Evidence map›Paper›PMID 36983136›Full record

ArticleJournal of clinical medicine2023

Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence.

Rebeca Lorca, Andrea Aparicio, Juan Gómez, Rut Álvarez-Velasco, Isaac Pascual, Pablo Avanzas, Francisco González-Urbistondo, Alberto Alen, Daniel Vázquez-Coto, Mar González-Fernández and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. 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
0.9field-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. 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

14 authors at 3 institutions in 1 country.

Rebeca LorcaÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-7803-4011
Andrea AparicioÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Juan GómezInstituto de Investigación Sanitaria del Principado de Asturias, ISPA, 33011 Oviedo, Spain.ORCID 0000-0002-3318-4649
Rut Álvarez-VelascoÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-2837-7374
Isaac PascualÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0001-5433-1364
Pablo AvanzasÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-4958-6108
Francisco González-UrbistondoÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Alberto AlenÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-0771-4650
Daniel Vázquez-CotoLaboratorio de Genética, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Mar González-FernándezLaboratorio de Genética, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0009-0007-5465-6290
Claudia García-LagoLaboratorio de Genética, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Elías Cuesta-LlavonaInstituto de Investigación Sanitaria del Principado de Asturias, ISPA, 33011 Oviedo, Spain.ORCID 0000-0002-0924-0962
César MorísÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-2871-190X
Eliecer CotoInstituto de Investigación Sanitaria del Principado de Asturias, ISPA, 33011 Oviedo, Spain.ORCID 0000-0002-8649-9150
Hospital Universitario Central de Asturias · ESUniversidad de Oviedo · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ES

Funding

Spanish Instituto de Salud Carlos III (ISCIII) PI18/00719
6 · The paper itself

Abstract

Mitochondrial DNA (mtDNA) differs from the nuclear genome in many aspects: a maternal inheritance pattern; being more prone to acquire somatic de novo mutations, accumulative with age; and the possible coexistence of different mtDNA alleles (heteroplasmy). Mitochondria are key cellular organelles responsible for energy production and involved in complex mechanisms, including atherosclerosis. In this scenario, we aimed to evaluate mtDNA variants that could be associated with premature cardiovascular disease. We evaluated 188 consecutive patients presenting with premature myocardial infarction with ST elevation (STEMI) confirmed by coronary angiogram. mtDNA polymorphisms and clinical data were evaluated and compared with 271 individuals from the same population (control group). Tobacco consumption (80.85% vs. 21.21%,

Indexed as

atherosclerotic cardiovascular disease (ACVS)cardiovascular preventiongenetic testingmitochondrial DNA (mtDNA)

Identifiers

PMID36983136
PMCPMC10053235
OpenAlexW4323667800

What Socratic 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 Socratic graph.