Primiano Guido, Luigetti Marco, Righi Delia, Romano Angela, Leonardi Luca, Guglielmino Valeria, Forcina Francesca, Ceccanti Marco, Inghilleri Maurizio, Manganelli Fiore, Tozza Stefano, Sciarrone Maria Ausilia, Vitali Francesca, Sabino Andrea, Manco Carlo, Stufano Angela, Stromillo Maria Laura, De Stefano Nicola, Calabresi Paolo, Plantone Domenico
Dipartimento di Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Eur J Neurol. 2025 Jun;32(6):e70215. doi: 10.1111/ene.70215.
Neurofilament light chains (NfL) represent reliable serum biomarkers of neuroaxonal injury. Due to their low serum levels, precise detection methods are critical. This study aimed to scrutinize the comparability of two techniques: Single Molecule Array (SiMoA) and Ella automated immunoassay, analyzing serum NfL levels in ATTRv presymptomatic subjects and polyneuropathy patients.
Blood samples were processed and analyzed using commercial Ella and SiMoA kits. Statistical analysis included the Wilcoxon signed-rank test, Spearman correlation, Bland-Altman, and Passing-Bablok regression. ANCOVA models were used to compare NfL levels between cohorts.
The study measured serum NfL levels in 55 symptomatic and 55 presymptomatic ATTRv subjects. Median NfL concentrations were significantly higher with Ella (median 27.5 pg/mL) than SiMoA (median 15.9 pg/mL). Both methods showed a strong positive correlation (r = 0.8, p < 0.001), but Ella overestimated NfL by 42%. Bland-Altman analysis revealed a mean bias of 15.4 pg/mL, with limits of agreement between -41.1 and 72.0 pg/mL. The slope of the Passing-Bablok regression line was 0.58, and the intercept was 3.48 pg/mL, suggesting that the Ella platform tends to overestimate NfL concentrations compared to the SiMoA platform, especially at higher concentrations. Both methods effectively distinguished presymptomatic from symptomatic patients (p < 0.001 for both).
Our findings underscore that both platforms are effective in measuring serum NfL, with Ella consistently overestimating, especially at higher concentrations. The difference between the two platforms must be taken into account when deeming the concentrations as pathological or normal, as well as when conducting longitudinal studies.
神经丝轻链(NfL)是神经轴突损伤可靠的血清生物标志物。由于其血清水平较低,精确的检测方法至关重要。本研究旨在仔细审查两种技术的可比性:单分子阵列(SiMoA)和Ella自动化免疫测定法,分析转甲状腺素蛋白淀粉样变性(ATTRv)症状前受试者和多发性神经病患者的血清NfL水平。
使用商业化的Ella和SiMoA试剂盒对血样进行处理和分析。统计分析包括Wilcoxon符号秩检验、Spearman相关性分析、Bland-Altman分析和Passing-Bablok回归分析。采用协方差分析模型比较各队列之间的NfL水平。
该研究测量了55例有症状和55例无症状的ATTRv受试者的血清NfL水平。Ella检测的NfL浓度中位数(中位数为27.5 pg/mL)显著高于SiMoA(中位数为15.9 pg/mL)。两种方法均显示出强正相关性(r = 0.8,p < 0.001),但Ella对NfL的估计高估了42%。Bland-Altman分析显示平均偏差为15.4 pg/mL,一致性界限在-41.1至72.0 pg/mL之间。Passing-Bablok回归线的斜率为0.58,截距为3.48 pg/mL,表明与SiMoA平台相比,Ella平台倾向于高估NfL浓度,尤其是在较高浓度时。两种方法均能有效区分症状前患者和有症状患者(两者p均< 0.001)。
我们的研究结果强调,两个平台在测量血清NfL方面均有效,但Ella始终存在高估情况,尤其是在较高浓度时。在将浓度判定为病理性或正常时,以及进行纵向研究时,必须考虑两个平台之间的差异。