- Research article
- Open Access
OMERACT-based fibromyalgia symptom subgroups: an exploratory cluster analysis
Arthritis Research & Therapy volume 16, Article number: 463 (2014)
The aim of this study was to identify subsets of patients with fibromyalgia with similar symptom profiles using the Outcome Measures in Rheumatology (OMERACT) core symptom domains.
Female patients with a diagnosis of fibromyalgia and currently meeting fibromyalgia research survey criteria completed the Brief Pain Inventory, the 30-item Profile of Mood States, the Medical Outcomes Sleep Scale, the Multidimensional Fatigue Inventory, the Multiple Ability Self-Report Questionnaire, the Fibromyalgia Impact Questionnaire-Revised (FIQ-R) and the Short Form-36 between 1 June 2011 and 31 October 2011. Hierarchical agglomerative clustering was used to identify subgroups of patients with similar symptom profiles. To validate the results from this sample, hierarchical agglomerative clustering was repeated in an external sample of female patients with fibromyalgia with similar inclusion criteria.
A total of 581 females with a mean age of 55.1 (range, 20.1 to 90.2) years were included. A four-cluster solution best fit the data, and each clustering variable differed significantly (P <0.0001) among the four clusters. The four clusters divided the sample into severity levels: Cluster 1 reflects the lowest average levels across all symptoms, and cluster 4 reflects the highest average levels. Clusters 2 and 3 capture moderate symptoms levels. Clusters 2 and 3 differed mainly in profiles of anxiety and depression, with Cluster 2 having lower levels of depression and anxiety than Cluster 3, despite higher levels of pain. The results of the cluster analysis of the external sample (n = 478) looked very similar to those found in the original cluster analysis, except for a slight difference in sleep problems. This was despite having patients in the validation sample who were significantly younger (P <0.0001) and had more severe symptoms (higher FIQ-R total scores (P = 0.0004)).
In our study, we incorporated core OMERACT symptom domains, which allowed for clustering based on a comprehensive symptom profile. Although our exploratory cluster solution needs confirmation in a longitudinal study, this approach could provide a rationale to support the study of individualized clinical evaluation and intervention.
Despite chronic, widespread pain being its cardinal symptom, fibromyalgia (FM) actually presents as a heterogeneous symptom complex that remains poorly understood ,. In addition to pain, frequently occurring symptoms include fatigue, unrefreshing sleep, cognitive difficulties, headache, anxiety and depression . Patients with FM often present with varying combinations and degrees of severity of these symptoms, which further complicates the ability to understand FM and makes its study challenging . Stratifying patients into more homogeneous subgroups may facilitate better understanding of FM.
Several studies have reported homogeneous subgroups within samples of patients with FM discovered using the exploratory data-mining technique of cluster analysis -. Variables used to identify clusters in these studies have included sociodemographic variables, patient responses to self-report questionnaires, physiological and psychophysiological parameters, biomarkers, comorbidities and psychosocial functioning. For example, Giesecke et al. categorized patients with FM based on self-report measures and evoked pain testing . In their study, 97 patients were clustered into three subgroups: (1) extreme tenderness with normal mood, (2) low tenderness with moderate mood and (3) extreme tenderness with low mood. In another study, by de Souza et al., patients with FM were clustered into two groups based on their responses to the Fibromyalgia Impact Questionnaire (FIQ) . In that study, both clusters reported similar levels of pain, fatigue and stiffness, but differed on severity of morning tiredness, anxiety and depression. Similarly, Docampo et al. clustered a large sample of Spanish patients with FM into three groups using dimensions of symptomatology, comorbidities and clinical scales. These subgroups included (1) low symptomatology and comorbidities, (2) high symptomatology and comorbidities and (3) high symptomatology and low comorbidities. These studies illustrate the symptom spectrum and symptom combinations that are possible in a heterogeneous sample of patients carrying the same diagnosis, and the results are consistent with those of Loevinger et al. and Wilson et al. ,. It has also been reported that patients with FM belonging to different clusters may respond differently to pain rehabilitation. In separate studies, Verra et al. and Turk et al. demonstrated that (1) the same treatment can yield different responses, depending upon symptom constitution of a subgroup; and (2) tailoring treatment based on symptoms could improve treatment efficacy ,.
Although a wide range of variables have been used to identify clusters of patients with FM, few studies have included a comprehensive symptom profile. The Outcome Measures in Rheumatology (OMERACT) FM working group recommended 12 domains (including both symptoms and biomarkers) to be used in FM studies: pain, fatigue, sleep disturbance, depression, anxiety, stiffness, dyscognition, patient global impression of health, multidimensional functioning, tenderness, cerebrospinal fluid (CSF) biomarkers and pain-related neuroimaging markers (if available) . The OMERACT domains provide an all-inclusive list of symptoms that may be used to better understand FM. Our objective in the present study was to identify clusters within a heterogeneous sample of patients with FM using OMERACT symptom domains assessed with validated, self-report questionnaires. We then sought to validate our cluster results in an independent sample of patients with FM.
The study was approved by the Mayo Clinic Institutional Review Board, and all participants provided written informed consent.
