J Rheum Dis Treat ISSN: 2469-5726

• Abstract
• Keywords
• Introduction
• Patients and Methods
• Results
• Discussion
• Competing Interest
• Acknowledgments
• Table 1
• Table 2
• Table 3
• References

Download PDF
    

Journal of Rheumatic Diseases and Treatment

¹Department of Psychiatry, Tokyo Women's Medical University School of Medicine, Japan
²Kanagawa Psychiatric Center, Yokohama, Japan
³Institute of Rheumatology, Tokyo Women's Medical University, Japan

Abstract

Objective: Fatigue has been intensively studied in patients with systemic lupus erythematosus (SLE). However, previous studies have mostly included patients with long-term disease who have been treated with corticosteroids. We investigated fatigue in corticosteroid-naive patients with early-stage SLE.

Methods: Forty-three SLE inpatients without neuropsychiatric SLE manifestations and 30 healthy control subjects with similar demographic characteristics participated in this study. The Profile of Mood States (POMS) was used to assess fatigue, depression and anxiety. Results of clinical, laboratory, and neurological tests were compared and their relationship with fatigue was assessed.

Results: The prevalence of fatigue did not differ between patients (n = 8, 19%) and controls (n = 6, 20%; p = 0.556), and the severity of fatigue also did not differ between groups (p = 0.590). Using multiple logistic regression analysis, we identified POMS-anxiety (OR, 1.14; 95% CI, 1.019 - 1.273, p = 0.022) as an independent risk factor for fatigue in these patients. There were no relationships between fatigue, disease activity, and concentrations of inflammatory markers.

Conclusion: Our results indicate that fatigue does not occur more frequently in corticosteroid-naive patients with early-stage SLE than in the normal population, and that fatigue may be related to anxiety.

Keywords

Systemic lupus erythematosus, Fatigue, Anxiety, Corticosteroids

Introduction

Systemic lupus erythematosus (SLE) is a chronic relapsing/remitting autoimmune disease characterized by multisystem involvement and diverse manifestations. Fatigue is the most prevalent symptom, affecting up to 90% of patients with SLE [1]; it is also the most debilitating symptom reported by patients with SLE [2]. The fatigue associated with SLE decreases patient quality of life [3-6] and reduces their ability to work [7,8]. The origin of fatigue is multifactorial and, despite its high prevalence and adverse clinical, social, and economic effects, its pathophysiological mechanisms are still unclear. There are several comorbid conditions associated with fatigue: reduced physical activity [9,10], obesity [11], sleep disturbance [12], depression [13-15], depression and anxiety syndrome [13], pain [1,15], vitamin D deficiency [16], and fibromyalgia [17]. Disease activity also seems to be a major factor associated with fatigue, although this relationship has been inconsistent in SLE patients [1,13,15,18,19]. No associations between fatigue and levels of serum cytokines such as interleukin (IL)-2, IL-6, or interferon (IFN)-α have been reported [20]. The findings of brain imaging studies investigating fatigue in SLE patients have also yielded inconsistent results. These have included negative findings from studies using magnetic resonance imaging (MRI) [20] and single-photon emission computed tomography [21] and positive findings from a study that used a semi-quantitative radiologic scale on a T-2 weighted MRI to detect the relationship between white matter hyper intensities and fatigue [22]. Although fatigue occurs in SLE patients relatively early in the disease [23], to our knowledge no reports have focused on fatigue in patients with early disease who have not yet received corticosteroid therapy.

The purpose of this study was to clarify the prevalence of, and risk factors for, fatigue in corticosteroid-naive patients with early-stage SLE. We compared fatigue between these SLE patients and healthy control participants, and assessed the association of fatigue with patient psychological health and neurological/immunological variables.

Patients and Methods

Patients and controls

The participants in this study were the same as those described in our previous study, which focused on neurocognitive impairment in SLE [24]. These participants were Japanese patients who were admitted to the Institute of Rheumatology at the Tokyo Women's Medical University Aoyama Hospital between 2000 and 2006, and who met all of the following criteria: 1) diagnosed with SLE based on criteria defined by the American College of Rheumatology (ACR) [25], 2) no history of corticosteroid or other immunosuppressive therapy, 3) not unable to participate in the psychiatric interview or complete the neuropsychological tests and questionnaires because of poor physical condition, 4) except for adjustment disorder, no history of major psychiatric disorders including substance abuse, and 5) no history of neurologic illness (e.g., strokes, seizures, or head injury resulting in loss of consciousness). All patients were screened for current and previous major psychiatric conditions using the Structured Clinical Interview from the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Axis I Disorders, Non-patient Edition (With Psychotic Screening), Version 2.0 (SCID-I-NP) [26]. The study was approved by the ethics committee of Tokyo Women's Medical University. All participants gave their informed written consent.

