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Increased risk of chronic fatigue syndrome following psoriasis: a nationwide population-based cohort study

Abstract

Background

The onset of chronic fatigue syndrome (CFS) has been shown to be associated with several immunological conditions such as infections or atopy. The aim of this study was to clarify the risk of chronic fatigue syndrome following the diagnosis of psoriasis, an immune-related dermatological disease, by analyzing the National Health Insurance Research Database of Taiwan.

Method

2616 patients aged 20 years or older with newly diagnosed psoriasis during 2004–2008 and 10,464 participants without psoriasis were identified. Both groups were followed up until the diagnoses of CFS were made at the end of 2011.

Results

The relationship between psoriasis and the subsequent risk of CFS was estimated through Cox proportional hazards regression analysis, with the incidence density rates being 2.27 and 3.58 per 1000 person-years among the non-psoriasis and psoriasis populations, respectively (adjusted hazard ratio [HR] = 1.48, with 95% confidence interval [CI] 1.07–2.06). In the stratified analysis, the psoriasis group were consistently associated with a higher risk of CFS in male sex (HR = 2.05, 95% CI 1.31–3.20) and age group of ≥ 60 years old (HR = 2.32, 95% CI 1.33–4.06). In addition, we discovered that the significantly increased risk of CFS among psoriasis patients is attenuated after they receive phototherapy and/or immunomodulatory drugs.

Conclusions

The data from this population-based retrospective cohort study revealed that psoriasis is associated with an elevated risk of subsequent CFS, which is differentiated by sex and age.

Background

Chronic fatigue syndrome (CFS) is a condition characterized by functional impairment, fatigue and accompanying symptoms, with a prevalence of approximately 0.1% to 2.5%, a rough estimate since diagnostics and terminology are still inconsistent. Although CFS does not cause acute injury, the condition profoundly affects those who suffer from it, as both adult and adolescent patients with CFS have a substantially lower quality of life compared with the non-CFS population [1]. CFS may be preceded by infection, exposure to environmental toxins, significant physical or emotional trauma and recent vaccination [2]. Several theoretical etiologies of CFS have been proposed, such as chronic inflammation, mitochondrial dysfunction, elevated oxidative stress, hypocortisolism and hypofunctioning hypothalamic–pituitary–adrenal (HPA) axis [3]. Most patients with autoimmune disease, like systemic lupus erythematosus and multiple sclerosis, complained about the fatigue that also correlated to the disease activity. Among these factors, the relationship between CFS and immune reactions has become one of the most intensely studied aspects of this disease. We previously reported that several immunological events, such as atopy, the reactivation of varicella-zoster virus and inflammatory bowel disease, could significantly increase the risk of CFS among the general population, further strengthening the association between CFS and a disordered immune system [4,5,6].

Psoriasis is a systemic immune disease that presents with dermatological as well as ophthalmologic, endocrinological, cardiovascular, and rheumatologic manifestations [7]. Systemic inflammation is one of the key symptoms of psoriasis, causing elevated circulating reactive oxygen species and other symptoms [8]. Chronic dermatological conditions such as psoriasis are considered in the sense that the innate immune system can bring about fatigue in the form of autoimmune diseases, cellular stress responses, even cancer. Many of these conditions demonstrate inflammatory or autoimmune features. From this perspective, one would expect fatigue to be common in dermatological diseases, but this aspect is often overlooked. Furthermore, the severity of psoriasis is positively related to the level of inflammatory cytokines, which provide potentially powerful targets for treating psoriasis [9, 10]. Notably, previous studies have indicated that the proportion of patients with psoriasis complaining of fatigue is larger than that of the non-psoriasis cohort, and such fatigue can be relieved by administering medication that targets inflammatory cytokines [11].

In this population-based retrospective cohort study, the increased subsequent CFS risk in patients with psoriasis was identified and analyzed by using data from the Taiwan National Health Insurance Research Database (NHIRD). Other related factors, including sex, age, comorbidity, and the severity of psoriasis were also analyzed.

Methods

Data sources

The NHIRD was established in 1996 and holds reimbursement claims data from the single-payer National Health Insurance (NHI) program, which was launched in 1995 and which covered approximately 99% of Taiwan’s population by the end of 2014. The NHI medical reimbursement claims database is managed by the National Health Research Institutes in Taiwan. The dataset used for this study was the Longitudinal Health Insurance Database 2000 (LHID 2000), a cohort of 1 million randomly sampled participants in the NHI system from 1996 to 2000, which includes their reimbursement information until the end of 2011. The LHID 2000 contains comprehensive information, including demographics, clinical visits, prescription details, and diagnostic codes, which is based on the International Classification of Diseases, Ninth revision, Clinical Modification (ICD-9-CM).

The reimbursement data on patient identities and institutions were scrambled cryptographically by the NHIRD to protect the privacy of the beneficiaries. The research ethics committee of the institutional review board of China Medical University, Taichung, Taiwan exempted this study from full review (CMUH104-REC2-115).

