Evidence map›Paper›PMID 33935094›Full record

Trial reportJournal of Alzheimer's disease : JAD2021

Paraoxonase 1, B Vitamins Supplementation, and Mild Cognitive Impairment.

Joanna Perła-Kaján, Olga Włoczkowska, Anetta Zioła-Frankowska, Marcin Frankowski, A David Smith, Celeste A de Jager, Helga Refsum, Hieronim Jakubowski

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of Alzheimer's disease : JAD, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
6.3field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Homocysteine Thiolactone Detoxifying Enzymes and Alzheimer's Disease.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Proteomic Exploration of Paraoxonase 1 Function in Health and Disease.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 4 countries.

Joanna Perła-KajánDepartment of Biochemistry and Biotechnology, Poznań University of Life Sciences, Poznań, Poland.
Olga WłoczkowskaDepartment of Biochemistry and Biotechnology, Poznań University of Life Sciences, Poznań, Poland.
Anetta Zioła-FrankowskaDepartment of Analytical Chemistry, Faculty of Chemistry, Adam Mickiewicz University, Poznań, Poland.
Marcin FrankowskiDepartment of Analytical and Environmental Chemistry, Faculty of Chemistry, Adam Mickiewicz University, Poznań, Poland.
A David SmithOPTIMA, Department of Pharmacology, University of Oxford, Oxford, United Kingdom.
Celeste A de JagerOPTIMA, Department of Pharmacology, University of Oxford, Oxford, United Kingdom.
Helga RefsumDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Hieronim JakubowskiDepartment of Biochemistry and Biotechnology, Poznań University of Life Sciences, Poznań, Poland.
Adam Mickiewicz University in Poznań · PLUniversity of Life Sciences in Poznań · PLUniversity of Oxford · GBRutgers, The State University of New Jersey · USUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdentification 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.

objectiveWe tested a hypothesis that PON1 status predicts cognition in individuals with mild cognitive impairment (MCI).

methodsIndividuals 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 B12 (0.5 mg) and B6 (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.

resultsIn 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.

conclusionPON1 is a new factor associated with impaired cognition that can be ameliorated by B-vitamins in individuals with MCI.

Indexed as

AryldialkylphosphataseBrainCognitionCognitive DysfunctionDietary SupplementsDouble-Blind MethodFemaleFolic AcidHumansMagnetic Resonance ImagingMaleMass SpectrometryNeuropsychological TestsVitamin B 12Vitamin B 6Vitamin B ComplexAryldialkylphosphataseFolic AcidVitamin B 12Vitamin B 6Vitamin B ComplexBDNF V66M genotypebrain atrophycognitionironmild cognitive impairmentparaoxonphenyl acetatePON1 activityPON1 Q192R genotype

Identifiers

PMID33935094
PMCPMC8293656
OpenAlexW3159556442

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.