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« Previous AbstractVolatile organic compounds in bile can diagnose malignant biliary strictures in the setting of pancreatic cancer: a preliminary observation    Next AbstractVolatile Organic Compounds in Urine for Noninvasive Diagnosis of Malignant Biliary Strictures: A Pilot Study »

Gastrointest Endosc


Title:Volatile organic compounds in bile for early diagnosis of cholangiocarcinoma in patients with primary sclerosing cholangitis: a pilot study
Author(s):Navaneethan U; Parsi MA; Lourdusamy V; Bhatt A; Gutierrez NG; Grove D; Sanaka MR; Hammel JP; Stevens T; Vargo JJ; Dweik RA;
Address:"Department of Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, USA. Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA"
Journal Title:Gastrointest Endosc
Year:2015
Volume:20141212
Issue:4
Page Number:943 - 949
DOI: 10.1016/j.gie.2014.09.041
ISSN/ISBN:1097-6779 (Electronic) 0016-5107 (Print) 0016-5107 (Linking)
Abstract:"BACKGROUND: The diagnosis of cholangiocarcinoma (CCA) in patients with primary sclerosing cholangitis (PSC) is particularly difficult. The role of volatile organic compounds (VOCs) for diagnosis of CCA in patients with PSC is not known. OBJECTIVE: Our aim was to identify potential VOCs in the headspaces (gas above the sample) in bile that may predict CCA in patients with PSC. DESIGN: Prospective cross-sectional study. SETTING: Referral center. PATIENTS: A total of 32 patients undergoing ERCP for PSC and for CCA complicating PSC. INTERVENTIONS: ERCP, bile aspiration. MAIN OUTCOME MEASUREMENTS: Selected ion flow tube mass spectrometry was used to analyze the concentration of 22 prevalent VOCs in bile samples. Logistic regression analysis was performed to build a predictive model for diagnosis of CCA. RESULTS: Levels of several compounds (ethanol, acrylonitrile, acetonitrile, acetaldehyde, benzene, carbon disulfide, dimethyl sulfide, 2-propranolol) were significantly different in patients with CCA complicating PSC compared with those having PSC (P < .05). By using receiver operating characteristic curve analysis, we developed a model for the diagnosis of CCA adjusted for age and sex based on VOC levels of acrylonitrile, 3-methyl hexane, and benzene. The model (2.3239*log [acrylonitrile] + 0.9871*log [3-methyl hexane] + 0.8448*log [benzene]) < -0.12 identified the patients with CCA (area under the curve [AUC] = 0.89), with 90.5% sensitivity and 72.7% specificity (P = .02). LIMITATIONS: Sample size. CONCLUSION: The measurement of VOCs in biliary fluid may be useful to diagnose CCA in patients with PSC. A larger study with a longitudinal study design is required to confirm our pilot observations to diagnose CCA early in patients with PSC. ( CLINICAL TRIAL REGISTRATION NUMBER: NCT01565460.)"
Keywords:"Acrylonitrile/analysis Area Under Curve Benzene/analysis Bile/*chemistry Bile Duct Neoplasms/*diagnosis/metabolism Biomarkers, Tumor/*analysis Cholangiocarcinoma/*diagnosis/metabolism Cholangitis, Sclerosing/complications/*metabolism Cross-Sectional Studi;"
Notes:"MedlineNavaneethan, Udayakumar Parsi, Mansour A Lourdusamy, Vennisvasanth Bhatt, Amit Gutierrez, Norma G Grove, David Sanaka, Madhusudhan R Hammel, Jeffrey P Stevens, Tyler Vargo, John J Dweik, Raed A eng P01 HL107147/HL/NHLBI NIH HHS/ RR026231/RR/NCRR NIH HHS/ P01 HL081064/HL/NHLBI NIH HHS/ UL1TR 000439-06/TR/NCATS NIH HHS/ HL081064/HL/NHLBI NIH HHS/ U10 HL109250/HL/NHLBI NIH HHS/ HL107147/HL/NHLBI NIH HHS/ UL1 TR000439/TR/NCATS NIH HHS/ HL103453/HL/NHLBI NIH HHS/ P01 HL103453/HL/NHLBI NIH HHS/ R21 RR026231/RR/NCRR NIH HHS/ HL109250/HL/NHLBI NIH HHS/ Clinical Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2014/12/17 Gastrointest Endosc. 2015 Apr; 81(4):943-9.e1. doi: 10.1016/j.gie.2014.09.041. Epub 2014 Dec 12"

 
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