Ovarian hyperstimulation syndrome: pathophysiology and prevention
Open accessAbstract
Purpose To review and discuss the pathophysiology and prevention strategies for ovarian hyperstimulation syndrome (OHSS), which is a condition that may occur in up to 20% of the high risk women submitted to assisted reproductive technology cycles. Methods The English language literature on these topics were reviewed through PubMed and discussed with emphasis on recent data. Results The role of estradiol, luteinizing hormone, human chorionic gonadotropin (hCG), inflammatory mediators, the renin-angiotensin system and vascular endothelial growth factor is discussed in the pathophysiology of OHSS. In addition we consider the prevention strategies, including coasting, administration of albumin, renin-angiotensin system blockage, dopamine agonist administration, non-steroidal anti-inflammatory administration, GnRH antagonist protocols, reducing hCG dosage, replacement of hCG and in vitro maturation of oocytes (IVM). Conclusions Among the many prevention strategies that have been discussed, the current evidence points to the replacement of hCG by GnRH agonists in antagonist cycles and the performance of IVM procedures as the safest approaches.
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The ovary is the second largest source of systemic renin, and ovarian stimulation activates local RAS to produce more renin.
“The reason is that the ovary is the second largest source of systemic renin, and ovarian stimulation activates local RAS to produce more renin [31].”
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Sorted by citations
Park, K., Wei, J., Minissian, M., Bairey Merz, C. N., & Pepine, C. J. (2015) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-015-6597-2 · Cited by 40 · see citing works
Wei, L., Bo, L., Luo, C., Yin, N., Jiang, W., Qian, F., Zhou, A., Lu, X., Guo, H., & Mao, C. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03997-6 · Cited by 11 · see citing works
“It should be pointed out that the positive results of renin dose not refute the independence of ovarian RAS The reason is that the ovary is the second largest source of systemic renin, and ovarian stimulation activates local RAS to produce more renin [31].”
Background
- Authors
- Nastri, C. O., Ferriani, R. A., Rocha, I. A., & Martins, W. P.
- Affiliations
- Universidade de São Paulo (BR)
- Corresponding author
- Martins, Wellington P.
- Venue
- Journal of Assisted Reproduction and Genetics
- Published
- 2010-02
- Volume
- 27
- Issue
- 2-3
- Pages
- 121-128
- ISSN
- 0740-7769 (ISSN-L)
- 1058-0468
- 1573-7330
- PMC
- PMC2842872
- OpenAlex
- W1988775832
- Cited by
- 233
- References
- 0
- Citations by year
- 2026: 12 · 2025: 11 · 2024: 10 · 2023: 13 · 2022: 28 · 2021: 10 · 2020: 14 · 2019: 12 · 2018: 14 · 2017: 18 · 2016: 15 · 2015: 15 · 2014: 20 · 2013: 17 · 2012: 12
- FWCI
- 1.85
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Journal of Assisted Reproduction and Genetics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Scientific Electronic Library Online (São Paulo Research Foundation, Latin American and Caribbean Center on Health Sciences Information, Conselho Nacional de Desenvolvimento Científico e Tecnológico) (publishedVersion)
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Reproductive Biology and Fertility
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Health and Technologies
- Keywords
- ovarian hyperstimulation syndrome, pathophysiology, prevention, assisted reproduction, estradiol, luteinizing hormone, human chorionic gonadotropin, renin-angiotensin system, vascular endothelial growth factor, inflammatory mediators, coasting, albumin administration, GnRH antagonist protocol, dopamine agonists, nonsteroidal anti-inflammatory drugs
- MeSH terms
- Adult, Albumins, Angiotensin-Converting Enzyme Inhibitors, Anti-Inflammatory Agents, Non-Steroidal, Cells, Cultured, Estradiol, Female, Chorionic Gonadotropin, Humans, Interleukins, Luteinizing Hormone, Gonadotropin-Releasing Hormone, Oocytes, Ovulation Induction, Renin-Angiotensin System, Risk Factors, Ovarian Hyperstimulation Syndrome, Dopamine Agonists, Inflammation Mediators, Vascular Endothelial Growth Factor A, Angiotensin II Type 1 Receptor Blockers
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