Evidence map›Paper›PMID 39541803›Full record

ArticleNeurobiology of aging2025

Hypertension may associate with cerebral small vessel disease and infarcts through the pathway of intracranial atherosclerosis.

Marcelo Kenzo Naya Takahashi, Regina Silva Paradela, Lea Tenenholz Grinberg, Renata Elaine Paraizo Leite, Daniela Souza Farias-Itao, Vitor Ribeiro Paes, Maria Eduarda Braga, Michel Satya Naslavsky, Mayana Zatz, Wilson Jacob-Filho and 3 more

Abstract read
In one paragraph

Article in Neurobiology of aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
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

13 authors.

Marcelo Kenzo Naya TakahashiDivision of Geriatrics, University of Sao Paulo Medical School, Sao Paulo 01246-903, Brazil.
Regina Silva ParadelaDivision of Geriatrics, University of Sao Paulo Medical School, Sao Paulo 01246-903, Brazil.
Lea Tenenholz GrinbergDepartment of Pathology, University of São Paulo Medical School, Sao Paulo, SP 01246-903, Brazil; Memory and Aging Center, Weill Institute for Neurosciences, Dept. of Neurology, University of California San Francisco, CA 94158, USA.
Renata Elaine Paraizo LeiteDepartment of Pathology, University of São Paulo Medical School, Sao Paulo, SP 01246-903, Brazil.
Daniela Souza Farias-ItaoDepartment of Pathology, University of São Paulo Medical School, Sao Paulo, SP 01246-903, Brazil.
Vitor Ribeiro PaesDepartment of Pathology, University of São Paulo Medical School, Sao Paulo, SP 01246-903, Brazil.
Maria Eduarda BragaDivision of Geriatrics, University of Sao Paulo Medical School, Sao Paulo 01246-903, Brazil.
Michel Satya NaslavskyHuman Genome and Stem Cell Center, Biosciences Institute, University of Sao Paulo, Sao Paulo 05508-090, Brazil.
Mayana ZatzHuman Genome and Stem Cell Center, Biosciences Institute, University of Sao Paulo, Sao Paulo 05508-090, Brazil.
Wilson Jacob-FilhoDivision of Geriatrics, University of Sao Paulo Medical School, Sao Paulo 01246-903, Brazil.
Ricardo NitriniDepartment of Neurology, University of Sao Paulo Medical School, SP 01246-903, Brazil.
Carlos Augusto PasqualucciDepartment of Pathology, University of São Paulo Medical School, Sao Paulo, SP 01246-903, Brazil.
Claudia Kimie SuemotoDivision of Geriatrics, University of Sao Paulo Medical School, Sao Paulo 01246-903, Brazil. Electronic address: cksuemoto@usp.br.

Funding

Clinical Features and Neuropathological Basis of Sleep Wake Behavior in Alzheimer's and PSPR01AG060477 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Lea Tenenholz Grinberg, Thomas C Neylan · 2019 to 2026
$8.2M
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 AG053435NIA NIH HHS R01 AG060477
6 · The paper itself

Abstract

Hypertension, a major modifiable risk factor for cardiovascular diseases, is linked to late-life neurocognitive disorders such as vascular dementia and Alzheimer's disease (AD). This study explores the associations between hypertension, intracranial atherosclerotic disease (ICAD), cerebral small vessel disease (cSVD), and Alzheimer's disease neuropathologic change (ADNC) in a large community-based autopsy study. This cross-sectional study used data from the Biobank for Aging Studies of the University of São Paulo Medical School. Sociodemographic and clinical information was gathered from a reliable next-of-kin informant. Neurofibrillary tangles, neuritic plaques, lacunar infarcts, hyaline arteriolosclerosis, and cerebral amyloid angiopathy were evaluated. Causal mediation analyses with natural effect models were performed to examine indirect associations of hypertension with cerebrovascular pathologies and ADNC through morphometric measurements of intracranial artery lumen obstruction. Hypertensive participants (n = 354) presented a higher rate of stenosed arteries (obstruction ≥ 50 %), critically stenosed arteries (obstruction ≥ 70 %), and more severe ICAD, shown by higher maximum and mean obstruction indexes compared to nonhypertensive participants (n = 166). These measurements of atherosclerosis were associated with neurofibrillary tangles and cSVD lesions. Hypertension was indirectly associated with hyaline arteriolosclerosis and lacunar infarcts through the pathway of ICAD. Presenting hypertension indirectly increased the odds of displaying hyaline arteriolosclerosis by 26 % (95 % CI: 1.08, 1.45, p = 0.002) and lacunar infarcts by 17 % (95 % CI: 1.01, 1.35, p = 0.029). Cognitive and APOE ε4 carrier status did not alter the investigated associations. In this community sample, hypertension was indirectly associated with cSVD through ICAD.

Indexed as

Alzheimer DiseaseCerebral Small Vessel DiseasesHypertensionIntracranial ArteriosclerosisAgedAged, 80 and overCross-Sectional StudiesFemaleHumansMaleMiddle AgedNeurofibrillary TanglesBlood pressureCircle of WillisDementiaNeuropathologySmall vessel disease

Identifiers

PMID39541803
PMCPMC11864294

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.