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Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity
Aims/hypothesis It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with...
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Published in: | Diabetologia 2021-05, Vol.64 (5), p.1158-1168 |
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creator | Koh, Han-Chow E. van Vliet, Stephan Meyer, Gretchen A. Laforest, Richard Gropler, Robert J. Klein, Samuel Mittendorfer, Bettina |
description | Aims/hypothesis
It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with obesity. The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity.
Methods
We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [
2
H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [
15
O]H
2
O (to assess muscle perfusion) and [
18
F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition.
Results
We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg
−1
min
−1
in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg
−1
min
−1
, respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate (
r
2
= 0.65,
p
|
doi_str_mv | 10.1007/s00125-021-05383-w |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8336476</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2483819599</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-c0ba1e0aeeee6d84e64aaf060719060568bdb086d6cc5d0e44757bcab698cd0f3</originalsourceid><addsrcrecordid>eNp9kUuLFDEUhQtRnHb0D7iQgBs3pTeVVKp6I8igjjDgRsFdSKVuVWdMJWUeNr3yr5u2Z8bHwhCSwPnuuTecqnpK4SUF6F5FANq0NTS0hpb1rN7fqzaUs6YG3vT3q81Rr2kvvpxVj2K8BgDWcvGwOmOspZRz2FQ_LjFh8DM6NOlAjCs7ZmtcHZNZslUJRzLbrH1EktekviJRi3czGc00YUCXyJKjtkjm4PMajxY7VDbtDsSicmRFvxZVufH2uTdpR_yAsXR8XD2YlI345OY-rz6_e_vp4rK--vj-w8Wbq1rzjqdaw6AogsKyxNhzFFypCQR0dFvOVvTDOEAvRqF1OwJy3rXdoNUgtr0eYWLn1euT75qHBUdd5g7KyjWYRYWD9MrIvxVndnL232XPmOCdKAYvbgyC_5YxJrmYqNFa5dDnKBves55u2-22oM__Qa99Dq58TzYtdKwVgvNCNSdKBx9jwOluGArymK885StLvvJXvnJfip79-Y27kttAC8BOQCySmzH87v0f25-WebW1</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2507356644</pqid></control><display><type>article</type><title>Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity</title><source>Springer Nature</source><creator>Koh, Han-Chow E. ; van Vliet, Stephan ; Meyer, Gretchen A. ; Laforest, Richard ; Gropler, Robert J. ; Klein, Samuel ; Mittendorfer, Bettina</creator><creatorcontrib>Koh, Han-Chow E. ; van Vliet, Stephan ; Meyer, Gretchen A. ; Laforest, Richard ; Gropler, Robert J. ; Klein, Samuel ; Mittendorfer, Bettina</creatorcontrib><description>Aims/hypothesis
It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with obesity. The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity.
Methods
We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [
2
H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [
15
O]H
2
O (to assess muscle perfusion) and [
18
F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition.
Results
We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg
−1
min
−1
in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg
−1
min
−1
, respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate (
r
2
= 0.65,
p
< 0.05).
Conclusions/interpretation
Obesity-associated insulin resistance is generalised across all major muscles, and is not caused by alterations in muscle fibre type composition or perfusion. In addition, insulin-stimulated whole-body glucose disposal relative to fat-free mass provides a reliable index of muscle glucose uptake rate.
