There is consistent epidemiologic association between the presence of interstitial cystitis/ painful bladder syndrome (IC/PBS) and certain somatic syndromes (e.g., fibromyalgia, irritable bowel syndrome, chronic fatigue syndrome) and psychiatric illness (anxiety, depression). While these associations are well established, their clinical significance has not been evaluated. A central hypothesis of this MAPP Discovery Site proposal is that certain IC/PBS patients have central abnormalities of pain processing. If true, then patients with multiple co-morbidities could represent a more severe disease phenotype which would be associated with worse clinical outcomes. We hypothesize that over four years of study, about 25% of women will have progression of IC/PBS symptoms, and 25% will have symptom regression;and that IC/ PBS patients will have a high rate of co-morbid systemic somatic symptoms at baseline (35%), that they will develop other regional pain symptoms and syndromes over time, and that these co-morbidities will be associated with IC/PBS symptom progression. The coexistence of multiple pain syndromes in individual subjects will reinforce the idea that IC/PBS patients have a central disturbance in pain processing rather than a disorder confined to the bladder. We hypothesize that clinic based patients and community women who have both sought and not sought urologist care each represent a subset of the women with bladder and other co-morbid symptoms, and that they differ from each other in terms of predominance and severity of co-morbidities and psychosocial characteristics. Using research methods developed by our group as part of the ongoing RAND Interstitial Cystitis Epidemiology (RICE) Study, we propose to recruit and follow a community-based probability sample of women with IC/PBS symptoms in Michigan, Indiana and Ohio, and combine them with a convenience sample of female IC/PBS patients from the University of Michigan urology clinic. These samples will allow us to assess and follow subjects with various degrees of IC/PBS severity. These methods are easily applied to additional geographic regions, and we propose that this study be done as a collaborative project with other MAPP Discovery Sites.
Specific Aims :
AIM 1 - To study the natural history of IC/PBS.
AIM 2 - To identify risk factors associated with symptom progression in women with IC/ PBS.
AIM 3 - To assess factors associated with healthcare seeking in individuals with IC/PBS symptoms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01DK082345-02
Application #
7928827
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
2
Fiscal Year
2009
Total Cost
$222,947
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Sutcliffe, Siobhan; Jemielita, Thomas; Lai, H Henry et al. (2018) A Case-Crossover Study of Urological Chronic Pelvic Pain Syndrome Flare Triggers in the MAPP Research Network. J Urol 199:1245-1251
Harper, Daniel E; Ichesco, Eric; Schrepf, Andrew et al. (2018) Relationships between brain metabolite levels, functional connectivity, and negative mood in urologic chronic pelvic pain syndrome patients compared to controls: A MAPP research network study. Neuroimage Clin 17:570-578
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Lai, H Henry; Jemielita, Thomas; Sutcliffe, Siobhan et al. (2017) Characterization of Whole Body Pain in Urological Chronic Pelvic Pain Syndrome at Baseline: A MAPP Research Network Study. J Urol 198:622-631
Dagher, Adelle; Curatolo, Adam; Sachdev, Monisha et al. (2017) Identification of novel non-invasive biomarkers of urinary chronic pelvic pain syndrome: findings from the Multidisciplinary Approach to the Study of Chronic Pelvic Pain (MAPP) Research Network. BJU Int 120:130-142
Harte, Steven E; Ichesco, Eric; Hampson, Johnson P et al. (2016) Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula. Pain 157:1933-45

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