Evidence map›Paper›PMID 40878761›Full record

ArticleAmerican journal of hypertension2026

Associations of Blood Pressure Level and Variability With Cortical Thickness: A Cross-Sectional Analysis From the Maracaibo Aging Study.

Romeo De Leon, Shana Garza, Silvia Mejia-Arango, Kristina P Vatcheva, Sokratis Charisis, Claudia Satizabal, Luis J Mena, Joseph H Lee, Joseph D Terwilliger, Eron Manusov and 5 more

Abstract read
In one paragraph

Article in American journal of hypertension, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Romeo De LeonInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.
Shana GarzaInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.
Silvia Mejia-ArangoInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.
Kristina P VatchevaInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.
Sokratis CharisisGlenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases, UT Health San Antonio, San Antonio, Texas, USA.
Claudia SatizabalSouth Texas Alzheimer's Disease Research Center, Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Luis J MenaAcademic Unit of Information Technology Engineering, Polytechnic University of Sinaloa, Mazatlán, Mexico.
Joseph H LeeTaub Institute for Research on Alzheimer's Disease and the Aging Brain, Department of Neurology, Columbia University, New York, New York, USA.
Joseph D TerwilligerTaub Institute for Research on Alzheimer's Disease and the Aging Brain, Department of Neurology, Columbia University, New York, New York, USA.
Eron ManusovInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.
Sudha SeshadriSouth Texas Alzheimer's Disease Research Center, Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Jose GutierrezDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA.
Gladys E MaestreInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.
Adam M BrickmanTaub Institute for Research on Alzheimer's Disease and the Aging Brain, Department of Neurology, Columbia University, New York, New York, USA.ORCID 0000-0002-5125-8226
Jesus D MelgarejoInstitute of Neuroscience, Neuro and Behavioral Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.ORCID 0000-0002-1382-1153

Funding

Research Education CoreP30AG066462 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Andrew Franklin Teich · 2020 to 2026
$30.1M
South Texas Alzheimer's Disease Research CenterP30AG066546 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Sudha Seshadri · 2021 to 2026
$24.0M
Rio Grande Valley Alzheimer's Resource Center for Minority Aging Research: Partnerships for ProgressP30AG059305 · NIA · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI Gladys E. Maestre · 2018 to 2026
$5.8M
Integration of Socio-Spatial Data for Neighborhoods with Multi-omic profiles to Identify and Mitigate Factors Affecting Risk of ALzheimer's DiseaseDP1AG069870 · NIA · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI MAESTRE, GLADYS E. · 2020 to 2024
$3.6M
Gene-Environment Interactions in Cognition in Venezuelan FamiliesR01AG036469 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHACON, INARA, MAESTRE, GLADYS E. · 2011 to 2015
$2.7M
A longitudinal study of mid-to late-life blood pressure profiles as risk factors for Alzheimer´s disease in HispanicsR03AG054186 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAESTRE, GLADYS E., TERWILLIGER, JOSEPH DOUGLAS · 2016 to 2017
$163k
American Heart Association Career Development Award 25CDA1456235NIA NIH HHS DP1 AG069870NIA NIH HHS DP1AG069870NIA NIH HHS P30 AG059305NIA NIH HHS P30AG059305NIA NIH HHS P30 AG066462NIA NIH HHS P30 AG066546NIA NIH HHS P30AG066546NIA NIH HHS R01 AG036469NIA NIH HHS R01AG036469NIA NIH HHS R03 AG054186NIA NIH HHS R03AG054186NIH HHS
6 · The paper itself

Abstract

backgroundAlthough high blood pressure (BP) level and variability are associated with Alzheimer's disease (AD), their relationship with cortical thickness in brain regions that are associated with AD is unclear. Furthermore, the role of 24-h BP has not been examined. We investigated the associations of office and ambulatory BP measures with cortical thickness in brain regions implicated in AD.

methodsWe performed a cross-sectional analysis of 304 participants without dementia from a population-based study with office and 24-h BP and magnetic resonance imaging data. We considered cortical thickness values derived from 10 regions throughout the frontal, parietal, and temporal lobes, and the posterior cingulate cortex that are associated with risk and progression of AD. The association between BP and cortical thickness was tested using adjusted linear regression models.

resultsThe mean age was 58.1 years and 231 (76%) were women. Higher office systolic BP was associated with thinner temporal (β = -0.059; 95% confidence interval [CI], -0.112, -0.005) and posterior cingulate cortex (β = -0.095; 95% CI, -0.145, -0.045). 24-h and nighttime BP levels were associated with thinner seven regions, with β-estimates ranging from -0.103 (95% CI, -0.182, -0.012) to -0.045 (95% CI, -0.080, -0.010). A higher 24-h BP variability was associated with thinner middle frontal (β = -0.156; 95% CI, -0.282, -0.030) and middle temporal (β = -0.146; 95% CI, -0.268, -0.024) gyri, and posterior cingulate cortex (β = -0.134; 95% CI, -0.026, -0.009).

conclusionsIncreased ambulatory BP level and variability are associated with cortical thinning in regions associated with AD. Better BP evaluation with out-of-office approaches might reduce brain structural changes associated with AD.

Indexed as

AgingAlzheimer DiseaseBlood PressureBrain Cortical ThicknessCerebral CortexHypertensionAgedAge FactorsBlood Pressure Monitoring, AmbulatoryCircadian RhythmCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedAD signaturesambulatory blood pressure monitoringblood pressureblood pressure levelblood pressure variabilitybrain MRIhypertensionpopulation-based study

Identifiers

PMID40878761
PMCPMC12802946

What OpenQuestion holds

Textmetadata
LicenceTDM
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.