Of the 54 corticosteroid-naive patients with SLE who were admitted during the study period, one patient declined the invitation to participate, two were excluded based on the initial SCID-I-NP interview (criterion 4), and eight could not complete the neuropsychological tests (criterion 3). As a result, data from 43 patients were available for analysis.

Thirty healthy controls were recruited from hospital staff and their relatives for neuropsychological testing. All controls were Japanese women with no history of major psychiatric disorders or neurologic illnesses as determined by the SCID-I-NP and neurologic history-related questions. The demographics of the control group (age, education level, and personality profile) were similar to those of the SLE group. Demographic, clinical, and psychological characteristics of the SLE and control groups are shown in table 1.

Assessment of fatigue, depression and anxiety

The fatigue levels of both patients and controls were evaluated using the Profile of Mood States (POMS) [27] fatigue subscale. The POMS provides scores on six separate subscales: tension-anxiety, depression-dejection, anger-hostility, vigor, fatigue, and confusion. The validity and reliability of the Japanese version of the POMS have been previously confirmed [28]. The POMS fatigue subscale consists of seven items that are rated on a five-point Likert scale ranging from "not at all" (0) to "extremely" (4). Each POMS fatigue subscale has factorial integrity and can be used independently of the others [29]. Both the patients and the controls were also evaluated using the POMS depression-dejection and tension-anxiety subscales to assess their depression and anxiety, respectively. Raw scores from each subscale were converted to T-scores based on the normative data, and a T-score > 60 was considered positive. Patients also completed a questionnaire regarding fatigue using visual analog scales (VAS) for fatigue (0-100 mm, with 100 mm indicating the most severe fatigue).

Clinical/health assessment

Disease duration was defined as the time between the onset of SLE-attributable symptoms and the assessment for this study. Global SLE-disease activity was evaluated using the systemic lupus erythematosus disease activity index 2000 (SLEDAI-2K) [30] at the same time as the psychological assessment or within the preceding 10 days.

Daily-living activities were evaluated using the Eastern Cooperative Oncology Group Scale of Performance Status. Patients also completed a questionnaire regarding pain using a VAS (0-100 mm, with 100 mm being the most severe pain). Sleep disturbance levels were derived by summing the scores of three subscales for insomnia (initial, middle, and delayed insomnia, each value: 0-2) from the 17-item Hamilton Depression Rating Scale.

Immunological/neurological markers

Anti-ds-DNA antibodies and serum complement CH50 were measured as markers of disease activity. Based on published reports regarding fatigue in SLE [23,31,32], the following potentially relevant laboratory and neurologic variables were selected: antiphospholipid antibodies; cerebrospinal fluid (CSF) and serum concentrations of IL-6, IL-8, and IFN-α; the CSF immunoglobulin G [IgG] index; brain MRI images; and electroencephalograms (EEG). Of the 43 patients, 37 underwent cerebrospinal fluid tests, 41 had brain MRI, and 41 underwent EEG. These neuropsychological, laboratory, and neurological tests were completed within a week after admission and before corticosteroids or other immunosuppressive therapies were administered. Control participants completed the neuropsychological tests, but did not undergo brain MRI, EEG, or cerebrospinal fluid testing.

Statistical analyses

For the univariate analyses, the non-parametric Mann-Whitney U-test was used to identify differences between groups for continuous variables, and the Fisher exact test was used for categorical variables. To identify independent risk factors for fatigue in SLE patients, multiple logistic regression analysis was performed with forward stepwise variable selection. Variables from the univariate analyses with p < 0.25 were entered into a forward logistic regression model. Regression coefficients were used to calculate the odds ratios (ORs) and 95% confidence intervals (CIs) of the ORs. For all statistical analyses, p-values < 0.05 were considered statistically significant. We performed all analyses using SPSS® Statistics 17.0 (SPSS Inc., Chicago, IL, USA).

Results

Prevalence and severity of fatigue

The prevalence of fatigue did not differ between groups (patients: 19%, n = 8; controls: 20%, n = 6; p = 0.556). POMS scores for fatigue also did not differ between the SLE and the control groups (p = 0.590, Table 1). Mean (standard deviation, SD) scores for VAS fatigue in SLE patients were 33.0 (27.6) (range; 0-96). The VAS and POMS scores for fatigue showed a strong positive correlation (r = 0.623, p < 0.001).

