Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China

Jia-Xin Xu; Fen Lin; Yong-Hao Wu; Zi-Kai Chen; Yu-Bin Ma; Li-Ye Yang

doi:10.12998/wjcc.v11.i11.2443

Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China

World J Clin Cases. 2023 Apr 16;11(11):2443-2451. doi: 10.12998/wjcc.v11.i11.2443.

Authors

Jia-Xin Xu¹, Fen Lin¹, Yong-Hao Wu¹, Zi-Kai Chen², Yu-Bin Ma³, Li-Ye Yang⁴

Affiliations

¹ Precision Medical Center, Chaozhou Central Hospital, Chaozhou 521021, Guangdong Province, China.
² School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou 521021, Guangdong Province, China.
³ Department of Pediatrics, Chaozhou Central Hospital, Chaozhou 521021, Guangdong Province, China.
⁴ Precision Medical Lab Center, People's Hospital of Yangjiang, Yangjiang 529500, Guangdong Province, China. yangleeyee@sina.com.

Abstract

Background: Neonatal hyperbilirubinemia is one of the common diseases of newborns that typically presents with yellow staining of skin, resulting in sequelaes such as hearing loss, motor and intellectual development disorders, and even death. The pathogenic factors of neonatal hyperbilirubinemia are complex. Different cases of hyperbilirubinemia may have a single or mixed etiology.

Aim: To explore the etiological characteristics of severe hyperbilirubinemia in term newborns of eastern Guangdong of China.

Methods: Term newborns with severe hyperbilirubinemia in one hospital from January 2012 to December 2021 were retrospectively analyzed. The etiology was determined according to the laboratory results and clinical manifestations.

Results: Among 1602 term newborns with hyperbilirubinemia in eastern Guangdong of China, 32.20% (580/1602) was severe hyperbilirubinemia. Among the causes of severe hyperbilirubinemia, neonatal hemolysis accounted for 15.17%, breast milk jaundice accounted for 12.09%, infection accounted for 10.17%, glucose-6-phosphate dehydrogenase (G6PD) deficiency accounted for 9.14%, and the coexistence of multiple etiologies accounted for 6.55%, unknown etiology accounted for 41.72%. ABO hemolysis and G6PD deficiency were the most common causes in the 20 cases with bilirubin encephalopathy. 94 severe hyperbilirubinemia newborns were tested for uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1)*6 variant (rs4148323, c.211G>A, p.Arg71Gly), 9 cases were 211 G to A homozygous variant, 37 cases were 211 G to A heterozygous variant, and 48 cases were wild genotypes.

Conclusion: The main cause for severe hyperbilirubinemia and bilirubin encephalopathy in eastern Guangdong of China were the hemolytic disease of the newborns, G6PD deficiency and infection. UGT1A1 gene variant was also a high-risk factor for neonatal hyperbilirubinemia. Targeted prevention and treatment according to the etiology may reduce the occurrence of bilirubin encephalopathy and kernicterus.

Keywords: Etiology; Glucose-6-phosphate dehydrogenase deficiency; Severe hyperbilirubinemia; Term newborns; Uridine diphosphate glucuronosyl transferase 1A1.