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Drug discovery is costly and filled with uncertainty. Drug repurposing reduces time and costs by identifying new applications of a drug already approved or under investigation by the U.S. Food and Drug Administration. The FDA approved finasteride, under the brand name Proscar, in 1992 to treat benign prostate enlargement in men and again, in 1997, under the brand name Propecia, to treat male pattern hair loss.

Researchers at the University of Illinois Urbana–Champaign, U of I, recently found another potential use for finasteride: preventing cardiovascular diseases, or CVD. In a published in the Journal of Lipid Research, the team hypothesizes that finasteride will lower heart disease risk by cutting cholesterol levels.

The researchers studied the effects of finasteride on male mice and analyzed data from men who participated in the , or NHANES, between 2009 and 2016.

Finasteride is a 5-alpha-reductase inhibitor that prevents the conversion of testosterone into , or DHT, an active metabolite that plays a critical role in forming male sex organs, hair patterns and prostate growth.

Donald Molina, a graduate student at U of I and first author of the study, explained that low levels of testosterone in men are associated with higher CVD risk.

“As the drug acts on the levels of testosterone, we thought there might be an association between the drug and heart disease,” he said. “This was our starting point; we investigated how finasteride affected lipid profiles in humans.”

The team first analyzed the data deposited at NHANES and found that finasteride intake was associated with a reduction in total cholesterol and low-density cholesterol. 

“These results encouraged us to go for the animal studies,” Molina said.

The researchers used male mice genetically predisposed to atherosclerosis, a major underlying cause of heart disease. They fed the mice a high-fat, high-cholesterol diet for 12 weeks, and finasteride was administered in four increasing doses. They monitored cholesterol and other lipid levels and studied gene expression and lipid metabolome.

The mice on finasteride had lower cholesterol levels and showed delayed progression of atherosclerosis, reduced plasma triglycerides and less liver inflammation.

Jaume Amengual, an associate professor at U of I and lead author on the study, said the team thinks that, in the presence of finasteride, the liver degrades more lipids.

“The liver is burning more fat,” Amengual said. “We can also relate our findings to fatty liver disease. When you have a bad diet, you have a lot of fat accumulating in your liver, your liver will become inflamed and eventually develop into liver cirrhosis and even cancer. Therefore, we see in our experiment a decrease in the fat content in the liver and decreased liver inflammation. Not only did finasteride reduce levels of plasma cholesterol, it also improved how the liver was working in these mice.”

To bolster these findings, the researchers will need a detailed analysis of the effects of finasteride on a statistically relevant population and metabolic side effects such as levels of gut microbiota, as well as studies of its interactions with other drugs that target cholesterol synthesis or absorption.

 “One of the reasons why I became interested in this medication in the first place is because I have been taking this drug for hair loss since I was about 20,” Amengual said. “Even with limitations our study offers a stepping stone for repurposing finasteride for preventing cardiovascular diseases.”