Evidence map›Paper›PMID 25170295›Full record

ArticleInternational journal of medical sciences2014

Relationship between European mitochondrial haplogroups and chronic renal allograft rejection in patients with kidney transplant.

María Angeles Jiménez-Sousa, Eduardo Tamayo, María Guzmán-Fulgencio, Amanda Fernández-Rodríguez, María Heredia-Rodriguez, Mónica García-Álvarez, Jesús F Bermejo-Martin, Daniel Pineda-Tenor, Patricia Ruiz-Granado, Elisa Alvarez-Fuente and 3 more

Abstract read
In one paragraph

Article in International journal of medical sciences, 2014. 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
–field-weighted citation impact
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.

  1. Trial
  2. Review
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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

13 authors.

María Angeles Jiménez-Sousa1. Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología. Instituto de Salud Carlos III, Majadahonda, Spain.
Eduardo Tamayo2. Departamento de Anestesiología y Reanimación, Hospital Clínico Universitario, Valladolid, Spain.
María Guzmán-Fulgencio1. Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología. Instituto de Salud Carlos III, Majadahonda, Spain.
Amanda Fernández-Rodríguez1. Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología. Instituto de Salud Carlos III, Majadahonda, Spain.
María Heredia-Rodriguez2. Departamento de Anestesiología y Reanimación, Hospital Clínico Universitario, Valladolid, Spain.
Mónica García-Álvarez1. Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología. Instituto de Salud Carlos III, Majadahonda, Spain.
Jesús F Bermejo-Martin3. Unidad de Investigación Biomédica. Hospital Clínico Universitario-IECSCYL, Valladolid, Spain.
Daniel Pineda-Tenor1. Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología. Instituto de Salud Carlos III, Majadahonda, Spain.
Patricia Ruiz-Granado2. Departamento de Anestesiología y Reanimación, Hospital Clínico Universitario, Valladolid, Spain.
Elisa Alvarez-Fuente2. Departamento de Anestesiología y Reanimación, Hospital Clínico Universitario, Valladolid, Spain.
Esther Gómez-Sanchez2. Departamento de Anestesiología y Reanimación, Hospital Clínico Universitario, Valladolid, Spain.
José I Gómez-Herreras2. Departamento de Anestesiología y Reanimación, Hospital Clínico Universitario, Valladolid, Spain.
Salvador Resino1. Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología. Instituto de Salud Carlos III, Majadahonda, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial DNA variants may contribute to differences in mitochondrial function, leading to an altered immune system. The aim of this study was to analyze the relationship between mtDNA haplogroups and the development of chronic allograft dysfunction in patients with kidney transplant. A retrospective observational study was carried out on 261 patients who received kidney transplant (114 had stable transplant and 147 patients developed chronic allograft dysfunction). DNA samples were genotyped for 14 mtDNA polymorphisms by using Sequenom's MassARRAY platform (San Diego, CA, USA). Only European white patients within the N macro-cluster were included. Patients with haplogroups V (odds ratio (OR)=0.32; p=0.037) and J (OR=0.36; p=0.038) showed lower odds for developing CRAD than patients with haplogroup H. After adjusting for the most significant variables, haplogroups V and J tended to statistical significance (p=0.091 and p=0.067 respectively). This is a preliminary study in which mtDNA haplogroups seem to be implicated in susceptibility or protection for developing chronic allograft dysfunction.

Indexed as

Kidney TransplantationAdultDNA, MitochondrialFemaleGraft RejectionHaplotypesHumansMaleMiddle AgedPolymorphism, Single NucleotideRetrospective StudiesWhite PeopleDNA, Mitochondrialallograft rejectionkidney transplantmitochondrial haplogroupsmtDNASNPs

Identifiers

PMID25170295
PMCPMC4147638

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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.