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2008 | 55 | 2 | 371-380
Article title

Association analysis of vitamin D receptor gene polymorphisms with bone mineral density in young women with Graves' disease

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Abstracts
EN
Graves' (GD) hyperthyroidism induces accelerated bone turnover that leads to decreased bone mineral density (BMD). The role of the VDR gene in predisposition to primary osteoporosis has been recognized. Recent studies show associations between the VDR gene polymorphisms and susceptibility to autoimmune diseases. Here we analyzed if VDR gene polymorphisms: BsmI, ApaI, TaqI, and FokI may predispose women with Graves' hyperthyroidism to BMD reduction or to disease development. The subjects were 75 premenopausal female Polish patients with GD and 163 healthy women. The genotyping was performed by the use of the restriction fragment length polymorphism analysis (RFLP). We studied the association of the VDR polymorphisms and their haplotypes with patients' BMD and also SNPs and haplotypes association with Graves' disease. We found a strong linkage disequilibrium for the BsmI, ApaI, and TaqI polymorphims that formed three most frequent haplotypes in Graves' women: baT (47.9%), BAt (34.9%), and bAT (16.4%). We did not show statistically significant association of analyzed VDR polymorphisms or haplotypes with decreased bone mineral density in Graves' patients. However, the presence of F allele had a weak tendency to be associated with Graves' disease (with OR=1.93; 95% CI: 0.97-3.84; p=0.058). In conclusion: VDR gene polymorphisms do not predict the risk of decreased BMD in Polish women with Graves'. It may be speculated that the F allele carriers of the VDR-FokI polymorphism are predisposed to Graves' disease development.
Publisher

Year
Volume
55
Issue
2
Pages
371-380
Physical description
Dates
published
2008
received
2007-09-14
revised
2008-04-09
accepted
2008-04-23
(unknown)
2008-05-26
Contributors
  • Department of Family Medicine, Poznan University of Medical Sciences, Poznań, Poland
  • Department of Family Medicine, Poznan University of Medical Sciences, Poznań, Poland
  • Department of Family Medicine, Poznan University of Medical Sciences, Poznań, Poland
  • Institute of Human Genetics, Polish Academy of Sciences, Poznań, Poland
  • Endocrinology Outpatient Clinic of Juraszow Hospital, Poznań, Poland
  • Department of Biochemistry and Biotechnology, Poznan University of Agriculture, Poznań, Poland
References
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Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.bwnjournal-article-abpv55p371kz
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