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
. 1984;66(1):41-5.
doi: 10.1007/BF00275184.

Maternal ageing and aneuploid embryos--evidence from the mouse that biological and not chronological age is the important influence

Maternal ageing and aneuploid embryos--evidence from the mouse that biological and not chronological age is the important influence

J D Brook et al. Hum Genet. 1984.

Abstract

Maternal ageing remains the overwhelming factor in the aetiology of human aneuploidy. Whether aberrant meiotic chromosome segregation in the oocyte relates causally to ovarian physiological ageing or to some factor dependent on the passage of chronological time, remains to be determined. The present experimental studies in the mouse indicate the former. An earlier cessation of reproductive life, brought on by unilateral ovariectomy in CBA females, resulted in the earlier onset of irregular cyclicity and an earlier rise in aneuploidy. The results could not be explained on the basis of the "production line" hypothesis. The clinical implications are that the probability of conceiving a Down foetus will be determined by distance in time from the approaching menopause, rather than by the chronological age of the woman per se.

PubMed Disclaimer

References

    1. J Reprod Fertil. 1980 Nov;60(2):449-56 - PubMed
    1. Obstet Gynecol. 1978 Nov;52(5):617-24 - PubMed
    1. J Endocrinol. 1983 Jan;96(1):23-33 - PubMed
    1. Biol Reprod. 1979 Sep;21(2):491-5 - PubMed
    1. Ann Hum Genet. 1972 Nov;36(2):195-208 - PubMed

Publication types

LinkOut - more resources