Evidence map›Paper›PMID 29748367›Full record

ReviewCirculation research2018

PCSK9: From Basic Science Discoveries to Clinical Trials.

Michael D Shapiro, Hagai Tavori, Sergio Fazio

Open access · bronzeAbstract readReview
In one paragraph

Review in Circulation research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 149 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
149citing papers in PubMed, 2 pooled it
24.4field-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

149 citing papers in PubMed, 2 syntheses or guidelines pooled it, 280 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Review
  8. Article
  9. PCSK9 inhibitors conquer primary prevention: the VESALIUS-CV study.European heart journal supplements : journal of the European Society of Cardiology · 2026
    Article
  10. Enzyme-Assisted Synthesis and In Vitro Characterization of Bifunctional PCSK9 Inhibitors.Chembiochem : a European journal of chemical biology · 2026
    Article
  11. Genetic determinants of plasma lipids in Greenlanders.Current opinion in lipidology · 2026
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

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

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

3 authors at 1 institution in 1 country.

Michael D ShapiroFrom the Center for Preventive Cardiology, Knight Cardiovascular Institute, Oregon Health & Science University, Portland.
Hagai TavoriFrom the Center for Preventive Cardiology, Knight Cardiovascular Institute, Oregon Health & Science University, Portland.
Sergio FazioFrom the Center for Preventive Cardiology, Knight Cardiovascular Institute, Oregon Health & Science University, Portland. fazio@ohsu.edu.
Oregon Health & Science University · US

Funding

Functional and structural correlates of PCSK9 association with lipoproteinsR01HL132985 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI PAMIR, NATHALIE · 2016 to 2024
$4.2M
NHLBI NIH HHS R01 HL132985
6 · The paper itself

Abstract

Unknown 15 years ago, PCSK9 (proprotein convertase subtilisin/kexin type 9) is now common parlance among scientists and clinicians interested in prevention and treatment of atherosclerotic cardiovascular disease. What makes this story so special is not its recent discovery nor the fact that it uncovered previously unknown biology but rather that these important scientific insights have been translated into an effective medical therapy in record time. Indeed, the translation of this discovery to novel therapeutic serves as one of the best examples of how genetic insights can be leveraged into intelligent target drug discovery. The PCSK9 saga is unfolding quickly but is far from complete. Here, we review major scientific understandings as they relate to the role of PCSK9 in lipoprotein metabolism and atherosclerotic cardiovascular disease and the impact that therapies designed to inhibit its action are having in the clinical setting.

Indexed as

AnimalsAntibodies, MonoclonalAtherosclerosisCardiovascular DiseasesCholesterolDyslipidemiasHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLipoproteinsLiverMiceObservational Studies as TopicPCSK9 InhibitorsProprotein Convertase 9Protein Processing, Post-TranslationalRandomized Controlled Trials as TopicAntibodies, MonoclonalCholesterolHydroxymethylglutaryl-CoA Reductase InhibitorsLDLR protein, humanLipoproteinsPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9Receptors, LDLdyslipidemiashyperlipoproteinemia type IIlipid metabolismlipoproteinsreceptors, LDL

Identifiers

PMID29748367
PMCPMC5976255
OpenAlexW2801426688

What Socratic 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 Socratic graph.