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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 2 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-01-01 Epub Date: 2021-07-31 DOI: 10.1007/s12018-021-09277-8
Russell T Turner, Lara H Sattgast, Vanessa A Jimenez, Kathleen A Grant, Urszula T Iwaniec

Alcohol consumption is often reported to influence bone health in a dose-dependent manner where moderate alcohol intake is deemed beneficial and heavy drinking detrimental. However, this relationship may not be valid for individual alcohol consumers, as small quantities of alcohol can have detrimental skeletal effects and not all studies report clinically relevant bone loss with long-duration alcohol abuse. These discrepant findings suggest that factors beyond quantity of alcohol consumed contribute to the observed skeletal response. We propose that the interplay between intrinsic (e.g., age, sex, skeletal site) and extrinsic (e.g., age of onset of drinking, duration of drinking, comorbidities) factors influence the precise impact of alcohol consumption on bone health. In this review, we summarize literature reporting the effects of alcohol on the human skeleton. Based on the finding that alcohol alters the circulating levels of dozens of peptides shown to influence bone metabolism, we arrive at the conclusion that no single unifying mechanism adequately explains the diversity of reports or successfully predicts individuals most likely to be impacted favorably or unfavorably by alcohol consumption. We propose that a more holistic approach - in which drinking pattern and intrinsic factors are accounted for - is required to better understand and respond to the end organ effects of alcohol on the skeleton.

饮酒常被报道以剂量依赖的方式影响骨骼健康,适度饮酒被认为是有益的,而大量饮酒被认为是有害的。然而,这种关系可能并不适用于个人饮酒者,因为少量的酒精会对骨骼产生有害影响,而且并非所有的研究都报告了长期酗酒与临床相关的骨质流失。这些差异的发现表明,除了酒精摄入量之外,还有其他因素导致了观察到的骨骼反应。我们认为,内在因素(如年龄、性别、骨骼部位)和外在因素(如开始饮酒的年龄、饮酒持续时间、合并症)之间的相互作用会影响饮酒对骨骼健康的确切影响。在这篇综述中,我们总结了有关酒精对人体骨骼影响的文献报道。基于酒精会改变数十种影响骨代谢的多肽的循环水平这一发现,我们得出结论,没有单一的统一机制能够充分解释报告的多样性,也没有成功地预测最可能受到酒精消费有利或不利影响的个体。我们建议采用一种更全面的方法——将饮酒模式和内在因素考虑在内——以更好地理解和应对酒精对骨骼的最终器官影响。
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引用次数: 0
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
期刊
Clinical Reviews in Bone and Mineral Metabolism
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