Literature DB >> 10367040

Polymorphism of the vitamin D receptor gene and corticosteroid-related osteoporosis.

Y V Ho1, E M Briganti, Y Duan, R Buchanan, S Hall, E Seeman.   

Abstract

Corticosteroid therapy (CST) is associated with reduced intestinal calcium absorption, bone loss and increased fracture risk. As polymorphisms of the vitamin D receptor (VDR) gene may be associated with bone mineral density (BMD) and intestinal calcium absorption, we asked whether patients with a given VDR genotype receiving CST may be at increased or decreased risk for corticosteroid-related bone loss and osteoporosis. We measured areal BMD (g/cm2) by dual-energy X-ray absorptiometry in 193 women (50 premenopausal, 143 postmenopausal) and 70 men with rheumatoid arthritis (n = 44), obstructive airway diseases (n = 128) and other corticosteroid-treated diseases (n = 91). All patients received a cumulative dose greater than 1.8 g per year or a minimum of 5 mg daily of prednisolone or equivalent for at least 1 year. VDR alleles were typed by polymerase chain reaction assay based on the polymorphic BsmI and TaqI restriction sites. BMD in patients was expressed as a Z-score (mean +/- SEM) derived from age- and gender-matched controls. BMD was reduced in patients at the lumbar spine (bb, -0.52 +/- 0.12; Bb, -0.47 +/- 0.11; BB, -0.65 +/- 0.18 SD; p < 0.01), femoral neck (bb, -0.46 +/- 0.10; Bb, -0.34 +/- 0.10; BB, -0.54 +/- 0.14 SD; p < 0.01), Ward's triangle (bb, -0.44 +/- 0.10; Bb, -0.31 +/- 0.10; BB, -0.45 +/- 0.13 SD; p < 0.01), and trochanter (bb, -0.50 +/- 0.10; Bb, -0.30 +/- 0.10; BB, -0.44 +/- 0.14 SD; p < 0.01). However, there was no significant difference in the deficit in BMD in any of the genotypes, either before or after adjusting for age, sex, body mass index, disease type, age at onset of disease, disease duration, cumulative steroid dosage, smoking status and dietary calcium intake. Similarly, there were no detectable differences between the BsmI genotypes and the rate of bone loss in 79 patients with repeated BMD measurements at an interval of 4-48 months. The data suggest that the VDR genotypes may not be a means of identifying patients at greater risk of corticosteroid-related bone loss.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10367040     DOI: 10.1007/s001980050126

Source DB:  PubMed          Journal:  Osteoporos Int        ISSN: 0937-941X            Impact factor:   4.507


  6 in total

Review 1.  Bone involvement in exogenous hypercortisolism.

Authors:  L Sinigaglia; D Mazzocchi; M Varenna
Journal:  J Endocrinol Invest       Date:  2008-04       Impact factor: 4.256

2.  Relationship between glucocorticoid-induced osteoporosis and vitamin D receptor genotypes.

Authors:  Yuming Li; Lin Xu; Lingxun Shen; Likai Yu; Lulu Chen
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2002

3.  Vitamin D receptor gene polymorphism in rheumatoid arthritis and associated osteoporosis.

Authors:  Péter Rass; Angéla Pákozdi; Péter Lakatos; Erika Zilahi; Sándor Sipka; Gyula Szegedi; Zoltán Szekanecz
Journal:  Rheumatol Int       Date:  2006-01-31       Impact factor: 2.631

4.  Pharmacogenetic risk factors for altered bone mineral density and body composition in pediatric acute lymphoblastic leukemia.

Authors:  Mariël L te Winkel; Robert D van Beek; Sabine M P F de Muinck Keizer-Schrama; André G Uitterlinden; Wim C J Hop; Rob Pieters; Marry M van den Heuvel-Eibrink
Journal:  Haematologica       Date:  2009-12-16       Impact factor: 9.941

5.  Association of interleukin-6 promoter variant with bone mineral density in pre-menopausal women.

Authors:  Hye Won Chung; Jeong-Sun Seo; Sung Eun Hur; Hyung Lae Kim; Jun Yeon Kim; Ji Hyun Jung; Lyoung Hyo Kim; Byung Lae Park; Hyoung Doo Shin
Journal:  J Hum Genet       Date:  2003-04-18       Impact factor: 3.172

6.  Do the COL1A1 and Taq 1 vitamin D receptor polymorphisms have a role in identifying individuals at risk of developing osteoporosis?

Authors:  E McClean; G P R Archbold; H McA Taggart
Journal:  Ulster Med J       Date:  2003-05
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.