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Molecular epidemiologic study of citrin deficiency by screening for four reported pathogenic SLC25A13 variants in the Shaanxi and Guangdong provinces, China.

Authors :
Lin WX
Yaqub MR
Zhang ZH
Mao M
Zeng HS
Chen FP
Li WM
Cai WZ
Li YQ
Tan ZY
Sheng W
Li ZM
Tao XL
Li YX
Zhang JP
Han YB
Li Y
Duan WQ
Ye BN
Li YR
Song YZ
Source :
Translational pediatrics [Transl Pediatr] 2021 Jun; Vol. 10 (6), pp. 1658-1667.
Publication Year :
2021

Abstract

Background: Citrin deficiency (CD) is an autosomal recessive disease resulting from biallelic mutations of the SLC25A13 gene. This study aimed to investigate the molecular epidemiological features of CD in the Guangdong and Shaanxi provinces of China.<br />Methods: A total of 3,409 peripheral blood samples from Guangdong and 2,746 such samples from Shaanxi province were collected. Four prevalent SLC25A13 mutations NG_012247.2 (NM_014251.3): c.852_855del, c.1638_1660dup, c.615+5G>A, and c.1751-5_1751-4ins(2684) were screened by using the conventional polymerase chain reaction (PCR)/PCR-restriction fragment length polymorphism and newly-developed multiplex PCR methods, respectively. The mutated SLC25A13 allele frequencies, carrier frequencies, and CD morbidity rates were calculated and then compared with the Chi-square and Fisher's exact tests.<br />Results: The mutations were detected in 68 out of 6,818 SLC25A13 alleles in Guangdong and 29 out of 5,492 alleles in the Shaanxi population. The carrier frequencies were subsequently calculated to be 1/51 and 1/95, while the CD morbidity rates were 1/10,053 and 1/35,865, in the 2 populations, respectively. When compared with the Shaanxi population, Guangdong exhibited a higher frequency of mutated SLC25A13 allele (68/6,818 vs. 29/5,492, χ <superscript>2</superscript> =8.570, P=0.003) in general, with higher c.852_855del (54/6,818 vs. 13/5,492, χ <superscript>2</superscript> =17.328, P=0.000) but lower c.1751-5_1751 -4ins(2684) (2/6,818 vs. 9/5,492, P=0.015) allele frequencies. The distribution of c.615+5G>A and c.1638_1660dup between the 2 provinces, as well as all 4 prevalent mutations among different geographic regions within the 2 provinces, did not differed significantly.<br />Conclusions: Our findings depicted the CD molecular epidemiological features in Guangdong and Shaanxi populations, providing preliminary but significant laboratory evidences for the subsequent CD diagnosis and management in the 2 provinces of mainland China.<br />Competing Interests: Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tp-21-58). The authors have no conflicts of interest to declare.<br /> (2021 Translational Pediatrics. All rights reserved.)

Details

Language :
English
ISSN :
2224-4344
Volume :
10
Issue :
6
Database :
MEDLINE
Journal :
Translational pediatrics
Publication Type :
Academic Journal
Accession number :
34295780
Full Text :
https://doi.org/10.21037/tp-21-58