Risk factors for fatigue in SLE patients

Patients were divided into two groups according to the presence or absence of fatigue. Then, demographic, clinical, immunological/neurological variables (Table 2), and cumulative symptoms of SLEDAI-2K (Table 3) were compared between the two groups. Among these variables, scores for the following characteristics were significantly higher in patients with fatigue than in those without: performance status (p = 0.032), POMS-anxiety (p = 0.005), and POMS-depression (p = 0.009). Furthermore, pleurisy was present significantly more frequently in patients with fatigue than in those without (p = 0.037). Multiple logistic regression analysis showed that POMS-anxiety was the only independent risk factor for fatigue in SLE patients. The OR was 1.139 (95% CI, 1.019-1.273, p = 0.022; -2 log likelihood = 38.793; χ² = 6.290, p = 0.012; Nagelkerke R2 = 0.293).

Discussion

Our results showed that the prevalence and severity of fatigue did not differ between patients with early-stage SLE, even when free from the potential effects of corticosteroids, and healthy controls. Since fatigue has been reported to be the most prevalent symptom, affecting up to 90% of patients with SLE [1], findings from the present study suggested that fatigue in SLE patients may be associated with long-term disease-related or treatment-related factors.

The point prevalence of fatigue in patients with SLE has been reported to vary widely [1] this prevalence varies with the definition and instruments used to assess fatigue, which are inconsistent throughout the literature. The ad hoc Committee on SLE response criteria for fatigue has recommended the use of the 9-item Fatigue Severity Scale (FSS) [33] for assessing fatigue in SLE patients [34]. The reported percentages of SLE patients experiencing clinical fatigue assessed using the FSS, the most frequently used instrument in studies on SLE-related fatigue, range from 67% to 90% [2]. The prevalence of fatigue in patients with early-stage SLE in this study was markedly lower than that reported in SLE patients in several previous studies, although we could not directly compare our results with those of earlier works because we used POMS-fatigue in our study. We used the POMS so that separate evaluations of fatigue, depression, and anxiety were possible, because the symptoms of depression overlap with those of fatigue. Furthermore, the fact that patients with severe fatigue were excluded may have reduced the prevalence rate.

In the present study, fatigue was not independently related to the level of disease activity or any immunological/neurological markers, although most patients had overall disease activity (SLEDAI-2K ≥ 6 in 88.4%) that was moderate or high and free from the potential influence of medication. This finding was consistent with the findings of several previous studies that showed weak or no association between fatigue and disease activity [1,13,15,18]; although some studies have shown a significant positive association between these factors [19]. There is abundant evidence that many patients with chronic fatigue syndrome (CFS) may suffer from autoimmune response [35]. Thus, future long-term study may serve an important clue to study the pathogenesis of CFS.

Among psychological variables, depression has been consistently reported to be strongly associated with fatigue in SLE patients [14,15,19,22,36]; however, in our study the association between fatigue and depression did not reach significance after multivariate analysis. Instead, our multivariate analysis revealed an independent relationship between fatigue and anxiety. Anxiety alone has not previously been shown to be associated with fatigue in SLE patients, although the depression and anxiety complex assessed using the hospital anxiety and depression scale (HADS) has been reported to have an association with fatigue [13]. Furthermore, several studies have suggested an indirect association between fatigue and anxiety through evaluation of psychosocial variables such as helplessness [19], perceived lack of social support [15], or work disability [37,38]. In addition, most patients in this study were female. Females are at greater risk for depression and anxiety-related disorders in the general population [39].

The strengths of our study were the early-stage, corticosteroid-naive SLE population, comprehensive collection of psychological and biological data, and the use of multivariate statistical analyses to identify predictive factors for fatigue in patients with SLE. However, our study had several limitations. First, in this study we used the POMS subscale to evaluate fatigue, although this instrument had not been previously used for this purpose in the study of SLE [2]. Therefore, we could not directly compare the prevalence of fatigue found in our study to that found in previous studies. Second, this study lacked prospective long-term analysis, which could have been helpful for defining predictors of fatigue (e.g., comparison of levels of fatigue before and after corticosteroid administration). Third, because of its small sample size, the statistical power of our study to identify factors that predict fatigue was relatively low. Finally, because the results in our study were obtained from a limited population of relatively young female patients with early SLE, the findings may not be applicable to all SLE patients, particularly male or with longer disease duration.

In conclusion, the results of our study suggest that fatigue does not occur more frequently in corticosteroid-naive patients with early-stage SLE than in healthy controls, and that fatigue is associated with anxiety. There were no relationships between fatigue, disease activity, and inflammatory markers, even without the potential effects of corticosteroids. Further follow-up studies using larger sample sizes are needed.

