Materials and Methods: This cross-sectional study included 240 women aged 18–65 years who met the 2016 American College of Rheumatology criteria for FM and reported lower urinary tract symptoms for at least three months. OAB was diagnosed based on International Continence Society criteria using the OAB-V8 questionnaire (cut-off ≥8) and a three-day bladder diary. Psychiatric symptoms were assessed using the Hospital Anxiety and Depression Scale (HADS). FM severity was measured using the Widespread Pain Index (WPI), Symptom Severity Scale (SSS), and General Symptom Score (GSS). Patients were divided into FM+OAB and FM−OAB groups. Statistical comparisons and correlation analyses were performed.
Results: OAB was identified in 148 of 240 FM patients (61.7%). The FM+OAB group had significantly higher mean age (47.2 ± 7.4 vs. 41.5 ± 10.1 years, p < 0.001) and fibromyalgia diagnosis time (10.5 ± 8.7 vs. 6.3 ± 6.0 years, p < 0.001) compared to the FM−OAB group. Clinically significant anxiety and depression (HADS ≥8) were more prevalent in the FM+OAB group (52.1% vs. 27.3%, p = 0.006). FM+OAB patients also had higher scores for WPI, SSS, and GSS (all p < 0.001). HADS scores correlated positively with FM symptom severity and OAB-V8 scores (ρ = 0.30–0.42, p < 0.01).
Conclusion: Overactive bladder is highly prevalent among women with fibromyalgia and is associated with greater psychiatric burden and symptom severity. These findings suggest a shared underlying mechanism driven by central sensitization and emotional dysregulation. Routine screening for OAB and psychological distress in FM patients may enhance diagnostic accuracy and guide comprehensive, multidisciplinary treatment strategies.
The pathophysiology of FM and OAB is believed to share common mechanisms, most notably central sensitization-a state of amplified neural signaling in the central nervous system that leads to heightened pain and sensory perception [3,4]. In both disorders, dysregulation of the autonomic nervous system, altered pain processing, and neurogenic inflammation have been implicated. These shared neurobiological pathways suggest that OAB in FM may not merely be coincidental but rather a manifestation of overlapping central dysfunction [1,5,6].
In parallel, psychiatric comorbidities-particularly anxiety and depression-are prevalent in both FM and OAB populations. Up to 60–70% of FM patients experience clinically significant symptoms of depression or anxiety, which have been shown to exacerbate pain, fatigue, and somatic burden [7]. Similarly, psychological distress has been associated with increased urinary urgency and incontinence episodes in patients with OAB, potentially through heightened arousal, cortical hypervigilance, and altered bladder perception [8,9].
Although the independent associations of psychiatric symptoms with FM and OAB are well documented [7,9] limited data exist regarding their combined burden in patients experiencing both conditions [2,10]. In particular, the impact of psychiatric comorbidity on symptom severity and functional status in FM patients with OAB remains poorly understood [10,11]. Elucidating this relationship may inform the development of more integrative treatment strategies [3,9].
The present study aimed to investigate the prevalence and clinical significance of anxiety and depression in FM patients diagnosed with OAB, using validated screening instruments. We further evaluated the relationship between psychiatric symptom burden and FM/OAB severity to better understand the interplay between psychological distress and visceral-somatic sensitization in this patient population.
A total of 240 women aged 18-65 years who met the 2016 American College of Rheumatology (ACR) diagnostic criteria for fibromyalgia [12]. were included. All participants reported LUTS, including urgency, frequency, or nocturia, for a minimum duration of three months. Exclusion criteria included active urinary tract infection, pelvic organ pathology (such as interstitial cystitis or endometriosis), pregnancy, neurological disorders affecting bladder function, a history of pelvic surgery within the past six months, or any systemic condition mimicking OAB symptoms.
OAB was diagnosed according to the International Continence Society (ICS) criteria, defined as urinary urgency (≥3 episodes per week), with or without urgency incontinence, in the absence of urinary tract infection. The Turkish-validated Overactive Bladder Awareness Tool Version 8 (OAB-V8) was administered to all participants, with a score of ≥8 accepted as indicative of OAB [13]. Participants also completed a threeday bladder diary documenting daytime and nighttime voiding frequency, urgency episodes, and urinary incontinence.