Study population

This population-based cohort study investigated the association of psoriasis with the risk of CFS between two groups: a psoriasis group and a non-psoriasis group. Figure 1 is a flowchart indicating how the study population was selected. We identified patients who were newly diagnosed with psoriasis (ICD-9-CM 696) during 2004–2008 as the psoriasis group; the date of psoriasis diagnosis was considered the index date. To increase the validity of psoriasis diagnoses, we selected patients who received outpatient service and/or inpatient hospitalization at least 3 times. We further excluded patients with missing information on sex or age (n = 1), aged less than 20 years of age (n = 653), and/or with a prior diagnosis of CFS (ICD-9-CM 780.71) (n = 19) from the analysis. For each patient with psoriasis, four insured participants were randomly selected from among those without psoriasis and frequency-matched by sex, age (5-year span), and index year as the non-psoriasis group, using the same inclusion criteria as that of the psoriasis group. The patient and the public were not involved in our cohort study.

Fig. 1
figure1

The selection process of the participants in the two study group

Differentiating severity of psoriasis

Furthermore, patients with psoriasis were separated into mild psoriasis and severe psoriasis according to what treatments they received. Severe psoriasis was defined as patients receiving phototherapy (e.g., ultraviolet B (psoralen) and ultraviolet A) and/or immunomodulatory drugs (e.g., methotrexate, azathioprine, ciclosporin, oral retinoids, hydroxyurea, mycophenolate mofetil, tacrolimus, etanercept, adalimumab, and ustekinumab). Patients not receiving phototherapy and/or immunomodulatory drugs for psoriasis were classified as having mild psoriasis [12].

Demographic factors

Demographic factors consisted of sex and age (age groups of 20–39, 40–59, and ≥ 60 years). Medical records of comorbidities were obtained before the index date, which comprised of diabetes (ICD-9-CM 250), depression (ICD-9-CM 296.2, 296.3, 300.4, and 311), anxiety (ICD-9-CM 300.00), sleep disorder (ICD-9-CM 307.4 and 780.5), and renal disease (ICD-9-CM 580–589).

Follow up of participants

In our study, the primary outcome was the development of CFS (ICD-9-CM 780.71). The diagnostic criteria was based on the 1994 Fukuda definition, which requires a severe, persistent fatigue for at least 6 months with an addition of four or more symptoms, such as: unusual post-exertion fatigue, impaired memory or concentration, unrefreshing sleep, headache, muscle pain, joint pain, sore throat, and tender cervical nodes [4]. Both groups were tracked from the index date to the development of CFS, the end of 2011, or termination of the record due to either death or withdrawal from the insurance program.

Statistical analysis

The descriptive statistics of the two groups are presented as mean and standard deviation (SD) for continuous variables and as number and percentage for categorical variables. The difference in the distribution of these statistics between the two groups was assessed using the Student’s t test for continuous variables and the Pearson’s Chi-square test for categorical variables. We calculated the incidence of CFS in the two groups by dividing the number of CFS events with the total follow-up time (per 1000 person-years). The cumulative incidence curves of CFS occurrence were generated through the Kaplan–Meier method, and the difference in the curves was assessed through a log-rank test. Univariate and multivariate Cox proportional hazards regression models were applied to assess the risk of CFS and CFS-associated risk factors. The multivariate model was adjusted for sex, age, diabetes, depression, anxiety, sleep disorder, and renal disease. Sex-, age-, and comorbidity-stratified analyses were also performed to investigate the association between psoriasis and the risk of CFS. Finally, we examined the association between different severities of psoriasis and the risk of CFS. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to quantify the risk of CFS.

All statistical analyses were performed using SAS 9.4 (SAS System for Windows, SAS Institute, Cary, NC, USA). The results of comparisons with a two-sided P value of < 0.05 were considered to represent statistically significant differences.

Results

Demographics and comorbidities according to psoriasis status

Our study included 2616 patients with psoriasis and 10,464 participants without psoriasis. The comparison between demographics and comorbidities of the psoriasis and non-psoriasis groups are presented in Table 1. The mean age of patients with psoriasis was 45.2 (SD = 17.5) years, with a mild predominance in men (approximately 54.05%). In addition, patients with psoriasis suffered from more comorbidities such as diabetes, depression, anxiety, sleep disorder, and renal disease than did the participants without psoriasis.

Table 1 Demographic factors and comorbidities of study participants according to psoriasis status

Cumulative incidence of CFS

During the follow-up period, the number of patients diagnosed with CFS were: 50 patients with psoriasis (1.91%) and 126 participants without psoriasis (1.20%) as seen in Fig. 1. The cumulative incidence curves of CFS according to psoriasis status are illustrated in Fig. 2. A log-rank test was used to determine the cumulative incidence of CFS between the groups, showing that the cumulative incidence of CFS was significantly higher in the psoriasis group than in the non-psoriasis group (P = 0.006).

