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Stroke and dementia risk: A systematic review and metaâ analysis

dc.contributor.authorKuźma, Elżbieta
dc.contributor.authorLourida, Ilianna
dc.contributor.authorMoore, Sarah F.
dc.contributor.authorLevine, Deborah A.
dc.contributor.authorUkoumunne, Obioha C.
dc.contributor.authorLlewellyn, David J.
dc.date.accessioned2020-01-13T15:14:07Z
dc.date.available2020-01-13T15:14:07Z
dc.date.issued2018-11
dc.identifier.citationKuźma, Elżbieta ; Lourida, Ilianna; Moore, Sarah F.; Levine, Deborah A.; Ukoumunne, Obioha C.; Llewellyn, David J. (2018). "Stroke and dementia risk: A systematic review and metaâ analysis." Alzheimer’s & Dementia 14(11): 1416-1426.
dc.identifier.issn1552-5260
dc.identifier.issn1552-5279
dc.identifier.urihttps://hdl.handle.net/2027.42/152961
dc.description.abstractIntroductionStroke is an established risk factor for allâ cause dementia, though metaâ analyses are needed to quantify this risk.MethodsWe searched Medline, PsycINFO, and Embase for studies assessing prevalent or incident stroke versus a noâ stroke comparison group and the risk of allâ cause dementia. Random effects metaâ analysis was used to pool adjusted estimates across studies, and metaâ regression was used to investigate potential effect modifiers.ResultsWe identified 36 studies of prevalent stroke (1.9 million participants) and 12 studies of incident stroke (1.3 million participants). For prevalent stroke, the pooled hazard ratio for allâ cause dementia was 1.69 (95% confidence interval: 1.49â 1.92; P < .00001; I2 = 87%). For incident stroke, the pooled risk ratio was 2.18 (95% confidence interval: 1.90â 2.50; P < .00001; I2 = 88%). Study characteristics did not modify these associations, with the exception of sex which explained 50.2% of betweenâ study heterogeneity for prevalent stroke.DiscussionStroke is a strong, independent, and potentially modifiable risk factor for allâ cause dementia.
dc.publisherWiley Periodicals, Inc.
dc.publisherUniversity of York
dc.titleStroke and dementia risk: A systematic review and metaâ analysis
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelNeurology and Neurosciences
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/152961/1/alzjjalz2018063061.pdf
dc.identifier.doi10.1016/j.jalz.2018.06.3061
dc.identifier.sourceAlzheimer’s & Dementia
dc.identifier.citedreferenceA. Gamaldo, A. Moghekar, S. Kilada, S.M. Resnick, A.B. Zonderman, R. O’Brien. Effect of a clinical stroke on the risk of dementia in a prospective cohort. Neurology. 67: 2006; 1363 â 1369
dc.identifier.citedreferenceJ.P. Higgins, S. Green. Cochrane Handbook for Systematic Reviews of Interventions. 2011; John Wiley & Sons
dc.identifier.citedreferenceJ.P.T. Higgins, S.G. Thompson, J.J. Deeks, D.G. Altman. Measuring inconsistency in metaâ analyses. BMJ. 327: 2003; 557 â 560
dc.identifier.citedreferenceR.D. Riley, J.P. Higgins, J.J. Deeks. Interpretation of random effects metaâ analyses. BMJ. 342: 2011; d549
dc.identifier.citedreferenceC. Reitz, M.J. Bos, A. Hofman, P.J. Koudstaal, M.M. Breteler. Prestroke cognitive performance, incident stroke, and risk of dementia: the Rotterdam Study. Stroke. 39: 2008; 36 â 41
dc.identifier.citedreferenceS.S. Mirza, M.L. Portegies, F.J. Wolters, A. Hofman, P.J. Koudstaal, H. Tiemeier, et al. Higher education is associated with a lower risk of dementia after a Stroke or TIA. The Rotterdam Study. Neuroepidemiology. 46: 2016; 120 â 127
dc.identifier.citedreferenceAmerican Psychiatric Association Diagnostic and Statistical Manual of Mental Health Disorders (DSMâ IIIâ R). 1987; American Psychiatric Association: Washington, DC
