The Interplay of HIV and Long COVID in Sub-Saharan Africa: Mechanisms of Endothelial Dysfunction.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-09-01 Epub Date: 2024-07-03 DOI:10.1007/s11886-024-02087-6
Theresa Chikopela, Naome Mwesigwa, Sepiso K Masenga, Annet Kirabo, Cyndya A Shibao
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Abstract

Purpose of review: Long COVID affects approximately 5 million people in Africa. This disease is characterized by persistent symptoms or new onset of symptoms after an acute SARS-CoV-2 infection. Specifically, the most common symptoms include a range of cardiovascular problems such as chest pain, orthostatic intolerance, tachycardia, syncope, and uncontrolled hypertension. Importantly, these conditions appear to have endothelial dysfunction as the common denominator, which is often due to impaired nitric oxide (NO) mechanisms. This review discusses the role of mechanisms contributing to endothelial dysfunction in Long COVID, particularly in people living with HIV.

Recent findings: Recent studies have reported that increased inflammation and oxidative stress, frequently observed in Long COVID, may contribute to NO dysfunction, ultimately leading to decreased vascular reactivity. These mechanisms have also been reported in people living with HIV. In regions like Africa, where HIV infection is still a major public health challenge with a prevalence of approximately 26 million people in 2022. Specifically, endothelial dysfunction has been reported as a major mechanism that appears to contribute to cardiovascular diseases and the intersection with Long COVID mechanisms is of particular concern. Further, it is well established that this population is more likely to develop Long COVID following infection with SARS-CoV-2. Therefore, concomitant infection with SARS-CoV-2 may lead to accelerated cardiovascular disease. We outline the details of the worsening health problems caused by Long COVID, which exacerbate pre-existing conditions such as endothelial dysfunction. The overlapping mechanisms of HIV and SARS-CoV-2, particularly the prolonged inflammatory response and chronic hypoxia, may increase susceptibility to Long COVID. Addressing these overlapping health issues is critical as it provides clinical entry points for interventions that could improve and enhance outcomes and quality of life for those affected by both HIV and Long COVID in the region.

Abstract Image

撒哈拉以南非洲地区艾滋病病毒与长 COVID 的相互作用:内皮功能障碍的机制。
审查目的:长期 COVID 影响着非洲约 500 万人。这种疾病的特点是急性 SARS-CoV-2 感染后症状持续存在或新出现症状。具体而言,最常见的症状包括一系列心血管问题,如胸痛、正压性不耐受、心动过速、晕厥和无法控制的高血压。重要的是,这些症状的共同点似乎是内皮功能障碍,而内皮功能障碍往往是一氧化氮(NO)机制受损所致。本综述将讨论导致内皮功能障碍的机制在长 COVID 中的作用,尤其是在艾滋病毒感染者中的作用:最近的研究报告称,在 Long COVID 中经常观察到的炎症和氧化应激的增加可能会导致一氧化氮功能障碍,最终导致血管反应性降低。这些机制在艾滋病毒感染者中也有报道。在非洲等地区,艾滋病毒感染仍是一项重大的公共卫生挑战,2022 年的感染率约为 2600 万。具体而言,据报道,内皮功能障碍是导致心血管疾病的一个主要机制,与长 COVID 机制的交叉尤其令人担忧。此外,已经明确的是,这类人群在感染 SARS-CoV-2 后更有可能患上长 COVID。因此,同时感染 SARS-CoV-2 可能会加速心血管疾病的发生。我们概述了长COVID导致的健康问题恶化的详细情况,它加剧了原有的疾病,如内皮功能障碍。艾滋病毒和 SARS-CoV-2 的重叠机制,特别是长期炎症反应和慢性缺氧,可能会增加对 Long COVID 的易感性。解决这些重叠的健康问题至关重要,因为它为干预措施提供了临床切入点,可以改善和提高该地区同时受艾滋病毒和长COVID影响的人的治疗效果和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.20
自引率
4.30%
发文量
567
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