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HIV co-morbidity and ageing

机译:艾滋病毒合并症和老龄化

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摘要

As treatment for HIV infection needs to be used continuously and lifelong, issues concerning long-term outcomes, including those involving tolerability and safety of treatment, are gaining increasing importance. Although current combination antiretroviral therapy (cART) regimens are generally better tolerated than those in the early days of cART, treatment toxicity remains an important cause for discontinuation of (components) of treatment. Moreover, several of the potential toxicities of cART (including cardiovascular, metabolic, renal and bone toxicity) overlap with known ageing-associated co-morbidities. Given that our patient population with HIV is increasingly getting older as a result of the success of cART in reducing traditional HIV-associated morbidity and mortality, these co-morbidities are increasingly being seen and importantly influence patient management. Moreover, persons with HIV, in spite of having suppressed viraemia on cART seem to be at increased risk of the premature development of age-associated non-communicable co-morbidities, including cardiovascular, chronic kidney, liver and pulmonary disease, diabetes mellitus, osteoporosis, non-AIDS associated malignancies, and neurocognitive impairment. It has therefore been hypothesised that such individuals, despite effective cART, may be prone to accelerated ageing. The underlying pathogenesis is likely to be multifactorial and, apart from include sustained immune activation, both systemically and within the central nervous system. The presentation will review the current state of knowledge and investigation in this area.
机译:由于艾滋病毒感染的治疗需要持续不断地终身使用,因此涉及长期结果的问题,包括涉及治疗的耐受性和安全性的问题,变得越来越重要。尽管目前的抗逆转录病毒联合疗法(cART)方案通常比cART早期耐受性更好,但是治疗毒性仍然是中止治疗(成分)的重要原因。此外,cART的几种潜在毒性(包括心血管,代谢,肾脏和骨骼毒性)与已知的衰老相关合并症重叠。鉴于由于cART成功降低了与HIV相关的传统发病率和死亡率,我们的HIV感染者人口正日益老龄化,因此越来越多地发现这些合并症,并且对患者管理产生了重要影响。此外,尽管在cART上抑制了病毒血症,但艾滋病毒感染者似乎处于与年龄相关的非传染性合并症过早发展的风险中,这些合并症包括心血管疾病,慢性肾脏,肝脏和肺部疾病,糖尿病,骨质疏松症,非艾滋病相关的恶性肿瘤和神经认知障碍。因此,有假设认为,尽管有有效的cART,这类个体仍可能会加速衰老。潜在的发病机制可能是多因素的,除了全身和中枢神经系统内的持续免疫活化外。该演讲将回顾该领域的知识和研究现状。

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