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Decidual prolactin content and secretion at term: Correlations with the clinical data
Author(s) -
Andersen Jesper Rye,
Borggaard Birgit,
Olsen Elith Bjarne,
Stimpel Hans,
Nyholm Henrik Christian,
Schroeder Erik
Publication year - 1987
Publication title -
acta obstetricia et gynecologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 102
eISSN - 1600-0412
pISSN - 0001-6349
DOI - 10.3109/00016348709022062
Subject(s) - prolactin , decidua , gestation , medicine , endocrinology , pregnancy , amniotic fluid , decidual cells , andrology , fetus , placenta , hormone , biology , genetics
This study was conducted to describe the distributions of the initial decidual PRL content (D‐PRL) and the decidual PRL secretion (D‐PRL‐s) in vitro at term and to ascertain whether the clinical data might influence these decidual PRL measures and their correlation with the amniotic fluid PRL concentration (A‐PRL). Decidual tissue was obtained after 134 normal pregnancies at term. D‐PRL and D‐PRL‐s into the medium after an 8 h incubation were determined. The distributions of D‐PRL and D‐PRL‐s were skewed to the right. A logarithmic transformation generated symmetric distibutions. Eight women who were delivered by vacuum extraction due to intra‐uterine asphyxia had D‐PRL values similar those in normal vaginal parturition, whereas D‐PRL‐s values were significantly reduced (p < 0.02). No significant difference (p>0.05) was found in the decidual PRL measures in the vaginal deliveries between those receiving labor stimulating medication and those without, or between women who gave birth vaginally and women undergoing elective cesarean section. Stepwise multiple regression analyses of data obtained from 30 women who gave birth after uncomplicated or various pathological pregnancies showed logarithmically transformed A‐PRL to be closely correlated with D‐PRL, and these correlations were improved by including the week of gestation as a second step (p < 0.00001). After normal pregnancy, D‐PRL‐s was significantly correlated with D‐PRL (p < 0.01), and D‐PRL was correlated with the week of gestation (p < 0.05). None of the remaining clinical data improved the correlations. The results indicate that a logarithmic transformation is appropriate when evaluating D‐PRL and D‐PRL‐s at term and that special attention should be paid to the differences in week of gestation and deliveries complicated with intra‐uterine as Dhvxia.

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