Evidence map›Paper›PMID 32362031›Full record

ArticleExperimental physiology2020

Augmented resting beat-to-beat blood pressure variability in young, healthy, non-Hispanic black men.

Benjamin E Young, Jasdeep Kaur, Jennifer R Vranish, Brandi Y Stephens, Thales C Barbosa, Jane N Cloud, Jing Wang, David M Keller, Paul J Fadel

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Experimental physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04770155 (Vascular Dysfunction in Black Individuals), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 10% 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.

NCT04770155 early_phase1terminatednot on this mapstarted 2021, after this paper: background citation

Vascular Dysfunction in Black Individuals: Roles of Nitric Oxide and Endothelin-1

TypeinterventionalSponsorUniversity of Mississippi Medical CenterRan2021 to 2021Enrolled8ConditionsVascular Function, Racial DisparityArmsDietary Nitrates 400 mg, L-citrulline 3 g, Sildenafil 100 mg, Bosentan 125 mg
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Individuals with posttraumatic stress disorder have increased beat-to-beat blood pressure variability.American journal of physiology. Regulatory, integrative and comparative physiology · 2026
    Article
  5. Article
  6. Article
  7. Resting beat-to-beat blood pressure variability is preserved in young adults with major depressive disorder.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  8. Article
  9. Cardiac autonomic function in young, healthy adults: Influence of race and sex.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  10. Resting beat-to-beat blood pressure variability in humans: role of alpha-1 adrenergic receptors.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Augmented resting beat-to-beat blood pressure variability in patients with chronic kidney disease.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2023
    Article
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  17. Article
  18. Article
  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Benjamin E YoungDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.ORCID 0000-0003-0239-005X
Jasdeep KaurDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.ORCID 0000-0002-1264-6103
Jennifer R VranishDepartment of Integrative Physiology and Health Science, Alma College, Alma, MI, USA.
Brandi Y StephensDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.
Thales C BarbosaDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.ORCID 0000-0001-5776-3824
Jane N CloudDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.
Jing WangCollege of Nursing, University of Texas at Arlington, Arlington, TX, USA.
David M KellerDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.
Paul J FadelDepartment of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.ORCID 0000-0002-0115-0743
The University of Texas at Arlington · USAlma College · US

Funding

Targeting Sympathetic Overactivity in CKD patients: Mechanisms & Novel TherapiesR01HL127071 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI FADEL, PAUL J · 2016 to 2019
$1.7M
Sympathetic baroreflex control and vascular transduction in African AmericansR15HL130906 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI KELLER, DAVID M · 2016 to 2016
$377k
American College of Sports Medicine Doctoral Student Foundation GrantAmerican Heart Association Pre-Doctoral Fellowship 19PRE34380596NHLBI NIH HHS R01 HL127071NHLBI NIH HHS R15 HL130906The University of Texas at Arlington College of Nursing and Health Innovation
6 · The paper itself

Abstract

NEW

findingsWhat is the central question of this study? The prevalence of hypertension in black individuals exceeds that in other racial groups. Despite this well-known heightened risk, the underlying contributory factors remain incompletely understood. We hypothesized that young black men would exhibit augmented beat-to-beat blood pressure variability compared with white men and that black men would exhibit augmented total peripheral resistance variability. What is the main finding and its importance? We demonstrate that young, healthy black men exhibit greater resting beat-to-beat blood pressure variability compared with their white counterparts, which is accompanied by greater variability in total peripheral resistance. These swings in blood pressure over time might contribute to the enhanced cardiovascular risk profile in black individuals. ABSTRACT: The prevalence of hypertension in black (BL) individuals exceeds that in other racial groups. Recently, resting beat-to-beat blood pressure (BP) variability has been shown to predict cardiovascular risk and detect target organ damage better than ambulatory BP monitoring. Given the heightened risk in BL individuals, we hypothesized young BL men would exhibit augmented beat-to-beat BP variability compared with white (WH) men. Furthermore, given studies reporting reduced vasodilatation and augmented vasoconstriction in BL individuals, we hypothesized that BL men would exhibit augmented variability in total peripheral resistance (TPR). In 45 normotensive men (24 BL), beat-to-beat BP (Finometer) was measured during 10-20 min of quiet rest. Cardiac output and TPR were estimated (Modelflow method). Despite similar resting BP, BL men exhibited greater BP standard deviation (e.g. systolic BP SD; BL, 7.1 ± 2.2 mmHg; WH, 5.4 ± 1.5 mmHg; P = 0.006) compared with WH men, which was accompanied by a greater TPR SD (P = 0.003), but not cardiac output SD (P = 0.390). Other traditional measures of variability provided similar results. Histogram analysis indicated that BL men exhibited a greater percentage of cardiac cycles with BPs higher (> +10 mmHg higher) and lower (< -8 mmHg lower) than mean systolic BP compared with WH men (interaction, P < 0.001), which was accompanied by a greater percentage of cardiac cycles with high/low TPR (P < 0.001). In a subset of subjects (n = 30), reduced sympathetic baroreflex sensitivity was associated with augmented BP variability (r = -0.638, P < 0.001), whereas cardiac baroreflex sensitivity had no relationship (P = 0.447). Herein, we document an augmented beat-to-beat BP variability in young BL men, which coincided with fluctuations in vascular resistance and reduced sympathetic BRS.

Indexed as

Black or African AmericanBlood PressureVascular ResistanceAdultBaroreflexCardiac OutputHeartHeart RateHumansHypertensionMaleRestWhite PeopleYoung Adultafrican americanarterial baroreflexcardiac outputcaucasian americanracial differencestotal peripheral resistance

Identifiers

PMID32362031
PMCPMC7895300
OpenAlexW3023313991

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Registered trials

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.