Associations between epigenetic age acceleration and infertility

Author:

Lee Yunsung1ORCID,Bohlin Jon1,Page Christian M12,Nustad Haakon E13,Harris Jennifer R1,Magnus Per1,Jugessur Astanand14,Magnus Maria C1,Håberg Siri E1ORCID,Hanevik Hans I15

Affiliation:

1. Centre for Fertility and Health, Norwegian Institute of Public Health , Oslo, Norway

2. Department of Mathematics, Faculty of Mathematics and Natural Sciences, University of Oslo , Oslo, Norway

3. Deepinsight , Oslo, Norway

4. Department of Global Public Health and Primary Care, University of Bergen , Bergen, Norway

5. Fertility Department Sør, Telemark Hospital Trust , Porsgrunn, Norway

Abstract

AbstractSTUDY QUESTIONIs the use of ART, a proxy for infertility, associated with epigenetic age acceleration?SUMMARY ANSWERThe epigenetic age acceleration measured by Dunedin Pace of Aging methylation (DunedinPoAm) differed significantly between non-ART and ART mothers.WHAT IS KNOWN ALREADYAmong mothers who used ART, epigenetic age acceleration may be associated with low oocyte yield and poor ovarian response. However, the difference in epigenetic age acceleration between non-ART and ART mothers (or even fathers) has not been examined.STUDY DESIGN, SIZE, DURATIONThe Norwegian Mother, Father and Child Cohort Study (MoBa) recruited pregnant women and their partners across Norway at around 18 gestational weeks between 1999 and 2008. Approximately 95 000 mothers, 75 000 fathers and 114 000 children were included. Peripheral blood samples were taken from mothers and fathers at ultrasound appointments or from mothers at childbirth, and umbilical cord blood samples were collected from the newborns at birth.PARTICIPANTS/MATERIALS, SETTING, METHODSAmong the MoBa participants, we selected 1000 couples who conceived by coitus and 894 couples who conceived by IVF (n = 525) or ICSI (n = 369). We measured their DNA methylation (DNAm) levels using the Illumina MethylationEPIC array and calculated epigenetic age acceleration. A linear mixed model was used to examine the differences in five different epigenetic age accelerations between non-ART and ART parents.MAIN RESULTS AND THE ROLE OF CHANCEWe found a significant difference in the epigenetic age acceleration calculated by DunedinPoAm between IVF and non-ART mothers (0.021 years, P-value = 2.89E−06) after adjustment for potential confounders. Further, we detected elevated DunedinPoAm in mothers with tubal factor infertility (0.030 years, P-value = 1.34E−05), ovulation factor (0.023 years, P-value = 0.0018) and unexplained infertility (0.023 years, P-value = 1.39E−04) compared with non-ART mothers. No differences in epigenetic age accelerations between non-ART and ICSI fathers were found. DunedinPoAm also showed stronger associations with smoking, education and parity than the other four epigenetic age accelerations.LIMITATIONS, REASONS FOR CAUTIONWe were not able to determine the directionality of the causal pathway between the epigenetic age accelerations and infertility. Since parents’ peripheral blood samples were collected after conception, we cannot rule out the possibility that the epigenetic profile of ART mothers was influenced by the ART treatment. Hence, the results should be interpreted with caution, and our results might not be generalizable to non-pregnant women.WIDER IMPLICATIONS OF THE FINDINGSA plausible biological mechanism behind the reported association is that IVF mothers could be closer to menopause than non-ART mothers. The pace of decline of the ovarian reserve that eventually leads to menopause varies between females yet, in general, accelerates after the age of 30, and some studies show an increased risk of infertility in females with low ovarian reserve.STUDY FUNDING/COMPETING INTEREST(S)This study was partly funded by the Research Council of Norway (Women’s fertility, project no. 320656) and through its Centres of Excellence Funding Scheme (project no. 262700). M.C.M. has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement number 947684). The authors declare no conflict of interest.TRIAL REGISTRATION NUMBERN/A.

Funder

Research Council of Norway (Women’s

Centres of Excellence Funding Scheme

European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

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