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. 2016 Nov 16;14:151. doi: 10.1186/s12955-016-0550-3

Sleep quality in Chinese patients with rheumatoid arthritis: contributing factors and effects on health-related quality of life

Genkai Guo 1,#, Ting Fu 1,2,#, Rulan Yin 1,2, Lijuan Zhang 1,2, Qiuxiang Zhang 1,2, Yunfei Xia 1, Liren Li 2,, Zhifeng Gu 1,
PMCID: PMC5111274  PMID: 27852301

Abstract

Background

Poor sleep quality is common in rheumatoid arthritis (RA) patients and may lead to disease aggravation and decreased health-related quality of life (HRQoL). The increasing prevalence of poor sleep in RA patients is associated with adverse demographic, clinical, and psychological characteristics. However, there are currently no known reported studies related to the effects of sleep quality on HRQoL in RA patients from China. This cross-sectional study aims to evaluate the contributors of poor sleep and the effects of sleep quality on HRQoL in Chinese RA patients.

Methods

A self-report survey was administered to 131 RA patients and 104 healthy individuals using the Pittsburgh Sleep Quality Index (PSQI) for sleep quality. RA patients completed the Hospital Anxiety and Depression Scale for anxiety and depression, the 28-joint Disease Activity Score for disease activity, the 10 cm Visual Analog Scale for pain, the Health Assessment Questionnaire-Disability Index for functional capacity and the Short Form 36 health survey for HRQoL. Blood samples were taken to gain some biochemical indicators (e.g., erythrocyte sedimentation rate, C-reactive protein, rheumatoid factor, and anti-cyclic citrullinated peptide). Independent samples t-tests, Chi square analysis, logistic regression modeling and linear regression were used to analyze these data.

Results

Our results found that the prevalence of poor sleep (PSQI ≥ 5) was 78.6% and the mean global score of PSQI was 7.93 (SD 3.98) in patients, which were significantly higher than the controls (18.7% and 3.88 (SD 1.89), respectively). There were significant correlations among synthetic disease-modifying antirheumatic drugs, erythrocyte sedimentation rate, pain, disease activity, functional capacity, anxiety/depression and sleep quality in RA patients. Meanwhile, logistic regression models identified disease activity and depression as predictors of poor sleep quality. Poor RA sleepers had impaired HRQoL than good RA sleepers, and sleep quality was independently and significantly associated with social function and mental components summary.

Conclusions

The majority of Chinese RA patients suffered from poor sleep, which significantly impairs their HRQoL. The data suggested the need for holistic assessment and management of RA patients and the importance of objective interventions to improve their sleep quality and finally to improve their HRQoL.

Electronic supplementary material

The online version of this article (doi:10.1186/s12955-016-0550-3) contains supplementary material, which is available to authorized users.

Keywords: Rheumatoid Arthritis, Sleep quality, Quality of life, Depression, Disease activity

Background

Rheumatoid arthritis (RA) is a chronic, inflammatory, autoimmune disorder characterized by joint pain, joint swelling and destruction of synovial joints. RA influences about 0.5–1% of adults in industrialised countries and causes disability, pain, psychological problems and decreased quality of life [13]. Sleep quality is an important component of health-related quality of life (HRQoL), and it has been reported that sleep problems significantly negatively affect the HRQoL in patients with RA [4]. Therefore, identifying factors contributing to poor sleep quality and studying the effects of sleep quality on HRQoL in RA patients is of great importance.

Poor sleep is one of the most prevalent and burdening symptoms and can have debilitating effect on physical and/or mental function and health [5]. It has been reported that sleep problems occur in 54% − 70% of RA patients, including difficulty falling asleep, poor sleep quality, non restorative sleep, wakefulness, awakenings during the night and excessive daytime sleepiness [6, 7]. Importantly, poor sleep quality may contribute to greater pain, disease activity and mood disorders, creating a cascade of dysfunction for afflicted patients [8, 9]. It has been recognized that a number of influences, such as socioeconomic status, disease activity and psychological disorders may impact sleep health, which is common in the RA population [10, 11].

Despite the importance of sleep quality in RA patients, only a limited number of studies related to RA patients’ sleep quality have been conducted in China. The aim of this study is (1) to determine contributors of sleep quality in RA patients recruited from China; (2) to evaluate the effects of sleep quality on various dimensions of HRQoL in Chinese RA patients.

Methods

Participants

Patients who fulfilled the American College of Rheumatology (ACR) (2012) criteria for RA were recruited from the Affiliated Hospital of Nantong University from December 2014 and to December 2015 [12]. RA patients were outpatients or inpatients and healthy subjects were selected from a population attending for an annual examination. Patients were excluded based on either of the following: (1) they were less than 18 years old; (2) they did not complete questionnaires; (3) they had comorbidities (e.g., serious infections, or cardiac, respiratory, gastrointestinal, endocrine disease) that could influence disease activity; (4) they did not complete the measurements of disease activity and pain. Control subjects were excluded if they exhibited current or history of other systemic diseases or psychiatric disorders. The study was approved by the Ethics Committee of the Affiliated Hospital of Nantong University (2014-387), and written informed consents were obtained from all of the participants, according to the Declaration of Helsinki.

