Sputum proteomic signature of gastro-oesophageal reflux in patients with severe asthma
Gastro-oesophageal reflux disease (GORD) has long been associated with poor asthma control without an established cause-effect relationship. 610 asthmatics (421 severe/88 mild-moderate) and 101 healthy controls were assessed clinically and a subset of 154 severe asthmatics underwent proteomic analys...
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Veröffentlicht in: | Respiratory medicine 2019-04, Vol.150, p.66-73 |
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creator | Tariq, K. Schofield, J.P.R. Nicholas, B.L. Burg, D. Brandsma, J. Bansal, A.T. Wilson, S.J. Lutter, R. Fowler, S.J. Bakke Caruso, M. Dahlen, B. Horváth, I. Krug, N. Montuschi, P. Sanak, M. Sandström, T. Geiser, T. Pandis, I. Sousa, A.R. Adcock, I.M. Shaw, D.E. Auffray, C. Howarth, P.H. Sterk, P.J. Chung, K.F. Skipp, P.J. Dimitrov, B. Djukanović, R. |
description | Gastro-oesophageal reflux disease (GORD) has long been associated with poor asthma control without an established cause-effect relationship.
610 asthmatics (421 severe/88 mild-moderate) and 101 healthy controls were assessed clinically and a subset of 154 severe asthmatics underwent proteomic analysis of induced sputum using untargeted mass spectrometry, LC-IMS-MSE. Univariate and multiple logistic regression analyses (MLR) were conducted to identify proteins associated with GORD in this cohort.
When compared to mild/moderate asthmatics and healthy individuals, respectively, GORD was three- and ten-fold more prevalent in severe asthmatics and was associated with increased asthma symptoms and oral corticosteroid use, poorer quality of life, depression/anxiety, obesity and symptoms of sino-nasal disease. Comparison of sputum proteomes in severe asthmatics with and without active GORD showed five differentially abundant proteins with described roles in anti-microbial defences, systemic inflammation and epithelial integrity. Three of these were associated with active GORD by multiple linear regression analysis: Ig lambda variable 1–47 (p = 0·017) and plasma protease C1 inhibitor (p = 0·043), both in lower concentrations, and lipocalin-1 (p = 0·034) in higher concentrations in active GORD.
This study provides evidence which suggests that reflux can cause subtle perturbation of proteins detectable in the airways lining fluid and that severe asthmatics with GORD may represent a distinct phenotype of asthma.
•5 proteins different in severe asthmatics with GORD.•Ig lambda variable 1–47 was associated with active GORD in severe asthma.•Lipocalin-1 was associated with active GORD in severe asthma.•Plasma protease C1 inhibitor was associated with active GORD in severe asthma. |
doi_str_mv | 10.1016/j.rmed.2019.02.008 |
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610 asthmatics (421 severe/88 mild-moderate) and 101 healthy controls were assessed clinically and a subset of 154 severe asthmatics underwent proteomic analysis of induced sputum using untargeted mass spectrometry, LC-IMS-MSE. Univariate and multiple logistic regression analyses (MLR) were conducted to identify proteins associated with GORD in this cohort.
When compared to mild/moderate asthmatics and healthy individuals, respectively, GORD was three- and ten-fold more prevalent in severe asthmatics and was associated with increased asthma symptoms and oral corticosteroid use, poorer quality of life, depression/anxiety, obesity and symptoms of sino-nasal disease. Comparison of sputum proteomes in severe asthmatics with and without active GORD showed five differentially abundant proteins with described roles in anti-microbial defences, systemic inflammation and epithelial integrity. Three of these were associated with active GORD by multiple linear regression analysis: Ig lambda variable 1–47 (p = 0·017) and plasma protease C1 inhibitor (p = 0·043), both in lower concentrations, and lipocalin-1 (p = 0·034) in higher concentrations in active GORD.
This study provides evidence which suggests that reflux can cause subtle perturbation of proteins detectable in the airways lining fluid and that severe asthmatics with GORD may represent a distinct phenotype of asthma.
