Evidence map›Paper›PMID 28350821›Full record

ArticlePLoS medicine2017

Neuropathological diagnoses and clinical correlates in older adults in Brazil: A cross-sectional study.

Claudia K Suemoto, Renata E L Ferretti-Rebustini, Roberta D Rodriguez, Renata E P Leite, Luciana Soterio, Sonia M D Brucki, Raphael R Spera, Tarcila M Cippiciani, Jose M Farfel, Alexandre Chiavegatto Filho and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
8.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

88 citing papers in PubMed, 144 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The landscape of dementia research, diagnosis, treatment, and care in Latin America.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  8. Apolipoprotein E and Alzheimer's disease pathology in a diverse autopsy study.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  9. Celebrating neuropathology's contributions to Alzheimer's Disease Research Centers.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  10. Co-pathology in Alzheimer's disease and Lewy body disease and its association with neuropsychiatric symptoms.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  11. Lewy Body Dementia Research in Latin America: A Scoping Review.Movement disorders clinical practice · 2025
    Article
  12. Circulating Biomarkers for the Early Diagnosis of Alzheimer's Disease.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Gaps in biomedical research in frontotemporal dementia: A call for diversity and disparities focused research.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Review
  19. Article
  20. Article

28 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 1 institution in 2 countries.

Claudia K SuemotoBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.
Renata E L Ferretti-RebustiniBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.
Roberta D RodriguezBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.ORCID 0000-0002-6544-7861
Renata E P LeiteBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.ORCID 0000-0002-5878-398X
Luciana SoterioBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.ORCID 0000-0002-9399-8062
Sonia M D BruckiDepartment of Neurology, University of São Paulo Medical School, São Paulo, Brazil.ORCID 0000-0002-8303-6732
Raphael R SperaDepartment of Neurology, University of São Paulo Medical School, São Paulo, Brazil.ORCID 0000-0003-3066-3457
Tarcila M CippicianiDepartment of Neurology, University of São Paulo Medical School, São Paulo, Brazil.
Jose M FarfelBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.
Alexandre Chiavegatto FilhoDepartment of Epidemiology, School of Public Health, University of São Paulo, São Paulo, Brazil.
Michel Satya NaslavskyHuman Genome and Stem Cell Center, Biosciences Institute, University of São Paulo, São Paulo, Brazil.
Mayana ZatzHuman Genome and Stem Cell Center, Biosciences Institute, University of São Paulo, São Paulo, Brazil.ORCID 0000-0003-3970-8025
Carlos A PasqualucciBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.
Wilson Jacob-FilhoBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.
Ricardo NitriniBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.
Lea T GrinbergBrazilian Aging Brain Study Group, University of São Paulo Medical School, São Paulo, Brazil.ORCID 0000-0002-6809-0618
Universidade de São Paulo · BR

Funding

Neuropathological changes underlying clinical heterogeneity in Alzheimer diseaseK24AG053435 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRINBERG, LEA TENENHOLZ · 2016 to 2025
$1.8M
NIA NIH HHS K24 AG053435
6 · The paper itself

Abstract

backgroundClinicopathological studies are important in determining the brain lesions underlying dementia. Although almost 60% of individuals with dementia live in developing countries, few clinicopathological studies focus on these individuals. We investigated the frequency of neurodegenerative and vascular-related neuropathological lesions in 1,092 Brazilian admixed older adults, their correlation with cognitive and neuropsychiatric symptoms, and the accuracy of dementia subtype diagnosis. METHODS AND

findingsIn this cross-sectional study, we describe clinical and neuropathological variables related to cognitive impairment in 1,092 participants (mean age = 74 y, 49% male, 69% white, and mean education = 4 y). Cognitive function was investigated using the Clinical Dementia Rating (CDR) and the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE); neuropsychiatric symptoms were evaluated using the Neuropsychiatric Inventory (NPI). Associations between neuropathological lesions and cognitive impairment were investigated using ordinal logistic regression. We developed a neuropathological comorbidity (NPC) score and compared it to CDR, IQCODE, and NPI scores. We also described and compared the frequency of neuropathological diagnosis to clinical diagnosis of dementia subtype. Forty-four percent of the sample met criteria for neuropathological diagnosis. Among these participants, 50% had neuropathological diagnoses of Alzheimer disease (AD), and 35% of vascular dementia (VaD). Neurofibrillary tangles (NFTs), hippocampal sclerosis, lacunar infarcts, hyaline atherosclerosis, siderocalcinosis, and Lewy body disease were independently associated with cognitive impairment. Higher NPC scores were associated with worse scores in the CDR sum of boxes (β = 1.33, 95% CI 1.20-1.46), IQCODE (β = 0.14, 95% CI 0.13-0.16), and NPI (β = 1.74, 95% CI = 1.33-2.16). Compared to neuropathological diagnoses, clinical diagnosis had high sensitivity to AD and high specificity to dementia with Lewy body/Parkinson dementia. The major limitation of our study is the lack of clinical follow-up of participants during life.

conclusionsNFT deposition, vascular lesions, and high NPC scorewere associated with cognitive impairment in a unique Brazilian sample with low education. Our results confirm the high prevalence of neuropathological diagnosis in older adults and the mismatch between clinical and neuropathological diagnoses.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseBrazilCognitionCross-Sectional StudiesDementiaDementia, VascularFemaleHumansMaleMiddle Aged

Identifiers

PMID28350821
PMCPMC5369698
OpenAlexW2602399996

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.