Data for the exploratory cluster analysis were derived from survey responses of a sample of patients randomly selected from an existing FM registry that has been described previously . Briefly, the FM registry is composed of patients who have been seen at the Mayo Clinic with a diagnosis of FM since 1 January 2000 and have consented to enrollment in the registry. Participants were invited to participate by postal survey and completed a questionnaire package that included the Brief Pain Inventory (BPI) , the 30-item Profile of Mood States (30-item POMS) , the Medical Outcomes Study Sleep Scale (MOS-Sleep) , the Multidimensional Fatigue Inventory (MFI-20) , the Multiple Ability Self-report Questionnaire (MASQ) , the Revised Fibromyalgia Impact Questionnaire (FIQ-R)  and the 36-item Short Form survey (SF-36) . All instruments included are considered appropriate in meaningfully characterizing the multiple facets of FM as described by Williams and Arnold .
Only female respondents who met FM research survey criteria were included in the exploratory cluster analysis . Male respondents were excluded (n = 50), because the number of males in our sample was too small to analyze meaningfully, given evidence which suggests that the symptom experience for males with FM may differ from that of females -.
OMERACT-recommended symptom domains were assessed using either total scores or subscale scores of the questionnaires described below . Our goal was to select the scale or subscale that best represented the OMERACT symptom domain while eliminating the possibility of item overlap between symptom domains and clustering variables. For example, in the case of MFI-20, which includes physical fatigue, mental fatigue (related to cognition) and reduced motivation (related to mood), we purposefully selected physical fatigue to keep this symptom construct distinct. The subscales selected for each domain are shown in Table 1. Of the core OMERACT symptom domains, all except objective tenderness and patient global impression of change to treatment (which was not applicable, given that there was no treatment comparison) were available. Table 1 lists the measures used to operationalize OMERACT domains (that is, used for clustering) and those measures used as descriptive clinical outcomes against which the clusters were evaluated.
Pain (Brief Pain Inventory)
The BPI is a 15-item, validated self-report measure of chronic, non-cancer-related pain and assesses presence of pain, pain severity and pain interference. It yields two subscales: pain severity and pain interference. Scores on pain severity and pain interference range from 0 to 10, with higher scores indicating greater pain. Internal consistency for the Pain Severity score is 0.85 and that for the Interference scale is 0.88 . The BPI has been used in FM clinical trials and is considered an appropriate measure of pain in FM ,-. For this analysis, we selected the Pain Severity subscale to represent the OMERACT symptom domain of pain.
Depression and anxiety (30-item Profile of Mood States)
The 30-item POMS is a validated self-report measure of mood. It yields six subscales: (1) depression-dejection, (2) tension-anxiety, (3) fatigue-inertia, (4) vigor-activity, (5) anger-hostility and (6) confusion-bewilderment. Scores on each subscale range from 0 to 20, with higher scores indicating worse symptoms on all scales, except for the vigor-activity scale, on which lower scores indicate worse symptoms. Although the majority of publications describing POMS in FM have been based on the 65-item instrument, the 30-item POMS has an internal consistency of 0.69 to 0.88 and is considered a superior measure in general -. For this analysis, we selected the Depression-Dejection and Tension-Anxiety subscales to represent the OMERACT symptom domains of depression and anxiety.
Sleep disturbance (Medical Outcomes Study-Sleep scale)
The MOS-Sleep scale is a 12-item, validated, self-report measure that assesses six dimensions of sleep: (1) sleep disturbance, (2) sleep adequacy, (3) sleep quantity, (4) somnolence, (5) snoring and (6) awakening with shortness of breath or headache. It yields two summary indices: the Sleep Problems Index I (six items) and the Sleep Problems Index II (nine items). Scores on dimensions and summary indices range from 0 to 100, with higher scores indicating poorer sleep. The MOS-Sleep scale has an internal consistency of 0.7 in patients with FM . The MOS-Sleep scale has been used in many FM clinical trials and is considered an appropriate measure of sleep in FM -. For this analysis, we selected the Sleep Problems Index II to represent the OMERACT symptom domain of sleep disturbance.
Fatigue (Multidimensional Fatigue Inventory)
The MFI-20 is a 20-item validated self-report measure of fatigue and assesses general fatigue, physical fatigue, reduced activity, reduced motivation and mental fatigue . Subscale scores range from 4 to 20, with higher scores indicating greater fatigue. It has an internal consistency of 0.93 . The MFI-20 has been used in clinical trials of FM and chronic pain and is an appropriate measure of fatigue in FM ,,. For this analysis, we selected the MFI Physical Fatigue subscale to represent the OMERACT symptom domain of fatigue.
Dyscognition (Multiple Ability Self-report Questionnaire)
The MASQ is a 38-item self-report measure and assesses five cognitive domains: language, visuoperceptual, verbal memory, visual memory and attention . Scores on the cognitive domains range from 0 to 30 or 0 to 40, and the maximum total score is 190. Higher scores indicate greater perceived difficulties with cognition. The MASQ has an internal consistency of 0.92. It has been used in several FM clinical trials to measure change in perceived cognition -. For this analysis, we selected the MASQ total to represent the OMERACT symptom domain of dyscognition.
Stiffness (Revised Fibromyalgia Impact Questionnaire)
The FIQ-R is a 21-item, validated self-report measure that assesses the symptoms, physical functioning and overall impact of FM . Scores range from 0 to 100, with higher scores indicating greater symptom burden. It has an internal consistency of 0.95 and is the most commonly used outcome measure in FM clinical trials ,,,. For this analysis, we selected the FIQ-R Stiffness question to represent the OMERACT symptom domain of stiffness. Additionally, FIQ-R total scores (not used in the clustering) were compared across the subgroups identified by cluster analysis.
