Evidence map›Paper›PMID 27899485›Full record

ArticleDiabetes2017

Circulating MicroRNA-122 Is Associated With the Risk of New-Onset Metabolic Syndrome and Type 2 Diabetes.

Peter Willeit, Philipp Skroblin, Alexander R Moschen, Xiaoke Yin, Dorothee Kaudewitz, Anna Zampetaki, Temo Barwari, Meredith Whitehead, Cristina M Ramírez, Leigh Goedeke and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed, 2 pooled it
10.3field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 2 syntheses or guidelines pooled it, 252 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Metabolic diseases in the East Asian populations.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  20. Review

81 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 4 countries.

Peter WilleitKing's British Heart Foundation Centre, King's College London, London, U.K. peter.willeit@i-med.ac.at manuel.mayr@kcl.ac.uk.ORCID 0000-0002-1866-7159
Philipp SkroblinKing's British Heart Foundation Centre, King's College London, London, U.K.
Alexander R MoschenDepartment of Internal Medicine I (Endocrinology, Gastroenterology and Metabolic Diseases), Medical University of Innsbruck, Innsbruck, Austria.
Xiaoke YinKing's British Heart Foundation Centre, King's College London, London, U.K.
Dorothee KaudewitzKing's British Heart Foundation Centre, King's College London, London, U.K.
Anna ZampetakiKing's British Heart Foundation Centre, King's College London, London, U.K.
Temo BarwariKing's British Heart Foundation Centre, King's College London, London, U.K.
Meredith WhiteheadKing's British Heart Foundation Centre, King's College London, London, U.K.
Cristina M RamírezVascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT.
Leigh GoedekeVascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT.
Noemi RotllanVascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT.
Enzo BonoraDivision of Endocrinology, Diabetes, and Metabolic Diseases, University and Hospital Trust of Verona, Verona, Italy.
Alun D HughesInstitute of Cardiovascular Sciences, University College London, London, U.K.
Peter SanterDepartment of Laboratory Medicine, Bruneck Hospital, Bruneck, Italy.
Carlos Fernández-HernandoVascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, CT.
Herbert TilgDepartment of Internal Medicine I (Endocrinology, Gastroenterology and Metabolic Diseases), Medical University of Innsbruck, Innsbruck, Austria.
Johann WilleitDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Stefan KiechlDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Manuel MayrKing's British Heart Foundation Centre, King's College London, London, U.K. peter.willeit@i-med.ac.at manuel.mayr@kcl.ac.uk.
British Heart Foundation · GBInnsbruck Medical University · ATYale University · USKrankenhaus Bruneck · ITUniversity College London · GBUniversity of Verona · IT

Funding

Caveolin-1 in Lipoprotein Metabolism and Atherosclerosis.R01HL106063 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2011 to 2016
$2.5M
Role of microRNAs in lipid metabolism and cardiovascular diseaseR01HL107953 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2011 to 2016
$2.4M
MiR-33 and Aging: Implications for Metabolic SyndromeF31AG043318 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GOEDEKE, LEIGH · 2012 to 2014
$125k
Austrian Science Fund FWF J 3679British Heart Foundation CS/13/1/30327British Heart Foundation FS/13/18/30207British Heart Foundation FS/13/2/29892British Heart Foundation RG/16/14/32397British Heart Foundation SP/12/5/29574Diabetes UK 12/0004530NHLBI NIH HHS R01 HL106063NHLBI NIH HHS R01 HL107953NIA NIH HHS F31 AG043318
6 · The paper itself

Abstract

MicroRNA-122 (miR-122) is abundant in the liver and involved in lipid homeostasis, but its relevance to the long-term risk of developing metabolic disorders is unknown. We therefore measured circulating miR-122 in the prospective population-based Bruneck Study (n = 810; survey year 1995). Circulating miR-122 was associated with prevalent insulin resistance, obesity, metabolic syndrome, type 2 diabetes, and an adverse lipid profile. Among 92 plasma proteins and 135 lipid subspecies quantified with mass spectrometry, it correlated inversely with zinc-α-2-glycoprotein and positively with afamin, complement factor H, VLDL-associated apolipoproteins, and lipid subspecies containing monounsaturated and saturated fatty acids. Proteomics analysis of livers from antagomiR-122-treated mice revealed novel regulators of hepatic lipid metabolism that are responsive to miR-122 inhibition. In the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT, n = 155), 12-month atorvastatin reduced circulating miR-122. A similar response to atorvastatin was observed in mice and cultured murine hepatocytes. Over up to 15 years of follow-up in the Bruneck Study, multivariable adjusted risk ratios per one-SD higher log miR-122 were 1.60 (95% CI 1.30-1.96; P < 0.001) for metabolic syndrome and 1.37 (1.03-1.82; P = 0.021) for type 2 diabetes. In conclusion, circulating miR-122 is strongly associated with the risk of developing metabolic syndrome and type 2 diabetes in the general population.

Indexed as

AdultAgedAnimalsAntagomirsAtorvastatinBlotting, NorthernCarrier ProteinsComplement Factor HDiabetes Mellitus, Type 2DyslipidemiasFemaleGlycoproteinsHepatocytesHumansHydroxymethylglutaryl-CoA Reductase InhibitorsIncidenceAFM protein, humanantagomir-122AntagomirsAtorvastatinCarrier ProteinsComplement Factor HGlycoproteinsHydroxymethylglutaryl-CoA Reductase InhibitorsLipoproteins, VLDLMicroRNAsMIRN122 microRNA, humanMirn122 microRNA, mouseOligonucleotidesSerum AlbuminSerum Albumin, Human

Identifiers

PMID27899485
PMCPMC5248985
OpenAlexW2557910380

What OpenQuestion holds

Texttitle and abstract
LicenceTDM
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.