Evidence map›Paper›PMID 33023259›Full record

ReviewJournal of personalized medicine2020

The Genetics of Spondyloarthritis.

Roberto Díaz-Peña, Patricia Castro-Santos, Josefina Durán, Catalina Santiago, Alejandro Lucia

Open access · goldAbstract readReview
In one paragraph

Review in Journal of personalized medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Genetic Risk Scores for the Clinical Rheumatologist.Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. The Role of Aminopeptidase ERAP1 in Human Pathology-A Review.Current issues in molecular biology · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Advances of Genomic Medicine in Psoriatic Arthritis.Journal of personalized medicine · 2022
    Review
  17. Article
  18. Personalized Medicine in Autoimmune Diseases.Journal of personalized medicine · 2021
    Article
  19. Review
  20. 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

5 authors at 5 institutions in 2 countries.

Roberto Díaz-PeñaFaculty of Health Sciences, Universidad Autónoma de Chile, Talca 3460000, Chile.ORCID 0000-0002-0114-2292
Patricia Castro-SantosInmunología, Centro de Investigaciones Biomédicas (CINBIO), Universidad de Vigo, 36310 Vigo, Spain.
Josefina DuránDepartment of Rheumatology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago 7690000, Chile.ORCID 0000-0001-7376-7729
Catalina SantiagoFaculty of Sport Sciences, European University of Madrid, 28670 Madrid, Spain.
Alejandro LuciaFaculty of Sport Sciences, European University of Madrid, 28670 Madrid, Spain.
Pontificia Universidad Católica de Chile · CLResearch Institute Hospital 12 de Octubre · ESUniversidad Autónoma de Chile · CLUniversidade de Vigo · ESUniversidad Europea de Madrid · ES

Funding

Fondo Nacional de Desarrollo Científico y Tecnológico 11130198
6 · The paper itself

Abstract

The term spondyloarthritis (SpA) encompasses a group of chronic inflammatory diseases with common features in terms of clinical presentation and genetic predisposition. SpA is characterized by inflammation of the spine and peripheral joints, and is also be associated with extra-articular inflammatory manifestations such as psoriasis, uveitis, or inflammatory bowel disease (IBD). The etiology of SpA is not completely understood, but it is known to have a strong genetic component dominated by the human leukocyte antigen (HLA)-B27. In the last few years, our understanding of genetic susceptibility to SpA, particularly ankylosing spondylitis (AS), has greatly improved thanks to the findings derived from powered genome-wide association studies (GWAS) based on single nucleotide polymorphism (SNP) arrays. These studies have identified many candidate genes, therefore providing new potential directions in the exploration of disease mechanisms, especially with regard to the key role of the immune system in the pathogenesis of SpA. SpA is a complex disease where genetic variability, environmental factors, and random events interact to trigger pathological pathways. The aim of this review is to summarize current findings on the genetics of SpA, some of which might help to study new treatment approaches.

Indexed as

ankylosing spondylitisERAP1ethnic groupgeneticsgenome-wide association studiesHLA-B27KIRpolymorphismspondyloarthritis

Identifiers

PMID33023259
PMCPMC7711559
OpenAlexW3089343327

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.