Breath biomarkers for detection of human liver diseases: preliminary study

被引:109
作者
Sehnert, SS
Jiang, L
Burdick, JF
Risby, TH
机构
[1] Johns Hopkins Med Inst, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, Dept Surg, Baltimore, MD 21205 USA
关键词
breath carbonyl sulphide; carbon disulphide; dimethyl sulphide; isoprene; liver diseases; hepatocellular diseases; diseases of the bile duct; staging disease;
D O I
10.1080/13547500110118184
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chronic liver disease is initially occult, has multiple aetiologies, involves complex diagnostic questions, and requires follow-up because progression is likely. Blood tests and biopsies are generally used, but have disadvantages. We have developed a new test for liver disease based on abnormal concentrations of metabolic products detected in exhaled breath. This test can be used, in conjunction with other clinically accepted diagnostic protocols, to detect and classify chronic liver diseases. Samples of breath collected from spontaneously breathing human subjects (86 patients presenting with 13 liver diseases and 109 subjects with normal liver function) were concentrated cryogenically and analysed by wide-bore capillary gas chromatography using various detectors. The concentrations of various molecules in exhaled breath were examined for potential use as biomarkers of liver function. Subjects with chronic liver diseases could be differentiated from those with normal liver function by comparing levels of breath carbonyl sulphide, carbon disulphide and isoprene; these differences were confirmed and correlated by comparing the levels with standard clinical blood markers of liver damage. The presence of chronic liver failure can thus be detected with sensitivity and specificity by quantifying sulphur-containing compounds arising from the abnormal metabolism associated with liver disease. The breath test we have developed appears to distinguish between hepatocellular and biliary tract aetiologies, and allows staging for severity. This approach may provide the clinician with a simple, non-invasive technique for use in the screening of large populations and follow-up for patients with chronic liver disease.
引用
收藏
页码:174 / 187
页数:14
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