Competing Interest

The authors declare that they have no competing interests.

Acknowledgments

We thank Prof. Masako Hara for their helpful comments, Dr. Manabu Kawamoto for assisting in the ELISA assays, and Dr. Eisuke Inoue for statistical consultation.

References

1. Zonana-Nacach A, Roseman JM, McGwin G, Friedman AW, Baethge BA, et al. (2000) Systemic lupus erythematosus in three ethnic groups. VI: Factors associated with fatigue within 5 years of criteria diagnosis. LUMINA Study Group. LUpus in MInority populations: NAture vs Nurture. Lupus 9: 101-109.
   


2. Cleanthous S, Tyagi M, Isenberg DA, Newman SP (2012) What do we know about self-reported fatigue in systemic lupus erythematosus? Lupus 21: 465-476.
   


3. McElhone K, Abbott J, Teh LS (2006) A review of health related quality of life in systemic lupus erythematosus. Lupus 15: 633-643.
   


4. Da Costa D, Dritsa M, Bernatsky S, Pineau C, Menard HA, et al. (2006) Dimensions of fatigue in systemic lupus erythematosus: relationship to disease status and behavioral and psychosocial factors. J Rheumatol 33: 1282-1288.
   


5. Fortin PR, Abrahamowicz M, Neville C, du Berger R, Fraenkel L, et al. (1998) Impact of disease activity and cumulative damage on the health of lupus patients. Lupus 7: 101-107.
   


6. Wang C, Mayo NE, Fortin PR (2001) The relationship between health related quality of life and disease activity and damage in systemic lupus erythematosus. J Rheumatol 28: 525-532.
   


7. Al Dhanhani AM, Gignac MA, Su J, Fortin PR (2009) Work disability in systemic lupus erythematosus. Arthritis Rheum 61: 378-385.
   


8. Panopalis P, Yazdany J, Gillis JZ, Julian L, Trupin L, et al. (2008) Health care costs and costs associated with changes in work productivity among persons with systemic lupus erythematosus. Arthritis Rheum 59: 1788-1795.
   


9. Tench C, Bentley D, Vleck V, McCurdie I, White P, et al. (2002) Aerobic fitness, fatigue, and physical disability in systemic lupus erythematosus. J Rheumatol 29: 474-481.
   


10. Keyser RE, Rus V, Cade WT, Kalappa N, Flores RH, et al. (2003) Evidence for aerobic insufficiency in women with systemic Lupus erythematosus. Arthritis Rheum 49: 16-22.
    


11. Oeser A, Chung CP, Asanuma Y, Avalos I, Stein CM (2005) Obesity is an independent contributor to functional capacity and inflammation in systemic lupus erythematosus. Arthritis Rheum 52: 3651-3659.
    


12. Iaboni A, Ibanez D, Gladman DD, Urowitz MB, Moldofsky H (2006) Fatigue in systemic lupus erythematosus: contributions of disordered sleep, sleepiness, and depression. J Rheumatol 33: 2453-2457.
    


13. Tench CM, McCurdie I, White PD, D'Cruz DP (2000) The prevalence and associations of fatigue in systemic lupus erythematosus. Rheumatology (Oxford) 39: 1249-1254.
    


14. Omdal R, Waterloo K, Koldingsnes W, Husby G, Mellgren SI (2003) Fatigue in patients with systemic lupus erythematosus: the psychosocial aspects. J Rheumatol 30: 283-287.
    


15. Jump RL, Robinson ME, Armstrong AE, Barnes EV, Kilbourn KM, et al. (2005) Fatigue in systemic lupus erythematosus: contributions of disease activity, pain, depression, and perceived social support. J Rheumatol 32: 1699-1705.
    


16. Ruiz-Irastorza G, Gordo S, Olivares N, Egurbide MV, Aguirre C (2010) Changes in vitamin D levels in patients with systemic lupus erythematosus: Effects on fatigue, disease activity, and damage. Arthritis Care Res (Hoboken) 62: 1160-1165.
    


17. Taylor J, Skan J, Erb N, Carruthers D, Bowman S, et al. (2000) Lupus patients with fatigue-is there a link with fibromyalgia syndrome? Rheumatology (Oxford) 39: 620-623.
    


18. Burgos PI, Alarcon GS, McGwin G, Crews KQ, Reveille JD, et al. (2009) Disease activity and damage are not associated with increased levels of fatigue in systemic lupus erythematosus patients from a multiethnic cohort: LXVII. Arthritis Rheum 61: 1179-1186.
    