Patients were categorized into two groups based on the presence or absence of OAB: FM+OAB and FM-OAB. Fibromyalgia symptom burden was assessed using the Widespread Pain Index (WPI), Symptom Severity Scale (SSS), and General Symptom Score (GSS), applied during face-to-face evaluations by a physical medicine and rehabilitation specialist.
Psychiatric comorbidities were assessed using the Turkish version of the Hospital Anxiety and Depression Scale (HADS) [14]. This instrument consists of two subscales, each scored from 0 to 21, with a cut-off value of ≥8 indicating clinically relevant anxiety or depression.
Statistical Analysis
Statistical analyses were performed using IBM SPSS
Statistics for Windows, Version 25.0 (IBM Corp., Armonk, NY,
USA). Continuous variables were expressed as mean ± standard
deviation (SD), and categorical variables were presented as
frequencies and percentages. The Shapiro–Wilk test was used to
evaluate the normality of continuous variables.
Comparisons between the FM+OAB and FM-OAB groups were made using the independent samples Student's t-test for normally distributed variables and the Mann-Whitney U test for non-normally distributed variables. Categorical variables were compared using Pearson's chi-square test. Spearman's rank correlation coefficient (ρ) was used to assess the relationship between HADS scores and fibromyalgia-related symptom scores (WPI, SSS, GSS) and OAB severity (OAB-V8 score). A p-value <0.05 was considered statistically significant.
Participants in the FM+OAB group were significantly older (47.2±7.4 vs. 41.5±10.1 years; p<0.001) and had a longer duration of fibromyalgia (10.5±8.7 vs. 6.3±6.0 years; p<0.001) compared to the FM−OAB group. No significant difference was observed in educational attainment between the groups (p=0.142).
Clinically significant anxiety (HADS-A ≥8) and depression (HADS-D ≥8) were more common in the FM+OAB group than in the FM−OAB group (52.1% vs. 27.3%; p=0.006 for both). Mean HADS-anxiety scores were significantly higher in the FM+OAB group (10.2±3.1 vs. 7.5±2.8; p<0.001), as were HADS-depression scores (9.4±2.7 vs. 6.3±2.9; p<0.001).
Fibromyalgia symptom burden was also greater in the FM+OAB group. WPI scores were significantly higher (13.8±3.1 vs. 10.4±4.2; p<0.001), as were SSS (7.1±1.9 vs. 5.6±2.1; p< 0.001) and GSS scores (4.9±1.3 vs. 3.2±1.8; p<0.001). These comparisons are summarized in Table 1.
Table 1. Demographic and clinical characteristics of participants by OAB status
Correlation analyses demonstrated significant associations between psychiatric symptoms and fibromyalgia-related measures. HADS-anxiety scores showed moderate positive correlations with WPI (ρ=0.36), SSS (ρ=0.38), and GSS (ρ=0.34), all p<0.01. Similarly, HADS-depression scores correlated with WPI (ρ=0.30), SSS (ρ=0.41), and GSS (ρ=0.33), all p<0.01. In addition, both HADS subscales were positively associated with OAB severity as measured by OAB-V8 scores (ρ=0.42 and ρ=0.39 for anxiety and depression, respectively; p<0.001 for both). These results are presented in Table 2.
Table 2. Correlation between HADS scores and symptom measures
These findings suggest that FM patients with coexisting OAB experience a greater psychiatric and somatic symptom burden compared to those without OAB, with meaningful correlations between psychological distress and symptom severity across domains.
Previous studies have noted that genitourinary symptoms are commonly reported in individuals with FM, yet the underlying mechanisms have not been fully elucidated [1,2,6]. Central sensitization-a state of augmented responsiveness of the central nervous system to stimuli-has been proposed as a unifying pathophysiological framework linking FM and OAB [3,4]. Both disorders share features such as heightened pain perception [5], autonomic dysfunction [6], neurogenic inflammation, and impaired descending inhibitory control [4]. Neuroimaging studies have revealed overlapping activation in regions such as the insula, anterior cingulate cortex, and periaqueductal gray matter in response to both pain and urinary urgency, reinforcing the notion of shared central processing pathways [3,5].