Demographics and clinical characteristics

Demographic variables contain the following: body mass index (BMI), gender, age, marital status, education, occupation, and monthly income, smoking and alcohol use, which were obtained by a self-designed questionnaire. Clinical variables of disease duration, family history and medications use were obtained by asking patients or viewing medical records. Additional clinical variables of erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), rheumatoid factor (RF), and anti-cyclic citrullinated peptide (anti-CCP) were examined at the time of investigation. ESR and CRP were assessed by the Westergren method (mm/h) and the nephelometric method (mg/L), respectively. RF was measured by immunoturbidimetry using Cobas integra RFII (Roche Diagnostics GmbH, Mannheim, Germany) and anti-CCP was measured by enzyme linked immunosorbent assay (ELISA) using DIASTAT™ (Axis-Shield Diagnostics, Dundee, UK) [13].

Disease activity was estimated with the valid and reliable 28-joint Disease Activity Score (DAS28), incorporating 28 swollen and tender joint counts, patient’s assessment of disease activity (0–100 mm VAS, where 0 = not active at all and 100 = extremely active), ESR (mm/h) and CRP (mg/L) [14].

Pain was measured by the Visual Analogue Scale (VAS) to characterize clinical pain severity. Patients were asked to rate their experience of pain during the last week, each on a VAS of 0–10, with a higher score indicating more severe pain [15].

Functional capacity was measured by using the Health Assessment Questionnaire -Disability Index (HAQ-DI). The HAQ-DI assesses the patient’s perceived difficulty in completing tasks in eight categories-dressing, arising, eating, walking, hygiene, reach, grip, and usual activities. The eight category scores were averaged into an overall HAQ-DI score and may range from 0 (no disability) to 3 (completely disabled). The Chinese HAQ-DI is a reliable and valid instrument for studies measuring disability of patients with RA [16]. “The test-retest reliability coefficient was 0.84. Between dimensions measured in HAQ-DI, the highest test-retest reliability was observed for walking (Spearman correlation coefficient rs = 0.80) and the lowest was for eating (rs = 0.54). The internal consistency of the scale using Cronbach's alpha was high at 0.86” [16].

Assessment of psychological parameters

Psychological status was measured using the Hospital Anxiety and Depression Scale (HADS), which is divided into HADS-A and HADS-D, both of which containing seven intermingled items [17]. Each item had a 4-point Likert scale and was scored between 0 and 3. Scores for each subscale were constructed by summation, ranging 0 − 21. The Chinese version of HADS had acceptable internal consistency and test-retest reliability, with a Cronbach alpha of 0.85 and intraclass correlation coefficient of 0.90, respectively [18].

Assessment of self-reported life quality

Participants’ health status was assessed using the Short Form 36 health survey (SF-36) in the past 4 weeks. It assessed eight domains (scores range from 0 to 100, with higher scores indicating better health status): physical function (PF); role limitations due to physical problems (RP); body pain (BP); general health perception (GH); energy/vitality (VT); social function (SF); role limitations due to emotional problems (RE); mental health (MH). Z-transformed and normalized domain scores were grouped into Physical Component Summary (PCS) and Mental Component Summary (MCS) [19]. The questionnaire was culturally adapted and translated into Chinese. “Convergent validity and discriminant validity were satisfactory for all except the social functioning scale. Cronbach’s α coefficients ranged from 0.72 to 0.88 except 0.39 for the social functioning scale and 0.66 for the vitality scale. Two weeks test-retest reliability coefficients ranged from 0.66 to 0.94” [20].

Assessment of self-reported sleep quality

Sleep quality was examined by the Chinese version of Pittsburgh Sleep Quality Index (PSQI) during the month preceding, which includes 19 questions completed by the subject [21]. Previous studies have found that PSQI is a well-established, commonly used measure of sleep quality that has been applied across a range of adult populations, including those with RA and other medical conditions [22]. These 19 items were broken down into the following seven components: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disorders, use of hypnotics, and daytime dysfunction. The seven components were each scored from 0 (no difficulty) to 3 (severe difficulty), and summed, to give an overall score ranging from 0 to 21. Participants were dichotomized into a poor-sleep group if the PSQI was ≥5.0 and a good-sleep group if the PSQI was < 5.0 [23].

Data collection

Resultant Chinese paper-based questionnaires were used to administer all instruments under physician supervision. Administration was performed in a single sitting, lasting from 15 to 20 min. Pain and DAS28 were evaluated by the same clinician for all patients. Results were added to a computer database by two research assistants and double checked against the original data prior to analysis.

Data analysis

Descriptive statistics are provided using mean (±standard deviation (SD)) or number (percentage) depending on parametric distribution of measured variables. Potential demographic, clinic and psychological variables were screened using univariate tests of the group difference (poor sleepers versus good sleepers according to the PSQI), at a lenient level of significance without correction for multiple testing (alpha = 0.05). The differences in terms of continuous and categorical variables that are studied in RA patients who are grouped as poor sleepers and good sleepers were evaluated with the two-tailed t test and the chi-square test respectively, as well as the differences between the RA patients and the controls. All variables with a significant association with sleep quality by univariate tests were entered into a multiple stepwise logistic regression model with the dichotomous sleep quality measured by the PSQI as the dependent variable. The relations between quality of life and the other evaluation parameters were examined with Spearman rank correlation analysis. Linear regression analysis was used for each of the SF-36 components to determine independent association of sleep quality with quality of life in patients with RA after controlling for related factors, which have a significant association with each component of SF-36 by Spearman rank correlation analysis. Statistical significance was considered when p <0.05 (two-sided). All analyses were performed using SPSS version 20.0.

