Specific Biomarkers Differentiate Cerebral Malaria From Other Causes of Coma in African Children.

IF 4.1 2区 医学 Q2 IMMUNOLOGY
Shaban Mwangi, Claudia Gomes, Abdirahman I Abdi, Ana Rodriguez
{"title":"Specific Biomarkers Differentiate Cerebral Malaria From Other Causes of Coma in African Children.","authors":"Shaban Mwangi, Claudia Gomes, Abdirahman I Abdi, Ana Rodriguez","doi":"10.1093/infdis/jiag070","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Cerebral malaria (CM) is a serious complication of Plasmodium falciparum malaria that causes coma and, frequently, death. In malaria-endemic settings, a large percentage of the population presents with incidental P falciparum malaria parasitemia. In the absence of specific biomarkers for CM, when these individuals suffer from bacterial or viral infections causing coma, they are frequently misdiagnosed with CM.</p><p><strong>Methods: </strong>We have tested the specificity for CM of 2 candidate biomarkers for severe malaria, angiopoietin-like 4 (ANGPTL4) and inhibin-βE (INHBE), which are secreted by endothelial cells in response to P falciparum-infected erythrocytes. The levels of these biomarkers were determined retrospectively in the plasma of a cohort of 379 Kenyan children including cases of severe malaria caused by CM, respiratory distress, or severe anemia, as well as cases of nontraumatic coma of unknown cause.</p><p><strong>Results: </strong>ANGPTL4 and INHBE showed high specificity for severe malaria, including CM (area under the curve [AUC] 0.82), respiratory distress (AUC 0.86), and severe anemia (AUC 0.85), when compared to acute nontraumatic coma of nonmalarial etiology. Specificity was further increased when the biomarkers were used in combination with platelet levels (AUC 0.96). ANGPTL4 and INHBE are also predictors of death by CM (AUC 0.85).</p><p><strong>Conclusions: </strong>ANGPTL4 and INHBE could be developed as a diagnostic tool for the differentiation of comatose patients with CM from other causes of coma.</p>","PeriodicalId":50179,"journal":{"name":"Journal of Infectious Diseases","volume":" ","pages":"288-296"},"PeriodicalIF":4.1000,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13537156/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/infdis/jiag070","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Cerebral malaria (CM) is a serious complication of Plasmodium falciparum malaria that causes coma and, frequently, death. In malaria-endemic settings, a large percentage of the population presents with incidental P falciparum malaria parasitemia. In the absence of specific biomarkers for CM, when these individuals suffer from bacterial or viral infections causing coma, they are frequently misdiagnosed with CM.

Methods: We have tested the specificity for CM of 2 candidate biomarkers for severe malaria, angiopoietin-like 4 (ANGPTL4) and inhibin-βE (INHBE), which are secreted by endothelial cells in response to P falciparum-infected erythrocytes. The levels of these biomarkers were determined retrospectively in the plasma of a cohort of 379 Kenyan children including cases of severe malaria caused by CM, respiratory distress, or severe anemia, as well as cases of nontraumatic coma of unknown cause.

Results: ANGPTL4 and INHBE showed high specificity for severe malaria, including CM (area under the curve [AUC] 0.82), respiratory distress (AUC 0.86), and severe anemia (AUC 0.85), when compared to acute nontraumatic coma of nonmalarial etiology. Specificity was further increased when the biomarkers were used in combination with platelet levels (AUC 0.96). ANGPTL4 and INHBE are also predictors of death by CM (AUC 0.85).

Conclusions: ANGPTL4 and INHBE could be developed as a diagnostic tool for the differentiation of comatose patients with CM from other causes of coma.

特异性生物标志物区分非洲儿童脑疟疾和其他原因的昏迷。
背景:脑型疟疾(CM)是恶性疟原虫疟疾的一种严重并发症,可导致昏迷和死亡。在疟疾流行的环境中,很大比例的人口出现偶发恶性疟原虫疟疾寄生虫病。由于缺乏CM的特异性生物标志物,当这些个体遭受细菌或病毒感染导致昏迷时,他们经常被误诊为CM。方法:研究了恶性疟原虫感染红细胞后内皮细胞分泌的血管生成素样4 (Angiopoietin-like 4)和抑制素-βE (Inhibin-βE)两种候选疟疾生物标志物对CM的特异性。回顾性测定了379名肯尼亚儿童的血浆中这些生物标志物的水平,这些儿童包括由CM引起的严重疟疾病例、呼吸窘迫或严重贫血病例,以及原因不明的非创伤性昏迷病例。结果:与非疟疾病因的急性非创伤性昏迷相比,血管生成素样4和抑制素-βE对重症疟疾的特异性较高,包括CM (AUC 0.82)、呼吸窘迫(AUC 0.86)和严重贫血(AUC 0.85)。当生物标志物与血小板水平联合使用时,特异性进一步提高(AUC 0.96)。血管生成素样4和抑制素-βE也是CM死亡的预测因子(AUC 0.85)。结论:血管生成素样4和抑制素β e可作为CM昏迷患者与其他原因昏迷的鉴别诊断工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Infectious Diseases
Journal of Infectious Diseases 医学-传染病学
CiteScore
13.50
自引率
3.10%
发文量
449
审稿时长
2-4 weeks
期刊介绍: Published continuously since 1904, The Journal of Infectious Diseases (JID) is the premier global journal for original research on infectious diseases. The editors welcome Major Articles and Brief Reports describing research results on microbiology, immunology, epidemiology, and related disciplines, on the pathogenesis, diagnosis, and treatment of infectious diseases; on the microbes that cause them; and on disorders of host immune responses. JID is an official publication of the Infectious Diseases Society of America.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书