Controlled ovarian hyperstimulation - A state of endothelial activation

Citation
R. Orvieto et al., Controlled ovarian hyperstimulation - A state of endothelial activation, AM J REPROD, 44(5), 2000, pp. 257-260
Citations number
19
Categorie Soggetti
Immunology
Journal title
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY
ISSN journal
10467408 → ACNP
Volume
44
Issue
5
Year of publication
2000
Pages
257 - 260
Database
ISI
SICI code
1046-7408(200011)44:5<257:COH-AS>2.0.ZU;2-U
Abstract
PROBLEM: To aim of the study was to investigate whether controlled ovarian hyperstimulation (COH) causes endothelial activation and whether there is a correlation between endothelial activation and serum sex-steroid levels. METHOD OF STUDY: The study population consisted of 14 consecutive patients undergoing our routine IVF long gonadotropin-releasing hormone-analog proto col. Blood was drawn three times during the COH cycle: (1) day when adequat e suppression was obtained (Day-S); (2) on the day of or the day prior to h CG administration (Day-hCG); and (3) on the day of ovum pick-up (Day-OPU). The levels of sex steroids and plasma soluble endothelial (E)-selectin were compared among the time points. Soluble E-selectin was measured with a com mercial sandwich enzyme-linked immunosorbent assay. RESULTS: Soluble E-selectin levels were significantly higher on Day-OPU tha n Day-S and Day-hCG, whereas no difference was observed between Day-hCG and Day-S. No significant correlations were found between soluble E-selectin l evel and patient age, number of gonadotropin ampoules used, number of oocyt es retrieved, or serum estradiol, progesterone and human chorionic gonadotr opin levels. CONCLUSIONS: Human chorionic gonadotropin administration leads to endotheli al activation regardless of the degree of ovarian response. Further studies are required to elucidate the relationship between COH and endothelial act ivation. These findings may lead to new strategies for predicting and preve nting complications of COH, such as severe ovarian hyperstimulation syndrom e.