Evidence map›Paper›PMID 29545345›Full record

ArticleHaematologica2018

Circulating microRNAs as biomarkers of disease and typification of the atherothrombotic status in antiphospholipid syndrome.

Carlos Pérez-Sánchez, Iván Arias-de la Rosa, María Ángeles Aguirre, María Luque-Tévar, Patricia Ruiz-Limón, Nuria Barbarroja, Yolanda Jiménez-Gómez, María Carmen Ábalos-Aguilera, Eduardo Collantes-Estévez, Pedro Segui and 11 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Antiphospholipid Syndrome in Pregnancy: New and Old Pathogenetic Mechanisms.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. An Update on Antiphospholipid Syndrome.Current rheumatology reports · 2022
    Review
  14. Review
  15. Epigenetics, microRNA and Metabolic Syndrome: A Comprehensive Review.International journal of molecular sciences · 2021
    Review
  16. Review
  17. Review
  18. Inhibition of miR-383 suppresses oxidative stress and improves endothelial function by increasing sirtuin 1.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  19. Inflammation, Senescence and MicroRNAs in Chronic Kidney Disease.Frontiers in cell and developmental biology · 2020
    Article
  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

21 authors at 6 institutions in 3 countries.

Carlos Pérez-SánchezInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Iván Arias-de la RosaInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
María Ángeles AguirreInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
María Luque-TévarInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Patricia Ruiz-LimónInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Nuria BarbarrojaInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Yolanda Jiménez-GómezInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
María Carmen Ábalos-AguileraInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Eduardo Collantes-EstévezInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Pedro SeguiInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain.
Francisco VelascoUnidad de Gestión Clínica Hematología, Hospital Universitario Reina Sofía, Córdoba, Spain.
María Teresa HerranzServicio de Medicina Interna, Hospital Morales Meseguer, Murcia, Spain.
Jesús Lozano-HerreroServicio de Medicina Interna, Hospital Morales Meseguer, Murcia, Spain.
María Julia Hernandez-VidalServicio de Medicina Interna, Hospital Morales Meseguer, Murcia, Spain.
Constantino MartínezCentro Regional de Hemodonación, Universidad de Murcia, IMIB-Arrixaca, Spain.
Rocío González-ConejeroCentro Regional de Hemodonación, Universidad de Murcia, IMIB-Arrixaca, Spain.
Massimo RadinDepartment of Clinical and Biological Sciences, Center of Research of Immunopathology and Rare Diseases, Torino, Italy.
Savino SciasciaDepartment of Clinical and Biological Sciences, Center of Research of Immunopathology and Rare Diseases, Torino, Italy.
Irene CecchiDepartment of Clinical and Biological Sciences, Center of Research of Immunopathology and Rare Diseases, Torino, Italy.
María José CuadradoLupus Research Unit and St. Thomas' Hospital, London, UK.
Chary López-PedreraInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Spain rosario.lopez.exts@juntadeandalucia.es.
Instituto Maimónides de Investigación Biomédica de Córdoba · ESHospital General Universitario Morales Meseguer · ESUniversity of Turin · ITCentro Regional de Hemodonación · ESHospital Universitario Reina Sofía · ESSt Thomas' Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to identify the plasma miRNA profile of antiphospholipid syndrome (APS) patients and to investigate the potential role of specific circulating miRNAs as non-invasive disease biomarkers. Ninety APS patients and 42 healthy donors were recruited. Profiling of miRNAs by PCR-array in plasma of APS patients identified a set of miRNAs differentially expressed and collectively involved in clinical features. Logistic regression and ROC analysis identified a signature of 10 miRNA ratios as biomarkers of disease. In addition, miRNA signature was related to fetal loss, atherosclerosis, and type of thrombosis, and correlated with parameters linked to inflammation, thrombosis, and autoimmunity. Hard clustering analysis differentiated 3 clusters representing different thrombotic risk profile groups. Significant differences between groups for several miRNA ratios were found. Moreover, miRNA signature remained stable over time, demonstrated by their analysis three months after the first sample collection. Parallel analysis in two additional cohorts of patients, including thrombosis without autoimmune disease, and systemic lupus erythematosus without antiphospholipid antibodies, each displayed specific miRNA profiles that were distinct from those of APS patients.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAntiphospholipid SyndromeAtherosclerosisBiomarkersCase-Control StudiesCirculating MicroRNACohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisThrombosisBiomarkersCirculating MicroRNA

Identifiers

PMID29545345
PMCPMC5927979
OpenAlexW2793953170

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.