Division of Molecular Biology and Human Genetics, DST/NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
PLoS One. 2021 Apr 30;16(4):e0250944. doi: 10.1371/journal.pone.0250944. eCollection 2021.
Stroke is a common complication in children with tuberculous meningitis (TBM). Host proteins may give us insight into the mechanisms of stroke in TBM and serve as biomarkers for detection of stroke, however, they have not been widely explored. In this study, we compared the concentrations of cerebrospinal fluid (CSF) and serum proteins between children who had TBM-related stroke and children with TBM without stroke.
We collected CSF and serum from 47 children consecutively admitted to the Tygerberg Academic Hospital in Cape Town, South Africa between November 2016, and November 2017, on suspicion of having TBM. A multiplex platform was used to measure the concentrations of 69 host proteins in CSF and serum from all study participants.
After classification of study participants, 23 (48.9%) out of the 47 study participants were diagnosed with TBM, of which 14 (60.9%) demonstrated radiological arterial ischemic infarction. The levels of lipocalin-2, sRAGE, IP-10/ CXCL10, sVCAM-1, MMP-1, and PDGF-AA in CSF samples and the levels of D-dimer, ADAMTS13, SAA, ferritin, MCP-1/ CCL2, GDF-15 and IL-13 in serum samples were statistically different between children who had TBM-related stroke and children with TBM without stroke. After correcting for multiple testing, only the levels of sVCAM-1, MMP-1, sRAGE, and IP-10/ CXCL10 in CSF were statistically different between the two groups. CSF and serum protein biosignatures indicated stroke in children diagnosed with TBM with up to 100% sensitivity and 88.9% specificity.
Serum and CSF proteins may serve as biomarkers for identifying individuals with stroke amongst children diagnosed with TBM at admission and may guide us to understand the biology of stroke in TBM. This was a pilot study, and thus further investigations in larger studies are needed.
中风是结核性脑膜炎(TBM)患儿的常见并发症。宿主蛋白可以帮助我们了解 TBM 中风的机制,并作为中风检测的生物标志物,但尚未广泛探索。在这项研究中,我们比较了 TBM 相关中风患儿和 TBM 无中风患儿的脑脊液(CSF)和血清蛋白浓度。
我们收集了 2016 年 11 月至 2017 年 11 月期间连续入住南非开普敦 Tygerberg 学术医院的 47 名疑似患有 TBM 的儿童的 CSF 和血清。使用多重平台测量所有研究参与者 CSF 和血清中 69 种宿主蛋白的浓度。
在对研究参与者进行分类后,47 名研究参与者中有 23 名(48.9%)被诊断为 TBM,其中 14 名(60.9%)表现出放射学动脉缺血性梗死。CSF 样本中脂联素-2、sRAGE、IP-10/CXCL10、sVCAM-1、MMP-1 和 PDGF-AA 的水平以及血清样本中 D-二聚体、ADAMTS13、SAA、铁蛋白、MCP-1/CCL2、GDF-15 和 IL-13 的水平在 TBM 相关中风患儿和 TBM 无中风患儿之间存在统计学差异。在进行多重检验校正后,只有 CSF 中 sVCAM-1、MMP-1、sRAGE 和 IP-10/CXCL10 的水平在两组之间存在统计学差异。CSF 和血清蛋白生物标志物可用于识别诊断为 TBM 的儿童中风患者,灵敏度高达 100%,特异性为 88.9%。
血清和 CSF 蛋白可能作为生物标志物,用于识别入院时诊断为 TBM 的儿童中风患者,并有助于我们了解 TBM 中风的生物学机制。这是一项初步研究,因此需要在更大的研究中进一步研究。