Evidence map›Paper›PMID 34916904›Full record

ArticleFrontiers in neuroscience2021

The Influence of MTHFR Polymorphism on Gray Matter Volume in Patients With Amnestic Mild Cognitive Impairment.

Mengzhe You, Xia Zhou, Wenwen Yin, Ke Wan, Wei Zhang, Chenchen Li, Mingxu Li, Wenhao Zhu, Xiaoqun Zhu, Zhongwu Sun

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. In vivo validation of late-onset Alzheimer's disease genetic risk factors.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  6. Article
  7. bioRxiv : the preprint server for biology · 2023
    Article
  8. Controlling the Impact ofMedicina (Kaunas, Lithuania) · 2023
    Article
  9. Alzheimer's Disease: An Updated Overview of Its Genetics.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Review
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

10 authors at 2 institutions in 1 country.

Mengzhe YouDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xia ZhouDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Wenwen YinDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Ke WanDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Wei ZhangDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Chenchen LiDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Mingxu LiDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Wenhao ZhuDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xiaoqun ZhuDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Zhongwu SunDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Anhui Medical University · CNFirst Affiliated Hospital of Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The methylenetetrahydrofolate reductase (MTHFR) gene has been associated with Alzheimer's disease (AD) pathogenesis. Amnestic mild cognitive impairment (aMCI) represents a prodromal stage of dementia and involves a high risk of progression into AD. Although the effects of the apolipoprotein E (APOE) gene on structural alterations in aMCI have been widely investigated, the effects of MTHFR C677T and interaction effects of MTHFR × APOE genotypes on gray matter atrophy in aMCI remain largely unknown. In the present study, 60 aMCI patients and 30 healthy controls were enrolled, and voxel-based morphometry analysis was performed to inspect the effects of diagnosis, different genotypes, and their interactions on gray matter atrophy. The results showed that aMCI patients had significant gray matter atrophy involving the bilateral hippocampus, the right parahippocampal gyrus, and the left superior temporal gyrus compared with healthy controls. Besides, a substantial reduction in gray matter volume was observed in the right hippocampus region in APOE ε4 carriers from the aMCI group, compared with APOE ε4 non-carriers. A significant interaction was found between diagnosis and MTHFR C677T genotype on the right precuneus in healthy controls and aMCI patients not carrying APOE ε4 allele. Our findings may provide new evidence substantiating the genetic effects of MTHFR C677T on brain structural alternation in patients with aMCI.

Indexed as

Alzheimer’s diseaseamnestic mild cognitive impairmentapolipoprotein Emethylenetetrahydrofolate reductasevoxel-based morphometry

Identifiers

PMID34916904
PMCPMC8670096
OpenAlexW3215183749

What OpenQuestion holds

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LicenceCC BY
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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.