Evidence map›Paper›PMID 36362878›Full record

ArticleLife (Basel, Switzerland)2022

The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes.

Bernardette Estandia-Ortega, Miriam Erandi Reyna-Fabián, José Antonio Velázquez-Aragón, Ariadna González-Del Angel, Liliana Fernández-Hernández, Miguel Angel Alcántara-Ortigoza

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 24% 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, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  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 1 institution in 1 country.

Bernardette Estandia-OrtegaMolecular Biology Laboratory, Medical Research Sudirectorate, National Institute of Pediatrics, Mexico City 04530, Mexico.
Miriam Erandi Reyna-FabiánMolecular Biology Laboratory, Medical Research Sudirectorate, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0003-3123-8305
José Antonio Velázquez-AragónExperimental Oncology Laboratory, Experimental Medicine Subdirectorate, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0002-3617-8148
Ariadna González-Del AngelMolecular Biology Laboratory, Medical Research Sudirectorate, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0002-7096-0969
Liliana Fernández-HernándezMolecular Biology Laboratory, Medical Research Sudirectorate, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0002-4153-6966
Miguel Angel Alcántara-OrtigozaMolecular Biology Laboratory, Medical Research Sudirectorate, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0003-0592-8214
National Institute of Genomic Medicine · MX

Funding

Instituto Nacional de Pediatría, Secretaría de Salud Recursos Fiscales 2015-2019, Programa E022 Investigación y Desarrollo Tecnológico en Salud, Ciudad de México, México
6 · The paper itself

Abstract

The clinical diagnosis of oculo-auriculo-vertebral spectrum (OAVS) is established when microtia is present in association with hemifacial hypoplasia (HH) and/or ocular, vertebral, and/or renal malformations. Genetic and non-genetic factors have been associated with microtia/OAVS. Although the etiology remains unknown in most patients, some cases may have an autosomal dominant, autosomal recessive, or multifactorial inheritance. Among the possible genetic factors, gene−gene interactions may play important roles in the etiology of complex diseases, but the literature lacks related reports in OAVS patients. Therefore, we performed a gene−variant interaction analysis within five microtia/OAVS candidate genes (HOXA2, TCOF1, SALL1, EYA1 and TBX1) in 49 unrelated OAVS Mexican patients (25 familial and 24 sporadic cases). A statistically significant intergenic interaction (p-value < 0.001) was identified between variants p.(Pro1099Arg) TCOF1 (rs1136103) and p.(Leu858=) SALL1 (rs1965024). This intergenic interaction may suggest that the products of these genes could participate in pathways related to craniofacial alterations, such as the retinoic acid (RA) pathway. The absence of clearly pathogenic variants in any of the analyzed genes does not support a monogenic etiology for microtia/OAVS involving these genes in our patients. Our findings could suggest that in addition to high-throughput genomic approaches, future gene−gene interaction analyses could contribute to improving our understanding of the etiology of microtia/OAVS.

Indexed as

gene–gene interactionsMexican populationmicrotiaMultifactor Dimensionality Reduction (MDR)next-generation sequencingOAVS

Identifiers

PMID36362878
PMCPMC9693117
OpenAlexW4307940202

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.