Unbound MEDLINE

Association of anticardiolipin antibody and C677T in methylenetetrahydrofolate reductase mutation in women with recurrent spontaneous abortions: a new path to thrombophilia? São Paulo medical journal = Revista paulista de medicina. [Sao Paulo Med J] Journal article

 
TitleAssociation of anticardiolipin antibody and C677T in methylenetetrahydrofolate reductase mutation in women with recurrent spontaneous abortions: a new path to thrombophilia?
Author(s)Couto E, Barini R, Zaccaria R, Annicchino-Bizzacchi JM, Passini Junior R, Pereira BG, Silva JC, Pinto e Silva JL 
InstitutionUniversidade Estadual de Campinas, São Paulo, Brazil. egle@unicamp.br
SourceSao Paulo Med J 2005 Jan 2; 123(1):15-20.
MeSHAbortion, Habitual
Antibodies, Anticardiolipin
Biological Markers
Case-Control Studies
Enzyme-Linked Immunosorbent Assay
Female
Humans
Methylenetetrahydrofolate Reductase (NADPH2)
Mutation
Nucleic Acid Amplification Techniques
Polymerase Chain Reaction
Pregnancy
Pregnancy Complications, Hematologic
Research Support, Non-U.S. Gov't
Risk Factors
Thrombophilia
AbstractCONTEXT: Recurrent spontaneous abortion (RSA) has been associated with venous thrombosis in the mother. Acquired and inherited thrombophilia factors are possible causes.
OBJECTIVE: To evaluate the association between thrombogenic factors and recurrent spontaneous abortion. TYPE OF STUDY: Case-control study.
SETTING: Centro de Atenção Integral à Saúde da Mulher, Universidade Estadual de Campinas.
METHODS: 40 ml of blood was collected from 88 women attending an RSA clinic and 88 fertile women attending a family planning clinic, to evaluate the presence of acquired and inherited thrombophilia factors. Anticardiolipin antibodies (ACA), lupus anticoagulant and deficiencies of proteins C and S and antithrombin III were evaluated by enzyme-linked immunosorbent assay (ELISA), dilute Russell Viper Venom time (dRVVT), coagulometric and chromogenic methods. DNA was amplified by the polymerase chain reaction (PCR) to study factor V Leiden and G20210A mutations in the prothrombin gene and C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene. Data were analyzed using odds ratios and a regression model for age adjustment. Fishers exact test was used to evaluate statistical relationships between associated factors and RSA.
RESULTS: ACA was detected in 11 women with RSA and one fertile woman. Heterozygous C677T was detected in 59 women with RSA and 35 fertile women. Concomitant presence of ACA and C677T was found in eight women with RSA and no fertile women (p < 0.01).
DISCUSSION: The meaning of the association between C677T mutation in the MTHFR gene and ACA is still not clear. It is possible that an inherited factor that alone would not strongly predispose a woman to thrombosis could, when associated with an acquired factor, start the process and increase the likelihood of thrombosis expression.
CONCLUSIONS: ACA and C677T in the MTHFR gene are statistically associated with RSA. The association of these two conditions is a new finding in thrombogenic factors and RSA.
Languageeng
Pub Type(s)Journal Article
PubMed ID15821810
  
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