维生素D能减缓骨关节炎的进展吗

V. Ch, J. Prakash, Md. Tashfeen Ashraf, Varsha Gupta
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引用次数: 1

摘要

骨关节炎(OA)是一种慢性和普遍的关节疾病,导致软骨退行性变化。如今,维生素d作为一种具有广泛生物效应的重要成分正在崭露头角。这些研究正在评估维生素D对骨关节炎的有益作用,因此本研究计划分析i)选定对照和OA患者的维生素D水平,ii)监测CYP2R1, CYP3A4, CYP27B1, CYP24A1和CYP27A1的基因表达变化,这些基因的产物与维生素D代谢有关。我们的结果显示OA组与对照组的维生素d水平没有显著差异。对照组平均维生素D水平为35.9 ng/ml(3例维生素D<20g/ml), OA患者平均维生素D水平为35.66 ng/ml(3例维生素D<20ng/ml)。然而,与对照组相比,OA患者中CYP2R1、CYP3A4基因表达降低,CYP24A1、CYP27B1基因表达无变化,CYP27A1基因表达上调。我们没有观察到对照组和患者维生素D水平的显著差异,这表明原发性OA的发病可能不是由于维生素D缺乏,或者维生素D可能不是OA症状的原因。然而,它的补充可能对所有人都有治疗益处,包括对照组和患者,因为两者的维生素D水平都不是最佳的。细胞色素p450基因的低表达表明对OA患者有一定影响,但这些影响与年龄或绝经后阶段有关,因为在我们的研究中,我们无法获得年龄小于55岁且无任何合病的原发性OA患者,因此尚不清楚。55岁以下的OA多伴有糖尿病、高血压、甲状腺、肥胖、慢性胃肠疾病、肾脏或肝脏疾病、创伤等合并症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can Vitamin D Slow Progression of Osteoarthritis
Osteoarthritis (OA) is a chronic and prevalent joint disease resulting in degenerative changes in the cartilage. Now-a-days vitamin-D is emerging as an important component which has a wide biological effects. The studies are evaluating the beneficial effects of vitamin-D in osteoarthritis therefore the present investigation was planned to analyze i) levels of vitamin-D in selected controls and OA patients, ii) monitor gene expression changes in CYP2R1, CYP3A4, CYP27B1, CYP24A1 and CYP27A1, whose products are involved in vitamin D metabolism. Our result shows that there was no significant difference in the vitamin-D levels in OA versus controls. The mean vitamin D levels in controls was 35.9 ng/ml (3 had ViD<20g/ml) and in OA patients was 35.66 ng/ml (3 had Vit D<20ng/ml). However gene expression of CYP2R1, CYP3A4 was reduced CYP24A1, CYP27B1 showed no variation in expression and CYP27A1 was upregulated in OA patients as compared to control. We could not observe significant difference in the levels of vitamin D in control and patient showing that onset of primary OA may not be because of vitamin D deficiency or vitamin D may not be responsible for symptoms of OA. However its supplementation may have therapeutic benefits to all including control and patients as vitamin D levels are not optimum in both. Lower gene expression of cytochrome p 450 genes suggest some effects on OA patients but these are related to age or post-menopausal stage or OA is not clear as in our study we were unable to obtain primary OA patients without any comorbidity with <55 years of age. OA in less than 55 years are mostly associated with comorbid conditions as diabetes, hypertention, thyroid, obesity, chronic gastrointestinal disturbance, kidney or liver disease, with trauma etc.
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