•5 proteins different in severe asthmatics with GORD.•Ig lambda variable 1–47 was associated with active GORD in severe asthma.•Lipocalin-1 was associated with active GORD in severe asthma.•Plasma protease C1 inhibitor was associated with active GORD in severe asthma.</description><identifier>ISSN: 0954-6111</identifier><identifier>ISSN: 1532-3064</identifier><identifier>EISSN: 1532-3064</identifier><identifier>DOI: 10.1016/j.rmed.2019.02.008</identifier><identifier>PMID: 30961953</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Antiinfectives and antibacterials ; Anxiety ; Asthma ; Asthma - complications ; Asthma - epidemiology ; Asthma - metabolism ; Asthma - psychology ; Biomarkers ; Cause-effect relationships ; Complement component C1 ; Corticosteroids ; Disease control ; Endopeptidases - metabolism ; Esophagus ; European Union - organization & administration ; Female ; Gastroesophageal reflux ; Gastroesophageal Reflux - complications ; Gastroesophageal Reflux - diagnosis ; Gastroesophageal Reflux - epidemiology ; Humans ; Immunoglobulin lambda-Chains - metabolism ; Immunoglobulins ; Keratin ; Lipocalin ; Lipocalin 1 - metabolism ; Male ; Mass spectrometry ; Mass spectroscopy ; Mental depression ; Microorganisms ; Middle Aged ; Patients ; Phenotypes ; Prevalence ; Prospective Studies ; Protease Inhibitors - metabolism ; Proteinase inhibitors ; Proteins ; Proteomics - methods ; Quality of Life ; Questionnaires ; Regression analysis ; Respiratory diseases ; Scientific imaging ; Severity of Illness Index ; Signs and symptoms ; Sputum ; Sputum - metabolism</subject><ispartof>Respiratory medicine, 2019-04, Vol.150, p.66-73</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><rights>2019. Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-3b9a7910acffcd29cfa67c72b10c459d4f7bf6294adc0aab4f41c1f1b1f909e3</citedby><cites>FETCH-LOGICAL-c504t-3b9a7910acffcd29cfa67c72b10c459d4f7bf6294adc0aab4f41c1f1b1f909e3</cites><orcidid>0000-0003-2101-8843 ; 0000-0002-6733-0317 ; 0000-0002-5896-2072 ; 0000-0003-4106-8469 ; 0000-0002-4524-1663 ; 0000-0003-4542-6614</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0954611119300447$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,550,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30961953$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-158738$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:140663160$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Tariq, K.</creatorcontrib><creatorcontrib>Schofield, J.P.R.</creatorcontrib><creatorcontrib>Nicholas, B.L.</creatorcontrib><creatorcontrib>Burg, D.</creatorcontrib><creatorcontrib>Brandsma, J.</creatorcontrib><creatorcontrib>Bansal, A.T.</creatorcontrib><creatorcontrib>Wilson, S.J.</creatorcontrib><creatorcontrib>Lutter, R.</creatorcontrib><creatorcontrib>Fowler, S.J.</creatorcontrib><creatorcontrib>Bakke</creatorcontrib><creatorcontrib>Caruso, M.</creatorcontrib><creatorcontrib>Dahlen, B.</creatorcontrib><creatorcontrib>Horváth, I.</creatorcontrib><creatorcontrib>Krug, N.</creatorcontrib><creatorcontrib>Montuschi, P.</creatorcontrib><creatorcontrib>Sanak, M.</creatorcontrib><creatorcontrib>Sandström, T.</creatorcontrib><creatorcontrib>Geiser, T.</creatorcontrib><creatorcontrib>Pandis, I.</creatorcontrib><creatorcontrib>Sousa, A.R.</creatorcontrib><creatorcontrib>Adcock, I.M.</creatorcontrib><creatorcontrib>Shaw, D.E.</creatorcontrib><creatorcontrib>Auffray, C.</creatorcontrib><creatorcontrib>Howarth, P.H.</creatorcontrib><creatorcontrib>Sterk, P.J.</creatorcontrib><creatorcontrib>Chung, K.F.</creatorcontrib><creatorcontrib>Skipp, P.J.</creatorcontrib><creatorcontrib>Dimitrov, B.</creatorcontrib><creatorcontrib>Djukanović, R.</creatorcontrib><creatorcontrib>the U-BIOPRED Study Group</creatorcontrib><creatorcontrib>U-BIOPRED Study Group</creatorcontrib><title>Sputum proteomic signature of gastro-oesophageal reflux in patients with severe asthma</title><title>Respiratory medicine</title><addtitle>Respir Med</addtitle><description>Gastro-oesophageal reflux disease (GORD) has long been associated with poor asthma control without an established cause-effect relationship.
