Leg electrical resistance predicts venous blood viscosity and hematocrit.

Myrenne aggregometer Red blood cell aggregation Segmental bioelectrical impedance electrical conductance hematocrit light transmission

Journal

Clinical hemorheology and microcirculation
ISSN: 1875-8622
Titre abrégé: Clin Hemorheol Microcirc
Pays: Netherlands
ID NLM: 9709206

Informations de publication

Date de publication:
2019
Historique:
pubmed: 23 4 2019
medline: 12 10 2019
entrez: 23 4 2019
Statut: ppublish

Résumé

 We previously reported that whole body bioelectrical impedance analysis (BIA) measurements are correlated to some hemorheologic factors, suggesting a relationship between viscosity factors and electric properties of flowing blood not only in vitro but also in vivo. Recently we reported that with segmental BIA (analyzing the body considered as composed of 5 cylinders) predictive equations for various determinants of blood viscosity were closer than for the wole body. Another widely used BIA technique uses leg-to-leg impedance measurements so that two cylinders (the two legs) are analyzed. We investigated whether impedance measured with this technique (Tanita TBF-300) is also a predictor of blood viscosity factors. From viscometric measurements performed on venous blood drawn in recreative athletes over the range of shear rates 1 to 6000 s-1 (RHEOMETRE Anton Paar CP 50-1), we found a correlation between leg-leg resistance at 50 kHz (Rx[50 kHz]) and blood viscosity at 1000 s-1 (η1000= 0.0051 Rx[50 kHz] + 1.3265; r = 0.521 p = 0.028 yielding a prediction of η1000 (Bland Altman plot: bias 0.05 [RANGE - 0.24; 0.34]. Neither plasma viscosity nor the red cell rheology index «k» of Quemada's model are correlated with Rx[50 kHz], but hematocrit (Hct) does (Hct (%) = 0.0217 Rx[50 kHz] + 33.783; r = 0.480 p = 0.044) yielding a prediction of Hct (Bland Altman plot: bias - 0.11, [range - 1.67; 1.45]. The discrepancy between actual and predicted Hct is also correlated with resistance at 50 kHz (r = 0.575 p = 0.031) as does the discrepancy between actual and predicted Hct/viscosity ratio (r = -0.651 p = 0.006). Therefore, as other previously studied methods, leg to leg BIA predicts viscosity, suggesting that blood rheology may influence the passage of an electric current in the legs.

Identifiants

pubmed: 31006677
pii: CH199003
doi: 10.3233/CH-199003
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

397-402

Auteurs

Emmanuelle Varlet-Marie (E)

Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS, Université de Montpellier, Ecole Nationale Supérieure de Chimie de Montpellier, France.
Laboratoire de Biophysique & Bio-Analyses, Faculté de Pharmacie, Université de Montpellier, France.

Laurent Vachoud (L)

UMR QualiSud, Faculté de Pharmacie, Université de Montpellier, France.

Bénédicte Marion (B)

Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS, Université de Montpellier, Ecole Nationale Supérieure de Chimie de Montpellier, France.
Laboratoire de Biophysique & Bio-Analyses, Faculté de Pharmacie, Université de Montpellier, France.

Céline Roques (C)

Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS, Université de Montpellier, Ecole Nationale Supérieure de Chimie de Montpellier, France.
Laboratoire de Biophysique & Bio-Analyses, Faculté de Pharmacie, Université de Montpellier, France.

Thibault Fidani (T)

U1046 INSERM, UMR 9214 CNRS «Physiopathologie & Médecine Expérimentale du Coeur et des Muscles - PHYMEDEXP», Unité d'Explorations Métaboliques (CERAMM), Université de Montpellier, Département de Physiologie Clinique, Hôpital Lapeyronie CHRU Montpellier, France.

Constance Chevalier (C)

U1046 INSERM, UMR 9214 CNRS «Physiopathologie & Médecine Expérimentale du Coeur et des Muscles - PHYMEDEXP», Unité d'Explorations Métaboliques (CERAMM), Université de Montpellier, Département de Physiologie Clinique, Hôpital Lapeyronie CHRU Montpellier, France.

Jacques Mercier (J)

U1046 INSERM, UMR 9214 CNRS «Physiopathologie & Médecine Expérimentale du Coeur et des Muscles - PHYMEDEXP», Unité d'Explorations Métaboliques (CERAMM), Université de Montpellier, Département de Physiologie Clinique, Hôpital Lapeyronie CHRU Montpellier, France.

Eric Raynaud de Mauverger (E)

U1046 INSERM, UMR 9214 CNRS «Physiopathologie & Médecine Expérimentale du Coeur et des Muscles - PHYMEDEXP», Unité d'Explorations Métaboliques (CERAMM), Université de Montpellier, Département de Physiologie Clinique, Hôpital Lapeyronie CHRU Montpellier, France.

Jean-Frédéric Brun (JF)

U1046 INSERM, UMR 9214 CNRS «Physiopathologie & Médecine Expérimentale du Coeur et des Muscles - PHYMEDEXP», Unité d'Explorations Métaboliques (CERAMM), Université de Montpellier, Département de Physiologie Clinique, Hôpital Lapeyronie CHRU Montpellier, France.

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