The SF-36 version 2 is a 36-item, validated self-report measure that assesses disease burden . It consists of eight subscales and two summary scores (physical and mental components). Component scores range from 0 to 100, with higher scores indicating better health. The SF-36 has an internal consistency of 0.9 and has been used in FM clinical trials -. Similarly to the FIQ-R total score, the SF-36 component scores were not included in the clustering, but were used for comparison of symptom levels across clusters.
Fibromyalgia research survey criteria
The FM research survey criteria have been validated for use in epidemiologic and survey studies . It yields a widespread pain index (WPI) score (range, 0 to 19) and a symptom severity (SS) score of (0 to 12). Patients are classified as meeting FM research survey criteria if their WPI was ≥7 and SS was ≥5 or if their WPI was between 3 and 6 SS ≥9. Higher scores indicate more severe symptoms. WPI and SS scores were also compared across clusters.
Participants and measures in the external validation sample
To provide an external validation measure, we chose a separate sample of patients with FM (n = 478) who participated in the FM Treatment Program at Mayo Clinic but were not yet enrolled in the FM registry. Patients who participate in this program complete a comprehensive package of questionnaires. This comprehensive package includes the same measures used in the exploratory cluster analysis, with the exception of POMS and BPI. In this sample, in place of POMS, the severity of depression and anxiety were assessed with Patient Health Questionnaire (PHQ-9) and Generalized Anxiety Disorder 7-item scale (GAD-7), both of which are clinically validated measures -. Although BPI was not part this package, the Pain subscale of the FIQ provides a similar measure of pain severity and is considered appropriate to meaningfully characterize pain in FM, as described by Williams and Arnold . Similarly to the exploratory cluster sample, only female participants who met FM Research Survey Criteria were included. Importantly, medication use at the time of the survey (that is, the clinic visit) was available for participants included in the validation sample, whereas such data were not available in the original registry survey-based cluster sample.
Cluster analysis variables were standardized by subtracting the variable mean from each individual observation and dividing by the standard deviation. Hierarchical agglomerative clustering with Ward's method and squared Euclidean distances was used on the standardized data. The number of clusters was chosen by examining the dendrogram and based on clinical interpretability and usefulness. Clusters were subsequently compared on variables of interest using analysis of variance, followed by pairwise comparisons between clusters when the omnibus test was significant (that is, P <0.05). For pairwise comparisons, a Bonferroni adjustment to the 0.05 significance level was applied when interpreting P-values; because our analysis resulted in four clusters, and thus six pairwise comparisons, the Bonferroni P-value for interpreting pairwise significance tests was 0.05/6 = 0.0083. Analysis was performed using R  statistical software (version 2.15.0; R Foundation for Statistical Computing, Vienna, Austria) and JMP (version 10.0.0; SAS Institute, Cary, NC, USA). The same methods used for cluster analysis and comparison across clusters were applied to the validation sample. Because standardized variables (that is, z-scores) rather than raw scales were used for the cluster analysis, we felt it was reasonable to interpret and compare results from the validation and original samples, although a few of the specific instruments to measure individual symptoms differed between the two samples, as described above.
Exploratory cluster analysis
Of the 655 patients who met the inclusion criteria for the exploratory cluster analysis, 74 patients had missing data for one or more of the cluster analysis variables, yielding a final sample size of 581 patients for analysis. Demographic and symptom scales for the sample are summarized in Table 2.
Hierarchical agglomerative clustering on the standardized variables corresponding to fatigue, sleep, pain, function, stiffness, dyscognition, depression and anxiety resulted in a dendrogram that suggested meaningful information when the data were examined with between three and four clusters. The four-cluster solution largely divided the sample into severity levels, with cluster 1 reflecting the lowest average levels across all symptoms, cluster 4 reflecting the highest average levels across all symptoms and clusters 2 and 3 capturing generally moderate symptom levels. An important distinction between clusters 2 and 3 was their different profiles on the mental aspects of the disease, as cluster 2 clearly had lower levels of depression and anxiety than did cluster 3, despite cluster 2's having somewhat higher levels of pain, stiffness, dysfunction, sleep disturbance and fatigue (Figure 1A). Considering a three-cluster solution, clusters 1 and 2 would have remained together, which we felt would miss a clinically important difference revealed by the four-cluster solution because these two subgroups have significantly different levels of fatigue, sleep, pain, stiffness, function and dyscognition despite their similar levels of negative mood. Thus, the four-cluster solution was used for the subsequent analyses described below.
The four clusters were similar in size, with clusters 1 to 4 comprising 26%, 29%, 23% and 21% of the samples, respectively. Each of the clustering variables differed significantly between the four clusters (Table 3). The pairwise comparisons also showed significant differences of each cluster from every other cluster on all symptoms, with a few exceptions. Clusters 2 and 3 did not differ significantly on sleep problems (P = 0.16), and clusters 1 and 2 did not differ significantly on either depression (P = 0.23) or anxiety (P = 0.26).
