莱姆病患者脑脊液炎症和脑损伤标志物的前瞻性随访研究

Ivar Tjernberg, Paula Gyllemark, H. Zetterberg, K. Blennow, J. Ernerudh, P. Forsberg, J. Sjöwall, A. Henningsson
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引用次数: 2

摘要

摘要目的研究莱姆病(Lyme neuroborreliosis, LNB)患者脑脊液(CSF)炎症和脑损伤标志物的水平和动力学。方法在瑞典东南部的一项前瞻性临床研究中,招募了临床怀疑为LNB的成年患者。根据欧洲神经学协会联合会的指南对患者进行分类。明确的LNB病例在一个月后复查,包括再次检查脑脊液。研究常规实验室参数以及脑脊液中神经退行性标志物胶质原纤维酸性蛋白(GFAp)、总tau蛋白(t-tau)和神经丝轻蛋白(NFL)的水平,以及神经炎症标志物髓细胞可溶性触发受体2 (sTREM2)、YKL-40和CXCL13的水平。非lnb作为对照。另一组由无已知中枢神经系统疾病的脊髓麻醉受试者(SAS)组成。结果确诊LNB患者脑脊液sTREM2和CXCL13水平在诊断时明显高于非LNB患者(p<0.001)和SAS患者(p≤0.01)。此外,在抗生素治疗后的随访中,脑脊液中sTREM2、YKL-40和CXCL13的水平迅速下降。相比之下,脑脊液GFAp和t-tau水平在LNB组之间没有差异,治疗后也没有变化。结论虽然在有限数量的LNB患者中,结果表明LNB的诊断以小胶质细胞和神经炎症为主,而不是脑实质中枢神经系统损伤,抗生素治疗后迅速下降。研究结果提供了病理见解,并可能对脑脊液的鉴别诊断有价值。
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Cerebrospinal fluid markers of inflammation and brain injury in Lyme neuroborreliosis – a prospective follow-up study
Abstract Objectives The purpose of this study was to evaluate levels and kinetics of cerebrospinal fluid (CSF) markers of inflammation and brain injury in patients with Lyme neuroborreliosis (LNB). Methods Adult patients with clinically suspected LNB were enrolled, in a prospective clinical study in the South East of Sweden. Patients were classified according to the European Federation of Neurological Societies’ guidelines. Definite cases of LNB were re-examined one month later including a repeat CSF investigation. Routine laboratory parameters were investigated along with CSF levels of neurodegenerative markers glial fibrillary acidic protein (GFAp), total tau (t-tau) and neurofilament light protein (NFL), as well as neuroinflammatory markers soluble triggering receptor expressed on myeloid cells 2 (sTREM2), YKL-40 and CXCL13. Non-LNB served as controls. An additional comparison group consisted of spinal anesthesia subjects (SAS) without known central nervous system conditions. Results CSF levels of sTREM2 and CXCL13 were elevated in definite LNB patients at diagnosis compared with non-LNB patients (p<0.001) and SAS (p≤0.01). In addition, CSF levels of sTREM2, YKL-40 and CXCL13 rapidly declined in at follow-up after antibiotic treatment. In contrast, CSF levels of GFAp and t-tau did not differ across LNB groups, and did not change after treatment. Conclusions Although in a limited number of LNB patients, the results indicate a predominance of microglial and neuroinflammatory involvement rather than parenchymal CNS injury in CSF at diagnosis of LNB with a prompt decline after antibiotic treatment. The findings provide pathogenetic insights and may be of value in differential diagnosis of CSF findings.
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