Evidence map›Paper›PMID 41285406›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2026

Chronic kidney disease and cardiac remodeling potentiate cognitive impairment progression: disentangling the sex-specific cross talk of kidney-heart-brain axis.

Sneha S Pillai, Christopher H Morrell, Carla Rocha Dos Santos, Hari Vishal Lakhani, Bruno De Souza Goncalves, Duane G Pereira, Amrit Thakur, Ellen Thompson, Wen Wei, Asma Nayyar and 5 more

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

15 authors.

Sneha S PillaiDepartment of Surgery and Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.ORCID 0000-0001-5209-4836
Christopher H MorrellLaboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, United States.ORCID 0000-0001-5080-7142
Carla Rocha Dos SantosLaboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, United States.ORCID 0009-0005-7424-0626
Hari Vishal LakhaniDepartment of Surgery and Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.ORCID 0000-0002-5308-2164
Bruno De Souza GoncalvesDepartment of Surgery and Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.
Duane G PereiraDepartment of Surgery and Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.
Amrit ThakurDepartment of Cardiology, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.
Ellen ThompsonDepartment of Cardiology, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.ORCID 0000-0002-4029-5398
Wen WeiLaboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, United States.
Asma NayyarDepartment of Internal Medicine, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.
Zeid J KhitanDepartment of Nephrology, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.ORCID 0000-0003-1607-770X
Joseph I ShapiroDepartment of Medicine, University of Toledo, Toledo, Ohio, United States.
Edward G LakattaLaboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, United States.ORCID 0000-0002-4772-0035
Komal SodhiDepartment of Surgery and Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, United States.
Olga V FedorovaLaboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, United States.ORCID 0000-0002-2991-5285

Funding

Exploring the involvement of Na pump inhibitor marinobufagenin in the interactions between age-associated vascular and neurodegenerative processes in cognitive impairment and Alzheimer's diseaseZIAAG000846 · NIA · NATIONAL INSTITUTE ON AGING · PI FEDOROVA, OLGA V · 2016 to 2025
$17.7M
Sodium pump ligands in blood pressure regulation and profibrotic signaling in hypertension, chronic kidney disease and aging in males and femalesZIAAG000609 · NIA · NATIONAL INSTITUTE ON AGING · PI FEDOROVA, OLGA V · 2009 to 2025
$17.3M
SODIUM PUMP INHIBITORS IN CARDIOVASCULAR CONTROLZ01AG000609 · NIA · NATIONAL INSTITUTE ON AGING · PI BAGROV, ALEXEI Y · 1993 to 2008
$1.2M
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01 HL164460-01A1HHS | NIH | National Institute on Aging (NIA)Intramural NIH HHS Z01 AG000609Intramural NIH HHS Z99 AG999999Intramural NIH HHS ZIA AG000609Intramural NIH HHS ZIA AG000846Office of Research on Women's Health (ORWH) 736214
6 · The paper itself

Abstract

Chronic kidney disease (CKD)-mediated oxidative stress, uremic toxicity, inflammation, and cardiovascular (CV) damage connect the kidney-heart-brain axis that contributes to cognitive impairment (CI) and progression to major neurological disorders. Although the sex disparity has a profound impact on CKD epidemiology, its role in the progression of CI needs to be elucidated in detail. The present study aims to unravel the sex-specific cross talk of the kidney-heart-brain axis in CKD. CKD and control subjects, equally represented by both sexes, were included in a cross-sectional study that involved a community-dwelling rural population. CV and CKD parameters, Mini-Mental State Examination (MMSE), markers of fibrosis and neurodegeneration were assessed. We elucidated the sex-specific associations among these factors through linear regression and structural equation modeling (SE), or Path, analyses. Patients with CKD have higher blood pressure versus controls, and men with CKD exhibited a decline in cardiac function versus sex- and age-matched controls. Both men and women with CKD had lower MMSE scores versus controls, although cognitive performance in women with CKD was significantly better than that of men with CKD. Path analysis revealed a direct association of the plasma phosphorylated Tau protein (pTau) and the ratio of amyloid β-42 to amyloid β-40 with MMSE scores in women only. Pro-brain natriuretic peptide and pTau were associated with short-term memory, a part of the MMSE assessment, also in women only. Our findings will broaden the current understanding and clinical consequences of the pathophysiological interactions between kidney and CV damage with brain function in a sex-dependent manner that could prompt innovative pharmacological interventions.

Indexed as

BrainCognitionCognitive DysfunctionKidneyRenal Insufficiency, ChronicVentricular RemodelingAgedBiomarkersCase-Control StudiesCross-Sectional StudiesDisease ProgressionFemaleHumansMaleMiddle AgedRisk FactorsBiomarkersMAPT protein, humantau Proteinscardiovascular diseasechronic kidney diseasecognitive impairmentfluid biomarkerswoman’s health

Identifiers

PMID41285406
PMCPMC13268786

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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.