Association between polymorphisms in GGPS1 and RANKL genes and postmenopausal osteoporosis in Romanian women

IF 0.2
A. Ciubean, Laszlo Irsay, R. Ungur, V. Ciortea, Ileana Monica Borda, B. G. Dogaru, A. Trifa, A. Buzoianu
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引用次数: 0

Abstract

Objectives: This study aimed to assess the relationship between bone mineral density, fragility fractures, fracture risk and polymorphisms of two osteoporosis-candidate genes (GGPS1 and RANKL) in Romanian women with postmenopausal osteoporosis. Methods: An analytical, prospective, transversal, observational, case-control study on 364 postmenopausal women, of which 228 were previously diagnosed with osteoporosis, was carried out between June 2016 and August 2017 in Cluj Napoca, Romania. Clinical data and blood samples were collected from all study participants. Polymorphisms in GGPS1 and RANKL genes were genotyped using TaqMan SNP Genotyping assays, run on a QuantStudio 3 real-time PCR machine. Results: The CT genotype in GGPS1 rs10925503 was associated with significant lower bone mineral density values at lumbar spine and femoral neck sites and a higher fracture risk compared to controls. No significant association was found between genotypes of RANKL rs2277439 with bone mineral density or fracture risk compared to the healthy controls. Conclusions: Our study showed a strong association between low bone mineral density and genotype CT of GGPS1 rs10925503 polymorphisms. No association was found for RANKL rs2277439 polymorphism.
罗马尼亚妇女GGPS1和RANKL基因多态性与绝经后骨质疏松症的关系
目的:本研究旨在评估罗马尼亚绝经后骨质疏松妇女的骨密度、脆性骨折、骨折风险和两个骨质疏松候选基因(GGPS1和RANKL)多态性之间的关系。方法:2016年6月至2017年8月,在罗马尼亚克卢日-纳波卡对364名绝经后妇女进行了一项分析性、前瞻性、横向、观察性、病例对照研究,其中228名先前被诊断为骨质疏松症。从所有研究参与者中收集临床数据和血液样本。GGPS1和RANKL基因的多态性使用在QuantStudio3实时PCR机器上运行的TaqMan SNP基因分型分析进行基因分型。结果:与对照组相比,GGPS1 rs10925503的CT基因型与腰椎和股骨颈部位的骨密度值显著较低以及骨折风险较高有关。与健康对照组相比,RANKL rs2277439的基因型与骨密度或骨折风险之间没有发现显著关联。结论:我们的研究显示低骨密度与GGPS1 rs10925503多态性的基因型CT之间有很强的相关性。RANKL rs2277439多态性没有发现相关性。
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Balneo Research Journal
Balneo Research Journal REHABILITATION-
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