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Potential Serological Biomarkers of Cerebral Malaria

机译:脑型疟疾的潜在血清生物标志物

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摘要

Biomarkers have been used to diagnose and prognosticate the progress and outcome of many chronic diseases such as neoplastic and non communicable diseases. However, only recently did the field of malaria research move in the direction of actively identifying biomarkers that can accurately discriminate the severe forms of malaria. Malaria continues to be a deadly disease, killing close to a million people (mostly children) every year. One life-threatening complication of malaria is cerebral malaria (CM). Studies carried out in Africa have demonstrated that even with the best treatment, as high as 15–30% of CM patients die and about 10–24% of CM survivors suffer short-or long-term neurological impairment. The transition from mild malaria to CM can be sudden and requires immediate intervention. Currently, there is no biological test available to confirm the diagnosis of CM and its complications. It is hoped that development of biomarkers to identify CM patients and potential risk for adverse outcomes would greatly enhance better intervention and clinical management to improve the outcomes. We review here what is currently known regarding biomarkers for CM outcomes. A Pub Med literature search was performed using the following search terms: “malaria,” “cerebral malaria,” “biomarkers,” “mortality” and “neurological sequelae.” This search revealed a paucity of usable biomarkers for CM management. We propose three main areas in which researchers can attempt to identify CM biomarkers: 1) early biomarkers, 2) diagnostic biomarkers and 3) prognostic biomarkers.
机译:生物标志物已被用于诊断和预测许多慢性疾病的进展和结果,例如肿瘤性和非传染性疾病。但是,直到最近,疟疾研究领域才朝着积极识别可以准确地区分严重疟疾形式的生物标志物的方向发展。疟疾仍然是一种致命疾病,每年造成近一百万人死亡(主要是儿童)。疟疾的一种威胁生命的并发症是脑疟疾(CM)。在非洲进行的研究表明,即使采用最佳治疗方法,高达15–30%的CM患者会死亡,约10–24%的CM幸存者会遭受短期或长期的神经系统损害。从轻度疟疾到CM的过渡可能是突然的,需要立即进行干预。当前,没有可用于证实CM及其并发症的生物学测试。希望开发用于识别CM患者的生物标志物和不良后果的潜在风险将大大加强更好的干预和临床管理以改善结果。我们在这里回顾了有关CM结局的生物标志物的当前已知信息。使用以下搜索词进行Pub Med文献搜索:“疟疾”,“脑部疟疾”,“生物标记物”,“死亡率”和“神经后遗症”。该搜索揭示了用于CM管理的可用生物标记物很少。我们提出了研究人员可以尝试识别CM生物标志物的三个主要领域:1)早期生物标志物,2)诊断生物标志物和3)预后生物标志物。

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