Importantly, our study adds to the existing literature by highlighting the influence of psychological distress on the severity of both FM and OAB symptoms. Anxiety and depression are not only prevalent in these populations but have been shown to modulate symptom intensity, treatment response, and quality of life [7-10]. In our analysis, the strong association between HADS scores and WPI, SSS, and OAB-V8 scores suggests a bidirectional relationship: psychiatric burden may exacerbate somatic and visceral symptoms, while chronic symptomatology may, in turn, worsen psychological wellbeing. This reciprocal amplification reflects a classic pattern seen in other central sensitivity syndromes, including irritable bowel syndrome, chronic fatigue syndrome, and migraine [10,11,15].
From a clinical perspective, our results underscore the importance of integrated assessment and management strategies for FM patients, particularly those reporting LUTS. Systematic screening for OAB symptoms using simple tools such as the OAB-V8 [13], in conjunction with validated psychiatric scales like the HADS, can facilitate earlier recognition and tailored intervention. Multimodal treatment plans incorporating pharmacological (e.g., duloxetine, pregabalin) [16-18], behavioral (e.g., cognitive-behavioral therapy) [19], and physical (e.g., pelvic floor training) modalities [20,21] may be more effective than traditional symptom-based approaches.
This study has several strengths. It is one of the few to examine the relationship between OAB and psychiatric comorbidity in women with fibromyalgia using validated assessment tools, including the 2016 ACR criteria [12], ICSbased OAB definition, and the HADS [14]. The inclusion of a relatively large, well-characterized sample strengthens the reliability of the findings. Subgroup analysis between FM+OAB and FM−OAB allowed for clearer interpretation of psychiatric burden in relation to symptom severity.
However, some limitations should be noted. The crosssectional design prevents causal inference [22]. Reliance on self-reported data, including symptom scales and bladder diaries, may introduce recall bias. Objective urodynamic testing was not performed. Additionally, potential confounders such as medication use, sleep quality, and pain-related psychological factors were not systematically evaluated.
Ethics Committee Approval: Ethical approval for this study was obtained from University of Health Sciences, Umraniye Training and Research Hospital Clinical Research Ethics Committee (Approval number and date: 09.05.2025- B.10.1.TKH.4.34.H.GP.0.01/170).
Informed Consent: An informed consent was obtained from all the patients.
Publication: The results of the study were not published in full or in part in form of abstracts.
Peer-review: Externally peer-reviewed.
Authorship Contributions: Any contribution was not made by any individual not listed as an author. Concept – D.K., F.Y.S.; Design – D.K., S.D.; Supervision – D.K.; Resources – D.K., Z.Ö.A.; Materials – D.K., F.Y.S.; Data Collection and/or Processing – D.K., S.D.; Analysis and/or Interpretation – D.K.; Literature Search – D.K., F.Y.S., Z.Ö.A.; Writing Manuscript – D.K., S.D., F.Y.S; Critical Review – D.K., S.D., F.Y.S, Z.Ö.A.
Conflict of Interest: The authors declare that they have no conflicts of interest.
Financial Disclosure: The authors declare that this study received no financial support.
1) Puri BK, Lee GS. Overactive bladder symptoms in patients
with fibromyalgia: A systematic case-controlled study.
Rev Recent Clin Trials 2021;16(2):202-5.
https://doi.org/10.2174/1574887115999201006201328
2) Goldberg N, Tamam S, Weintraub AY. The association
between overactive bladder and fibromyalgia: A
systematic review and meta-analysis. Int J Gynaecol
Obstet 2022;159(3):630-41.
https://doi.org/10.1002/ijgo.14290
3) Reynolds WS, Dmochowski R, Wein A, Bruehl S. Does
central sensitization help explain idiopathic overactive
bladder? Nat Rev Urol 2016;13(8):481-91.
https://doi.org/10.1038/nrurol.2016.95
4) Woolf CJ. Central sensitization: implications for the
diagnosis and treatment of pain. Pain 2011;152(3
Suppl):S2-S15.
https://doi.org/10.1016/j.pain.2010.09.030
5) Gori MC, Onesti E, Ceccanti M, Cambieri C, Nasta L,
Cervigni M, et al. Central sensitization in the bladder pain
syndrome. JSM Pain Manag 2016;1(1):1004.
https://doi.org/10.47739/2578-3378/1004
6) Tüfekçi B, Sönmezer E, Bayrak Ö, Tüfekçi A. The
examination of variations in the pain characteristics
of women with overactive bladder syndrome. Grand J
Urol 2024;4(3):89–97.
https://doi.org/10.5505/GJU.2024.77699
7) Hadlandsmyth K, Dailey DL, Rakel BA, Zimmerman
MB, Vance CG, Merriwether EN, et al. Somatic symptom
presentations in women with fibromyalgia are differentially
associated with elevated depression and anxiety. J Health
Psychol 2020;25(6):819-29.
https://doi.org/10.1177/1359105317736577
8) Melotti IGR, Juliato CRT, Tanaka M, Riccetto CLZ.
