Microinfarct Pathology, Dementia, and Cognitive Systems
Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in community-dwelling older persons. Four hundred twenty-five subjects enrolled in the Religious Orders Study underwent annual clinical evaluat...
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Published in | Stroke (1970) Vol. 42; no. 3; pp. 722 - 727 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Hagerstown, MD
Lippincott Williams & Wilkins
01.03.2011
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Subjects | |
Online Access | Get full text |
ISSN | 0039-2499 1524-4628 1524-4628 |
DOI | 10.1161/STROKEAHA.110.595082 |
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Abstract | Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in community-dwelling older persons.
Four hundred twenty-five subjects enrolled in the Religious Orders Study underwent annual clinical evaluations, including 19 neuropsychological tests and assessment for dementia, and brain autopsy (39% men; mean age at death, 87; Mini-Mental State Examination score, 21). Neuropathologic examination documented the presence, number, and location of chronic microinfarcts on 6-μm hematoxylin-eosin-stained sections from cortical and subcortical regions. Multiple regression analyses adjusted for age at death, sex, education, macroscopic infarcts, Alzheimer disease pathology, and Lewy bodies.
Microinfarcts were present in 129 of 425 (30%) persons (54 cortical, 80 subcortical, 49 multiple); 58 of 129 (45%) of persons with microinfarcts did not exhibit macroscopic infarcts. Persons with microinfarcts had increased odds of dementia (OR, 1.77; 95% CI, 1.07-2.92), especially those persons with multiple cortical microinfarcts. Microinfarcts were also associated with lower average global cognition (estimate, -0.287; SE, 0.113; P=0.012), particularly for persons with multiple cortical microinfarcts. Microinfarcts were specifically associated with lower episodic memory (estimate, -0.279; SE, 0.138; P=0.044), semantic memory (estimate, -0.391; SE, 0.130; P=0.003), and perceptual speed (estimate, -0.400; SE, 0.117; P<0.001). In addition, single, multiple, and cortical microinfarcts were associated with worse semantic memory and perceptual speed (all P<0.028). Neither macroscopic infarcts nor AD pathology modified these associations (all P>0.154).
Microinfarcts are common, and persons with multiple cortical microinfarcts have higher odds of dementia. Microinfarcts are also associated with lower cognition, specifically perceptual speed and semantic and episodic memory. |
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AbstractList | BACKGROUND AND PURPOSE{MDASH}: Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in community-dwelling older persons. METHODS{MDASH}: Four hundred twenty-five subjects enrolled in the Religious Orders Study underwent annual clinical evaluations, including 19 neuropsychological tests and assessment for dementia, and brain autopsy (39% men; mean age at death, 87; Mini-Mental State Examination score, 21). Neuropathologic examination documented the presence, number, and location of chronic microinfarcts on 6- mu m hematoxylin-eosin-stained sections from cortical and subcortical regions. Multiple regression analyses adjusted for age at death, sex, education, macroscopic infarcts, Alzheimer disease pathology, and Lewy bodies. RESULTS{MDASH}: Microinfarcts were present in 129 of 425 (30%) persons (54 cortical, 80 subcortical, 49 multiple); 58 of 129 (45%) of persons with microinfarcts did not exhibit macroscopic infarcts. Persons with microinfarcts had increased odds of dementia (OR, 1.77; 95% CI, 1.07-2.92), especially those persons with multiple cortical microinfarcts. Microinfarcts were also associated with lower average global cognition (estimate, -0.287; SE, 0.113; P=0.012), particularly for persons with multiple cortical microinfarcts. Microinfarcts were specifically associated with lower episodic memory (estimate, -0.279; SE, 0.138; P=0.044), semantic memory (estimate, -0.391; SE, 0.130; P=0.003), and perceptual speed (estimate, -0.400; SE, 0.117; P<0.001). In addition, single, multiple, and cortical microinfarcts were associated with worse semantic memory and perceptual speed (all P<0.028). Neither macroscopic infarcts nor AD pathology modified these associations (all P>0.154). CONCLUSIONS{MDASH}: Microinfarcts are common, and persons with multiple cortical microinfarcts have higher odds of dementia. Microinfarcts are also associated with lower cognition, specifically perceptual speed and semantic and episodic memory. Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in community-dwelling older persons. Four hundred twenty-five subjects enrolled in the Religious Orders Study underwent annual clinical evaluations, including 19 neuropsychological tests and assessment for dementia, and brain autopsy (39% men; mean age at death, 87; Mini-Mental State Examination score, 21). Neuropathologic examination documented the presence, number, and location of chronic microinfarcts on 6-μm hematoxylin-eosin-stained sections from cortical and subcortical regions. Multiple regression analyses adjusted for age at death, sex, education, macroscopic infarcts, Alzheimer disease pathology, and Lewy bodies. Microinfarcts were present in 129 of 425 (30%) persons (54 cortical, 80 subcortical, 49 multiple); 58 of 129 (45%) of persons with microinfarcts did not exhibit macroscopic infarcts. Persons with microinfarcts had increased odds of dementia (OR, 1.77; 95% CI, 1.07-2.92), especially those persons with multiple cortical microinfarcts. Microinfarcts were also associated with lower average global cognition (estimate, -0.287; SE, 0.113; P=0.012), particularly for persons with multiple cortical microinfarcts. Microinfarcts were specifically associated with lower episodic memory (estimate, -0.279; SE, 0.138; P=0.044), semantic memory (estimate, -0.391; SE, 0.130; P=0.003), and perceptual speed (estimate, -0.400; SE, 0.117; P<0.001). In addition, single, multiple, and cortical microinfarcts were associated with worse semantic memory and perceptual speed (all P<0.028). Neither macroscopic infarcts nor AD pathology modified these associations (all P>0.154). Microinfarcts are common, and persons with multiple cortical microinfarcts have higher odds of dementia. Microinfarcts are also associated with lower cognition, specifically perceptual speed and semantic and episodic memory. Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in community-dwelling older persons.BACKGROUND AND PURPOSELittle is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in community-dwelling older persons.Four hundred twenty-five subjects enrolled in the Religious Orders Study underwent annual clinical evaluations, including 19 neuropsychological tests and assessment for dementia, and brain autopsy (39% men; mean age at death, 87; Mini-Mental State Examination score, 21). Neuropathologic examination documented the presence, number, and location of chronic microinfarcts on 6-μm hematoxylin-eosin-stained sections from cortical and subcortical regions. Multiple regression analyses adjusted for age at death, sex, education, macroscopic infarcts, Alzheimer disease pathology, and Lewy bodies.METHODSFour hundred twenty-five subjects enrolled in the Religious Orders Study underwent annual clinical evaluations, including 19 neuropsychological tests and assessment for dementia, and brain autopsy (39% men; mean age at death, 87; Mini-Mental State Examination score, 21). Neuropathologic examination documented the presence, number, and location of chronic microinfarcts on 6-μm hematoxylin-eosin-stained sections from cortical and subcortical regions. Multiple regression analyses adjusted for age at death, sex, education, macroscopic infarcts, Alzheimer disease pathology, and Lewy bodies.Microinfarcts were present in 129 of 425 (30%) persons (54 cortical, 80 subcortical, 49 multiple); 58 of 129 (45%) of persons with microinfarcts did not exhibit macroscopic infarcts. Persons with microinfarcts had increased odds of dementia (OR, 1.77; 95% CI, 1.07-2.92), especially those persons with multiple cortical microinfarcts. Microinfarcts were also associated with lower average global cognition (estimate, -0.287; SE, 0.113; P=0.012), particularly for persons with multiple cortical microinfarcts. Microinfarcts were specifically associated with lower episodic memory (estimate, -0.279; SE, 0.138; P=0.044), semantic memory (estimate, -0.391; SE, 0.130; P=0.003), and perceptual speed (estimate, -0.400; SE, 0.117; P<0.001). In addition, single, multiple, and cortical microinfarcts were associated with worse semantic memory and perceptual speed (all P<0.028). Neither macroscopic infarcts nor AD pathology modified these associations (all P>0.154).RESULTSMicroinfarcts were present in 129 of 425 (30%) persons (54 cortical, 80 subcortical, 49 multiple); 58 of 129 (45%) of persons with microinfarcts did not exhibit macroscopic infarcts. Persons with microinfarcts had increased odds of dementia (OR, 1.77; 95% CI, 1.07-2.92), especially those persons with multiple cortical microinfarcts. Microinfarcts were also associated with lower average global cognition (estimate, -0.287; SE, 0.113; P=0.012), particularly for persons with multiple cortical microinfarcts. Microinfarcts were specifically associated with lower episodic memory (estimate, -0.279; SE, 0.138; P=0.044), semantic memory (estimate, -0.391; SE, 0.130; P=0.003), and perceptual speed (estimate, -0.400; SE, 0.117; P<0.001). In addition, single, multiple, and cortical microinfarcts were associated with worse semantic memory and perceptual speed (all P<0.028). Neither macroscopic infarcts nor AD pathology modified these associations (all P>0.154).Microinfarcts are common, and persons with multiple cortical microinfarcts have higher odds of dementia. Microinfarcts are also associated with lower cognition, specifically perceptual speed and semantic and episodic memory.CONCLUSIONSMicroinfarcts are common, and persons with multiple cortical microinfarcts have higher odds of dementia. Microinfarcts are also associated with lower cognition, specifically perceptual speed and semantic and episodic memory. |
