Evidence map›Paper›PMID 40471971›Full record

Observational studyPloS one2025

Vascular dysfunction is associated with major adverse cardiovascular events in prediabetes: A cohort study.

Dariya Kozlova, Colin Gimblet, Linder Wendt, Sadaf Akbari, Adeyinka Taiwo, Sanjana Dayal, Patrick Ten Eyck, Anna Stanhewicz, Joel Trinity, Diana Jalal

Abstract readObservational Study
In one paragraph

Observational study in PloS one, 2025. 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

10 authors.

Dariya KozlovaDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America.
Colin GimbletDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America.
Linder WendtInstitute for Clinical and Translational Science, University of Iowa, Iowa City, Iowa, United States of America.ORCID https://orcid.org/0000-0003-1832-0486
Sadaf AkbariDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America.ORCID https://orcid.org/0000-0003-2485-7693
Adeyinka TaiwoDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America.
Sanjana DayalDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America.
Patrick Ten EyckInstitute for Clinical and Translational Science, University of Iowa, Iowa City, Iowa, United States of America.ORCID https://orcid.org/0000-0002-5041-0708
Anna StanhewiczDepartment of Health and Human Physiology, University of Iowa, Iowa City, Iowa, United States of America.
Joel TrinityDepartment of Medicine, University of Utah, Salt Lake City, Utah, United States of America.
Diana JalalDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America.ORCID https://orcid.org/0000-0002-1975-8650

Funding

University of Iowa Institute for Clinical and Translational ScienceUM1TR004403 · NCATS · UNIVERSITY OF IOWA · PI Marlan R Hansen, Patricia Winokur · 2023 to 2026
$16.1M
BLRD VA I01 BX007087NCATS NIH HHS UM1 TR004403
6 · The paper itself

Abstract

backgroundPrediabetes is a growing public health concern that increases the risk of major adverse cardiovascular events (MACE). Vascular dysfunction worsens with hyperglycemia and is associated with MACE in several high-risk populations. However, it is unknown whether vascular dysfunction contributes to MACE in prediabetes. We hypothesized that vascular dysfunction is associated with elevated risk of MACE in prediabetes.

methodsWe conducted an observational study of 5742 adults (age 54.9 ± 11.5 years, 54% female) in the Framingham Offspring and Generation III cohorts. Prediabetes was defined using the ADA criteria. Endothelial function was determined via brachial artery flow-mediated dilation (BA-FMD), aortic stiffness via carotid-femoral pulse wave velocity (cfPWV), and coronary artery calcium (CAC) score via computed tomography. Stepwise selection models evaluated BA-FMD, cfPWV, and CAC score by prediabetes status. The association of BA-FMD, cfPWV, and CAC score with time to MACE was assessed via Cox proportional hazards regression.

resultsIndividuals with prediabetes had lower BA-FMD and higher cfPWV and CAC score (p < 0.001). In stepwise selection models, age, sex, smoking history, systolic blood pressure, triglycerides, high-density lipoprotein, low-density lipoprotein, and fasting glucose related to vascular dysfunction. After adjusting for traditional cardiovascular risk factors, BA-FMD (HR [95% CI], 0.93 [0.90,0.97]; p < 0.001) and CAC score >100 [HR [95% CI], 4.15 [2.24, 7.70]; p < 0.001)] were associated with MACE in prediabetes while cfPWV was not (p = 0.051).

conclusionsVascular dysfunction measured by BA-FMD independently associates with MACE in prediabetes. Therapies that target vascular dysfunction may reduce CVD risk in prediabetes.

Indexed as

Cardiovascular DiseasesPrediabetic StateAdultAgedBrachial ArteryCohort StudiesEndothelium, VascularFemaleHumansMaleMiddle AgedPulse Wave AnalysisRisk FactorsVascular Stiffness

Identifiers

PMID40471971
PMCPMC12140275

What Socratic holds

Textmetadata
LicenceCC0
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 Socratic graph.