Evidence map›Paper›PMID 24019627›Full record

ArticleIndian journal of human genetics2013

The effect of FokI vitamin D receptor polymorphism on bone mineral density in Jordanian perimenopausal women.

Raed M Kanan

Abstract read
In one paragraph

Article in Indian journal of human genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

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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, 13 citations in OpenAlex.

  1. Article
  2. A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
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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

1 author at 1 institution in 1 country.

Raed M KananDepartment of Biotechnology and Genetic Engineering, Philadelphia University, Amman, Jordan.
Philadelphia University · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextOsteoporosis is a polygenic, multifactorial disease that is characterized by demineralization of bone, and thus presented with decreasing bone mineral mass. Vitamin D receptor (VDR) gene polymorphisms in the 3'-end region (as determined by the enzymes BsmI and ApaI) have been inconsistently associated with bone mineral mass. Another important VDR start codon polymorphism (as determined by the enzyme FokI) has been found to be related to adult bone mineral density (BMD) in pre-and post-menopausal American women.

aimsThis study aims to investigate the prevalence of the FokI VDR gene polymorphism in Jordanian perimenopausal women and study its relationship with bone mineral density. MATERIALS AND

methodsDNA was isolated from 90 controls (Mean age = 50.41 ± 1.29 y), and 120 patients with symptomatic vertebral fractures (Mean age = 49.14 ± 3.19 y). Restriction Fragment Length Polymorphism (RFLP) analysis of FokI was performed on DNA samples. STATISTICAL ANALYSIS: Data was analyzed using SPSS v19 and Microsoft Excel 2007.

resultsThe results showed that in controls, the FF (-0.70 ± 0.51) genotype is associated with high lumbar spine BMD Z-score as compared to Ff (-1.25 ± 0.26) and ff (-1.66 ± 0.47) genotypes (P = 0.0095). In patients, the ff genotype was associated with lower lumbar spine BMD in T-score (-2.31 ± 0.17) and Z-score (-1.56 ± 0.09) genotypes (P = 0.031). No significant association was seen in the femoral neck BMD.

conclusionFokI polymorphism may be associated with low BMD in our studied population; however, further studies including other polymorphisms and large sample number are needed.

Indexed as

dbSNP rs10735810Jordanosteoporosisvitamin D receptor

Identifiers

PMID24019627
PMCPMC3758732
OpenAlexW2076923707

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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.