Results

Patient characteristics

As four RA patients and five healthy individuals did not complete the questionnaires, 131 RA patients (19 males and 112 females) and 104 healthy individuals (16 males and 88 females) were enrolled in the current study. Table 1 presents the baseline participant characteristics included in our study. Of the 131 RA patients included in this analysis, 85.5% were female and the mean (SD) age was 54.7(11.5) years. Almost 98.5% RA patients were treated with synthetic Disease-Modifying Antirheumatic Drugs (DMARD) and the mean (SD) ESR was 28.47 (27.64) mm/h. There was no significant difference in the age, gender, BMI, marital status, education, occupation, income/month, alcohol and smoke between the RA individuals and the controls (p > 0.05).

Table 1.

Baseline characteristics of RA patients and the healthy controls

Variables Cases (n = 131) Controls (n = 104) p
Gender, female, N (%) 112 (85.5) 88 (84.6) 0.79
BMI (kg/m2), Mean ± SD 22.5 ± 3.12 22.84 ± 2.81 0.432
Age (years), Mean ± SD 54.5 ± 11.5 54.77 ± 11.20 0.851
Monthly income (yuan), N (%) 0.973
 <1000 67 (51.1) 55 (52.9)
 1000-3000 47 (35.9) 35 (33.7)
 3000-5000 13 (9.9) 10 (9.6)
 >5000 4 (3.1) 4 (3.8)
Marital status, N (%) 0.411
 Single 7 (5.3) 11 (10.6)
 Married 118 (90.1) 90 (86.5)
 Divorced 1 (0.8) 1 (1.0)
 Widowed 5 (3.8) 2 (1.9)
Education, N (%) 0.571
 ≤9 years 93 (71.0) 70 (76.9)
 >9 years 38 (29.0) 34 (23.1)
Occupation, N (%) 0.757
 Employed 102 (77.9) 80 (80.8)
 Unemployed 29 (22.1) 24 (19.2)
Alcohol use, yes, N (%) 24 (18.3) 19 (18.3) 1.000
Smoking use, yes, N (%) 10 (7.6) 10 (9.6) 0.642
Disease duration (years), Mean ± SD 8.7 ± 9.1
Family history, yes, N (%) 10 (7.6)
Medications use, N (%)
 NSAIDs 692 (52.7)
 Synthetic DMARDs 129 (98.5)
 Biologic DMARDs 11 (8.4)
 Glucocorticoid 62 (47.3)
ESR (mm/h), Mean ± SD 28.47 ± 27. 64
CRP (mg/L), Mean ± SD 16.61 ± 24.51
RF positive, N (%) 102 (77.9)
anti-CCP positive, N (%) 91 (69.5)
DAS28, Mean ± SD 3.96 ± 1.44
HAQ-DI, Mean ± SD 0.50 ± 0.61
Total pain (VAS), Mean ± SD 4.32 ± 2.76
Nocturnal pain (VAS), Mean ± SD 3.95 ± 3.22
HADS-A, Mean ± SD 9.12 ± 2.79
HADS-D, Mean ± SD 8.74 ± 2.46

Data are means ± SD for continuous variables, or percentages for categorical variables

p values were obtained with the chi-square test for categorical variables and the two-tailed t test for continuous variables

BMI Body Mass Index, NSAID Nonsteroidal anti-Inflammatory Drugs, DMARD Disease-Modifying Antirheumatic Drugs, ESR Erythrocyte Sedimentation Rate, CRP C-reactive Protein, RF Rheumatoid Factor, anti-CCP anti-cyclic citrullinated peptide, DAS28 Disease Activity Score in 28 Joints, HAQ-DI Health Assessment Questionnaire-Disability Index, VAS Visual Analog Scale, HADS Hospital Anxiety and Depression Scale, SF-36 the Medical Outcomes Study Short Form 36, PCS Physical Components Summary, MCS Mental Components Summary, PSQI Pittsburgh Sleep Quality Index

Self-reported sleep quality

In the present study, we found that 103 of the 131 patients with RA had a high risk for poor sleep quality. The results demonstrated that the prevalence of poor sleep (PSQI ≥ 5) in RA patients (78.6%) was higher than in the controls (18.7%) and the total PSQI score of patients with RA was significantly higher than that of the controls (7.93 ± 3.98 versus 3.88 ± 1.89; p < 0.01). Table 2 summarized the global score and the component scale scores of the PSQI for our RA sample in comparison with controls. The data showed that five of the seven components of PSQI in RA patients were significantly different from the controls: subjective sleep quality, sleep latency, habitual sleep efficiency, sleep disorders and use of hypnotics.

Table 2.

