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Mechanism of impaired glucose tolerance in patients with neoplasia.

The disappearance rate (k) of i.v. glucose was measured in cachectic and non-cachectic cancer patients and tumour-free controls. The respective k values were found to be 1.06 +/- 0.27 (mean +/- s.d.), 1.64 +/- 0.34 and 1.63 +/- 0.23. Of the other parameters measured, only plasma albumin level was fo...

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Autores principales: Jasani, B., Donaldson, L. J., Ratcliffe, J. G., Sokhi, G. S.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009725/
https://www.ncbi.nlm.nih.gov/pubmed/698044
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author Jasani, B.
Donaldson, L. J.
Ratcliffe, J. G.
Sokhi, G. S.
author_facet Jasani, B.
Donaldson, L. J.
Ratcliffe, J. G.
Sokhi, G. S.
author_sort Jasani, B.
collection PubMed
description The disappearance rate (k) of i.v. glucose was measured in cachectic and non-cachectic cancer patients and tumour-free controls. The respective k values were found to be 1.06 +/- 0.27 (mean +/- s.d.), 1.64 +/- 0.34 and 1.63 +/- 0.23. Of the other parameters measured, only plasma albumin level was found to vary significantly amongst the 3 categories, the mean level being the lowest in cachectic cancer patients. The means of total plasma protein, fasting blood glucose and plasma liver enzyme concentrations were similar in the 3 groups. Glucagon, a potent insulin secretogogue, failed to augment the fasting insulin level in cachectic but did so in non-cachectic cancer patients. Taken together, the findings suggest that the reduced glucose tolerance in patients with neoplasia is due to impairment of insulin release exhibited predominantly by ill-nourished advanced cancer patients having a moderate to sever degree of hypoalbuminemia.
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spelling pubmed-20097252009-09-10 Mechanism of impaired glucose tolerance in patients with neoplasia. Jasani, B. Donaldson, L. J. Ratcliffe, J. G. Sokhi, G. S. Br J Cancer Research Article The disappearance rate (k) of i.v. glucose was measured in cachectic and non-cachectic cancer patients and tumour-free controls. The respective k values were found to be 1.06 +/- 0.27 (mean +/- s.d.), 1.64 +/- 0.34 and 1.63 +/- 0.23. Of the other parameters measured, only plasma albumin level was found to vary significantly amongst the 3 categories, the mean level being the lowest in cachectic cancer patients. The means of total plasma protein, fasting blood glucose and plasma liver enzyme concentrations were similar in the 3 groups. Glucagon, a potent insulin secretogogue, failed to augment the fasting insulin level in cachectic but did so in non-cachectic cancer patients. Taken together, the findings suggest that the reduced glucose tolerance in patients with neoplasia is due to impairment of insulin release exhibited predominantly by ill-nourished advanced cancer patients having a moderate to sever degree of hypoalbuminemia. Nature Publishing Group 1978-08 /pmc/articles/PMC2009725/ /pubmed/698044 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Jasani, B.
Donaldson, L. J.
Ratcliffe, J. G.
Sokhi, G. S.
Mechanism of impaired glucose tolerance in patients with neoplasia.
title Mechanism of impaired glucose tolerance in patients with neoplasia.
title_full Mechanism of impaired glucose tolerance in patients with neoplasia.
title_fullStr Mechanism of impaired glucose tolerance in patients with neoplasia.
title_full_unstemmed Mechanism of impaired glucose tolerance in patients with neoplasia.
title_short Mechanism of impaired glucose tolerance in patients with neoplasia.
title_sort mechanism of impaired glucose tolerance in patients with neoplasia.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009725/
https://www.ncbi.nlm.nih.gov/pubmed/698044
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