Fig. 2
figure2

Cumulative incidence curves of chronic fatigue syndrome for groups with and without psoriasis

Incidence density rate of CFS among psoriasis status, demographic factors, and comorbidities

The incidence density rate of CFS was higher, 3.58 per 1000 person-years among the patients with psoriasis compared with the 2.27 per 1000 person-years among participants without psoriasis. After adjustment for sex, age, and comorbidity, the adjusted HR of developing CFS was 1.48 times (95% CI 1.07–2.06) greater for patients with psoriasis than for the participants without psoriasis (Table 2). The incidence density rate of CFS is also increased with age. Compared with the younger patients (aged 20–39 years), the risk of developing CFS was 1.64-fold (95% CI 1.10–2.45) higher in those ≥ 60 years old. In the multivariate model, the risk of developing CFS was higher for the patients with a sleep disorder (adjusted HR = 2.17, 95% CI 1.53–3.08).

Table 2 Cox-model-measured hazard ratios and 95% confidence intervals of chronic fatigue syndrome associated with psoriasis and covariates

When stratified by sex, the results indicated that men with psoriasis had a higher risk of developing CFS than did those without psoriasis (adjusted HR = 2.05, 95% CI 1.31–3.20; Table 3). When stratified by age group, the results indicated that the patients with psoriasis had a higher risk of CFS compared with the participants without psoriasis aged ≥ 60 years (adjusted HR = 2.32, 95% CI 1.33–4.06). When stratified by comorbidity status, the patients with psoriasis had a higher risk of CFS compared to the non- psoriasis group without comorbidity (adjusted HR = 1.66, 95% CI 1.03–2.67).

Table 3 Incidence density rates and hazard ratios of chronic fatigue syndrome according to psoriasis status stratified by sex, age, and comorbidity

Incidence density rate of CFS based on severity of psoriasis

Moreover, associations between different severities of psoriasis and the risk of CFS were examined, as shown in Table 4. Patients with mild psoriasis had a higher risk of CFS than did the participants without psoriasis (adjusted HR = 1.46, 95% CI 1.02–2.09). However, patients with severe psoriasis were found to have insignificant risk of developing CFS compared with the participants without psoriasis (adjusted HR = 1.59, 95% CI 0.83–3.03).

Table 4 Incidence density rates and hazard ratios of chronic fatigue syndrome for different severities of psoriasis

Discussion

This population-based retrospective cohort study indicated that the psoriasis group significantly increases the incidence of CFS compared with the non-psoriasis group (Table 2, Fig. 2). Such findings are consistent with those of previous studies [13]. Furthermore, we also discovered that both male and older psoriasis patients have a higher HR of developing CFS according to subgroup analysis (Table 3), which has not been described in previous studies to our knowledge.

According to our study, men with psoriasis are more likely to be diagnosed with CFS (Table 3). Previous studies have shown that the severity of fatigue is worse in women with CFS, whereas other studies have concluded that men and women do not differ in this aspect [13, 14]. However, the prevalence of CFS is higher among both the adult and adolescent female populations (who exhibit additional symptoms such as a spastic colon and neck pain, with peak age of 30 to 50) than among men [15]. From these findings, it is suggested that the incidence of psoriasis raises the risk of CFS among men but with a lower prevalence and severity of CFS in comparison to women. The cause of this phenomenon may be sex-based differences in immune responses, which can be influenced by hormones, genetics, and other sex factors. For example, several previous studies have addressed the risk of psoriatic arthritis, which may be slightly higher in men than in women due to the potential role of hormonal influences in the pathogenesis of psoriatic arthritis- pregnancy and estrogen levels were suggested as protective factors of developing psoriatic arthritis [16]. However, these detailed mechanisms and immunomodulating effects of sex hormones require further investigations [17].

Among individuals ≥ 60 years old, psoriasis patients have an incidence rate of CFS that more than doubles in that of the non-psoriasis population, indicating that the effect of psoriasis on the etiology of CFS is significant in populations with advancing age (Table 3). The incidence rate of psoriasis has a bimodal distribution that illustrates two subtypes of psoriasis, with early-onset psoriasis being considered more genetically related [18]. Those with early- and late-onset psoriasis also have different clinical manifestations, comorbidities, reactions to treatment, and even psychological traits [19]. In addition, eruptive guttate psoriasis is often observed to follow an streptococcal infection by 2 to 3 weeks, and is believed to be an infection-induced disease [20]. CFS may be preceded by an acute or a chronic infection (viral, bacterial or parasitic) [2]. The decline of immune function in aging immune system may be contribute to development of CFS in patient with psoriasis by increased rate of infection. The mechanisms of late-onset psoriasis are poorly understood, and its association with CFS discovered in this study may provide insight for future studies.

