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Article

Association Between Polymorphisms of VDR, COL1A1, and LCT Genes and Bone Mineral Density in Belarusian Women With Severe Postmenopausal Osteoporosis

by
Pavel Marozik
1,
Irma Mosse
1,
Vidmantas Alekna
2,3,
Ema Rudenko
4,
Marija Tamulaitienė
2,5,*,
Heorhi Ramanau
6,
Vaidilė Strazdienė
3,5,
Volha Samokhovec
4,
Maxim Ameliyanovich
1,
Nikita Byshnev
1,
Alexander Gonchar
1,
Liubov Kundas
1 and
Krystsina Zhur
1
1
Institute of Genetics and Cytology NAS Belarus, Belarus
2
Faculty of Medicine, Vilnius University, Lithuania
3
State Research Institute Centre for Innovative Medicine, Lithuania
4
Belarusian Medical Academy of Postgraduate Education, Belarus
5
National Osteoporosis Centre, Lithuania
6
Gomel State Medical University, Belarus
*
Author to whom correspondence should be addressed.
Medicina 2013, 49(4), 28; https://doi.org/10.3390/medicina49040028
Submission received: 6 November 2012 / Accepted: 30 April 2013 / Published: 5 May 2013

Abstract

Background and Objective. Variation of osteoporosis in the population is the result of an interaction between the genotype and the environment, and the genetic causes of osteoporosis are being widely investigated. The aim of this study was to analyze the association between the polymorphisms of the vitamin D receptor (VDR), type I collagen (COL1A1), and lactase (LCT) genes and severe postmenopausal osteoporosis as well as bone mineral density (BMD).
Material and Methods.
A total of 54 women with severe postmenopausal osteoporosis and 77 controls (mean age, 58.3 years [SD, 6.2] and 56.7 years [SD, 7.42], respectively) were included into the study. The subjects were recruited at the City Center for Osteoporosis Prevention (Minsk, Belarus). Dual-energy x-ray absorptiometry was used to measure bone mineral density at the lumbar spine and the femoral neck. Severe osteoporosis was diagnosed in the women with the clinical diagnosis of postmenopausal osteoporosis and at least 1 fragility fracture. The control group included women without osteoporosis. Polymorphic sites in osteoporosis predisposition genes (ApaI, BsmI, TaqI, and Cdx2 of the VDR gene, G2046T of the COL1A1 gene, and T-13910C of the LCT gene) were determined using the polymerase chain reaction on the deoxyribonucleic acid isolated from dried bloodspots.
Results
. The data showed that the ApaI and BsmI polymorphisms of the VDR gene and T- 13910C of the LCT gene were associated with severe postmenopausal osteoporosis in the analyzed Belarusian women (P<0.01). A statistically significant positive correlation between the VDR risk genotypes ApaI and TaqI and bone mineral density was found (P<0.05).
Conclusions
. The findings of this study suggest that at least the ApaI and BsmI polymorphisms of the VDR gene and T-13910C of the LCT gene are associated with the risk of postmenopausal osteoporosis in our sample of the Belarusian women.
Keywords: bone mineral density; genes; polymorphisms; osteoporosis bone mineral density; genes; polymorphisms; osteoporosis

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MDPI and ACS Style

Marozik, P.; Mosse, I.; Alekna, V.; Rudenko, E.; Tamulaitienė, M.; Ramanau, H.; Strazdienė, V.; Samokhovec, V.; Ameliyanovich, M.; Byshnev, N.; et al. Association Between Polymorphisms of VDR, COL1A1, and LCT Genes and Bone Mineral Density in Belarusian Women With Severe Postmenopausal Osteoporosis. Medicina 2013, 49, 28. https://doi.org/10.3390/medicina49040028

AMA Style

Marozik P, Mosse I, Alekna V, Rudenko E, Tamulaitienė M, Ramanau H, Strazdienė V, Samokhovec V, Ameliyanovich M, Byshnev N, et al. Association Between Polymorphisms of VDR, COL1A1, and LCT Genes and Bone Mineral Density in Belarusian Women With Severe Postmenopausal Osteoporosis. Medicina. 2013; 49(4):28. https://doi.org/10.3390/medicina49040028

Chicago/Turabian Style

Marozik, Pavel, Irma Mosse, Vidmantas Alekna, Ema Rudenko, Marija Tamulaitienė, Heorhi Ramanau, Vaidilė Strazdienė, Volha Samokhovec, Maxim Ameliyanovich, Nikita Byshnev, and et al. 2013. "Association Between Polymorphisms of VDR, COL1A1, and LCT Genes and Bone Mineral Density in Belarusian Women With Severe Postmenopausal Osteoporosis" Medicina 49, no. 4: 28. https://doi.org/10.3390/medicina49040028

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