Evidence map›Paper›PMID 32429343›Full record

ReviewNutrients2020

Naturally Occurring PCSK9 Inhibitors.

Maria Pia Adorni, Francesca Zimetti, Maria Giovanna Lupo, Massimiliano Ruscica, Nicola Ferri

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
10.4field-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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Review
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  11. Article
  12. Article
  13. Male-specific amelioration of lipid metabolism by edible insectFood chemistry. Molecular sciences · 2025
    Article
  14. Review
  15. Article
  16. Naturally Occurring PCSK9 Inhibitors: An Updated Review.Molecules (Basel, Switzerland) · 2025
    Review
  17. Review
  18. Review
  19. 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

5 authors at 3 institutions in 1 country.

Maria Pia AdorniDepartment of Medicine and Surgery-Unit of Neurosciences, University of Parma, 43125 Parma, Italy.
Francesca ZimettiDipartimento di Scienze degli Alimenti e del Farmaco, Università di Parma, 43124 Parma, Italy.ORCID 0000-0002-6665-263X
Maria Giovanna LupoDipartimento di Scienze del Farmaco, Università degli Studi di Padova, 35121 Padova, Italy.
Massimiliano RuscicaDipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, 20122 Milan, Italy.ORCID 0000-0002-0195-7061
Nicola FerriDipartimento di Scienze del Farmaco, Università degli Studi di Padova, 35121 Padova, Italy.ORCID 0000-0001-8898-7441
University of Padua · ITUniversity of Parma · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic, epidemiological and pharmacological data have led to the conclusion that antagonizing or inhibiting Proprotein convertase subtilisin/kexin type 9 (PCSK9) reduces cardiovascular events. This clinical outcome is mainly related to the pivotal role of PCSK9 in controlling low-density lipoprotein (LDL) cholesterol levels. The absence of oral and affordable anti-PCSK9 medications has limited the beneficial effects of this new therapeutic option. A possible breakthrough in this field may come from the discovery of new naturally occurring PCSK9 inhibitors as a starting point for the development of oral, small molecules, to be used in combination with statins in order to increase the percentage of patients reaching their LDL-cholesterol target levels. In the present review, we have summarized the current knowledge on natural compounds or extracts that have shown an inhibitory effect on PCSK9, either in experimental or clinical settings. When available, the pharmacodynamic and pharmacokinetic profiles of the listed compounds are described.

Indexed as

PCSK9 InhibitorsBerberineCholesterol, LDLEnzyme InhibitorsHumansPhytochemicalsProprotein Convertase 9Receptors, LDLBerberineCholesterol, LDLEnzyme InhibitorsPCSK9 InhibitorsPCSK9 protein, humanPhytochemicalsProprotein Convertase 9Receptors, LDLberberinecholesterolHNF1αnutraceuticalsPCSK9SREBP

Identifiers

PMID32429343
PMCPMC7284437
OpenAlexW3025949713

What Socratic 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 Socratic graph.