| Literature DB >> 26272057 |
Cécile L Overman1, Marianne B Kool2, José A P Da Silva3, Rinie Geenen2,4.
Abstract
Fatigue is a common, disabling, and difficult-to-manage problem in rheumatic diseases. Prevalence estimates of fatigue within rheumatic diseases vary considerably. Data on the prevalence of severe fatigue across multiple rheumatic diseases using a similar instrument is missing. Our aim was to provide an overview of the prevalence of severe fatigue across a broad range of rheumatic diseases and to examine its association with clinical and demographic variables. Online questionnaires were filled out by an international sample of 6120 patients (88 % female, mean age 47) encompassing 30 different rheumatic diseases. Fatigue was measured with the RAND(SF)-36 Vitality scale. A score of ≤35 was taken as representing severe fatigue (90 % sensitivity and 81 % specificity for chronic fatigue syndrome). Severe fatigue was present in 41 to 57 % of patients with a single inflammatory rheumatic disease such as rheumatoid arthritis, systemic lupus erythematosus, ankylosing spondylitis, Sjögren's syndrome, psoriatic arthritis, and scleroderma. Severe fatigue was least prevalent in patients with osteoarthritis (35 %) and most prevalent in patients with fibromyalgia (82 %). In logistic regression analysis, severe fatigue was associated with having fibromyalgia, having multiple rheumatic diseases without fibromyalgia, younger age, lower education, and language (French: highest prevalence; Dutch: lowest prevalence). In conclusion, one out of every two patients with a rheumatic disease is severely fatigued. As severe fatigue is detrimental to the patient, the near environment, and society at large, unraveling the underlying mechanisms of fatigue and developing optimal treatment should be top priorities in rheumatologic research and practice.Entities:
Keywords: Fatigue; Fibromyalgia; Osteoarthritis; Rheumatic diseases; Rheumatoid arthritis; Vitality
Mesh:
Year: 2015 PMID: 26272057 PMCID: PMC4752960 DOI: 10.1007/s10067-015-3035-6
Source DB: PubMed Journal: Clin Rheumatol ISSN: 0770-3198 Impact factor: 2.980
Characteristics of the 6120 patients with rheumatic diseases
| Female sex, | 5391 | (88) |
| Age, mean ± SD | 47 | ±12 |
| Men | 50 | ±12 |
| Women | 46 | ±12 |
| Years of education, | ||
| ≤14 years | 2673 | (44) |
| >14 years | 2959 | (48) |
| Unknown | 488 | (8) |
| Marital status, | ||
| Single | 963 | (16) |
| Married or in a steady relationship | 4480 | (73) |
| Separated or widowed | 662 | (11) |
| Unknown | 15 | (0) |
| Language, | ||
| Dutch | 1871 | (31) |
| English | 739 | (12) |
| French | 787 | (13) |
| German | 560 | (9) |
| Portuguese | 725 | (12) |
| Spanish | 1438 | (23) |
| Disease duration, median, interquartile range | 5 | 2–11 |
| Rheumatic disease, | ||
| Fibromyalgia | 2993 | (49) |
| Osteoarthritis | 1249 | (20) |
| Rheumatoid arthritis | 1054 | (17) |
| Systemic lupus erythematosus | 804 | (13) |
| Ankylosing spondylitis/Bechterew’s disease | 621 | (10) |
| Sjögren’s syndrome | 567 | (9) |
| Psoriatic arthritis | 240 | (4) |
| Scleroderma | 147 | (2) |
| Polymyalgia rheumatica | 93 | (2) |
| Ehlers-Danlos syndrome or hypermobility syndrome | 85 | (1) |
| Juvenile idiopathic arthritis | 81 | (1) |
| Gout or pseudogout | 62 | (1) |
| Mixed connective tissue disease | 56 | (1) |
| Tietze’s syndrome/costochondritis | 54 | (1) |
| Another rheumatic diseaseb | 149 | (2) |
aDue to patients with more than one rheumatic disease, the sum of percentages mentioned per rheumatic disease exceeds 100 %
bThe most mentioned diseases in the category “another rheumatic disease” are osteoporosis (n = 22), Behçet’s disease (n = 21), Still’s disease (n = 21), sarcoidosis (n = 18), undifferentiated spondyloarthropathy (n = 15), and dermatomyositis (n = 11)
Fig. 1Prevalence of severe fatigue [RAND(SF)-Vitality score ≤35] in patients with rheumatic diseases. Of the 6120 patients, 6034 had a SF-Vitality score; the number of patients with a missing score ranged per rheumatic disease group from 3 to 16. “A single other rheumatic disease” included all diagnoses which did not reach the minimum of 75 patients to represent a specific rheumatic population. Patients with multiple rheumatic diseases were divided into a group with fibromyalgia and a group without fibromyalgia as one of the diagnoses
Logistic regression model examining associations with severe fatigue (RAND(SF)-Vitality ≤35)
|
| Wald statistic |
| Odds ratio | |
|---|---|---|---|---|
| Fibromyalgia | 1.35 (0.07) | 368.16*** | 0.23 | 3.86 |
| Multiple rheumatic diseases without FMb | 0.49 (0.11) | 20.95*** | 0.05 | 1.63 |
| Disease durationc | −0.27 (0.08) | 11.60** | 0.04 | 0.76 |
| Genderd | −0.12 (0.10) | 1.69 | 0.00 | 0.88 |
| Age | −0.01 (0.003) | 11.15** | 0.04 | 0.99 |
| Years of educatione | −0.30 (0.07) | 19.87*** | 0.05 | 0.74 |
| Marital statusf | ||||
| Single | −0.08 (0.09) | 0.93 | 0.00 | 0.92 |
| Separated/widowed | 0.01 (0.11) | 0.03 | 0.00 | 1.01 |
| Languageg | ||||
| English | 1.12 (0.12) | 88.44*** | 0.11 | 3.08 |
| French | 1.81 (0.13) | 208.62*** | 0.17 | 6.11 |
| German | 0.94 (0.12) | 65.64*** | 0.09 | 2.57 |
| Portuguese | 0.34 (0.11) | 10.46** | 0.03 | 1.41 |
| Spanish | 0.74 (0.08) | 78.35*** | 0.10 | 2.09 |
* = p < 0.05; ** = p < 0.01; *** = p < 0.001; “Variance” explained by the total model, Nagelkerke’s R 2 = 0.23
a r is the logistic pseudo partial correlation, i.e., the explanatory value attributable to a single independent variable after taking into account all other independent variables
bHaving multiple rheumatic diseases without fibromyalgia (FM): yes = 1, no = 0
cDisease duration is log transformed
dGender: male = 1 and female = 0
eYears of education: >14 years = 1, ≤14 years = 0
fMarital status: two dummy variables with “in a relationship” as reference category
gLanguage: five dummy variables with Dutch as reference category