Literature DB >> 31278756

Prenatal diagnosis of methylmalonic aciduria from amniotic fluid using genetic and biochemical approaches.

Xing Ji1,2, Huanhuan Wang1,2, Jun Ye1,2, Wenjuan Qiu1,2, Huiwen Zhang1,2, Lili Liang1,2, Bing Xiao1,2, Mengyao Dai1,2, Yan Xu1,2, Ting Chen1,2, Feng Xu1,2, Yingwei Chen2, Weiping Ye2, Xuefan Gu1,2, Lei Wang2, Lianshu Han1,2.   

Abstract

OBJECTIVES: This study reported the clinical prenatal diagnosis experience of families affected by methylmalonic acidemia (MMA) evaluated at a single prenatal diagnosis center over 8 years, and the reliability of a biochemical approach for prenatal diagnosis was analyzed.
METHODS: Prenatal diagnosis data for 187 MMA families referred to our center from 2009 to 2016 were reviewed retrospectively. The results of the genetic analysis and biochemical approach were compared.
RESULTS: A total of 41 MMA-affected pregnancies (21%) were identified. The biochemical analysis could identify the true status of 99.5% of fetuses. The diagnostic sensitivities of the propionylcarnitine (C3) level, the C3 to acetylcarnitine (C2) ratio (C3/C2), the methylmalonic acid, and methylcitrate levels in the amniotic fluid were 95.1%, 100%, 100%, and 82.9%, respectively, and the specificities were 98.7%, 99.3%, 97.4%, and 96.7%, respectively.
CONCLUSIONS: The biochemical analysis could be optionally used in the prenatal diagnosis of MMA, especially in cases where the genetic results are inconclusive. Among the four tested biochemical markers, C3/C2 appeared to be the most reliable.
© 2019 John Wiley & Sons, Ltd.

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Year:  2019        PMID: 31278756     DOI: 10.1002/pd.5519

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  7 in total

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

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7.  Noninvasive Prenatal Testing of Methylmalonic Acidemia cblC Type Using the cSMART Assay for MMACHC Gene Mutations.

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  7 in total

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