Intestinal β-carotene bioconversion in humans is determined by a new single-sample, plasma isotope ratio method and compared with traditional and modified area-under-the-curve methods
The vitamin A value (bioefficacy) of provitamin A carotenoids is determined by absorption of the carotenoid (bioavailability) and its subsequent conversion to retinol (bioconversion). Here we show that intestinal bioconversion of β-carotene can be estimated based on analysis of a single plasma sampl...
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Published in | Archives of biochemistry and biophysics Vol. 653; pp. 121 - 126 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.09.2018
Elsevier |
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ISSN | 0003-9861 1096-0384 1096-0384 |
DOI | 10.1016/j.abb.2018.06.015 |
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Abstract | The vitamin A value (bioefficacy) of provitamin A carotenoids is determined by absorption of the carotenoid (bioavailability) and its subsequent conversion to retinol (bioconversion). Here we show that intestinal bioconversion of β-carotene can be estimated based on analysis of a single plasma sample collected 6 h after subjects ingest a test dose of stable isotope-labeled β-carotene from the ratio of retinyl esters to retinyl esters plus β-carotene. Plasma isotope ratio predictions of bioconversion ranged from 50 to– 93% (mean 76%) for 45 healthy young adults with low vitamin A stores. Results were the same as predictions made by a traditional area-under-the-curve method calculated from 0 to– 8 h or a modified area-under-the-curve method calculated from 0 to– 12 h. The modified method may provide better estimates of bioconversion between 8 and 24 h after ingestion of a carotenoid dose when stable isotopes cannot be used due to cost or logistics. Furthermore, because the plasma isotope ratio method requires only one blood sample and no isolation of triglyceride-rich lipoproteins, its use will facilitate estimation of provitamin A carotenoid bioconversion in human subjects and especially children, in whom repeated blood sampling is not feasible. |
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AbstractList | The vitamin A value (bioefficacy) of provitamin A carotenoids is determined by absorption of the carotenoid (bioavailability) and its subsequent conversion to retinol (bioconversion). Here we show that intestinal bioconversion of β-carotene can be estimated based on analysis of a single plasma sample collected 6 h after subjects ingest a test dose of stable isotope-labeled β-carotene from the ratio of retinyl esters to retinyl esters plus β-carotene. Plasma isotope ratio predictions of bioconversion ranged from 50 to– 93% (mean 76%) for 45 healthy young adults with low vitamin A stores. Results were the same as predictions made by a traditional area-under-the-curve method calculated from 0 to– 8 h or a modified area-under-the-curve method calculated from 0 to– 12 h. The modified method may provide better estimates of bioconversion between 8 and 24 h after ingestion of a carotenoid dose when stable isotopes cannot be used due to cost or logistics. Furthermore, because the plasma isotope ratio method requires only one blood sample and no isolation of triglyceride-rich lipoproteins, its use will facilitate estimation of provitamin A carotenoid bioconversion in human subjects and especially children, in whom repeated blood sampling is not feasible. The vitamin A value (bioefficacy) of provitamin A carotenoids is determined by absorption of the carotenoid (bioavailability) and its subsequent conversion to retinol (bioconversion). Here we show that intestinal bioconversion of β-carotene can be estimated based on analysis of a single plasma sample collected 6 h after subjects ingest a test dose of stable isotope-labeled β-carotene from the ratio of retinyl esters to retinyl esters plus β-carotene. Plasma isotope ratio predictions of bioconversion ranged from 50 to- 93% (mean 76%) for 45 healthy young adults with low vitamin A stores. Results were the same as predictions made by a traditional area-under-the-curve method calculated from 0 to- 8 h or a modified area-under-the-curve method calculated from 0 to- 12 h. The modified method may provide better estimates of bioconversion between 8 and 24 h after ingestion of a carotenoid dose when stable isotopes