Researchers discover direct link between placental function and future metabolic disorders

NewsGuard 100/100 Score

Researchers at the University of Colorado Anschutz Medical Campus have discovered a direct association between placental function in pregnant women and future metabolic disorders in children and adults, a finding that could lead to earlier intervention and diagnosis of disease.

We've known for some time that many major diseases in adults like diabetes and cardiovascular disease are at least partly caused by problems during fetal life. For example, it has been shown that 50% of all type-2 diabetes in young adults are caused by exposure to the intrauterine environment in pregnant women with obesity and/or gestational diabetes."

Thomas Jansson, MD, PhD, Study's Senior Author, Professor of Obstetrics & Gynecology, University of Colorado School of Medicine

In this study, published this month in the journal Diabetes, Jansson and the paper's lead author Madeline Rose Keleher, PhD, of the Colorado School of Public Health's LEAD Center (Lifecourse, Epidemiology of Adiposity & Diabetes) have uncovered more about the placenta's role in the future health of a child.

"We are the first to discover associations between placental function and blood pressure, body fat and triglyceride levels in children between the ages of 4-6 years old," Jansson said. "These markers often signal risks for future heart disease, diabetes and obesity."

The researchers used the Healthy Start longitudinal pre-birth cohort study which enrolled 1,410 healthy pregnant women between 2010-2014. The children are now 4-6-years-old.

"What's unique is the time frame. We didn't just stop at newborns," Keleher said. "We followed the kids for one year then four to six years. We see this isn't something they simply outgrow. We will continue to follow them when they are eight to ten years old."

A healthy intrauterine environment is largely determined by the placenta, which nourishes the fetus and protects it against the mother's immune system. Changes in the placenta like inflammation or insulin signaling, the researchers said, can set the stage for later disease.

The study revealed that the placental IGF-1 receptor protein was associated with serum triglycerides in children which could lead to obesity or diabetes later. Other proteins in the placenta were shown to have associations with increased fat tissue on the arms and thighs of children.

"All of these showed a novel link between placental function and long-term metabolic outcomes," Keleher said.

According to Jansson, if doctors discover that a placenta is not functioning properly during pregnancy they may be able to intervene.

"If we know the placenta is impaired or changed during pregnancy we can design interventions to modulate that function and decrease the risk to the fetus," he said. "Treating pregnant women is always difficult but the placenta is accessible whereas the fetus is largely inaccessible."

The findings could ultimately lead to a kind of personalized medicine that begins before birth.

"I think a better understanding of the mechanisms linking placental function to childhood and adult metabolic disease risk may offer innovative avenues to preventing them in future generations," Keleher said.

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Expanding research and clinical options for children with cancer