Literature DB >> 15908288

Prenatal diagnosis for organic acid disorders using two mass spectrometric methods, gas chromatography mass spectrometry and tandem mass spectrometry.

Yuki Hasegawa1, Misako Iga, Masahiko Kimura, Yosuke Shigematsu, Seiji Yamaguchi.   

Abstract

We performed prenatal diagnosis of organic acid disorders using two mass spectrometric methods; gas chromatography mass spectrometry (GC/MS) and tandem mass spectrometry (ESI/MS/MS). Of 28 cases whose amniotic fluid was tested, 11 cases were diagnosed as "affected". All cases whose samples were diagnosed as "unaffected" were confirmed to have no symptoms or abnormalities in urinary organic acid analysis after birth. Of the 11 "affected" cases, two cases were missed by ESI/MS/MS but not by GC/MS. When the stability of metabolites in amniotic fluid was checked, it was found that acylcarnitines degraded in one week at room temperature, whereas organic acids such as methylmalonate or methylcitrate were stable for at least 14 days. Prenatal diagnosis by analysis using simultaneous two or more methods may be more reliable, though attention should be paid to sample transportation conditions.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15908288     DOI: 10.1016/j.jchromb.2005.04.020

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  6 in total

1.  Prenatal Diagnosis of Isovaleric Acidemia From Amniotic Fluid Using Genetic and Biochemical Approaches.

Authors:  Si Ding; Lili Liang; Wenjuan Qiu; Huiwen Zhang; Bing Xiao; Liping Dong; Wenjun Ji; Feng Xu; Zhuwen Gong; Xuefan Gu; Lei Wang; Lianshu Han
Journal:  Front Genet       Date:  2022-06-30       Impact factor: 4.772

Review 2.  Current medical research with the application of coupled techniques with mass spectrometry.

Authors:  Joanna Kałużna-Czaplińska
Journal:  Med Sci Monit       Date:  2011-05

3.  A fetus with mitochondrial trifunctional protein deficiency: Elevation of 3-OH-acylcarnitines in amniotic fluid functionally assured the genetic diagnosis.

Authors:  Ryosuke Bo; Yuki Hasegawa; Kenji Yamada; Hironori Kobayashi; Takeshi Taketani; Seiji Fukuda; Seiji Yamaguchi
Journal:  Mol Genet Metab Rep       Date:  2015-12-05

4.  Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduria.

Authors:  Yupeng Liu; Zhehui Chen; Lulu Kang; Ruxuan He; Jinqing Song; Yi Liu; Chunyan Shi; Junya Chen; Hui Dong; Yao Zhang; Yanyan Ma; Tongfei Wu; Qiao Wang; Yuan Ding; Xiyuan Li; Dongxiao Li; Mengqiu Li; Ying Jin; Jiong Qin; Yanling Yang
Journal:  PLoS One       Date:  2022-03-31       Impact factor: 3.240

5.  Variable phenotypes and outcomes associated with the MMACHC c.609G>A homologous mutation: long term follow-up in a large cohort of cases.

Authors:  Ruxuan He; Ruo Mo; Ming Shen; Lulu Kang; Jinqing Song; Yi Liu; Zhehui Chen; Hongwu Zhang; Hongxin Yao; Yupeng Liu; Yao Zhang; Hui Dong; Ying Jin; Mengqiu Li; Jiong Qin; Hong Zheng; Yongxing Chen; Dongxiao Li; Haiyan Wei; Xiyuan Li; Huifeng Zhang; Min Huang; Chunyan Zhang; Yuwu Jiang; Desheng Liang; Yaping Tian; Yanling Yang
Journal:  Orphanet J Rare Dis       Date:  2020-08-03       Impact factor: 4.123

6.  Biochemical and genetic approaches to the prenatal diagnosis of propionic acidemia in 78 pregnancies.

Authors:  Mengyao Dai; Bing Xiao; Huiwen Zhang; Jun Ye; Wenjuan Qiu; Hong Zhu; Lei Wang; Lili Liang; Xia Zhan; Wenjun Ji; Yu Wang; Yongguo Yu; Xuefan Gu; Lianshu Han
Journal:  Orphanet J Rare Dis       Date:  2020-10-07       Impact factor: 4.123

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.