610 asthmatics (421 severe/88 mild-moderate) and 101 healthy controls were assessed clinically and a subset of 154 severe asthmatics underwent proteomic analysis of induced sputum using untargeted mass spectrometry, LC-IMS-MSE. Univariate and multiple logistic regression analyses (MLR) were conducted to identify proteins associated with GORD in this cohort.
When compared to mild/moderate asthmatics and healthy individuals, respectively, GORD was three- and ten-fold more prevalent in severe asthmatics and was associated with increased asthma symptoms and oral corticosteroid use, poorer quality of life, depression/anxiety, obesity and symptoms of sino-nasal disease. Comparison of sputum proteomes in severe asthmatics with and without active GORD showed five differentially abundant proteins with described roles in anti-microbial defences, systemic inflammation and epithelial integrity. Three of these were associated with active GORD by multiple linear regression analysis: Ig lambda variable 1–47 (p = 0·017) and plasma protease C1 inhibitor (p = 0·043), both in lower concentrations, and lipocalin-1 (p = 0·034) in higher concentrations in active GORD.
This study provides evidence which suggests that reflux can cause subtle perturbation of proteins detectable in the airways lining fluid and that severe asthmatics with GORD may represent a distinct phenotype of asthma.
•5 proteins different in severe asthmatics with GORD.•Ig lambda variable 1–47 was associated with active GORD in severe asthma.•Lipocalin-1 was associated with active GORD in severe asthma.•Plasma protease C1 inhibitor was associated with active GORD in severe asthma.</description><subject>Adult</subject><subject>Antiinfectives and antibacterials</subject><subject>Anxiety</subject><subject>Asthma</subject><subject>Asthma - complications</subject><subject>Asthma - epidemiology</subject><subject>Asthma - metabolism</subject><subject>Asthma - psychology</subject><subject>Biomarkers</subject><subject>Cause-effect relationships</subject><subject>Complement component C1</subject><subject>Corticosteroids</subject><subject>Disease control</subject><subject>Endopeptidases - metabolism</subject><subject>Esophagus</subject><subject>European Union - organization & administration</subject><subject>Female</subject><subject>Gastroesophageal reflux</subject><subject>Gastroesophageal Reflux - complications</subject><subject>Gastroesophageal Reflux - diagnosis</subject><subject>Gastroesophageal Reflux - epidemiology</subject><subject>Humans</subject><subject>Immunoglobulin lambda-Chains - metabolism</subject><subject>Immunoglobulins</subject><subject>Keratin</subject><subject>Lipocalin</subject><subject>Lipocalin 1 - metabolism</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Mental depression</subject><subject>Microorganisms</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Phenotypes</subject><subject>Prevalence</subject><subject>Prospective Studies</subject><subject>Protease Inhibitors - metabolism</subject><subject>Proteinase inhibitors</subject><subject>Proteins</subject><subject>Proteomics - methods</subject><subject>Quality of Life</subject><subject>Questionnaires</subject><subject>Regression analysis</subject><subject>Respiratory diseases</subject><subject>Scientific imaging</subject><subject>Severity of Illness Index</subject><subject>Signs and symptoms</subject><subject>Sputum</subject><subject>Sputum - 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complications</topic><topic>Asthma - epidemiology</topic><topic>Asthma - metabolism</topic><topic>Asthma - psychology</topic><topic>Biomarkers</topic><topic>Cause-effect relationships</topic><topic>Complement component C1</topic><topic>Corticosteroids</topic><topic>Disease control</topic><topic>Endopeptidases - metabolism</topic><topic>Esophagus</topic><topic>European