The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing

Abstract

by Janet R. Zhou,Ross Ridsdale,Lauren MacNeil,Margaret Lilley,Stephanie Hoang,Susan Christian,Pamela Blumenschein,Vanessa Wolan,Aisha Bruce,Gurpreet Singh,Nicola Wright,Jillian S. Parboosingh,Ryan E. Lamont andIveta Sosova
Int. J. Neonatal Screen. 2021, 7(4), 78; https://doi.org/10.3390/ijns7040078 - 2022
Cited by 6 | Viewed by 3950
Abstract
Sickle cell disease (SCD), a group of inherited red blood cell (RBC) disorders caused by pathogenic variants in the beta-globin gene (HBB), can cause lifelong disabilities and/or early mortality. If diagnosed early, preventative measures significantly reduce adverse outcomes related to SCD. In Alberta, Canada, SCD was added to the newborn screening (NBS) panel in April 2019. The primary conditions screened for are sickle cell anemia (HbS/S), HbS/C disease, and HbS/β thalassemia. In this study, we retrospectively analyzed the first 19 months of SCD screening performance, as well as described our approach for screening of infants that have received a red blood cell transfusion prior to collection of NBS specimen. Hemoglobins eluted from dried blood spots were analyzed using the Bio-Rad™ VARIANT nbs analyzer (Bio-Rad Laboratories, Inc., Hercules, CA, USA). Targeted sequencing of HBB was performed concurrently in samples from all transfused infants. During the period of this study, 43 of 80,314 screened infants received a positive NBS result for SCD, and of these, 34 were confirmed by diagnostic testing, suggesting a local SCD incidence of 1:2400 births. There were 608 infants with sickle cell trait, resulting in a carrier frequency of 1:130. Over 98% of non-transfused infants received their NBS results within 10 days of age. Most of the 188 transfused infants and 2 infants who received intrauterine transfusions received their final SCD screen results within 21 ± 10 d of birth. Our SCD screening algorithm enables detection of affected newborns on the initial NBS specimen, independent of the reported blood transfusion status. Full article
► Show Figures
13 pages, 1183 KiB
Open AccessArticle