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
Review
. 2021 Jul 14;162(2):R19-R33.
doi: 10.1530/REP-21-0022.

Mechanisms of ovarian aging

Affiliations
Review

Mechanisms of ovarian aging

Selena U Park et al. Reproduction. .

Abstract

Ovarian aging in women correlates with the progressive loss of both the number and quality of oocytes. When these processes occur early or are accelerated, their clinical correlates are diminished ovarian reserve and/or premature ovarian insufficiency. Both these conditions have important consequences for the reproductive and general health of women, including infertility. Although there are many contributing factors, the molecular mechanisms underlying many of the processes associated with ovarian aging have not been fully elucidated. In this review, we highlight some of the most critical factors that impact oocyte quantity and quality with advancing age. We discuss chromosomal factors including cohesion deterioration and mis-segregation, errors in meiotic recombination, and decreased stringency of the spindle assembly checkpoint. DNA damage, telomere changes, reactive oxygen species and mitochondrial dysfunction as they relate to ovarian aging, and well-known gene mutations associated with primary ovarian insufficiency and diminished ovarian reserve are also discussed. Additionally, studies investigating recently acknowledged cytoplasmic factors associated with ovarian aging including protein metabolic dysregulation and microenvironmental alterations in the ovary are presented. We use both mouse and human studies to support the roles these factors play in physiologic and expedited ovarian aging, and we propose directions for future studies. A better understanding of the molecular basis of ovarian aging will ultimately lead to diagnostic and therapeutic advancements that would provide women with information to make earlier choices about their reproductive health.

PubMed Disclaimer

Conflict of interest statement

Declaration of interest

The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of this review.

Figures

Figure 1
Figure 1
A multitude of physiological factors can diminish the quantity and quality of the ovarian reserve and lead to ovarian aging. Each factor is explained further under subheadings in the text.
Figure 2
Figure 2
Schematic of folliculogenesis. During the stages of follicle development, granulosa cells (depicted by dashed lines) proliferate in layers around the growing oocyte. Many primordial and antral follicles undergo atresia during this process. Ovulation occurs when the egg is released at the time of follicle rupture during the antral follicle stage (antral cavity is depicted in blue). Following ovulation, a corpus luteum forms from the remaining antral follicle. If the egg is not fertilized, the follicle will undergo luteal regression and ultimately be degraded.

Similar articles

Cited by

References

    1. AlAsiri S, Basit S, Wood-Trageser MA, Yatsenko SA, Jeffries EP, Surti U, Ketterer DM, Afzal S, Ramzan K, Faiyaz-Ul Haque M et al. 2015. Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability. Journal of Clinical Investigation 125 258–262. (10.1172/JCI78473) - DOI - PMC - PubMed
    1. Allen JW 2010. Fertility and Pregnancy: an Epidemiologic Perspective:Oxford, NY: Oxford University Press.
    1. ASRM 2020. Testing and interpreting measures of ovarian reserve: a committee opinion. Fertility and Sterility 98 1407–1415. (10.1016/j.fertnstert.2020.09.134) - DOI - PubMed
    1. Baker TG 1963. A quantitative and cytological study of germ cells in human ovaries. Proceedings of the Royal Society of London: Series B, Biological Sciences 158 417–433. (10.1098/rspb.1963.0055) - DOI - PubMed
    1. Banks N, Patounakis G, Devine K, DeCherney AH, Widra E, Levens ED, Whitcomb BW & Hill MJ 2016. Is FMR1 CGG repeat length a predictor of in vitro fertilization stimulation response or outcome? Fertility and Sterility 105 1537.e8–1546.e8. (10.1016/j.fertnstert.2016.02.011) - DOI - PMC - PubMed

Publication types