The impact of chronic hepatitis B viral infection on gastrointestinal motility

被引:12
作者
Chen, CY [1 ]
Lu, CL [1 ]
Chang, FY [1 ]
Huang, YS [1 ]
Lee, FY [1 ]
Lu, RH [1 ]
Kang, LJ [1 ]
Lee, SD [1 ]
机构
[1] Vet Gen Hosp, Div Gastroenterol, Dept Med, Taipei 11252, Taiwan
关键词
gastrointestinal motility; gastrointestinal transit; hepatitis B; liver cirrhosis; oro-caecal transit time (OCTT);
D O I
10.1097/00042737-200012090-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives Disturbed gastrointestinal (GI) motility probably exists in alcoholic cirrhotic patients; however, the influence of chronic hepatitis B virus (HBV) infection on GI motility remains unknown, The purpose of this prospective study was to determine the impact of chronic HBV infection on human GI transit, and to explore the possible patient factors modulating GI motility. Methods We used a non-invasive hydrogen breath test measuring the oro-caecal transit time (OCTT) to assess the GI motility in 45 asymptomatic HBV carriers, 26 patients with chronic hepatitis B, 23 patients with HBV-related liver cirrhosis, and 45 age- and sex-matched healthy volunteers. Their clinical symptoms and various blood parameters, such as platelet count, prothrombin time, etc, were recorded. Plasma substance P, nitrate/nitrite and endothelin-l levels were also measured. Results The OCTTs in controls, HBV carriers, chronic hepatitis B and liver cirrhosis patients were (mean +/- SEM) 78.4 +/- 5.8, 80.9 +/- 4.2, 93.9 +/- 8.8 and 106.5 +/- 12.4 min, respectively. The OCTT was delayed in patients with HBV-related liver cirrhosis compared to that of controls (P=0.039), Among the cirrhotic patients, presentation with ascites delayed OCTT (145.7 +/- 27.2 versus 91.3 +/- 11.9 min, P=0.039). Neither Child-Pugh grade, portal hypertension, various blood parameters, plasma substance P, nitrate/nitrite or endothelin-l levels had any influence on OCTT. Conclusions HBV infection alone does not alter GI motility, whereas the patients with liver cirrhosis may have delayed GI motility. Ascites is most likely a factor responsible for the delayed GI transit among chronic HBV-infected subjects. (C) 2000 Lippincott Williams & Wilkins.
引用
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页码:995 / 1000
页数:6
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