Comparison of the components of PSQI in cases and controls

PSQI components score Cases (n = 131) Controls (n = 104) p
Subjective sleep quality 1.23 ± 0.74 0.63 ± 0.73 <0.001
Sleep latency 1.70 ± 1.04 0.70 ± 0.74 <0.001
Sleep duration 0.80 ± 1.05 0.70 ± 1.00 0.451
Habitual sleep efficiency 1.16 ± 1.19 0.15 ± 0.41 <0.001
Sleep disorders 1.65 ± 0.69 0.90 ± 0.72 <0.001
Use of sleep medications 0.52 ± 1.04 0.06 ± 0.27 <0.001
Daytime dysfunction 0.88 ± 0.74 0.73 ± 0.80 0.148
Total 7.93 ± 3.98 3.88 ± 1.89 <0.001

Data are means (standard deviation) for continuous variables

p values were obtained with the two-tailed t test

Differences between good and poor sleepers in RA patients

As shown in Table 3, a number of demographic, clinical and psychological variables were tested for possible differences between good sleepers and poor sleepers in patients. Poor sleepers had higher disease activity scores, higher level of ESR, severer total/nocturnal pain, higher degree of depression and anxiety, with a trend toward lower functional capacity as well, compared with good sleepers (p < 0.05). In addition, the percentage of synthetic DMARDs use in good sleep patients was significant higher than that of poor sleep patients (p < 0.05).

Table 3.

Comparison between poor and good sleepers in RA patients

Variables PSQI < 5 (n = 28) PSQI ≥ 5 (n = 103) p
Female 22 (78.6) 90 (87.4) 0.240
BMI (kg/m2) 22.88 ± 3.40 22.39 ± 3.01 0.347
Age (years) 54.79 ± 12.08 54.38 ± 11.45 0.872
Disease duration (years) 8.21 ± 8.99 8.83 ± 9.15 0.749
Monthly income (yuan) 0.141
 <1000 12 (426.9) 55 (53.4)
 1000-3000 9 (32.1) 38 (36.9)
 3000-5000 6 (21.4) 7 (6.8)
 >5000 1 (3.6) 3 (2.9)
Marital status 0.273
 Single 1 (3.6) 5 (4.9)
 Married 25 (89.3) 94 (91.3)
 Divorced 1 (3.6) 0 (0)
 Widowed 1 (3.6) 4 (3.9)
Education 0.240
 ≤9 years 17 (60.7) 76 (73.8)
 >9 years 11 (39.3) 27 (26.2)
Occupation 0.798
 Employed 21 (75.0) 81 (78.6)
 Unemployed 7 (25.0) 22 (21.4)
Smoking use, yes 4 (14.3) 6 (5.8) 0.220
Alcohol use, yes 4 (14.3) 20 (19.4) 0.783
Family history 2 (7.1) 8 (7.8) 1.000
Medications use
 NSAIDs 17 (60.7) 52 (50.5) 0.396
 Synthetic DMARDs 26 (92.9) 103 (100.0) 0.044
 Biologic DMARDs 2 (7.1) 9 (8.7) 1.000
 Glucocorticoid 11 (39.3) 512 (49.5) 0.396
ESR (mm/h) 19.14 ± 15.96 31.00 ± 29.39 0.006
CRP (mg/dl) 12.36 ± 25.00 17.7668 ± 24.37 0.336
RF positive 19 (67.9) 84 (80.6) 0.198
anti-CCP positive 19 (67.9) 72 (69.9) 0.821
DAS28 3.15 ± 1.39 4.17 ± 1.38 0.001
HAQ-DI 0.20 ± 0.38 0.52 ± 0.65 0.002
Total pain (VAS) 2.96 ± 1.86 4.69 ± 2.85 0.001
Nocturnal pain (VAS) 2.66 ± 2.54 4.30 ± 3.30 0.007
HADS-A 8.00 ± 2.46 9.42 ± 2.81 0.016
HADS-D 7.25 ± 1.76 9.03 ± 2.49 0.001

Data are means ± SD for continuous variables, or percentages for categorical variables

p values were obtained with the chi-square test for categorical variables and the two-tailed t test for continuous variables

BMI Body Mass Index, NSAID Nonsteroidal anti-Inflammatory Drugs, DMARD Disease-Modifying Antirheumatic Drugs, ESR Erythrocyte Sedimentation Rate, CRP C-reactive Protein, anti-CCP anti-cyclic citrullinated peptide, RF Rheumatoid Factor, DAS28 Disease Activity Score in 28 Joints, HAQ-DI Health Assessment Questionnaire-Disability Index, VAS Visual Analog Scale, HADS Hospital Anxiety and Depression Scale, SF-36 the Medical Outcomes Study Short Form 36, PCS Physical Components Summary, MCS Mental Components Summary, PSQI Pittsburgh Sleep Quality Index

Determinants of self-reported sleep quality in RA patients

We used stepwise multiple logistic regression analysis to investigate predictors of sleep quality, as indicated in Table 4. We found that HADS-D(β = 0.340, p < 0.01) and DAS28 (β = 0.520, p < 0.01) were the predictors of sleep quality.

Table 4.

Stepwise multiple logistic regression analysis of demographic, medical and psychological variables in relation to PSQI in RA patients

Predictors β SE p Exp(B) 95%CI
Lower Upper
HADS-D 0.340 0.122 0.007 1.406 1.106 1.786
DAS-28 0.520 0.193 0.004 1.681 1.152 2.453

p values were obtained with stepwise multiple logistic regression analysis

DAS28 Disease Activity Score in 28 Joints, HADS Hospital Anxiety and Depression Scale, PSQI Pittsburgh Sleep Quality Index

Effects of self-reported sleep quality on HRQoL

Comparison of poor sleepers and good sleepers in terms of HRQoL was summarized in Table 5. Patients with poor sleep quality had significantly lower HRQoL in all domains of the SF-36 scale. The relations between HRQoL and the other evaluation parameters were examined with Spearman rank correlation analysis (Additional file 1: Table S1). Considering observed associations of demographic, disease-related and psychological factors with sleep quality, we conducted linear regression analysis for each of the SF-36 components to determine independent association of sleep quality with quality of life after controlling for related factors, which have a significant association with each component of SF-36 by Spearman rank correlation analysis. The results showed that sleep quality was independently and significantly associated with SF (β = -0.204, p = 0.012) and MCS (β = -0.158, p = 0.037). Sleep quality was not significantly associated with the remained components of SF-36 (Table 6).

