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Incorporation of second‐tier tests and secondary biomarkers to improve positive predictive value (PPV) rate in newborn metabolic screening program
Authors:Sarang Younesi,Bahareh Yazdani,Mohammad Mahdi Taheri Amin,Pourandokht Saadati,Soudabeh Jamali,Mohammad‐  Hossein Modarresi,Shahram Savad,Saloomeh Amidi,Homayoun Razavi,Soudeh Ghafouri‐  Fard
Affiliation:1. Nilou Laboratory, Tehran Iran ; 2. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran Iran ; 3. Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran Iran
Abstract:BackgroundNowadays, 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.MethodsThis 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).ResultsStatistical 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%.ConclusionThis 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.
Keywords:mass spectrometry, neonatal screening, second‐  tier biomarkers
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