Clinically relevant variables external to the cluster creation were compared across clusters, and the results are given in Table 4. FIQ Impact was significantly different for each cluster (all P-values <0.0001), except for cluster 2 versus cluster 3, which had very similar levels (mean, 11.5 vs 11.7; P =0.76). Similarly, clusters 2 and 3 had similar FIQ Total scores (mean, 58.1 vs 57.7). This underscores the point that both clusters have a globally "moderate" level of symptoms, although the drivers appear to be more physical in cluster 2 and more mental in cluster 3. The SF-36 mental composite score differed significantly for each cluster, and the physical composite score differed for every cluster comparison except cluster 2 versus cluster 4 (mean, 26.2 vs 25.6; P = 0.53).
Interestingly, patients in clusters 1 and 2, who had the lowest levels of depression and anxiety, were also significantly older than those in clusters 3 and 4. Body mass index (BMI) varied somewhat across clusters, but the only pairwise comparison that reached statistical significance was for cluster 1 versus 2 (mean, 28.6 vs 31.5; P = 0.0008).
External sample validation
A total of 478 female patients who met the FM research survey criteria were included in the validation sample. The mean age of the participants was 46.5 (±13.1) years, mean BMI was 30.2 (±7.8) kg/m2 and the mean FIQ Total score was 60.0 (±17.4). Compared to the original sample, the validation sample was significantly younger (P <0.0001), had a similar BMI (P = 0.74) and had a higher FIQ Total score (P = 0.0004).
As with the exploratory cluster analysis, the dendrogram of the hierarchical clustering solution for the validation sample suggested four clusters. The four clusters comprised 24%, 32%, 21% and 23% of the sample, respectively. The four-cluster solution from the validation sample similarly divided the sample into severity levels, with cluster 1 demonstrating the lowest symptom severity and cluster 4 having the highest symptom severity (Figure 1B). Similarly to the exploratory cluster analysis, each of the clustering variables differed significantly among the four clusters (Table 5). The pairwise comparisons also showed significant differences of each cluster from every other cluster on all symptoms, with a few exceptions. Clusters 1 and 2 did not differ significantly on anxiety (P = 0.96) or depression (P = 0.07). Clusters 3 and 4 did not differ significantly on depression (P = 0.53). The symptom profiles looked very similar to those found in the original cluster analysis sample, with a slight difference for sleep problems, which did not differ significantly between clusters 2 and 3 in the original sample but were significantly worse for cluster 3 vs cluster 2 in the validation sample.
The FIQ-Total and SF-36 scores serve as external benchmarks for the cluster differentiation. As with the original cluster sample, these scores are consistent with our interpretation of the clusters, specifically that cluster 1 shows a globally low symptom level, cluster 4 shows a globally high symptom level and clusters 2 and 3 are both generally moderate at the global level based on FIQ-Total scores (Table 6), whereas the SF-36 Mental component score differentiated clusters 2 and 3.
The percentage of patients on work disability also differed significantly between clusters (P <0.0001). Cluster 1 had the lowest percentage of patients on work disability (9.6%), clusters 2 and 3 had a greater number of patients on work disability (18.6% and 19.1% of patients, respectively) and cluster 4 had the greatest percentage of patients on work disability (33.1%).
Medication use across clusters is described in Table 6. In regard to serotonin norepinephrine reuptake inhibitors (SNRIs) and α2δ ligands, classes that include the US Food and Drug Administration-approved medications for FM, cluster 4 had the highest percentage of patients taking both SNRIs (44%) and α2δ ligands (22%), in comparison to cluster 1, which had 30% of patients receiving SNRIs and 20% taking α2δ ligands. Opioid use was significantly different across clusters, with 53% of patients in cluster 4 using opioids in comparison with 18% in cluster 1. Similarly, use of benzodiazepines was different across clusters, with 49% of patients in cluster 3 and 44% in cluster 4 taking benzodiazepines, in comparison to 19% of patients in cluster 1 and 21% in cluster 2.
In the exploratory cluster analysis, we identified four unique clusters using self-report questionnaires representing eight core OMERACT symptom domains (fatigue, sleep disturbance, pain, function, stiffness, dyscognition, depression and anxiety). The four subgroups that were derived from this cluster analysis included (1) a generally low symptom intensity group (cluster 1); (2) a moderate symptom, low anxiety and low depression group (cluster 2); (3) a moderate symptom, higher anxiety and higher depression group (cluster 3); and (4) a generally high symptom intensity group (cluster 4). Despite the fact that the validation sample consisted of younger patients with higher FM symptom severity, the cluster solution in this sample was similar to the exploratory cluster analysis.
Our results share common themes with previous cluster analysis studies in patients with FM. For example, in the cluster analyses by Wilson et al. , Loevinger et al.  and de Souza et al. , there appear to be at least one subgroup of patients who have high physical and psychological symptoms (similar to our cluster 4) and one subgroup with less psychological distress and low levels of physical symptoms (similar to our cluster 1). Notably, our results are quite similar to those of Wilson et al. in that we also identified four clusters: one cluster that was low on all symptom domains, two clusters that were moderate on physical domains but distinguished by differences on psychological factors, and one cluster that was high on all symptom domains . Although clusters 2 and 3 had overall moderate levels of symptoms, the severity of depression and anxiety was the distinguishing factor, which is consistent with the findings reported by Loevinger et al.  and de Souza et al.  in that psychological distress may be one factor that differentiates clusters.