dc.identifier.citedreferenceAmerican Psychiatric Association Diagnostic and Statistical Manual. 4th ed.. 2000; American Psychiatric Association: Washington, DC, Text Revision (DSMâ IVâ TR)
dc.identifier.citedreferenceWorld Health Organization The ICDâ 10 Classification of Mental and Behavioural Disorders: Clinical Descriptions and Diagnostic Guidelines. 1992; World Health Organization
dc.identifier.citedreferenceS.G. Aguilarâ Navarro, A.J. Mimenzaâ Alvarado, J.A. Avilaâ Funes, T. Juarezâ Cedillo, C. Bernalâ Lopez, C.G. Hernandezâ Favela. Clinical and demographic predictors of conversion to dementia in Mexican elderly with mild cognitive impairment. Rev Invest Clin. 69: 2017; 33 â 39
dc.identifier.citedreferenceD.E. Barnes, A.S. Beiser, A. Lee, K.M. Langa, A. Koyama, S.R. Preis, et al. Development and validation of a brief dementia screening indicator for primary care. Alzheimers Dement. 10: 2014; 656 â 665.e1
dc.identifier.citedreferenceC. Brayne, C. Gill, F.A. Huppert, C. Barkley, E. Gehlhaar, D.M. Girling, et al. Vascular risks and incident dementia: Results from a cohort study of the very old. Dement Geriatr Cogn Disord. 9: 1998; 175 â 180
dc.identifier.citedreferenceD.G. Bruce, W.A. Davis, S.E. Starkstein, T.M. Davis. Midâ life predictors of cognitive impairment and dementia in type 2 diabetes mellitus: The Fremantle Diabetes Study. J Alzheimers Dis. 3: 2014; S63 â S70
dc.identifier.citedreferenceR. Chen, Z. Hu, L. Wei, Y. Ma, Z. Liu, J.R. Copeland. Incident Dementia in a Defined Older Chinese Population. PLoS One. 6: 2011; e24817
dc.identifier.citedreferenceF. Clerici, B. Caracciolo, I. Cova, S.F. Imperatori, L. Maggiore, D. Galimberti, et al. Does vascular burden contribute to the progression of mild cognitive impairment to dementia?. Dement Geriatr Cogn Disord. 34: 2012; 235 â 243
dc.identifier.citedreferenceP. Corraini, V.W. Henderson, A.G. Ording, L. Pedersen, E. Horvathâ Puho, H.T. Sorensen. Longâ Term Risk of Dementia Among Survivors of Ischemic or Hemorrhagic Stroke. Stroke. 48: 2017; 180 â 186
dc.identifier.citedreferenceV.C. Crooks, J. Lubben, D.B. Petitti, D. Little, V. Chiu. Social Network, Cognitive Function, and Dementia Incidence among elderly women. Am J Public Health. 98: 2008; 1221 â 1227
dc.identifier.citedreferenceR.F. de Bruijn, M.J. Bos, M.L. Portegies, A. Hofman, O.H. Franco, P.L. Koudstaal, et al. The potential for prevention of dementia across two decades: The prospective, populationâ based Rotterdam Study. BMC Med. 13: 2015; 132
dc.identifier.citedreferenceC. DeCarli, D. Mungas, D. Harvey, B. Reed, M. Weiner, H. Chui, et al. Memory impairment, but not cerebrovascular disease, predicts progression of MCI to dementia. Neurology. 63: 2004; 220 â 227
dc.identifier.citedreferenceD.W. Desmond, J.T. Moroney, M. Sano, Y. Stern. Incidence of dementia after ischemic stroke: Results of a longitudinal study. Stroke. 33: 2002; 2254 â 2260
dc.identifier.citedreferenceH.H. Dodge, C.C. Chang, I.M. Kamboh, M. Ganguli. Risk of Alzheimer’s disease incidence attributable to vascular disease in the population. Alzheimers Dement. 7: 2011; 356 â 360
dc.identifier.citedreferenceB. Downer, A. Kumar, S.P. Veeranki, H.B. Mehta, M. Raji, K.S. Markides. Mexicanâ American dementia nomogram: Development of a dementia risk index for Mexicanâ American older adults. J Am Geriatr Soc. 64: 2016; e265 â e269
dc.identifier.citedreferenceM. Ganguli, C.â W. Lee, B.E. Snitz, T.F. Hughes, E. McDade, C.â C.H. Chang. Rates and risk factors for progression to incident dementia vary by age in a population cohort. Neurology. 84: 2015; 72 â 80
dc.identifier.citedreferenceL.B. Hassing, A.K. Dahl, V. Thorvaldsson, S. Berg, M. Gatz, N.L. Redersen, et al. Overweight in midlife and risk of dementia: A 40â year followâ up study. Int J Obes (2005). 33: 2009; 893 â 898
