Association between genotype and phenotype in children with Phenylalanine hydroxylase deficiency in Lianyungang area.
10.3760/cma.j.cn511374-20241125-00620
- Author:
Shuang LIU
1
,
2
;
Qin ZHENG
;
Dandan CUI
;
Wei WANG
;
Leilei WANG
;
Guanghua LUO
Author Information
1. Clinical Medical Research Center, the Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, China. shineroar@
2. com.
- Publication Type:Journal Article
- MeSH:
Humans;
Phenylalanine Hydroxylase/genetics*;
Female;
Phenylketonurias/enzymology*;
Male;
Phenotype;
Genotype;
Child;
Infant;
Infant, Newborn;
Child, Preschool;
China;
Mutation;
Alleles
- From:
Chinese Journal of Medical Genetics
2025;42(6):648-659
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the spectrum of genetic variants and phenotypes of Phenylalanine hydroxylase deficiency (PAHD) in Lianyungang area and the correlation between genotype and phenotypes among the patients.
METHODS:Eighty children with Hyperphenylalaninemia (HPA) diagnosed at the Lianyungang Branch of Jiangsu Provincial Newborn Screening Center between January 2015 and December 2022 were enrolled. Peripheral blood samples were collected for genetic analysis using next generation sequencing (NGS), Sanger sequencing, and multiplex ligation-dependent probe amplification (MLPA) to identify the variants of PAH gene. Clinical and phenotypic data were concurrently analyzed to investigate the correlation between the types of PAH gene variant and phenotypes. This study was approved by the Medical Ethics Committee of Lianyungang Maternal and Child Health Care Hospital (Ethics No.: XM2022041).
RESULTS:PAH gene variants were identified in 93.75% (75/80) of the children, classified as PAHD cases, while 6.25% (5/80) harbored PTS gene variants. Of the 150 PAH alleles from 75 PAHD children, a total of 152 variants (55 distinct types) were detected, with a detection rate of 100%. 80.26% (122/152) of the variants were located in exons, with the main types being missense variants (67.11%, 102/152). 53.29% (81/152) of coding sequence variants have occurred in the PAH gene's catalytic center region, while 19.74% (30/152) of the variants involved non-coding sequences. The phenotypes of the 75 PAHD children were evenly distributed. The re-screened Phe concentrations and Phe/Tyr ratios of classic-phenylketonuria (CPKU) and mild-phenylketonuria (MPKU) patients were markedly higher than initial screening values (P < 0.001, P < 0.001; P = 0.004, P = 0.016). The genotypes of the PAHD patients mostly occurred as compound heterozygotes, and different mutation positions and variant types have significantly affected the phenotypes (P = 0.042, P = 0.045). APV/GPV genotype-phenotype analysis of 61 patients showed high consistency between predicted and actual phenotypes (κ = 0.755, P < 0.001).
CONCLUSION:PAH gene variants were detected in most HPA children from Lianyungang area. The location and type of PAH gene variants has correlated with the severity of the phenotype, and the non-coding sequence variants and non-missense variants may aggravate the phenotype, and the APV/GPV model has predicted the phenotype with high consistency with the actual phenotype.