Our preliminary cluster solution is further supported by FIQ-R and SF-36 scores, which serve as external benchmarks. Cluster 1 in both samples had the lowest mean FIQ-R total score, which also fell within the mild symptom severity range described for the FIQ-R (score 0 to <39) . Compared to this finding, cluster 4 fell in the severe symptom severity range for the FIQ-R (≥59 to 100). Similarly, cluster 1 in both samples had the best physical and mental composite scores on the SF-36, and score ranges appeared relatively close to healthy population norms (50 ± 10) . Cluster 4 in both samples had the worst physical and mental composite scores, indicating the poorest levels of physical and mental health. Using disability status as yet another external benchmark of symptom burden and/or impact, we found that the percentage of patients on work disability significantly increased (P <0.0001) as symptom severity increased across clusters.
We were not able to compare medication use across clusters in our exploratory sample (as medication use at the time of the survey was not available). When we compared medication use in the validation sample, however, cluster 1 had the lowest percentage using any medications for FM and cluster 4 had the highest percentage. Although this finding was somewhat surprising, it demonstrates that patients in cluster 4, despite being on multiple medications (patients in cluster 4 were taking an average of 3.4 medications each), had the highest level of symptom burden. This indicates that symptom severity in cluster 4 is not driven by the lack treatment, but rather it may be indicative of the symptom severity spectrum of FM.
In contrast to clusters 1 and 4, clusters 2 and 3 (both exploratory and validation samples) had similar levels of total FIQ-R symptom severity. The cluster differentiation between clusters 2 and 3 was driven primarily by anxiety and depression, with cluster 3 having significantly higher levels. Comparison of medication use in the validation sample indicated that there were no significant differences in medication use between clusters 2 and 3, except with regard to use of benzodiazepines, which was significantly higher in cluster 3 (P <0.0001). This indicates that the differences in depression and anxiety that distinguished clusters 2 and 3 were not due to one cluster being differentially treated. In fact, patients in cluster 3 were taking more medications for anxiety (benzodiazepines) compared to cluster 2 and had more severe anxiety.
In support of these results, the SF-36 Mental scores indicated better mental health in cluster 2 compared to cluster 3 in both samples. However, the SF-36 Physical scores were higher in cluster 2 compared to cluster 3 in both samples. A reason for this might be that the increased BMI in cluster 2 could be associated with poorer physical function. Although BMI was significantly higher in cluster 2 in the exploratory sample, the difference in the validation sample did not reach statistical significance.
We recognize several limitations to this study. First, despite identification of four clusters, the sample is cross-sectional and the longitudinal stability of these clusters is unknown. One published study on the longitudinal behavior of FM symptoms over the course of 5.5 years indicated that pain, fatigue and sleep demonstrated small longitudinal fluctuations over time at the group level, but showed significant within-patient variability . A second limitation is that objective biomarkers recommended by OMERACT, such as tenderness, CSF biomarkers and functional imaging, were not available and therefore could not be included in the clustering. A third limitation is that, based on our inclusion criteria, we cannot comment on the generalizability of our results to community samples or men with FM, given our sample of female patients with FM identified through a clinical registry. Fourth, variables such as those included by Docampo et al. (sociodemographic characteristics, medications, comorbidities and personal or family history) that we were unable to include , and our questionnaire selection could influence clustering; however, the rationale for our use of these variables was based on the OMERACT recommendations, and care was taken to avoid any overlap between items representing symptom domains. Despite this, both our results and those of Docampo et al. suggest that varying symptom combinations are present in a heterogeneous sample of patients with FM.
Our study corroborates previous cluster reports, but also distinguishes itself by being the first study of its kind to incorporate a comprehensive spectrum of symptoms, as recommended by the OMERACT FM working group. We acknowledge that this cluster solution needs longitudinal study and that the feasibility and outcomes of this approach must be assessed before any conclusions regarding its clinical implications can be made; however, the present study is a first step toward this goal.
AV and TLH conceived of and designed the study, collected and analyzed data and wrote the manuscript. MOW collected and analyzed data and wrote the manuscript. DJC, DLB, RPB and DAW conceived of and designed the study and critically revised the manuscript. All authors read and approved the final manuscript.
Body mass index
Brief Pain Inventory
Revised Fibromyalgia Impact Questionnaire
Generalized Anxiety Disorder 7-item scale
Multiple Ability Self-report Questionnaire
Multidimensional Fatigue Inventory
Medical Outcomes Study Sleep Scale
Outcome Measures in Rheumatology
Patient Health Questionnaire
Profile of Mood States
36-item Short Form survey
Serotonin norepinephrine reuptake inhibitor
Selective serotonin reuptake inhibitor
Widespread Pain Index
Fibromyalgia: poorly understood; treatments are disappointing.Prescrire Int 2009, 18:169-173.,
Clauw DJ, Arnold LM, McCarberg BH: The science of fibromyalgia. Mayo Clin Proc. 2011, 86: 907-911. 10.4065/mcp.2011.0206.
Wolfe F, Clauw DJ, Fitzcharles MA, Goldenberg DL, Katz RS, Mease P, Russell AS, Russell IJ, Winfield JB, Yunus MB: The American College of Rheumatology preliminary diagnostic criteria for fibromyalgia and measurement of symptom severity. Arthritis Care Res. 2010, 62: 600-610. 10.1002/acr.20140.
Bennett RM, Russell J, Cappelleri JC, Bushmakin AG, Zlateva G, Sadosky A: Identification of symptom and functional domains that fibromyalgia patients would like to see improved: a cluster analysis. BMC Musculoskelet Disord. 2010, 11: 134-10.1186/1471-2474-11-134.
de Souza JB, Goffaux P, Julien N, Potvin S, Charest J, Marchand S: Fibromyalgia subgroups: profiling distinct subgroups using the Fibromyalgia Impact Questionnaire: a preliminary study. Rheumatol Int. 2009, 29: 509-515. 10.1007/s00296-008-0722-5.
