Breath Biopsy Assessment of Liver Disease Using an Exogenous Volatile Organic Compound—Toward Improved Detection of Liver Impairment
Liver cirrhosis and its complication - hepatocellular carcinoma (HCC) - have been associated with increased exhaled limonene. It is currently unclear whether this increase is more strongly associated with the presence of HCC or with the severity of liver dysfunction. We compared the exhaled breath o...
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Veröffentlicht in: | Clinical and translational gastroenterology 2020-09, Vol.11 (9), p.e00239-e00239 |
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creator | Ferrandino, Giuseppe Orf, Isabel Smith, Rob Calcagno, Marzia Thind, Anita Kaur Debiram-Beecham, Irene Williams, Megan Gandelman, Olga de Saedeleer, Alexandra Kibble, Graham Lydon, Anne Marie Mayhew, Chris A. Allsworth, Max Boyle, Billy van der Schee, Marc P. Allison, Michael Hoare, Matthew Snowdon, Victoria K. |
description | Liver cirrhosis and its complication - hepatocellular carcinoma (HCC) - have been associated with increased exhaled limonene. It is currently unclear whether this increase is more strongly associated with the presence of HCC or with the severity of liver dysfunction.
We compared the exhaled breath of 40 controls, 32 cirrhotic patients, and 12 cirrhotic patients with HCC using the Breath Biopsy platform. Breath samples were analyzed by thermal desorption-gas chromatography-mass spectrometry. Limonene levels were compared between the groups and correlated to bilirubin, albumin, prothrombin time international normalized ratio, and alanine aminotransferase.
Breath limonene concentration was significantly elevated in subjects with cirrhosis-induced HCC (M: 82.1 ng/L, interquartile range [IQR]: 16.33-199.32 ng/L) and cirrhosis (M: 32.6 ng/L, IQR: 6.55-123.07 ng/L) compared with controls (M: 6.2 ng/L, IQR: 2.62-9.57 ng/L) (P value = 0.0005 and 0.0001, respectively) with no significant difference between 2 diseased groups (P value = 0.37). Levels of exhaled limonene correlated with serum bilirubin (R = 0.25, P value = 0.0016, r = 0.51), albumin (R = 0.58, P value = 5.3e-8, r = -0.76), and international normalized ratio (R = 0.29, P value = 0.0003, r = 0.51), but not with alanine aminotransferase (R = 0.01, P value = 0.36, r = 0.19).
Exhaled limonene levels are primarily affected by the presence of cirrhosis through reduced liver functional capacity, as indicated by limonene correlation with blood metrics of impaired hepatic clearance and protein synthesis capacity, without further alterations observed in subjects with HCC. This suggests that exhaled limonene is a potential non-invasive marker of liver metabolic capacity (see Visual abstract, Supplementary Digital Content 1, http://links.lww.com/CTG/A388). |
doi_str_mv | 10.14309/ctg.0000000000000239 |
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We compared the exhaled breath of 40 controls, 32 cirrhotic patients, and 12 cirrhotic patients with HCC using the Breath Biopsy platform. Breath samples were analyzed by thermal desorption-gas chromatography-mass spectrometry. Limonene levels were compared between the groups and correlated to bilirubin, albumin, prothrombin time international normalized ratio, and alanine aminotransferase.
Breath limonene concentration was significantly elevated in subjects with cirrhosis-induced HCC (M: 82.1 ng/L, interquartile range [IQR]: 16.33-199.32 ng/L) and cirrhosis (M: 32.6 ng/L, IQR: 6.55-123.07 ng/L) compared with controls (M: 6.2 ng/L, IQR: 2.62-9.57 ng/L) (P value = 0.0005 and 0.0001, respectively) with no significant difference between 2 diseased groups (P value = 0.37). Levels of exhaled limonene correlated with serum bilirubin (R = 0.25, P value = 0.0016, r = 0.51), albumin (R = 0.58, P value = 5.3e-8, r = -0.76), and international normalized ratio (R = 0.29, P value = 0.0003, r = 0.51), but not with alanine aminotransferase (R = 0.01, P value = 0.36, r = 0.19).
