Literature DB >> 20499271

No mitochondrial DNA deletions but more D-loop point mutations in repeated pregnancy loss.

Seyed Mohammad Seyedhassani1, Massoud Houshmand, Seyed Mehdi Kalantar, Glayol Modabber, Abbas Aflatoonian.   

Abstract

PURPOSE: repeated pregnancy loss (RPL) occurs in 1 out of 300 couples, and the cause of about 50% of them remains idiopathic. Mitochondria have an important role in human development through ATP production and their involvement in apoptosis.
METHODS: 96 RPL and 96 control females were used to investigate the frequency of deletions and point mutations in the displacement loop (D-loop) on mitochondria. Multiplex PCR and DNA sequencing methods were used to detect possible variations in the mitochondrial DNA (mtDNA).
RESULTS: no deletions but a high frequency of point mutations were found in RPL females; among 129 variations observed in RPL, 22 mutations were significant (P < 0.05) and the insertion of C in nucleotide 114 was novel.
CONCLUSION: high rate of mutations in D-loop of mtDNA was observed in maternal blood, a fact that may have a direct or indirect role in inducing RPL. The results can be used in the assessment of RPL and designing possible treatments for improving assisted reproduction.

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Year:  2010        PMID: 20499271      PMCID: PMC2995430          DOI: 10.1007/s10815-010-9435-2

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


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