cannot be used due to cost or logistics. Furthermore, because the plasma isotope ratio method requires only one blood sample and no isolation of triglyceride-rich lipoproteins, its use will facilitate estimation of provitamin A carotenoid bioconversion in human subjects and especially children, in whom repeated blood sampling is not feasible.The vitamin A value (bioefficacy) of provitamin A carotenoids is determined by absorption of the carotenoid (bioavailability) and its subsequent conversion to retinol (bioconversion). Here we show that intestinal bioconversion of β-carotene can be estimated based on analysis of a single plasma sample collected 6 h after subjects ingest a test dose of stable isotope-labeled β-carotene from the ratio of retinyl esters to retinyl esters plus β-carotene. Plasma isotope ratio predictions of bioconversion ranged from 50 to- 93% (mean 76%) for 45 healthy young adults with low vitamin A stores. Results were the same as predictions made by a traditional area-under-the-curve method calculated from 0 to- 8 h or a modified area-under-the-curve method calculated from 0 to- 12 h. The modified method may provide better estimates of bioconversion between 8 and 24 h after ingestion of a carotenoid dose when stable isotopes cannot be used due to cost or logistics. Furthermore, because the plasma isotope ratio method requires only one blood sample and no isolation of triglyceride-rich lipoproteins, its use will facilitate estimation of provitamin A carotenoid bioconversion in human subjects and especially children, in whom repeated blood sampling is not feasible. |
Author | Green, Joanne Balmer Oxley, Anthony Green, Michael H. Ford, Jennifer Lynn Lietz, Georg |
AuthorAffiliation | b Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK a Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802, United States |
AuthorAffiliation_xml | – name: a Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802, United States – name: b Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK |
Author_xml | – sequence: 1 givenname: Jennifer Lynn orcidid: 0000-0002-1740-5704 surname: Ford fullname: Ford, Jennifer Lynn organization: Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802, United States – sequence: 2 givenname: Michael H. surname: Green fullname: Green, Michael H. organization: Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802, United States – sequence: 3 givenname: Joanne Balmer surname: Green fullname: Green, Joanne Balmer organization: Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802, United States – sequence: 4 givenname: Anthony surname: Oxley fullname: Oxley, Anthony organization: Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK – sequence: 5 givenname: Georg surname: Lietz fullname: Lietz, Georg email: georg.lietz@newcastle.ac.uk organization: Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29958897$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1194/jlr.D021139 10.1093/ajcn/56.1.128 10.3945/jn.111.140756 10.1093/ajcn/62.1.110 10.3945/jn.113.187674 10.3945/jn.117.252361 10.3945/ajcn.112.034850 10.1016/S0021-9150(99)00397-4 10.1172/JCI105468 10.1093/ajcn/77.1.12 10.1096/fj.08-121962 10.1194/jlr.D040204 10.1017/S0007114514000166 10.3945/ajcn.2010.28674G 10.1146/annurev.nutr.22.010402.102834 10.3109/00365516709090648 10.1146/annurev.nutr.18.1.19 10.3945/jn.116.233486 10.1093/ajcn/71.6.1545 10.1016/S0955-2863(97)00060-0 10.1093/ajcn/75.5.900 |
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Keywords | Vitamin A Area under the curve Carotenoid bioconversion Carotenoid bioefficacy β-Carotene |
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SubjectTerms | Adult Area Under Curve Area under the curve beta Carotene - metabolism beta-carotene bioavailability Biological Availability Biotransformation blood sampling Carotenoid bioconversion Carotenoid bioefficacy children Chromatography, Liquid - methods esters Female Humans ingestion Intestinal Mucosa - metabolism isotope labeling Isotopes lipoproteins Male prediction stable isotopes Tandem Mass Spectrometry - methods Vitamin A Vitamin A - blood Young Adult young adults β-Carotene |
Title | Intestinal β-carotene bioconversion in humans is determined by a new single-sample, plasma isotope ratio method and compared with traditional and modified area-under-the-curve methods |
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