First genetic risk factor found for erectile dysfunction

For the first time, a team of researchers has found a specific place in the human genome where variations can raise a person’s risk of erectile dysfunction. The discovery is a significant advancement in the understanding of the genetics underlying erectile dysfunction. The study, Genetic variation in the SIM1 locus is associated with erectile dysfunction, was published Oct. 8 in the journal Proceedings of the National Academy of Sciences.

“This study points to a new research direction for erectile dysfunction that could help us identify other key genetic variants that trigger the disease and lead to investigations to better understand the precise mechanisms by which they operate,” said Hunter Wessells, chair of urology at the University of Washington School of Medicine and one of the study’s principal investigators. “Hopefully, this will translate into better treatments and, importantly, prevention approaches for the men and their partners who often suffer silently with this condition.

“This is the first time there’s ever been any strong evidence that there’s actually a genetic component (to ED) independent of all those other possible causes. This changes everything,” Wessells said.

Erectile dysfunction, the inability to obtain and maintain an erection sufficient for sexual activity, is a common and costly condition of men of primarily middle and older ages. The disease is linked to many causes, such as neurological, hormonal and vascular factors. New therapeutics  are needed because about half of all men don’t respond to available pharmaceutical treatments.

The new study found that variations in a specific place in the genome, called a genetic locus, near the SIM1 gene are significantly associated with an increased risk of erectile dysfunction. The researchers ruled out that the risk was due to other known risk factors for erectile dysfunction, such as body mass index, or differences in how men describe their erectile dysfunction. By demonstrating a biological role for the genetic location in regulating sexual function,  the study strongly suggested that these variations can cause erectile dysfunction.

The two-year study highlights the potential of targeting variations in the SIM1 locus on the genome in developing new erectile dysfunction treatments.

“We found the association so strong, that it gave us confidence this wasn’t by chance,” Wessells said of the genetic connection.

Genetics had been suspected as a factor in about one-third of erectile dysfunction cases, but researchers had failed to make an association with any specific genomic locations until now. The study found that variations in the SIM1 locus were associated with a 26 percent increased risk of erectile dysfunction. This risk was independent of known erectile dysfunction risk factors. Replicating the association replicated in the U.K. Biobank sample provided strong confirmation of the findings.

The researchers conducted a genome-wide association study in two large and diverse cohorts to investigate genetic contributors to the risk of erectile dysfunction. The first cohort included 36,648 men from the Genetic Epidemiology Research on Adult Health and Aging cohort. The findings in the that cohort were then verified in a cohort of 222,358 men from the UK Biobank. The existence of these genetic banks finally made this research possible, said Wessells, who has been studying this topic for 15 years.

An actual clinical treatment for erectile dysfunction, based on these findings, is yesars in the future. The next step, Wessells said, it to take these results, and test it against an even larger database, and against laboratory computer models.

Erectile dysfunction has been difficult to study in part because of the differences in how patients report their symptoms. To overcome this challenge, the study looked to see whether the SIM1 locus was a risk factor when considering differences in how men reported their erectile dysfunction to their doctors. The study found that this location was indeed a risk factor for erectile dysfunction, whether the disorder was defined through clinical diagnoses, prescriptions history, or self-reported by study participants.

Data were provided by the Kaiser Permanente Research Bank from its collection, which includes the Kaiser Permanente Research Program on Genes, Environment, and Health and the GERA data. The study was funded by the National Institutes of Health (RC2 AG036607), the Robert Wood Johnson Foundation, the Wayne and Gladys Valley Foundation, The Ellison Medical Foundation, and the Kaiser Permanente Community Benefits Program. Access to data used in this study may be obtained by application to the KPRB via This article was supported in part by a grant from the National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK104764).

The study was a collaboration the UW School of Medicine, Kaiser Permanente Northern California,  UCSF and the University of Utah. Co-authors from the UW School of Medicine include Melody R. Palmer and Gail Jarvik. Co-authors on the study from the Division of Research include Jie Yin, Jun Shan and Khanh K. Thai. Co-authors from the University of California, San Francisco, include Navneet Matharu, Thomas J. Hoffmann, Xujia Zhou and Nadav Ahituv. Co-author James M. Hotaling is from the University of Utah School of Medicine.

The material in this press release comes from the originating research organization. Content may be edited for style and length. Have a question? Let us know.


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