3, 2004 and March 29, 2009, we included 218 patients (median age 67·5 years) without pre-existing dementia who were alive at 6 months follow-up. 63 patients developed new-onset dementia leading to an incidence rate of 14·2% (95% CI 10·0–19·3) at 1 year after intracerebral haemorrhage, and incidence reached 28·3% (22·4–34·5) at 4 years. The incidence of new-onset dementia was more than two times higher in patients with lobar intracerebral haemorrhage (incidence at 1 year 23·4%, 14·6–33·3) than for patients with non-lobar intracerebral haemorrhage (incidence at 1 year 9·2%, 5·1–14·7). Disseminated superficial siderosis (subhazard ratio [SHR] 7·45, 95% CI 4·27–12·99), cortical atrophy score (SHR per 1-point increase 2·61, 1·70–4·01), a higher number of cerebral microbleeds (SHR for >5 cerebral microbleeds 2·33, 1·38–3·94), and older age (SHR per 10-year increase 1·34, 1·00–1·79) were risk factors of new-onset dementia. Interpretation There is a substantial risk of incident dementia in dementia-free survivors of spontaneous intracerebral haemorrhage; our results suggest that underlying cerebral amyloid angiopathy is a contributing factor to the occurrence of new-onset dementia. Future clinical trials including patients with intracerebral haemorrhage should assess cognitive endpoints. Funding French Ministry of Education, Research, and Technology, Adrinord, Inserm U1171.</description><identifier>ISSN: 1474-4422</identifier><identifier>EISSN: 1474-4465</identifier><identifier>DOI: 10.1016/S1474-4422(16)00130-7</identifier><identifier>PMID: 27133238</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Age ; Aged ; Aged, 80 and over ; Biomarkers ; Cerebral Hemorrhage - complications ; Cerebral Hemorrhage - diagnostic imaging ; Cerebral Hemorrhage - epidemiology ; Cognition & reasoning ; Cognitive ability ; Cohort Studies ; Dementia ; Dementia - diagnostic imaging ; Dementia - epidemiology ; Dementia - etiology ; Female ; Hemorrhage ; Humans ; Magnetic Resonance Imaging ; Male ; Medical prognosis ; Middle Aged ; Mortality ; Neurology ; Population ; Stroke ; Surveys and Questionnaires ; Tomography Scanners, X-Ray Computed</subject><ispartof>Lancet neurology, 2016-07, Vol.15 (8), p.820-829</ispartof><rights>Elsevier Ltd</rights><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Jul 01, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-3f633706b963958d5fcc560a515b2f25f4bbb65b204b32ca53fcfa7719455c5e3</citedby><cites>FETCH-LOGICAL-c533t-3f633706b963958d5fcc560a515b2f25f4bbb65b204b32ca53fcfa7719455c5e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1474442216001307$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27133238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moulin, Solène, MD</creatorcontrib><creatorcontrib>Labreuche, Julien, Bst</creatorcontrib><creatorcontrib>Bombois, Stéphanie, PhD</creatorcontrib><creatorcontrib>Rossi, Costanza, PhD</creatorcontrib><creatorcontrib>Boulouis, Gregoire, MD</creatorcontrib><creatorcontrib>Hénon, Hilde, PhD</creatorcontrib><creatorcontrib>Duhamel, Alain, Prof</creatorcontrib><creatorcontrib>Leys, Didier, Prof</creatorcontrib><creatorcontrib>Cordonnier, Charlotte, Prof</creatorcontrib><title>Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study</title><title>Lancet neurology</title><addtitle>Lancet Neurol</addtitle><description>Summary Background Dementia occurs in at least 10% of patients within 1 year after stroke. However, the risk of dementia after spontaneous intracerebral haemorrhage that accounts for about 15% of all strokes has not been investigated in prospective studies. We aimed to determine the incidence of dementia and risk factors after an intracerebral haemorrhage. Methods We did a prospective observational cohort study in patients with spontaneous intracerebral haemorrhage from the