Psoriasis is generally considered an autoimmune disease without clearly identified autoantigens and thus exhibits systemic manifestations of a dysfunctional innate and adaptive immune system, most biological agents used to treat severe psoriasis affect Th1 or Th17 pathways [21]. Innate immunity is also believed to be vital in the biological mechanisms of fatigue, with altered activities of B cells, regulatory T cells, and NK cells being identified among populations with CFS [22]. For example, activation of innate immunity can lead to increases in the expression of proinflammatory cytokines (PICs), which can not only cause inflammation, but also induce behavioral changes such as fatigue by affecting the cytokine receptors in the brain [23]. In a 2015 review I. Skoie et al. discussed the phenomenon of fatigue in psoriasis and summarized that previous clinical trials of several biologics, for example TNF-α inhibitors adalimumab or etanercept, that target the innate immunity pathway have shown reductions in the severity of fatigue in psoriasis patients. Only three of the mentioned studies utilized the Functional Assessment of Chronic Illness Therapy Fatigue subscale (FACIT-F), but all of the studies still revealed a clinically significant improvement of fatigue [11]. In our study, we compared the non-psoriasis population with patients who were and were not receiving phototherapy and/or immunomodulatory drugs (Table 4). The patients who did not receive phototherapy and/or immunomodulatory drugs had significantly higher HRs of CFS than did the patients who received these interventions, further confirming the effect of such treatments on fatigue and indirectly indicating the role of immunity in the etiology of CFS.

One of the most researched types of CFS pathophysiology is the dysregulation of the HPA axis. Abnormal adrenocortical activity has been reported among CFS patients since 1981 [24]. We previously reported that burn injury can disturb HPA axis and increase risk of subsequent CFS [25]. The HPA axis provides the body with the capability to respond to stress, which is a self-regulated feedback system that maintains homeostasis [26]. This feedback system includes the paraventricular nucleus of the hypothalamus, pituitary, and adrenal glands. Positive feedback from the hypothalamus to the adrenal gland provided by mediating hormones such as the corticotropin-releasing hormone, arginine vasopressin, and adrenocorticotropic hormone (ACTH) stimulates the cortisol secretion of the adrenal gland. However, circulating cortisol suppresses the secretion of upstream hormones through the binding of the mineralocorticoid receptor (MR) and glucocorticoid receptor (GR) implementation of the feedback loops of the HPA axis [27]. Several reviews have suggested that the abnormality of the HPA axis might be a common feature among the CFS population [28]. For example, hypocortisolaemia [24], loss of the diurnal peak of ACTH and cortisol levels [24, 28], and blunted responsiveness of the HPA axis during a challenge test have all been reported [29]. Some authors have hypothesized that the fundamental cause of the impaired HPA response of CFS might be over-activity of the GR and MR, which leads to increased suppression of the hypothalamus and anterior pituitary components [30]. Although typical symptoms of CFS can be presented in those with hypocortisolemia, the altered HPA-axis function potentially reduces the capacity of HPA hormones to counteract the immune system. As a result, an inflammatory response may be easily triggered by slight stressors [31]. Subsequent PIC storms, such as secretion of IL-6, have been correlated with sustained fatigue and other symptoms that are exhibited by CFS patients [32, 33]. Immune activation markers of CFS include increased levels of PICs such as tumor necrosis factors TNFα, IL-6, IL-1β [34]. Recent studies have suggested that levels of IL-1 and TNFα have a significantly positive correlation with fatigue, autonomic symptoms, and flu-like symptoms [35]. Some clinical trials of treating CFS with biological agent have been emerging, Rituximab has had the best improvement rates in chronic fatigue syndrome (CFS) in randomised placebo-controlled and open studies [36, 37]. Since the diagnostic criteria in CFS is still debatable, HPA-axis dysregulation seems to play a crucial role in the pathophysiology of CFS. Due to the varied and often debilitating manifestations displayed by these patients, the etiology of CFS is most likely multifactorial encompassing several body systems, diseases, or even genetic predisposition and thus, finding a treatment that works for every CFS patient is a challenging task. Multidisciplinary rehabilitation treatment is effective at reducing long-term fatigue severity in patients with CFS [38, 39], the intent is to build an increased awareness and consciousness of healthy bodily symptoms and their relation to physical function, psychological wellbeing, and social interaction. Yet with a renewed interest in this previously rather shunned condition, setting a clear diagnostic criterion has become a priority, with the development of what might be the first diagnostic test under way [40].

