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Table 1 Community-based, autopsy studies are required to estimate the prevalence and incidence of mixed Alzheimer disease/vascular brain injury

From: Clinical and imaging features of mixed Alzheimer and vascular pathologies

Autopsy study

N

Mean age (years)

Diagnosis of AD

Diagnosis of VBI or VCI

Prevalence of mixed

Interaction between VBI and AD on risk of dementia

Neuropsychology

Nun Study [7]

102

87 (76-100)

Khachaturian plaque criteria

Number of infarcts > or <1.5 cm

39% (24/61) of dementia cases were mixed

Number of tangles and number of lacunes exert independent additive effect on MMSE and likelihood of dementia

MMSE

CERAD

ROS [8,9]

550

87

Mean number of neurofibrillary tangles, neuritic plaques, and diffuse plaques in five lobes

Number of macroscopic and microscopic infarcts

28% of dementia cases were mixed

AD and VBI pathology have additive effect on odds of dementia

 

MAP [8,9]

425

87

Mean number of neurofibrillary tangles, neuritic plaques, and diffuse plaques in five lobes

Number of macroscopic and microscopic infarcts

44% of dementia cases were mixed

  

BLSA [10]

179

87.6 ± 7.1

CERAD

Macroscopic infarcts

Hemispheral infarcts alone or with AD account for 35% of dementia cases

In subjects with intermediate AD pathology scores, a single macroscopic hemispheral infarct was sufficient to cause dementia

Blessed Memory Information Concentration Test

Braak and Braak stage

Microscopic infarcts

BLSA [11]

200

Atherosclerosis (0-3) of coronary, aorta, and intracranial vessels

45% have remote infarct

68% of cases have atherosclerosis, which increased the odds of dementia independent of AD pathology or cerebral infarcts

175 complete autopsies, including heart and aorta

MRC CFAS [12]

N = 456

87 (SD = 7): range 66 to 100 (63% ≥85)

CERAD scale (0-3)

Regional infarcts (>1 cm)

 

Association between AD pathology and cognitive status goes down with age

MMSE

243 dementia

Diffuse plaques, neuritic plaques, tangles, atrophy

AGECAT

183 without dementia

Small vessel disease: lacunes, microinfarcts, white matter change

Association between atrophy and age continues to go up

30 unknown

MRC CFAS [13]

Self-reported vascular risk factors

 

Vascular risk factors were not associated with an increased burden of AD pathology at death in old age

26% of non dementia cases had CVA; 43% of dementia cases had CVA

CC75 + C [14]

224

91

CERAD

 

22% of 113 dementia cases

  

Hisayama [15]

N = 469

 

CERAD

NINDS-AIREN

4.7% of dementia cases were mixed

  

275 incident dementia cases

NIA-Reagan

(164 autopsies)

HAAS [16]

N = 443

86 ± 5.2

Mean number of neurofibrillary tangles and neuritic plaques over 20 fields in 4 lobes

High correlations noted between MBIs and lacunar infarcts (Spearman r = 0.45, P < 0.0001)

14.2% of dementia cases were mixed

No correlation between AD and microvascular lesions

CASI

(72-90+)

HAAS [17]

N = 436

 

Number of infarcts > or <1.0 cm, microinfarcts

MBI found in 72% of demented and 61% of non-demented

144 with dementia

292 without dementia

MBI and AD exert independent additive effects on cognition

  1. AD, Alzheimer disease; AGECAT, Automated Geriatric Examination for Computer Assisted Taxonomy; BLSA, Baltimore Longitudinal Aging Study; CASI, Cognitive Abilities Screening Instrument; CC75 + C, Cambridge City Over-75 s Cohort; CERAD, Consortium to Establish a Registry for Alzheimer Disease; CFAS, Cognitive Function and Ageing Study; CVA, cerebrovascular accident; HAAS, Honolulu Asia Aging Study; MAP, Rush Memory and Aging Project; MBI, microscopic brain infarct; MMSE, Mini-Mental State Exam; MRC, Medical Research Council; NIA, National Institute on Aging; NINDS-AIREN, National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche et l’Enseignement en Neurosciences; ROS, Rush Religious Order Study; SD, standard deviation; VBI, vascular brain injury; VCI, vascular cognitive impairment.