Risk of congenital malformations in live-born singletons conceived after intracytoplasmic sperm injection: a Nordic study from the CoNARTaS group.


Journal

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

Informations de publication

Date de publication:
11 2023
Historique:
received: 28 02 2023
revised: 02 07 2023
accepted: 03 07 2023
medline: 30 10 2023
pubmed: 14 7 2023
entrez: 13 7 2023
Statut: ppublish

Résumé

To investigate whether the risk of major congenital malformations is higher in live-born singletons conceived with intracytoplasmic sperm injection (ICSI) compared with in vitro fertilization (IVF)? Nordic register-based cohort study. Cross-linked data from Medical Birth Registers and National ART and Patient Registers in Denmark, Norway and Sweden. Data were included from the year the first child conceived using ICSI was born: Sweden, 1992; Denmark, 1994; and Norway, 1996. Data were included until 2014 for Denmark and 2015 for Norway and Sweden. All live-born singletons conceived using fresh ICSI (n = 32,484); fresh IVF (n = 47,178); without medical assistance (n = 4,804,844); and cryo-ICSI (n = 7,200) during the study period. Different in vitro conception methods, and cryopreservation of embryos. Risk of major congenital malformations on the basis of International Classification of Diseases codes. The European Concerted Action on Congenital Anomalies and Twins was used to differentiate between major and minor malformations. Among singletons conceived using fresh ICSI, 6.0% had a major malformation, compared with 5.3% of children conceived using fresh IVF; 4.2% of children conceived without medical assistance; and 4.9% of children conceived using cryo-ICSI; adjusted odds ratio (AOR) 1.07 (95% confidence interval [CI] 1.01-1.14) in ICSI vs. IVF; and AOR 1.28 (95% CI, 1.23-1.35) in ICSI vs. no medical assistance; and AOR 1.11 (95% CI, 0.99-1.26) in ICSI fresh vs. cryo-ICSI. When malformations were grouped by different organ systems, children conceived using ICSI had a higher risk of respiratory and chromosomal malformations compared with children conceived using IVF, but there were very few cases in each group. When categorizing children conceived using ICSI according to treatment indication (male factor infertility only vs. other indications), we found a higher risk of hypospadias when ICSI was performed because of male factor infertility only (AOR 1.85 [95% CI 1.03-332]). The indications for ICSI changed over time, as male factor infertility did not remain the primary indication for ICSI throughout the study period. In this large cohort study, we found the risk of major malformations in live-born singletons to be slightly higher after fresh ICSI compared with fresh IVF. These findings should be considered when choosing the assisted reproductive technology method for couples without male factor infertility.

Identifiants

pubmed: 37442533
pii: S0015-0282(23)00684-2
doi: 10.1016/j.fertnstert.2023.07.003
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1033-1041

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests A.K.A.H. has nothing to disclose. S.O. has nothing to disclose. U.B.W has nothing to disclose. A.T. has nothing to disclose. S.R. has nothing to disclose. L.B.R. has nothing to disclose. C.B. received funding from Ferring Pharmaceuticals AB and honoraria from Gedeon Richter, Ferring Pharmaceuticals AB, and Merck A/S outside the submitted work. M.G. has nothing to disclose. J.L.F. has nothing to disclose. A.P. has received funding from Gedeon Richter, Ferring Pharmaceuticals, and Merck A/S; consulting fees from Preglem, Novo Nordisk, Ferring, Gedeon Richter, Cryos, and Merck A/S; honoraria from Gedeon Richter, Ferring Pharmaceuticals, Merck A/S, Theramex, and Organon; travel support from Gedeon Richter; an advisory board for Preglem; and nonfinancial support from Gedeon Richter outside the submitted work.

Auteurs

Anna-Karina Aaris Henningsen (AA)

Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark. Electronic address: ahen0024@regionh.dk.

Signe Opdahl (S)

Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.

Ulla-Britt Wennerholm (UB)

Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.

Aila Tiitinen (A)

Department of Obstetrics and Gynecology, University of Helsinki, Helsinki University Hospital, Helsinki, Finland.

Steen Rasmussen (S)

Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Liv Bente Romundstad (LB)

Spiren Fertility Clinic, Trondheim, Norway.

Christina Bergh (C)

Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.

Mika Gissler (M)

Department of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland; Region Stockholm, Academic Primary Health Care Centre, Stockholm, Sweden; Karolinska Institute, Stockholm, Sweden.

Julie Lyng Forman (JL)

Section of Biostatistics, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

Anja Pinborg (A)

Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

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