Evidence map›Paper›PMID 39982362›Full record

ReviewPathophysiology : the official journal of the International Society for Pathophysiology2025

Association Between Vitamin D Receptor BsmI Polymorphism and Low Bone Mineral Density in Postmenopausal Women in the MENA Region.

Tara Al-Barazenji, Asma Allouch, Nedhal Al Husaini, Sondos Yousef, Wisam Nabeel Ibrahim, Amal Al-Haidose, Hatem Zayed, Atiyeh M Abdallah

Erratum issuedAbstract readReview
In one paragraph

Review in Pathophysiology : the official journal of the International Society for Pathophysiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Tara Al-BarazenjiDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.ORCID 0000-0002-4817-4873
Asma AllouchDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.
Nedhal Al HusainiDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.ORCID 0009-0003-2781-1591
Sondos YousefDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.
Wisam Nabeel IbrahimDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.ORCID 0000-0001-6008-1947
Amal Al-HaidoseDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.ORCID 0009-0000-8705-0198
Hatem ZayedDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.ORCID 0000-0001-8838-6638
Atiyeh M AbdallahDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha 2713, Qatar.ORCID 0000-0003-4812-956X

Funding

Qatar University QUCP-CHS-2022-551
6 · The paper itself

Abstract

BACKGROUND/

objectivesLow bone mineral density increases the risk of bone fractures, and this condition is especially common in postmenopausal women. Genetic factors significantly influence bone mineral density. This meta-analysis examined the relationship between vitamin D receptor (VDR) gene polymorphisms (BsmI, ApaI, and TaqI) and bone mineral density in postmenopausal women in the Middle East and North Africa (MENA) region.

methodsThe PubMed, Embase, Scopus, and Web of Science databases were searched from inception to March 2024 for case-control studies on VDR BsmI, ApaI, and TaqI polymorphisms and their relationship with low bone density. Associations with low bone mineral density were tested with respect to different genetic models (dominant, recessive, allelic) using RevMan v5.3.

resultsThe meta-analysis included seven studies for BsmI, six for ApaI, and seven for TaqI, representing 704/689 cases/controls for BsmI, 914/711 for ApaI, and 974/895 for TaqI. No significant association was found between VDR polymorphisms and low bone mineral density in postmenopausal women, except in the dominant model (CC + CG vs. GG) for the BsmI variant (OR = 1.27, 95% CI: 1.01-1.59,

conclusionsWe found a modest association between the BsmI polymorphism and increased risk of low bone mineral density (BMD) in postmenopausal women from the MENA region, suggesting its potential as a biomarker. No associations were observed for ApaI or TaqI. These findings highlight the complex genetic-environmental interactions influencing BMD.

Indexed as

ApaI polymorphismBsmI polymorphismlow BMDmeta-analysisosteoporosis and osteopeniapostmenopausalTaqI polymorphismvitamin D receptor

Identifiers

PMID39982362
PMCPMC11843856

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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.