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Role of Activins in Embryo Implantation and Diagnosis of Ectopic Pregnancy: a Review

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Publisher Biomed Central
Date 2014 Nov 26
PMID 25421645
Citations 7
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Abstract

Embryo implantation is a major prerequisite for the successful establishment of pregnancy. Ectopic implantation outside the intrauterine cavity and the development of ectopic pregnancy (EP) is a major cause of maternal morbidity and occasionally mortality during the first trimester. EP may be induced by failure of tubal transport and/or increased tubal receptivity. Activins, their type II receptors and follistatin have been localised in the human endometrial and tubal epithelium and they are major regulators of endometrial and tubal physiology during the menstrual cycle. Pathological expression of activins and their binding protein, follistatin, was observed in tissue and serum samples collected from EP. Several studies with different designs investigated the diagnostic value of a single measurement of serum activin-A in the differentiation between normal intrauterine and failing early pregnancy and the results are controversial. Nevertheless, the diagnostic value of activins in EP, including the other activin isoforms (activin-B and -AB) and follistatin, merits further research. This review appraises the data to date researching the role of activins in the establishment of normal pregnancy and, pathogenesis and diagnosis of tubal EP.

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References
1.
Refaat B, Bahathiq A, Sockanathan S, Stewart R, Wells M, Ledger W . Production and localization of activins and activin type IIA and IIB receptors by the human endosalpinx. Reproduction. 2004; 128(2):249-55. DOI: 10.1530/rep.1.00156. View

2.
Hajenius P, Mol F, Mol B, Bossuyt P, Ankum W, van der Veen F . Interventions for tubal ectopic pregnancy. Cochrane Database Syst Rev. 2007; (1):CD000324. PMC: 7043290. DOI: 10.1002/14651858.CD000324.pub2. View

3.
Brown C, Woodruff T, Matzuk M . Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functions. Nat Genet. 2000; 25(4):453-7. DOI: 10.1038/78161. View

4.
Thompson T, Lerch T, Cook R, Woodruff T, Jardetzky T . The structure of the follistatin:activin complex reveals antagonism of both type I and type II receptor binding. Dev Cell. 2005; 9(4):535-43. DOI: 10.1016/j.devcel.2005.09.008. View

5.
Cartwright J, Duncan W, Critchley H, Horne A . Serum biomarkers of tubal ectopic pregnancy: current candidates and future possibilities. Reproduction. 2009; 138(1):9-22. DOI: 10.1530/REP-09-0060. View