Exhaled limonene levels are primarily affected by the presence of cirrhosis through reduced liver functional capacity, as indicated by limonene correlation with blood metrics of impaired hepatic clearance and protein synthesis capacity, without further alterations observed in subjects with HCC. This suggests that exhaled limonene is a potential non-invasive marker of liver metabolic capacity (see Visual abstract, Supplementary Digital Content 1, http://links.lww.com/CTG/A388).</description><identifier>ISSN: 2155-384X</identifier><identifier>EISSN: 2155-384X</identifier><identifier>DOI: 10.14309/ctg.0000000000000239</identifier><identifier>PMID: 33094960</identifier><language>eng</language><publisher>United States: Wolters Kluwer</publisher><subject>Adult ; Age ; Aged ; Aged, 80 and over ; Biomarkers - analysis ; Breath Tests ; Carcinoma, Hepatocellular - diagnosis ; Carcinoma, Hepatocellular - pathology ; Carcinoma, Hepatocellular - physiopathology ; Case-Control Studies ; Cross-Sectional Studies ; Female ; Humans ; Limonene - analysis ; Liver ; Liver - pathology ; Liver - physiopathology ; Liver cancer ; Liver cirrhosis ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - pathology ; Liver Cirrhosis - physiopathology ; Liver diseases ; Liver Function Tests - methods ; Liver Neoplasms - diagnosis ; Liver Neoplasms - pathology ; Liver Neoplasms - physiopathology ; Male ; Metabolism ; Middle Aged ; Prospective Studies ; Severity of Illness Index ; Surveillance ; Volatile Organic Compounds - analysis</subject><ispartof>Clinical and translational gastroenterology, 2020-09, Vol.11 (9), p.e00239-e00239</ispartof><rights>Wolters Kluwer</rights><rights>2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4842-5afd77bc333691599bf965f35e15be2bda7d46a445ed07947065c2c8774a10a43</citedby><cites>FETCH-LOGICAL-c4842-5afd77bc333691599bf965f35e15be2bda7d46a445ed07947065c2c8774a10a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498135/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498135/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33094960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ferrandino, Giuseppe</creatorcontrib><creatorcontrib>Orf, Isabel</creatorcontrib><creatorcontrib>Smith, Rob</creatorcontrib><creatorcontrib>Calcagno, Marzia</creatorcontrib><creatorcontrib>Thind, Anita Kaur</creatorcontrib><creatorcontrib>Debiram-Beecham, Irene</creatorcontrib><creatorcontrib>Williams, Megan</creatorcontrib><creatorcontrib>Gandelman, Olga</creatorcontrib><creatorcontrib>de Saedeleer, Alexandra</creatorcontrib><creatorcontrib>Kibble, Graham</creatorcontrib><creatorcontrib>Lydon, Anne Marie</creatorcontrib><creatorcontrib>Mayhew, Chris A.</creatorcontrib><creatorcontrib>Allsworth, Max</creatorcontrib><creatorcontrib>Boyle, Billy</creatorcontrib><creatorcontrib>van der Schee, Marc P.</creatorcontrib><creatorcontrib>Allison, Michael</creatorcontrib><creatorcontrib>Hoare, Matthew</creatorcontrib><creatorcontrib>Snowdon, Victoria K.</creatorcontrib><title>Breath Biopsy Assessment of Liver Disease Using an Exogenous Volatile Organic Compound—Toward Improved Detection of Liver Impairment</title><title>Clinical and translational gastroenterology</title><addtitle>Clin Transl Gastroenterol</addtitle><description>Liver cirrhosis and its complication - hepatocellular carcinoma (HCC) - have been associated with increased exhaled limonene. It is currently unclear whether this increase is more strongly associated with the presence of HCC or with the severity of liver dysfunction.
We compared the exhaled breath of 40 controls, 32 cirrhotic patients, and 12 cirrhotic patients with HCC using the Breath Biopsy platform. Breath samples were analyzed by thermal desorption-gas chromatography-mass spectrometry. Limonene levels were compared between the groups and correlated to bilirubin, albumin, prothrombin time international normalized ratio, and alanine aminotransferase.
Breath limonene concentration was significantly elevated in subjects with cirrhosis-induced HCC (M: 82.1 ng/L, interquartile range [IQR]: 16.33-199.32 ng/L) and cirrhosis (M: 32.6 ng/L, IQR: 6.55-123.07 ng/L) compared with controls (M: 6.2 ng/L, IQR: 2.62-9.57 ng/L) (P value = 0.0005 and 0.0001, respectively) with no significant difference between 2 diseased groups (P value = 0.37). Levels of exhaled limonene correlated with serum bilirubin (R = 0.25, P value = 0.0016, r = 0.51), albumin (R = 0.58, P value = 5.3e-8, r = -0.76), and international normalized ratio (R = 0.29, P value = 0.0003, r = 0.51), but not with alanine aminotransferase (R = 0.01, P value = 0.36, r = 0.19).
