Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/28809
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dc.contributor.authorVANHOVE, Karolien-
dc.contributor.authorGIESEN, Pieter-
dc.contributor.authorOWOKOTOMO, Olajumoke Evangelina-
dc.contributor.authorMESOTTEN, Liesbet-
dc.contributor.authorLOUIS, Evelyne-
dc.contributor.authorSHKEDY, Ziv-
dc.contributor.authorTHOMEER, Michiel-
dc.contributor.authorADRIAENSENS, Peter-
dc.date.accessioned2019-07-24T16:53:37Z-
dc.date.available2019-07-24T16:53:37Z-
dc.date.issued2018-
dc.identifier.citationBMC CANCER, 18 (Art N° 868)-
dc.identifier.issn1471-2407-
dc.identifier.urihttp://hdl.handle.net/1942/28809-
dc.description.abstractBackground: Pulmonary imaging often identifies suspicious abnormalities resulting in supplementary diagnostic procedures. This study aims to investigate whether the metabolic fingerprint of plasma allows to discriminate between patients with lung inflammation and patients with lung cancer. Methods: Metabolic profiles of plasma from 347 controls, 269 cancer patients and 108 patients with inflammation were obtained by H-1-NMR spectroscopy. Models to discriminate between groups were trained by PLS-LDA. A test set was used for independent validation. A ROC curve was built to evaluate the diagnostic performance of potential biomarkers. Results: Sensitivity, specificity, PPV and NPV of PET-CT to diagnose cancer are 96, 23, 76 and 71%. Metabolic profiles differentiate between cancer and inflammation with a sensitivity of 89%, a specificity of 87% and a MCE of 12%. Removal of the glutamate metabolite results in an increase of MCE (38%) and a decrease of both sensitivity and specificity (62%), demonstrating the importance of glutamate for discrimination. At the cut-off point <= 0.31 on the ROC curve, the relative glutamate concentration discriminates between cancer and inflammation with a sensitivity of 85%, a specificity of 81%, and an AUC of 0.88. PPV and NPV are 92 and 69%. In PET-positive patients with a relative glutamate level 0.31 the sensitivity to diagnose cancer reaches 100% with a PPV of 94%. In PET-negative patients, a relative glutamate level > 031 increases the specificity of PET from 23% to 58% and results in a high NPV of 100%. In case of discrepancy between SUVmax and the glutamate concentration, lung cancer is missed in 19% of the cases. Conclusion: This study indicates that the H-1-NMR-derived relative plasma concentration of glutamate allows discrimination between lung cancer and lung inflammation. A glutamate level <= 0.31 in PET-positive patients corresponds to the diagnosis of lung cancer with a higher specificity and PPV than PET-CT. Glutamate levels > 0.31 in patients with PET negative lung lesions is likely to correspond with inflammation. Caution is needed for patients with conflicting SUVmax values and glutamate concentrations. Confirmation is needed in a prospective study with external validation and by another analytical technique such as HPLC-MS.-
dc.language.isoen-
dc.publisherBMC-
dc.rightsThe Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0-
dc.subject.otherLung cancer; Lung inflammation; 1 H-NMR; Metabolic phenotype; Glutamate; ROC-
dc.subject.otherLung cancer; Lung inflammation; H-1-NMR; Metabolic phenotype; Glutamate; ROC-
dc.titleThe plasma glutamate concentration as a complementary tool to differentiate benign PET-positive lung lesions from lung cancer-
dc.typeJournal Contribution-
dc.identifier.volume18-
local.format.pages12-
local.bibliographicCitation.jcatA1-
dc.description.notes[Vanhove, K.; Mesotten, L.; Thomeer, M.] Hasselt Univ, Fac Med & Life Sci, Martelarenlaan 42, B-3500 Hasselt, Belgium. [Vanhove, K.] Algemeen Ziekenhuis Vesalius, Dept Resp Med, Hazelereik 51, B-3700 Tongeren, Belgium. [Giesen, P.; Owokotomo, O. E.; Shkedy, Z.] Hasselt Univ, Inst Biostat & Stat Bioinformat, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium. [Mesotten, L.] Ziekenhuis Oost Limburg, Dept Nucl Med, Schiepse Bos 6, B-3600 Genk, Belgium. [Louis, E.] Univ Hosp Leuven, Dept Resp Med, Herestr 49, B-3000 Leuven, Belgium. [Thomeer, M.] Ziekenhuis Oost Limburg, Dept Resp Med, Schiepse Bos 6, B-3600 Genk, Belgium. [Adriaensens, P.] Hasselt Univ, Inst Mat Res, Appl & Analyt Chem, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium.-
local.publisher.placeLONDON-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr868-
dc.identifier.doi10.1186/s12885-018-4755-1-
dc.identifier.isi000443891900009-
item.contributorVANHOVE, Karolien-
item.contributorGIESEN, Pieter-
item.contributorOWOKOTOMO, Olajumoke Evangelina-
item.contributorMESOTTEN, Liesbet-
item.contributorLOUIS, Evelyne-
item.contributorSHKEDY, Ziv-
item.contributorTHOMEER, Michiel-
item.contributorADRIAENSENS, Peter-
item.fullcitationVANHOVE, Karolien; GIESEN, Pieter; OWOKOTOMO, Olajumoke Evangelina; MESOTTEN, Liesbet; LOUIS, Evelyne; SHKEDY, Ziv; THOMEER, Michiel & ADRIAENSENS, Peter (2018) The plasma glutamate concentration as a complementary tool to differentiate benign PET-positive lung lesions from lung cancer. In: BMC CANCER, 18 (Art N° 868).-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
item.validationecoom 2019-
crisitem.journal.eissn1471-2407-
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