Graphical abstract</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-021-05383-w</identifier><identifier>PMID: 33511440</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adult ; Antidepressants ; Biological Transport - drug effects ; Biopsy ; Diabetes ; Fat-free body mass ; Female ; Fluorodeoxyglucose F18 ; Glucose ; Glucose - metabolism ; Glucose - pharmacokinetics ; Glucose Clamp Technique ; Human Physiology ; Humans ; Insulin ; Insulin - metabolism ; Insulin - pharmacology ; Insulin resistance ; Insulin Resistance - physiology ; Internal Medicine ; Male ; Medicine ; Medicine & Public Health ; Metabolic Diseases ; Middle Aged ; Muscle, Skeletal - diagnostic imaging ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - pathology ; Muscles ; Obesity ; Obesity - diagnostic imaging ; Obesity - metabolism ; Obesity - pathology ; Perfusion ; Positron emission tomography ; Quadriceps muscle ; Quadriceps Muscle - diagnostic imaging ; Quadriceps Muscle - drug effects ; Quadriceps Muscle - metabolism ; Quadriceps Muscle - pathology ; Thinness - diagnostic imaging ; Thinness - metabolism ; Thinness - pathology</subject><ispartof>Diabetologia, 2021-05, Vol.64 (5), p.1158-1168</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-c0ba1e0aeeee6d84e64aaf060719060568bdb086d6cc5d0e44757bcab698cd0f3</citedby><cites>FETCH-LOGICAL-c474t-c0ba1e0aeeee6d84e64aaf060719060568bdb086d6cc5d0e44757bcab698cd0f3</cites><orcidid>0000-0001-8992-555X ; 0000-0002-0238-1439 ; 0000-0003-4784-4967 ; 0000-0001-9268-3993 ; 0000-0001-7127-1156 ; 0000-0003-0049-2677 ; 0000-0002-6550-0570</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33511440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koh, Han-Chow E.</creatorcontrib><creatorcontrib>van Vliet, Stephan</creatorcontrib><creatorcontrib>Meyer, Gretchen A.</creatorcontrib><creatorcontrib>Laforest, Richard</creatorcontrib><creatorcontrib>Gropler, Robert J.</creatorcontrib><creatorcontrib>Klein, Samuel</creatorcontrib><creatorcontrib>Mittendorfer, Bettina</creatorcontrib><title>Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><addtitle>Diabetologia</addtitle><description>Aims/hypothesis
It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with obesity. The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity.
Methods
We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [
2
H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [
15
O]H
2
O (to assess muscle perfusion) and [
18
F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition.
Results
We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg
−1
min
−1
in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg
−1
min
−1
, respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate (
r
2
= 0.65,
p
< 0.05).
Conclusions/interpretation
Obesity-associated insulin resistance is generalised across all major muscles, and is not caused by alterations in muscle fibre type composition or perfusion. In addition, insulin-stimulated whole-body glucose disposal relative to fat-free mass provides a reliable index of muscle glucose uptake rate.
Graphical abstract</description><subject>Adult</subject><subject>Antidepressants</subject><subject>Biological Transport - drug effects</subject><subject>Biopsy</subject><subject>Diabetes</subject><subject>Fat-free body mass</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Glucose - pharmacokinetics</subject><subject>Glucose Clamp Technique</subject><subject>Human Physiology</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Insulin - pharmacology</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - physiology</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Middle Aged</subject><subject>Muscle, Skeletal - diagnostic imaging</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - pathology</subject><subject>Muscles</subject><subject>Obesity</subject><subject>Obesity - diagnostic imaging</subject><subject>Obesity - metabolism</subject><subject>Obesity - pathology</subject><subject>Perfusion</subject><subject>Positron emission tomography</subject><subject>Quadriceps muscle</subject><subject>Quadriceps Muscle - diagnostic imaging</subject><subject>Quadriceps Muscle - drug effects</subject><subject>Quadriceps Muscle - metabolism</subject><subject>Quadriceps Muscle - pathology</subject><subject>Thinness - diagnostic imaging</subject><subject>Thinness - metabolism</subject><subject>Thinness - pathology</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kUuLFDEUhQtRnHb0D7iQgBs3pTeVVKp6I8igjjDgRsFdSKVuVWdMJWUeNr3yr5u2Z8bHwhCSwPnuuTecqnpK4SUF6F5FANq0NTS0hpb1rN7fqzaUs6YG3vT3q81Rr2kvvpxVj2K8BgDWcvGwOmOspZRz2FQ_LjFh8DM6NOlAjCs7ZmtcHZNZslUJRzLbrH1EktekviJRi3czGc00YUCXyJKjtkjm4PMajxY7VDbtDsSicmRFvxZVufH2uTdpR_yAsXR8XD2YlI345OY-rz6_e_vp4rK--vj-w8Wbq1rzjqdaw6AogsKyxNhzFFypCQR0dFvOVvTDOEAvRqF1OwJy3rXdoNUgtr0eYWLn1euT75qHBUdd5g7KyjWYRYWD9MrIvxVndnL232XPmOCdKAYvbgyC_5YxJrmYqNFa5dDnKBves55u2-22oM__Qa99Dq58TzYtdKwVgvNCNSdKBx9jwOluGArymK885StLvvJXvnJfip79-Y27kttAC8BOQCySmzH87v0f25-WebW1</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Koh, Han-Chow E.