Exhaled limonene levels are primarily affected by the presence of cirrhosis through reduced liver functional capacity, as indicated by limonene correlation with blood metrics of impaired hepatic clearance and protein synthesis capacity, without further alterations observed in subjects with HCC. This suggests that exhaled limonene is a potential non-invasive marker of liver metabolic capacity (see Visual abstract, Supplementary Digital Content 1, http://links.lww.com/CTG/A388).</description><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers - analysis</subject><subject>Breath Tests</subject><subject>Carcinoma, Hepatocellular - diagnosis</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Carcinoma, Hepatocellular - physiopathology</subject><subject>Case-Control Studies</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Limonene - analysis</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver - physiopathology</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver Cirrhosis - physiopathology</subject><subject>Liver diseases</subject><subject>Liver Function Tests - methods</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - pathology</subject><subject>Liver Neoplasms - physiopathology</subject><subject>Male</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Severity of Illness Index</subject><subject>Surveillance</subject><subject>Volatile Organic Compounds - analysis</subject><issn>2155-384X</issn><issn>2155-384X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkc9u1DAQxiMEolXpI4AsceGS4r9xfEFqtwUqrdRLi7hZTjLJuiR2sJNdeuPEE_CEPAletpSllqwZaX7zjcdflr0k-IRwhtXbeupO8P6hTD3JDikRImcl__x0Lz_IjmO83UIc01Kp59kBSxpcFfgw-3EWwEwrdGb9GO_QaYwQ4wBuQr5FS7uGgM5tBBMB3UTrOmQcuvjmO3B-juiT781ke0BXoTPO1mjhh9HPrvn1_ee135jQoMthDH4NDTqHCerJevdPOdWMDdtpL7JnrekjHN_Ho-zm_cX14mO-vPpwuThd5jUvOc2FaRspq5oxVigilKpaVYiWCSCiAlo1Rja8MJwLaLBUXOJC1LQupeSGYMPZUfZupzvO1QBNnUYH0-sx2MGEO-2N1f9XnF3pzq-15KokTCSBN_cCwX-dIU56sLGGvjcO0o9oygUnuKCFTOjrR-itn4NL62kqsOSFFEQlSuyoOvgYA7QPjyFY_zFbJ7P1Y7NT36v9TR66_lqbAL4DNr6fIMQv_byBoFdg-mmlMZEUJzKneBuTaJ4uoew37MG3zA</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Ferrandino, Giuseppe</creator><creator>Orf, Isabel</creator><creator>Smith, Rob</creator><creator>Calcagno, Marzia</creator><creator>Thind, Anita Kaur</creator><creator>Debiram-Beecham, Irene</creator><creator>Williams, Megan</creator><creator>Gandelman, Olga</creator><creator>de Saedeleer, Alexandra</creator><creator>Kibble, Graham</creator><creator>Lydon, Anne Marie</creator><creator>Mayhew, Chris A.</creator><creator>Allsworth, Max</creator><creator>Boyle, Billy</creator><creator>van der Schee, Marc P.</creator><creator>Allison, Michael</creator><creator>Hoare, Matthew</creator><creator>Snowdon, Victoria K.</creator><general>Wolters Kluwer</general><general>Wolters Kluwer Health Medical Research, Lippincott Williams & Wilkins</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>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200901</creationdate><title>Breath Biopsy Assessment of Liver Disease Using an Exogenous Volatile Organic Compound—Toward Improved Detection of Liver Impairment</title><author>Ferrandino, Giuseppe ; Orf, Isabel ; Smith, Rob ; Calcagno, Marzia ; Thind, Anita Kaur ; Debiram-Beecham, Irene ; Williams, Megan ; Gandelman, Olga ; de Saedeleer, Alexandra ; Kibble, Graham ; Lydon, Anne Marie ; Mayhew, Chris A. ; Allsworth, Max ; Boyle, Billy ; van der Schee, Marc P. ; Allison, Michael ; Hoare, Matthew ; Snowdon, Victoria K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4842-5afd77bc333691599bf965f35e15be2bda7d46a445ed07947065c2c8774a10a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers - analysis</topic><topic>Breath Tests</topic><topic>Carcinoma, Hepatocellular - diagnosis</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Carcinoma, Hepatocellular - physiopathology</topic><topic>Case-Control Studies</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Limonene - analysis</topic><topic>Liver</topic><topic>Liver - pathology</topic><topic>Liver - physiopathology</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver Cirrhosis - physiopathology</topic><topic>Liver diseases</topic><topic>Liver Function Tests - methods</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - pathology</topic><topic>Liver Neoplasms - physiopathology</topic><topic>Male</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Severity of Illness Index</topic><topic>Surveillance</topic><topic>Volatile Organic Compounds - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferrandino, Giuseppe</creatorcontrib><creatorcontrib>Orf, Isabel</creatorcontrib><creatorcontrib>Smith, Rob</creatorcontrib><creatorcontrib>Calcagno, Marzia</creatorcontrib><creatorcontrib>Thind, Anita Kaur</creatorcontrib><creatorcontrib>Debiram-Beecham, Irene</creatorcontrib><creatorcontrib>Williams, Megan</creatorcontrib><creatorcontrib>Gandelman, Olga</creatorcontrib><creatorcontrib>de Saedeleer, Alexandra</creatorcontrib><creatorcontrib>Kibble, Graham</creatorcontrib><creatorcontrib>Lydon, Anne Marie</creatorcontrib><creatorcontrib>Mayhew, Chris A.