Use of Intra-uterine Injection of Platelet-rich Plasma (PRP) for Endometrial Receptivity and Thickness: a Literature Review of the Mechanisms of Action.
Marco MouannessShelena Ali-BynomJanelle JackmanSerin SeckinZaher MerhiPublished in: Reproductive sciences (Thousand Oaks, Calif.) (2021)
Endometrial receptivity and thickness play an important role in achieving a pregnancy. Intrauterine autologous platelet-rich plasma (PRP) infusion has been used in infertile women with recurrent implantation failure (RIF) and thin endometrial lining thickness (EMT). Literature search was performed in PubMed for studies including in vitro, animal, and human studies as well as in abstracts presented at national conferences. Animal studies demonstrated a decrease in the expression of inflammatory markers and fibrosis, and increased endometrial proliferation rate, increased expression of proliferative genes, and increased pregnancy rates. The in vitro studies showed that PRP was associated with increased stromal and mesenchymal cell proliferation, increased expression of regenerative enzymes, and enhancement in cell migration. In infertile women undergoing assisted reproductive technology, one randomized clinical trial showed that PRP intrauterine infusion improved EMT, implantation rate, and clinical pregnancy rate (CPR) in patients with thin EMT, while 3 other trials involving subjects with RIF showed conflicting results related to CPR. Case series and cohort studies showed conflicting results pertaining to CPR. Data to date suggest that PRP may be beneficial in improving endometrial thickness and endometrial receptivity. However, further large prospective and high-quality trials are needed to assert its effect and to identify the population of patients that would benefit the most.
Keyphrases
- platelet rich plasma
- endometrial cancer
- cardiac arrest
- poor prognosis
- optical coherence tomography
- epithelial mesenchymal transition
- pregnancy outcomes
- cell proliferation
- polycystic ovary syndrome
- cardiopulmonary resuscitation
- cell migration
- stem cells
- case control
- bone marrow
- preterm birth
- mesenchymal stem cells
- low dose
- systematic review
- endothelial cells
- newly diagnosed
- signaling pathway
- binding protein
- ejection fraction
- clinical trial
- cell cycle
- pulmonary tuberculosis
- pregnant women
- adipose tissue
- cell therapy
- chronic kidney disease
- electronic health record
- dna methylation
- mycobacterium tuberculosis
- genome wide
- big data
- patient reported outcomes
- skeletal muscle
- drug induced
- ultrasound guided