Giesecke T, Williams DA, Harris RE, Cupps TR, Tian X, Tian TX, Gracely RH, Clauw DJ: Subgrouping of fibromyalgia patients on the basis of pressure-pain thresholds and psychological factors. Arthritis Rheum. 2003, 48: 2916-2922. 10.1002/art.11272.
Loevinger BL, Shirtcliff EA, Muller D, Alonso C, Coe CL: Delineating psychological and biomedical profiles in a heterogeneous fibromyalgia population using cluster analysis. Clin Rheumatol. 2012, 31: 677-685. 10.1007/s10067-011-1912-1.
Rutledge DN, Mouttapa M, Wood PB: Symptom clusters in fibromyalgia: potential utility in patient assessment and treatment evaluation. Nurs Res. 2009, 58: 359-367. 10.1097/NNR.0b013e3181b499d2.
Verra ML, Angst F, Brioschi R, Lehmann S, Keefe FJ, Staal JB, de Bie RA, Aeschlimann A: Does classification of persons with fibromyalgia into Multidimensional Pain Inventory subgroups detect differences in outcome after a standard chronic pain management program?. Pain Res Manag. 2009, 14: 445-453.
Wilson HD, Robinson JP, Turk DC: Toward the identification of symptom patterns in people with fibromyalgia. Arthritis Rheum. 2009, 61: 527-534. 10.1002/art.24163.
Docampo E, Collado A, Escaramís G, Carbonell J, Rivera J, Vidal J, Alegre J, Rabionet R, Estivill X: Cluster analysis of clinical data identifies fibromyalgia subgroups. PLoS One. 2013, 8: e74873-10.1371/journal.pone.0074873.
Turk DC, Okifuji A, Sinclair JD, Starz TW: Differential responses by psychosocial subgroups of fibromyalgia syndrome patients to an interdisciplinary treatment. Arthritis Care Res. 1998, 11: 397-404. 10.1002/art.1790110511.
Mease PJ, Arnold LM, Crofford LJ, Williams DA, Russell IJ, Humphrey L, Abetz L, Martin SA: Identifying the clinical domains of fibromyalgia: contributions from clinician and patient Delphi exercises. Arthritis Rheum. 2008, 59: 952-960. 10.1002/art.23826.
Whipple MO, McAllister SJ, Oh TH, Luedtke CA, Toussaint LL, Vincent A: Construction of a US fibromyalgia registry using the Fibromyalgia Research Survey criteria. Clin Trans Sci. 2013, 6: 398-399. 10.1111/cts.12056.
Cleeland CS, Ryan KM: Pain assessment: global use of the Brief Pain Inventory. Ann Acad Med Singapore. 1994, 23: 129-138.
McNair DM, Lorr M, Droppleman LF: EdITS Manual for the Profile of Mood States. 1992, Educational and Industrial Testing Service, San Diego, CA
Cappelleri JC, Bushmakin AG, McDermott AM, Dukes E, Sadosky A, Petrie CD, Martin S: Measurement properties of the medical outcomes study sleep scale in patients with fibromyalgia. Sleep Med. 2009, 10: 766-770. 10.1016/j.sleep.2008.09.004.
Smets EM, Garssen B, Bonke B, De Haes JC: The Multidimensional Fatigue Inventory (MFI) psychometric qualities of an instrument to assess fatigue. J Psychosom Res. 1995, 39: 315-325. 10.1016/0022-3999(94)00125-O.
Seidenberg M, Haltiner A, Taylor MA, Hermann BB, Wyler A: Development and validation of a Multiple Ability Self-Report Questionnaire. Clin Exp Neuropsychol. 1994, 16: 93-104. 10.1080/01688639408402620.
Bennett RM, Friend R, Jones KD, Ward R, Han BK, Ross RL: The Revised Fibromyalgia Impact Questionnaire (FIQR): validation and psychometric properties. Arthritis Res Ther. 2009, 11: R120-10.1186/ar2783.
Ware JE: SF-36 health survey update. Spine. 2000, 25: 3130-3139. 10.1097/00007632-200012150-00008.
Williams DA, Arnold LM: Measures of fibromyalgia: Fibromyalgia Impact Questionnaire (FIQ), Brief Pain Inventory (BPI), Multidimensional Fatigue Inventory (MFI-20), Medical Outcomes Study (MOS) Sleep Scale, and Multiple Ability Self-Report Questionnaire (MASQ). Arthritis Care Res. 2011, 63: S86-S97. 10.1002/acr.20531.
Wolfe F, Clauw DJ, Fitzcharles MA, Goldenberg DL, Häuser W, Katz RS, Mease P, Russell AS, Russell IJ, Winfield JB: Fibromyalgia criteria and severity scales for clinical and epidemiological studies: a modification of the ACR Preliminary Diagnostic Criteria for Fibromyalgia. J Rheumatol. 2011, 38: 1113-1122. 10.3899/jrheum.100594.
Aparicio VA, Ortega FB, Carbonell-Baeza A, Femia P, Tercedor P, Ruiz JR, Delgado-Fernández M: Are there gender differences in quality of life and symptomatology between fibromyalgia patients?. Am J Mens Health. 2012, 6: 314-319. 10.1177/1557988312436872.
