Erectile dysfunction(ED), 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. Genetics also are suspected as a
factor in about one-third of erectile dysfunction cases,
but researchers have failed to make an association with
any specific genomic locations until now. 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 ED, such as
body mass index, or differences in how men describe
their erectile dysfunction. The study found that
variations in the SIM1 locus were associated with a 26
percent increased risk of ED. It 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 ED to their doctors. The study found that this
location was indeed a risk factor for ED, whether the
disorder was defined through clinical diagnoses,
prescriptions history, or study participant self-report.
The study then identified a biological role for this
location in ED susceptibility. The SIM1 gene is known to
be part of a signaling pathway that plays a central role
in body weight regulation and sexual function. Research
team shows that the implicated location physically
interacts with the promoter of the SIM1 gene, and that
variants in this location alter the function of a master
gene regulator, called an enhancer. The promoter is like
a light switch, and an enhancer acts like the fuse box.
Because the ED risk locus showed enhancer activity and
interacted with the SIM1 promoter, the risk locus likely
influences the expression of the SIM1 gene, turning it
on and off when needed. The study highlights the
potential of SIM1 as a target for the development of new
treatments for ED, which are needed because about half
of all men who try currently available pharmaceutical
treatments for ED don't respond to them. Lead researcher
said that, this study points to a new research direction
for ED 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.
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