Atlanta Research and Education Foundation, Decatur, GA, USA.
Dis Markers. 2011;31(6):327-35. doi: 10.3233/DMA-2011-0854.
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.
生物标志物已被用于诊断和预测许多慢性疾病(如肿瘤和非传染性疾病)的进展和结果。然而,直到最近,疟疾研究领域才开始积极寻找能够准确区分疟疾严重程度的生物标志物。疟疾仍然是一种致命的疾病,每年导致近 100 万人(大多数是儿童)死亡。疟疾的一种危及生命的并发症是脑型疟疾(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 患者仍会死亡,约 10-24%的 CM 幸存者会出现短期或长期的神经损伤。从轻度疟疾到 CM 的转变可能是突然的,需要立即干预。目前,尚无生物学检测方法可用于确诊 CM 及其并发症。希望开发出识别 CM 患者和不良结局潜在风险的生物标志物,将极大地促进更好的干预和临床管理,以改善结局。我们在此回顾了目前关于 CM 结局的生物标志物的研究进展。我们使用以下搜索词在 Pub Med 文献数据库中进行了文献检索:“疟疾”、“脑型疟疾”、“生物标志物”、“死亡率”和“神经后遗症”。这一检索结果显示,目前可用于 CM 管理的生物标志物非常有限。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,3)预后生物标志物。