dc.identifier.citedreferenceK.M. Hayden, P.P. Zandi, C.G. Lyketsos, A.S. Khachaturian, L.A. Bastian, G. Charoonruk, et al. Vascular risk factors for incident Alzheimer disease and vascular dementia: The Cache County study. Alzheimer Dis Assoc Disord. 20: 2006; 93 â 100
dc.identifier.citedreferenceH.C. Hendrie, A. Hake, K. Lane, C. Purnell, F. Unverzagt, V. Smithâ Gamble, et al. Statin Use, Incident Dementia and Alzheimer Disease in Elderly African Americans. Ethn Dis. 25: 2015; 345 â 354
dc.identifier.citedreferenceP. Hobson, J. Meara. Cognitive function and mortality in a communityâ based elderly cohort of firstâ ever stroke survivors and control subjects. J Stroke Cerebrovasc Dis. 19: 2010; 382 â 387
dc.identifier.citedreferenceR. Peters, R. Poulter, N. Beckett, F. Forette, R. Fagard, J. Potter, et al. Cardiovascular and biochemical risk factors for incident dementia in the Hypertension in the Very Elderly Trial. J Hypertens. 27: 2009; 2055 â 2062
dc.identifier.citedreferenceF.W. Unverzagt, L.T. Guey, R.N. Jones, M. Marsiske, J.W. King, V.G. Wadley, et al. ACTIVE cognitive training and rates of incident dementia. J Int Neuropsychol Soc. 18: 2012; 669 â 677
dc.identifier.citedreferenceA. Dregan, C.D. Wolfe, M.C. Gulliford. Does the influence of stroke on dementia vary by different levels of prestroke cognitive functioning?: A cohort study. Stroke. 44: 2013; 3445 â 3451
dc.identifier.citedreferenceP.F. Hsu, W.H. Pan, B.S. Yip, R.C. Chen, H.M. Cheng, S.Y. Chuang. Câ reactive protein predicts incidence of dementia in an elderly Asian community cohort. JAMDA. 18: 2017; 277.e7 â 277.e11
dc.identifier.citedreferenceC.S. Ivan, S. Seshadri, A. Beiser, R. Au, C.S. Kase, M. Kellyâ Hayes, et al. Dementia after stroke: The Framingham Study. Stroke. 35: 2004; 1264 â 1268
dc.identifier.citedreferenceY.P. Jin, S. Di Legge, T. Ostbye, J.W. Feightner, V. Hachinski. The reciprocal risks of stroke and cognitive impairment in an elderly population. Alzheimers Dement. 2: 2006; 171 â 178
dc.identifier.citedreferenceJ.â H. Kim, Y. Lee. Dementia and death after stroke in older adults during a 10â year followâ up: Results from a competing risk model. J Nutr Health Aging. 22: 2018; 297 â 301
dc.identifier.citedreferenceN.â C. Li, A. Lee, R.A. Whitmer, M. Kivipelto, E. Lawler, L.E. Kazis, et al. Use of angiotensin receptor blockers and risk of dementia in a predominantly male population: Prospective cohort analysis. BMJ. 340: 2010
dc.identifier.citedreferenceP. Nordstrom, A. Nordstrom, M. Eriksson, L.O. Wahlund, Y. Gustafson. Risk factors in late adolescence for youngâ onset dementia in men: A nationwide cohort study. JAMA Intern Med. 173: 2013; 1612 â 1618
dc.identifier.citedreferenceS. Rastas, T. Pirttila, K. Mattila, A. Verkkoniemi, K. Juva, L. Niinisto, et al. Vascular risk factors and dementia in the general population aged >85 years: Prospective populationâ based study. Neurobiol Aging. 31: 2010; 1 â 7
dc.identifier.citedreferenceL. Zhu, L. Fratiglioni, Z. Guo, H. Basun, E.H. Corder, B. Winblad, et al. Incidence of dementia in relation to stroke and the apolipoprotein E epsilon4 allele in the very old. Findings from a populationâ based longitudinal study. Stroke. 31: 2000; 53 â 60
dc.identifier.citedreferenceL. Rouch, P. Cestac, O. Hanon, C. Cool, C. Helmer, B. Bouhanick, et al. Antihypertensive drugs, prevention of cognitive decline and dementia: a systematic review of observational studies, randomized controlled trials and metaâ analyses, with discussion of potential mechanisms. CNS Drugs. 29: 2015; 113 â 130
dc.identifier.citedreferenceG.C. Román. Vascular dementia prevention: A risk factor analysis. Cerebrovasc Dis. 2: 2005; 91 â 100
