Post-stroke dementia - a comprehensive review

被引:469
作者
Mijajlovic, Milija D. [1 ]
Pavlovic, Aleksandra [1 ]
Brainin, Michael [2 ]
Heiss, Wolf-Dieter [3 ]
Quinn, Terence J. [4 ]
Ihle-Hansen, Hege B. [5 ,6 ]
Hermann, Dirk M. [7 ]
Ben Assayag, Einor [8 ,9 ]
Richard, Edo [10 ]
Thiel, Alexander [11 ,12 ]
Kliper, Efrat [8 ,9 ]
Shin, Yong-Il [13 ]
Kim, Yun-Hee [14 ]
Choi, SeongHye [15 ]
Jung, San [16 ]
Lee, Yeong-Bae [17 ]
Sinanovic, Osman [18 ]
Levine, Deborah A. [19 ,20 ]
Schlesinger, Ilana [21 ,22 ]
Mead, Gillian [23 ]
Milosevic, Vuk [24 ]
Leys, Didier [25 ]
Hagberg, Guri [5 ,6 ]
Ursin, Marie Helene [5 ,6 ]
Teuschl, Yvonne [2 ]
Prokopenko, Semyon [26 ]
Mozheyko, Elena [26 ]
Bezdenezhnykh, Anna [26 ]
Matz, Karl [2 ]
Aleksic, Vuk [27 ]
Muresanu, DafinFior [28 ]
Korczyn, Amos D. [29 ]
Bornstein, Natan M. [8 ,9 ]
机构
[1] Univ Belgrade, Neurol Clin, Clin Ctr Serbia, Sch Med, Dr Subotica 6, Belgrade 11000, Serbia
[2] Danube Univ Krems, Dept Clin Neurosci & Prevent Med, Krems, Austria
[3] Max Planck Inst Metab Res, Cologne, Germany
[4] Univ Glasgow, Inst Cardiovasc & Med Sci, Glasgow, Lanark, Scotland
[5] Oslo Univ Hosp, Dept Internal Med, Ulleval, Norway
[6] Vestre Viken Hosp Trust, Baerum Hosp, Dept Med Res, Baerum, Norway
[7] Univ Hosp Essen, Dept Neurol, Essen, Germany
[8] Tel Aviv Sourasky Med Ctr, Dept Neurol, Stroke Unit, Tel Aviv, Israel
[9] Shaare Zedek Med Ctr, Jerusalem, Israel
[10] Radboud Univ Nijmegen, Med Ctr, Dept Neurol, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[11] McGill Univ, Dept Neurol & Neurosurg, SMBD Jewish Gen Hosp, Montreal, PQ, Canada
[12] Lady Davis Inst Med Res, Montreal, PQ, Canada
[13] Pusan Natl Univ, Sch Med, Dept Rehabil Med, Busan, South Korea
[14] Sungkyunkwan Univ, Dept Phys & Rehabil Med, Sch Med,Ctr Prevent & Rehabil, Heart Vasc & Stroke Inst,Samsung Med Ctr, Seoul, South Korea
[15] Inha Univ, Sch Med, Dept Neurol, Inchon, South Korea
[16] Hallym Univ, Med Ctr, Kang Nam Sacred Heart Hosp, Seoul, South Korea
[17] Gachon Univ, Gil Med Ctr, Dept Neurol, Inchon, South Korea
[18] Univ Tuzla, Dept Neurol, Univ Clin Ctr Tuzla, Sch Med, Tuzla 75000, Bosnia & Herceg
[19] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[20] VA Ann Arbor Healthcare Syst, Ann Arbor, MI USA
[21] Rambam Hlth Care Campus, Dept Neurol, Haifa, Israel
[22] Technion Fac Med, Haifa, Israel
[23] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Midlothian, Scotland
[24] Clin Ctr Nis, Clin Neurol, Nish, Serbia
[25] Univ Lille, Dept Neurol, INSERM, Fac Med,Lille Univ Hosp,U1171, Lille, France
[26] Krasnoyarsk State Med Univ, Dept Neurol & Med Rehabil, Krasnoyarsk, Russia
[27] Clin Hosp CenterZemun, Dept Neurosurg, Belgrade, Serbia
[28] Iuliu Hatieganu Univ Med & Pharm, Dept Clin Neurosci, Cluj Napoca, Romania
[29] Tel Aviv Univ, Dept Neurol, IL-69978 Ramat Aviv, Israel
关键词
Cognitive impairment; Dementia; Definitions and classification; Diagnosis; Neuroimaging; Interventions; Biomarkers; Stroke; TRANSIENT ISCHEMIC ATTACK; VASCULAR COGNITIVE IMPAIRMENT; LIFE-STYLE INTERVENTIONS; PLACEBO-CONTROLLED TRIAL; ACE-I/D POLYMORPHISM; SMALL-VESSEL DISEASE; BLOOD-PRESSURE; METHODOLOGICAL FACTORS; ALZHEIMER-DISEASE; APOLIPOPROTEIN-E;
D O I
10.1186/s12916-017-0779-7
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Post-stroke dementia (PSD) or post-stroke cognitive impairment (PSCI) may affect up to one third of stroke survivors. Various definitions of PSCI and PSD have been described. We propose PSD as a label for any dementia following stroke in temporal relation. Various tools are available to screen and assess cognition, with few PSD-specific instruments. Choice will depend on purpose of assessment, with differing instruments needed for brief screening (e.g., Montreal Cognitive Assessment) or diagnostic formulation (e.g., NINDS VCI battery). A comprehensive evaluation should include assessment of pre-stroke cognition (e.g., using Informant Questionnaire for Cognitive Decline in the Elderly), mood (e.g., using Hospital Anxiety and Depression Scale), and functional consequences of cognitive impairments (e.g., using modified Rankin Scale). A large number of biomarkers for PSD, including indicators for genetic polymorphisms, biomarkers in the cerebrospinal fluid and in the serum, inflammatory mediators, and peripheral microRNA profiles have been proposed. Currently, no specific biomarkers have been proven to robustly discriminate vulnerable patients ('at risk brains') from those with better prognosis or to discriminate Alzheimer's disease dementia from PSD. Further, neuroimaging is an important diagnostic tool in PSD. The role of computerized tomography is limited to demonstrating type and location of the underlying primary lesion and indicating atrophy and severe white matter changes. Magnetic resonance imaging is the key neuroimaging modality and has high sensitivity and specificity for detecting pathological changes, including small vessel disease. Advanced multi-modal imaging includes diffusion tensor imaging for fiber tracking, by which changes in networks can be detected. Quantitative imaging of cerebral blood flow and metabolism by positron emission tomography can differentiate between vascular dementia and degenerative dementia and show the interaction between vascular and metabolic changes. Additionally, inflammatory changes after ischemia in the brain can be detected, which may play a role together with amyloid deposition in the development of PSD. Prevention of PSD can be achieved by prevention of stroke. As treatment strategies to inhibit the development and mitigate the course of PSD, lowering of blood pressure, statins, neuroprotective drugs, and anti-inflammatory agents have all been studied without convincing evidence of efficacy. Lifestyle interventions, physical activity, and cognitive training have been recently tested, but large controlled trials are still missing.
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