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Int Neurourol J > Volume 17(2); 2013 > Article
Kwon and Chang: Pain, Catastrophizing, and Depression in Chronic Prostatitis/Chronic Pelvic Pain Syndrome


Persistent and disabling pain is the hallmark of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS). However, disease severity (as measured by objective indexes such as those that use radiography or serology) is only marginally related to patients’ reports of pain severity, and pain-related presentation can differ widely among individuals with CP/CPPS. Increasing evidence in support of the biopsychosocial model of pain suggests that cognitive and emotional processes are crucial contributors to inter-individual differences in the perception and impact of pain. This review describes the growing body of literature relating depression and catastrophizing to the experience of pain and pain-related sequelae in CP/CPPS. Depression and catastrophizing are consistently associated with the reported severity of pain, sensitivity to pain, physical disability, poor treatment outcomes, and inflammatory disease activity and potentially with early mortality. A variety of pathways, from cognitive to behavioral to neuro-physiological, seem to mediate these deleterious effects. Collectively, depression and catastrophizing are critically important variables in understanding the experience of pain in patients with CP/CPPS. Pain, depression, and catastrophizing might all be uniquely important therapeutic targets in the multimodal management of a range of such conditions.



    Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) is a common male chronic pain condition. Its prevalence ranges from 9% to 16% worldwide and from 5% to 25% in Korea [13]. CP/CPPS presents with various voiding symptoms, perineal or suprapubic pain, erectile dysfunction or sexual disturbance, and psychological problems such as depression and catastrophizing, which have a negative impact on health-related quality of life (QoL) [4,5]. However, the etiology of CP/CPPS is uncertain. Various theories have been hypothesized, such as inflammation, pathogen and host-specific factors, pelvic floor tension myalgia, and differences in systemic pressure sensitivity [68]. It has been suggested that this condition has significant psychological components, because most CP/CPPS patients have depression and catastrophizing [9]. It has also been suggested that stress is a potent factor in the development, prolongation, and perpetuation of the symptoms in the condition known generally as chronic prostatitis [10].
    The severity of stress has been reported to depend on individual perception or subjective interpretation of causative factors rather than on the contents or frequency of the factors causing stress [11]. That is, individual coping strategies for each stress and cognitive assessment of stress have been suggested to significantly affect stress progression [12]. Coping strategies refer to cognitive and behavioral efforts that are used to satisfy external or internal demands, and they have been known to act as regulators between stress and psychological disorders or physical diseases [13]. Therefore, in addition to stress frequency, differences in stress perception and coping strategies should be considered as factors causing or deteriorating stress symptoms in patients with CP/CPPS.
    Physical disease and psychiatric disorders coexist in CP/CPPS [14], with as many as 78% of patients with CP/CPPS reporting depression [15] and 60% meeting the criteria for a major depressive disorder [16]. Furthermore, greater depression and not having a partner for support were associated with poorer CP/ CPPS outcomes [5]. Adding to the depression concern, CP/CPPS pain and QoL outcomes are predicted by a particular set of psychosocial risk factors, including low social support and pain catastrophizing [5,17,18]. Pain catastrophizing is associated with chronic pain and it may be a key component in the clinical phenotypic classification of male urologic chronic pelvic pain [19,20]. Catastrophizing is the tendency to employ a set of pain-associated cognitive appraisals referred to as ruminative (“can’t keep it out of my mind”), magnifying (“makes me think about other pains”), and helpless (“there is nothing I can do”) when undergoing or anticipating pain [21]. Catastrophizing is associated with anxiety and depression but is considered a unique factor in pain [18,21]. With control for urinary symptoms and depression, catastrophizing was the strongest biopsychosocial predictor of CP/CPPS pain and was shown to be a robust predictor of diminished mental status QoL in men with CP/CPPS [17,18]. CP/CPPS research supports the necessity and rationale for a specific cognitive behavioral treatment model. There has been interest in considering psychosocial treatments [18,22] and approaches to reduce the psychosocial risk factors associated with poor CP/CPPS outcomes [23]. Although the concept of “psychogenic” pain has (appropriately) been abandoned, it is clear that negative emotional processes such as depression and catastrophizing can increase the level of pain perceived by patients with CP/CPPS through a range of mechanisms, which we review here.


