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Expanded Newborn Screening for Inborn Errors of Metabolism in Hong Kong: Results and Outcome of a 7 Year Journey

Authors :
Kiran Moti Belaramani
Toby Chun Hei Chan
Edgar Wai Lok Hau
Matthew Chun Wing Yeung
Anne Mei Kwun Kwok
Ivan Fai Man Lo
Terry Hiu Fung Law
Helen Wu
Sheila Suet Na Wong
Shirley Wai Lam
Gladys Ha Yin Ha
Toby Pui Yee Lau
Tsz Ki Wong
Venus Wai Ching Or
Rosanna Ming Sum Wong
Wong Lap Ming
Jasmine Chi Kwan Chow
Eric Kin Cheong Yau
Antony Fu
Josephine Shuk Ching Chong
Ho Chung Yau
Grace Wing Kit Poon
Kwok Leung Ng
Kwong Tat Chan
Yuen Yu Lam
Joannie Hui
Chloe Miu Mak
Cheuk Wing Fung
Source :
International Journal of Neonatal Screening, Vol 10, Iss 1, p 23 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

Abstract

Newborn screening (NBS) is an important public health program that aims to identify pre-symptomatic healthy babies that will develop significant disease if left undiagnosed and untreated. The number of conditions being screened globally is expanding rapidly in parallel with advances in technology, diagnosis, and treatment availability for these conditions. In Hong Kong, NBS for inborn errors of metabolism (NBSIEM) began as a pilot program in October 2015 and was implemented to all birthing hospitals within the public healthcare system in phases, with completion in October 2020. The number of conditions screened for increased from 21 to 24 in April 2016 and then to 26 in October 2019. The overall recruitment rate of the NBS program was 99.5%. In the period between October 2015 and December 2022, 125,688 newborns were screened and 295 were referred back for abnormal results. The recall rate was reduced from 0.26% to 0.12% after the implementation of second-tier testing. An inherited metabolic disorder (IMD) was eventually confirmed in 47 infants, making the prevalence of IMD in Hong Kong 1 in 2674. At the time of the NBS result, 78.7% of the newborns with IMD were asymptomatic. There were two deaths reported: one newborn with methylmalonic acidemia cobalamin B type (MMACblB) died after the initial crisis and another case of carnitine palmitoyltransferase II deficiency (CPTII) died at 18 months of age after metabolic decompensation. The most common IMD noted were disorders of fatty acid oxidation metabolism (40%, 19 cases), closely followed by disorders of amino acid metabolism (38%, 18 cases), with carnitine uptake defect (19.1%, 9 cases) and citrullinemia type II (17%, 8 cases) being the two most common IMD picked up by the NBSIEM in Hong Kong. Out of the all the IMDs identified, 19.1% belonged to diverse ethnic groups. False negative cases were reported for citrullinemia type II and congenital adrenal hyperplasia during this period.

Details

Language :
English
ISSN :
2409515X
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
International Journal of Neonatal Screening
Publication Type :
Academic Journal
Accession number :
edsdoj.9e174954a012423e9418a84e92790b6e
Document Type :
article
Full Text :
https://doi.org/10.3390/ijns10010023