[Vitamin D Receptor Gene Polymorphisms in Female Adolescent Idiopathic Scoliosis Patients]
Overview
Affiliations
Objective: To investigate the association of vitamin D receptor (VDR) gene polymorphisms with abnormal growth pattern and low bone mass in adolescent idiopathic scoliosis (AIS) patients.
Methods: Peripheral blood samples were obtained from 164 female patients with AIS, aged 14.4 +/- 2 (9 - 20), and 122 age-matched healthy girls. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used to detect the VDR gene distributions.
Results: The frequency of Bb genotype was significantly higher in the AIS patients than in the controls (P < 0.01). The frequency of B alleles of the AIS patients was significantly higher than that of the controls (P < 0.01). In AIS patients, the expression rate of Aa genotype of the AIS patients with the body mass index (BMI) > or = 18 kg/m(2) was significantly higher than those with the BMI < 18 kg/m(2) (P < 0.05), and the expression rate of Bb genotype of the AIS patients with the BMI < 18 kg/m(2) and arm span < 160 cm was significantly higher than that of the AIS patients with the BMI > or = 18 kg/m(2) and arm span > or = 160 cm (P < 0.05).
Conclusion: The BsmI site polymorphism of vitamin D receptor gene may be associated with abnormal growth pattern and low bone mass in girls with AIS.
Prevalence of 25-OH-Vitamin D and Calcium Deficiency in Adolescent Idiopathic Scoliosis.
Herdea A, Charkaoui A, Ulici A J Med Life. 2020; 13(2):260-264.
PMID: 32728404 PMC: 7378343. DOI: 10.25122/jml-2020-0101.
Tuncel G, Temel S, Ergoren M Mol Biol Rep. 2019; 46(3):3349-3355.
PMID: 30977086 DOI: 10.1007/s11033-019-04796-6.
Dai J, Lv Z, Huang J, Cheng P, Fang H, Chen A Eur Spine J. 2018; 27(9):2175-2183.
PMID: 29728923 DOI: 10.1007/s00586-018-5614-0.
Yin X, Wang H, Guo J, Zhang L, Zhang Y, Li L Medicine (Baltimore). 2018; 97(2):e9627.
PMID: 29480871 PMC: 5943872. DOI: 10.1097/MD.0000000000009627.
Noshchenko A, Hoffecker L, Lindley E, Burger E, Cain C, Patel V World J Orthop. 2015; 6(7):537-58.
PMID: 26301183 PMC: 4539477. DOI: 10.5312/wjo.v6.i7.537.