Objectives. Studies of male chronic pelvic pain syndrome (CPPS) have genera
lly centered on the pathologic features of the prostate rather than on the
neurology of pain. Electrodiagnostic studies examine the integrity of somat
osensory nerve pathways consisting of large, group A fibers. Heat sensation
and visceral (autonomic) pain is mediated through small, unmyelinated C fi
bers, which can be tested cutaneously by thermal sensory analysis. We hypot
hesized that CPPS pain is mediated by these small C fibers.
Methods. All subjects and controls had no history of neurologic disease and
had normal neurologic examinations. Phase I: 14 patients with CPPS underwe
nt electrodiagnostic testing using pudendal somatosensory evoked potentials
and bulbocavernosus reflex latency measurements. Phase II: 31 patients wit
h CPPS and 14 controls underwent thermal sensory analysis testing on the pe
rineum and anterior thigh using noxious heat stimuli. Subjects used a compu
ter-generated visual analog scale to dynamically report their discomfort. T
he peak and slope of the computer-generated visual analog scale were analyz
ed.
Results. Phase I: two patients had delayed latency of the somatosensory evo
ked potentials, but additional evaluation with magnetic resonance imaging r
evealed no definable lesion. Phase II: with thermal sensory analysis, men w
ith CPPS reported higher intensity pain at lower temperatures [P = 0.03). M
en with CPPS also had higher peak computer-generated visual analog scale sc
ores on perineal testing. No difference in thermal testing on the anterior
thigh was found between the two groups.
Conclusions. Large, myelinated somatic fibers do not play a significant rol
e in the pathophysiology of CPPS. Patients with CPPS have an altered sensat
ion of perineal pain elicited by heat, which may represent a C-fiber-mediat
ed effect. UROLOGY 58: 246-250, 2001. (C) 2001, Elsevier Science Inc.