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Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment

BACKGROUND: Identification of modifiable risk factors that affect cognitive decline is important for the development of preventive and treatment strategies. Status of paraoxonase 1 (PON1), a high-density lipoprotein-associated enzyme, may play a role in the development of neurological diseases, incl...

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Autores principales: Perła-Kaján, Joanna, Włoczkowska, Olga, Zioła-Frankowska, Anetta, Frankowski, Marcin, Smith, A. David, de Jager, Celeste A., Refsum, Helga, Jakubowski, Hieronim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293656/
https://www.ncbi.nlm.nih.gov/pubmed/33935094
http://dx.doi.org/10.3233/JAD-210137
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author Perła-Kaján, Joanna
Włoczkowska, Olga
Zioła-Frankowska, Anetta
Frankowski, Marcin
Smith, A. David
de Jager, Celeste A.
Refsum, Helga
Jakubowski, Hieronim
author_facet Perła-Kaján, Joanna
Włoczkowska, Olga
Zioła-Frankowska, Anetta
Frankowski, Marcin
Smith, A. David
de Jager, Celeste A.
Refsum, Helga
Jakubowski, Hieronim
author_sort Perła-Kaján, Joanna
collection PubMed
description BACKGROUND: Identification of modifiable risk factors that affect cognitive decline is important for the development of preventive and treatment strategies. Status of paraoxonase 1 (PON1), a high-density lipoprotein-associated enzyme, may play a role in the development of neurological diseases, including Alzheimer’s disease. OBJECTIVE: We tested a hypothesis that PON1 status predicts cognition in individuals with mild cognitive impairment (MCI). METHODS: Individuals with MCI (n = 196, 76.8-years-old, 60% women) participating in a randomized, double-blind placebo-controlled trial (VITACOG) were assigned to receive a daily dose of folic acid (0.8 mg), vitamin B(12) (0.5 mg) and B(6) (20 mg) (n = 95) or placebo (n = 101) for 2 years. Cognition was analyzed by neuropsychological tests. Brain atrophy was quantified in a subset of participants (n = 168) by MRI. PON1 status, including PON1 Q192R genotype, was determined by quantifying enzymatic activity of PON1 using paraoxon and phenyl acetate as substrates. RESULTS: In the placebo group, baseline phenylacetate hydrolase (PhAcase) activity of PON1 (but not paraoxonase activity or PON1 Q192R genotype) was significantly associated with global cognition (Mini-Mental State Examination, MMSE; Telephone Inventory for Cognitive Status-modified, TICS-m), verbal episodic memory (Hopkins Verbal Learning Test-revised: Total Recall, HVLT-TR; Delayed Recall, HVLT-DR), and attention/processing speed (Trail Making A and Symbol Digits Modalities Test, SDMT) at the end of study. In addition to PhAcase, baseline iron and triglycerides predicted MMSE, baseline fatty acids predicted SDMT, baseline anti-N-Hcy-protein autoantibodies predicted TICS-m, SDMT, Trail Making A, while BDNF V66M genotype predicted HVLT-TR and HVLT-DR scores at the end of study. B-vitamins abrogated associations of PON1 and other variables with cognition. CONCLUSION: PON1 is a new factor associated with impaired cognition that can be ameliorated by B-vitamins in individuals with MCI.
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spelling pubmed-82936562021-08-05 Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment Perła-Kaján, Joanna Włoczkowska, Olga Zioła-Frankowska, Anetta Frankowski, Marcin Smith, A. David de Jager, Celeste A. Refsum, Helga Jakubowski, Hieronim J Alzheimers Dis Research Article BACKGROUND: Identification of modifiable risk factors that affect cognitive decline is important for the development of preventive and treatment strategies. Status of paraoxonase 1 (PON1), a high-density lipoprotein-associated enzyme, may play a role in the development of neurological diseases, including Alzheimer’s disease. OBJECTIVE: We tested a hypothesis that PON1 status predicts cognition in individuals with mild cognitive impairment (MCI). METHODS: Individuals with MCI (n = 196, 76.8-years-old, 60% women) participating in a randomized, double-blind placebo-controlled trial (VITACOG) were assigned to receive a daily dose of folic acid (0.8 mg), vitamin B(12) (0.5 mg) and B(6) (20 mg) (n = 95) or placebo (n = 101) for 2 years. Cognition was analyzed by neuropsychological tests. Brain atrophy was quantified in a subset of participants (n = 168) by MRI. PON1 status, including PON1 Q192R genotype, was determined by quantifying enzymatic activity of PON1 using paraoxon and phenyl acetate as substrates. RESULTS: In the placebo group, baseline phenylacetate hydrolase (PhAcase) activity of PON1 (but not paraoxonase activity or PON1 Q192R genotype) was significantly associated with global cognition (Mini-Mental State Examination, MMSE; Telephone Inventory for Cognitive Status-modified, TICS-m), verbal episodic memory (Hopkins Verbal Learning Test-revised: Total Recall, HVLT-TR; Delayed Recall, HVLT-DR), and attention/processing speed (Trail Making A and Symbol Digits Modalities Test, SDMT) at the end of study. In addition to PhAcase, baseline iron and triglycerides predicted MMSE, baseline fatty acids predicted SDMT, baseline anti-N-Hcy-protein autoantibodies predicted TICS-m, SDMT, Trail Making A, while BDNF V66M genotype predicted HVLT-TR and HVLT-DR scores at the end of study. B-vitamins abrogated associations of PON1 and other variables with cognition. CONCLUSION: PON1 is a new factor associated with impaired cognition that can be ameliorated by B-vitamins in individuals with MCI. IOS Press 2021-06-01 /pmc/articles/PMC8293656/ /pubmed/33935094 http://dx.doi.org/10.3233/JAD-210137 Text en © 2021 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Perła-Kaján, Joanna
Włoczkowska, Olga
Zioła-Frankowska, Anetta
Frankowski, Marcin
Smith, A. David
de Jager, Celeste A.
Refsum, Helga
Jakubowski, Hieronim
Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment
title Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment
title_full Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment
title_fullStr Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment
title_full_unstemmed Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment
title_short Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment
title_sort paraoxonase 1, b vitamins supplementation, and mild cognitive impairment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293656/
https://www.ncbi.nlm.nih.gov/pubmed/33935094
http://dx.doi.org/10.3233/JAD-210137
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