    A number of small cohort studies have investigated the impact of CP/CPPS on men with regard to QoL, sexual function, and psychological aspects (Table 1) [5,16]. In the National Institutes of Health (NIH) Chronic Prostatitis Cohort study, McNaughton Collins et al. [24] reported an association of reduction in mental and physical items of the Short Form-12 QoL measures with increasing severities of CP/CPPS symptoms. Another study, in a large healthy population, indicated that bladder symptoms, including urinary frequency and incomplete emptying, have a greater detrimental effect on QoL than do pain symptoms. A further study, which evaluated the management of CP/CPPS patients in primary care settings, showed that worse QoL is associated with greater pain and urinary symptoms and that pelvic pain is associated with worse QoL than urinary symptoms [25]. On the basis of the results from the 463 men enrolled in the NIH Chronic Prostatitis Cohort Study, which included data from seven clinical centers, Tripp et al. [5] indicated that the severity of pelvic pain can be strongly predicted by depressive symptoms, beyond the contributions of urinary symptom scores and age. Recently, a case-control study conducted by Clemens et al. [26] also showed that depression and panic disorder are significantly more common in men with CP/CPPS than in controls. Many patients with pelvic pain reported continuing symptoms of depression and anxiety despite receiving treatment medications. These findings suggest that the mental health disorders may be more difficult to treat in patients with urologic pain syndromes [26]. Pelvic pain and urinary symptoms both contribute to reduced QoL and depressive mood experienced by CP/CPPS patients [27].
    The first study examining catastrophizing in CP/CPPS was conducted by the NIH Chronic Prostatitis Collaborative Research Network (CPCRN) Study Group [18,28], which found that catastrophizing was correlated with greater disability, higher urinary scores, depressive symptoms, and pain. Furthermore, catastrophizing was a significant predictor of pain when the analysis was controlled for demographic and psychosocial variables. Another recent study showed that diminished mental status QoL was predicted by greater helplessness catastrophizing and lower social support from friends and family, beyond the demographic, medical status, and other psychosocial variables in the analyses [17]. Furthermore, Tripp et al. [29] showed that an adolescent male sample (aged 16 to 19 years) reported a prevalence of at least mild prostatitis-like symptoms at 8.3%, with 3% reporting a pain domain score of >7.
    Pain, urinary symptoms, depressive symptoms, and catastrophizing were all correlated with poorer QoL and the catastrophizing magnification domain was the lone predictor of poorer QoL after control for pain and urinary scores. These findings have increased the desire to model treatment of urologic chronic pelvic pain syndromes from a framework that manages individual patients through the use of a multimodal therapy approach. UPOINT (urological, psychosocial, organ-specific, infection, neurological, and tenderness of skeletal muscles) is a 6-point clinical classification system that includes a psychosocial domain (i.e., catastrophizing) [30].


    Acute (category I) and chronic (category II) bacterial prostatitis are the best understood and least common of the prostatitis syndromes. CP/CPPS, with or without inflammation, is the third category of prostatitis syndromes. In CP/CPPS type IIIA (with inflammation), urine, semen, and other fluids from the prostate show no evidence of infection. Type IIIB (no inflammation) is regarded as the most common but also the least understood [31]. The fourth category of prostatitis is asymptomatic inflammatory prostatitis in which white blood cells are present in the semen but there is no pain.

