Optimal dual calcium and cholecalciderol dosages for osteoporotic fracture risk patients

Khaled Mohammad, Juma Husain, Bani Hani1, Bani Hani, Sinan Ibrahim Alghamaz, Madher Ali, Mohammad Doumi, Rami Mohamad Salem, Aldarawshe, Suhib Fayiz, Naim Dawaghreh, Ahmed Mahmoud Mohammed, Ali Alboun, Kholoud Muhsen Al Quraan
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Abstract

Background: Vitamin D is crucial for musculoskeletal health, promoting calcium absorption, osteoid tissue mineralization, and muscle function. Insufficient levels can lead to bone dystrophy, muscle weakness, and osteoporotic fractures. Aims: This research investigates the correlation between bone mineral density and osteoporotic fracture risk, including positive and negative influences, and aims to determine the optimal vitamin D level. Methods: This retrospective observational study examined 206 Jordanian rehabilitation and rheumatology clinic patients from September to November 2021. The participants were post-menopausal women and men over 60. The Age-adjusted Charlson Co-Morbidity Index and Functionality Grade system was used to assess participants' co-morbidity burden and functionality. DEXA scans assessed participants' proximal femoral hip and anteroposterior spine. Participants were divided into two Vit D groups: those below 30 ng/ml and those above 30. Results were compared using a Chi Square test. The study examined correlations, total variations, and Vit D prediction quality using logistic regression analyses. SPSS 23.0 was used for statistical analysis with a 5% significance level. Results: A binary logistic regression model was employed to simulate the correlation between the vitamin D levels of patients and their bone mineral density. The model indicated a 61.39% likelihood of having a fH_BMD (femoral head bone mineral density) equal to or greater than 0.755 g/cm2 when the vitamin D level is at its optimal value of 27.25 ng/ml. The model indicated a 27.25% likelihood of a fHOPF risk-free tool with a value of ≥3% when the optimal vitamin D level is 27.25 ng/ml. The model indicated a 17.74% likelihood of experiencing a significant osteoporotic fracture within the next 10 years. Conclusion: The findings of our study demonstrated a direct correlation between elevated levels of vitamin D and improved bone mineral quality indices that were examined. The serum 25-OH Cholecalciferol levels are more likely to have a beneficial effect on bone health status.
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骨质疏松性骨折风险患者的最佳钙和胆碱酯酶双重剂量
背景:维生素 D 对肌肉骨骼健康至关重要,可促进钙吸收、骨组织矿化和肌肉功能。维生素 D 含量不足会导致骨质疏松、肌肉无力和骨质疏松性骨折。目的:本研究调查了骨矿物质密度与骨质疏松性骨折风险之间的相关性,包括正面和负面影响,并旨在确定最佳维生素 D 水平。研究方法这项回顾性观察研究对 2021 年 9 月至 11 月期间的 206 名约旦康复和风湿病诊所患者进行了调查。参与者为绝经后女性和 60 岁以上男性。研究采用年龄调整后的夏尔森共病指数和功能分级系统来评估参与者的共病负担和功能。DEXA 扫描评估了参与者的股骨近端髋关节和前胸脊柱。参与者被分为两个维生素 D 组:低于 30 纳克/毫升和高于 30 纳克/毫升。研究结果通过 Chi Square 检验进行比较。研究采用逻辑回归分析法对相关性、总变化和 Vit D 预测质量进行了检验。统计分析采用 SPSS 23.0,显著性水平为 5%。结果采用二元逻辑回归模型模拟患者维生素 D 水平与其骨矿物质密度之间的相关性。模型显示,当维生素 D 水平达到 27.25 纳克/毫升的最佳值时,fH_BMD(股骨头骨矿密度)大于或等于 0.755 克/平方厘米的可能性为 61.39%。该模型显示,当维生素 D 的最佳水平为 27.25 纳克/毫升时,fHOPF 无风险工具值≥3% 的可能性为 27.25%。模型显示,在未来 10 年内发生重大骨质疏松性骨折的可能性为 17.74%。结论我们的研究结果表明,维生素 D 水平的升高与骨矿物质质量指标的改善直接相关。血清 25-OH 胆钙化醇水平更有可能对骨骼健康状况产生有益影响。
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