Markers of inflammation and disuse in vastus lateralis of chronic obstructive pulmonary disease patients

Background  Disuse and/or local inflammation in the muscle cannot be excluded as potential influences for the decreased muscle force in patients hospitalised due to an acute chronic obstructive pulmonary disease (COPD) exacerbation. This study aims to compare expression levels of markers of disuse (...

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Veröffentlicht in:European journal of clinical investigation 2007-11, Vol.37 (11), p.897-904
Hauptverfasser: Crul, T., Spruit, M. A., Gayan-Ramirez, G., Quarck, R., Gosselink, R., Troosters, T., Pitta, F., Decramer, M.
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container_end_page 904
container_issue 11
container_start_page 897
container_title European journal of clinical investigation
container_volume 37
creator Crul, T.
Spruit, M. A.
Gayan-Ramirez, G.
Quarck, R.
Gosselink, R.
Troosters, T.
Pitta, F.
Decramer, M.
description Background  Disuse and/or local inflammation in the muscle cannot be excluded as potential influences for the decreased muscle force in patients hospitalised due to an acute chronic obstructive pulmonary disease (COPD) exacerbation. This study aims to compare expression levels of markers of disuse (insulin‐like growth factor‐1 (IGF‐I), MyoD and myogenin) and inflammation [interleukin‐6 (IL‐6), IL‐8 and tumour necrosis factor‐alpha (TNF‐α)] in the muscle of hospitalised and stable COPD patients and healthy elderly. Material and methods  Muscle biopsies (m. vastus lateralis) were taken in 14 hospitalised COPD patients (aged 68 ± 8), 11 clinically stable COPD patients (aged 68 ± 9) and seven healthy subjects (aged 70 ± 7) to analyse local mRNA expression levels of IL‐6, IL‐8, TNF‐α, IGF‐I and protein expression levels of IGF‐I, MyoD and myogenin. Relationships of these expression levels with lung and skeletal muscle function were investigated. Results  IGF‐I mRNA and MyoD protein levels were significantly lower in hospitalised patients compared to healthy subjects. MyoD protein levels were positively related to quadriceps force. Muscle IL‐6 and IL‐8 expression in hospitalised patients was similar compared to stable patients and healthy subjects and was not related to expression levels of muscle markers of disuse or quadriceps force. Muscle TNF‐α and myogenin were not detected. Conclusion  Decreased expression levels of muscle IGF‐I and MyoD in hospitalised patients suggest a potential influence of disuse in the increased muscle weakness during an acute COPD exacerbation. This study did not find any evidence supporting local inflammation via IL‐6, IL‐8 and/or TNF‐α in the vastus lateralis muscle of COPD patients.
doi_str_mv 10.1111/j.1365-2362.2007.01867.x
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A. ; Gayan-Ramirez, G. ; Quarck, R. ; Gosselink, R. ; Troosters, T. ; Pitta, F. ; Decramer, M.</creator><creatorcontrib>Crul, T. ; Spruit, M. A. ; Gayan-Ramirez, G. ; Quarck, R. ; Gosselink, R. ; Troosters, T. ; Pitta, F. ; Decramer, M.</creatorcontrib><description>Background  Disuse and/or local inflammation in the muscle cannot be excluded as potential influences for the decreased muscle force in patients hospitalised due to an acute chronic obstructive pulmonary disease (COPD) exacerbation. This study aims to compare expression levels of markers of disuse (insulin‐like growth factor‐1 (IGF‐I), MyoD and myogenin) and inflammation [interleukin‐6 (IL‐6), IL‐8 and tumour necrosis factor‐alpha (TNF‐α)] in the muscle of hospitalised and stable COPD patients and healthy elderly. Material and methods  Muscle biopsies (m. vastus lateralis) were taken in 14 hospitalised COPD patients (aged 68 ± 8), 11 clinically stable COPD patients (aged 68 ± 9) and seven healthy subjects (aged 70 ± 7) to analyse local mRNA expression levels of IL‐6, IL‐8, TNF‐α, IGF‐I and protein expression levels of IGF‐I, MyoD and myogenin. Relationships of these expression levels with lung and skeletal muscle function were investigated. Results  IGF‐I mRNA and MyoD protein levels were significantly lower in hospitalised patients compared to healthy subjects. MyoD protein levels were positively related to quadriceps force. Muscle IL‐6 and IL‐8 expression in hospitalised patients was similar compared to stable patients and healthy subjects and was not related to expression levels of muscle markers of disuse or quadriceps force. Muscle TNF‐α and myogenin were not detected. Conclusion  Decreased expression levels of muscle IGF‐I and MyoD in hospitalised patients suggest a potential influence of disuse in the increased muscle weakness during an acute COPD exacerbation. 