Siqueira-E-Silva Beatriz Nogueira, de Sousa Luciana Pereira, Rosa-Gonçalves Pamela, da Silva Rízia Maria, Martins Yuri Chaves, Brasil Patrícia, Daniel-Ribeiro Cláudio Tadeu
Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Pesquisa em Malária, Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio Grande do Norte, Centro de Biociências, Departamento de Microbiologia e Parasitologia, Natal, RN, Brasil.
Mem Inst Oswaldo Cruz. 2025 Feb 3;120:e240223. doi: 10.1590/0074-02760240223. eCollection 2025.
Malaria, caused by Plasmodium spp., remains a major public health problem. Cerebral malaria is its deadliest form, with a 15-25% mortality rate, despite artemisinin-based treatments. In addition, the World Health Organization (WHO) strictly defines cerebral malaria as the presence of coma, 1 h after a seizure or the correction of hypoglycemia, in patients with P. falciparum parasitemia. Consequently, 25% of survivors experience neurocognitive and behavioral sequelae, particularly in children. However, more recently, neurocognitive and behavioral impairments were also reported in severe non-cerebral malaria, non-severe malaria, and even during asymptomatic Plasmodium infection. Such impairments have been observed in school-aged children, the elderly, and in animal models without classic cerebral malaria pathology. Additionally, mild vasogenic edema has been detected in neuroimaging of patients with severe non-cerebral and non-severe P. falciparum malaria. Therefore, given that approximately 98% of malaria cases in the world are non-severe, neurocognitive and behavioral sequelae may account for a significant proportion of global malaria morbidity. Taken together, these observations suggest that systemic inflammation from malaria, even without traditional cerebral malaria signs, can disrupt brain function and lead to long-term sequelae. We propose that the current definition of cerebral malaria may not fully capture the observed evidence and a new conceptualization is necessary to encompass these findings.
由疟原虫属引起的疟疾仍然是一个主要的公共卫生问题。尽管有基于青蒿素的治疗方法,但脑型疟疾是其最致命的形式,死亡率为15%至25%。此外,世界卫生组织(WHO)将脑型疟疾严格定义为恶性疟原虫血症患者在癫痫发作或低血糖纠正1小时后出现昏迷。因此,25%的幸存者会出现神经认知和行为后遗症,尤其是儿童。然而,最近有报告称,在严重非脑型疟疾、非严重疟疾甚至无症状疟原虫感染期间也出现了神经认知和行为障碍。在学龄儿童、老年人以及没有典型脑型疟疾病理的动物模型中都观察到了这种障碍。此外,在严重非脑型和非严重恶性疟原虫疟疾患者的神经影像学检查中发现了轻度血管源性水肿。因此,鉴于世界上约98%的疟疾病例为非严重病例,神经认知和行为后遗症可能在全球疟疾发病率中占很大比例。综上所述,这些观察结果表明,即使没有传统的脑型疟疾症状,疟疾引起的全身炎症也会扰乱脑功能并导致长期后遗症。我们认为,目前脑型疟疾的定义可能无法完全涵盖所观察到的证据,需要一种新的概念来包含这些发现。