Abstract

The mechanisms underlying the rapidly reversible brain swelling described in patients with cerebral malaria (CM) are unknown. Using a 1.5-Tesla (T) magnetic resonance imaging (MRI) scanner, we undertook an observational study in Rourkela, India, of 11 Indian patients hospitalized with CM and increased brain volume. Among the 11 cases, there were 5 adults and 6 children. All patients had reduced consciousness and various degrees of cortical swelling at baseline. The latter was predominately posterior in distribution. The findings on diffusion-weighted imaging (DWI) and apparent diffusion coefficient (ADC) maps were consistent with vasogenic edema in all cases. Reversibility after 48 to 72h was observed in >90% of cases. DWI/ADC mismatch suggested the additional presence of cytotoxic edema in the basal nuclei of 5 patients; all of these had perfusion parameters consistent with vascular engorgement and not with ischemic infarcts. Our results suggest that an impairment of the blood-brain barrier is responsible for the brain swelling in CM. In 5 cases, vasogenic edema occurred in conjunction with changes in the basal nuclei consistent with venous congestion, likely to be caused by the sequestration of Plasmodium falciparum-infected erythrocytes. While both mechanisms have been individually postulated to play an important role in the development of CM, this is the first demonstration of their concurrent involvement in different parts of the brain. The clinical and radiological characteristics observed in the majority of our patients are consistent with posterior reversible encephalopathy syndrome (PRES), and we show for the first time a high frequency of PRES in the context of CM. IMPORTANCE The pathophysiology and molecular mechanisms underlying cerebral malaria (CM) are still poorly understood. Recent neuroimaging studies demonstrated that brain swelling is a common feature in CM and a major contributor to death in pediatric patients. Consequently, determining the precise mechanisms responsible for this swelling could open new adjunct therapeutic avenues in CM patients. Using an MRI scanner with a higher resolution than the ones used in previous reports, we identified two distinct origins of brain swelling in both adult and pediatric patients from India, occurring in distinct parts of the brain. Our results support the hypothesis that both endothelial dysfunction and microvascular obstruction by Plasmodium falciparum-infected erythrocytes make independent contributions to the pathogenesis of CM, providing opportunities for novel therapeutic interventions.

Highlights

  • IMPORTANCE The pathophysiology and molecular mechanisms underlying cerebral malaria (CM) are still poorly understood

  • Magnetic resonance imaging (MRI) facilities have become increasingly accessible in countries where malaria is endemic, creating new opportunities to investigate the mechanisms underlying the occurrence of CM in living patients [1]

  • By allowing the comparison of specific parameters between CM patients who survive and those who succumb to the disease, the systematic use of magnetic resonance imaging (MRI) in an extensive study performed in patients from Malawi demonstrated the importance of increased brain volume as a major contributor to death in pediatric CM

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Summary

Introduction

IMPORTANCE The pathophysiology and molecular mechanisms underlying cerebral malaria (CM) are still poorly understood. By allowing the comparison of specific parameters between CM patients who survive and those who succumb to the disease, the systematic use of MRI in an extensive study performed in patients from Malawi demonstrated the importance of increased brain volume as a major contributor to death in pediatric CM. The cerebral swelling is transient and quickly reversible with routine treatment in survivors but is associated with progression to herniation and respiratory arrest in fatal cases [2] This general mechanism is consistent with the rapid and complete recovery observed in the majority of surviving cases, and while various hypotheses have been suggested, the cellular pathogenesis underlying the rapidly reversible coma in CM remains unknown [3,4,5]. We performed serial brain scans in 11 patients with CM from India who presented with increased brain volume on MRI to investigate the pathophysiology of brain swelling in CM

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