Vitamin D receptor gene polymorphism influence on lumbar intervertebral disc degeneration

福基 医学 塔奇 单核苷酸多态性 腰椎 骨化三醇受体 椎间盘 病理 基因分型 腰痛 基因多态性 基因型 解剖 内科学 多态性(计算机科学) 基因 受体 遗传学 生物 替代医学
作者
Przemysław A. Pękala,Małgorzata Jasińska,Dominik Taterra,Katelyn M. Skoczen,Agata Jarosz,Tomasz Konopka,Marios Loukas,Jerzy Walocha,Krzysztof A. Tomaszewski,Grzegorz Lis
出处
期刊:Clinical Anatomy [Wiley]
卷期号:35 (6): 738-744 被引量:3
标识
DOI:10.1002/ca.23877
摘要

Intervertebral disc (IVD) degeneration is a multifaceted pathology that is the main morphological cause of lower back pain. This study aimed to determine the link between the vitamin D receptor gene single nucleotide polymorphisms (SNPs) and degenerative processes of the lumbar spine. The complete lumbar spinal columns were collected from 100 Caucasian cadavers via ventral dissection. The specimens for the histological analysis were harvested from the L5/S1 IVDs and endplates. Then, the tissues were cut into slices, inserted into paraffin blocks, and stained. The histology was evaluated according to the Boos' protocol. Moreover, TaqI(rs731236), FokI(rs2228570), and ApaI(rs7975232) genotyping were performed. Lastly, the histological scores for different genotypes were analyzed. The overall Boos' score in the study group was 12.49. It consisted of a mean IVD score of 7.46 and endplate score of 5.39. The determination of the SNPs was successful in 99 specimens and had a distribution of all alleles in accordance with the Hardy-Weinberg equilibrium. No significant differences in overall histological degeneration scores were found between samples from donors with different genotypes. However, in subgroup analysis of specific regions on the IVD, the significant difference was found in posterior inner anulus fibrosus for ApaI. The results of this study suggest that one must be careful when interpreting the results of the clinical and/or radiological studies on vitamin D receptor gene polymorphisms and lumbar spine degeneration risk, because such a relationship, if present, is likely to be very subtle.
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