    A Symptom Complex Rather Than a Specific Disease

    CP/CPPS symptoms can vary without warning, with most men reporting acute pain attacks, longstanding persistent pain, or a combination [32]. CP/CPPS pain is localized to urogenital regions (perineum, pelvic area, and/or genitalia) [33,34]. Similar to other chronically painful conditions, the pain in CP/CPPS does not correspond strongly with medical findings [35]. Although CP/CPPS patients may include those with inflammatory prostate findings, no pathognomonic, histologic, or radiologic findings exist for confirmatory diagnosis. The important reality is that no postulated molecular mechanism explains the symptoms of CP/CPPS. Several case series show lack of CP/CPPS symptom improvement after end organ removal (cystectomy and prostatectomy) [36,37]. Thus, CP/CPPS is a symptom complex rather than a specific disease [38,39].
    The NIH definition of CP/CPPS is pelvic pain for 3 of the previous 6 months, with or without voiding symptoms and with no evidence of uropathogenic bacterial infection [32]. Symptoms of CP/CPPS do not routinely remit, with 66% of subjects in community-based samples experiencing symptoms 1 year later [32], and tertiary care patients showing no drop in their pain, depression, or catastrophizing over a multi-year assessment [40]. Treatment successes in CP/CPPS have been described as dismal, with strategies based on sequential mono-therapies considered suboptimal for patients with long histories of severe CP/CPPS [31]. The QoL of individuals with CP/CPPS is diminished to a level comparable to that experienced by patients with severe congestive heart failure, myocardial infarction, unstable angina, hemodialysis-dependent end-stage renal disease, or active Crohn’s disease [24,41].
    Thus, CP/CPPS is a heterogeneous condition in terms of its clinical manifestation and, most likely, its underlying mechanism. This heterogeneity is evidenced by four critical observations: 1) the clinical presentation of patients varies from one patient to the next, 2) a single patient may have symptoms that fluctuate over time [42], 3) varying etiological mechanisms (e.g., infection, inflammation, and nerve damage) may account for the observed pathology in the same patient and between patients [43], and 4) the symptoms of CP/CPPS overlap with those of irritable bowel syndrome, fibromyalgia, chronic fatigue syndrome, and other chronic pain disorders [44].

    Mechanistic Insight Into CP/CPPS Through Phenotyping

    There is a need for the development of a deeper mechanistic understanding of the etiology and progression of CP/CPPS [45]. Phenotyping is one way to address the knowledge deficit that exists and will improve mechanistic understanding of the syndrome. Phenotyping research explores the etiology and mechanisms of disease and fluctuations in symptoms and pathology over time [46]. A phenotyping system provides a platform through which associations can be made between genotypes and phenotypes. To make these associations, there must be a system for consistently defining and characterizing phenotypes. Thus, new genetic findings can then be placed into a preexisting system and matched and associated with specific clinical presentations.

    UPOINT: evaluation of a novel CP/CPPS phenotyping system

    In 2009, Nickel and Shoskes [47] introduced UPOINT, an original system that categorizes CP/CPPS symptoms in six domains: urological, psychosocial, organ-specific, infection, neurological, and tenderness of skeletal muscles. It accords broadly with the NIH Chronic Prostatitis Symptom Index (NIH-CPSI) scale, which currently serves as the standardized symptom severity questionnaire in CP/CPPS. However, it is important to note that CP/CPPS, by definition, is a chronic pain syndrome and therefore is encapsulated by the pain domain [44,48]. Thus, a high total NIH-CPSI score may not necessarily reflect pain severity as captured by a high pain-domain score but could result from a high voiding score (representing voiding dysfunction). In such a case, UPOINT is not a sensitive measure of chronic pain symptoms, a hallmark that defines CP/CPPS. Besides, the concordance of UPOINT domains with the NIH-CPSI score is most likely a byproduct of the similarities in scope and approach between the two systems. UPOINT was created on the basis of studies conducted with the use of the NIH-CPSI.
    In reality, the UPOINT system emerged because clinical trials (evaluating α-blockers, pentosan polysulfate, and pregabalin) failed to detect a significant difference between intervention and placebo, but significant differences were observed in secondary outcomes, such as QoL [44,47]. Therefore, it appeared feasible to define cohorts on the basis of secondary outcomes and to establish treatment guidelines for each group. However, the unknown optimal duration of therapy and the placebo effect limit the generalizability of these results [19]. Importantly, UPOINT is limited by the strength of correlation between symptoms and disease mechanisms and provides little improvement in mechanistically driven treatment outcomes when compared with the NIH-CPSI. Lastly, because a single physician examined and diagnosed all the patients, the UPOINT study has the risk of having a biased cohort. Commendably, however, UPOINT recognizes and seeks to address the heterogeneity present in patients with CP/CPPS.

