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Study: ‘Fatty Liver’ in Fetus Can Result in Childhood Obesity, Other Problems

March 12, 2018
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Peter Nathanielsz directs UW’s Wyoming Pregnancy and Life Course Health Center. (UW Photo)

New research published in the Journal of Physiology indicates that an obese pregnant mother and exposure to a high-fat, high-sugar diet during pregnancy produces a “fatty liver” in the fetus, potentially predisposing children to obesity, metabolic and cardiovascular disorders later in life.

The research -- which was co-led by Peter Nathanielsz of the University of Wyoming’s Wyoming Pregnancy and Life Course Health Center -- aims to understand the cellular mechanisms involved in laying down fat in the liver of a fetus, leading to a “fatty liver.” This knowledge is essential to developing strategies to combat childhood obesity, according to a media release from The Physiological Society.

“This research is important as, throughout the world, over 50 percent of women of reproductive age are overweight or obese,” Nathanielsz says. “Maternal obesity, combined with high-fat, high-sugar diets, makes it more likely that children will suffer from liver disease and face health problems such as obesity and heart disease later in life.”

The research aims to shed light on the mechanisms underlying the link between obese pregnant mothers and obesity in their children, a poorly understood concept called developmental programming. This study found that when a fetus develops in an obese pregnant mother, fat accumulates in its liver, and many metabolic pathways are disturbed.

This is the first study to report that important recently discovered microRNAs (a DNA product that modifies protein synthesis) play a role in this increased deposition of fat in the liver in humans’ closest relatives, the nonhuman primates. The observations of this study may explain why children of obese mothers live shorter lives than the offspring of normal-weight mothers.

In order to determine which genes were changed in the fetal liver of obese pregnant monkeys and to identify which microRNAs regulate these genes, genomic and epigenomic methods were used. The altered cellular signaling pathways were identified using bioinformatics approaches, and microscopic studies were conducted to quantify the amount of stored fat and sugar present in the liver cells, as well as assessing their shape, which is an indicator of liver cell health.

“It wasn’t until we saw the microscope slides for the staining of liver sections, showing very high amounts of lipid in fetuses of obese mothers, that we realized the dramatic impact of maternal obesity at such an early developmental time point,” Nathanielsz says. “Histological analyses of these livers showing the condition steatosis underlined the detrimental impact of maternal obesity on the developing fetus.”

While there is always some fat in the liver, when the liver fat increases above normal, an individual is said to have a “fatty liver.” As the amount of liver fat increases, troubles begin. If this symptom is dealt with early enough, it can be reversed; however, if fat deposition persists, the damage can lead to liver scarring and even later-life liver cancer.

The Texas Biomedical Research Institute, Wake Forest Baptist Medical Centre, Indiana University School of Medicine and the University of Texas Health Science Center also were involved in the research.

Although the researchers were able to see significant changes in many cellular functional pathways, the study may have been limited in its ability to show significant changes during even early stages of subjects. A major principle of developmental programming is that significant changes may lie dormant, only to emerge under stress or when hormones begin to change with puberty or aging.

The researchers plan to investigate metabolic and cardiovascular health of monkey offspring of obese mothers, including liver function at regular intervals across the life course to follow the progress of these fetal changes. This will allow them to assess whether unwanted consequences of maternal obesity can pass across generations from mother to daughter to grandchildren. They also plan to identify interventions that can reverse these unwanted changes using the same technologies employed in this study.

Contact Us

Institutional Communications

Bureau of Mines Building, Room 137

Laramie

Laramie, WY 82071

Phone: (307) 766-2929

Email: cbaldwin@uwyo.edu

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