Evidence map›Paper›PMID 31036794›Full record

ArticleJournal of clinical medicine2019

The rs1126616 Single Nucleotide Polymorphism of the Osteopontin Gene Is Independently Associated with Cardiovascular Events in a Chronic Kidney Disease Cohort.

Serafí Cambray, Rajesh Kumar Galimudi, Milica Bozic, Marcelino Bermúdez-López, Isabel Rodríguez, José M Valdivielso

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Dentoalveolar Alterations in an Adenine-Induced Chronic Kidney Disease Mouse Model.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Article
  4. Review
  5. 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 2 institutions in 1 country.

Serafí CambrayVascular and Renal Translational Research Group, Biomedical Research Institute, IRBLLEIDA, and RedinRen-ISCIII, 25198 Lleida, Spain. seracc@yahoo.es.
Rajesh Kumar GalimudiVascular and Renal Translational Research Group, Biomedical Research Institute, IRBLLEIDA, and RedinRen-ISCIII, 25198 Lleida, Spain. rajeshgkumar26@gmail.com.
Milica BozicVascular and Renal Translational Research Group, Biomedical Research Institute, IRBLLEIDA, and RedinRen-ISCIII, 25198 Lleida, Spain. bozicm@medicina.udl.cat.
Marcelino Bermúdez-LópezVascular and Renal Translational Research Group, Biomedical Research Institute, IRBLLEIDA, and RedinRen-ISCIII, 25198 Lleida, Spain. mbermudez@irblleida.cat.
Isabel RodríguezBone and Mineral Research Unit, RedinRen-ISCIII, Hospital Universitario Central de Asturias, Universidad de Oviedo, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain. isabelrodriguez2710@gmail.com.ORCID 0000-0001-7213-1411
José M ValdivielsoVascular and Renal Translational Research Group, Biomedical Research Institute, IRBLLEIDA, and RedinRen-ISCIII, 25198 Lleida, Spain. valdivielso@irblleida.cat.
Instituto de Salud Carlos III · ESUniversidad de Oviedo · ES

Funding

Instituto de Salud Carlos III PI10/00173Instituto de Salud Carlos III PI16/01354Instituto de Salud Carlos III RD16/0009
6 · The paper itself

Abstract

Chronic kidney disease (CKD) is associated with a higher risk of cardiovascular events (CVE), partly due to the higher burden of atherosclerosis. Circulating Osteopontin (OPN) levels have been also shown to have a potential role in the development of atherosclerosis. Indeed, CKD patients show an increase in circulating OPN levels, but their effect of CKD-related atherosclerosis is not clear. Polymorphisms in the OPN gene (

Indexed as

atherosclerotic plaquecardiovascular eventchronic kidney diseaseOsteopontinOsteopontin gene (SPP1)polymorphisms

Identifiers

PMID31036794
PMCPMC6571716
OpenAlexW2942969066

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.