19. Tayer WG, Nicassio PM, Weisman MH, Schuman C, Daly J (2001) Disease status predicts fatigue in systemic lupus erythematosus. J Rheumatol 28: 1999-2007.
    


20. Omdal R, Mellgren SI, Koldingsnes W, Jacobsen EA, Husby G (2002) Fatigue in patients with systemic lupus erythematosus: lack of associations to serum cytokines, antiphospholipid antibodies, or other disease characteristics. J Rheumatol 29: 482-486.
    


21. Omdal R, Sjoholm H, Koldingsnes W, Sundsfjord JA, Jacobsen EA, et al. (2005) Fatigue in patients with lupus is not associated with disturbances in cerebral blood flow as detected by SPECT. J Neurol 252: 78-83.
    


22. Harboe E, Greve OJ, Beyer M, Goransson LG, Tjensvoll AB, et al. (2008) Fatigue is associated with cerebral white matter hyperintensities in patients with systemic lupus erythematosus. J Neurol Neurosurg Psychiatry 79: 199-201.
    


23. Ramsey-Goldman R, Rothrock N (2010) Fatigue in systemic lupus erythematosus and rheumatoid arthritis. PM R 2: 384-392.
    


24. Nishimura K, Omori M, Katsumata Y, Sato E, Gono T, et al. (2015) Neurocognitive impairment in corticosteroid-naive patients with active systemic lupus erythematosus: a prospective study. J Rheumatol 42: 441-448.
    


25. Hochberg MC (1997) Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 40: 1725.
    


26. First MB, Spitzer RL, Gibbon M, Spizer RS, Williams JBW (2002) Structured clinical interview for DSM-IV-TR Axis I disorders, research version, non-patient edition (SCID-I/NP). New York: Biometrics Research, New York State Psychiatric Institute.
    


27. McNair DM, Lorr M, Droppleman LF (1992) Manual for the Profile of Mood Status (POMS), revised. San Diego Educational and Industrial Testing Service (EdITS).
    


28. Yokoyama K, Araki S, Kawakami N, Tkakeshita T (1990) Production of the Japanese edition of profile of mood states (POMS): assessment of reliability and validity. Nihon Koshu Eisei Zasshi 37: 913-918.
    


29. Norcross JC, Guadagnoli E, Prochaska JO (1984) Factor structure of the Profile of Mood States (POMS): two partial replications. J Clin Psychol 40: 1270-1277.
    


30. Gladman DD, Ibanez D, Urowitz MB (2002) Systemic lupus erythematosus disease activity index 2000. J Rheumatol 29: 288-291.
    


31. Morris G, Berk M, Walder K, Maes M (2015) Central pathways causing fatigue in neuro-inflammatory and autoimmune illnesses. BMC Med 13: 28.
    


32. Ahn GE, Ramsey-Goldman R (2012) Fatigue in systemic lupus erythematosus. Int J Clin Rheumtol 7: 217-227.
    


33. Krupp LB, LaRocca NG, Muir-Nash J, Steinberg AD (1989) The fatigue severity scale. Application to patients with multiple sclerosis and systemic lupus erythematosus. Arch Neurol 46: 1121-1123.
    


34. Ad Hoc Committee on Systemic Lupus Erythematosus Response Criteria for Fatigue (2007) Measurement of fatigue in systemic lupus erythematosus: a systematic review. Arthritis Rheum 57: 1348-1357.
    


35. Morris G, Berk M, Galecki P, Maes M (2014) The emerging role of autoimmunity in myalgic encephalomyelitis/chronic fatigue syndrome (ME/cfs). Mol Neurobiol 49: 741-756.
    


36. Klingberg E, Wallerstedt SM, Torstenson T, Hawi G, Forsblad-d'Elia H (2009) The use of complementary and alternative medicine in outpatients with inflammatory rheumatic diseases in Sweden. Scand J Rheumatol 38: 472-480.
    


37. Baker K, Pope J, Fortin P, Silverman E, Peschken C; 1000 Faces of Lupus Investigators; CaNIOS (Canadian Network for Improved Outcomes in SLE) (2009) Work disability in systemic lupus erythematosus is prevalent and associated with socio-demographic and disease related factors. Lupus 18: 1281-1288.
    


38. Utset TO, Chohan S, Booth SA, Laughlin JC, Kocherginsky M, et al. (2008) Correlates of formal work disability in an urban university systemic lupus erythematosus practice. J Rheumatol 35: 1046-1052.
    


39. Parker G, Brotchie H (2010) Gender differences in depression. Int Rev Psychiatry 22: 429-436.