Literature DB >> 20357240

Maternal methylenetetrahydrofolate reductase (MTHFR) homozygosity and neonatal outcome: follow-up of 42 pregnancies at risk.

Laura Pogliani1, Luisa Muggiasca, Luisa Arrigoni, Edoardo Rossi, Gianvincenzo Zuccotti.   

Abstract

From February 2006 to March 2008, 42 pregnant women homozygous for the 677CT-methylenetetrahydrofolate reductase (MTHFR) allele were recruited in our obstetrics service for pregnancy at risk. All had antithrombotic prophylaxis with low-dose aspirin and/or low-molecular-weight heparin, supplemented with folic acid. In all, 2 women lost the fetus and 4 were lost to follow-up before delivery. A total of 36 women delivered term infants who all underwent transfontanellar ultrasonography within 24 hours of birth. Six (16.6%) had ischemic or hemorrhagic cerebral lesions. No differences were observed in gestational age, birth weight, or umbilical cord pH between the 30 healthy infants and the 6 with cerebral lesions. Neonatal outcomes were negative in spite of maternal folic acid supplementation and antithrombotic prophylaxis during pregnancy. This suggests a relationship between maternal homozygous mutation in the 677CT-MTHFR allele and neonatal cerebral lesions.

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Year:  2010        PMID: 20357240     DOI: 10.1177/0883073809344622

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  5 in total

1.  Maternal Interleukin Genotypes Are Associated With NICU Outcomes Among Low-Birth-Weight Infants.

Authors:  Kelley L Baumgartel; Maureen W Groer; Susan M Cohen; Dianxu Ren; Diane L Spatz; Yvette P Conley
Journal:  Biol Res Nurs       Date:  2016-09-20       Impact factor: 2.522

2.  Candidate single-nucleotide polymorphisms and cerebral palsy: A case-control study.

Authors:  Xiao-Guang He; Q I Peng; Yan-Hua Chen; Ting He; Hui Huang; Ze-Ke Ma; Xue-Jin Fan; Ling Luo; Shao-Ji Liu; Xiao-Mei Lu
Journal:  Biomed Rep       Date:  2015-09-25

3.  Thrombus obstructing the right ventricle outflow tract in a neonate with methylenetetrahydrofolate reductase 677TT genotype.

Authors:  Lubica Kovacikova; Peter Skrak; Martin Zahorec
Journal:  Eur J Pediatr       Date:  2011-03-08       Impact factor: 3.183

4.  Cerebral ultrasound abnormalities in offsprings of women with C677T homozygous mutation in the MTHFR gene: a prospective study.

Authors:  Laura Pogliani; Chiara Cerini; Francesca Penagini; Piergiorgio Duca; Chiara Mameli; Gian Vincenzo Zuccotti
Journal:  World J Pediatr       Date:  2014-06-28       Impact factor: 2.764

5.  Hyperhomocysteinemia and MTHFR polymorphisms as antenatal risk factors of white matter abnormalities in two cohorts of late preterm and full term newborns.

Authors:  Lucia M Marseglia; Antonio Nicotera; Vincenzo Salpietro; Elisa Giaimo; Giovanna Cardile; Maria Bonsignore; Angela Alibrandi; Daniela Caccamo; Sara Manti; Gabriella D'Angelo; Carmelo Mamì; Gabriella Di Rosa
Journal:  Oxid Med Cell Longev       Date:  2015-02-10       Impact factor: 6.543

  5 in total

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