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A.</creatorcontrib><creatorcontrib>Gayan-Ramirez, G.</creatorcontrib><creatorcontrib>Quarck, R.</creatorcontrib><creatorcontrib>Gosselink, R.</creatorcontrib><creatorcontrib>Troosters, T.</creatorcontrib><creatorcontrib>Pitta, F.</creatorcontrib><creatorcontrib>Decramer, M.</creatorcontrib><title>Markers of inflammation and disuse in vastus lateralis of chronic obstructive pulmonary disease patients</title><title>European journal of clinical investigation</title><addtitle>Eur J Clin Invest</addtitle><description>Background  Disuse and/or local inflammation in the muscle cannot be excluded as potential influences for the decreased muscle force in patients hospitalised due to an acute chronic obstructive pulmonary disease (COPD) exacerbation. This study aims to compare expression levels of markers of disuse (insulin‐like growth factor‐1 (IGF‐I), MyoD and myogenin) and inflammation [interleukin‐6 (IL‐6), IL‐8 and tumour necrosis factor‐alpha (TNF‐α)] in the muscle of hospitalised and stable COPD patients and healthy elderly. Material and methods  Muscle biopsies (m. vastus lateralis) were taken in 14 hospitalised COPD patients (aged 68 ± 8), 11 clinically stable COPD patients (aged 68 ± 9) and seven healthy subjects (aged 70 ± 7) to analyse local mRNA expression levels of IL‐6, IL‐8, TNF‐α, IGF‐I and protein expression levels of IGF‐I, MyoD and myogenin. Relationships of these expression levels with lung and skeletal muscle function were investigated. Results  IGF‐I mRNA and MyoD protein levels were significantly lower in hospitalised patients compared to healthy subjects. MyoD protein levels were positively related to quadriceps force. Muscle IL‐6 and IL‐8 expression in hospitalised patients was similar compared to stable patients and healthy subjects and was not related to expression levels of muscle markers of disuse or quadriceps force. Muscle TNF‐α and myogenin were not detected. Conclusion  Decreased expression levels of muscle IGF‐I and MyoD in hospitalised patients suggest a potential influence of disuse in the increased muscle weakness during an acute COPD exacerbation. This study did not find any evidence supporting local inflammation via IL‐6, IL‐8 and/or TNF‐α in the vastus lateralis muscle of COPD patients.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>COPD</subject><subject>Cross-Sectional Studies</subject><subject>disuse</subject><subject>exacerbation</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>inflammation</subject><subject>Insulin-Like Growth Factor I</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-8 - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Muscular Atrophy - physiopathology</subject><subject>MyoD Protein</subject><subject>Pneumology</subject><subject>Pulmonary Disease, Chronic Obstructive - blood</subject><subject>Pulmonary Disease, Chronic Obstructive - physiopathology</subject><subject>Quadriceps Muscle - physiopathology</subject><subject>RNA, Messenger - isolation &amp; purification</subject><subject>skeletal muscle</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><issn>0014-2972</issn><issn>1365-2362</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtP3DAURq2qFUwpf6Hypt0l9TvJootqoBSJPhYgJDaWY98IT51kaid0-Pd1mBFs640t33Ourz4jhCkpaV6fNiXlShaMK1YyQqqS0FpV5e4VWj0XXqMVIVQUrKnYMXqb0oYQUlPOjtAxreqaC0ZW6P67ib8hJjx22A9dMH1vJj8O2AwOO5_mBPkeP5g0zQkHM0E0wT_h9j6Og7d4bNMUZzv5B8DbOfTjYOLj4oLJ8ja3g2FK79CbzoQEp4f9BN18Pb9efyuufl5crr9cFVYSWhXWSiVc66RUoJxpXAeyA8Etrxy0FDgV4DpFKgAjmJGCgm2Y49SxjrcZPEEf9323cfwzQ5p075OFEMwA45y0qoVUdb2A9R60cUwpQqe30fd5dE2JXlLWG72EqZcw9ZKyfkpZ77L6_vDG3PbgXsRDrBn4cABMsiZ00QzWpxeuYYRJwTL3ec_99QEe_3sAfb6-XE7ZL_a-TxPsnv38pTpXK6lvf1zos4aI67tfd7nPP470qnA</recordid><startdate>200711</startdate><enddate>200711</enddate><creator>Crul, T.</creator><creator>Spruit, M. 