Psoriasis is a chronic inflammatory disease that increases the prevalence of a variety of psychosomatic disorders [41]. In 1985, Arnetz et al. demonstrated that after a stress test, lower cortisol levels were seen in psoriasis patients than in the control (non-psoriasis) population [42]. Another study of 102 psoriasis patients’ salivary cortisol values revealed that bedtime cortisol levels were correlated with psoriasis severity, as measured by the Psoriasis Area Severity Index (PASI) [43]. Other researchers have observed hypocortisolemia in psoriasis patients in high-stress populations [44]. All of these results indicate a correlation between psoriasis and cortisol levels, suggesting that an HPA-axis dysfunction might play a crucial role in psoriasis patients when their bodies are managing stress [42]. Subsequent release of PICs could aggravate psoriasis [45], and theoretically, typical symptoms of CFS. Although the exact mechanism of the impairment of the HPA-axis function in psoriasis and CFS patients is not yet clear, some CFS patients may benefit from therapy that is intended to restore HPA-axis function. Low-dose oral hydrocortisone supplement therapy was administered in an RCT study, which showed improvement of CFS symptoms in the experimental group. However, suppression of adrenal glucocorticoid responsiveness limited the practical use of this therapy for treating CFS [46]. In future studies, more applicable rehabilitation programs or pharmacologic agents that recover the responsiveness of the HPA-axis in CFS patients merit exploration.

Chronic fatigue syndrome patients have clinical depression and/or anxiety [47]. Psychosocial stress and mental illness are comorbidities of psoriasis, including anxiety disorder, depression, social phobia, alcoholism, sexual dysfunction and somatoform symptoms. However, the neurobiological, psychological and social interactions in patients with psoriasis and potential psychological and mental comorbidities that have not been fully understood yet [48, 49]. Several inflammatory and pathogenic pathways in depression have been proposed, such as reduced brain monoaminergic transmission (e.g., serotonin, norepinephrine), increased proinflammatory cytokines (e.g., IL-1, IL-6, IL-17, TNFα), reduced neurotrophic factors, elevated oxidative stress and dysregulation of HPA-axis, which are similar to CFS [50]. In addition, some evidence showed biologic DMARDs (e.g., methotrexate), which is used to treat severe psoriasis, had the highest rates of depression, anxiety and suicidal ideation [51]. The psychosocial and mental correlations between CFS and psoriasis are necessary to be determined in future studies.

Since 99.9% of Taiwan’s population is currently enrolled, coverage of the Taiwan NHI program is highly comprehensive. This high percentage of enrollment minimized the selection bias in our study. Furthermore, we attest to the reliability and accuracy of the diagnoses by clinical physicians due to the scrutiny of peer review and medical reimbursement specialists for insurance claim purposes.

Our study had some limitations. First, the complications of both psoriasis and CFS and their severity (based on PASI), have not been considered in this study because of the limited information gathered from the NHIRD. Whether the severity of psoriasis and the risk of CFS are positively associated has yet to be determined. Second, patients’ histories (including symptoms, occupation status, family history), serum laboratory data, and related clinical variables were unavailable because of the anonymity of the data from the NHIRD, which prevented our group from analyzing the relationships among psoriasis, CFS, serum C-reactive protein levels, and other detailed data. Third, the studied population was mainly composed of East Asians living in Taiwan. Whether ethnic or geographic discrepancies exist within this population requires further examination. In addition, the relationships between CFS and different subtypes or manifestations of psoriasis (such as psoriatic arthritis) which have not been discussed, will be the focus of our future study. Fourth, the duration of our study was between 2004 and 2008, and although multiple diagnostic criteria were developed for CFS in recent years, we still chose to include the participants based on the widely- accepted 1994 Fukuda definition. Thus, patients who were diagnosed with CFS by other criteria were not included in our study.

Conclusion

Psoriasis significantly increases the risk of CFS, especially in men and the aging population. These increased risks can be attenuated in patients who receive phototherapy or immunomodulatory drugs.

Availability of data and materials

The data underlying this study is from the National Health Insurance Research database (NHIRD). Interested researchers can obtain the data through formal application to the Ministry of Health and Welfare, Taiwan.

Abbreviations

CFS:

chronic fatigue syndrome

HPA axis:

hypothalamic–pituitary–adrenal axis

NHIRD:

National Health Insurance Research Database

LHID:

Longitudinal Health Insurance Database

SD:

standard deviation

HRs:

hazard ratios

CIs:

confidence intervals

PICs:

proinflammatory cytokines

ACTH:

adrenocorticotropic hormone

MR:

mineralocorticoid receptor

GR:

glucocorticoid receptor

TNFα:

tumor necrosis factor α

IL-1:

interleukin-1

IL-6:

interleukin-6

IL-1β:

interleukin-1β

References

  1. 1.

    Winger A, Kvarstein G, Wyller VB, Ekstedt M, Sulheim D, Fagermoen E, Smastuen MC, Helseth S. Health related quality of life in adolescents with chronic fatigue syndrome: a cross-sectional study. Health Qual Life Outcomes. 2015;13:96.

  2. 2.

    International Association for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis. Chronic fatigue syndrome/myalgic encephalomyelitis: primer for clinical practitioners. 2014.

