Evidence map›Paper›PMID 35722629›Full record

ArticlePharmacogenomics and personalized medicine2022

Inducible Nitric Oxide Synthase iNOS-954-G>C and Ex16+14-C>T Gene Polymorphisms and Susceptibility to Vitiligo in the Saudi Population.

Fahad Al-Harthi, Ghaleb Bin Huraib, Md Mustafa, Yasser Al-Qubaisy, Naif Al-Nomair, Nour Abdurrahman, Abdulrahman Al-Asmari

Open access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Fahad Al-HarthiDeparment of Dermatology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Ghaleb Bin HuraibScientific Research Center, Health service directorate, Riyadh, Saudi Arabia.
Md MustafaScientific Research Center, Health service directorate, Riyadh, Saudi Arabia.ORCID 0000-0001-7768-6651
Yasser Al-QubaisyDeparment of Dermatology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Naif Al-NomairDeparment of Dermatology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Nour AbdurrahmanDeparment of Dermatology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Abdulrahman Al-AsmariScientific Research Center, Health service directorate, Riyadh, Saudi Arabia.
Riyadh Armed Forces Hospital · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Vitiligo is an acquired pigmentary skin disorder with regional disappearance of melanocytes. Multigenic inheritance has been proposed in the pathogenesis of vitiligo. The present study aimed to investigate the possible association of inducible nitric oxide synthase polymorphisms iNOS-954-G/C (rs1800482 G>C) and iNOS-Ex16+14-C/T (rs2297518 C>T) with vitiligo in the Saudi population, if any. Methods: We included 120 vitiligo cases and an equal number of age matched healthy controls. Polymerase chain reaction with restriction fragment length polymorphism method was used for the analysis of genetic polymorphisms. Results: The heterozygous (GC), (GC + CC) combined genotype and variant allele; C allele of rs1800482 G>C were associated significantly ( Conclusion: The heterozygous (GC), (GC+CC) combined genotype and variants allele; C allele of rs1800482 G>C, may cause overproduction of NO, which has been linked to melanocyte loss by increasing oxidative stress and decreasing melanocyte adhesion to the extracellular matrix components, and thus could be an associative risk factor for vitiligo.

Indexed as

genetic polymorphismnitric oxidenitric oxide synthasenon-segmentalrs1800482 G>Crs2297518 C>Tvitiligo

Identifiers

PMID35722629
PMCPMC9205318
OpenAlexW4282572332

What OpenQuestion holds

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Registered trials

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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.