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


Journal

Experimental physiology
ISSN: 1469-445X
Titre abrégé: Exp Physiol
Pays: England
ID NLM: 9002940

Informations de publication

Date de publication:
07 2020
Historique:
received: 09 02 2020
accepted: 24 04 2020
pubmed: 4 5 2020
medline: 29 9 2021
entrez: 4 5 2020
Statut: ppublish

Résumé

What 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. 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.

Identifiants

pubmed: 32362031
doi: 10.1113/EP088535
pmc: PMC7895300
mid: NIHMS1599411
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1102-1110

Subventions

Organisme : American College of Sports Medicine Doctoral Student Foundation Grant
Organisme : NHLBI NIH HHS
ID : R15 HL130906
Pays : United States
Organisme : American Heart Association Pre-Doctoral Fellowship
ID : 19PRE34380596
Organisme : The University of Texas at Arlington College of Nursing and Health Innovation
Organisme : NHLBI NIH HHS
ID : R01 HL127071
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The Authors. Experimental Physiology © 2020 The Physiological Society.

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Auteurs

Benjamin E Young (BE)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

Jasdeep Kaur (J)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

Jennifer R Vranish (JR)

Department of Integrative Physiology and Health Science, Alma College, Alma, MI, USA.

Brandi Y Stephens (BY)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

Thales C Barbosa (TC)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

Jane N Cloud (JN)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

Jing Wang (J)

College of Nursing, University of Texas at Arlington, Arlington, TX, USA.

David M Keller (DM)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

Paul J Fadel (PJ)

Department of Kinesiology, University of Texas at Arlington, Arlington, TX, USA.

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Classifications MeSH