    DABBEC: moving toward a mechanistically predictive phenotyping system

    Allsop et al. [49] proposed the DABBEC (dimitrakoff, allsop, brook, bhai, erstad, and cohen) phenotyping system (DPS) as a clinically useful method for phenotyping patients, designing clinical trials, and evaluating the efficacy of mechanistically driven treatments for CP/CPPS. This system incorporates a view of CP/CPPS as both a localized and a systemic condition. The DPS consists of four scoring domains: the NIH-CPSI, localized-versus-systemic, hypothalamic-pituitary-adrenal axis/sympathetic nervous system (HPA/SNA), and CYP21a2 phenotype.
    Following a clinical diagnosis of CP/CPPS, as recommended by the CPCRN guidelines [50], the authors suggest that clinicians administer questionnaire instruments to assess the patient’s constitutional, psychological, and cognitive symptom domains. This symptom domain phenotyping will be helpful in identifying comorbidities, such as depression, anxiety, and catastrophizing conditions that are highly prevalent in patients with CP/ CPPS. CPCRN recommends that such patients receive multi-modal therapy in the context of multidisciplinary teams of psychologists, neurologists, and internists.

    Psychosocial Domain of UPOINT

    The following psychosocial questionnaires may be useful if it is believed that psychosocial parameters may be important on the basis of probing questions asked during the history taking.

    Patient health questionnaire

    This self-administered tool provides an assessment of depression and anxiety [51]. We summed the responses on the depressive symptoms section to create a depressive symptoms index of 0–27, with higher scores representing greater depressive symptoms.

    Pain catastrophizing scale (PCS)

    This scale assesses three measures of negative thoughts associated with pain: rumination or worry, magnification, and helplessness [52]. Rumination and magnification tend to be considered reactionary or proximal cognitive responses to pain experience, whereas helplessness may develop at a later time following ruminative or magnifying thoughts about pain. Helplessness is associated with feelings of despair and represents the internal belief that one cannot manage one’s pain. The PCS is reliable [53], and catastrophizing has been shown to be a significant psychological predictor of both pain [18] and QoL [17] for patients with CP/CPPS.
    Patients with chronic pain often have maladaptive coping mechanisms (for example, catastrophizing) and may suffer from depression, anxiety, or stress or have a history of sexual or other physical abuse. Psychometric evaluations of men with CP/CPPS compared with healthy control men showed significantly higher scores on all assessments except type A behavior. Especially notable were the highest differential rankings for somatization, depression, psychoticism, and phobic anxiety in men with CP/CPPS [54]. These observations of psychological disturbances in men with CP/CPPS were anticipated and in agreement with earlier reports [10,18,5558].


    Increasing Pain Severity and Sensitivity

    Catastrophizing is a robust pain predictor across clinical and nonclinical samples [18] and is important in understanding CP/CPPS outcomes. The first study examining catastrophizing in CP/CPPS found it to be associated with greater disability, depression, urinary symptoms, and pain [18]. Furthermore, helplessness catastrophizing was the strongest pain predictor, even when urinary symptoms and depression were controlled for. In another study, CP/CPPS QoL determinants showed that diminished mental health status was predicted by greater helplessness catastrophizing and lower social support from friends and family, beyond all demographic, medical status, and other competing psychosocial variables [24]. Helplessness catastrophizing is a predominant pain and QoL predictor in CP/CPPS and is expressed by patients reporting longer pain durations (e.g., 4–7 years) [59]. It is worth noting that the relationship between helplessness and pain is not specific to CP/CPPS and is likely to be a manifestation of suffering from long-term pain. Thus, it might be expected that those suffering in the earlier stages of chronicity may manifest different interrelating factors. For example, the male adolescent community-dwelling sample in Canada (16–19 years old) reported a high prevalence of chronic prostatitis-like symptoms (8.3%) [29], with pain, urinary symptoms, depressive symptoms, and catastrophizing all being associated with diminished QoL. Ancillary analyses also indicated that the magnification subscale for catastrophizing (e.g., “I keep thinking of other painful events”) was the lone predictor of poorer QoL when the analysis was controlled for urinary status and pain.

