Wienholt Louise, Kane Alisa, Adelstein Stephen, Richardson Alexander, Kothur Kavitha, Brilot Fabienne, Dale Russell C
Department of Clinical Immunology and Allergy, Royal Prince Alfred Hospital, Camperdown, NSW, Australia; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Department of Clinical Immunology and Allergy, Royal Prince Alfred Hospital, Camperdown, NSW, Australia; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Pathology. 2021 Oct;53(6):753-758. doi: 10.1016/j.pathol.2020.11.011. Epub 2021 Mar 19.
The analysis of cerebrospinal fluid (CSF) is routinely used in the diagnostic work-up of a range of inflammatory, infective, and congenital neurological conditions. Many diagnostic tests used in this analysis have poor sensitivity; as such, we investigated the utility of CSF free light chain (FLC) analysis as an adjunct to currently used assays in a paediatric population with neurological disorders. Kappa (κ) and lambda (λ) FLC levels were quantitated in blinded CSF samples by two nephelometric platforms. Results were correlated to clinical diagnoses and classified according to inflammatory/infective or non-inflammatory pathogenesis. FLC results were also compared to currently used CSF diagnostic tests including oligoclonal bands (OCB), CSF IgG and albumin levels, and differential cell count. Of 70 samples analysed, 29 (41%) had an inflammatory or infective diagnosis and 41 (59%) presented with a range of non-inflammatory aetiologies. Thirteen patients had elevated κFLC or λFLC as detected on the IMMAGE 800, defined as greater than the detection limit of the assay (0.600 mg/L for CSF κFLC, and 0.490 mg/L for CSF λFLC), and of these 12 (92%) had an inflammatory disease (sensitivity 41.4%, specificity 97.6%). On the BN II using optimal cut-offs of 0.27 mg/L and 0.12 mg/L for CSF κFLC and λFLC respectively, 24 (34%) patients had elevated results, of which 21 (88%) had an inflammatory disease (sensitivity 72.4%, specificity 92.7%). Analysis of FLC correlated better with diagnostic classification of the diseases than OCB, cell counts and CSF IgG levels. The results of this study support the use of CSF FLC analysis in the diagnosis of paediatric neuroinflammatory conditions.
脑脊液(CSF)分析常用于一系列炎症性、感染性和先天性神经系统疾病的诊断检查。该分析中使用的许多诊断测试灵敏度较低;因此,我们研究了脑脊液游离轻链(FLC)分析作为目前儿科神经系统疾病检测方法辅助手段的效用。通过两个比浊法平台对盲法脑脊液样本中的κ(κ)和λ(λ)FLC水平进行定量分析。结果与临床诊断相关,并根据炎症/感染性或非炎症性发病机制进行分类。FLC结果还与目前使用的脑脊液诊断测试进行比较,包括寡克隆带(OCB)、脑脊液IgG和白蛋白水平以及细胞分类计数。在分析的70个样本中,29个(41%)有炎症或感染性诊断,41个(59%)呈现一系列非炎症性病因。在IMMAGE 800上检测到13例患者的κFLC或λFLC升高,定义为高于检测限(脑脊液κFLC为0.600mg/L,脑脊液λFLC为0.490mg/L),其中12例(92%)患有炎症性疾病(灵敏度41.4%,特异性97.6%)。在BN II上,分别使用脑脊液κFLC和λFLC的最佳临界值0.27mg/L和0.12mg/L,24例(34%)患者结果升高,其中21例(88%)患有炎症性疾病(灵敏度72.4%,特异性92.7%)。与OCB、细胞计数和脑脊液IgG水平相比,FLC分析与疾病的诊断分类相关性更好。本研究结果支持脑脊液FLC分析在儿科神经炎症性疾病诊断中的应用。