Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Oct 1;30(10):1053-1057.
doi: 10.1097/GME.0000000000002238. Epub 2023 Aug 22.

Association of senescence-associated secretory phenotype proteins with ovarian reserve among middle-aged/older women

Affiliations

Association of senescence-associated secretory phenotype proteins with ovarian reserve among middle-aged/older women

Ji-Won Shin et al. Menopause. .

Abstract

Objective: This study aimed to examine the association of circulating senescence-associated secretory phenotype proteins, secreted by senescent cells, with indicators of women's ovarian reserve.

Methods: This secondary analysis of cross-sectional baseline survey data was undertaken by the Korean Genome and Epidemiology Study Cardiovascular Disease Association Study. A total of 223 women (aged 40-82 y), without any history of oophorectomy, hysterectomy, or other medical conditions that could lower the ovarian reserve, were enrolled in this analysis. Chronological age (years), menopausal status, and serum anti-müllerian hormone (ng/mL) level were used to assess the associations among biological aging, accelerated menopausal aging, and ovarian reserve.

Results: Of the 223 women participants (53.4 ± 11.0 y), 147 (46.4 ± 3.9 y) and 76 (67.0 ± 6.9 y) were premenopausal and postmenopausal, respectively. Serum levels of senescence-associated secretory phenotype proteins were generally higher in postmenopausal, than in premenopausal, women. In the analyses adjusted for chronological age and body mass index, 17 senescence-associated secretory phenotype proteins were associated with menopausal status. However, in premenopausal women, no association trends with the level of anti-müllerian hormone were detected for a total of 28 senescence-associated secretory phenotype proteins.

Conclusions: In a cohort of middle-aged/older women, the level of circulating senescence-associated secretory phenotype proteins indicated chronological age and menopausal status. Yet, serum levels of senescence-associated secretory phenotype protein potentially have limited predictive value for ascertaining ovarian reserve in premenopausal women.

PubMed Disclaimer

Conflict of interest statement

Financial disclosure/conflicts of interest: None reported.

References

    1. Campisi J. Aging, cellular senescence, and cancer. Annu Rev Physiol 2013;75:685–705. doi: 10.1146/annurev-physiol-030212-183653 - DOI
    1. van Deursen JM. The role of senescent cells in ageing. Nature 2014;509:439–446. doi: 10.1038/nature13193 - DOI
    1. Coppé JP, Patil CK, Rodier F, et al. Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor. PLoS Biol 2008;6:2853–2868. doi: 10.1371/journal.pbio.0060301 - DOI
    1. Palmer AK, Xu M, Zhu Y, et al. Targeting senescent cells alleviates obesity-induced metabolic dysfunction. Aging Cell 2019;18:e12950. doi: 10.1111/acel - DOI
    1. Farr JN, Xu M, Weivoda MM, et al. Targeting cellular senescence prevents age-related bone loss in mice. Nat Med 2017;23:1072–1079. doi: 10.38/nm.4385 - DOI

Publication types

Substances

LinkOut - more resources