    Enhanced Inflammatory Disease Activity

    One experimental study also confirmed that chronic stress in rats can specifically induce histological inflammation of the prostate [60]. In patients with CP/CPPS there appear to be some direct, measurable effects of stress or stress decreases on cytokine levels. Chronic activation of the physiologic stress response augments the release of proinflammatory cytokines and prostaglandins that may contribute to CP/CPPS [61]. In CP/CPPS patients, the degree of spousal concern and support as well as an effort to distract the patient from symptoms correlates with lower seminal plasma interleukin (IL)-6 and IL-10 concentrations [62]. Also, patients with depression have been shown to have lower levels of IL-10 in peripheral blood mononuclear cells than do control subjects [63]. Thus, stress changes appear to have measurable effects on proinflammatory cytokine levels in patients with CP/CPPS, which suggests that there may be a link with histologic inflammation of the prostate [64].


    The mechanisms underlying the association of psychosocial factors with CP/CPPS remain unclear. It was suggested that stress accompanied by depression and catastrophizing is a potent factor in the development, prolongation, and perpetuation of CP/CPPS symptoms [10,28]. For the sake of clarify, Fig. 1 simplifies the presentation of these factors as independent factors and the pathways as unidirectional, but the discussion below demonstrates our increasing knowledge of the interdependencies of these mechanisms.

    Alterations in Central Nervous System (CNS) Processing

    Incoming signals in the CNS are subject to modulation (both facilitation and inhibition) at a variety of sites. One of the mechanisms by which catastrophizing and depression are thought to influence the experience of pain is by promoting sensitization or by interfering with endogenous pain inhibition in the CNS [65], a hypothesis that can be readily investigated by using noninvasive functional neuroimaging methods such as functional magnetic resonance imaging (fMRI). Among patients with fibromyalgia, for example, those who catastrophized most showed the greatest extent of activation in pain-processing brain areas such as the anterior cingulate and dorsolateral prefrontal cortex during the administration of calibrated noxious stimuli [66]. A recent fMRI study revealed specific pain-related brain activation in patients with CP/CPPS, thus suggesting an ongoing reorganization of the brain circuitry [67]. In a related fMRI study of individuals with major depression, catastrophizing cognitions such as perceived helplessness were related to stronger activation of the amygdala (a key component of the limbic system) during both pain and anticipation of pain [68]. Finally, inducing a depressed mood state increased subjects’ level of catastrophizing, impaired their emotion-regulation neurocircuitry, and amplified their cortical responses to a noxious stimulus [69].
    Taken together, these functional neuroimaging studies highlight the roles of negative cognitive and emotional processes in amplifying the transmission of pain-related signals in the cortex. Interestingly, one study showed that CP/CPPS is associated with a reduction of relative gray matter in the anterior cingulate cortex [70]. Assuming a core function in pain suppression, the relative reduction in gray matter volume provides evidence of gray matter changes as sequelae of chronic neuroanatomical pain susceptibility. Such evidence supports the findings of corresponding publications regarding chronic back pain, phantom pain, migraine, fibromyalgia, and irritable bowel syndrome [7173]. Moreover, these structural changes in the brain may be most closely associated with depression and emotional aspects of chronic pain [74,75].
    We believe that advanced imaging methods, such as brain fMRI and neuroimaging, can provide a unique bridge to disease staging in CP/CPPS. Establishing a universal staging system will provide a uniform language and system of communication among different working groups in terms of the natural history of the disease, progression, and treatment outcomes in clinical trials of CP/CPPS treatments.

