Is serum-soluble vascular endothelial growth factor receptor-1 of importance in unexplained infertility?
Observational
OA: closed
CC0
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This study found that elevated VEGF and altered VEGF/sVEGFR-1 ratios in infertile women during natural and IVF cycles may contribute to unexplained infertility by impairing implantation.
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Abstract
OBJECTIVE: To analyze the role of vascular endothelial growth factor (VEGF) and its naturally occurring circulating antagonist, soluble VEGF receptor-1 (sVEGFR-1), in infertility. VEGF is a key angiogenic factor in the endometrial and ovarian cyclic processes that are crucial for fertility and sVEGFR-1 impairs its function and fertility in animals - less is known as regards human fertility.
DESIGN: Case-control study.
SETTING: University Central Hospital, a tertiary referral center.
POPULATION: Women with unexplained infertility (n=15) and fertile controls (n=10) had serial blood samples collected during their natural cycles, and the infertile women during a subsequent in vitro fertilization (IVF) cycle.
METHODS: Enzyme-linked immunosorbent assay was used for this study.
MAIN OUTCOME MEASURES: Concentrations of VEGF and sVEGFR-1 in the natural cycles and of sVEGFR-1 during a subsequent IVF cycle.
RESULTS: Plasma VEGF concentrations showed no cyclicity in fertile women, but were higher in the infertile group at the midluteal phase. Serum sVEGFR-1 concentrations were similar between the groups and between natural and IVF cycles. However, in infertile women, concentrations of sVEGFR-1 increased from the follicular phase to the luteal phase. In the follicular phase infertile women had a high ratio of VEGF/sVEGFR-1, which was decreased in the luteal phase. Both findings were associated with failure to achieve pregnancy in subsequent IVF cycles.
CONCLUSIONS: One cause of unexplained infertility may be unbalanced secretion of sVEGFR-1 with concomitant changes in free VEGF during the transition from the follicular to the luteal phase. This aberration may be related to impaired implantation.
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References (34)
- Antiangiogenic agents are effective inhibitors of endometriosis via openalex
- Circulating levels of free and total vascular endothelial growth factor (VEGF)-A, soluble VEGF receptors-1 and -2, and angiogenin during ovarian stimulation in non-human primates and women via openalex
- Expression of Vascular Endothelial Growth Factor and Its Receptors in the Human Corpus Luteum during the Menstrual Cycle and in Early Pregnancy via openalex
- Ovarian steroid regulation of vascular endothelial growth factor in the human endometrium: implications for angiogenesis during the menstrual cycle and in the pathogenesis of endometriosis via openalex
- Ovarian steroid regulation of vascular endothelial growth factor in the human endometrium: implications for angiogenesis during the menstrual cycle and in the pathogenesis of endometriosis via openalex
- Vascular endothelial growth factor and its soluble receptor in ovarian pathology via openalex
- Vascular endothelial growth factor production by human luteinized granulosa cells in vitro via openalex
- doi:10.3892/ijmm.2.4.465 via openalex
- doi:10.1093/molehr/5.5.452 via openalex
- doi:10.1210/en.138.11.4748 via openalex
- doi:10.1046/j.1365-2265.1999.00618.x via openalex
- doi:10.1210/en.142.7.3244 via openalex
- doi:10.1095/biolreprod56.2.489 via openalex
- doi:10.1038/bjc.1998.655 via openalex
- doi:10.1210/endo.142.7.8258 via openalex
- doi:10.1093/humrep/16.4.621 via openalex
- doi:10.1080/0951359042000199878 via openalex
- doi:10.1210/jcem.85.10.6888 via openalex
- doi:10.1210/endo.138.11.5500 via openalex
- doi:10.1016/j.ejogrb.2004.01.034 via openalex
- doi:10.1210/jc.83.12.4177 via openalex
- doi:10.1093/humrep/12.6.1280 via openalex
- doi:10.1095/biolreprod59.6.1540 via openalex
- doi:10.1038/nm0398-336 via openalex
- doi:10.1093/molehr/6.11.993 via openalex
- doi:10.1016/s0015-0282(98)00447-6 via openalex
- doi:10.1016/j.fertnstert.2003.10.025 via openalex
- doi:10.1111/j.8755-8920.2000.430105.x via openalex
- doi:10.1210/jcem.83.12.5296 via openalex
- doi:10.1095/biolreprod67.4.1305 via openalex
- doi:10.1016/s0188-4409(01)00323-x via openalex
- doi:10.1210/jcem.84.10.6025 via openalex
- doi:10.1016/j.mce.2006.11.015 via openalex
- W148216960 via openalex
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