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A. ; Gayan-Ramirez, G. ; Quarck, R. ; Gosselink, R. ; Troosters, T. ; Pitta, F. ; Decramer, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5017-cc564dbd556e6da9dfe5fe43c37deb1e314edf607eea42a541ec92d31d2f3be43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>COPD</topic><topic>Cross-Sectional Studies</topic><topic>disuse</topic><topic>exacerbation</topic><topic>Female</topic><topic>General aspects</topic><topic>Humans</topic><topic>inflammation</topic><topic>Insulin-Like Growth Factor I</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-8 - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscular Atrophy - physiopathology</topic><topic>MyoD Protein</topic><topic>Pneumology</topic><topic>Pulmonary Disease, Chronic Obstructive - blood</topic><topic>Pulmonary Disease, Chronic Obstructive - physiopathology</topic><topic>Quadriceps Muscle - physiopathology</topic><topic>RNA, Messenger - isolation &amp; purification</topic><topic>skeletal muscle</topic><topic>Tumor Necrosis Factor-alpha - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Crul, T.</creatorcontrib><creatorcontrib>Spruit, M. A.</creatorcontrib><creatorcontrib>Gayan-Ramirez, G.</creatorcontrib><creatorcontrib>Quarck, R.</creatorcontrib><creatorcontrib>Gosselink, R.</creatorcontrib><creatorcontrib>Troosters, T.</creatorcontrib><creatorcontrib>Pitta, F.</creatorcontrib><creatorcontrib>Decramer, M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Crul, T.</au><au>Spruit, M. A.</au><au>Gayan-Ramirez, G.</au><au>Quarck, R.</au><au>Gosselink, R.</au><au>Troosters, T.</au><au>Pitta, F.</au><au>Decramer, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Markers of inflammation and disuse in vastus lateralis of chronic obstructive pulmonary disease patients</atitle><jtitle>European journal of clinical investigation</jtitle><addtitle>Eur J Clin Invest</addtitle><date>2007-11</date><risdate>2007</risdate><volume>37</volume><issue>11</issue><spage>897</spage><epage>904</epage><pages>897-904</pages><issn>0014-2972</issn><eissn>1365-2362</eissn><abstract>Background  Disuse and/or local inflammation in the muscle cannot be excluded as potential influences for the decreased muscle force in patients hospitalised due to an acute chronic obstructive pulmonary disease (COPD) exacerbation. This study aims to compare expression levels of markers of disuse (insulin‐like growth factor‐1 (IGF‐I), MyoD and myogenin) and inflammation [interleukin‐6 (IL‐6), IL‐8 and tumour necrosis factor‐alpha (TNF‐α)] in the muscle of hospitalised and stable COPD patients and healthy elderly. Material and methods  Muscle biopsies (m. vastus lateralis) were taken in 14 hospitalised COPD patients (aged 68 ± 8), 11 clinically stable COPD patients (aged 68 ± 9) and seven healthy subjects (aged 70 ± 7) to analyse local mRNA expression levels of IL‐6, IL‐8, TNF‐α, IGF‐I and protein expression levels of IGF‐I, MyoD and myogenin. Relationships of these expression levels with lung and skeletal muscle function were investigated. Results  IGF‐I mRNA and MyoD protein levels were significantly lower in hospitalised patients compared to healthy subjects. MyoD protein levels were positively related to quadriceps force. Muscle IL‐6 and IL‐8 expression in hospitalised patients was similar compared to stable patients and healthy subjects and was not related to expression levels of muscle markers of disuse or quadriceps force. Muscle TNF‐α and myogenin were not detected. Conclusion  Decreased expression levels of muscle IGF‐I and MyoD in hospitalised patients suggest a potential influence of disuse in the increased muscle weakness during an acute COPD exacerbation. This study did not find any evidence supporting local inflammation via IL‐6, IL‐8 and/or TNF‐α in the vastus lateralis muscle of COPD patients.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17883420</pmid><doi>10.1111/j.1365-2362.2007.01867.x</doi><tpages>8</tpages></addata></record>
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subjects Adult
Aged
Biological and medical sciences
Biomarkers - blood
Chronic obstructive pulmonary disease, asthma
COPD
Cross-Sectional Studies
disuse
exacerbation
Female
General aspects
Humans
inflammation
Insulin-Like Growth Factor I
Interleukin-6 - blood
Interleukin-8 - blood
Male
Medical sciences
Middle Aged
Muscular Atrophy - physiopathology
MyoD Protein
Pneumology
Pulmonary Disease, Chronic Obstructive - blood
Pulmonary Disease, Chronic Obstructive - physiopathology
Quadriceps Muscle - physiopathology
RNA, Messenger - isolation & purification
skeletal muscle
Tumor Necrosis Factor-alpha - blood
title Markers of inflammation and disuse in vastus lateralis of chronic obstructive pulmonary disease patients
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