Literature DB >> 2414312

Discordant and variable production of human chorionic gonadotropin and its free alpha- and beta-subunits in early pregnancy.

D L Hay.   

Abstract

Monoclonal antibodies specific to dimer hCG (alpha beta), free beta-subunit (beta hCG), free alpha-subunit (alpha hCG), and total beta hCG (dimer + free beta hCG) were used to monitor discordant production of hCG and its subunits during the early stages of embryo implantation. Sera collected 3 to 22 days postovum retrieval were assayed from patients participating in an in vitro fertilization program. In the majority of patients with ongoing pregnancies (n = 16), rising levels using the dimer hCG assay were first detected at an average time of 9.2 days post retrieval compared to 8.3 days for the total beta hCG assay and 6.5 days for the free beta hCG assays. Between days 5 to 9 after retrieval, the rises in the total beta hCG assay were due to predominantly free beta hCG subunit production. The proportion of total beta hCG levels due to free beta hCG subunits declined progressively from day 9 to less than 5% by day 22. Free alpha hCG levels remained low with rising levels first detected from day 18. A second group of patients (n = 12) had delayed, slowly rising levels in the total beta hCG assay which were first detected at an average of 12.4 days and associated with mainly biochemical pregnancies (n = 10). In these patients, rising total beta hCG levels were due to predominantly free beta hCG production. The subsequent loss of their pregnancy may be due to poor luteal support associated with delayed rises in dimer hCG levels. In nonconceptual cycles (n = 47) no significant rises were detected in dimer or free hCG subunits. Although the major form of hCG in circulation is dimer hCG, the origin of free beta hCG production in the early stages of implantation may be due to poorly differentiated trophoblastic tissue. Thus falling levels of free beta hCG subunits associated with increasing dimer hCG production may reflect increasing alpha hCG production by the proliferating layer of cytotrophoblastic cells.

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Year:  1985        PMID: 2414312     DOI: 10.1210/jcem-61-6-1195

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  5 in total

1.  Measurement of human chorionic gonadotropin during early pregnancy: a comparison of two immunoradiometric assays.

Authors:  P L Matson; M C Newman; D Morroll; S A Troup; B A Lieberman
Journal:  J In Vitro Fert Embryo Transf       Date:  1990-06

2.  How positive is a positive pregnancy test?

Authors:  T Lind; P G Whittaker
Journal:  Br Med J (Clin Res Ed)       Date:  1988-03-12

3.  Serial evaluation of vasopressin release and thirst in human pregnancy. Role of human chorionic gonadotrophin in the osmoregulatory changes of gestation.

Authors:  J M Davison; E A Shiells; P R Philips; M D Lindheimer
Journal:  J Clin Invest       Date:  1988-03       Impact factor: 14.808

4.  Predictive value of plasma human chorionic gonadotrophin beta subunit in diagnosing ectopic pregnancy after in vitro fertilisation and embryo transfer.

Authors:  S H Okamoto; D L Healy; L M Morrow; P A Rogers; A O Trounson; E C Wood
Journal:  Br Med J (Clin Res Ed)       Date:  1987-03-14

5.  Urinary gonadotropin fragment (UGF) measurements in the diagnosis and management of ovarian cancer.

Authors:  L A Cole; J H Nam
Journal:  Yale J Biol Med       Date:  1989 Jul-Aug
  5 in total

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