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Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults
Scope: B vitamers are co-enzymes involved in key physiological processes including energy production, one-carbon, and macronutrient metabolism. Studies profiling B vitamers simultaneously in parent–child dyads are scarce. Profiling B vitamers in parent–child dyads enables an insightful determination...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001009/ https://www.ncbi.nlm.nih.gov/pubmed/33801409 http://dx.doi.org/10.3390/nu13030821 |
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author | Andraos, Stephanie Jones, Beatrix Wall, Clare Thorstensen, Eric Kussmann, Martin Cameron-Smith, David Lange, Katherine Clifford, Susan Saffery, Richard Burgner, David Wake, Melissa O’Sullivan, Justin |
author_facet | Andraos, Stephanie Jones, Beatrix Wall, Clare Thorstensen, Eric Kussmann, Martin Cameron-Smith, David Lange, Katherine Clifford, Susan Saffery, Richard Burgner, David Wake, Melissa O’Sullivan, Justin |
author_sort | Andraos, Stephanie |
collection | PubMed |
description | Scope: B vitamers are co-enzymes involved in key physiological processes including energy production, one-carbon, and macronutrient metabolism. Studies profiling B vitamers simultaneously in parent–child dyads are scarce. Profiling B vitamers in parent–child dyads enables an insightful determination of gene–environment contributions to their circulating concentrations. We aimed to characterise: (a) parent–child dyad concordance, (b) generation (children versus adults), (c) age (within the adult subgroup (age range 28–71 years)) and (d) sex differences in plasma B vitamer concentrations in the CheckPoint study of Australian children. Methods and Results: 1166 children (11 ± 0.5 years, 51% female) and 1324 parents (44 ± 5.1 years, 87% female) took part in a biomedical assessment of a population-derived longitudinal cohort study: The Growing Up in Australia’s Child Health CheckPoint. B vitamer levels were quantified by UHPLC/MS-MS. B vitamer levels were weakly concordant between parent–child pairs (10–31% of variability explained). All B vitamer concentrations exhibited generation-specificity, except for flavin mononucleotide (FMN). The levels of thiamine, pantothenic acid, and 4-pyridoxic acid were higher in male children, and those of pantothenic acid were higher in male adults compared to their female counterparts. Conclusion: Family, age, and sex contribute to variations in the concentrations of plasma B vitamers in Australian children and adults. |
format | Online Article Text |
id | pubmed-8001009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80010092021-03-28 Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults Andraos, Stephanie Jones, Beatrix Wall, Clare Thorstensen, Eric Kussmann, Martin Cameron-Smith, David Lange, Katherine Clifford, Susan Saffery, Richard Burgner, David Wake, Melissa O’Sullivan, Justin Nutrients Article Scope: B vitamers are co-enzymes involved in key physiological processes including energy production, one-carbon, and macronutrient metabolism. Studies profiling B vitamers simultaneously in parent–child dyads are scarce. Profiling B vitamers in parent–child dyads enables an insightful determination of gene–environment contributions to their circulating concentrations. We aimed to characterise: (a) parent–child dyad concordance, (b) generation (children versus adults), (c) age (within the adult subgroup (age range 28–71 years)) and (d) sex differences in plasma B vitamer concentrations in the CheckPoint study of Australian children. Methods and Results: 1166 children (11 ± 0.5 years, 51% female) and 1324 parents (44 ± 5.1 years, 87% female) took part in a biomedical assessment of a population-derived longitudinal cohort study: The Growing Up in Australia’s Child Health CheckPoint. B vitamer levels were quantified by UHPLC/MS-MS. B vitamer levels were weakly concordant between parent–child pairs (10–31% of variability explained). All B vitamer concentrations exhibited generation-specificity, except for flavin mononucleotide (FMN). The levels of thiamine, pantothenic acid, and 4-pyridoxic acid were higher in male children, and those of pantothenic acid were higher in male adults compared to their female counterparts. Conclusion: Family, age, and sex contribute to variations in the concentrations of plasma B vitamers in Australian children and adults. MDPI 2021-03-02 /pmc/articles/PMC8001009/ /pubmed/33801409 http://dx.doi.org/10.3390/nu13030821 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Andraos, Stephanie Jones, Beatrix Wall, Clare Thorstensen, Eric Kussmann, Martin Cameron-Smith, David Lange, Katherine Clifford, Susan Saffery, Richard Burgner, David Wake, Melissa O’Sullivan, Justin Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults |
title | Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults |
title_full | Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults |
title_fullStr | Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults |
title_full_unstemmed | Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults |
title_short | Plasma B Vitamers: Population Epidemiology and Parent-Child Concordance in Children and Adults |
title_sort | plasma b vitamers: population epidemiology and parent-child concordance in children and adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001009/ https://www.ncbi.nlm.nih.gov/pubmed/33801409 http://dx.doi.org/10.3390/nu13030821 |
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