Buskila D, Neumann L, Alhoashle A, Abu-Shakra M: Fibromyalgia syndrome in men. Semin Arthritis Rheum. 2000, 30: 47-51. 10.1053/sarh.2000.8363.
Castro-Sánchez AM, Matarán-Peñarrocha GA, López-Rodríguez MM, Lara-Palomo IC, Arendt-Nielsen L, Fernández-de-las-Peñas C: Gender differences in pain severity, disability, depression, and widespread pressure pain sensitivity in patients with fibromyalgia syndrome without comorbid conditions. Pain Med. 2012, 13: 1639-1647. 10.1111/j.1526-4637.2012.01523.x.
Hooten WM, Townsend CO, Decker PA: Gender differences among patients with fibromyalgia undergoing multidisciplinary pain rehabilitation. Pain Med. 2007, 8: 624-632. 10.1111/j.1526-4637.2006.00202.x.
Mease P, Arnold LM, Choy EH, Clauw DJ, Crofford LJ, Glass JM, Martin SA, Morea J, Simon L, Strand CV, Williams DA: Fibromyalgia syndrome module at OMERACT 9: domain construct. J Rheumatol. 2009, 36: 2318-2329. 10.3899/jrheum.090367.
Cleeland CS: The Brief Pain Inventory: User Guide. 2009, Charles S Cleeland, Houston, TX
Arnold LM, Rosen A, Pritchett YL, D’Souza DN, Goldstein DJ, Iyengar S, Wernicke JF: A randomized, double-blind, placebo-controlled trial of duloxetine in the treatment of women with fibromyalgia with or without major depressive disorder. Pain. 2005, 119: 5-15. 10.1016/j.pain.2005.06.031.
Chappell AS, Bradley LA, Wiltse C, Detke MJ, D’Souza DN, Spaeth M: A six-month double-blind, placebo-controlled, randomized clinical trial of duloxetine for the treatment of fibromyalgia. Int J Gen Med. 2008, 1: 91-102. 10.2147/IJGM.S3979.
Mease PJ, Spaeth M, Clauw DJ, Arnold LM, Bradley LA, Russell IJ, Kajdasz DK, Walker DJ, Chappell AS: Estimation of minimum clinically important difference for pain in fibromyalgia. Arthritis Care Res. 2011, 63: 821-826. 10.1002/acr.20449.
Russell IJ, Mease PJ, Smith TR, Kajdasz DK, Wohlreich MM, Detke MJ, Walker DJ, Chappell AS, Arnold LM: Efficacy and safety of duloxetine for treatment of fibromyalgia in patients with or without major depressive disorder: Results from a 6-month, randomized, double-blind, placebo-controlled, fixed-dose trial. Pain. 2008, 136: 432-444. 10.1016/j.pain.2008.02.024.
Bourgeois A, LeUnes A, Meyers M: Full-scale and short-form of the Profile of Mood States: a factor analytic comparison. J Sport Behav. 2010, 33: 355-376.
Malin K, Littlejohn GO: Psychological control is a key modulator of fibromyalgia symptoms and comorbidities. J Pain Res. 2012, 5: 463-471.
Katz RS, Heard AR, Mills M, Leavitt F: The prevalence and clinical impact of reported cognitive difficulties (fibrofog) in patients with rheumatic disease with and without fibromyalgia. J Clin Rheumatol. 2004, 10: 53-58. 10.1097/01.rhu.0000120895.20623.9f.
Arnold LM, Russell IJ, Diri EW, Duan WR, Young JP, Sharma U, Martin SA, Barrett JA, Haig G: A 14-week, randomized, double-blinded, placebo-controlled monotherapy trial of pregabalin in patients with fibromyalgia. J Pain. 2008, 9: 792-805. 10.1016/j.jpain.2008.03.013.
Crofford LJ, Rowbotham MC, Mease PJ, Russell IJ, Dworkin RH, Corbin AE, Young JP, LaMoreaux LK, Martin SA, Sharma U: Pregabalin for the treatment of fibromyalgia syndrome: results of a randomized, double-blind, placebo-controlled trial. Arthritis Rheum. 2005, 52: 1264-1273. 10.1002/art.20983.
Martin S, Chandran A, Zografos L, Zlateva G: Evaluation of the impact of fibromyalgia on patients' sleep and the content validity of two sleep scales. Health Qual Life Outcomes. 2009, 7: 64-10.1186/1477-7525-7-64.
Lin JMS, Brimmer DJ, Maloney EM, Nyarko E, BeLue R, Reeves WC: Further validation of the Multidimensional Fatigue Inventory in a US adult population sample. Popul Health Metr. 2009, 7: 18-10.1186/1478-7954-7-18.
Clauw DJ, Mease P, Palmer RH, Gendreau RM, Wang Y: Milnacipran for the treatment of fibromyalgia in adults: a 15-week, multicenter, randomized, double-blind, placebo-controlled, multiple-dose clinical trial. Clin Ther. 2008, 30: 1988-2004. 10.1016/j.clinthera.2008.11.009.
Arnold LM, Wang F, Ahl J, Gaynor PJ, Wohlreich MM: Improvement in multiple dimensions of fatigue in patients with fibromyalgia treated with duloxetine: Secondary analysis of a randomized, placebo-controlled trial. Arthritis Res Ther. 2011, 13: R86-10.1186/ar3359.
