Literature DB >> 16796900

[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].

Xin Liu1, Pu Dai, De-liang Huang, Hui-jun Yuan, Wei-min Li, Ju-yang Cao, Fei Yu, Rui-ning Zhang, Hong-yan Lin, Xiu-hui Zhu, Yong He, You-jun Yu, Kun Yao.   

Abstract

OBJECTIVE: To explore the necessity of large-scale screening of mtDNA A1555G mutation in prevention of aminoglycoside antibiotic induced deafness (AAID) and to develop a feasible method to prevent AAID.
METHODS: A total of 1836 patients with non-syndromic hearing impairment (NSHI), 1352 students of schools for deaf-mutes in 11 provinces and municipality in China, 413 out-patients, and 71 persons from the families with maternal relatives suffering from AAID, underwent questionnaire survey and/or PCR for A-to-G mutation at nucleotide 1555 of the mitochondrial genome.
RESULTS: Sixty three patients with mtDNA A1555G mutation were found among the 1836 NSHI patients. Fifty-two maternal pedigrees were identified. 536 cases with normal hearing from these pedigrees were informed to avoid using aminoglycoside antibiotics (AmAn).
CONCLUSION: Large-scale screening of mtDNA A1555G mutation and relevant health education to avoid use of AmAn are effective to prevent ototoxicity in the A1555G carriers and their maternal relatives.

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Year:  2006        PMID: 16796900

Source DB:  PubMed          Journal:  Zhonghua Yi Xue Za Zhi        ISSN: 0376-2491


  6 in total

1.  Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.

Authors:  Pu Dai; Li-Hui Huang; Guo-Jian Wang; Xue Gao; Chun-Yan Qu; Xiao-Wei Chen; Fu-Rong Ma; Jie Zhang; Wan-Li Xing; Shu-Yan Xi; Bin-Rong Ma; Ying Pan; Xiao-Hua Cheng; Hong Duan; Yong-Yi Yuan; Li-Ping Zhao; Liang Chang; Ru-Zhen Gao; Hai-Hong Liu; Wei Zhang; Sha-Sha Huang; Dong-Yang Kang; Wei Liang; Ke Zhang; Hong Jiang; Yong-Li Guo; Yi Zhou; Wan-Xia Zhang; Fan Lyu; Ying-Nan Jin; Zhen Zhou; Hong-Li Lu; Xin Zhang; Ping Liu; Jia Ke; Jin-Sheng Hao; Hai-Meng Huang; Di Jiang; Xin Ni; Mo Long; Luo Zhang; Jie Qiao; Cynthia Casson Morton; Xue-Zhong Liu; Jing Cheng; De-Min Han
Journal:  Am J Hum Genet       Date:  2019-09-26       Impact factor: 11.025

2.  A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China.

Authors:  Junzhen Zhu; Qinying Cao; Ning Zhang; Jun Ge; Donglan Sun; Qingqi Feng
Journal:  Intractable Rare Dis Res       Date:  2015-08

3.  Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing.

Authors:  Pingsen Zhao; Lifang Lin; Liubing Lan
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

4.  Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.

Authors:  Yongyi Yuan; Yiwen You; Deliang Huang; Jinghong Cui; Yong Wang; Qiang Wang; Fei Yu; Dongyang Kang; Huijun Yuan; Dongyi Han; Pu Dai
Journal:  J Transl Med       Date:  2009-09-10       Impact factor: 5.531

5.  Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.

Authors:  Yi Jiang; Shasha Huang; Tao Deng; Lihua Wu; Juan Chen; Dongyang Kang; Xiufeng Xu; Ruiyu Li; Dongyi Han; Pu Dai
Journal:  PLoS One       Date:  2015-08-07       Impact factor: 3.240

6.  Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening.

Authors:  Cai-Xia Li; Qian Pan; Yong-Gang Guo; Yan Li; Hua-Fang Gao; Di Zhang; Hao Hu; Wan-Li Xing; Keith Mitchelson; Kun Xia; Pu Dai; Jing Cheng
Journal:  Hum Mutat       Date:  2008-02       Impact factor: 4.878

  6 in total

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