Evidence map›Paper›PMID 28316001›Full record

ArticleMolecular biology reports2017

Associations of polymorphisms in the candidate genes for Alzheimer's disease BIN1, CLU, CR1 and PICALM with gestational diabetes and impaired glucose tolerance.

Gabriela Vacínová, D Vejražková, P Lukášová, O Lischková, K Dvořáková, R Rusina, I Holmerová, H Vaňková, J Včelák, B Bendlová and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Frontiers in dementia · 2022
    Article
  6. Article
  7. Article
  8. 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

11 authors at 3 institutions in 1 country.

Gabriela VacínováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic. gvacinova@endo.cz.
D VejražkováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
P LukášováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
O LischkováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
K DvořákováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
R RusinaThomayer Hospital, Prague, Czech Republic.
I HolmerováFaculty of Humanities, Charles University in Prague, Prague, Czech Republic.
H VaňkováFaculty of Humanities, Charles University in Prague, Prague, Czech Republic.
J VčelákDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
B BendlováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
M VaňkováDepartment of Molecular Endocrinology, Institute of Endocrinology, Národní 8, Prague, 116 94, Czech Republic.
Institute of Endocrinology · CZCharles University · CZThomayer University Hospital · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common type of dementia, with a prevalence that is rising every year. AD is associated with type 2 diabetes mellitus (T2DM) and insulin resistance, and is therefore sometimes called "type 3 diabetes mellitus". The aim of this study was to examine whether the variants of some candidate genes involved in the development of AD, namely BIN1 (rs744373), CLU (rs11136000), CR1 (rs3818361), and PICALM (rs3851179), are related to several disorders of glucose metabolism-gestational diabetes (GDM), T2DM and impaired glucose tolerance (IGT). Our study included 550 women with former GDM and 717 control women, 392 patients with T2DM and 180 non-diabetic controls, and 117 patients with IGT and 630 controls with normal glucose tolerance. Genotyping analysis was performed using specially-designed TaqMan assays. No significant associations of the genetic variants rs744373 in BIN1, rs11136000 in CLU, or rs3818361 in CR1 were found with GDM, T2DM or IGT, but rs3851179 in PICALM was associated with an increased risk of GDM. The frequency of the AD risk-associated C allele was significantly higher in the GDM group compared to controls: OR 1.21; 95% CI (1.03-1.44). This finding was not apparent in T2DM and IGT; conversely, the C allele of the PICALM SNP was protective for IGT: OR 0.67; 95% CI (0.51-0.89). This study demonstrates an association between PICALM rs3851179 and GDM as well as IGT. However, elucidation of the possible role of this gene in the pathogenesis of GDM requires further independent studies.

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAllelesAlzheimer DiseaseClusterinDiabetes, GestationalDiabetes Mellitus, Type 2FemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenetic VariationGlucose IntoleranceHumansMiddle AgedAdaptor Proteins, Signal TransducingBIN1 protein, humanCLU protein, humanClusterinCR1 protein, humanMonomeric Clathrin Assembly ProteinsNuclear ProteinsPICALM protein, humanReceptors, Complement 3bTumor Suppressor ProteinsAlzheimer’s diseaseGestational diabetes mellitusGlucose metabolismImpaired glucose tolerancePolymorphismsType 2 diabetes mellitus

Identifiers

PMID28316001
OpenAlexW2595824080

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.