  3. 3.

    Romano GF, Tomassi S, Russell A, Mondelli V, Pariante CM. Fibromyalgia and chronic fatigue: the underlying biology and related theoretical issues. Adv Psychosom Med. 2015;34:61–77.

  4. 4.

    Tsai SY, Yang TY, Chen HJ, Chen CS, Lin WM, Shen WC, Kuo CN, Kao CH. Increased risk of chronic fatigue syndrome following herpes zoster: a population-based study. Eur J Clin Microbiol Infect Dis. 2014;33(9):1653–9.

  5. 5.

    Yang TY, Kuo HT, Chen HJ, Chen CS, Lin WM, Tsai SY, Kuo CN, Kao CH. Increased risk of chronic fatigue syndrome following atopy: a population-based study. Medicine. 2015;94(29):e1211.

  6. 6.

    Tsai SY, Chen HJ, Lio CF, Kuo CF, Kao AC, Wang WS, Yao WC, Chen C, Yang TY. Increased risk of chronic fatigue syndrome in patients with inflammatory bowel disease: a population-based retrospective cohort study. J Transl Med. 2019;17(1):55.

  7. 7.

    Armstrong AW, Harskamp CT, Armstrong EJ. Psoriasis and the risk of diabetes mellitus: a systematic review and meta-analysis. JAMA Dermatol. 2013;149(1):84–91.

  8. 8.

    Reich K. The concept of psoriasis as a systemic inflammation: implications for disease management. J Eur Acad Dermatol Venereol. 2012;26(s2):3–11.

  9. 9.

    Dowlatshahi E, Voort E, Arends L, Nijsten T. Markers of systemic inflammation in psoriasis: a systematic review and meta-analysis. Br J Dermatol. 2013;169(2):266–82.

  10. 10.

    Rácz E, Prens EP, Kurek D, Kant M, de Ridder D, Mourits S, Baerveldt EM, Ozgur Z, van IJcken WF, Laman JD. Effective treatment of psoriasis with narrow-band UVB phototherapy is linked to suppression of the IFN and Th17 pathways. J Investig Dermatol. 2011;131(7):1547–58.

  11. 11.

    Skoie I, Ternowitz T, Jonsson G, Norheim K, Omdal R. Fatigue in psoriasis: a phenomenon to be explored. Br J Dermatol. 2015;172(5):1196–203.

  12. 12.

    Tsai SY, Chen HJ, Lio CF, Ho HP, Kuo CF, Jia X, Chen C, Chen YT, Chou YT, Yang TY, Sun FJ, Shi L (2017) Increased risk of herpes zoster in patients with psoriasis: a population-based retrospective cohort study. PLoS ONE 12(8):e0179447.

  13. 13.

    Verhoeven E, Kraaimaat F, Van De Kerkhof P, Van Weel C, Duller P, Van Der Valk P, Van Den Hoogen H, Bor J, Schers H, Evers A. Prevalence of physical symptoms of itch, pain and fatigue in patients with skin diseases in general practice. Br J Dermatol. 2007;156(6):1346–9.

  14. 14.

    Sampogna F, Chren M, Melchi C, Pasquini P, Tabolli S, Abeni D. Age, gender, quality of life and psychological distress in patients hospitalized with psoriasis. Br J Dermatol. 2006;154(2):325–31.

  15. 15.

    Nacul LC, Lacerda EM, Pheby D, Campion P, Molokhia M, Fayyaz S, Leite JC, Poland F, Howe A, Drachler ML. Prevalence of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in three regions of England: a repeated cross-sectional study in primary care. BMC Med. 2011;9(1):91.

  16. 16.

    Wilson FC, Icen M, Crowson CS, McEvoy MT, Gabriel SE, Kremers HM. Incidence and clinical predictors of psoriatic arthritis in patients with psoriasis: a population-based study. Arthritis Rheum. 2009;61(2):233–9.

  17. 17.

    Markle JG, Frank DN, Mortin-Toth S, Robertson CE, Feazel LM, Rolle-Kampczyk U, von Bergen M, McCoy KD, Macpherson AJ, Danska JS. Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity. Science. 2013;339(6123):1084–8.

  18. 18.

    Parisi R, Symmons DP, Griffiths CE, Ashcroft DM. Global epidemiology of psoriasis: a systematic review of incidence and prevalence. J Investig Dermatol. 2013;133(2):377–85.

  19. 19.

    Griffiths C, Christophers E, Szumski A, Jones H, Mallbris L. Impact of early versus late disease onset on treatment response to etanercept in patients with psoriasis. Br J Dermatol. 2015;173:1271–3.

  20. 20.

    Schon MP, Boehncke WH. Psoriasis. N Engl J Med. 2005;352(18):1899–912.

  21. 21.

    Nestle FO, Kaplan DH, Barker J. Psoriasis. N Engl J Med. 2009;361(5):496–509.

