El Osta Marven, Naubourg Pierre, Grunewald Olivier, Renom Gilles, Ducoroy Patrick, Périni Jean Marc
Biomaneo, 22B boulevard Winston Churchill, F-21000 Dijon, France.
Newborn Screening Laboratory, Biology and Pathology Center, Lille University Medical Centre, F-59000 Lille, France.
Int J Neonatal Screen. 2019 Aug 31;5(3):31. doi: 10.3390/ijns5030031. eCollection 2019 Sep.
Previous research has shown that a MALDI-MS technique can be used to screen for sickle cell disease (SCD), and that a system combining automated sample preparation, MALDI-MS analysis and classification software is a relevant approach for first-line, high-throughput SCD screening. In order to achieve a high-throughput "plug and play" approach while detecting "non-standard" profiles that might prompt the misclassification of a sample, we have incorporated various sets of alerts into the decision support software. These included "biological alert" indicators of a newborn's clinical status (e. g., detecting samples with no or low HbA), and "technical alerts" indicators for the most common non-standard profiles, i.e., those which might otherwise lead to sample misclassification. We evaluated these alerts by applying them to two datasets (produced by different laboratories). Despite the random generation of abnormal spectra by one-off technical faults or due to the nature and quality of the samples, the use of alerts fully secured the process of automatic sample classification. Firstly, cases of β-thalassemia were detected. Secondly, after a visual check on the tagged profiles and reanalysis of the corresponding biological samples, all the samples were correctly reclassified without prompting further alerts. All of the samples for which the results were not tagged were well classified (i.e., sensitivity and specificity = 1). The alerts were mainly designed for detecting false-negative classifications; all the FAS samples misclassified by the software as FA (a false negative) were marked with an alert. The implementation of alerts in the NeoScreening Laboratory Information Management System's decision support software opens up perspectives for the safe, reliable, automated classification of samples, with a visual check solely on abnormal results or samples. It should now be possible to evaluate the combination of the NeoSickle analytical solution and the NeoScreening Laboratory Information Management System in a real-life, prospective study of first-line SCD screening.
先前的研究表明,基质辅助激光解吸/电离质谱(MALDI-MS)技术可用于筛查镰状细胞病(SCD),并且结合自动样品制备、MALDI-MS分析和分类软件的系统是一线高通量SCD筛查的一种相关方法。为了在检测可能导致样品误分类的“非标准”谱型时实现高通量的“即插即用”方法,我们在决策支持软件中纳入了各种警报集。这些警报包括新生儿临床状态的“生物学警报”指标(例如,检测无HbA或低HbA的样品),以及最常见非标准谱型的“技术警报”指标,即那些否则可能导致样品误分类的谱型。我们通过将这些警报应用于两个数据集(由不同实验室产生)来对其进行评估。尽管一次性技术故障或由于样品的性质和质量会随机产生异常光谱,但使用警报完全确保了自动样品分类过程。首先,检测到了β地中海贫血病例。其次,在对标记的谱型进行目视检查并对相应的生物样品进行重新分析后,所有样品都被正确重新分类,且未引发进一步警报。所有未标记结果的样品都被正确分类(即灵敏度和特异性 = 1)。这些警报主要用于检测假阴性分类;软件误分类为FA(假阴性)的所有FAS样品都被标记了警报。在新生儿筛查实验室信息管理系统的决策支持软件中实施警报,为安全、可靠、自动的样品分类开辟了前景,只需对异常结果或样品进行目视检查。现在应该可以在一线SCD筛查的实际前瞻性研究中评估NeoSickle分析解决方案和新生儿筛查实验室信息管理系统的组合。