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Article

Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis

  • Authors:
    • Xiu‑Fang Yang
    • Guo‑Sheng Liu
    • Min‑Xu Li
  • View Affiliations / Copyright

    Affiliations: Department of Neonatology, Zhongshan People's Hospital Affiliated to Sun Yat‑sen University, Zhongshan, Guangdong 528403, P.R. China, Department of Neonatology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong 510630, P.R. China, Dongguan Maternal and Child Health Center, Dongguan, Guangdong 523000, P.R. China
  • Pages: 2361-2365
    |
    Published online on: October 14, 2015
       https://doi.org/10.3892/etm.2015.2800
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Abstract

The aim of this study was to investigate mutations of multidrug resistance 3 (MDR3) exons 9 and 23 in infants with parenteral nutrition‑associated cholestasis (PNAC). A total of 41 infants with PNAC were enrolled in the study. Genomic DNA was extracted from the peripheral venous blood leukocytes of each patient and MDR3 exons 9 and 23 were amplified by polymerase chain reaction. One patient was identified who carried a frameshift mutation in MDR3 exon 23 (C.2793) that was caused by the insertion of a single adenine residue, while mutations were not found in MDR3 exon 23 in the other 40 patients. The clinical features of the patient with the MDR3 exon 23 frameshift mutation included high serum γ-glutamyl transferase levels, the absence of biliary dilatation and deformity in magnetic resonance cholangiopancreatography, and abnormal electrical capacitance tomography imaging of the liver. No mutations in MDR3 exon 9 were identified in any of the patients. All 41 PNAC patients recovered following oral ursodeoxycholic acid treatment. The C.2793 frameshift mutation in MDR3 exon 23 is potentially associated with the development of PNAC in infants.
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Copy and paste a formatted citation
Spandidos Publications style
Yang XF, Liu GS and Li MX: Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis. Exp Ther Med 10: 2361-2365, 2015.
APA
Yang, X., Liu, G., & Li, M. (2015). Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis. Experimental and Therapeutic Medicine, 10, 2361-2365. https://doi.org/10.3892/etm.2015.2800
MLA
Yang, X., Liu, G., Li, M."Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis". Experimental and Therapeutic Medicine 10.6 (2015): 2361-2365.
Chicago
Yang, X., Liu, G., Li, M."Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis". Experimental and Therapeutic Medicine 10, no. 6 (2015): 2361-2365. https://doi.org/10.3892/etm.2015.2800
Copy and paste a formatted citation
x
Spandidos Publications style
Yang XF, Liu GS and Li MX: Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis. Exp Ther Med 10: 2361-2365, 2015.
APA
Yang, X., Liu, G., & Li, M. (2015). Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis. Experimental and Therapeutic Medicine, 10, 2361-2365. https://doi.org/10.3892/etm.2015.2800
MLA
Yang, X., Liu, G., Li, M."Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis". Experimental and Therapeutic Medicine 10.6 (2015): 2361-2365.
Chicago
Yang, X., Liu, G., Li, M."Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis". Experimental and Therapeutic Medicine 10, no. 6 (2015): 2361-2365. https://doi.org/10.3892/etm.2015.2800
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