Prognosis of Intracerebral Haemorrhage (PITCH) cohort who were admitted to Lille University Hospital, Lille, France. We included patients aged 18 years and older with parenchymal haemorrhage on the first CT scan. Exclusion criteria were pure intraventricular haemorrhage; intracerebral haemorrhage resulting from intracranial vascular malformation, intracranial venous thrombosis, head trauma, or tumour; haemorrhagic transformation within an infarct; and referral from other hospitals. Median follow-up was 6 years. We studied risk factors (clinical and neuroradiological [MRI] biomarkers) of new-onset dementia as per a prespecified subgroup analysis, according to intracerebral haemorrhage location. Dementia diagnosis was based on the National Institute on Aging-Alzheimer's Association criteria for all-cause dementia. We did multivariable analyses using competing risk analyses, with death during follow-up as a competing event. Findings From the 560 patients with spontaneous intracerebral haemorrhage enrolled in the PITCH cohort between Nov 3, 2004 and March 29, 2009, we included 218 patients (median age 67·5 years) without pre-existing dementia who were alive at 6 months follow-up. 63 patients developed new-onset dementia leading to an incidence rate of 14·2% (95% CI 10·0–19·3) at 1 year after intracerebral haemorrhage, and incidence reached 28·3% (22·4–34·5) at 4 years. The incidence of new-onset dementia was more than two times higher in patients with lobar intracerebral haemorrhage (incidence at 1 year 23·4%, 14·6–33·3) than for patients with non-lobar intracerebral haemorrhage (incidence at 1 year 9·2%, 5·1–14·7). Disseminated superficial siderosis (subhazard ratio [SHR] 7·45, 95% CI 4·27–12·99), cortical atrophy score (SHR per 1-point increase 2·61, 1·70–4·01), a higher number of cerebral microbleeds (SHR for >5 cerebral microbleeds 2·33, 1·38–3·94), and older age (SHR per 10-year increase 1·34, 1·00–1·79) were risk factors of new-onset dementia. Interpretation There is a substantial risk of incident dementia in dementia-free survivors of spontaneous intracerebral haemorrhage; our results suggest that underlying cerebral amyloid angiopathy is a contributing factor to the occurrence of new-onset dementia. Future clinical trials including patients with intracerebral haemorrhage should assess cognitive endpoints. Funding French Ministry of Education, Research, and Technology, Adrinord, Inserm U1171.</description><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers</subject><subject>Cerebral Hemorrhage - complications</subject><subject>Cerebral Hemorrhage - diagnostic imaging</subject><subject>Cerebral Hemorrhage - epidemiology</subject><subject>Cognition & reasoning</subject><subject>Cognitive ability</subject><subject>Cohort Studies</subject><subject>Dementia</subject><subject>Dementia - diagnostic imaging</subject><subject>Dementia - epidemiology</subject><subject>Dementia - etiology</subject><subject>Female</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Neurology</subject><subject>Population</subject><subject>Stroke</subject><subject>Surveys and Questionnaires</subject><subject>Tomography Scanners, X-Ray Computed</subject><issn>1474-4422</issn><issn>1474-4465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkctuFDEQRS0EIg_4BJAlNsmig9_uZgGKAgSkSCwga8vtLjNO-jGx3ZHm7-OZHoKUTVYuW6euq-5F6B0lZ5RQ9fE3FVpUQjB2QtUpIZSTSr9Ah_tnJV8-1owdoKOUbghhVNT0NTpgmnLOeH2Irr_CAGMOFseQbrH1GSJO62nMdoRpTjiMOVoHEdpoe7yyMEwxruxf-IQtXscprcHlcA_YTaspZpzy3G3eoFfe9gne7s9jdP3925-LH9XVr8ufF-dXlZOc54p7xbkmqm0Ub2TdSe-cVMRKKlvmmfSibVtVaiJazpyV3DtvtaaNkNJJ4MfoZNEtg9zNkLIZQnLQ98vwhtakVozRhj2P6kZLQSklBf3wBL2Z5jiWRRaKKKZ0oeRCuWJCiuDNOobBxo2hxGwjMruIzNZ_U267iMy27_1efW4H6B67_mVSgC8LAMW5-wDRJBdgdNCFWLw23RSe_eLzEwXXhzE429_CBtL_bUxihiwiWw2qdgqaPwBQT7RH</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Moulin, Solène, MD</creator><creator>Labreuche, Julien, Bst</creator><creator>Bombois, Stéphanie, PhD</creator><creator>Rossi, Costanza, PhD</creator><creator>Boulouis, Gregoire, MD</creator><creator>Hénon, Hilde, PhD</creator><creator>Duhamel, Alain, Prof</creator><creator>Leys, Didier, Prof</creator><creator>Cordonnier, Charlotte, Prof</creator><general>Elsevier