Literature DB >> 2503176

Inhibin: a new circulating marker of hydatidiform mole?

T Yohkaichiya1, T Fukaya, H Hoshiai, A Yajima, D M de Kretser.   

Abstract

OBJECTIVE: To define the concentrations of inhibin in serum and tissue of patients with hydatidiform mole and assess their value as a clinical marker of the condition.
DESIGN: Prospective study of new patients with hydatidiform mole, comparison of paired observations, and case-control analysis.
SETTING: A university hospital, two large public hospitals, and a private women's clinic in Japan. PATIENTS: Seven consecutive referred patients seen over four months with newly diagnosed complete hydatidiform mole, including one in whom the mole was accompanied by viable twin fetuses (case excluded from statistical analysis because of unique clinical features). All patients followed up for six months after evacuation of molar tissue. END POINT: Correlation of serum inhibin concentrations with trophoblastic disease.
MEASUREMENTS AND MAIN RESULTS: Serum concentrations of inhibin, human chorionic gonadotrophin, and follicle stimulating hormone were compared before and seven to 10 days after evacuation of the mole. Before evacuation the serum inhibin concentrations (median 8.3 U/ml; 95% confidence interval 2.4 to 34.5) were significantly greater than in 21 normal women at the same stage of pregnancy (2.8 U/ml; 2.1 to 3.6), and inhibin in molar tissue was also present in high concentrations (578 U/ml cytosol; 158 to 1162). Seven to 10 days after evacuation inhibin concentrations in serum samples from the same patients declined significantly to values (0.4 U/ml; 0.1 to 1.4) similar to those seen in the follicular phase of normal menstrual cycles. None of the four patients whose serum inhibin concentrations were 0.4 U/ml or less after evacuation developed persistent trophoblastic disease. Though serum human chorionic gonadotrophin concentrations declined after evacuation (6.6 x 10(3) IU/l; 0.8 x 10(3) to 32.6 x 10(3], they remained far higher than in non-pregnant women. Serum follicle stimulating hormone concentrations remained suppressed.
CONCLUSIONS: In this small study serum inhibin concentrations higher than those found in the early follicular phase one to two weeks after evacuation of a hydatidiform mole seemed to be specific for persistent trophoblastic disease. Further data are needed to confirm these promising results.

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Year:  1989        PMID: 2503176      PMCID: PMC1836764          DOI: 10.1136/bmj.298.6689.1684

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


  10 in total

1.  Further observations on the excretion of chorionic gonadotrophin by women with hydatidiform mole.

Authors:  B M HOBSON
Journal:  J Obstet Gynaecol Br Emp       Date:  1958-04

2.  The human placenta: a novel source of inhibin.

Authors:  R I McLachlan; D L Healy; D M Robertson; H G Burger; D M de Kretser
Journal:  Biochem Biophys Res Commun       Date:  1986-10-30       Impact factor: 3.575

3.  Inhibin A-subunit cDNAs from porcine ovary and human placenta.

Authors:  K E Mayo; G M Cerelli; J Spiess; J Rivier; M G Rosenfeld; R M Evans; W Vale
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

4.  Circulating immunoactive inhibin in the luteal phase and early gestation of women undergoing ovulation induction.

Authors:  R I McLachlan; D L Healy; D M Robertson; H G Burger; D M de Kretser
Journal:  Fertil Steril       Date:  1987-12       Impact factor: 7.329

5.  Metastatic gestational trophoblastic disease: experience at the New England Trophoblastic Disease Center, 1965 to 1985.

Authors:  B DuBeshter; R S Berkowitz; D P Goldstein; D W Cramer; M R Bernstein
Journal:  Obstet Gynecol       Date:  1987-03       Impact factor: 7.661

6.  Prognostic characteristics of serum human chorionic gonadotropin titer regression following molar pregnancy.

Authors:  J B Schlaerth; C P Morrow; O A Kletzky; R H Nalick; G A D'Ablaing
Journal:  Obstet Gynecol       Date:  1981-10       Impact factor: 7.661

7.  Comparison of inhibin immunological and in vitro biological activities in human serum.

Authors:  D M Robertson; C G Tsonis; R I McLachlan; D J Handelsman; R Leask; D T Baird; A S McNeilly; S Hayward; D L Healy; J K Findlay
Journal:  J Clin Endocrinol Metab       Date:  1988-09       Impact factor: 5.958

8.  Circulating immunoreactive inhibin levels during the normal human menstrual cycle.

Authors:  R I McLachlan; D M Robertson; D L Healy; H G Burger; D M de Kretser
Journal:  J Clin Endocrinol Metab       Date:  1987-11       Impact factor: 5.958

9.  Localization, secretion, and action of inhibin in human placenta.

Authors:  F Petraglia; P Sawchenko; A T Lim; J Rivier; W Vale
Journal:  Science       Date:  1987-07-10       Impact factor: 47.728

10.  Isolation of inhibin from bovine follicular fluid.

Authors:  D M Robertson; L M Foulds; L Leversha; F J Morgan; M T Hearn; H G Burger; R E Wettenhall; D M de Kretser
Journal:  Biochem Biophys Res Commun       Date:  1985-01-16       Impact factor: 3.575

  10 in total
  3 in total

Review 1.  Recent advances in the human physiology of inhibin secretion.

Authors:  D M de Kretser; D M Robertson; G P Risbridger
Journal:  J Endocrinol Invest       Date:  1990 Jul-Aug       Impact factor: 4.256

Review 2.  New aspects of placental endocrinology.

Authors:  F Petraglia; L Calzà; G C Garuti; L Giardino; B M De Ramundo; S Angioni
Journal:  J Endocrinol Invest       Date:  1990-04       Impact factor: 4.256

3.  Serum levels of dimeric activin A are not a marker of placental tumors in the course of chemotherapy.

Authors:  P Florio; S Luisi; E Casarosa; A R Genazzani; P Pautier; C Lhommé; J M Bidart; P G Driul; F Petraglia
Journal:  J Endocrinol Invest       Date:  1998-03       Impact factor: 4.256

  3 in total

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