Literature DB >> 25891513

Analysis of breath volatile organic compounds in children with chronic liver disease compared to healthy controls.

Katharine Eng1, Naim Alkhouri, Frank Cikach, Nishaben Patel, Chen Yan, David Grove, Rocio Lopez, Ellen Rome, Raed A Dweik.   

Abstract

Breath testing is increasingly being used as a non-invasive diagnostic tool for disease states across medicine. The purpose of this study was to compare the levels of volatile organic compounds (VOCs) as measured by mass spectrometry in healthy children and children with chronic liver disease (CLD). Patients between the ages of 6 and 21 were recruited for the study. Control subjects were recruited from a general pediatric population during well-child visits, while patients with CLD were recruited from pediatric gastroenterology clinic visits. The diagnosis of CLD was confirmed by clinical, laboratory, and/or histologic data. A single exhaled breath was collected and analyzed by means of selected-ion flow-tube mass spectrometry per protocol. A total of 104 patients were included in the study (49 with CLD and 55 healthy controls). Of the patients with CLD, 20 had advanced liver fibrosis (F3-F4). In the CLD cohort, levels of exhaled 1-decene, 1-heptene, 1-octene and 3 methylhexane were found to be significantly higher when compared to the control population (p < 0.001, p = 0.035, p < 0.001 and p = 0.004, respectively). Exhaled 1-nonene, (E)-2-nonene, and dimethyl sulfide levels were found to be significantly lower in patients with CLD patients when compared to controls (p < 0.001, p < 0.001 and p = 0.007, respectively). By utilizing a combination of five of the VOCs, the accuracy for predicting the presence of CLD was excellent (AUROC = 0.97). Our study demonstrates that children with CLD have a unique pattern of exhaled VOCs. Utilization of a combination of these VOCs represents a promising non-invasive diagnostic tool and may provide further insight into the pathophysiologic processes and pathways leading to pediatric liver disease. Further analysis of these compounds in external cohorts are needed to validate our findings.

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Year:  2015        PMID: 25891513     DOI: 10.1088/1752-7155/9/2/026002

Source DB:  PubMed          Journal:  J Breath Res        ISSN: 1752-7155            Impact factor:   3.262


  11 in total

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Authors:  L M Wirtz; S Kreuer; T Volk; T Hüppe
Journal:  Med Klin Intensivmed Notfmed       Date:  2019-02-06       Impact factor: 0.840

Review 2.  Novel methods in pulmonary hypertension phenotyping in the age of precision medicine (2015 Grover Conference series).

Authors:  Jarrod W Barnes; Adriano R Tonelli; Gustavo A Heresi; Jennie E Newman; Noël E Mellor; David E Grove; Raed A Dweik
Journal:  Pulm Circ       Date:  2016-12       Impact factor: 3.017

3.  Human breath metabolomics using an optimized non-invasive exhaled breath condensate sampler.

Authors:  Konstantin O Zamuruyev; Alexander A Aksenov; Alberto Pasamontes; Joshua F Brown; Dayna R Pettit; Soraya Foutouhi; Bart C Weimer; Michael Schivo; Nicholas J Kenyon; Jean-Pierre Delplanque; Cristina E Davis
Journal:  J Breath Res       Date:  2016-12-22       Impact factor: 3.262

4.  The breath print represents a novel biomarker of malnutrition in pulmonary arterial hypertension: A proof of concept study.

Authors:  Jacob T Mey; Mary C Rath; Kathleen McLaughlin; Marianne Galang; Kathryn Lynch; Jaime DiMattio; Hillary Nason; Shengping Yang; Celia A Melillo; David E Grove; Adriano R Tonelli; Gustavo A Heresi; John P Kirwan; Raed A Dweik
Journal:  JPEN J Parenter Enteral Nutr       Date:  2021-11-12       Impact factor: 3.896

5.  Power-efficient self-cleaning hydrophilic condenser surface for portable exhaled breath condensate (EBC) metabolomic sampling.

Authors:  Konstantin O Zamuruyev; Alexander J Schmidt; Eva Borras; Mitchell M McCartney; Michael Schivo; Nicholas J Kenyon; Jean-Pierre Delplanque; Cristina E Davis
Journal:  J Breath Res       Date:  2018-06-08       Impact factor: 3.262

6.  Blinded Validation of Breath Biomarkers of Lung Cancer, a Potential Ancillary to Chest CT Screening.

Authors:  Michael Phillips; Thomas L Bauer; Renee N Cataneo; Cassie Lebauer; Mayur Mundada; Harvey I Pass; Naren Ramakrishna; William N Rom; Eric Vallières
Journal:  PLoS One       Date:  2015-12-23       Impact factor: 3.240

7.  Exhaled volatile substances mirror clinical conditions in pediatric chronic kidney disease.

Authors:  Juliane Obermeier; Phillip Trefz; Josephine Happ; Jochen K Schubert; Hagen Staude; Dagmar-Christiane Fischer; Wolfram Miekisch
Journal:  PLoS One       Date:  2017-06-01       Impact factor: 3.240

8.  Breath Metabolomics Provides an Accurate and Noninvasive Approach for Screening Cirrhosis, Primary, and Secondary Liver Tumors.

Authors:  Galen Miller-Atkins; Lou-Anne Acevedo-Moreno; David Grove; Raed A Dweik; Adriano R Tonelli; J Mark Brown; Daniela S Allende; Federico Aucejo; Daniel M Rotroff
Journal:  Hepatol Commun       Date:  2020-04-26

9.  Exhaled volatile organic compounds analysis in clinical pediatrics: a systematic review.

Authors:  Rosa A Sola Martínez; José M Pastor Hernández; Óscar Yanes Torrado; Manuel Cánovas Díaz; Teresa de Diego Puente; María Vinaixa Crevillent
Journal:  Pediatr Res       Date:  2020-09-12       Impact factor: 3.756

Review 10.  Electronic Noses for Well-Being: Breath Analysis and Energy Expenditure.

Authors:  Julian W Gardner; Timothy A Vincent
Journal:  Sensors (Basel)       Date:  2016-06-23       Impact factor: 3.576

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