Evidence map›Paper›PMID 33250642›Full record

ReviewSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society2020

The potential of Atorvastatin for chronic lung diseases therapy.

Alaa S Tulbah

Open access · hybridAbstract readReview
In one paragraph

Review in Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Design and Characterization of Atorvastatin Dry Powder Formulation as a potential Lung Cancer Treatment.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2021
    Article
  13. 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

1 author at 1 institution in 1 country.

Alaa S TulbahDepartment of Pharmaceutics, College of Pharmacy, Umm Al Qura University, Makkah, Saudi Arabia.
Umm al-Qura University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atorvastatin (ATO) is of the statin class and is used as an orally administered lipid-lowering drug. ATO is a reversible synthetic competitive inhibitor of 3-hydroxy-3-methyl-glutaryl-CoA (HMG-CoA) reductase thus leading to a reduction in cholesterol synthesis. It has recently been demonstrated that ATO has different pharmacological actions, which are unrelated to its lipid-lowering effects and has the ability to treat chronic airway diseases. This paper reviews the potential of ATO as an anti-inflammatory, antioxidant, and anti-proliferative agent after oral or inhaled administration. This paper discusses the advantages and disadvantages of using ATO under conditions associated with those found in the airways. This treatment could potentially be used to support the formulating of ATO as an inhaler for the treatment of chronic respiratory diseases.

Indexed as

AA, Allergic asthmaAP-1, Activator protein-1ATO, AtorvastatinAtorvastatinBALF, Bronchoalveolar lavage fluidCCL7, Chemokine ligand 7CI, Confidence interval°C/min, Temperature in degrees per minutesCOPD, Chronic obstructive pulmonary diseaseCRP, C-reactive proteinCS, Cigarettes smokeCYP3A4/5, Cytochrome Metabolic enzymes3A4/5FPP, FarnesylpyrophosphateGEF, Guanine nucleotide exchange factorsGGPP, GeranylgeranylpyrophosphateG, GramIL, InterleukinsInflammationInhalelog D, Coefficient values octanol/waterLog P, Partition coefficientm2, Square metermg/day, Milligram per daymg, Milligramml, MillilitresMMPs, Matrix-metalloproteaseMVA, Mevalonic acidNADPH, Nicotinamide adenine dinucleotide phosphateNaOH, Sodium hydroxideNCSCL, Non-small cell lung cancerNF-κB, Nuclear factor kappaNOS, Nitric oxide synthaseOATP, Organic anion transporting polypeptideOralOxidationPEG, Polyethylene glycol%, PercentagepH, Measure of the acidity or basicity of an aqueous solutionpKa, Dissociation constantPPE, Porcine pancreatic elastaseRespiratory diseasesROS, Reactive oxygen speciesSAS, Supercritical antisolventSphK1, Sphingosine kinase 1s, SecondTGF, Transforming growth factorTNF-a, Tumour necrosis factor alphaTSC, Tuberous sclerosisUDP, Uridine diphosphateUV, Ultraviolet lightVEGF, Vascular endothelial cell growth factorVLDL, Very low-density lipoproteinsv/v, Volume per volumeWHO, World Health Organizationμg/day, Microgram per dayμg, Microgramμg/mL, Microgram per millilitreμM, Micromolar

Identifiers

PMID33250642
PMCPMC7679442
OpenAlexW3086138664

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.