Literature DB >> 33838095

Birth prevalence of tetrahydrobiopterin deficiency in China: data from the national newborn screening program, 2013-2019.

Xuelian Yuan1, Jun Zhu1,2, Hanmin Liu3,4, Liangcheng Xiang2, Yongna Yao2, Qi Li2, Kui Deng1,2, Xiaohong Li1,4,5.   

Abstract

BACKGROUND: Tetrahydrobiopterin deficiency (BH4D), a less common form of hyperphenylalaninemia (HPA), can lead to severe developmental retardation if untreated. Little has been reported on the prevalence of BH4D among live births worldwide. This study examined its prevalence across China and between geographical areas within the country.
METHODS: We analyzed data from the Chinese national screening program for HPA in newborns between 2013 and 2019. BH4D prevalence was examined by province, region and the entire country. Provincial-level prevalence was estimated from the number of confirmed BH4D cases and screened newborns, after adjusting for HPA-positive recall rate. Regional- and national-level prevalences were estimated by summing provincial-level prevalences after weighting them by the number of live births. A Poisson distribution was assumed in order to calculate 95% confidence intervals (CIs) for prevalence.
RESULTS: Among 107,078,115 newborns screened for HPA in China, 380 with BH4D were identified, corresponding to a total prevalence of 3.8 per 1,000,000 live births. Prevalence was higher in eastern regions (5.9 per 1,000,000) and northern regions (4.1 per 1,000,000) of China than in southern regions (1.6 per 1,000,000) or northwestern regions (1.7 per 1,000,000). Across the entire country, 3.9% cases of HPA were diagnosed as BH4D, and this proportion reached as high as 15.1% in the southern part of the country.
CONCLUSIONS: These first insights into BH4D prevalence across China suggest slightly higher prevalence than in other countries, and it varies substantially by region. More attention should be paid to early diagnosis and timely treatment of BH4D.
© 2021 Xuelian Yuan et al., published by De Gruyter, Berlin/Boston.

Entities:  

Keywords:  geographical; newborn screening; prevalence; tetrahydrobiopterin deficiency

Mesh:

Year:  2021        PMID: 33838095     DOI: 10.1515/jpem-2021-0077

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  Identification and molecular analysis of 11 cases of the PTS gene variants associated with tetrahydrobiopterin deficiency.

Authors:  Lulu Li; Haihe Yang; Jinqi Zhao; Nan Yang; Lifei Gong; Yue Tang; Yuanyuan Kong
Journal:  Front Genet       Date:  2022-09-12       Impact factor: 4.772

  1 in total

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