Evidence map›Paper›PMID 35736408›Full record

ArticleMetabolites2022

Folate Related Pathway Gene Analysis Reveals a Novel Metabolic Variant Associated with Alzheimer's Disease with a Change in Metabolic Profile.

Jaleel Miyan, Charlotte Buttercase, Emma Beswick, Salma Miyan, Ghazaleh Moshkdanian, Naila Naz

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

6 authors at 2 institutions in 2 countries.

Jaleel MiyanDivision of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine & Health, The University of Manchester, 3.540 Stopford Building, Oxford Road, Manchester M13 9PT, UK.ORCID 0000-0002-1835-0143
Charlotte ButtercaseDivision of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine & Health, The University of Manchester, 3.540 Stopford Building, Oxford Road, Manchester M13 9PT, UK.ORCID 0000-0002-1078-2160
Emma BeswickLifecodeGX Ltd., 409 Royle Building, London N1 7SH, UK.
Salma MiyanDivision of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine & Health, The University of Manchester, 3.540 Stopford Building, Oxford Road, Manchester M13 9PT, UK.
Ghazaleh MoshkdanianDivision of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine & Health, The University of Manchester, 3.540 Stopford Building, Oxford Road, Manchester M13 9PT, UK.
Naila NazDivision of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine & Health, The University of Manchester, 3.540 Stopford Building, Oxford Road, Manchester M13 9PT, UK.
University of Manchester · GBKashan University of Medical Sciences · IR

Funding

African Healthcare Development Trust NACharles Wolfson Charitable Trust NA
6 · The paper itself

Abstract

Metabolic disorders may be important potential causative pathways to Alzheimer's disease (AD). Cerebrospinal fluid (CSF) decreasing output, raised intracranial pressure, and ventricular enlargement have all been linked to AD. Cerebral folate metabolism may be a key player since this is significantly affected by such changes in CSF, and genetic susceptibilities may exist in this pathway. In the current study, we aimed to identify whether any single nucleotide polymorphism (SNPs) affecting folate and the associated metabolic pathways were significantly associated with AD. We took a functional nutrigenomics approach to look for SNPs in genes for the linked folate, methylation, and biogenic amine neurotransmitter pathways. Changes in metabolism were found with the SNPs identified. An abnormal SNP in methylene tetrahydrofolate dehydrogenase 1 (

Indexed as

Alzheimer’s diseasecerebrospinal fluidfolateMTHFD1single nucleotide polymorphism

Identifiers

PMID35736408
PMCPMC9230919
OpenAlexW4281478530

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.