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脑型疟疾患者的磁共振成像揭示了大脑不同部位独特的致病过程。

Magnetic Resonance Imaging of Cerebral Malaria Patients Reveals Distinct Pathogenetic Processes in Different Parts of the Brain.

作者信息

Mohanty Sanjib, Benjamin Laura A, Majhi Megharay, Panda Premanand, Kampondeni Sam, Sahu Praveen K, Mohanty Akshaya, Mahanta Kishore C, Pattnaik Rajyabardhan, Mohanty Rashmi R, Joshi Sonia, Mohanty Anita, Turnbull Ian W, Dondorp Arjen M, Taylor Terrie E, Wassmer Samuel C

机构信息

Center for the Study of Complex Malaria in India, Ispat General Hospital, Rourkela, Odisha, India.

Brain Infections Group, Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom.

出版信息

mSphere. 2017 Jun 7;2(3). doi: 10.1128/mSphere.00193-17. eCollection 2017 May-Jun.

DOI:10.1128/mSphere.00193-17
PMID:28596990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5463026/
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 72 h 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 -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. 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 -infected erythrocytes make independent contributions to the pathogenesis of CM, providing opportunities for novel therapeutic interventions.

摘要

脑型疟疾(CM)患者中出现的快速可逆性脑肿胀的潜在机制尚不清楚。我们使用一台1.5特斯拉(T)的磁共振成像(MRI)扫描仪,在印度鲁尔克拉对11名因CM住院且脑容量增加的印度患者进行了一项观察性研究。11例患者中,有5名成人和6名儿童。所有患者在基线时均意识减退且存在不同程度的皮质肿胀,后者主要分布在后部。所有病例的扩散加权成像(DWI)和表观扩散系数(ADC)图结果均与血管源性水肿一致。超过90%的病例在48至72小时后出现可逆性。DWI/ADC不匹配提示5例患者基底核存在额外的细胞毒性水肿;所有这些患者的灌注参数均与血管充血一致,而非缺血性梗死。我们的结果表明,血脑屏障受损是CM脑肿胀的原因。在5例患者中,血管源性水肿与基底核变化同时出现,符合静脉淤血,可能是由感染红细胞的滞留所致。虽然这两种机制各自都被推测在CM的发展中起重要作用,但这是首次证明它们同时累及大脑的不同部位。我们大多数患者观察到的临床和放射学特征与后部可逆性脑病综合征(PRES)一致,并且我们首次显示在CM背景下PRES的高发生率。脑型疟疾(CM)的病理生理学和分子机制仍知之甚少。最近的神经影像学研究表明,脑肿胀是CM的常见特征,也是儿科患者死亡的主要原因。因此,确定导致这种肿胀的确切机制可能为CM患者开辟新的辅助治疗途径。使用一台分辨率高于以往报告中所用设备的MRI扫描仪,我们在来自印度的成人和儿科患者中确定了脑肿胀的两个不同起源,分别发生在大脑的不同部位。我们的结果支持以下假设,即内皮功能障碍和感染红细胞导致的微血管阻塞对CM的发病机制都有独立贡献,为新型治疗干预提供了机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/7ce68620e135/sph0031722930004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/055d3917c96c/sph0031722930001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/b09cc5ea3429/sph0031722930002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/0733283a77af/sph0031722930003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/7ce68620e135/sph0031722930004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/055d3917c96c/sph0031722930001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/b09cc5ea3429/sph0031722930002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/0733283a77af/sph0031722930003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/5463026/7ce68620e135/sph0031722930004.jpg

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