Evidence map›Paper›PMID 39683539›Full record

ArticleNutrients2024

Bone Fracture Incidence in Postmenopausal Women: Results of a 10 Year Follow Up in a RAC-OST-POL Study of rs1544410, rs7975232 and rs731236 Polymorphisms.

Elżbieta Tabor, Sylwia Górczyńska-Kosiorz, Wojciech Pluskiewicz, Janusz Gumprecht

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Elżbieta TaborDepartment of Internal Medicine, Diabetology and Nephrology Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.ORCID 0000-0001-6958-9050
Sylwia Górczyńska-KosiorzDepartment of Internal Medicine, Diabetology and Nephrology Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.ORCID 0000-0001-6669-7216
Wojciech PluskiewiczMetabolic Bone Diseases Unit, Department of Internal Medicine, Diabetology and Nephrology Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.
Janusz GumprechtDepartment of Internal Medicine, Diabetology and Nephrology Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.

Funding

Medical University of Silesia PCN-1-176/N/2/K
6 · The paper itself

Abstract

backgroundThe clinical significance of the genetic influence of vitamin D receptor polymorphisms has still not been well-analyzed.

objectivesTo verify whether rs1544410, rs7975232 and rs731236 polymorphisms are associated with a higher 10-year fracture risk in postmenopausal women.

methodsThe study group was a subset of a pre-defined population as part of the broader epidemiological research called the RAC-OST-POL Study and consisted of 358 postmenopausal women, chosen randomly from Racibórz (Poland) inhabitants (mean baseline age 65 ± 6.9 years, BMI 31.2 ± 5.5 kg/m

resultsWe did not find statistically significant main effects on the fracture incidence of single-polymorphism variants. However, there were some significant findings dependent on the co-existence of these polymorphisms and medical factors. Women with a positive history of parental fracture and configuration of CC rs7975232, AA rs731236 and CC rs1544410 had a higher fracture incidence. The risk of bone fracture was also significantly higher in the group of heterozygotes of AC rs7975232 if their BMI value was in the categories of normal weight or overweight, or if they were treated with calcium or vitamin D.

conclusionsPolymorphisms of rs1544410, rs7975232 and rs731236 are connected with the fracture incidence in postmenopausal women. Nevertheless, its influence should be considered with co-existing clinical factors, especially paternal fracture history, prior fracture, BMI value, any osteoporotic treatment or calcium/vit. D supplementation.

Indexed as

Fractures, BonePolymorphism, Single NucleotidePostmenopauseReceptors, CalcitriolAgedFemaleFollow-Up StudiesGenetic Predisposition to DiseaseHumansIncidenceMiddle AgedOsteoporosis, PostmenopausalOsteoporotic FracturesRisk FactorsReceptors, CalcitriolVDR protein, humanbone fracturefracture riskgenetic polymorphismgenotypinglong-term follow uppaternalpostmenopausal osteoporosisVDR

Identifiers

PMID39683539
PMCPMC11643942

What Socratic holds

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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 Socratic graph.