Union - organization & administration</topic><topic>Female</topic><topic>Gastroesophageal reflux</topic><topic>Gastroesophageal Reflux - complications</topic><topic>Gastroesophageal Reflux - diagnosis</topic><topic>Gastroesophageal Reflux - epidemiology</topic><topic>Humans</topic><topic>Immunoglobulin lambda-Chains - metabolism</topic><topic>Immunoglobulins</topic><topic>Keratin</topic><topic>Lipocalin</topic><topic>Lipocalin 1 - metabolism</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Mental depression</topic><topic>Microorganisms</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Phenotypes</topic><topic>Prevalence</topic><topic>Prospective Studies</topic><topic>Protease Inhibitors - metabolism</topic><topic>Proteinase inhibitors</topic><topic>Proteins</topic><topic>Proteomics - methods</topic><topic>Quality of Life</topic><topic>Questionnaires</topic><topic>Regression analysis</topic><topic>Respiratory diseases</topic><topic>Scientific imaging</topic><topic>Severity of Illness Index</topic><topic>Signs and symptoms</topic><topic>Sputum</topic><topic>Sputum - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tariq, K.</creatorcontrib><creatorcontrib>Schofield, J.P.R.</creatorcontrib><creatorcontrib>Nicholas, B.L.</creatorcontrib><creatorcontrib>Burg, D.</creatorcontrib><creatorcontrib>Brandsma, J.</creatorcontrib><creatorcontrib>Bansal, A.T.</creatorcontrib><creatorcontrib>Wilson, S.J.</creatorcontrib><creatorcontrib>Lutter, R.</creatorcontrib><creatorcontrib>Fowler, S.J.</creatorcontrib><creatorcontrib>Bakke</creatorcontrib><creatorcontrib>Caruso, M.</creatorcontrib><creatorcontrib>Dahlen, B.</creatorcontrib><creatorcontrib>Horváth, I.</creatorcontrib><creatorcontrib>Krug, N.</creatorcontrib><creatorcontrib>Montuschi, P.</creatorcontrib><creatorcontrib>Sanak, M.</creatorcontrib><creatorcontrib>Sandström, T.</creatorcontrib><creatorcontrib>Geiser, T.</creatorcontrib><creatorcontrib>Pandis, I.</creatorcontrib><creatorcontrib>Sousa, A.R.</creatorcontrib><creatorcontrib>Adcock, I.M.</creatorcontrib><creatorcontrib>Shaw, D.E.</creatorcontrib><creatorcontrib>Auffray, C.</creatorcontrib><creatorcontrib>Howarth, P.H.</creatorcontrib><creatorcontrib>Sterk, P.J.</creatorcontrib><creatorcontrib>Chung, K.F.</creatorcontrib><creatorcontrib>Skipp, P.J.</creatorcontrib><creatorcontrib>Dimitrov, B.</creatorcontrib><creatorcontrib>Djukanović, R.</creatorcontrib><creatorcontrib>the U-BIOPRED Study Group</creatorcontrib><creatorcontrib>U-BIOPRED Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Umeå universitet</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Respiratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tariq, K.</au><au>Schofield, J.P.R.</au><au>Nicholas, B.L.</au><au>Burg, D.</au><au>Brandsma, J.</au><au>Bansal, A.T.</au><au>Wilson, S.J.</au><au>Lutter, R.</au><au>Fowler, S.J.</au><au>Bakke</au><au>Caruso, M.</au><au>Dahlen, B.</au><au>Horváth, I.</au><au>Krug, N.</au><au>Montuschi, P.</au><au>Sanak, M.</au><au>Sandström, T.</au><au>Geiser, T.</au><au>Pandis, I.</au><au>Sousa, A.R.</au><au>Adcock, I.M.</au><au>Shaw, D.E.</au><au>Auffray, C.</au><au>Howarth, P.H.</au><au>Sterk, P.J.</au><au>Chung, K.F.</au><au>Skipp, P.J.</au><au>Dimitrov, B.</au><au>Djukanović, R.</au><aucorp>the U-BIOPRED Study Group</aucorp><aucorp>U-BIOPRED Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sputum proteomic signature of gastro-oesophageal reflux in patients with severe asthma</atitle><jtitle>Respiratory medicine</jtitle><addtitle>Respir Med</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>150</volume><spage>66</spage><epage>73</epage><pages>66-73</pages><issn>0954-6111</issn><issn>1532-3064</issn><eissn>1532-3064</eissn><abstract>Gastro-oesophageal reflux disease (GORD) has long been associated with poor asthma control without an established cause-effect relationship.
