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Irritable
bowel syndrome (IBS) is a very common gastrointestinal condition which
is present in up to 17% of the general population. The classic gastrointestinal
symptoms of IBS are chronic or recurrent abdominal pain and/or discomfort
and associated alterations in bowel habits. However, many individuals
with IBS also suffer from non-gastrointestinal symptoms. Rheumatologic
symptoms, such as skin rashes, muscle contraction headache and myalgias,
have been reported in two-thirds of IBS patients. Previous studies have
found that IBS typically overlaps with fibromyalgia syndrome (FM) in the
same patient, suggesting a common cause. FM occurs in up to 60% of patients
with irritable bowel syndrome (IBS). Up to 70% of patients with a diagnosis
of FM have symptoms of IBS. Following arthritis, FM is the most common
condition seen in community rheumatologic practice. It is a common pain
disorder in which the presence of multiple muscular tender points is associated
with characteristic symptoms of generalized muscle aching, stiffness,
fatigue and an abnormal sleep pattern. The diagnosis of FM is presently
defined by criteria established by the American College of Rheumatology.
Although
IBS is a chronic visceral (bowel) pain condition and FM is a chronic somatic
(muscle) pain disorder, IBS and FM have common clinical characteristics:
(1) the majority of patients associate stressful life events with the
onset or exacerbation of symptoms, (2) the majority of patients complain
of disturbed sleep and fatigue, (3) psychotherapy and behavioral therapies
are efficacious in treating symptoms, and (4) certain medications can
treat symptoms of both conditions. It has been suggested that IBS and
FM have a common cause and that specific physiologic alterations may be
responsible for the symptoms seen in these two conditions.
The UCLA
Neuroenteric Disease Program is presently conducting research studies
comparing the physiologic responses to visceral (bowel) or somatic (muscle)
stimulus in individuals with IBS alone, FM alone, and both IBS and FM
(IBS + FM). By comparing the responses of these three groups, we can learn
about more about how chronic visceral and somatic pain are processed in
these conditions.
The investigators
at the UCLA Neuroenteric Disease Program have recently completed somatic
perception studies in female patients with IBS alone, both IBS + FM, and
healthy individuals. The responses to pressure which was placed on particular
muscle tender points was measured. Like FM patients, patients with IBS
+ FM demonstrate somatic hyperalgesia (increased somatic pain sensation).
However, patients with IBS alone have somatic hypoalgesia (decreased somatic
pain sensation). This study demonstrates that while IBS patients have
increased sensitivity to visceral pain, they are less sensitive to somatic
pain.
UCLA
studies evaluating visceral sensation have also been performed in these
patients using a balloon catheter placed in the rectum and lower large
intestine (colon). The balloon catheter is connected to a computerized
pump which inflates the balloon and thus reaches specific pressure levels
in the bowel. The patient’s sensations in response to the balloon inflation
can be measured. In a recent study published in the journal Gastroenterology,
the investigators at the UCLA Neuroenteric Disease Program showed that
IBS patients have an altered perceptual response to irritation of the
gastrointestinal tract by repetitive distention (inflation of balloon
catheter). IBS patients have an increased sensitivity to balloon distention
in the rectum, while healthy individuals do not. These findings suggest
a compromised ability to activate the body’s own pain inhibition systems
to counter-act the irritation of the gastrointestinal tract. The results
of this study were also discussed in a previous issue of this newsletter
(volume 1, issue 1, Spring 1997). Patients with both IBS + FM also demonstrate
an altered perceptual response to balloon inflation in the gastrointestinal
tract, but to a lesser degree than patients with IBS alone. These data
suggest that IBS have altered perceptual responses to visceral and somatic
pain/discomfort and the coexistence of FM alters these perceptual responses.
To determine
if an alteration in how the brain processes visceral and somatic pain
information in IBS and FM, the investigators at the UCLA Neuroenteric
Disease Program are comparing the brain responses to visceral and somatic
stimuli in patients with IBS alone, IBS + FM, and FM alone. Brain responses
are assessed by positron emission tomography (PET) which can measure blood
flow to brain areas in response to a particular stimulus. During this
study, a visceral stimulus (balloon inflation in the rectum) and a somatic
stimulus (pressure applied to a somatic tender point) are given. Results
have shown that in response to a rectal balloon inflation, IBS patients
exhibit activation in a portion of the brain which is called the prefrontal
cortex. This brain area is involved in the attention and arousal to a
particular stimulus and also in memory retrieval of past pain experiences.
Patients with IBS + FM have activation in this same brain region to a
somatic stimulus but not to a rectal stimulus. Most of the IBS + FM patients
reported greater muscular pain due to FM than abdominal pain from IBS
at the time of the PET study. These findings suggests that brain’s mechanisms
of attention/arousal are activated in response to visceral pain in IBS,
but in response to somatic pain in patients with coexistent FM.
In summary,
clinical characteristics and a significant overlap of symptoms suggest
that the functional syndromes IBS and FM may have a common etiology. Visceral
and somatic perception studies and PET imaging have demonstrated that
each of these conditions have specific responses to painful stimuli and
that patients with both IBS and FM may have responses to somatic and visceral
stimuli that are uniquely different from that of IBS alone and FM alone.
Further studies including PET, visceral perception tests, and sleep studies
are being completed in patients with IBS and/or FM. Hopefully, these studies
will improve the understanding of chronic visceral and somatic pain conditions
and lead to more effective treatment.
If you
would like to learn more about our research program, or if you are interested
in participating in one of our ongoing IBS and fibromyalgia studies, please
contact our clinical trials office at (310) 268-3432.
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