Owen RT: Milnacipran hydrochloride: its efficacy, safety and tolerability profile in fibromyalgia syndrome. Drugs Today (Barc). 2008, 44: 653-660. 10.1358/dot.2008.44.9.1256003.
Branco JC, Bannwarth B, Failde I, Abello Carbonell J, Blotman F, Spaeth M, Saraiva F, Nacci F, Thomas E, Caubère JP, Le Lay K, Taieb C, Matucci-Cerinic M: Prevalence of fibromyalgia: a survey in five European countries. Semin Arthritis Rheum. 2010, 39: 448-453. 10.1016/j.semarthrit.2008.12.003.
Mease PJ, Clauw DJ, Gendreau RM, Rao SG, Kranzler J, Chen W, Palmer RH: The efficacy and safety of milnacipran for treatment of fibromyalgia: a randomized, double-blind, placebo-controlled trial. J Rheumatol. 2009, 36: 398-409. 10.3899/jrheum.080734. A published erratum appears in J Rheumatol 2009, 36:661
Arnold LM, Hess EV, Hudson JI, Welge JA, Berno SE, Keck PE: A randomized, placebo-controlled, double-blind, flexible-dose study of fluoxetine in the treatment of women with fibromyalgia. Am J Med. 2002, 112: 191-197. 10.1016/S0002-9343(01)01089-0.
Arnold LM, Gendreau RM, Palmer RH, Gendreau JF, Wang Y: Efficacy and safety of milnacipran 100 mg/day in patients with fibromyalgia: results of a randomized, double-blind, placebo-controlled trial. Arthritis Rheum. 2010, 62: 2745-2756. 10.1002/art.27559.
Da Costa D, Dobkin PL, Fitzcharles MA, Fortin PR, Beaulieu A, Zummer M, Senécal JL, Goulet JR, Rich E, Choquette D, Clarke AE: Determinants of health status in fibromyalgia: a comparative study with systemic lupus erythematosus. J Rheumatol. 2000, 27: 365-372.
Neumann L, Berzak A, Buskila D: Measuring health status in Israeli patients with fibromyalgia syndrome and widespread pain and healthy individuals: utility of the Short Form 36-item health survey (SF-36). Semin Arthritis Rheum. 2000, 29: 400-408. 10.1053/sarh.2000.7171.
Tüzün EH, Albayrak G, Eker L, Sözay S, Daşkapan A: A comparison study of quality of life in women with fibromyalgia and myofascial pain syndrome. Disabil Rehabil. 2004, 26: 198-202. 10.1080/09638280310001639696.
Löwe B, Decker O, Müller S, Brähler E, Schellberg D, Herzog W, Herzberg PY: Validation and standardization of the Generalized Anxiety Disorder Screener (GAD-7) in the general population. Med Care. 2008, 46: 266-274. 10.1097/MLR.0b013e318160d093.
Spitzer RL, Kroenke K, Williams JBW, Löwe B: A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med. 2006, 166: 1092-1097. 10.1001/archinte.166.10.1092.
Smarr KL, Keefer AL: Measures of depression and depressive symptoms: Beck Depression Inventory-II (BDI-II), Center for Epidemiologic Studies Depression Scale (CES-D), Geriatric Depression Scale (GDS), Hospital Anxiety and Depression Scale (HADS), and Patient Health Questionnaire-9 (PHQ-9). Arthritis Care Res. 2011, 63: S454-S466. 10.1002/acr.20556.
R: A Language and Environment for Statistical Computing. 2012, R Foundation for Statistical Computing, Vienna, Austria
Schaefer C, Chandran A, Hufstader M, Baik R, McNett M, Goldenberg D, Gerwin R, Zlateva G: The comparative burden of mild, moderate and severe fibromyalgia: results from a cross-sectional survey in the United States. Health Qual Life Outcomes. 2011, 9: 71-10.1186/1477-7525-9-71.
Walitt B, Fitzcharles MA, Hassett AL, Katz RS, Häuser W, Wolfe F: The longitudinal outcome of fibromyalgia: a study of 1555 patients. J Rheumatol. 2011, 38: 2238-2246. 10.3899/jrheum.110026.
This study was supported in part by the Center for Translational Science Activities (CTSA) at the Mayo Clinic. This center is funded in part by a grant from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH) (RR024150). The manuscript contents are solely the responsibility of the authors and do not necessarily represent the official views of CTSA, NCRR or NIH. The funders had no role in the study design, data collection and analysis, decision to publish or manuscript preparation. The study data were collected and managed using REDCap electronic data capture tools hosted at the Mayo Clinic. REDCap (Research Electronic Data Capture) is a secure, web-based application designed to support data capture for research studies by providing (1) an intuitive interface for validated data entry, (2) audit trails for tracking data manipulation and export procedures, (3) automated export procedures for seamless data downloads to common statistical packages and (4) procedures for importing data from external sources.
The authors declare that they have no competing interests.
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Vincent, A., Hoskin, T.L., Whipple, M.O. et al. OMERACT-based fibromyalgia symptom subgroups: an exploratory cluster analysis. Arthritis Res Ther 16, 463 (2014). https://doi.org/10.1186/s13075-014-0463-7
- Fibromyalgia Impact Questionnaire
- Brief Pain Inventory
- Multidimensional Fatigue Inventory
- Mental Composite Score