  22. 22.

    Brenu EW, Huth TK, Hardcastle SL, Fuller K, Kaur M, Johnston S, Ramos SB, Staines DR, Marshall-Gradisnik SM. Role of adaptive and innate immune cells in chronic fatigue syndrome/myalgic encephalomyelitis. Int Immunol. 2014;26(4):233–42.

  23. 23.

    Dantzer R, Kelley KW. Twenty years of research on cytokine-induced sickness behavior. Brain Behav Immun. 2007;21(2):153–60.

  24. 24.

    Poteliakhoff A. Adrenocortical activity and some clinical findings in acute and chronic fatigue. J Psychosom Res. 1981;25(2):91–5.

  25. 25.

    Tsai SY, Lin CL, Shih SC, Hsu CW, Leong KH, Kuo CF, Lio CF, Chen YT, Hung YJ, Shi L. Increased risk of chronic fatigue syndrome following burn injuries. J Transl Med. 2018;16(1):342.

  26. 26.

    Lanfumey L, Mongeau R, Cohen-Salmon C, Hamon M. Corticosteroid-serotonin interactions in the neurobiological mechanisms of stress-related disorders. Neurosci Biobehav Rev. 2008;32(6):1174–84.

  27. 27.

    Cleare AJ. The neuroendocrinology of chronic fatigue syndrome. Endocr Rev. 2003;24(2):236–52.

  28. 28.

    Papadopoulos AS, Cleare AJ. Hypothalamic–pituitary–adrenal axis dysfunction in chronic fatigue syndrome. Nat Rev Endocrinol. 2012;8(1):22–32.

  29. 29.

    Van Den Eede F, Moorkens G, Hulstijn W, Van Houdenhove B, Cosyns P, Sabbe BG, Claes SJ. Combined dexamethasone/corticotropin-releasing factor test in chronic fatigue syndrome. Psychol Med. 2008;38(7):963–73.

  30. 30.

    Jerjes WK, Taylor NF, Wood PJ, Cleare AJ. Enhanced feedback sensitivity to prednisolone in chronic fatigue syndrome. Psychoneuroendocrinology. 2007;32(2):192–8.

  31. 31.

    Martinon F, Mayor A, Tschopp J. The inflammasomes: guardians of the body. Annu Rev Immunol. 2009;27:229–65.

  32. 32.

    Arnold MC, Papanicolaou DA, O’Grady JA, Lotsikas A, Dale JK, Straus SE, Grafman J. Using an interleukin-6 challenge to evaluate neuropsychological performance in chronic fatigue syndrome. Psychol Med. 2002;32(6):1075–89.

  33. 33.

    Miller GE, Chen E, Sze J, Marin T, Arevalo JM, Doll R, Ma R, Cole SW. A functional genomic fingerprint of chronic stress in humans: blunted glucocorticoid and increased NF-kappaB signaling. Biol Psychiatry. 2008;64(4):266–72.

  34. 34.

    Broderick G, Fuite J, Kreitz A, Vernon SD, Klimas N, Fletcher MA. A formal analysis of cytokine networks in chronic fatigue syndrome. Brain Behav Immun. 2010;24(7):1209–17.

  35. 35.

    Maes M, Twisk FN, Kubera M, Ringel K. Evidence for inflammation and activation of cell-mediated immunity in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): increased interleukin-1, tumor necrosis factor-alpha, PMN-elastase, lysozyme and neopterin. J Affect Disord. 2012;136(3):933–9.

  36. 36.

    Fluge O, Bruland O, Risa K, Storstein A, Kristoffersen EK, Sapkota D, Naess H, Dahl O, Nyland H, Mella O. Benefit from B-lymphocyte depletion using the anti-CD20 antibody rituximab in chronic fatigue syndrome. A double-blind and placebo-controlled study. PLoS ONE. 2011;6(10):e26358.

  37. 37.

    Fluge O, Risa K, Lunde S, Alme K, Rekeland IG, Sapkota D, Kristoffersen EK, Sorland K, Bruland O, Dahl O, et al. B-lymphocyte depletion in myalgic encephalopathy/chronic fatigue syndrome. An open-label phase II study with rituximab maintenance treatment. PLoS ONE. 2015;10(7):e0129898.

  38. 38.

    Vos-Vromans DC, Smeets RJ, Huijnen IP, Koke AJ, Hitters WM, Rijnders LJ, Pont M, Winkens B, Knottnerus JA. Multidisciplinary rehabilitation treatment versus cognitive behavioural therapy for patients with chronic fatigue syndrome: a randomized controlled trial. J Intern Med. 2016;279(3):268–82.

  39. 39.

    Vos-Vromans D, Evers S, Huijnen I, Koke A, Hitters M, Rijnders N, Pont M, Knottnerus A, Smeets R. Economic evaluation of multidisciplinary rehabilitation treatment versus cognitive behavioural therapy for patients with chronic fatigue syndrome: a randomized controlled trial. PLoS ONE. 2017;12(6):e0177260.