</creator><creator>van Vliet, Stephan</creator><creator>Meyer, Gretchen A.</creator><creator>Laforest, Richard</creator><creator>Gropler, Robert J.</creator><creator>Klein, Samuel</creator><creator>Mittendorfer, Bettina</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8992-555X</orcidid><orcidid>https://orcid.org/0000-0002-0238-1439</orcidid><orcidid>https://orcid.org/0000-0003-4784-4967</orcidid><orcidid>https://orcid.org/0000-0001-9268-3993</orcidid><orcidid>https://orcid.org/0000-0001-7127-1156</orcidid><orcidid>https://orcid.org/0000-0003-0049-2677</orcidid><orcidid>https://orcid.org/0000-0002-6550-0570</orcidid></search><sort><creationdate>20210501</creationdate><title>Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity</title><author>Koh, Han-Chow E. ; van Vliet, Stephan ; Meyer, Gretchen A. ; Laforest, Richard ; Gropler, Robert J. ; Klein, Samuel ; Mittendorfer, Bettina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-c0ba1e0aeeee6d84e64aaf060719060568bdb086d6cc5d0e44757bcab698cd0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Antidepressants</topic><topic>Biological Transport - drug effects</topic><topic>Biopsy</topic><topic>Diabetes</topic><topic>Fat-free body mass</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Glucose - pharmacokinetics</topic><topic>Glucose Clamp Technique</topic><topic>Human Physiology</topic><topic>Humans</topic><topic>Insulin</topic><topic>Insulin - metabolism</topic><topic>Insulin - pharmacology</topic><topic>Insulin resistance</topic><topic>Insulin Resistance - physiology</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic Diseases</topic><topic>Middle Aged</topic><topic>Muscle, Skeletal - diagnostic imaging</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - pathology</topic><topic>Muscles</topic><topic>Obesity</topic><topic>Obesity - diagnostic imaging</topic><topic>Obesity - metabolism</topic><topic>Obesity - pathology</topic><topic>Perfusion</topic><topic>Positron emission tomography</topic><topic>Quadriceps muscle</topic><topic>Quadriceps Muscle - diagnostic imaging</topic><topic>Quadriceps Muscle - drug effects</topic><topic>Quadriceps Muscle - metabolism</topic><topic>Quadriceps Muscle - pathology</topic><topic>Thinness - diagnostic imaging</topic><topic>Thinness - metabolism</topic><topic>Thinness - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koh, Han-Chow E.</creatorcontrib><creatorcontrib>van Vliet, Stephan</creatorcontrib><creatorcontrib>Meyer, Gretchen A.</creatorcontrib><creatorcontrib>Laforest, Richard</creatorcontrib><creatorcontrib>Gropler, Robert J.</creatorcontrib><creatorcontrib>Klein, Samuel</creatorcontrib><creatorcontrib>Mittendorfer, Bettina</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koh, Han-Chow E.</au><au>van Vliet, Stephan</au><au>Meyer, Gretchen A.</au><au>Laforest, Richard</au><au>Gropler, Robert J.</au><au>Klein, Samuel</au><au>Mittendorfer, Bettina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity</atitle><jtitle>Diabetologia</jtitle><stitle>Diabetologia</stitle><addtitle>Diabetologia</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>64</volume><issue>5</issue><spage>1158</spage><epage>1168</epage><pages>1158-1168</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>Aims/hypothesis
It has been proposed that muscle fibre type composition and perfusion are key determinants of insulin-stimulated muscle glucose uptake, and alterations in muscle fibre type composition and perfusion contribute to muscle, and consequently whole-body, insulin resistance in people with obesity. The goal of the study was to evaluate the relationships among muscle fibre type composition, perfusion and insulin-stimulated glucose uptake rates in healthy, lean people and people with obesity.
