首页> 外文期刊>Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA >Diagnosis, prevention, and treatment of bone fragility in people living with HIV: a position statement from the Swiss Association against Osteoporosis
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Diagnosis, prevention, and treatment of bone fragility in people living with HIV: a position statement from the Swiss Association against Osteoporosis

机译:艾滋病毒患者中骨脆性的诊断,预防和治疗:瑞士骨质疏松症协会的立场声明

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摘要

Life expectancy of people living with HIV (PLWH) is reaching similar length as in the general population. Accordingly, age-related comorbidities, including osteoporosis, are increasing. Fracture risk is higher and increases approximately 10years earlier in PLWH. Classical risk factors of bone fragility are highly prevalent in PLWH but factors specific for HIV infection itself and the type of antiretroviral therapy (ART) (triple combination antiretroviral therapy) regimen (especially tenofovir and protease inhibitors) also contribute to bone loss. The majority of bone loss occurs during virus activity and at initiation of ART (immune reconstitution) and is associated with an increase of bone resorption (upregulation RANKL). Recent data indicate that calcium and vitamin D supplements as ART initiation lower BMD loss. The reduction of tenofovir plasma concentrations with tenofovir alafenamide attenuates BMD loss but it remains unknown whether it will contribute to reduce fracture risk. Hence, special considerations for the management of bone fragility in PLWH are warranted. Based on the current state of epidemiology and pathophysiology of osteoporosis in PLWH, we provide the consensus of the Swiss Association against Osteoporosis on best practice for diagnosis, prevention, and management of osteoporosis in this population. Periodic assessment of fracture risk is indicated in all HIV patients and general preventive measures should be implemented. All postmenopausal women, men above 50years of age, and patients with other clinical risk for fragility fractures qualify for BMD measurement. An algorithm clarifies when treatment with bisphosphonates and review of ART regimen in favour of more bone-friendly options are indicated.
机译:艾滋病毒(PLWH)的人们预期寿命与一般人群相似。因此,具有骨质疏松症,包括骨质疏松症的年龄相关的可变性,正在增加。骨折风险较高,PLWH早些时候增加了大约10年。骨质脆性的经典风险因素在PLWH中普遍普遍,但艾滋病毒感染本身的因素和抗逆转录病毒治疗(第三次组合抗逆转录病毒治疗)方案(特别是替诺福韦和蛋白酶抑制剂)也有助于骨质损失。在病毒活性期间和艺术的开始(免疫重建)期间发生大部分骨丢失,并且与骨吸收增加有关(上调RANKL)。最近的数据表明钙和维生素D补充剂作为艺术启动较低的BMD损失。用替诺福韦阿拉芬酰胺的替替洛韦血浆浓度降低衰减BMD损失,但仍然有助于降低骨折风险。因此,保证了PLWH中骨脆性管理的特殊考虑因素。基于PLWH骨质疏松症的流行病学和病理生理学的现状,我们提供瑞士骨质疏松症的综合协商症,以对该人群诊断,预防和管理骨质疏松症的最佳实践。所有HIV患者都表明了骨折风险的定期评估,并应实施一般预防措施。所有绝经后妇女,50年龄以上的男性,以及其他临床风险的疾病骨折患者有资格获得BMD测量。指出了一种算法阐明了用双膦酸盐治疗和艺术方案的治疗,有利于更有骨头友好的选择。

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