Impact of diabetes and obesity on the prostate and urethra: implications to
improved bladder dysfunction understanding and treatment.
Authors Christ GJ, Bushman W, Fraser MO
Submitted By Wade Bushman on 3/31/2010
Status Published
Journal The Journal of urology
Year 2009
Date Published 12/1/2009
Volume : Pages 182 : S38 - S44
PubMed Reference 19846131
Abstract PURPOSE: Alterations in bladder function are well documented in response to
diabetes and obesity. Nonetheless, clinical manifestations of bladder
dysfunction are diverse and the efficacy of available therapy is suboptimal.
Since the bladder is only 1 component of the lower urinary tract, we explored
existing evidence for the potential contribution(s) of other major lower urinary
tract structures to diabetes and obesity related bladder dysfunction, namely the
prostate and the urethra. MATERIALS AND METHODS: We performed a MEDLINE database
search of the relevant literature. RESULTS: A relatively large literature exists
on bladder dysfunction and the urethra. However, when additional search terms
were added, such as prostate, diabetes and obesity, there was a dramatic
decrease in the number of retrieved citations. These observations are consistent
with the vanishingly small available literature on the impact of diabetes on
prostatic biology and urethral function, and their potential impact on bladder
physiology/dysfunction. The available literature documents significant
alterations in prostatic biology and urethral function in the setting of
diabetes and/or obesity. CONCLUSIONS: The observed diversity in diabetes and
obesity related bladder dysfunction, and the variable efficacy of currently
available treatments may be related at least in part to the differential impact
of these disease states on the complex integration of bladder function with
other structural components of the lower urinary tract, namely the urethra and
the prostate. More comprehensive investigations of this system should lead to
improved understanding of the mechanistic basis for the observed pathophysiology
and identify novel treatment regimens.


Investigators with authorship
NameInstitution
Wade BushmanUniversity of Wisconsin-Madison
Matthew FraserDuke University Medical Center

Complications