Ltd</general><general>Elsevier Limited</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>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20160701</creationdate><title>Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study</title><author>Moulin, Solène, MD ; Labreuche, Julien, Bst ; Bombois, Stéphanie, PhD ; Rossi, Costanza, PhD ; Boulouis, Gregoire, MD ; Hénon, Hilde, PhD ; Duhamel, Alain, Prof ; Leys, Didier, Prof ; Cordonnier, Charlotte, Prof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-3f633706b963958d5fcc560a515b2f25f4bbb65b204b32ca53fcfa7719455c5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers</topic><topic>Cerebral Hemorrhage - complications</topic><topic>Cerebral Hemorrhage - diagnostic imaging</topic><topic>Cerebral Hemorrhage - epidemiology</topic><topic>Cognition & reasoning</topic><topic>Cognitive ability</topic><topic>Cohort Studies</topic><topic>Dementia</topic><topic>Dementia - diagnostic imaging</topic><topic>Dementia - epidemiology</topic><topic>Dementia - etiology</topic><topic>Female</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Neurology</topic><topic>Population</topic><topic>Stroke</topic><topic>Surveys and Questionnaires</topic><topic>Tomography Scanners, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moulin, Solène, MD</creatorcontrib><creatorcontrib>Labreuche, Julien, Bst</creatorcontrib><creatorcontrib>Bombois, Stéphanie, PhD</creatorcontrib><creatorcontrib>Rossi, Costanza, PhD</creatorcontrib><creatorcontrib>Boulouis, Gregoire, MD</creatorcontrib><creatorcontrib>Hénon, Hilde, PhD</creatorcontrib><creatorcontrib>Duhamel, Alain, Prof</creatorcontrib><creatorcontrib>Leys, Didier, Prof</creatorcontrib><creatorcontrib>Cordonnier, Charlotte, Prof</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</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>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Lancet Titles</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 Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing & Allied Health Premium</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 One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Lancet neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moulin, Solène, MD</au><au>Labreuche, Julien, Bst</au><au>Bombois, Stéphanie, PhD</au><au>Rossi, Costanza, PhD</au><au>Boulouis, Gregoire, MD</au><au>Hénon, Hilde, PhD</au><au>Duhamel, Alain, Prof</au><au>Leys, Didier, Prof</au><au>Cordonnier, Charlotte, Prof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study</atitle><jtitle>Lancet neurology</jtitle><addtitle>Lancet Neurol</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>15</volume><issue>8</issue><spage>820</spage><epage>829</epage><pages>820-829</pages><issn>1474-4422</issn><eissn>1474-4465</eissn><coden>LANCAO</coden><abstract>Summary Background Dementia occurs in at least 10% of patients within 1 year after stroke. However, the risk of dementia after spontaneous intracerebral haemorrhage that accounts for about 15% of all strokes has not been investigated in prospective studies. We aimed to determine the incidence of dementia and risk factors after an intracerebral haemorrhage. Methods We did a prospective observational cohort study in patients with spontaneous intracerebral haemorrhage from the Prognosis of Intracerebral Haemorrhage (PITCH) cohort who were admitted to Lille University Hospital, Lille, France. We included