Evidence map›Paper›PMID 33834868›Full record

ReviewAmerican journal of physiology. Heart and circulatory physiology2021

Mitochondrial contributions to vascular endothelial dysfunction, arterial stiffness, and cardiovascular diseases.

Danielle L Kirkman, Austin T Robinson, Matthew J Rossman, Douglas R Seals, David G Edwards

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Heart and circulatory physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
6.3field-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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 127 citations in OpenAlex.

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36 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

5 authors at 4 institutions in 1 country.

Danielle L KirkmanDepartment of Kinesiology and Health Sciences, Virginia Commonwealth University, Richmond, Virginia.ORCID 0000-0003-1648-0662
Austin T RobinsonSchool of Kinesiology, Auburn University, Auburn, Alabama.ORCID 0000-0001-8250-3952
Matthew J RossmanDepartment of Integrative Physiology, University of Colorado, Boulder, Colorado.
Douglas R SealsDepartment of Integrative Physiology, University of Colorado, Boulder, Colorado.
David G EdwardsDepartment of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware.ORCID 0000-0002-5098-6678
University of Colorado Boulder · USAuburn University · USUniversity of Delaware · USVirginia Commonwealth University · US

Funding

University of Colorado Aging Training GrantT32AG000279 · NIA · UNIVERSITY OF COLORADO DENVER · PI Kerrie Moreau · 2001 to 2026
$10.1M
Aging and Arterial Dysfunction with a Western Diet: Exercise and AMPKR01HL107120 · NHLBI · UNIVERSITY OF COLORADO · PI SEALS, DOUGLAS R · 2011 to 2014
$1.6M
Exercise and Vascular Function in Chronic Kidney DiseaseR01HL113514 · NHLBI · UNIVERSITY OF DELAWARE · PI EDWARDS, DAVID G · 2013 to 2015
$1.2M
Sodium Nitrite Supplementation for Improving Physiological Function in Patients with Chronic Kidney DiseaseK01DK115524 · NIDDK · UNIVERSITY OF COLORADO · PI ROSSMAN, MATTHEW J · 2018 to 2023
$1.1M
Racial Differences in Serum Sodium and Blood Pressure RegulationK01HL147998 · NHLBI · TRUSTEES OF INDIANA UNIVERSITY · PI ROBINSON, AUSTIN TYLER · 2019 to 2023
$705k
NHLBI NIH HHS K01 HL147998NHLBI NIH HHS L30 HL154374NHLBI NIH HHS R01 HL107120NHLBI NIH HHS R01 HL113514NIA NIH HHS T32 AG000279NIDDK NIH HHS K01 DK115524
6 · The paper itself

Abstract

Cardiovascular disease (CVD) affects one in three adults and remains the leading cause of death in America. Advancing age is a major risk factor for CVD. Recent plateaus in CVD-related mortality rates in high-income countries after decades of decline highlight a critical need to identify novel therapeutic targets and strategies to mitigate and manage the risk of CVD development and progression. Vascular dysfunction, characterized by endothelial dysfunction and large elastic artery stiffening, is independently associated with an increased CVD risk and incidence and is therefore an attractive target for CVD prevention and management. Vascular mitochondria have emerged as an important player in maintaining vascular homeostasis. As such, age- and disease-related impairments in mitochondrial function contribute to vascular dysfunction and consequent increases in CVD risk. This review outlines the role of mitochondria in vascular function and discusses the ramifications of mitochondrial dysfunction on vascular health in the setting of age and disease. The adverse vascular consequences of increased mitochondrial-derived reactive oxygen species, impaired mitochondrial quality control, and defective mitochondrial calcium cycling are emphasized, in particular. Current evidence for both lifestyle and pharmaceutical mitochondrial-targeted strategies to improve vascular function is also presented.

Indexed as

AnimalsCardiovascular DiseasesEndothelium, VascularHumansMitochondriaOxidative StressReactive Oxygen SpeciesVascular StiffnessReactive Oxygen Speciesendotheliummitochondriavascularvascular stiffness

Identifiers

PMID33834868
PMCPMC8163660
OpenAlexW3145407809

What Socratic holds

Textmetadata
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.