Batte Anthony, Nakulima Violah, Namazzi Ruth, Aujo Judith Caroline, Starr Michelle C, Schwaderer Andrew L, Lintner-Rivera Michael, Ahumwire Avias, Ogwal Daniel, Tenywa Emmanuel, Oyang William, Ssenkusu John M, Bangirana Paul, Idro Richard, Kalyesubula Robert, Dreyer Gavin, McCulloch Mignon, Bassat Quique, John Chandy C, Goldstein Stuart L, Conroy Andrea L
Child Health and Development Centre, Makerere University College of Health Sciences, Kampala, Uganda.
ISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
BMC Nephrol. 2025 Jul 15;26(1):390. doi: 10.1186/s12882-025-04333-7.
Severe malaria (SM) remains a leading cause of child mortality and an important global contributor to acute kidney injury (AKI), which can progress to chronic kidney disease (CKD) in some survivors. Notably, 80% of AKI deaths occur in low- and middle-income countries (LMIC). Despite this burden, the mechanisms and recovery trajectory of SM associated AKI remain poorly understood. There is a critical need to define the etiology and pathophysiology of SM-AKI, uncover pathways of maladaptive repair, identify risk factors for CKD, and evaluate long-term health and development.
This prospective multi-site cohort study will enroll children at three sites in Uganda: Mulago National Referral and Teaching Hospital, Jinja Regional Referral Hospital, and Lira Regional Referral Hospital. We aim to recruit 750 children with severe malaria and 375 community controls between 3 months of age and < 16 years. Participants will be followed for two years. Children with severe malaria will be assessed at 1-, 2-, and 4-months to evaluate short-term kidney recovery and 12- and 24-months to assess kidney function and health-related quality of life. The study will investigate short-term and long-term kidney disease risk factors following severe malaria. We will characterize host pathways involved in maladaptive kidney repair, focusing on mechanisms related to cell stress, angiogenesis, and tubulointerstitial injury. Additionally, we will assess the impact of AKI and persistent kidney disease on morbidity, mortality, and health-related quality of life. Cognitive and behavioral assessments, along with brain magnetic resonance imaging (MRI), will be used to evaluate the effects of AKI on brain injury and edema.
This study will generate key insights into the prevalence of persistent kidney disease following SM-AKI and identify risk factors for CKD to inform clinical follow-up. Defining specific pathways involved with maladaptive repair in severe malaria will provide the foundation for targeted interventions to promote adaptive recovery. The research has the potential to transform long-term health outcomes following SM-AKI.
ISRCTN10885288.
重症疟疾(SM)仍然是儿童死亡的主要原因,也是急性肾损伤(AKI)的一个重要全球病因,在一些幸存者中,急性肾损伤可能会进展为慢性肾脏病(CKD)。值得注意的是,80%的急性肾损伤死亡发生在低收入和中等收入国家(LMIC)。尽管有如此负担,但重症疟疾相关急性肾损伤的机制和恢复轨迹仍知之甚少。迫切需要明确重症疟疾相关急性肾损伤的病因和病理生理学,揭示适应性不良修复的途径,确定慢性肾脏病的危险因素,并评估长期健康和发育情况。
这项前瞻性多中心队列研究将在乌干达的三个地点招募儿童:穆拉戈国家转诊和教学医院、金贾地区转诊医院和利拉地区转诊医院。我们的目标是招募750名患有重症疟疾的儿童和375名年龄在3个月至16岁以下的社区对照。参与者将被随访两年。患有重症疟疾的儿童将在1个月、2个月和4个月时接受评估,以评估短期肾脏恢复情况,并在12个月和24个月时评估肾功能和与健康相关的生活质量。该研究将调查重症疟疾后短期和长期的肾脏疾病危险因素。我们将描述参与适应性不良肾脏修复的宿主途径,重点关注与细胞应激、血管生成和肾小管间质损伤相关的机制。此外,我们将评估急性肾损伤和持续性肾脏疾病对发病率、死亡率和与健康相关的生活质量的影响。认知和行为评估以及脑磁共振成像(MRI)将用于评估急性肾损伤对脑损伤和水肿的影响。
这项研究将对重症疟疾相关急性肾损伤后持续性肾脏疾病的患病率产生关键见解,并确定慢性肾脏病的危险因素,为临床随访提供依据。明确重症疟疾中与适应性不良修复相关的特定途径将为促进适应性恢复的靶向干预提供基础。该研究有可能改变重症疟疾相关急性肾损伤后的长期健康结局。
ISRCTN10885288。