patients aged 18 years and older with parenchymal haemorrhage on the first CT scan. Exclusion criteria were pure intraventricular haemorrhage; intracerebral haemorrhage resulting from intracranial vascular malformation, intracranial venous thrombosis, head trauma, or tumour; haemorrhagic transformation within an infarct; and referral from other hospitals. Median follow-up was 6 years. We studied risk factors (clinical and neuroradiological [MRI] biomarkers) of new-onset dementia as per a prespecified subgroup analysis, according to intracerebral haemorrhage location. Dementia diagnosis was based on the National Institute on Aging-Alzheimer's Association criteria for all-cause dementia. We did multivariable analyses using competing risk analyses, with death during follow-up as a competing event. Findings From the 560 patients with spontaneous intracerebral haemorrhage enrolled in the PITCH cohort between Nov 3, 2004 and March 29, 2009, we included 218 patients (median age 67·5 years) without pre-existing dementia who were alive at 6 months follow-up. 63 patients developed new-onset dementia leading to an incidence rate of 14·2% (95% CI 10·0–19·3) at 1 year after intracerebral haemorrhage, and incidence reached 28·3% (22·4–34·5) at 4 years. The incidence of new-onset dementia was more than two times higher in patients with lobar intracerebral haemorrhage (incidence at 1 year 23·4%, 14·6–33·3) than for patients with non-lobar intracerebral haemorrhage (incidence at 1 year 9·2%, 5·1–14·7). Disseminated superficial siderosis (subhazard ratio [SHR] 7·45, 95% CI 4·27–12·99), cortical atrophy score (SHR per 1-point increase 2·61, 1·70–4·01), a higher number of cerebral microbleeds (SHR for >5 cerebral microbleeds 2·33, 1·38–3·94), and older age (SHR per 10-year increase 1·34, 1·00–1·79) were risk factors of new-onset dementia. Interpretation There is a substantial risk of incident dementia in dementia-free survivors of spontaneous intracerebral haemorrhage; our results suggest that underlying cerebral amyloid angiopathy is a contributing factor to the occurrence of new-onset dementia. Future clinical trials including patients with intracerebral haemorrhage should assess cognitive endpoints. Funding French Ministry of Education, Research, and Technology, Adrinord, Inserm U1171.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27133238</pmid><doi>10.1016/S1474-4422(16)00130-7</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1474-4422 |
ispartof | Lancet neurology, 2016-07, Vol.15 (8), p.820-829 |
issn | 1474-4422 1474-4465 |
language | eng |
recordid | cdi_proquest_miscellaneous_1808622192 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Age Aged Aged, 80 and over Biomarkers Cerebral Hemorrhage - complications Cerebral Hemorrhage - diagnostic imaging Cerebral Hemorrhage - epidemiology Cognition & reasoning Cognitive ability Cohort Studies Dementia Dementia - diagnostic imaging Dementia - epidemiology Dementia - etiology Female Hemorrhage Humans Magnetic Resonance Imaging Male Medical prognosis Middle Aged Mortality Neurology Population Stroke Surveys and Questionnaires Tomography Scanners, X-Ray Computed |
title | Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T17%3A21%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dementia%20risk%20after%20spontaneous%20intracerebral%20haemorrhage:%20a%20prospective%20cohort%20study&rft.jtitle=Lancet%20neurology&rft.au=Moulin,%20Sol%C3%A8ne,%20MD&rft.date=2016-07-01&rft.volume=15&rft.issue=8&rft.spage=820&rft.epage=829&rft.pages=820-829&rft.issn=1474-4422&rft.eissn=1474-4465&rft.coden=LANCAO&rft_id=info:doi/10.1016/S1474-4422(16)00130-7&rft_dat=%3Cproquest_cross%3E1808622192%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1797506267&rft_id=info:pmid/27133238&rft_els_id=S1474442216001307&rfr_iscdi=true |