The effects of pregnancy, its progression, and its cessation on human (maternal) biological aging

Affiliations

¹ Yale Child Study Center, Yale School of Medicine, New Haven, CT, USA; Department of Obstetrics Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT, USA.
² Department Genes and Environment, Max Planck Institute of Psychiatry, Munich, Germany.
³ Development, Health and Disease Research Program, University of California, Irvine, Irvine, CA, USA; Department of Pediatrics, University of California, Irvine, Irvine, CA, USA.
⁴ Development, Health and Disease Research Program, University of California, Irvine, Irvine, CA, USA; Department of Pediatrics, University of California, Irvine, Irvine, CA, USA; Department of Medical Psychology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
⁵ Development, Health and Disease Research Program, University of California, Irvine, Irvine, CA, USA; Department of Pediatrics, University of California, Irvine, Irvine, CA, USA; Departments of Psychiatry & Human Behavior, Obstetrics & Gynecology, and Epidemiology, University of California, Irvine, Irvine, CA, USA.
⁶ Yale Child Study Center, Yale School of Medicine, New Haven, CT, USA; Department of Obstetrics Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT, USA. Electronic address: kieran.odonnell@yale.edu.

PMID: 38521058
PMCID: PMC11774303
DOI: 10.1016/j.cmet.2024.02.016

The effects of pregnancy, its progression, and its cessation on human (maternal) biological aging

Hung Pham et al. Cell Metab. 2024.

. 2024 May 7;36(5):877-878.

doi: 10.1016/j.cmet.2024.02.016. Epub 2024 Mar 22.

Authors

Affiliations

¹ Yale Child Study Center, Yale School of Medicine, New Haven, CT, USA; Department of Obstetrics Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT, USA.
² Department Genes and Environment, Max Planck Institute of Psychiatry, Munich, Germany.
³ Development, Health and Disease Research Program, University of California, Irvine, Irvine, CA, USA; Department of Pediatrics, University of California, Irvine, Irvine, CA, USA.
⁴ Development, Health and Disease Research Program, University of California, Irvine, Irvine, CA, USA; Department of Pediatrics, University of California, Irvine, Irvine, CA, USA; Department of Medical Psychology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
⁵ Development, Health and Disease Research Program, University of California, Irvine, Irvine, CA, USA; Department of Pediatrics, University of California, Irvine, Irvine, CA, USA; Departments of Psychiatry & Human Behavior, Obstetrics & Gynecology, and Epidemiology, University of California, Irvine, Irvine, CA, USA.
⁶ Yale Child Study Center, Yale School of Medicine, New Haven, CT, USA; Department of Obstetrics Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT, USA. Electronic address: kieran.odonnell@yale.edu.

PMID: 38521058
PMCID: PMC11774303
DOI: 10.1016/j.cmet.2024.02.016

No abstract available

PubMed Disclaimer

Conflict of interest statement

Declaration of interests The authors declare no competing interests.

References

1. Parikh NI, Gonzalez JM, Anderson CAM, Judd SE, Rexrode KM, Hlatky MA, Gunderson EP, Stuart JJ, and Vaidya D; American Heart Association Council on Epidemiology and Prevention; Council on Arteriosclerosis, Thrombosis and Vascular Biology; Council on Cardiovascular and Stroke Nursing; and the Stroke Council (2021). Adverse Pregnancy Outcomes and Cardiovascular Disease Risk: Unique Opportunities for Cardiovascular Disease Prevention in Women: A Scientific Statement From the American Heart Association. Circulation 143, e902–e916. 10.1161/CIR.0000000000000961. - DOI - PubMed
1. Poganik JR, Zhang B, Baht GS, Tyshkovskiy A, Deik A, Kerepesi C, Yim SH, Lu AT, Haghani A, Gong T, et al. (2023). Biological age is increased by stress and restored upon recovery. Cell Metab. 35, 807–820.e5. 10.1016/j.cmet.2023.03.015. - DOI - PMC - PubMed
1. Toepfer P, O’Donnell KJ, Entringer S, Garg E, Heim CM, Lin DTS, MacIsaac JL, Kobor MS, Meaney MJ, Provenç al N., et et al. (2019). Dynamic DNA methylation changes in the maternal oxytocin gene locus (OXT) during pregnancy predict postpartum maternal intrusiveness. Psychoneuroendocrinology 103, 156–162. 10.1016/j.psyneuen.2019.01.013. - DOI - PMC - PubMed
1. Higgins-Chen AT, Thrush KL, Wang Y, Minteer CJ, Kuo PL, Wang M, Niimi P, Sturm G, Lin J, Moore AZ, et al. (2022). A computational solution for bolstering reliability of epigenetic clocks: Implications for clinical trials and longitudinal tracking. Nat. Aging 2, 644–661. 10.1038/s43587-022-00248-2. - DOI - PMC - PubMed
1. Lu AT, Binder AM, Zhang J, Yan Q, Reiner AP, Cox SR, Corley J, Harris SE, Kuo PL, Moore AZ, et al. (2022). DNA methylation GrimAge version 2. Aging (Albany NY) 14, 9484–9549. 10.18632/aging.204434. - DOI - PMC - PubMed

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions

Grants and funding

LinkOut - more resources

Full Text Sources
- Elsevier Science
- PubMed Central
Medical
- MedlinePlus Health Information

Save citation to file

Email citation

Add to Collections

Add to My Bibliography

Your saved search

Create a file for external citation management software

Your RSS Feed

The effects of pregnancy, its progression, and its cessation on human (maternal) biological aging

Affiliations

The effects of pregnancy, its progression, and its cessation on human (maternal) biological aging

Authors

Affiliations

Conflict of interest statement

References

Publication types

MeSH terms

Grants and funding

LinkOut - more resources

Full Text Sources

Medical