</creatorcontrib><creatorcontrib>Allsworth, Max</creatorcontrib><creatorcontrib>Boyle, Billy</creatorcontrib><creatorcontrib>van der Schee, Marc P.</creatorcontrib><creatorcontrib>Allison, Michael</creatorcontrib><creatorcontrib>Hoare, Matthew</creatorcontrib><creatorcontrib>Snowdon, Victoria K.</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content 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>Clinical and translational gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferrandino, Giuseppe</au><au>Orf, Isabel</au><au>Smith, Rob</au><au>Calcagno, Marzia</au><au>Thind, Anita Kaur</au><au>Debiram-Beecham, Irene</au><au>Williams, Megan</au><au>Gandelman, Olga</au><au>de Saedeleer, Alexandra</au><au>Kibble, Graham</au><au>Lydon, Anne Marie</au><au>Mayhew, Chris A.</au><au>Allsworth, Max</au><au>Boyle, Billy</au><au>van der Schee, Marc P.</au><au>Allison, Michael</au><au>Hoare, Matthew</au><au>Snowdon, Victoria K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Breath Biopsy Assessment of Liver Disease Using an Exogenous Volatile Organic Compound—Toward Improved Detection of Liver Impairment</atitle><jtitle>Clinical and translational gastroenterology</jtitle><addtitle>Clin Transl Gastroenterol</addtitle><date>2020-09-01</date><risdate>2020</risdate><volume>11</volume><issue>9</issue><spage>e00239</spage><epage>e00239</epage><pages>e00239-e00239</pages><issn>2155-384X</issn><eissn>2155-384X</eissn><abstract>Liver cirrhosis and its complication - hepatocellular carcinoma (HCC) - have been associated with increased exhaled limonene. It is currently unclear whether this increase is more strongly associated with the presence of HCC or with the severity of liver dysfunction.
We compared the exhaled breath of 40 controls, 32 cirrhotic patients, and 12 cirrhotic patients with HCC using the Breath Biopsy platform. Breath samples were analyzed by thermal desorption-gas chromatography-mass spectrometry. Limonene levels were compared between the groups and correlated to bilirubin, albumin, prothrombin time international normalized ratio, and alanine aminotransferase.
Breath limonene concentration was significantly elevated in subjects with cirrhosis-induced HCC (M: 82.1 ng/L, interquartile range [IQR]: 16.33-199.32 ng/L) and cirrhosis (M: 32.6 ng/L, IQR: 6.55-123.07 ng/L) compared with controls (M: 6.2 ng/L, IQR: 2.62-9.57 ng/L) (P value = 0.0005 and 0.0001, respectively) with no significant difference between 2 diseased groups (P value = 0.37). Levels of exhaled limonene correlated with serum bilirubin (R = 0.25, P value = 0.0016, r = 0.51), albumin (R = 0.58, P value = 5.3e-8, r = -0.76), and international normalized ratio (R = 0.29, P value = 0.0003, r = 0.51), but not with alanine aminotransferase (R = 0.01, P value = 0.36, r = 0.19).
Exhaled limonene levels are primarily affected by the presence of cirrhosis through reduced liver functional capacity, as indicated by limonene correlation with blood metrics of impaired hepatic clearance and protein synthesis capacity, without further alterations observed in subjects with HCC. This suggests that exhaled limonene is a potential non-invasive marker of liver metabolic capacity (see Visual abstract, Supplementary Digital Content 1, http://links.lww.com/CTG/A388).</abstract><cop>United States</cop><pub>Wolters Kluwer</pub><pmid>33094960</pmid><doi>10.14309/ctg.0000000000000239</doi><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adult Age Aged Aged, 80 and over Biomarkers - analysis Breath Tests Carcinoma, Hepatocellular - diagnosis Carcinoma, Hepatocellular - pathology Carcinoma, Hepatocellular - physiopathology Case-Control Studies Cross-Sectional Studies Female Humans Limonene - analysis Liver Liver - pathology Liver - physiopathology Liver cancer Liver cirrhosis Liver Cirrhosis - diagnosis Liver Cirrhosis - pathology Liver Cirrhosis - physiopathology Liver diseases Liver Function Tests - methods Liver Neoplasms - diagnosis Liver Neoplasms - pathology Liver Neoplasms - physiopathology Male Metabolism Middle Aged Prospective Studies Severity of Illness Index Surveillance Volatile Organic Compounds - analysis |
title | Breath Biopsy Assessment of Liver Disease Using an Exogenous Volatile Organic Compound—Toward Improved Detection of Liver Impairment |
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