There is accumulating evidence indicating that the presence of malignant disease is accompanied by profound changes of liver metabolism in the cancer-bearing host. We previously reported [P. C. Dagnelie, J. D. Bell, -S. C. R. Williams, T. E. Bates, P. D. Abel and C. S. Foster, Br. J. Cancer 67, 1303
Quantitative P-31 MR spectroscopy of the liver in alcoholic cirrhosis
β Scribed by Vasanthan Rajanayagam; Roland R. Lee; Zvi Ackerman; William G. Bradley; Brian D. Ross
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 751 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1053-1807
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β¦ Synopsis
Abstract
To determine the cause of reduced urea synthesis in cirrhosis, absolute concentrations of phosphorus metabolites in the human liver have been measured in vivo with magnetic resonance (MR) spectroscopy. Oneβdimensional chemical shift imaging was used to obtain phosphorusβ31 spectra from five healthy volunteers and five patients with alcoholic cirrhosis. A reference standard included in all studies enabled the calculation of absolute concentrations. In contrast to hepatic metabolite ratios, absolute concentrations reveal that in the cirrhotic patients, concentrations of adenosine triphosphate (ATP) were significantly reduced and concentrations of phosphomonoesters slightly reduced. Intracellular pH was unchanged. Histologic evidence suggests that the amount of ATP per cell was unchanged and could not account for the reduced urea production. Instead, urea synthesis depends on the functional liver cell mass, which was reduced by 31% in alcoholic cirrhosis. Quantitative in vivo Pβ31 MR spectroscopy of liver has potential clinical applications and can supplement the more generally used Pβ31 metabolite ratios.
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