Prednisolone treatment reduces endometrial spiral artery development in women with recurrent miscarriage
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Date
Authors
Lash, Gendie
Bulmer, Judith
Innes, Barbara
Drury, Josephine A
Robson, Stephen
Quenby, Siobhan
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Volume Title
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Kluwer Academic Publishers
Abstract
Background Uterine natural killer (uNK) cells and
endometrial blood vessel maturation are increased in the
luteal phase of the menstrual cycle in a subset of women
with recurrent miscarriage (RM). uNK cell numbers are
reduced after treatment with prednisolone (20 mg/day for
3 weeks).
Hypotheses Prednisolone treatment reduces endometrial
vascular maturation and angiogenic growth factor expression in women with RM with increased uNK cells.
Methods Endometrial biopsies (n = 18 paired samples)
from women with RM at LH ? 7 before and during
prednisolone treatment (20 mg/day for 3 weeks) were snap
frozen. Total RNA and cDNA was prepared and used in a
human angiogenesis RT-PCR superarray (84 genes, n = 6
pairs) with results validated using RT-PCR (n = 15 pairs).
Immunohistochemistry (n = 15 pairs) was performed for
Factor VIII, a-smooth muscle actin (a-SMA) and myosin
heavy chain (MyHC) and the total number of vessels and
the percentage of vessels completely surrounded by
vascular smooth muscle cells (VSMCs) were determined.
Results During prednisolone treatment there was no
change in the total number of endometrial blood vessels but the percentage of vessels completely surrounded by
VSMCs was decreased (a-SMA P\0.0001; MyHC
P\0.0001). Endometrial EGF and STAB 1 expression
was decreased during prednisolone treatment in samples
from woman who went on to have a live birth.
Conclusions The effect of prednisolone therapy for some
women with RM may be due to altered endometrial
angiogenic growth factor expression and reduced blood
vessel maturation.
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Angiogenesis
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2099-12-31
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