Hammond Charles K, Kanzie Perpetual, Martyn-Dickens Charles, Ocran Edward Ebo
Department of Child Health, School of Medical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana; Department of Child Health, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
Department of Child Health, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
Semin Pediatr Neurol. 2025 Jul;54:101205. doi: 10.1016/j.spen.2025.101205. Epub 2025 Jun 19.
HIV affects both the central and peripheral nervous systems, resulting in a wide range of neurological complications due to direct viral effects, chronic inflammation, opportunistic infections, and adverse effects of antiretroviral therapy (ART), collectively referred to as neuroAIDS. In children, the underdeveloped blood-brain barrier heightens the vulnerability of the brain to neuroAIDS, impacting cognitive and motor development. Even HIV-exposed, uninfected children exhibit neurodevelopmental delays. Chronic infection leads to a sustained viral presence in the cerebrospinal fluid, resulting in neuroinflammation. HIV encephalopathy (HIVE) remains a major concern, causing developmental regression, cognitive impairment, and motor dysfunction. Although the prevalence of HIVE has declined with the advent of combination antiretroviral therapy, rates remain high in low-resource settings. Opportunistic infections such as tuberculous meningitis, viral encephalitis, and fungal infections are prevalent among children with HIV-AIDS. Children with HIV are also at risk for cerebrovascular diseases, neurocognitive impairments, and neuropsychiatric conditions such as mood disorders and high-risk behaviors. Epilepsy and peripheral neuropathy are more common in children with HIV, with ART regimens sometimes contributing to neuropathy. Early ART initiation remains crucial in improving neurodevelopmental outcomes. Careful drug selection and adequate treatment of opportunistic infections before ART initiation are important to prevent drug-drug interactions and immune reconstitution inflammatory syndrome, respectively. While treatment progress has improved neurological outcomes, disparities in access to healthcare continue to impact children in resource-limited settings.
人类免疫缺陷病毒(HIV)会影响中枢神经系统和周围神经系统,由于病毒的直接作用、慢性炎症、机会性感染以及抗逆转录病毒疗法(ART)的不良反应,导致一系列神经并发症,统称为神经艾滋病(neuroAIDS)。在儿童中,发育不完善的血脑屏障会增加大脑对神经艾滋病的易感性,影响认知和运动发育。即使是暴露于HIV但未感染的儿童也会出现神经发育迟缓。慢性感染会导致脑脊液中持续存在病毒,从而引发神经炎症。HIV脑病(HIVE)仍然是一个主要问题,会导致发育倒退、认知障碍和运动功能障碍。尽管随着联合抗逆转录病毒疗法的出现,HIVE的患病率有所下降,但在资源匮乏地区,其发病率仍然很高。机会性感染,如结核性脑膜炎、病毒性脑炎和真菌感染,在患有HIV艾滋病的儿童中很常见。感染HIV的儿童也有患脑血管疾病、神经认知障碍以及神经精神疾病(如情绪障碍和高危行为)的风险。癫痫和周围神经病变在感染HIV的儿童中更为常见,ART方案有时会导致神经病变。尽早开始ART对于改善神经发育结局仍然至关重要。在开始ART之前,仔细选择药物并充分治疗机会性感染,分别对于预防药物相互作用和免疫重建炎症综合征很重要。虽然治疗进展改善了神经学结局,但在资源有限的环境中,获得医疗保健的差距继续影响着儿童。