Evidence map›Paper›PMID 37202765›Full record

ArticleBMC medical genomics2023

Vitamin D receptor gene polymorphism and polycystic ovary syndrome susceptibility.

Ibrahim A Albahlol, Mustafa Neamatallah, Mohamed Saad Serria, Abdel-Hady El-Gilany, Yomna A Setate, Nashwa M Alkasaby, Sally Abdallah Mostafa, Mahmoud Abdelaziz, Hossam Elazab, Omar A Ammar

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. The Link BetweenBioMed research international · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Journal of obstetrics and gynaecology of India · 2025
    Article
  9. Article
  10. Article
  11. The Impact of Vitamin D Receptor Gene Polymorphisms (Medicina (Kaunas, Lithuania) · 2024
    Article
  12. Association of candidate gene (Journal of the Turkish German Gynecological Association · 2024
    Article
  13. Article
  14. Article
  15. Molecular role of non-exonic variants inFrontiers in endocrinology · 2023
    Article
  16. 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

10 authors at 3 institutions in 1 country.

Ibrahim A AlbahlolDepartment of Obstetrics and Gynecology, Jouf College of Medicine, Jouf University, Mansoura College of Medicine, Mansoura University, Mansoura, SA, Egypt.
Mustafa NeamatallahDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mohamed Saad SerriaDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Abdel-Hady El-GilanyDepartment of Public Health and Preventive Medicine, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Yomna A SetateInfection Control Unit, Mansoura Specialized Hospital (MSH), Mansoura, Egypt.
Nashwa M AlkasabyDepartments of Medical Microbiology & Immunology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Sally Abdallah MostafaDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mahmoud AbdelazizOncology Center, Mansoura University, Mansoura, Egypt.
Hossam ElazabDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Omar A AmmarBasic Science Department, Delta University for Science and Technology, Gamasa, Egypt. omar.ammar@deltauniv.edu.eg.
Mansoura University · EGDelta University for Science and Technology · EGMansoura University Hospital · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolycystic ovary syndrome (PCOS) is the most common endocrinopathy in women. This study was designed to investigate the associations of vitamin D receptor (VDR) gene variants with PCOS risk and the severity of the disease phenotype among Egyptian women.

methodsIn this study, 185 women with PCOS and 207 fertile women as controls were recruited. Cases were divided into phenotype groups based on their clinical and paraclinical features. Clinical and laboratory data were measured in the patient and control groups. All individuals were genotyped for nine single-nucleotide polymorphisms (SNPs) located across the VDR gene using Taq

resultsWomen with PCOS were significantly (P ≤ 0.001) higher body mass index (BMI) (22.77 ± 2.5) than controls (21.68 ± 1.85 kg/m

conclusionsThe findings of this study indicate that variations in the VDR gene were associated with an increased risk of PCOS in Egyptian women.

Indexed as

Polycystic Ovary SyndromeCase-Control StudiesFemaleFollicle Stimulating HormoneGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideReceptors, CalcitriolTestosteroneFollicle Stimulating HormoneReceptors, CalcitriolTestosteroneVDR protein, humanGene polymorphismsPCOSSNPVitamin D receptor

Identifiers

PMID37202765
PMCPMC10197246
OpenAlexW4377047437

What OpenQuestion 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 OpenQuestion graph.