dc.identifier.citedreferenceM. Barber, R. Tait, J. Scott, A. Rumley, G. Lowe, D. Stott. Dementia in subjects with atrial fibrillation: Hemostatic function and the role of anticoagulation. J Thromb Haemost. 2: 2004; 1873 â 1878
dc.identifier.citedreferenceT.J. Bunch, H.T. May, T.L. Bair, B.G. Crandall, M.J. Cutler, J.D. Day, et al. Atrial fibrillation patients treated with longâ term warfarin anticoagulation have higher rates of all dementia types compared with patients receiving longâ term Warfarin for other indications. J Am Heart Assoc. 5 (7): 2016; e003932
dc.identifier.citedreferenceY. Béjot, C. Aboaâ Eboulé, J. Durier, O. Rouaud, A. Jacquin, E. Ponavoy, et al. Prevalence of early dementia after firstâ ever stroke. Stroke. 42: 2011; 607 â 612
dc.identifier.citedreferenceR.N. Kalaria, R. Akinyemi, M. Ihara. Stroke injury, cognitive impairment and vascular dementia. Biochim Biophys Acta. 1862: 2016; 915 â 925
dc.identifier.citedreferenceM. Garciaâ Alloza, J. Gregory, K.V. Kuchibhotla, S. Fine, Y. Wei, C. Ayata, et al. Cerebrovascular lesions induce transient βâ amyloid deposition. Brain. 134: 2011; 3697 â 3707
dc.identifier.citedreferenceK.P. Doyle, M.S. Buckwalter. Does B lymphocyteâ mediated autoimmunity contribute to postâ stroke dementia?. Brain Behav Immun. 64: 2016; 1 â 8
dc.identifier.citedreferenceS.N. Whitehead, G. Cheng, V.C. Hachinski, D.F. Cechetto. Progressive increase in infarct size, neuroinflammation, and cognitive deficits in the presence of high levels of amyloid. Stroke. 38: 2007; 3245 â 3250
dc.identifier.citedreferenceW.D. Heiss, G.A. Rosenberg, A. Thiel, J. de Reuck. Neuroimaging in vascular cognitive impairment: A stateâ ofâ theâ art review. BMC Med. 14: 2016; 174
dc.identifier.citedreferenceS.D.J. Makin, S. Turpin, M.S. Dennis, J.M. Wardlaw. Cognitive impairment after lacunar stroke: Systematic review and metaâ analysis of incidence, prevalence and comparison with other stroke subtypes. J Neurol Neurosurg Psychiatr. 84: 2013; 893 â 900
dc.identifier.citedreferenceJ.B. Pinkston, N. Alekseeva, E. González Toledo. Stroke and dementia. Neurol Res. 31: 2009; 824 â 831
dc.identifier.citedreferenceG.M. Savva, B.C. Stephan. Epidemiological studies of the effect of stroke on incident dementia: A systematic review. Stroke. 41: 2010; e41 â e46
dc.identifier.citedreferenceS.T. Pendlebury, P.M. Rothwell. Prevalence, incidence, and factors associated with preâ stroke and postâ stroke dementia: A systematic review and metaâ analysis. Lancet Neurol. 8: 2009; 1006 â 1018
dc.identifier.citedreferenceJ. Zhou, J.â T. Yu, H.â F. Wang, X.â F. Meng, C.â C. Tan, J. Wang, et al. Association between stroke and Alzheimer’s disease: Systematic review and metaâ analysis. J Alzheimers Dis. 43: 2015; 479 â 489
dc.identifier.citedreferenceV. Bellou, L. Belbasis, I. Tzoulaki, L.T. Middleton, J.P. Ioannidis, E. Evangelou. Systematic evaluation of the associations between environmental risk factors and dementia: An umbrella review of systematic reviews and metaâ analyses. Alzheimers Dement. 13: 2017; 406 â 418
dc.identifier.citedreferenceCentre for Reviews and Dissemination (CRD) Systematic Reviews: CRD’s Guidance for Undertaking Reviews in Health Care. Centre for Reviews and Dissemination. 2009; University of York: York, UK
dc.identifier.citedreferenceB.H. Thomas, D. Ciliska, M. Dobbins, S. Micucci. A process for systematically reviewing the literature: Providing the research evidence for public health nursing interventions. Worldviews Evid Based Nurs. 1: 2004; 176 â 184
dc.identifier.citedreferenceJ.J. Deeks, J.P.T. Higgins, D.G. Altman. Chapter 9: Analysing data and undertaking metaâ analyses J.P.T. Higgins, S. Green. Cochrane Handbook for Systematic Reviews of Interventions. 2008; John Wiley & Sons: Chichester (UK)
