Evidence mapPaperPMID 36834701Full record

ReviewInternational journal of molecular sciences2023

Pharmacometabolomics for the Study of Lipid-Lowering Therapies: Opportunities and Challenges.

Erica Gianazza, Maura Brioschi, Ada Iezzi, Giuseppe Paglia, Cristina Banfi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. A bezafibrate bearing Pt(IV) prodrug triggers ferroptosis via modulating lipid metabolism in lung cancer cells.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Proteomics and Metabolomics in Biomedicine.International journal of molecular sciences · 2023
    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 2 institutions in 1 country.

Erica GianazzaMonzino Cardiologic Center, IRCCS, 20138 Milan, Italy.ORCID 0000-0003-2370-947X
Maura BrioschiMonzino Cardiologic Center, IRCCS, 20138 Milan, Italy.
Ada IezziMonzino Cardiologic Center, IRCCS, 20138 Milan, Italy.
Giuseppe PagliaSchool of Medicine and Surgery, University of Milano-Bicocca, 20854 Vedano al Lambro, Italy.ORCID 0000-0003-4724-6801
Cristina BanfiMonzino Cardiologic Center, IRCCS, 20138 Milan, Italy.ORCID 0000-0003-3346-9879
Centro Cardiologico Monzino · ITUniversity of Milano-Bicocca · IT

Funding

Ministero della Salute 2764191
6 · The paper itself

Abstract

Lipid-lowering therapies are widely used to prevent the development of atherosclerotic cardiovascular disease (ASCVD) and related mortality worldwide. "Omics" technologies have been successfully applied in recent decades to investigate the mechanisms of action of these drugs, their pleiotropic effects, and their side effects, aiming to identify novel targets for future personalized medicine with an improvement of the efficacy and safety associated with the treatment. Pharmacometabolomics is a branch of metabolomics that is focused on the study of drug effects on metabolic pathways that are implicated in the variation of response to the treatment considering also the influences from a specific disease, environment, and concomitant pharmacological therapies. In this review, we summarized the most significant metabolomic studies on the effects of lipid-lowering therapies, including the most commonly used statins and fibrates to novel drugs or nutraceutical approaches. The integration of pharmacometabolomics data with the information obtained from the other "omics" approaches could help in the comprehension of the biological mechanisms underlying the use of lipid-lowering drugs in view of defining a precision medicine to improve the efficacy and reduce the side effects associated with the treatment.

Indexed as

Drug-Related Side Effects and Adverse ReactionsHydroxymethylglutaryl-CoA Reductase InhibitorsHumansHypolipidemic AgentsLipidsPrecision MedicineHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsLipidsatherosclerotic cardiovascular diseaselipid-lowering drugsmetabolomicsstatins

Identifiers

PMID36834701
PMCPMC9960554
OpenAlexW4319600572

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.