Evidence map›Paper›PMID 31664702›Full record

ArticleMolecular neurobiology2020

Familial Alzheimer's Disease and Recessive Modifiers.

Jorge I Vélez, Francisco Lopera, Claudia T Silva, Andrés Villegas, Lady G Espinosa, Oscar M Vidal, Claudio A Mastronardi, Mauricio Arcos-Burgos

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.3field-weighted citation impact, top 43% 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, 14 citations in OpenAlex.

  1. NovelWorld journal of radiology · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Genetics, Functions, and Clinical Impact of Presenilin-1 (PSEN1) Gene.International journal of molecular sciences · 2022
    Review
  11. 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 3 institutions in 1 country.

Jorge I VélezUniversidad del Norte, Barranquilla, Colombia.ORCID http://orcid.org/0000-0002-3146-7899
Francisco LoperaNeuroscience Research Group, University of Antioquia, Medellín, Colombia.ORCID http://orcid.org/0000-0003-3986-1484
Claudia T SilvaNeuroscience Research Group, University of Antioquia, Medellín, Colombia.ORCID http://orcid.org/0000-0001-8172-5860
Andrés VillegasNeuroscience Research Group, University of Antioquia, Medellín, Colombia.
Lady G EspinosaINPAC Research Group, Fundación Universitaria Sanitas, Bogotá, Colombia.
Oscar M VidalUniversidad del Norte, Barranquilla, Colombia.ORCID http://orcid.org/0000-0002-7807-1242
Claudio A MastronardiINPAC Research Group, Fundación Universitaria Sanitas, Bogotá, Colombia.ORCID http://orcid.org/0000-0002-0777-9075
Mauricio Arcos-BurgosGrupo de Investigación en Psiquiatría (GIPSI), Departamento de Psiquiatría, Instituto de Investigaciones Médicas (IIM), Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia. mauricio.arcos@udea.edu.co.ORCID http://orcid.org/0000-0002-8529-0574
Universidad de Antioquia · COFundación Universitaria Sanitas · COUniversidad del Norte · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is progressive brain disorder that affects ~ 50 million people worldwide and has no current effective treatment. AD age of onset (ADAOO) has shown to be critical for the identification of genes that modify the appearance of AD signs and symptoms in a specific population. We clinically characterized and whole-exome genotyped 71 individuals with AD from the Paisa genetic isolate, segregating the (PSEN1) E280A dominant fully penetrant mutation, and analyzed the potential recessive effects of ~ 50,000 common functional genomic variants to the ADAOO. Standard quality control and filtering procedures were applied, and recessive single- and multi-locus linear mixed-effects models were used. We identified genetic variants in the SLC9C1, CSN1S1, and LOXL4 acting recessively to delay ADAOO up to ~ 11, ~ 6, and ~ 9 years on average, respectively. In contrast, the CC recessive genotype in marker DHRS4L2-rs2273946 accelerates ADAOO by ~ 8 years. This study, reports new recessive variants modifying ADAOO in PSEN1 E280A mutation carriers. This set of genes are implicated in important biological processes and molecular functions commonly affected by genes associated with the etiology of AD such as APP, APOE, and CLU. Future functional studies using modern techniques such as induced pluripotent stem cells will allow a better understanding of the over expression and down regulation of these recessive modifier variants and hence the pathogenesis of AD. These results are important for prediction of AD and ultimately, substantial to develop new therapeutic strategies for individuals at risk or affected by AD.

Indexed as

AdultAlzheimer DiseaseBrainExomeFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMutationRiskAge of onsetAlzheimer’s diseaseGenetic InteractionsGenetic IsolatesPSEN1Recessive Mutations

Identifiers

PMID31664702
PMCPMC7031188
OpenAlexW2982546484

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.