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Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test

OBJECTIVE: Limited data from pharmacokinetic studies in underweight and severely malnourished children have indicated an impaired activity of their hepatic enzymes. We used the caffeine breath test to assess the metabolising activity of cytochrome P450 1A2 (CYP1A2) enzyme in underweight children. ME...

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Autores principales: Oshikoya, K A, Sammons, H, Smith, K, Choonara, I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483790/
https://www.ncbi.nlm.nih.gov/pubmed/25897037
http://dx.doi.org/10.1136/archdischild-2014-308017
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author Oshikoya, K A
Sammons, H
Smith, K
Choonara, I
author_facet Oshikoya, K A
Sammons, H
Smith, K
Choonara, I
author_sort Oshikoya, K A
collection PubMed
description OBJECTIVE: Limited data from pharmacokinetic studies in underweight and severely malnourished children have indicated an impaired activity of their hepatic enzymes. We used the caffeine breath test to assess the metabolising activity of cytochrome P450 1A2 (CYP1A2) enzyme in underweight children. METHODS: Underweight children from the paediatric outpatient clinic, Lagos State University Teaching Hospital, Ikeja in Nigeria, were studied. After an overnight fast, 15 underweight children took 3 mg/kg labelled caffeine orally. Breath samples were collected in duplicate at −20, −10 and −1 min and at 15 min intervals for 2 h. The mean cumulative per cent dose recovered (CPDR) of labelled caffeine in the expired carbon dioxide was determined over the study period. This was repeated after 2–6 weeks of nutritional rehabilitation. RESULTS: The mean areas under the enrichment-time curve before and after nutritional rehabilitation were 0.539±0.320 and 0.620±0.322 atom per cent excess minute, respectively. The difference between the two values was not statistically significant (p=0.528). The mean CPDR in the exhaled carbon dioxide of the underweight children over a period of 2 h was 7.56±4.01% and 7.95±3.68% before and after nutritional rehabilitation, respectively, and there was no significant difference in the mean values (p=0.603). CONCLUSIONS: The metabolism of caffeine was not significantly affected in underweight children compared with after 2–6 weeks of nutritional rehabilitation. This suggests that hepatic CYP1A2-metabolising activity was not significantly impaired in underweight children.
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spelling pubmed-44837902015-07-10 Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test Oshikoya, K A Sammons, H Smith, K Choonara, I Arch Dis Child Drug Therapy OBJECTIVE: Limited data from pharmacokinetic studies in underweight and severely malnourished children have indicated an impaired activity of their hepatic enzymes. We used the caffeine breath test to assess the metabolising activity of cytochrome P450 1A2 (CYP1A2) enzyme in underweight children. METHODS: Underweight children from the paediatric outpatient clinic, Lagos State University Teaching Hospital, Ikeja in Nigeria, were studied. After an overnight fast, 15 underweight children took 3 mg/kg labelled caffeine orally. Breath samples were collected in duplicate at −20, −10 and −1 min and at 15 min intervals for 2 h. The mean cumulative per cent dose recovered (CPDR) of labelled caffeine in the expired carbon dioxide was determined over the study period. This was repeated after 2–6 weeks of nutritional rehabilitation. RESULTS: The mean areas under the enrichment-time curve before and after nutritional rehabilitation were 0.539±0.320 and 0.620±0.322 atom per cent excess minute, respectively. The difference between the two values was not statistically significant (p=0.528). The mean CPDR in the exhaled carbon dioxide of the underweight children over a period of 2 h was 7.56±4.01% and 7.95±3.68% before and after nutritional rehabilitation, respectively, and there was no significant difference in the mean values (p=0.603). CONCLUSIONS: The metabolism of caffeine was not significantly affected in underweight children compared with after 2–6 weeks of nutritional rehabilitation. This suggests that hepatic CYP1A2-metabolising activity was not significantly impaired in underweight children. BMJ Publishing Group 2015-07 2015-04-20 /pmc/articles/PMC4483790/ /pubmed/25897037 http://dx.doi.org/10.1136/archdischild-2014-308017 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Drug Therapy
Oshikoya, K A
Sammons, H
Smith, K
Choonara, I
Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
title Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
title_full Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
title_fullStr Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
title_full_unstemmed Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
title_short Lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
title_sort lack of a significant change in caffeine metabolism in underweight children as determined by the caffeine breath test
topic Drug Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483790/
https://www.ncbi.nlm.nih.gov/pubmed/25897037
http://dx.doi.org/10.1136/archdischild-2014-308017
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