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Licensed Unlicensed Requires Authentication Published by De Gruyter June 30, 2021

Neonatal maple syrup urine disease in China: two novel mutations in the BCKDHB gene and literature review

  • Hong‐Hua Jiang , Yan Guo , Xian Shen , Ying Wang , Ting-Ting Dai , Hui Rong , Rui Cheng EMAIL logo and Fei Zhao EMAIL logo

Abstract

Objectives

To report two novel mutations in the BCKDHB gene with Maple syrup urine disease (MSUD) and compare their data with 52 cases of MSUD reported in the available Chinese literature.

Methods

Clinical data of a case of a newborn with MSUD was retrospectively studied. Literatures on MSUD in the local medical journals from January 1990 till December 2019 in China were reviewed.

Results

Two novel BCKDHB mutations c.90_91insCTGGCGCGGGG (p.Phe35TrpfsTer41) and c.80_90del (p.Ala32PhefsTer48) were identified. We found a total of 52 cases of MSUD reports so far. A total of 49 cases had the symptom of poor feeding (94.2%), 50 cases showed poor responses to stimulation (96.2%), 21 cases had odor of maple syrup (40.3%), 29 cases had seizures (55.7%), and 13 cases had respiratory failure (25.0%). The average of the blood ammonia was 127.2 ± 75.0 μmol/L. A total of 18 cases reported the gene testing, among of them 9 cases of BCKDHA mutations, 6 cases of BCKDHB mutations, and 2 cases of DBT mutations. A total of 13 cases (25%) were treated with mechanical ventilation, 50 cases (96.2%) with protein-restricted diet and l-carnitine, 29 cases with thiamine, and only 2 cases were treated with blood purification. Finally, 19 patients (36.5%) were died, 21 cases (40.4%) were improved after treatments.

Conclusions

The clinical phenotype of neonatal MSUD in China belongs to the classical type currently. Suspected patients should have blood or urine branched-chain amino acid levels tested and brain MRI as early as possible to enable early diagnosis, thus improvement in prognosis.


Corresponding authors: Rui Cheng, Department of Neonatology, Nanjing Children’s Hospital of Nanjing Medical University, 72 Guangzhou Road, Nanjing, Jiangsu 210008, China, E-mail: ; and Fei Zhao, Department of Nephrology, Nanjing Children’s Hospital of Nanjing Medical University, 72 Guangzhou Road, Nanjing, Jiangsu 210008, China, E-mail:
Rui Cheng and Fei Zhao contributed equally to this work.

Acknowledgments

Our heartfelt thanks go to all doctors and nurses in the Department of Neonatology of Nanjing Children’s Hospital for the cooperation during the patient’s hospitalization. The authors are grateful to the patient and their parents for their contribution to the study. We would like to thank Kangso (Beijing) Medical Laboratory for technical support.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The local Institutional Review Board deemed the study exempt from review.

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Received: 2020-12-31
Accepted: 2021-05-31
Published Online: 2021-06-30
Published in Print: 2021-09-27

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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