Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (21)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Hashimoto, K.
Right arrow Articles by Murata, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hashimoto, K.
Right arrow Articles by Murata, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 14, No. 7, 1872-1874, July 1999
© 1999 European Society of Human Reproduction and Embryology

The factor V Leiden mutation in Japanese couples with recurrent spontaneous abortion

Kazumasa Hashimoto1,2,5, Yoshie Shizusawa2, Koichiro Shimoya2,3, Kazutomo Ohashi2, Takashi Shimizu4, Chihiro Azuma2 and Yuji Murata2

1 Department of Obstetrics and Gynecology, Case Western Reserve University at Metro Health Medical Center, 2500 Metro Health Drive, Cleveland, OH 44109–1998, USA, 2 Department of Obstetrics and Gynecology, Faculty of Medicine, Osaka University 2–2, Yamadaoka, Suita, Osaka, 565-0871, 3 Department of Obstetrics and Gynecology, Osaka Police Hospital, 10–31 Kitayama-cho, Tennouji-ku, Osaka 543-8502 and 4 Shimizu Women's Clinic, 2–2–4 Minamiguchi, Takarazuka, Hyogo, 665-0011, Japan

Thrombosis of placental vessels can be a major cause of recurrent spontaneous abortion (RSA). The factor V Leiden (FVL) mutation, a single point mutation in the factor V gene, is the most common genetic predisposition to thrombosis in European countries and the United States. However, even among Caucasian populations, the association between the FVL mutation and RSA is still controversial. The objectives of the present study were to investigate the prevalence of the FVL mutation in Japanese women who have experienced RSA and to clarify the contribution of the FVL mutation to recurrent miscarriages. A total of 52 Japanese women with a history of three or more consecutive idiopathic first trimester miscarriages and 41 of their male partners were studied. The control group consisted of 55 parous women without obstetric complications. Peripheral blood cell DNA was examined for the presence of the FVL alleles by polymerase chain reaction with Mnl I restriction fragment length polymorphisms. None of the 52 women with RSA and the 41 partners carried the mutation. We also found no subject carrying the FVL alleles in the control group. These results suggest that the FVL alleles are not concentrated in women with RSA at least to clinically significant levels and that there is no apparent association between the FVL mutation and RSA in our Japanese population.

Key words: factor V Leiden mutation/recurrent spontaneous abortion

5 To whom correspondence should be addressed


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Arch Intern MedHome page
G. Kovalevsky, C. R. Gracia, J. A. Berlin, M. D. Sammel, and K. T. Barnhart
Evaluation of the Association Between Hereditary Thrombophilias and Recurrent Pregnancy Loss: A Meta-analysis
Arch Intern Med, March 8, 2004; 164(5): 558 - 563.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
J. K. Lynch, K. B. Nelson, C. J. Curry, and J. K. Grether
Cerebrovascular Disorders in Children With the Factor V Leiden Mutation
J Child Neurol, October 1, 2001; 16(10): 735 - 744.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.