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New potential marker for obesity found

Date:
May 11, 2016
Source:
University of Kentucky
Summary:
A potential new biological marker for the development of obesity has been found, along with a possible target for obesity prevention and treatment, report scientists.
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A new study led by University of Kentucky researchers and published in Nature shows a potential new biological marker for the development of obesity and a possible target for obesity prevention and treatment.

Neurotensin (NT), a peptide produced mainly in the gastrointestinal tract and central nervous system, is released with fat ingestion and facilitates fatty acid absorption in the intestine. Previous research has shown that NT can also stimulate the growth of various cancers and increased fasting levels of pro-NT (an NT precursor hormone) are associated with development of cardiovascular disease and breast cancer.

The new Nature study examined data from the Malmö Diet and Cancer Study, a population-based, prospective epidemiologic cohort of 28,449 men and women who were followed for an average of 16.5±1.5 years. The analysis showed that obese and insulin-resistant subjects have significantly elevated levels of fasting pro-NT, and the risk of developing obesity was doubled in non-obese subjects who had fasting pro-NT at the highest concentrations compared to subjects with the lowest concentrations.

The study further used animal models to show that a deficiency in NT protects against obesity, insulin resistance and fatty liver disease associated with high fat consumption, thus identifying NT as a potential early marker of future obesity and a novel therapeutic target for this disease.

University of Kentucky Markey Cancer Center Director Dr. Mark Evers, a surgical oncologist and professor in the UK Department of Surgery, led the study in collaboration with other investigators from the University of Kentucky, the University of Massachusetts, and the University of Lund in Malmö, Sweden.

"Our findings have redefined how we view the role of NT," said Evers, whose laboratory has been studying this peptide for over two decades. "NT appears to be a metabolically 'thrifty' peptide which increases the absorption of ingested fats; however, with the abundance of fats in typical Western diets, NT can have a detrimental effect by contributing to increased obesity and related metabolic disorders."

Additionally, because NT can contribute to the growth of certain cancers and is now linked with obesity, Evers speculates that increased NT may contribute to the higher incidence of certain cancers associated with obesity. Building on the findings from this study, future research at the University of Kentucky will examine this possible link.

Worldwide, more than 1.7 billion people are overweight, with a body mass index (BMI) higher than 25, or obese (BMI higher than 30). Additionally, more than 2.5 million deaths are attributed to the consequences of obesity each year.


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Materials provided by University of Kentucky. Note: Content may be edited for style and length.


Journal Reference:

  1. Jing Li, Jun Song, Yekaterina Y. Zaytseva, Yajuan Liu, Piotr Rychahou, Kai Jiang, Marlene E. Starr, Ji Tae Kim, Jennifer W. Harris, Frederique B. Yiannikouris, Wendy S. Katz, Peter M. Nilsson, Marju Orho-Melander, Jing Chen, Haining Zhu, Timothy Fahrenholz, Richard M. Higashi, Tianyan Gao, Andrew J. Morris, Lisa A. Cassis, Teresa W. -M. Fan, Heidi L. Weiss, Paul R. Dobner, Olle Melander, Jianhang Jia, B. Mark Evers. An obligatory role for neurotensin in high-fat-diet-induced obesity. Nature, 2016; DOI: 10.1038/nature17662

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University of Kentucky. "New potential marker for obesity found." ScienceDaily. ScienceDaily, 11 May 2016. <www.sciencedaily.com/releases/2016/05/160511142343.htm>.
University of Kentucky. (2016, May 11). New potential marker for obesity found. ScienceDaily. Retrieved April 24, 2024 from www.sciencedaily.com/releases/2016/05/160511142343.htm
University of Kentucky. "New potential marker for obesity found." ScienceDaily. www.sciencedaily.com/releases/2016/05/160511142343.htm (accessed April 24, 2024).

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