dc.identifier.citedreferenceT. Cochrane. Review Manager (RevMan) 5.3. 2008; The Nordic Cochrane Centre: Copenhagen
dc.identifier.citedreferenceY.P. Jin, T. Ostbye, J.W. Feightner, S. Di Legge, V. Hachinski. Joint effect of stroke and APOE 4 on dementia risk: the Canadian Study of Health and Aging. Neurology. 70: 2008; 9 â 16
dc.identifier.citedreferenceE. Kokmen, J.P. Whisnant, W.M. O’Fallon, C.P. Chu, C.M. Beard. Dementia after ischemic stroke: A populationâ based study in Rochester, Minnesota (1960â 1984). Neurology. 46: 1996; 154 â 159
dc.identifier.citedreferenceL.H. Kuller, O.L. Lopez, A. Newman, N.J. Beauchamp, G. Burke, C. Dulberg, et al. Risk factors for dementia in the cardiovascular health cognition study. Neuroepidemiology. 22: 2003; 13 â 22
dc.identifier.citedreferenceG. Li, Y.C. Shen, C.H. Chen, Y.W. Zhau, S.R. Li, M. Lu. A threeâ year followâ up study of ageâ related dementia in an urban area of Beijing. Acta Psychiatr Scand. 83: 1991; 99 â 104
dc.identifier.citedreferenceM. Liebetrau, B. Steen, I. Skoog. Stroke in 85â yearâ olds: Prevalence, incidence, risk factors, and relation to mortality and dementia. Stroke. 34: 2003; 2617 â 2622
dc.identifier.citedreferenceM. Noale, F. Limongi, S. Zambon, G. Crepaldi, S. Maggi. Incidence of dementia: Evidence for an effect modification by gender. The ILSA Study. Int Psychogeriatr. 25: 2013; 1867 â 1876
dc.identifier.citedreferenceC. Qiu, W. Xu, B. Winblad, L. Fratiglioni. Vascular risk profiles for dementia and Alzheimer’s disease in very old people: A populationâ based longitudinal study. J Alzheimers Dis. 20: 2010; 293 â 300
dc.identifier.citedreferenceL.A. Simons, J. Simons, J. McCallum, Y. Friedlander. Lifestyle factors and risk of dementia: Dubbo Study of the elderly. Med J Aust. 184: 2006; 68 â 70
dc.identifier.citedreferenceV.K. Srikanth, J.F. Anderson, G.A. Donnan, M.M. Saling, E. Didus, R. Alpitsis, et al. Progressive dementia after firstâ ever stroke: A communityâ based followâ up study. Neurology. 63: 2004; 785 â 792
dc.identifier.citedreferenceV.K. Srikanth, S.J. Quinn, G.A. Donnan, M.M. Saling, A.G. Thrift. Longâ term cognitive transitions, rates of cognitive change, and predictors of incident dementia in a populationâ based firstâ ever stroke cohort. Stroke. 37: 2006; 2479 â 2483
dc.identifier.citedreferenceH.â H. Tsai, R.â F. Yen, C.â L. Lin, C.â H. Kao. Increased risk of dementia in patients hospitalized with acute kidney injury: A nationwide populationâ based cohort study. PLoS One. 12: 2017; e0171671
dc.identifier.citedreferenceK. Walters, S. Hardoon, I. Petersen, S. Illife, R.Z. Omar, I. Nazareth, et al. Predicting dementia risk in primary care: Development and validation of the Dementia Risk Score using routinely collected data. BMC Med. 14: 2016; 6
dc.identifier.citedreferenceM. Yamada, Y. Mimori, F. Kasagi, T. Miyachi, T. Ohshita, H. Sasaki. Incidence and risks of dementia in Japanese women: Radiation Effects Research Foundation Adult Health Study. J Neurol Sci. 283: 2009; 57 â 61
dc.identifier.citedreferenceA.G. Yip, C. Brayne, F.E. Matthews. Risk factors for incident dementia in England and Wales: The Medical Research Council Cognitive Function and Ageing Study. A populationâ based nested caseâ control study. Age Ageing. 35: 2006; 154 â 160
dc.identifier.citedreferenceL.B. Zahodne, N. Schupf, A.M. Brickman, R. Mayeux, M.M. Wall, Y. Stern, et al. Dementia risk and protective factors differ in the context of memory trajectory groups. J Attend Disord. 52: 2016; 1013 â 1020
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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