Author | Leurgans, Sue E. Schneider, Julie A. Barnes, Lisa L. Arvanitakis, Zoe Bennett, David A. |
AuthorAffiliation | 4 Department of Pathology, Rush University Medical Center, Chicago, IL 3 Department of Behavioral Sciences, Rush University Medical Center, Chicago, IL 2 Department of Neurological Sciences, Rush University Medical Center, Chicago, IL 1 Rush Alzheimer’s Disease Center, Rush University Medical Center, Chicago, IL |
AuthorAffiliation_xml | – name: 1 Rush Alzheimer’s Disease Center, Rush University Medical Center, Chicago, IL – name: 3 Department of Behavioral Sciences, Rush University Medical Center, Chicago, IL – name: 2 Department of Neurological Sciences, Rush University Medical Center, Chicago, IL – name: 4 Department of Pathology, Rush University Medical Center, Chicago, IL |
Author_xml | – sequence: 1 givenname: Zoe surname: Arvanitakis fullname: Arvanitakis, Zoe organization: From the Rush Alzheimer's Disease Center (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Neurological Sciences (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Behavioral Sciences (L.L.B.), and Department of Pathology (J.A.S.), Rush University Medical Center, Chicago, IL – sequence: 2 givenname: Sue E. surname: Leurgans fullname: Leurgans, Sue E. organization: From the Rush Alzheimer's Disease Center (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Neurological Sciences (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Behavioral Sciences (L.L.B.), and Department of Pathology (J.A.S.), Rush University Medical Center, Chicago, IL – sequence: 3 givenname: Lisa L. surname: Barnes fullname: Barnes, Lisa L. organization: From the Rush Alzheimer's Disease Center (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Neurological Sciences (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Behavioral Sciences (L.L.B.), and Department of Pathology (J.A.S.), Rush University Medical Center, Chicago, IL – sequence: 4 givenname: David A. surname: Bennett fullname: Bennett, David A. organization: From the Rush Alzheimer's Disease Center (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Neurological Sciences (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Behavioral Sciences (L.L.B.), and Department of Pathology (J.A.S.), Rush University Medical Center, Chicago, IL – sequence: 5 givenname: Julie A. surname: Schneider fullname: Schneider, Julie A. organization: From the Rush Alzheimer's Disease Center (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Neurological Sciences (Z.A., S.E.L., L.L.B., D.A.B., J.A.S.), Department of Behavioral Sciences (L.L.B.), and Department of Pathology (J.A.S.), Rush University Medical Center, Chicago, IL |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23916830$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/21212395$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/0022-510X(70)90063-8 10.3233/JAD-2009-1178 10.1161/01.str.0000237236.88823.47 10.1136/jnnp.73.6.672 10.1016/S0140-6736(00)03589-3 10.1212/01.wnl.0000271090.28148.24 10.3233/JAD-2009-1227 10.1097/WAD.0b013e318199fc7a 10.1212/01.WNL.0000055863.87435.B2 10.1002/ana.21413 10.1212/WNL.59.2.198 10.1002/ana.21706 10.1111/j.1749-6632.2000.tb06373.x 10.1161/01.str.0000110791.51378.4e 10.1111/j.1749-6632.2002.tb04794.x 10.1002/ana.21208 10.1037/0882-7974.17.2.179 10.1212/WNL.39.9.1159 10.1212/01.WNL.0000042478.08543.F7 10.1002/ana.21142 10.1212/WNL.34.7.939 10.3233/JAD-2009-1182 10.1097/WAD.0b013e3181a6bed5 10.1056/NEJMoa070972 10.1093/jnen/59.11.931 |
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Snippet | Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global cognition, and 5 cognitive systems in... BACKGROUND AND PURPOSE{MDASH}: Little is known about the role of microinfarcts in dementia and cognition. We examined microinfarcts and dementia, global... |
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SubjectTerms | Age Aged Aged, 80 and over Alzheimer Disease - etiology Alzheimer Disease - pathology Alzheimer's disease Autopsy Biological and medical sciences Brain Cerebral Infarction - complications Cerebral Infarction - diagnosis Cerebral Infarction - pathology Cognition Disorders - diagnosis Cognition Disorders - etiology Cognition Disorders - pathology Cognitive ability Dementia - diagnosis Dementia - etiology Dementia - pathology Dementia disorders Female Follow-Up Studies Humans Lewy bodies Longitudinal Studies Male Medical sciences Memory Metabolic diseases Microcirculation Multiple regression analysis Neurodegenerative diseases Neurology Other metabolic disorders Pigments (porphyrias, hyperbilirubinemias...) Semantics Stroke Vascular diseases and vascular malformations of the nervous system |
Title | Microinfarct Pathology, Dementia, and Cognitive Systems |
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