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CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women

The single nucleotide polymorphisms (SNPs) rs3808607, rs2072183, rs2032582, and rs1761667 are associated with coenzyme Q(10) (CoQ(10)) bioavailability in women after long-term CoQ(10) supplementation. However, the beneficial aspects of the association between these SNPs and CoQ(10) supplementation r...

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Autores principales: Takahashi, Michiyo, Kinoshita, Tetsu, Maruyama, Koutatsu, Suzuki, Toshikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268390/
https://www.ncbi.nlm.nih.gov/pubmed/35807759
http://dx.doi.org/10.3390/nu14132579
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author Takahashi, Michiyo
Kinoshita, Tetsu
Maruyama, Koutatsu
Suzuki, Toshikazu
author_facet Takahashi, Michiyo
Kinoshita, Tetsu
Maruyama, Koutatsu
Suzuki, Toshikazu
author_sort Takahashi, Michiyo
collection PubMed
description The single nucleotide polymorphisms (SNPs) rs3808607, rs2072183, rs2032582, and rs1761667 are associated with coenzyme Q(10) (CoQ(10)) bioavailability in women after long-term CoQ(10) supplementation. However, the beneficial aspects of the association between these SNPs and CoQ(10) supplementation remain unknown. We investigated their relationship using the subjective quality of life score SF-36 by reanalyzing previous data from 92 study participants who were receiving ubiquinol (a reduced form of CoQ(10)) supplementation for 1 year. Two-way repeated-measures analysis of variance revealed a significant interaction between rs1761667 and the SF-36 scores of role physical (p = 0.016) and mental health (p = 0.017) in women. Subgrouping of participants based on the above four SNPs revealed significant interactions between these SNPs and the SF-36 scores of general health (p = 0.045), role emotional (p = 0.008), and mental health (p = 0.019) and increased serum CoQ(10) levels (p = 0.008), suggesting that the benefits of CoQ(10) supplementation, especially in terms of psychological parameters, are genotype-dependent in women. However, significant interactions were not observed in men. Therefore, inclusion of SNP subgrouping information in clinical trials of CoQ(10) supplementation may provide conclusive evidence supporting other beneficial health effects exerted by the association between these SNPs and CoQ(10) on women.
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spelling pubmed-92683902022-07-09 CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women Takahashi, Michiyo Kinoshita, Tetsu Maruyama, Koutatsu Suzuki, Toshikazu Nutrients Article The single nucleotide polymorphisms (SNPs) rs3808607, rs2072183, rs2032582, and rs1761667 are associated with coenzyme Q(10) (CoQ(10)) bioavailability in women after long-term CoQ(10) supplementation. However, the beneficial aspects of the association between these SNPs and CoQ(10) supplementation remain unknown. We investigated their relationship using the subjective quality of life score SF-36 by reanalyzing previous data from 92 study participants who were receiving ubiquinol (a reduced form of CoQ(10)) supplementation for 1 year. Two-way repeated-measures analysis of variance revealed a significant interaction between rs1761667 and the SF-36 scores of role physical (p = 0.016) and mental health (p = 0.017) in women. Subgrouping of participants based on the above four SNPs revealed significant interactions between these SNPs and the SF-36 scores of general health (p = 0.045), role emotional (p = 0.008), and mental health (p = 0.019) and increased serum CoQ(10) levels (p = 0.008), suggesting that the benefits of CoQ(10) supplementation, especially in terms of psychological parameters, are genotype-dependent in women. However, significant interactions were not observed in men. Therefore, inclusion of SNP subgrouping information in clinical trials of CoQ(10) supplementation may provide conclusive evidence supporting other beneficial health effects exerted by the association between these SNPs and CoQ(10) on women. MDPI 2022-06-22 /pmc/articles/PMC9268390/ /pubmed/35807759 http://dx.doi.org/10.3390/nu14132579 Text en © 2022 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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Takahashi, Michiyo
Kinoshita, Tetsu
Maruyama, Koutatsu
Suzuki, Toshikazu
CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women
title CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women
title_full CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women
title_fullStr CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women
title_full_unstemmed CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women
title_short CYP7A1, NPC1L1, ABCB1, and CD36 Polymorphisms Associated with Coenzyme Q(10) Availability Affect the Subjective Quality of Life Score (SF-36) after Long-Term CoQ(10) Supplementation in Women
title_sort cyp7a1, npc1l1, abcb1, and cd36 polymorphisms associated with coenzyme q(10) availability affect the subjective quality of life score (sf-36) after long-term coq(10) supplementation in women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268390/
https://www.ncbi.nlm.nih.gov/pubmed/35807759
http://dx.doi.org/10.3390/nu14132579
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