Table 5.

Comparison between poor and good sleepers in RA patients

Variables PSQI < 5 (n = 28) PSQI ≥ 5(n = 103) p
PF 69.82 ± 28.07 54.27 ± 28.43 0.015
RP 41.07 ± 48.70 17.23 ± 32.09 0.020
BP 60.79 ± 24.72 44.91 ± 25.54 0.004
GH 54.86 ± 21.70 38.29 ± 19.72 <0.001
VT 63.39 ± 17.69 48.59 ± 18.03 <0.001
SF 75.89 ± 26.12 58.62 ± 26.55 0.003
RE 54.76 ± 46.45 31.39 ± 41.96 0.012
MH 71.29 ± 18.48 58.56 ± 17.56 0.002
SF-36 PCS 56.63 ± 24.63 38.68 ± 19.95 0.001
SF-36 MCS 66.33 ± 22.72 49.30 ± 20.27 0.001

p values were obtained with the two-tailed t test for continuous variables

PF physical function, RP role limitations due to physical problems, BP body pain, GH general health perception, VT energy/vitality. SF social function, RE role limitations due to emotional problems, MH mental health, PCS Physical Components Summary, MCS Mental Components Summary, PSQI Pittsburgh Sleep Quality Index

Table 6.

Linear regression analysis of sleep quality on each of the SF-36 components

SF-36 components β p
PFa 0.057 0.471
RPb -0.018 0.836
BPc -0.060 0.383
GHd -0.016 0.067
VTe -0.097 0.255
SFf -0.204 0.012
REg -0.151 0.091
MHh -0.068 0.397
PCSi -0.045 0.527
MCSg -0.158 0.037

p values were obtained with multiple linear regression analysis

acontrolled for income, disease duration, ESR, CRP, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. bcontrolled for income, synthetic DMARDs, CRP, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. ccontrolled for income, synthetic DMARDs, CRP, RF, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. dcontrolled for age, alcohol, disease duration, synthetic DMARDs, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. econtrolled for income, disease duration, ESR, CRP, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. fcontrolled for age, income, synthetic DMARDs, ESR, CRP, RF positive, anti-CCP positive, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. gcontrolled for age, income, synthetic DMARDs, ESR, CRP, RF positive, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. hcontrolled for occupation, income, ESR, CRP, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS. icontrolled for income, disease duration, synthetic DMARDs, ESR, CRP, DAS28, total pain, nocturnal pain, HAQ-DI, and HADS

Discussion

Sleep problems are common in patients with chronic diseases and the prevalence of poor sleep is high in RA patients compared to controls [2426]. In the current study, 78.6% of RA patients suffered from poor sleep, and disease activity and depression were independent predictors of poor sleep quality in RA patients. What is more, poor RA sleepers had impaired HRQoL than good RA sleepers and sleep quality was independently and significantly associated with HRQoL. To our knowledge, this is the first examination of the effects of sleep quality on HRQoL in Chinese RA patients.

It has been reported that several factors of demographic, clinical and psychogenic variables have an influence on sleep quality [2729]. In our study, patients with a PSQI score ≥5 were found to have significantly more frequently use synthetic DMARDs. However, Nicassio PM et al. examining sleep disturbance in RA patients have found no association between synthetic DMARDs and sleep quality [30]. While, one study has shown that YORA (age at disease onset ≤ 65 years) patients reported more sleep disorders and received significantly more synthetic DMARDs than LORA (age at disease onset > 65 years) RA patients [31]. In our present study, the majority of RA patients were under 65 years and 98.5% patients had synthetic DMARDs, which may account for the differences in our findings compared to other reported findings [30].

An increasing number of studies have indicated that psychological disorders are risk factors for sleep quality [4, 32, 33]. It has been reported that 20% − 30% of RA patients have significant mood problems [9, 34]. Psychological disorders especially depression aggravate the numerous health-related comorbidities that are related to RA such as disability and limitations in quality of life [35, 36]. In the present study, we also found that poor-sleep patients had significantly higher levels of HADS-A and HADS-D scores compared with good-sleep patients. Interestingly, logistic regression analysis indicated that depression was a major contributor to sleep quality, which is consistent with previous studies [28, 30]. The data suggested the need for systemic psychiatric screening and management and the importance of targeted interventions to help RA patients get rid of sleep problems [30]. At present, some non-pharmacological treatments, such as intermittent aerobic exercise, can relieve depression and anxiety, as well as improving sleep quality in RA patients [37]. Meanwhile, it is reported that sleep management including sleep education and cognitive-behavioral interventions can improve physical/mental wellness and sleep quality [38].

