Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans

Abstract Insulin increases muscle microvascular perfusion and enhances tissue insulin and nutrient delivery. Our aim was to determine phenotypic traits that foretell human muscle microvascular insulin responses. Hyperinsulinemic euglycemic clamps were performed in 97 adult humans who were lean and h...

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Autores principales: Kaitlin M. Love, Linda A. Jahn, Lee M. Hartline, James T. Patrie, Eugene J. Barrett, Zhenqi Liu
Formato: article
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/b4056d7b9f8e47e6b3c79ddc7099260d
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spelling oai:doaj.org-article:b4056d7b9f8e47e6b3c79ddc7099260d2021-12-02T15:56:56ZInsulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans10.1038/s41598-021-90935-82045-2322https://doaj.org/article/b4056d7b9f8e47e6b3c79ddc7099260d2021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-90935-8https://doaj.org/toc/2045-2322Abstract Insulin increases muscle microvascular perfusion and enhances tissue insulin and nutrient delivery. Our aim was to determine phenotypic traits that foretell human muscle microvascular insulin responses. Hyperinsulinemic euglycemic clamps were performed in 97 adult humans who were lean and healthy, had class 1 obesity without comorbidities, or controlled type 1 diabetes without complications. Insulin-mediated whole-body glucose disposal rates (M-value) and insulin-induced changes in muscle microvascular blood volume (ΔMBV) were determined. Univariate and multivariate analyses were conducted to examine bivariate and multivariate relationships between outcomes, ΔMBV and M-value, and predictor variables, body mass index (BMI), total body weight (WT), percent body fat (BF), lean body mass, blood pressure, maximum consumption of oxygen (VO2max), plasma LDL (LDL-C) and HDL cholesterol, triglycerides (TG), and fasting insulin (INS) levels. Among all factors, only M-value (r = 0.23, p = 0.02) and VO2max (r = 0.20, p = 0.047) correlated with ΔMBV. Conversely, INS (r = − 0.48, p ≤ 0.0001), BF (r = − 0.54, p ≤ 0.001), VO2max (r = 0.5, p ≤ 0.001), BMI (r = − 0.40, p < 0.001), WT (r = − 0.33, p = 0.001), LDL-C (r = − 0.26, p = 0.009), TG (r = − 0.25, p = 0.012) correlated with M-value. While both ΔMBV (p = 0.045) and TG (p = 0.03) provided significant predictive information about M-value in the multivariate regression model, only M-value was uniquely predictive of ΔMBV (p = 0.045). Thus, both M-value and VO2max correlated with ΔMBV but only M-value provided unique predictive information about ΔMBV. This suggests that metabolic and microvascular insulin responses are important predictors of one another, but most metabolic insulin resistance predictors do not predict microvascular insulin responses.Kaitlin M. LoveLinda A. JahnLee M. HartlineJames T. PatrieEugene J. BarrettZhenqi LiuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Kaitlin M. Love
Linda A. Jahn
Lee M. Hartline
James T. Patrie
Eugene J. Barrett
Zhenqi Liu
Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
description Abstract Insulin increases muscle microvascular perfusion and enhances tissue insulin and nutrient delivery. Our aim was to determine phenotypic traits that foretell human muscle microvascular insulin responses. Hyperinsulinemic euglycemic clamps were performed in 97 adult humans who were lean and healthy, had class 1 obesity without comorbidities, or controlled type 1 diabetes without complications. Insulin-mediated whole-body glucose disposal rates (M-value) and insulin-induced changes in muscle microvascular blood volume (ΔMBV) were determined. Univariate and multivariate analyses were conducted to examine bivariate and multivariate relationships between outcomes, ΔMBV and M-value, and predictor variables, body mass index (BMI), total body weight (WT), percent body fat (BF), lean body mass, blood pressure, maximum consumption of oxygen (VO2max), plasma LDL (LDL-C) and HDL cholesterol, triglycerides (TG), and fasting insulin (INS) levels. Among all factors, only M-value (r = 0.23, p = 0.02) and VO2max (r = 0.20, p = 0.047) correlated with ΔMBV. Conversely, INS (r = − 0.48, p ≤ 0.0001), BF (r = − 0.54, p ≤ 0.001), VO2max (r = 0.5, p ≤ 0.001), BMI (r = − 0.40, p < 0.001), WT (r = − 0.33, p = 0.001), LDL-C (r = − 0.26, p = 0.009), TG (r = − 0.25, p = 0.012) correlated with M-value. While both ΔMBV (p = 0.045) and TG (p = 0.03) provided significant predictive information about M-value in the multivariate regression model, only M-value was uniquely predictive of ΔMBV (p = 0.045). Thus, both M-value and VO2max correlated with ΔMBV but only M-value provided unique predictive information about ΔMBV. This suggests that metabolic and microvascular insulin responses are important predictors of one another, but most metabolic insulin resistance predictors do not predict microvascular insulin responses.
format article
author Kaitlin M. Love
Linda A. Jahn
Lee M. Hartline
James T. Patrie
Eugene J. Barrett
Zhenqi Liu
author_facet Kaitlin M. Love
Linda A. Jahn
Lee M. Hartline
James T. Patrie
Eugene J. Barrett
Zhenqi Liu
author_sort Kaitlin M. Love
title Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
title_short Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
title_full Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
title_fullStr Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
title_full_unstemmed Insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
title_sort insulin-mediated muscle microvascular perfusion and its phenotypic predictors in humans
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/b4056d7b9f8e47e6b3c79ddc7099260d
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