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Clinical Reviews in Bone and Mineral Metabolism最新文献

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Effect of Oxidative Stress on Bone Remodeling in Periprosthetic Osteolysis 氧化应激对假体周围骨溶解骨重建的影响
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-03 DOI: 10.1007/s12018-021-09278-7
E. Galliera, L. Massaccesi, G. Banfi, E. De Vecchi, V. Ragone, M. C. Corsi Romanelli
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引用次数: 4
Making Sense of the Highly Variable Effects of Alcohol on Bone 理解酒精对骨骼的高度可变影响
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-07-31 DOI: 10.1007/s12018-021-09277-8
R. Turner, Lara H. Sattgast, Vanessa A. Jimenez, K. Grant, U. Iwaniec
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引用次数: 1
Insights into the Perspective Correlation Between Vitamin D and Regulation of Hormones: Thyroid and Parathyroid Hormones 透视维生素D与激素调节的相关性:甲状腺和甲状旁腺激素
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-12-01 DOI: 10.1007/s12018-021-09279-6
M. Abed, F. Alassaf, M. Qazzaz, M. Alfahad, Mahmood H. M. Jasim
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引用次数: 1
Adipokines and Chronic Rheumatic Diseases: from Inflammation to Bone Involvement 脂肪因子与慢性风湿病:从炎症到骨受累
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-12-01 DOI: 10.1007/s12018-021-09275-w
D. Cici, A. Corrado, C. Rotondo, R. Colia, F. Cantatore
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引用次数: 3
Towards a Standard Approach to Assess Tibial Bone Loss Following Total Knee Arthroplasty 评估全膝关节置换术后胫骨骨丢失的标准方法
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-12-01 DOI: 10.1007/s12018-021-09276-9
T. Anijs, I. Kouwert, N. Verdonschot, D. Janssen
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引用次数: 2
Current and Emerging Therapies for Pediatric Bone Diseases 儿童骨病的当前和新兴治疗方法
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-08-15 DOI: 10.1007/s12018-020-09272-5
Supamit Ukarapong, Tossaporn Seeherunvong, G. Berkovitz
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引用次数: 3
Can Periodontal Disease Be Considered Linked to Obesity and Lipoinflammation? Mechanisms Involved in the Pathogenesis Occurrence 牙周病可以被认为与肥胖和炎症有关吗?发病机制
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-08-13 DOI: 10.1007/s12018-020-09273-4
V. Nicolin, F. Costantinides, Erica Vettori, F. Berton, G. Marchesi, R. Rizzo, R. Di Lenarda
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引用次数: 1
Periodontitis and Rheumatoid Arthritis: the Common Thread 牙周炎和类风湿关节炎:共同点
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-08-09 DOI: 10.1007/s12018-020-09271-6
Namrata S. Jajoo, Anup U. Shelke, R. Bajaj
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引用次数: 3
Type 2 Diabetes Mellitus and Osteoarthritis: the Role of Glucose Transporters 2型糖尿病和骨关节炎:葡萄糖转运蛋白的作用
IF 1.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-05-16 DOI: 10.1007/s12018-020-09270-7
Hadis Ashrafizadeh, Mohadeseh Ashrafizadeh, A. A. Oroojan
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引用次数: 4
Bone Metabolism in SARS-CoV-2 Disease: Possible Osteoimmunology and Gender Implications. SARS-CoV-2 疾病中的骨代谢:可能的骨免疫学和性别影响
IF 0.8 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2020-01-01 Epub Date: 2020-09-01 DOI: 10.1007/s12018-020-09274-3
Gianmaria Salvio, Claudio Gianfelice, Francesca Firmani, Stefano Lunetti, Giancarlo Balercia, Gilberta Giacchetti

Even though inflammatory conditions are known to exert adverse effects on bone metabolism, there are no published data regarding SARS-CoV-2 infection and subsequent fracture risk. We present a brief review of the molecular mechanisms linking inflammatory diseases to increased fracture risk/osteoporosis and of the therapeutic strategies that can prevent bone resorption in patients with inflammatory disease, focusing on the RANK-RANKL system. We also make some considerations on gender differences in infection response and on their implications for survival and for the consequences of COVID-19. Several inflammatory cytokines, especially IL-1, IL-6, and TNF-α, stimulate osteoclast activity, favoring bone resorption through the RANK-RANKL system. Data from the previous SARS-CoV outbreak suggest that the present disease also has the potential to act directly on bone resorption units, although confirmation is clearly needed. Even though the available data are limited, the RANK-RANKL system may provide the best therapeutic target to prevent bone resorption after COVID-19 disease. Vitamin D supplementation in case of deficiency could definitely be beneficial for bone metabolism, as well as for the immune system. Supplementation of vitamin D in case of deficiency could be further advantageous. In COVID-19 patients, it would be useful to measure the bone metabolism markers and vitamin D. Targeting the RANK-RANKL system should be a priority, and denosumab could represent a safe and effective choice. In the near future, every effort should be made to investigate the fracture risk after SARS-CoV-2 infection.

尽管众所周知炎症会对骨代谢产生不利影响,但目前还没有关于 SARS-CoV-2 感染和后续骨折风险的公开数据。我们简要回顾了炎症性疾病与骨折风险/骨质疏松症增加之间的分子机制,以及可以防止炎症性疾病患者骨吸收的治疗策略,重点是 RANK-RANKL 系统。我们还对感染反应的性别差异及其对生存和 COVID-19 后果的影响进行了一些思考。几种炎症细胞因子,尤其是 IL-1、IL-6 和 TNF-α,可刺激破骨细胞的活性,通过 RANK-RANKL 系统促进骨吸收。上一次 SARS-CoV 爆发的数据表明,目前的疾病也有可能直接作用于骨吸收单位,但显然还需要证实。尽管现有数据有限,但 RANK-RANKL 系统可能是预防 COVID-19 疾病后骨吸收的最佳治疗目标。在缺乏维生素 D 的情况下补充维生素 D 肯定对骨代谢和免疫系统有益。在缺乏维生素 D 的情况下补充维生素 D 可能更有好处。针对 RANK-RANKL 系统的治疗应优先考虑,而地诺单抗可能是一种安全有效的选择。在不久的将来,应尽一切努力研究 SARS-CoV-2 感染后的骨折风险。
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引用次数: 0
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Clinical Reviews in Bone and Mineral Metabolism
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