610 asthmatics (421 severe/88 mild-moderate) and 101 healthy controls were assessed clinically and a subset of 154 severe asthmatics underwent proteomic analysis of induced sputum using untargeted mass spectrometry, LC-IMS-MSE. Univariate and multiple logistic regression analyses (MLR) were conducted to identify proteins associated with GORD in this cohort.
When compared to mild/moderate asthmatics and healthy individuals, respectively, GORD was three- and ten-fold more prevalent in severe asthmatics and was associated with increased asthma symptoms and oral corticosteroid use, poorer quality of life, depression/anxiety, obesity and symptoms of sino-nasal disease. Comparison of sputum proteomes in severe asthmatics with and without active GORD showed five differentially abundant proteins with described roles in anti-microbial defences, systemic inflammation and epithelial integrity. Three of these were associated with active GORD by multiple linear regression analysis: Ig lambda variable 1–47 (p = 0·017) and plasma protease C1 inhibitor (p = 0·043), both in lower concentrations, and lipocalin-1 (p = 0·034) in higher concentrations in active GORD.
This study provides evidence which suggests that reflux can cause subtle perturbation of proteins detectable in the airways lining fluid and that severe asthmatics with GORD may represent a distinct phenotype of asthma.
•5 proteins different in severe asthmatics with GORD.•Ig lambda variable 1–47 was associated with active GORD in severe asthma.•Lipocalin-1 was associated with active GORD in severe asthma.•Plasma protease C1 inhibitor was associated with active GORD in severe asthma.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30961953</pmid><doi>10.1016/j.rmed.2019.02.008</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2101-8843</orcidid><orcidid>https://orcid.org/0000-0002-6733-0317</orcidid><orcidid>https://orcid.org/0000-0002-5896-2072</orcidid><orcidid>https://orcid.org/0000-0003-4106-8469</orcidid><orcidid>https://orcid.org/0000-0002-4524-1663</orcidid><orcidid>https://orcid.org/0000-0003-4542-6614</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0954-6111 |
ispartof | Respiratory medicine, 2019-04, Vol.150, p.66-73 |
issn | 0954-6111 1532-3064 1532-3064 |
language | eng |
recordid | cdi_swepub_primary_oai_swepub_ki_se_480642 |
source | MEDLINE; Elsevier ScienceDirect Journals; SWEPUB Freely available online; EZB Electronic Journals Library |
subjects | Adult Antiinfectives and antibacterials Anxiety Asthma Asthma - complications Asthma - epidemiology Asthma - metabolism Asthma - psychology Biomarkers Cause-effect relationships Complement component C1 Corticosteroids Disease control Endopeptidases - metabolism Esophagus European Union - organization & administration Female Gastroesophageal reflux Gastroesophageal Reflux - complications Gastroesophageal Reflux - diagnosis Gastroesophageal Reflux - epidemiology Humans Immunoglobulin lambda-Chains - metabolism Immunoglobulins Keratin Lipocalin Lipocalin 1 - metabolism Male Mass spectrometry Mass spectroscopy Mental depression Microorganisms Middle Aged Patients Phenotypes Prevalence Prospective Studies Protease Inhibitors - metabolism Proteinase inhibitors Proteins Proteomics - methods Quality of Life Questionnaires Regression analysis Respiratory diseases Scientific imaging Severity of Illness Index Signs and symptoms Sputum Sputum - metabolism |
title | Sputum proteomic signature of gastro-oesophageal reflux in patients with severe asthma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T17%3A31%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sputum%20proteomic%20signature%20of%20gastro-oesophageal%20reflux%20in%20patients%20with%20severe%20asthma&rft.jtitle=Respiratory%20medicine&rft.au=Tariq,%20K.&rft.aucorp=the%20U-BIOPRED%20Study%20Group&rft.date=2019-04-01&rft.volume=150&rft.spage=66&rft.epage=73&rft.pages=66-73&rft.issn=0954-6111&rft.eissn=1532-3064&rft_id=info:doi/10.1016/j.rmed.2019.02.008&rft_dat=%3Cproquest_swepu%3E2206230283%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2203689137&rft_id=info:pmid/30961953&rft_els_id=S0954611119300447&rfr_iscdi=true |