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将二线检测和次要生物标志物纳入新生儿代谢筛查计划,以提高阳性预测值(PPV)率。

Incorporation of second-tier tests and secondary biomarkers to improve positive predictive value (PPV) rate in newborn metabolic screening program.

机构信息

Nilou Laboratory, Tehran, Iran.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

J Clin Lab Anal. 2022 Jul;36(7):e24471. doi: 10.1002/jcla.24471. Epub 2022 May 2.

Abstract

BACKGROUND

Nowadays, neonatal screening has become an essential part of routine newborn care in the world. This is a non-invasive evaluation that evaluated inborn errors of metabolisms (IEMs) using tandem mass spectrometry (LC-MS/MS) for the evaluation of the baby's risk of certain metabolic disorders.

METHODS

This retrospective study was conducted on 39987 Iranian newborns who were referred to Nilou Medical Laboratory, Tehran, Iran, for newborn screening programs of IEMs. We incorporated second-tier tests and secondary biomarkers to improve positive predictive value (PPV).

RESULTS

Statistical data were recorded via call interviewing in 6-8 months after their screening tests. The overall prevalence of IEM was 1:975. The mean age of all participants was 3.9 ± 1.1 days; 5.1% of participants were over 13 days and 7.7% were preterm or underweight. A total of 11384 (29.4%) of the cases were born in a consanguineous family. The type of delivery was the cesarean section in 8332 (51.3%) valid cases. The neonatal screening results had an overall negative predictive value (NPV) of 100% and the overall PPV of 40.2%. The false-positive rate was 0.15%.

CONCLUSION

This study showed a high incidence of metabolic disease due to a high rate of consanguineous marriages in Iran and indicated that incorporation of second-tier tests and secondary biomarkers improves PPV of neonatal screening programs.

摘要

背景

如今,新生儿筛查已成为世界范围内常规新生儿护理的重要组成部分。这是一种非侵入性评估,使用串联质谱(LC-MS/MS)评估婴儿罹患某些代谢紊乱的风险,评估先天代谢错误(IEM)。

方法

本回顾性研究纳入了 39987 名伊朗新生儿,他们因 IEM 新生儿筛查项目被转诊至伊朗德黑兰 Nilou 医学实验室。我们纳入了二级测试和次要生物标志物,以提高阳性预测值(PPV)。

结果

通过筛查后 6-8 个月的电话访谈记录统计数据。IEM 的总患病率为 1:975。所有参与者的平均年龄为 3.9±1.1 天;5.1%的参与者超过 13 天,7.7%为早产儿或体重不足。共有 11384 例(29.4%)病例来自近亲家庭。有效病例中 8332 例(51.3%)为剖宫产。新生儿筛查结果的总体阴性预测值(NPV)为 100%,总体阳性预测值(PPV)为 40.2%。假阳性率为 0.15%。

结论

本研究显示由于伊朗近亲结婚率较高,代谢疾病的发病率较高,表明纳入二级测试和次要生物标志物可提高新生儿筛查项目的 PPV。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2664/9279966/dadffd89757f/JCLA-36-e24471-g001.jpg

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