Previous study has found that disease activity has a vital effect on sleep quality in RA patients [33, 34]. Westhovens et al. examining sleep problems in patients with RA have found a positive and independent association between disease activity and sleep quality [29]. Our study has shown poor-sleep patients had significantly higher levels of disease activity compared with good-sleep patients. Importantly, logistic regression analysis indicated that disease activity is a major contributor to sleep quality, which is consistent with previous studies from Turkey and Korea [4, 27]. Additionally, the ESR was found to be associated with sleep quality in our study, which was in line with prior research reports [4]. It is possible that ESR more closely correlated with polysomnography parameters recorded during sleep hypoxic episodes and moderate and severe obstructive sleep apnea were independently associated with an elevated ESR [39]. Also, there was a positive correlation between sleep quality and pain in RA patients, which was also found in our study [32]. Unexpectedly, pain did not contribute to poor sleep quality in the logistic regression analysis of our study, which was different from a previous study [30]. The possible explanation may be that the active inflammatory disease and the resulting pain are treated and the arthritic process is stopped, which resulted in less influence than other variables on sleep quality [40]. Similar to the results of Wolfe et al., the data in the present study support that functional capacity is associated with sleep quality [32]. The inability to perform the daily activities may cause depression and lead to poor sleep quality in RA patients [41]. After administration of the IL-6 receptor antagonist tocilizumab in patients with RA, changes in PSQI score over time were correlated significantly with HAQ-DI changes and marginally with changes in fatigue [42]. Therefore, IL-6 may play an important role in the mechanism of sleep quality.

HRQoL is considered as one of the main outcome measures for RA patients and sleep quality represents a central component of HRQoL in RA patients [4]. Several studies have shown that individuals with RA have poorer quality of life compared to the general population, in both the emotional and physical domains [43, 44]. We found diminished HRQoL in poor sleepers in all dimensions of SF-36 compared with good sleepers. Association between sleep quality remained significant for SF and MCS after controlling for demographic, disease-related and psychological factors. It is of interest that RA patients had poorer HRQoL, including general health, physical health, mental health and sleep [45]. Associations of sleep problems with pain and fatigue in RA patients are also reported by some previous studies [46]. It must be noted that fatigue and pain in RA patients are multidimensional with physical and mental health. The HRQoL instrument we used in our study was not comprehensive in this regard, which may explain our results.

Though we reported the relationship between the demographic, clinical, psychological characteristics and sleep quality and the effects of sleep quality on HRQoL in Chinese patients with RA, we also had several limitations: (1) We just measure sleep quality and psychological factors with self-report questionnaires. (2) Since the sample size was rather small and was from a single clinic of rheumatology, findings of this study cannot be generalized to all RA patients in our society. (3) The cross-sectional design of our study does not allow examining causal relationships between variables. Further studies with expanded sample sizes, objective sleep measures and prospective studies on RA patients’ quality of sleep should be conducted to support the development of effective interventions to improve their sleep quality.

Conclusions

In summary, this is the first known evaluation of the contributors of poor sleep quality and the effects of sleep quality on RA patients’ HRQoL in China. The present study has found that the quality of sleep was very poor in RA patients and that poor sleep quality may significantly impair their HRQoL. The results of this research provided evidence of the importance of disease activity and depression in explaining sleep quality in patients with RA. The results emphasize the need for systemic psychiatric screening, holistic assessment and targeted intervention/management of RA patients to improve their sleep quality and finally improve their HRQoL.

Acknowledgments

We want to thank Yan Sang, Haixia Cao, Guijuan Feng, Yan Meng, Zhimin Lu, Jing Wang, Juan Ji, and Biyu Shen for their assistance with this study.

Funding

The study was supported by the College graduate research and innovation of Jiangsu Province (YKZZ15-0353) and the Nantong University Graduate Innovation Program (YKC15075).

Availability of data and materials

We have attached the databases described in the manuscript to make it available for testing by reviewers. However, we are sorry that we can’t share our data now. Because we are a team and other members of our group have been doing some further researches. Some part of the results in this manuscript is the basis of their study. However, their research is not over now and their articles have not been written or published.

Authors’ contributions

GG and TF have contributed to study design, data collection, data analysis, interpretation of results, preparation of the manuscript. RY, LZ, QZ and YX have contributed to data collection and data analysis; LL and ZG have contributed to study design, preparation of the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

The study was approved by the Ethics Committee of the Affiliated Hospital of Nantong University (2014-387), and written informed consents were obtained from all of the participants, according to the Declaration of Helsinki.

Abbreviations

ACR

American college of rheumatology

anti-CCP

anti-Cyclic Citrullinated Peptide

BMI

Body mass index

BP

Body pain

CRP

C-reactive protein

DAS28

Disease activity score in 28 joints

DMARD

Disease-modifying antirheumatic drugs

ELISA

Enzyme linked immunosorbent assay

ESR

Erythrocyte sedimentation rate

GH

General health perception

HADS

Hospital anxiety and depression scale

HAQ-DI

Health assessment questionnaire-disability index

HRQoL

Health-related quality of life

MCS

Mental components summary

MH

Mental health

NSAID

Nonsteroidal anti-Inflammatory Drugs

PCS

Physical components summary

PF

Physical function

PSQI

Pittsburgh sleep quality index

RA

Rheumatoid arthritis

RE

Role limitations due to emotional problems

RF

Rheumatoid factor

RP

Role limitations due to physical problems

SF

Social function

SF-36

The short form 36 health survey

VAS

Visual analog scale

VT

Energy/Vitality

Additional file

Additional file 1: Table S1. (58.5KB, doc)

Correlation coefficients between components of SF-36 and PSQI (Spearman rho). (DOC 58 kb)

Contributor Information

Genkai Guo, Email: guogenkai@126.com.

