Journal
CLINICAL BIOCHEMISTRY
Volume 42, Issue 4-5, Pages 380-386Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.clinbiochem.2008.12.003
Keywords
Homocysteine; Recurrent pregnancy loss; Methylene tetrahydrofolate reductase; Polymorphism; DNA damage
Categories
Funding
- Government of India
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Objectives: To investigate the association of parental hyperhomocysteinemia, C677T Methylene tetrahydrofolate reductase (MTHFR) polymorphism and DNA damage with recurrent pregnancy loss (RPL). Design and methods: A case-control study. Reverse phase HPLC, PCR-RFLP and Cytokinesis blocked micronuclei assay were used to assess total plasma homocysteine, C677T MTHFR polymorphism and DNA damage respectively. Student t-test, ANOVA and Fisher exact test were used for statistical analysis. Results: Maternal [mean: 11.6 +/- 5.0 versus 8.6 +/- 4.2 mu mol/L, odds ratio (OR): 4.48] and paternal [mean: 19.6 +/- 9.5 versus 14.2 +/- 7.4 mu mol/L, OR: 6.92] hyperhomocysteinemia, paternal age [OR: 1.16], paternal MTHFR 677T allele [OR: 2.30] and DNA damage were found to increase the risk for RPL. DNA damage showed positive correlation with plasma homocysteine and MTHFR 677T allele. Conclusions: Parental hyperhomocysteinemia, paternal age, paternal C677T MTHFR polymorphism and DNA damage are fisk factors for RPL. DNA damage showed positive correlation with plasma homocysteine and MTHFR 677T allele. (C) 2008 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
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