Age-related infertility may be caused by scarred ovaries

Saturday, August 6, 2016

Washington: Women’s decreased ability to produce healthy eggs as they become older may be due to excessive scarring and inflammation in their ovaries, reports a new Northwestern Medicine study in mice.

This is the first study to show the ovarian environment ages and that aging affects the quality of eggs it produces. These findings could result in new treatments that preserve fertility by delaying ovarian aging.

Most reproductive research focuses on women’s eggs and trying to understand why their number and quality deteriorate as a woman enters her forties. Deteriorating eggs contribute to infertility, miscarriages and birth defects.

But in this study scientists examined the reproductive age-related changes that occur in the environment in which the eggs develop, known as the ovarian stroma. The environment in which cells grow and develop can greatly influence their quality and function, but surprisingly little is known about how the ovarian stroma changes with age.

“Under the microscope, eggs from reproductively young and old animals may look identical, but the environment in which they are growing is completely different,” said lead study author Francesca Duncan, executive director of the Centre for Reproductive Science at Northwestern University Feinberg School of Medicine. “Ovaries from reproductively old mice are fibrotic and inflamed. There is no way this environment won’t impact the eggs growing in it, and it very likely contributes to their decrease in quality.”

The study is published in the journal Reproduction. Duncan led the study when she was at the University of Kansas Medical Centre.

In this study, researchers analysed ovarian tissue from populations of reproductively “young” (equivalent to women in their early twenties) and “old” mice (equivalent to women ages 38-45). They consistently identified fibrosis in the reproductively “old” mice. This age period is associated with a decline in reproductive function and egg quality in both humans and mice. In some reproductively “old” mice, up to 35 percent of the ovarian tissue was fibrotic.

Researchers also found a type of immune cell (multinucleated macrophage giant cells) in the ovaries of reproductively “old” mice only. When found in other tissues, these cells are associated with chronic inflammation. They also found ovaries from mice of advanced reproductive age expressed genes and produced proteins that are highly inflammatory.

“Our work establishes fibrosis and inflammation as hallmarks of the aging ovary and lays the foundation for considering the use of anti-fibrotic or anti-inflammatory treatments to delay or counteract the impact of reproductive aging,” said Duncan, also an associate research professor in obstetrics and gynaecology at Feinberg.

“People tend to overlook that the egg is growing in a complex environment, and no one has taken a deep look at what is happening to that environment with age,” Duncan added. “It’s an underappreciated area.”

The findings have broader implications for women’s health because ovarian fibrosis is a key feature of polycystic ovary syndrome, a common endocrine system disorder among women of reproductive age, and is also a consequence of chemotherapy and radiation, Duncan said.

Duncan’s research team is currently investigating how to therapeutically target the ovarian environment to improve reproductive function.

Categories: Reproductive Medicine, RESEARCH

Tags: , , , , , ,

  More from Reproductive Medicine

Age-related infertility may be caused by scarred ovaries


Real-time imaging of embryo development could pave the way for more effective human reproduction therapies


Genetic pattern linked to IVF failure identified


Scientists develop motorised ‘spermbots’ to maximise fertility chances


Forget IVF, another way to have a baby soon


Data reveals frozen embryos as successful as fresh embryos in IVF

Comments »

No comments yet.

Name (required)
E-mail (required - never shown publicly)
URI
Your Comment (smaller size | larger size)
You may use <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong> in your comment.