Ting Fu, Email: 13861992963@163.com.

Rulan Yin, Email: lanchy4@126.com.

Lijuan Zhang, Email: 13861993170@163.com.

Qiuxiang Zhang, Email: 13861993173@163.com.

Yunfei Xia, Email: xiayf1986@163.com.

Liren Li, Email: larry017@163.com.

Zhifeng Gu, Phone: 13706291941, Email: guzhifeng@126.com.

References

  • 1.Matcham F, Scott IC, Rayner L, Hotopf M, Kingsley GH, Norton S, et al. The impact of rheumatoid arthritis on quality-of-life assessed using the SF-36: a systematic review and meta-analysis. Semin Arthritis Rheum. 2014;44:123–130. doi: 10.1016/j.semarthrit.2014.05.001. [DOI] [PubMed] [Google Scholar]
  • 2.Scott DL, Wolfe F, Huizinga TW. Rheumatoid arthritis. Lancet. 2010;376(9746):1094–1108. doi: 10.1016/S0140-6736(10)60826-4. [DOI] [PubMed] [Google Scholar]
  • 3.Kojima M, Kojima T, Ishiguro N, Oguchi T, Oba M, Tsuchiya H, et al. Psychosocial factors, disease status, and quality of life in patients with rheumatoid arthritis. J Psychosom Res. 2009;67(5):425–431. doi: 10.1016/j.jpsychores.2009.01.001. [DOI] [PubMed] [Google Scholar]
  • 4.Sariyildiz MA, Batmaz I, Bozkurt M, Bez Y, Cetincakmak MG, Yazmalar L, et al. Sleep quality in rheumatoid arthritis: relationship between the disease severity, depression, functional status and the quality of life. J Clin Med Res. 2014;6(1):44–52. doi: 10.4021/jocmr1648w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Løppenthin K, Esbensen BA, Jennum P, Østergaard M, Tolver A, Thomsen T, et al. Sleep quality and correlates of poor sleep in patients with rheumatoid arthritis. Clin Rheumatol. 2015;34(12):2029–2039. doi: 10.1007/s10067-015-2875-4. [DOI] [PubMed] [Google Scholar]
  • 6.Abad VC, Sarinas PS, Guilleminault C. Sleep and rheumatologic disorders. Sleep Med Rev. 2008;12(3):211–228. doi: 10.1016/j.smrv.2007.09.001. [DOI] [PubMed] [Google Scholar]
  • 7.Drewes AM, Nielsen KD, Hansen B, Taagholt SJ, Bjerregard K, Svendsen L. A longitudinal study of clinical symptoms and sleep parameters in rheumatoid arthritis. Rheumatology(Oxford) 2000;39(11):1287–1289. doi: 10.1093/rheumatology/39.11.1287. [DOI] [PubMed] [Google Scholar]
  • 8.Stephenson E, Delongis A, Esdaile JM, Lehman AJ. Depressive symptoms and rheumatoid arthritis: spouse empathic responding as a buffer. Arthritis Care Res (Hoboken) 2014;66(4):532–541. doi: 10.1002/acr.22161. [DOI] [PubMed] [Google Scholar]
  • 9.Covic T, Tyson G, Spencer D, Howe G. Depression in rheumatoid arthritis patients: demographic, clinical, and psychological predictors. J Psychosom Res. 2006;60(5):469–476. doi: 10.1016/j.jpsychores.2005.09.011. [DOI] [PubMed] [Google Scholar]
  • 10.Xu Y, Zhang L, Huang A, Zhao Y, Liu Y. An investigation of sleep disturbance and related factors in rheumatoid arthritis patients. Zhonghua Nei Ke Za Zhi. 2015;54(11):927–930. [PubMed] [Google Scholar]
  • 11.Goes AC, Reis LA, Silva MB, Kahlow BS, Skare TL. Rheumatoid arthritis and sleep quality. Rev Bras Reumatol. 2016;S0482–5004(16):30046–30048. doi: 10.1016/j.rbre.2016.07.011. [DOI] [PubMed] [Google Scholar]
  • 12.Radner H, Neogi T, Smolen JS, Aletaha D. Performance of the 2010 ACR/EULAR classification criteria for rheumatoid arthritis: a systematic literature review. Ann Rheum Dis. 2014;73(1):114–123. doi: 10.1136/annrheumdis-2013-203284. [DOI] [PubMed] [Google Scholar]
  • 13.Kim HH, Kim J, Park SH, Kim SK, Kim OD, Choe JY. Correlation of anti-cyclic citrullinated antibody with hand joint erosion score in rheumatoid arthritis patients. Korean J Intern Med. 2010;25(2):201–206. doi: 10.3904/kjim.2010.25.2.201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Prevoo ML, van ‘t Hof MA, Kuper HH, van Leeuwen MA, van de Putte LB, van Riel PL. Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis. Arthritis Rheum. 1995;38(1):44–48. doi: 10.1002/art.1780380107. [DOI] [PubMed] [Google Scholar]
  • 15.Sokka T, Kankainen A, Hannonen P. Scores for functional disability in patients with rheumatoid arthritis are correlated at higher levels with pain scores than with radiographic scores. Arthritis Rheum. 2000;43(2):386–389. doi: 10.1002/1529-0131(200002)43:2&#x0003c;386::AID-ANR19&#x0003e;3.0.CO;2-Z. [DOI] [PubMed] [Google Scholar]
