香港扩大新生儿先天性代谢异常筛查:七年历程的结果和成果

IF 4 Q1 GENETICS & HEREDITY International Journal of Neonatal Screening Pub Date : 2024-03-11 DOI:10.3390/ijns10010023
K. Belaramani, T. 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, J. Chow, E. Yau, A. Fu, Josephine Shuk Ching Chong, H. Yau, G. Poon, K. Ng, Kwong-tat Chan, Y. Lam, Joannie Hui, Chloe Miu Mak, C. Fung
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引用次数: 0

摘要

新生儿疾病筛查(NBS)是一项重要的公共卫生计划,其目的是发现无症状前的健康婴儿,如果不及时诊断和治疗,这些婴儿将发展成重大疾病。随着技术、诊断和治疗手段的进步,全球接受筛查的疾病数量也在迅速增加。在香港,先天性代谢异常新生儿筛查(NBSIEM)于 2015 年 10 月开始试点,并分阶段在公立医疗系统内的所有分娩医院实施,将于 2020 年 10 月完成。2016 年 4 月,筛查病种从 21 种增至 24 种,2019 年 10 月增至 26 种。新生儿筛查计划的总体招募率为 99.5%。在 2015 年 10 月至 2022 年 12 月期间,125688 名新生儿接受了筛查,295 名新生儿因结果异常而被转回。实施二级检测后,召回率从 0.26% 降至 0.12%。最終有 47 名嬰兒證實患有遺傳性代謝障礙,令香港的遺傳性代謝障礙發病率為每 2674 名嬰兒中有 1 名患有這種障礙。在国家新生儿筛查结果出来时,78.7%的新生儿无症状。据报告,有两名新生儿死亡:一名患有甲基丙二酸血症钴胺 B 型(MMACblB)的新生儿在最初的危象后死亡,另一名患有肉碱棕榈酰转移酶 II 缺乏症(CPTII)的新生儿在 18 个月大时因代谢失调而死亡。最常见的IMD是脂肪酸氧化代谢紊乱(40%,19例),紧随其后的是氨基酸代谢紊乱(38%,18例),肉碱摄取缺陷(19.1%,9例)和瓜氨酸血症II型(17%,8例)是NBSIEM在香港发现的两种最常见的IMD。在所有被识别的IMD中,19.1%属于不同的种族群体。在这期间,曾有瓜氨酸血症II型和先天性肾上腺增生症的假阴性个案报告。
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Expanded Newborn Screening for Inborn Errors of Metabolism in Hong Kong: Results and Outcome of a 7 Year Journey
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.
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来源期刊
International Journal of Neonatal Screening
International Journal of Neonatal Screening Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
20.00%
发文量
56
审稿时长
11 weeks
期刊最新文献
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