Discovery of asprosin, new hormone could have potential implications in treatment of diabetes

What started as a search for answers for patients suffering from a rare genetic condition called neonatal progeroid syndrome (NPS) that keeps the body from accumulating fat, among other symptoms, has now turned into a discovery that could potentially impact the lives of millions of people living with type 2 diabetes. The findings appear in the journal Cell.

Dr. Atul Chopra, a medical geneticist at Baylor College of Medicine, and senior author of the report, first identified two patients with this rare disorder in 2013 (only a handful of patients had been described to have this disorder worldwide, and its cause was unknown). At that time, whole genome/exome sequencing was only just being used to find answers for previously unsolvable medical/genetic mysteries. Chopra’s long-standing interest was in understanding disorders of energy metabolism, and NPS patients with extremely low levels of body fat piqued his imagination. Both patients had lived their entire lives with this “mysterious” disorder and Chopra, recognizing that technology was finally available to attack this problem, invited both to the genetics clinic at Texas Children’s Hospital for initial interviews and tests.

Using whole exome sequencing, Chopra and colleagues discovered the genetic mutation that appeared to be responsible for NPS. However, how that mutation resulted in the disorder was still unknown. Taking this problem to the laboratory, the researchers were able to figure out that these mutations prevented the patients from generating a previously unknown hormone. This newly discovered hormone, named asprosin, appears to be generated by fat. It travels to the liver where it instructs the liver to release glucose into the blood stream. NPS patients with abnormally low levels of asprosin are unable to do this and display low blood glucose and insulin.

In the opposite direction, patients with obesity/diabetes who have high blood glucose and insulin display higher than normal levels of asprosin. Using this information, the researchers determined that they could develop an antibody against it, and use that antibody to neutralize asprosin, a process called immunologic sequestration. This way they could potentially reduce the amount of glucose released by the liver, resulting in the pancreatic cells needing to release less insulin.

“We began to wonder, could this be a way to treat diabetes?” said Chopra.

To test this concept, they treated diabetic mice with this antibody and found that even a single dose of the antibody worked well to reduce their insulin levels back toward the normal range. When such mice were treated for a longer period of time, their insulin resistance completely normalized.

“This result brought us full circle. We started with an extremely rare genetic disorder, and using information learned from those patients, discovered a new hormone that can be targeted to treat a different disease that affects many more people. If humans with diabetes respond the same way to the asprosin antibody that diabetic mice do, this discovery could result in a new treatment for diabetes, which affects millions of people,” said Chopra, who also is a Caroline Weiss Law scholar and assistant professor of molecular and cellular biology and of molecular and human genetics at Baylor. “Therein lies the value in studying rare human genetic disorders. Sometimes such an endeavor can impact many more people beyond the original small cohort of patients one began with.”

One of the NPS patients this story started with, Abigail Solomon of Austin, Texas, is very excited about these findings. “Dr. Chopra’s work not only paves the way to find a treatment for people with my disorder – NPS, something I have lived with my entire life – but also a treatment for diabetes. I feel proud and honored to have been given an opportunity to participate in this process,” said Solomon, who is now a student at The University of Texas at Austin.

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