Evidence map›Paper›PMID 30250222›Full record

ArticleScientific reports2018

Circulating microRNAs -192 and -194 are associated with the presence and incidence of diabetes mellitus.

Andrea Jaeger, Lukas Zollinger, Christoph H Saely, Axel Muendlein, Ioannis Evangelakos, Dimitris Nasias, Nikoleta Charizopoulou, Jonathan D Schofield, Alaa Othman, Handrean Soran and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
–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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

13 authors.

Andrea JaegerInstitute for Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland.
Lukas ZollingerInstitute for Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland.
Christoph H SaelyVorarlberg Institute for Vascular Investigation and Treatment (VIVIT), Feldkirch, Austria.
Axel MuendleinVorarlberg Institute for Vascular Investigation and Treatment (VIVIT), Feldkirch, Austria.
Ioannis EvangelakosUniversity of Crete Medical School and Institute of Molecular Biology and Biotechnology-FORTH, Heraklion, Greece.
Dimitris NasiasUniversity of Crete Medical School and Institute of Molecular Biology and Biotechnology-FORTH, Heraklion, Greece.
Nikoleta CharizopoulouUniversity of Crete Medical School and Institute of Molecular Biology and Biotechnology-FORTH, Heraklion, Greece.
Jonathan D SchofieldCardiovascular Trials Unit, The Old St Mary's Hospital, Central Manchester University Hospitals, Manchester, United Kingdom.
Alaa OthmanInstitute for Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland.
Handrean SoranCardiovascular Trials Unit, The Old St Mary's Hospital, Central Manchester University Hospitals, Manchester, United Kingdom.
Dimitris KardassisUniversity of Crete Medical School and Institute of Molecular Biology and Biotechnology-FORTH, Heraklion, Greece.
Heinz DrexelVorarlberg Institute for Vascular Investigation and Treatment (VIVIT), Feldkirch, Austria.
Arnold von EckardsteinInstitute for Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland. arnold.voneckardstein@usz.ch.

Funding

European Commission (EC) RESOLVE, Project no: 305707Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) CRSII3_154420Universität Zürich (University of Zurich) ZIHP grant
6 · The paper itself

Abstract

We sought to identify circulating microRNAs as biomarkers of prevalent or incident diabetes. In a pilot study of 18 sex- and age-matched patients with metabolic syndrome, nine of whom developed diabetes during 6 years of follow-up, an array of 372 microRNAs discovered significantly elevated serum levels of microRNAs -122, -192, -194, and -215 in patients who developed diabetes mellitus type 2 (T2DM). In two cross-sectional validation studies, one encompassing sex- and age-matched groups of patients with T2DM, impaired fasting glucose (IFG) and euglycemic controls (n = 43 each) and the other 53 patients with type 1 diabetes and 54 age- and BMI-matched euglycemic controls, serum levels of miR-192, miR-194, and mi215 were significantly higher in diabetic subjects than in probands with euglycemia or IFG. In a longitudinal study of 213 initially diabetes-free patients of whom 35 developed diabetes during 6 years of follow-up, elevated serum levels of microRNAs 192 and 194 were associated with incident T2DM, independently of fasting glucose, HbA1c and other risk factors. Serum levels of miR-192 and miR-194 were also elevated in diabetic Akt2 knockout mice compared to wild type mice. In conclusion, circulating microRNAs -192 and -194 are potential biomarkers for risk of diabetes.

Indexed as

AgedAnimalsDiabetes Mellitus, Type 2FemaleHumansKaplan-Meier EstimateMaleMetabolic SyndromeMiceMice, KnockoutMicroRNAsMiddle AgedPilot ProjectsPrediabetic StateProto-Oncogene Proteins c-aktAkt2 protein, mouseMicroRNAsMIRN122 microRNA, humanMIRN192 microRNA, humanMIRN194 microRNA, humanMIRN215 microRNA, humanProto-Oncogene Proteins c-akt

Identifiers

PMID30250222
PMCPMC6155281

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.