Moschetti Estelle, Venet Mélany, Thibaudin Lise, Moreau Amelie, Gonzalo Philippe, Camdessanche Jean-Philippe, Tholance Yannick
Department of Biochemistry, University Hospital of Saint-Etienne, France.
Department of Neurology, University Hospital of Saint-Etienne, France; and.
Neurol Neuroimmunol Neuroinflamm. 2025 Sep;12(5):e200451. doi: 10.1212/NXI.0000000000200451. Epub 2025 Jul 22.
Biological analyses are crucial for diagnosing multiple sclerosis (MS), notably detection of oligoclonal bands (OCBs) of immunoglobulin G in CSF. Kappa free light chain (KFLC) quantification in serum and CSF has recently been proposed as an additional test. In a rational medicoeconomic approach, identifying algorithms or biomarkers is important. The objective of this study was, therefore, to evaluate the correlation between CSF kappa free light chain (KFLC)/total CSF protein ratio (KFLC/Prot) and OCB status and its performance in diagnosing MS.
KFLC measurements were performed prospectively with each OCB analysis, and the data were interpreted retrospectively. A total of 814 clinical cases were included: 153 with MS or clinically isolated syndrome (CIS), 181 with other inflammatory neurologic diseases, and 480 with noninflammatory neurologic diseases. Performances of KFLC/Prot in predicting OCB status, diagnosing MS, and estimating evolution of CIS to MS were evaluated and compared with those of other KFLC parameters, i.e., KFLC index, and with OCB and IgG parameters.
KFLC/Prot and KFLC index performed similarly in predicting OCB status, with a sensitivity of 80.2% and a specificity of 93.4% at a threshold >0.21% for KFLC/Prot (area under the curve: 0.93). The percentage of agreement between OCB status and KFLC/Prot was 91.2%. Using KFLC and KFLC/Prot initially could reduce OCB testing by 68% and quantitative tests by 48.4%. For diagnosing MS/CIS, KFLC/Prot performed similar to or slightly worse than the KFLC index but always outperformed IgG, OCB, and KFLC. For this indication, the optimal threshold for KFLC/Prot was >0.24%. It is important to note that KFLC/Prot was the most predictive parameter for CIS progression to MS.
To conclude, KFLC/Prot is as an easier and cost-effective alternative for predicting OCB status and CIS progression to MS and assisting in the diagnosis of MS.
This study provides Class II evidence that the KFLC/Protein ratio accurately distinguishes patients with CSF OCBs from those without CSF OCBs and patients with MS from those with other neurologic disorders.
生物学分析对于多发性硬化症(MS)的诊断至关重要,尤其是脑脊液中免疫球蛋白G寡克隆带(OCB)的检测。血清和脑脊液中κ游离轻链(KFLC)定量检测最近被提议作为一项附加检测。在合理的医学经济学方法中,识别算法或生物标志物很重要。因此,本研究的目的是评估脑脊液κ游离轻链(KFLC)/脑脊液总蛋白比值(KFLC/Prot)与OCB状态之间的相关性及其在MS诊断中的性能。
在每次OCB分析时前瞻性地进行KFLC测量,并对数据进行回顾性解读。共纳入814例临床病例:153例患有MS或临床孤立综合征(CIS),181例患有其他炎性神经系统疾病,480例患有非炎性神经系统疾病。评估KFLC/Prot在预测OCB状态、诊断MS以及估计CIS向MS演变方面的性能,并与其他KFLC参数(即KFLC指数)以及OCB和IgG参数进行比较。
KFLC/Prot和KFLC指数在预测OCB状态方面表现相似,KFLC/Prot阈值>0.21%时,敏感性为80.2%,特异性为93.4%(曲线下面积:0.93)。OCB状态与KFLC/Prot之间的一致率为91.2%。最初使用KFLC和KFLC/Prot可减少68%的OCB检测和48.4%的定量检测。对于诊断MS/CIS,KFLC/Prot的表现与KFLC指数相似或略差,但始终优于IgG、OCB和KFLC。对于该指征,KFLC/Prot的最佳阈值>0.24%。需要注意的是,KFLC/Prot是CIS进展为MS的最具预测性的参数。
总之,KFLC/Prot是预测OCB状态和CIS进展为MS以及辅助MS诊断的一种更简便且具有成本效益的替代方法。
本研究提供了II类证据,即KFLC/蛋白比值能准确区分脑脊液中有OCB的患者与无OCB的患者,以及MS患者与其他神经系统疾病患者。