Associations of polymorphisms in the vitamin D receptor gene (BsmI and FokI) with bone mineral density in postmenopausal women in Malta
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作者:
C. Vidal
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机构:University of Malta Medical School,Department of Pathology
C. Vidal
C. Grima
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机构:University of Malta Medical School,Department of Pathology
C. Grima
M. Brincat
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机构:University of Malta Medical School,Department of Pathology
M. Brincat
N. Megally
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机构:University of Malta Medical School,Department of Pathology
N. Megally
A. Xuereb-Anastasi
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机构:University of Malta Medical School,Department of Pathology
A. Xuereb-Anastasi
机构:
[1] University of Malta Medical School,Department of Pathology
[2] St Luke’s Hospital,Department of Obstetrics and Gynaecology
[3] University of Malta,Institute of Health Care
来源:
Osteoporosis International
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2003年
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14卷
关键词:
Bone mineral density;
Maltese;
Osteoporosis;
Postmenopausal women;
VDR gene polymorphisms;
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摘要:
Previous studies have suggested that variations in the vitamin D receptor (VDR) gene are related to bone mineral density (BMD). In this study, the T→C transition in the start codon and the G→A polymorphism at the 3′ end of the VDR gene, identified by endonucleases FokI and BsmI, respectively, were analysed and correlated with BMD in postmenopausal Maltese women (n=104). Genotype frequencies observed for the VDR start codon polymorphism (SCP) were CC: 60.4%; CT: 30.7% and TT: 8.9%, while those observed for the 3′ in this study were GG: 16.4%; GA: 51.9%; AA: 31.7%. In postmenopausal women, both lumbar and femoral BMD were observed to be highest in CC homozygotes for the FokI genotype and in GG homozygotes for the BsmI genotype, although in both groups the difference between the genotypes was not statistically significant, even after adjusting BMD for age, BMI and years since menopause. No evidence of linkage disequilibrium between the two alleles was observed.
机构:
Tunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Mongi Slim Hosp, Dept Rheumatol, La Marsa, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Karray, Emna Fakhfakh
Ben Dhifallah, Imen
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Tunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Ben Dhifallah, Imen
Ben Abdelghani, Kawther
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机构:
Mongi Slim Hosp, Dept Rheumatol, La Marsa, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Ben Abdelghani, Kawther
Ben Ghorbel, Imed
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机构:
La Rabta Hosp, Dept Internal Med, Tunis, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Ben Ghorbel, Imed
Khanfir, Monia
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机构:
La Rabta Hosp, Dept Internal Med, Tunis, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Khanfir, Monia
Houman, Habib
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La Rabta Hosp, Dept Internal Med, Tunis, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Houman, Habib
Hamzaoui, Kamel
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Tunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia
Hamzaoui, Kamel
Zakraoui, Leith
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机构:
Mongi Slim Hosp, Dept Rheumatol, La Marsa, TunisiaTunis El Manar Univ, Sch Med, Homeostasis & Cell Dysfunct Unit Res UR 99 08 40, Tunis, Tunisia