Severe depression and anxiety in women with overactive
bladder. Neurourol Urodyn 2018;37(1):223-8.
https://doi.org/10.1002/nau.23277
9) Lai H, Gardner V, Vetter J, Andriole GL. Correlation
between psychological stress levels and the severity of
overactive bladder symptoms. BMC Urol 2015;15:14.
https://doi.org/10.1186/s12894-015-0009-6
10) Gong H, Huang S. Associations of overactive bladder
(OAB) with suicidal ideation incidence and all-cause
mortality among the U.S. population. BMC Psychiatry
2024;24(1):641.
https://doi.org/10.1186/s12888-024-06107-1
11) Mahjani B, Koskela LR, Batuure A, Gustavsson Mahjani
C, Janecka M, Hultman CM, et al. Systematic review and
meta-analysis identify significant relationships between
clinical anxiety and lower urinary tract symptoms. Brain
Behav 2021;11(9):e2268.
https://doi.org/10.1002/brb3.2268
12) Wolfe F, Clauw DJ, Fitzcharles MA, Goldenberg DL,
Häuser W, Katz RL, et al. 2016 Revisions to the 2010/2011
fibromyalgia diagnostic criteria. Semin Arthritis Rheum
2016;46(3):319-29.
https://doi.org/ 10.1016/j.semarthrit.2016.08.012
13) Tarcan T, Mangır N, Özgür MÖ, Akbal C. OAB‑V8 aşırı
aktif mesane sorgulama formu validasyon çalışması.
Üroloji Bülteni 2012;21(2):113‑6.
14) Aydemir Ö, Güvenir T, Küey L, Kültür S. Hastane
anksiyete ve depresyon ölçeği Türkçe formunun
geçerlilik ve güvenilirlik çalışması. Türk Psikiyatri
Dergisi 1997;8(4):280–7.
15) Kindler LL, Bennett RM, Jones KD. Central sensitivity
syndromes: mounting pathophysiologic evidence to link
fibromyalgia with other common chronic pain disorders.
Pain Manag Nurs 2011;12(1):15-24.
https://doi.org/10.1016/j.pmn.2009.10.003
16) Perahia DG, Pritchett YL, Desaiah D, Raskin J. Efficacy
of duloxetine in painful symptoms: an analgesic or
antidepressant effect? Int Clin Psychopharmacol
2006;21(6):311-7.
https://doi.org/10.1097/01.yic.0000224782.83287.3c
17) Arnold LM, Russell IJ, Diri EW, Duan WR, Young JP Jr,
Sharma U, et al. A 14-week, randomized, double-blinded,
placebo-controlled monotherapy trial of pregabalin in
patients with fibromyalgia. J Pain 2008;9(9):792-805.
https://doi.org/10.1016/j.jpain.2008.03.013
18) Steers WD, Herschorn S, Kreder KJ, Moore K, Strohbehn
K, Yalcin I, et al. Duloxetine compared with placebo for
treating women with symptoms of overactive bladder.
BJU Int 2007;100(2):337-45.
https://doi.org/10.1111/j.1464-410X.2007.06980.x
19) Funada S, Watanabe N, Goto T, Negoro H, Akamatsu S,
Ueno K, et al. Cognitive behavioral therapy for overactive
bladder in women: study protocol for a randomized
controlled trial. BMC Urol 2020;10:129.
https://doi.org/10.1186/s12894-020-00697-0
20) Hay-Smith EJ, Bø Berghmans LC, Hendriks HJ, de Bie RA,
van Waalwijk van Doorn ES. Pelvic floor muscle training
for urinary incontinence in women. Cochrane Database
Syst Rev 2001;(1):CD001407. doi: 10.1002/14651858.
CD001407. Update in: Cochrane Database Syst Rev. 2007
Jul 18;(1):CD001407.
https://doi.org/10.1002/14651858.CD001407