Serum luteal phase progesterone in women undergoing frozen embryo transfer in assisted conception: a systematic review and meta-analysis.


Journal

Fertility and sterility
ISSN: 1556-5653
Titre abrégé: Fertil Steril
Pays: United States
ID NLM: 0372772

Informations de publication

Date de publication:
12 2021
Historique:
received: 02 04 2021
revised: 30 06 2021
accepted: 02 07 2021
pubmed: 14 8 2021
medline: 22 12 2021
entrez: 13 8 2021
Statut: ppublish

Résumé

To investigate the association between luteal serum progesterone levels and frozen embryo transfer (FET) outcomes. Systematic review and meta-analysis. Not applicable. Women undergoing FET. We conducted electronic searches of MEDLINE, PubMed, CINAHL, EMBASE, the Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, Web of Science, ClinicalTrials.gov, and grey literature (not widely available) from inception to March 2021 to identify cohort studies in which the serum luteal progesterone level was measured around the time of FET. Ongoing pregnancy or live birth rate, clinical pregnancy rate, and miscarriage rate. Among the studies analyzing serum progesterone level thresholds <10 ng/mL, a higher serum progesterone level was associated with increased rates of ongoing pregnancy or live birth (relative risk [RR] 1.47, 95% confidence interval [CI] 1.28 to 1.70), higher chance of clinical pregnancy (RR 1.31, 95% CI 1.16 to 1.49), and lower risk of miscarriage (RR 0.62, 95% CI 0.50 to 0.77) in cycles using exclusively vaginal progesterone and blastocyst embryos. There was uncertainty about whether progesterone thresholds ≥10 ng/mL were associated with FET outcomes in sensitivity analyses including all studies, owing to high interstudy heterogeneity and wide CIs. Our findings indicate that there may be a minimum clinically important luteal serum concentration of progesterone required to ensure an optimal endocrine milieu during embryo implantation and early pregnancy after FET treatment. Future clinical trials are required to assess whether administering higher-dose luteal phase support improves outcomes in women with a low serum progesterone level at the time of FET. CRD42019157071.

Identifiants

pubmed: 34384594
pii: S0015-0282(21)00577-X
doi: 10.1016/j.fertnstert.2021.07.002
pii:
doi:

Substances chimiques

Progesterone 4G7DS2Q64Y

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1534-1556

Subventions

Organisme : Department of Health
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

Auteurs

Pedro Melo (P)

Tommy's National Centre for Miscarriage Research, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, United Kingdom; CARE Fertility Birmingham, Edgbaston, United Kingdom. Electronic address: pedro.melo1@nhs.net.

Yealin Chung (Y)

Tommy's National Centre for Miscarriage Research, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, United Kingdom; CARE Fertility Birmingham, Edgbaston, United Kingdom.

Oonagh Pickering (O)

Tommy's National Centre for Miscarriage Research, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, United Kingdom.

Malcolm J Price (MJ)

Institute of Applied Health Research, University of Birmingham, Edgbaston, United Kingdom; National Institute for Health Research Birmingham Biomedical Research Centre, University Hospitals Birmingham National Health Service Foundation Trust and University of Birmingham, Birmingham, United Kingdom.

Simon Fishel (S)

CARE Fertility Nottingham, Nottingham, United Kingdom; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.

Mohammed Khairy (M)

CARE Fertility Birmingham, Edgbaston, United Kingdom.

Charles Kingsland (C)

CARE Fertility Liverpool, Liverpool, United Kingdom.

Philip Lowe (P)

CARE Fertility Manchester, Manchester, United Kingdom.

Georgios Petsas (G)

CARE Fertility Sheffield, Sheffield, United Kingdom.

Madhurima Rajkhowa (M)

CARE Fertility Birmingham, Edgbaston, United Kingdom.

Victoria Sephton (V)

CARE Fertility Chester, Chester, United Kingdom.

Amanda Tozer (A)

CARE Fertility London, London, United Kingdom.

Simon Wood (S)

CARE Fertility Chester, Chester, United Kingdom.

Elena Labarta (E)

Human Reproduction Department, Instituto Valenciano de Infertilidad - Reproductive Medicine Associates, Valencia, Spain.

Mark Wilcox (M)

CARE Fertility Nottingham, Nottingham, United Kingdom.

Adam Devall (A)

Tommy's National Centre for Miscarriage Research, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, United Kingdom.

Ioannis Gallos (I)

Tommy's National Centre for Miscarriage Research, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, United Kingdom.

Arri Coomarasamy (A)

Tommy's National Centre for Miscarriage Research, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, United Kingdom; CARE Fertility Birmingham, Edgbaston, United Kingdom.

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Classifications MeSH