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Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels

Elevated homocysteine (Hcy) levels are a risk factor for vascular diseases. Recently, increases in ultraviolet radiation (UVR) have been linked to decreased Hcy levels. This relationship may be mediated by the status of UVR-responsive vitamins, vitamin D and folate, and/or genetic variants influenci...

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Autores principales: Jones, Patrice, Lucock, Mark, Martin, Charlotte, Thota, Rohith, Garg, Manohar, Yates, Zoe, Scarlett, Christopher J., Veysey, Martin, Beckett, Emma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284830/
https://www.ncbi.nlm.nih.gov/pubmed/32443475
http://dx.doi.org/10.3390/nu12051455
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author Jones, Patrice
Lucock, Mark
Martin, Charlotte
Thota, Rohith
Garg, Manohar
Yates, Zoe
Scarlett, Christopher J.
Veysey, Martin
Beckett, Emma
author_facet Jones, Patrice
Lucock, Mark
Martin, Charlotte
Thota, Rohith
Garg, Manohar
Yates, Zoe
Scarlett, Christopher J.
Veysey, Martin
Beckett, Emma
author_sort Jones, Patrice
collection PubMed
description Elevated homocysteine (Hcy) levels are a risk factor for vascular diseases. Recently, increases in ultraviolet radiation (UVR) have been linked to decreased Hcy levels. This relationship may be mediated by the status of UVR-responsive vitamins, vitamin D and folate, and/or genetic variants influencing their levels; however, this has yet to be examined. Therefore, the independent and interactive influences of environmental UVR, vitamin D and folate levels and related genetic variants on Hcy levels were examined in an elderly Australian cohort (n = 619). Red blood cell folate, 25-hydroxyvitamin D (25(OH)D), and plasma Hcy levels were determined, and genotyping for 21 folate and vitamin D-related variants was performed. Erythemal dose rate accumulated over six-weeks (6W-EDR) and four-months (4M-EDR) prior to clinics were calculated as a measure of environmental UVR. Multivariate analyses found interactions between 6W-EDR and 25(OH)D levels (p(interaction) = 0.002), and 4M-EDR and MTHFD1-rs2236225 (p(interaction) = 0.006) in predicting Hcy levels. The association between 6W-EDR and Hcy levels was found only in subjects within lower 25(OH)D quartiles (<33.26 ng/mL), with the association between 4M-EDR and Hcy occurring only in subjects carrying the MTHFD1-rs2236225 variant. 4M-EDR, 6W-EDR, and MTHFD1-rs2236225 were also independent predictors of Hcy. Findings highlight nutrient–environment and gene–environment interactions that could influence the risk of Hcy-related outcomes.
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spelling pubmed-72848302020-06-15 Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels Jones, Patrice Lucock, Mark Martin, Charlotte Thota, Rohith Garg, Manohar Yates, Zoe Scarlett, Christopher J. Veysey, Martin Beckett, Emma Nutrients Article Elevated homocysteine (Hcy) levels are a risk factor for vascular diseases. Recently, increases in ultraviolet radiation (UVR) have been linked to decreased Hcy levels. This relationship may be mediated by the status of UVR-responsive vitamins, vitamin D and folate, and/or genetic variants influencing their levels; however, this has yet to be examined. Therefore, the independent and interactive influences of environmental UVR, vitamin D and folate levels and related genetic variants on Hcy levels were examined in an elderly Australian cohort (n = 619). Red blood cell folate, 25-hydroxyvitamin D (25(OH)D), and plasma Hcy levels were determined, and genotyping for 21 folate and vitamin D-related variants was performed. Erythemal dose rate accumulated over six-weeks (6W-EDR) and four-months (4M-EDR) prior to clinics were calculated as a measure of environmental UVR. Multivariate analyses found interactions between 6W-EDR and 25(OH)D levels (p(interaction) = 0.002), and 4M-EDR and MTHFD1-rs2236225 (p(interaction) = 0.006) in predicting Hcy levels. The association between 6W-EDR and Hcy levels was found only in subjects within lower 25(OH)D quartiles (<33.26 ng/mL), with the association between 4M-EDR and Hcy occurring only in subjects carrying the MTHFD1-rs2236225 variant. 4M-EDR, 6W-EDR, and MTHFD1-rs2236225 were also independent predictors of Hcy. Findings highlight nutrient–environment and gene–environment interactions that could influence the risk of Hcy-related outcomes. MDPI 2020-05-18 /pmc/articles/PMC7284830/ /pubmed/32443475 http://dx.doi.org/10.3390/nu12051455 Text en © 2020 by the authors. 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/).
spellingShingle Article
Jones, Patrice
Lucock, Mark
Martin, Charlotte
Thota, Rohith
Garg, Manohar
Yates, Zoe
Scarlett, Christopher J.
Veysey, Martin
Beckett, Emma
Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels
title Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels
title_full Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels
title_fullStr Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels
title_full_unstemmed Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels
title_short Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels
title_sort independent and interactive influences of environmental uvr, vitamin d levels, and folate variant mthfd1-rs2236225 on homocysteine levels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284830/
https://www.ncbi.nlm.nih.gov/pubmed/32443475
http://dx.doi.org/10.3390/nu12051455
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