    HPA Axis Dysfunction

    Depression and catastrophizing can also influence HPA axis responses. Studies have shown that HPA dysregulation may lead to abnormalities of inflammatory responses, resulting in chronic inflammatory and pain conditions such as interstitial cystitis or CP/CPPS [58,76]. Men with CP/CPPS have a greater slope of the awakening cortisol response than do age-matched healthy controls, which suggests a dysfunctional HPA axis [58]. The awakening cortisol response serves as a useful index of adrenocortical activity, which provides important information on the activation of the HPA axis. The relatively high intraindividual stability of the awakening cortisol response when measured over repeated days partly reflects a personal trait. However, HPA axis responses can be influenced by environmental factors including depression and catastrophizing and can serve as an indicator of allostatic load. Allostatic load can take the form of alteration in diurnal cortisol rhythm. Systemic cortisol modulates several systems including the balance between cellular and humoral immunity, or the HPA feedback system. HPA axis dysregulation can be manifested either as pathologically decreased or increased cortisol responses. Some abnormalities may lead to dysregulation of inflammatory responses, resulting in chronic inflammatory and pain conditions such as fibromyalgia and interstitial cystitis [76,77]. These symptomatically varied conditions share a common feature of lowered activity of the HPA axis. Blunted awakening cortisol responses are also reported in subjects with burnout or persistent sciatic pain after discectomy [78,79]. These conditions are the opposite of the augmented awakening cortisol response that we have observed in patients with CPPS. Several other studies have also shown an association between increased cortisol levels after awakening and psychological variables in chronically stressed individuals owing to work overload [80,81].
    Depression and catastrophizing appear to have a similar pattern of HPA axis dysregulation. Whereas hypercortisolism is associated with clinical depression, this observation has also been made in the nonclinical range of depression in healthy young men [82]. The consistent observation that hypercortisolism and depression appear together has led many authors to suggest that increased cortisol levels can cause depressive symptoms and that depressive symptoms can be reversed with anti-depressant actions on HPA regulation [82]. Psychological stress has long been implicated as contributory to the etiology or exacerbation of CP/CPPS [2,10]. Prospective studies have associated perceived stress longitudinally with pain intensity and have examined cognitive/behavioral variables, such as catastrophizing, as predictors of greater pain intensity and disability [18].

    Genetic Influence

    CP/CPPS and depression and catastrophizing may also originate from a shared genetic susceptibility. Among all categories of depression and catastrophizing, panic disorder was mentioned as being highly associated with CP/CPPS. Some prior studies documented that patients with panic disorder were more likely to have symptoms of bladder pain syndrome/interstitial cystitis (BPS/IC) [83,84], which may represent the same underlying condition as CP/CPPS [26]. The possible common genetic susceptibility shared by BPS/IC and depression and catastrophizing might be linked to the Barrington nucleus, which provides an anatomical substrate for coregulation of pelvic visceral symptoms and mental activity in the prosencephalon [85]. Depression and catastrophizing and panic disorder are often comorbid with one another owing to the similarity of their causes, meaning that those who suffer from one often suffer from the other, or will later in life. Therefore, despite the lack of genetic data regarding the association between CP/CPPS and depression and catastrophizing, a common genetic vulnerability might be one possible explanation.
    Several studies hint at a potential genetic underpinning for some of the overlap between pain, depression, and catastrophizing. Recent work has focused on the gene coding for catechol O-methyltransferase (COMT), an enzyme that degrades catecholamines (which in turn affect the functioning of endogenous opioid systems). To date, certain COMT genotypes have been associated with widespread pain [86], depression [87], and enhanced sensitivity to pain [88]. A daily diary study in patients with fibromyalgia reported a significant interaction between COMT genotype and pain fluctuations, such that individuals with the “high pain sensitivity” genotype experienced a greater decline in positive emotion on days when pain was elevated than did individuals with other COMT genotypes. Similarly, in a prospective study of joint pain [89], COMT genotype interacted with individual differences in catastrophizing to predict long-term pain outcomes. Subjects with high levels of catastrophizing reported the most severe persistent pain, but only if they also had a COMT profile that reflected high pain sensitivity [89]. That finding indicates that genetic influences might moderate the impact of psychosocial factors on pain outcomes. We believe that future studies will identify additional biomarkers, provide validation to existing biomarkers, and elucidate additional pathogenetic mechanisms in CP/CPPS.


