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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 39 Issue 4
Apr.  2023
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Article Contents

Research advances in the treatment of Crigler-Najjar syndrome

DOI: 10.3969/j.issn.1001-5256.2023.04.035
Research funding:

National Natural Science Foundation of China (81930061);

Key Project of the Technical Innovation Plan of Southwest Hospital (SWH2016ZDCX1007)

More Information
  • Corresponding author: DENG Guohong, gh_deng@hotmail.com (ORCID: 0000-0003-1263-7220)
  • Received Date: 2022-08-14
  • Accepted Date: 2022-10-14
  • Published Date: 2023-04-20
  • Crigler-Najjar syndrome (CNS) is an autosomal recessive disorder in which the content of plasma unconjugated bilirubin is increased due to the reduction or complete deficiency of the activity of bilirubin uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1), classified as CNS type Ⅰ and Ⅱ. CNS type Ⅰ is the most severe, which will develop into kernicterus, damage the brain nervous system, and even threaten the life of patients. This article introduces six CNS treatment techniques, including phototherapy, plasma exchange, drug therapy, liver transplantation, hepatocyte transplantation and gene therapy. The applicable patient types, treatment effects and existing deficiencies of each technique were summarized. Phototherapy, plasma exchange, drug therapy and hepatocyte transplantation can temporarily control serum levels and reduce the risk of jaundice, but cannot completely restore UGT1A1 enzyme activity; liver transplantation is currently the only treatment option for CNS type Ⅰ patients, but is limited by suitable liver donors and post-operative immune rejection. Gene therapy has the most promising application in the treatment of genetic disorders such as CNS, which can provide more viable therapeutic techniques for CNS patients.

     

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