  40. 40.

    Maxmen A. A reboot for chronic fatigue syndrome research. Nature. 2018;553(7686):14–7.

  41. 41.

    Dominguez PL, Han J, Li T, Ascherio A, Qureshi AA. Depression and the risk of psoriasis in US women. J Eur Acad Dermatol Venereol. 2013;27(9):1163–7.

  42. 42.

    Arnetz BB, Fjellner B, Eneroth P, Kallner A. Stress and psoriasis: psychoendocrine and metabolic reactions in psoriatic patients during standardized stressor exposure. Psychosom Med. 1985;47(6):528–41.

  43. 43.

    Brunoni AR, Santos IS, Sabbag C, Lotufo PA, Bensenor IM. Psoriasis severity and hypothalamic–pituitary–adrenal axis function: results from the CALIPSO study. Braz J Med Biol Res. 2014;47(12):1102–6.

  44. 44.

    Evers AW, Verhoeven EW, Kraaimaat FW, de Jong EM, de Brouwer SJ, Schalkwijk J, Sweep FC, van de Kerkhof PC. How stress gets under the skin: cortisol and stress reactivity in psoriasis. Br J Dermatol. 2010;163(5):986–91.

  45. 45.

    Basavaraj KH, Navya MA, Rashmi R. Stress and quality of life in psoriasis: an update. Int J Dermatol. 2011;50(7):783–92.

  46. 46.

    McKenzie R, O’Fallon A, Dale J, Demitrack M, Sharma G, Deloria M, Garcia-Borreguero D, Blackwelder W, Straus SE. Low-dose hydrocortisone for treatment of chronic fatigue syndrome: a randomized controlled trial. JAMA. 1998;280(12):1061–6.

  47. 47.

    Komaroff AL, Buchwald DS. Chronic fatigue syndrome: an update. Annu Rev Med. 1998;49:1–13.

  48. 48.

    Kurd SK, Troxel AB, Crits-Christoph P, Gelfand JM. The risk of depression, anxiety, and suicidality in patients with psoriasis: a population-based cohort study. Arch Dermatol. 2010;146(8):891–5.

  49. 49.

    Wohlrab J, Fiedler G, Gerdes S, Nast A, Philipp S, Radtke MA, Thaci D, Koenig W, Pfeiffer AF, Harter M, et al. Recommendations for detection of individual risk for comorbidities in patients with psoriasis. Arch Dermatol Res. 2013;305(2):91–8.

  50. 50.

    Miller AH, Raison CL. The role of inflammation in depression: from evolutionary imperative to modern treatment target. Nat Rev Immunol. 2016;16(1):22–34.

  51. 51.

    de Oliveira Ribeiro NP, de Mello Schier AR, Ornelas AC, de Oliveira CMP, Nardi AE, Silva AC. Anxiety, depression and suicidal ideation in patients with rheumatoid arthritis in use of methotrexate, hydroxychloroquine, leflunomide and biological drugs. Compr Psychiatry. 2013;54(8):1185–9.

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Acknowledgements

We would like to extend acknowledgements to Fang-Ju Sun, M.S at fjsun.b612@mmh.org.tw for her help with statistical advice and to the organizations that have funded this project.

Funding

This study is supported in part by Taiwan Ministry of Health and Welfare Clinical Trial Center (MOHW108-TDU-B-212-133004), China Medical University Hospital, Academia Sinica Stroke Biosignature Project (BM10701010021), MOST Clinical Trial Consortium for Stroke (MOST 107-2321-B-039-004), Tseng-Lien Lin Foundation, Taichung, Taiwan, and Katsuzo and Kiyo Aoshima Memorial Funds, Japan.; The Department of Medical Research at Mackay Memorial Hospital (MMH-105-87; MMH-106-81; MMH-107-71; MMH-107-102; MMH-107-135).

Author information

WW, ST, HC had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: ST, CC, CL. Acquisition, analysis, or interpretation of data: ST, HC. Drafting of the manuscript: All authors. Critical revision of the manuscript for important: ST, CK, YTW, KL. Intellectual content: ST, CL, CC. Statistical analysis: HC. Obtained funding: ST, HC, WW. Administrative, technical, or material support: All authors. Study supervision: ST, WW. Submission: ST, KL. All authors read and approved the final manuscript.

Correspondence to Shin-Yi Tsai or Wei-Sheng Wang.

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Ethics approval and consent to participate

This study was approved by the Institutional Review Board of China Medical University (CMUH104-REC2-115) and the Institutional Review Board of MacKay Memorial Hospital (16MMHIS074).

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Keywords

  • Chronic fatigue syndrome
  • Psoriasis
  • National health programs
  • Immune system diseases