    Following on the clinical necessity of these findings, a psychotherapy model was proposed that targeted the empirically supported CP/CPPS psychosocial risk factors (depression and catastrophizing) [30], and a study was conducted to examine the treatment feasibility of a risk factor reduction intervention [90]. Specifically, we sought to determine the feasibility of a cognitive-behavioral symptom management program for the acute improvement of psychosocial risk factors of diminished QoL in patients with CP/CPPS. In the study, mean baseline scores showed significant linear reductions in pain, disability, and catastrophizing over time. In addition, positive but modest changes were made in depressive symptoms and social support. The study also showed that follow-up scores for QoL were improved and CP/CPPS symptoms significantly reduced. Furthermore, the baseline to 8-week termination analysis showed that score changes for CP/CPPS symptoms and psychosocial risk factors were predicted by reductions in catastrophizing. We concluded that psychosocial management programs can target and significantly reduce several empirically supported psychosocial risk factors associated with poorer CP/CPPS outcomes, but a randomized controlled trial with longitudinal follow-up is needed.


    The literature on catastrophizing and depression in patients with CP/CPPS strongly implicates these factors as having a profound long-term influence on the shaping of pain responses and pain outcomes. To date, abundant evidence suggests that depression and catastrophizing about pain can serve as prospective markers of risk for negative pain-related endpoints, including severe physical disability, disease progression, and lack of improvement following surgical and other interventions. Further research in this area should help to tailor analgesic interventions to individual characteristics, and it seems likely that catastrophizing and depression will be important factors to consider in the selection of individualized treatments. Collectively, catastrophizing and depression are complex biopsychosocial constructs that exert their detrimental effects via multiple overlapping pathways. Fortunately, psychological interventions, particularly cognitive-behavioral therapy, can evidently reduce catastrophizing and depression in some groups of CP/CPPS patients. In the future, it will be important to evaluate the potential long-term benefits of reducing catastrophizing and depression in patients with CP/CPPS, with a particular focus on studies of tailored early intervention that may help to move patients from a high-risk to a relatively lower risk profile to improve long-term pain outcomes.


    No potential conflict of interest relevant to this article was reported.


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    Fig. 1
    Depression and catastrophizing: influence on pain-related outcomes. Depression and catastrophizing comprise overlapping yet distinct sets of negative emotional processes. These factors influence a broad spectrum of pain-related outcomes via a variety of pathways. CNS, central nervous system.
    Table 1
    Examples of adverse outcomes of depression and catastrophizing in studies
    Sample Outcome Study
      Patients with CP/CPPS Prostatitis patients were employed but reported that their symptoms greatly interfered with their sexual/romantic relationships, and half of the prostatitis patients met criteria for major depression Egan and Krieger (1994) [16]
      Patients with CP/CPPS An association of reduction in mental and physical items of the Short Form-12 QoL measures with increasing severities of CP/CPPS symptoms McNaughton Collins et al. (2001) [24]
      Patients with CP/CPPS The severity of pelvic pain can be strongly predicted by depressive symptoms, beyond the contributions of urinary symptom scores and age Tripp et al. (2004) [5]
      Case control study Depression and panic disorder are significantly more common in men with CP/CPPS than in controls Clemens et al. (2008) [26]
      Population-based study CP patients experienced an increased risk of depressive disorder compared with non-CP patients during a 3-year follow-up period Chung et al. (2011) [7]
      Cohort study CP/CPPS patients had depression, anxiety, and higher perception of stress Ahn et al. (2012) [28]
      Patients with CP/CPPS Catastrophizing was a significant pain predictor when demographic and psychosocial variables were controlled Tripp et al. (2006) [18]
      Patients with CP/CPPS Diminished mental status QoL was predicted by greater helplessness catastrophizing and lower social support from friends and family, beyond the demographic, medical status, and other psychosocial variables in the analyses Nickel et al. (2008) [17]
      Adolescent male Adolescent male sample (aged 16 to 19 years) reported a prevalence of at least mild prostatitis-like symptoms at 8.3%, with 3% reporting a pain domain score of >7. Catastrophizing was correlated with diminished QoL Tripp et al. (2009) [29]

    CP/CPPS, chronic prostatitis/chronic pelvic pain syndrome; QoL, quality of life.

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