Evidence map›Paper›PMID 27073746›Full record

ArticleAmerican journal of neurodegenerative disease2016

Association study between the DNMT3A -448A>G polymorphism and risk of Alzheimer's disease in Caucasians of Italian origin.

Pierpaola Tannorella, Andrea Stoccoro, Gloria Tognoni, Ubaldo Bonuccelli, Lucia Migliore, Fabio Coppedè

Open access · greenAbstract read
In one paragraph

Article in American journal of neurodegenerative disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Association of Polymorphisms in Genes Involved in One-Carbon Metabolism withInternational journal of molecular sciences · 2019
    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 1 country.

Pierpaola TannorellaDepartment of Translational Research and New Technologies in Medicine and Surgery, Section of Medical Genetics, University of Pisa Via Roma 55, 56126 Pisa, Italy.
Andrea StoccoroDepartment of Translational Research and New Technologies in Medicine and Surgery, Section of Medical Genetics, University of PisaVia Roma 55, 56126 Pisa, Italy; Doctoral School in Genetics Oncology and Clinical Medicine, University of SienaSiena, Italy.
Gloria TognoniUnit of Neurology, Department of Neuroscience, Pisa University Hospital Via Roma 67, 56126 Pisa, Italy.
Ubaldo BonuccelliUnit of Neurology, Department of Neuroscience, Pisa University HospitalVia Roma 67, 56126 Pisa, Italy; Department of Clinical and Experimental Medicine, University of Pisa, Neurological ClinicVia Roma 67, 56126 Pisa, Italy.
Lucia MiglioreDepartment of Translational Research and New Technologies in Medicine and Surgery, Section of Medical Genetics, University of PisaVia Roma 55, 56126 Pisa, Italy; Interdepartmental Research Center Nutrafood "Nutraceuticals and Food for Health", University of PisaVia del Borghetto 80, 56124 Pisa, Italy.
Fabio CoppedèDepartment of Translational Research and New Technologies in Medicine and Surgery, Section of Medical Genetics, University of PisaVia Roma 55, 56126 Pisa, Italy; Interdepartmental Research Center Nutrafood "Nutraceuticals and Food for Health", University of PisaVia del Borghetto 80, 56124 Pisa, Italy.
University of Pisa · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence points to an epigenetic contribution in Alzheimer's disease (AD) pathogenesis. In this regard, variants and polymorphisms of DNA methyltransferase genes (DNMTs) are being investigated for their contribution to cognitive decline and dementia, but results are still scarce or controversial. In the present study we genotyped 710 Caucasian subjects of Italian descent, including 320 late-onset AD (LOAD) patients, 70 individuals with amnestic Mild Cognitive Impairment (MCI), and 320 matched healthy controls, for the presence of a functional DNMT3A -448A>G (rs1550117) polymorphism, searching for association with disease risk. In addition, we searched for correlation between the studied polymorphism and circulating levels of folate, homocysteine (hcy) and vitamin B12, all involved in DNA methylation reactions and available from 189 LOAD patients and 186 matched controls. Both allele and genotype frequencies of rs1550117 were closely similar between MCI, LOAD and control subjects, and no association with dementia or pre-dementia conditions was observed. Plasma hcy levels were significantly higher (p = 0.04) and serum folate levels significantly lower (p = 0.01) in LOAD than in controls, but no difference in circulating folate, hcy or vitamin B12 levels was seen between carriers and non-carriers of the minor DNMT3A -448A allele. Collectively, present results confirmed previous associations of increased hcy and decreased folate with LOAD risk, but do not support an association between the DNMT3A -448A>G polymorphism and AD in our population.

Indexed as

Alzheimer’s diseaseDNMT3A -448A>G polymorphismepigeneticsfolatehomocysteineMild Cognitive Impairmentrs1550117

Identifiers

PMID27073746
PMCPMC4788735
OpenAlexW2399564585

What OpenQuestion holds

Textmetadata
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.