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感染艾滋病毒/艾滋病者的骨骼健康:现状与未来潜在策略的最新情况

Bone Health in People Living with HIV/AIDS: An Update of Where We Are and Potential Future Strategies.

作者信息

Ahmed Musaab, Mital Dushyant, Abubaker Nuha Eljaili, Panourgia Maria, Owles Henry, Papadaki Ioanna, Ahmed Mohamed H

机构信息

College of Medicine, Ajman University, Ajman P.O. Box 346, United Arab Emirates.

Center of Medical and Bio-Allied Health Sciences Research, Ajman University, Ajman P.O. Box 346, United Arab Emirates.

出版信息

Microorganisms. 2023 Mar 19;11(3):789. doi: 10.3390/microorganisms11030789.

Abstract

The developments in Human Immunodeficiency Virus (HIV) treatment and in the care of people living with HIV (PLWHIV) and Acquired Immunodeficiency Syndrome (AIDS) over the last three decades has led to a significant increase in life expectancy, on par with HIV-negative individuals. Aside from the fact that bone fractures tend to occur 10 years earlier than in HIV-negative individuals, HIV is, per se, an independent risk factor for bone fractures. A few available antiretroviral therapies (ARVs) are also linked with osteoporosis, particularly those involving tenofovir disoproxil fumarate (TDF). HIV and hepatitis C (HCV) coinfection is associated with a greater risk of osteoporosis and fracture than HIV monoinfection. Both the Fracture Risk Assessment Tool (FRAX) and measurement of bone mineral density (BMD) via a DEXA scan are routinely used in the assessment of fracture risk in individuals living with HIV, as bone loss is thought to start between the ages of 40 and 50 years old. The main treatment for established osteoporosis involves bisphosphonates. Supplementation with calcium and vitamin D is part of clinical practice of most HIV centers globally. Further research is needed to assess (i) the cut-off age for assessment of osteoporosis, (ii) the utility of anti-osteoporotic agents in PLWHIV and (iii) how concomitant viral infections and COVID-19 in PLWHIV can increase risk of osteoporosis.

摘要

在过去三十年中,人类免疫缺陷病毒(HIV)治疗以及HIV感染者(PLWHIV)和获得性免疫缺陷综合征(AIDS)护理方面的进展,使预期寿命显著提高,与HIV阴性个体相当。除了骨折往往比HIV阴性个体早10年发生这一事实外,HIV本身就是骨折的一个独立危险因素。一些可用的抗逆转录病毒疗法(ARV)也与骨质疏松症有关,特别是那些涉及富马酸替诺福韦二吡呋酯(TDF)的疗法。与单纯HIV感染相比,HIV与丙型肝炎病毒(HCV)合并感染会增加患骨质疏松症和骨折的风险。骨折风险评估工具(FRAX)和通过双能X线吸收法(DEXA)扫描测量骨矿物质密度(BMD),在评估HIV感染者的骨折风险时经常使用,因为骨质流失被认为在40至50岁之间开始。已确诊骨质疏松症的主要治疗方法包括使用双膦酸盐。补充钙和维生素D是全球大多数HIV治疗中心临床实践的一部分。需要进一步研究来评估:(i)评估骨质疏松症的临界年龄;(ii)抗骨质疏松药物在HIV感染者中的效用;(iii)HIV感染者中合并的病毒感染和COVID-19如何增加骨质疏松症的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3612/10052733/e4fefdbe17f7/microorganisms-11-00789-g001.jpg

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