Evidence map›Paper›PMID 31280192›Full record

ReviewIn vivo (Athens, Greece)

Pharmacogenetic Implications of eNOS Polymorphisms (

Angela Cozma, Adriana Fodor, Olga Hilda Orasan, Romana Vulturar, Dorel Samplelean, Vasile Negrean, Crina Muresan, Ramona Suharoschi, Adela Sitar-Taut

Open access · diamondAbstract readReview
In one paragraph

Review in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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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

9 authors at 3 institutions in 1 country.

Angela Cozma *University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Adriana Fodor *University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Olga Hilda Orasan *University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Romana VulturarUniversity of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Dorel SampleleanUniversity of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Vasile NegreanUniversity of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Crina MuresanUniversity of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca, Faculty of Food Science &Technology, Cluj-Napoca, Romania.
Ramona SuharoschiUniversity of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca, Faculty of Food Science &Technology, Cluj-Napoca, Romania ramona.suharoschi@usamvcluj.ro.
Adela Sitar-TautUniversity of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Iuliu Hațieganu University of Medicine and Pharmacy · ROUniversity of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca · ROSpitalul Clinic CF Cluj-Napoca · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial nitric oxide synthase (NOS3 or eNOS) is the enzyme responsible for the highest production of nitric oxide, with the greatest impact on the cardiovascular system, encoded by the eNOS gene, which presents various polymorphisms. ENOS gene polymorphisms play an important role in the response to drugs affecting nitric oxide (NO) signaling. This review discusses the pharmacogenetic impact of eNOS polymorphisms on the response to drugs affecting NO activity: angiotensin converting enzyme inhibitors, angiotensin II receptor antagonists, calcium blockers, beta-blockers, diuretics, phosphodiesterase inhibitors, and statins. The identification of biomarkers that accurately predict particular phenotypes is a challenge that needs additional large studies, in different populations. Efforts should be oriented towards a more accurate evaluation of the effects of eNOS genetic variants on biochemical parameters reflecting eNOS gene expression and enzymatic activity, in different diseases, as well as following drug treatment. This approach will allow for a better understanding of the role of eNOS genetic variants in cardiovascular disease progression and for cardiovascular drug therapy optimization.

Indexed as

AllelesAmino Acid SubstitutionPharmacogenomic VariantsPolymorphism, Single NucleotideAnimalsBiomarkersCardiovascular AgentsCardiovascular DiseasesCardiovascular SystemGene Expression RegulationGenetic Association StudiesGenetic Predisposition to DiseaseHumansNitric OxideNitric Oxide Synthase Type IIIPharmacogeneticsBiomarkersCardiovascular AgentsNitric OxideNitric Oxide Synthase Type IIINOS3 protein, humanCardiovascular drugeNOSnitric oxidepharmacogeneticspolymorphismsreview

Identifiers

PMID31280192
PMCPMC6689342
OpenAlexW2954369823

What OpenQuestion holds

Textmetadata
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.