Methods
We measured insulin-stimulated whole-body glucose disposal and glucose uptake and perfusion rates in five major muscle groups (erector spinae, obliques, rectus abdominis, hamstrings, quadriceps) in 15 healthy lean people and 37 people with obesity by using the hyperinsulinaemic–euglycaemic clamp procedure in conjunction with [
2
H]glucose tracer infusion (to assess whole-body glucose disposal) and positron emission tomography after injections of [
15
O]H
2
O (to assess muscle perfusion) and [
18
F]fluorodeoxyglucose (to assess muscle glucose uptake). A biopsy from the vastus lateralis was obtained to assess fibre type composition.
Results
We found: (1) a twofold difference in glucose uptake rates among muscles in both the lean and obese groups (rectus abdominis: 67 [51, 78] and 32 [21, 55] μmol kg
−1
min
−1
in the lean and obese groups, respectively; erector spinae: 134 [103, 160] and 66 [24, 129] μmol kg
−1
min
−1
, respectively; median [IQR]) that was unrelated to perfusion or fibre type composition (assessed in the vastus only); (2) the impairment in insulin action in the obese compared with the lean group was not different among muscle groups; and (3) insulin-stimulated whole-body glucose disposal expressed per kg fat-free mass was linearly related with muscle glucose uptake rate (
r
2
= 0.65,
p
< 0.05).
Conclusions/interpretation
Obesity-associated insulin resistance is generalised across all major muscles, and is not caused by alterations in muscle fibre type composition or perfusion. In addition, insulin-stimulated whole-body glucose disposal relative to fat-free mass provides a reliable index of muscle glucose uptake rate.
Graphical abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33511440</pmid><doi>10.1007/s00125-021-05383-w</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-8992-555X</orcidid><orcidid>https://orcid.org/0000-0002-0238-1439</orcidid><orcidid>https://orcid.org/0000-0003-4784-4967</orcidid><orcidid>https://orcid.org/0000-0001-9268-3993</orcidid><orcidid>https://orcid.org/0000-0001-7127-1156</orcidid><orcidid>https://orcid.org/0000-0003-0049-2677</orcidid><orcidid>https://orcid.org/0000-0002-6550-0570</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Springer Nature |
subjects | Adult Antidepressants Biological Transport - drug effects Biopsy Diabetes Fat-free body mass Female Fluorodeoxyglucose F18 Glucose Glucose - metabolism Glucose - pharmacokinetics Glucose Clamp Technique Human Physiology Humans Insulin Insulin - metabolism Insulin - pharmacology Insulin resistance Insulin Resistance - physiology Internal Medicine Male Medicine Medicine & Public Health Metabolic Diseases Middle Aged Muscle, Skeletal - diagnostic imaging Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscles Obesity Obesity - diagnostic imaging Obesity - metabolism Obesity - pathology Perfusion Positron emission tomography Quadriceps muscle Quadriceps Muscle - diagnostic imaging Quadriceps Muscle - drug effects Quadriceps Muscle - metabolism Quadriceps Muscle - pathology Thinness - diagnostic imaging Thinness - metabolism Thinness - pathology |
title | Heterogeneity in insulin-stimulated glucose uptake among different muscle groups in healthy lean people and people with obesity |
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