  • 16.Koh ET, Seow A, Pong LY, Koh WH, Chan L, Howe HS, et al. Cross cultural adaptation and validation of the Chinese Health Assessment Questionnaire for use in rheumatoid arthritis. J Rheumatol. 1998;25(9):1705–1708. [PubMed] [Google Scholar]
  • 17.Bjelland I, Dahl AA, Haug TT, Neckelmann D. The validity of the Hospital Anxiety and Depression Scale. An updated literature review. J Psychosom Res. 2002;52(2):69–77. doi: 10.1016/S0022-3999(01)00296-3. [DOI] [PubMed] [Google Scholar]
  • 18.Wang W, Chair SY, Thompson DR, Twinn SF. A psychometric evaluation of the Chinese version of the Hospital Anxiety and Depression Scale in patients with coronary heart disease. J Clin Nurs. 2009;18(13):2436–2443. doi: 10.1111/j.1365-2702.2009.02807.x. [DOI] [PubMed] [Google Scholar]
  • 19.Emery P, Kavanaugh A, Bao Y, Ganguli A, Mulani P. Comprehensive disease control (CDC): what does achieving CDC mean for patients with rheumatoid arthritis? Ann Rheum Dis. 2014;74(12):2165–2174. doi: 10.1136/annrheumdis-2014-205302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Li L, Wang HM, Shen Y. Chinese SF-36 Health Survey: translation, cultural adaptation, validation, and normalisation. J Epidemiol Community Health. 2003;57(4):259–263. doi: 10.1136/jech.57.4.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Liu XC, Tang MQ. Reliability and validity of the Pittsburgh sleep quality index. Chin J Psychiatry. 1996;29(02):103–107. [Google Scholar]
  • 22.Cole JC, Motivala SJ, Buysse DJ, Oxman MN, Levin MJ, Irwin MR. Validation of a 3-factor scoring model for the Pittsburgh sleep quality index in older adults. Sleep. 2006;29(1):112–116. doi: 10.1093/sleep/29.1.112. [DOI] [PubMed] [Google Scholar]
  • 23.Buysse DJ, Reynolds CF, 3rd, Monk TH, Berman SR, Kupfer DJ. The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research. Psychiatry Res. 1989;28(2):193–213. doi: 10.1016/0165-1781(89)90047-4. [DOI] [PubMed] [Google Scholar]
  • 24.Drewes AM. Pain and sleep disturbances with special reference to fibromyalgia and rheumatoid arthritis. Rheumatology (Oxford) 1999;38(11):1035–1038. doi: 10.1093/rheumatology/38.11.1035. [DOI] [PubMed] [Google Scholar]
  • 25.Sivertsen B, Krokstad S, Overland S, Mykletun A. The epidemiology of insomnia: associations with physical and mental health. The HUNT-2 study. J Psychosom Res. 2009;67(2):109–116. doi: 10.1016/j.jpsychores.2009.05.001. [DOI] [PubMed] [Google Scholar]
  • 26.Louie GH, Tektonidou MG, Caban-Martinez AJ, Ward MM. Sleep disturbances in adults with arthritis: prevalence, mediators, and subgroups at greatest risk. Data from the 2007 National Health Interview Survey. Arthritis Care Res (Hoboken) 2011;63(2):247–260. doi: 10.1002/acr.20362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Son CN, Choi G, Lee SY, Lee JM, Lee TH, Jeong HJ, et al. Sleep quality in rheumatoid arthritis, and its association with disease activity in a Korean population. Korean J Intern Med. 2015;30(3):384–390. doi: 10.3904/kjim.2015.30.3.384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Purabdollah M, Lakdizaji S, Rahmani A, Hajalilu M, Ansarin K. Relationship between Sleep Disorders, Pain and Quality of Life in Patients with Rheumatoid Arthritis. J Caring Sci. 2015;4(3):233–241. doi: 10.15171/jcs.2015.024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Westhovens R, Van der Elst K, Matthys A, Tran M, Gilloteau I. Sleep problems in patients with rheumatoid arthritis. J Rheumatol. 2014;41(1):31–40. doi: 10.3899/jrheum.130430. [DOI] [PubMed] [Google Scholar]
  • 30.Nicassio PM, Ormseth SR, Kay M, Custodio M, Irwin MR, Olmstead R, et al. The contribution of pain and depression to self-reported sleep disturbance in patients with rheumatoid arthritis. Pain. 2012;153(1):107–112. doi: 10.1016/j.pain.2011.09.024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Huscher D, Sengler C, Gromnica-Ihle E, Bischoff S, Eidner T, Ochs W, et al. Clinical presentation, burden of disease and treatment in young-onset and late-onset rheumatoid arthritis: a matched-pairs analysis taking age and disease duration into account. Clin Exp Rheumatol. 2013;31(2):256–262. [PubMed] [Google Scholar]
  • 32.Wolfe F, Michaud K, Li T. Sleep disturbance in patients with rheumatoid arthritis: evaluation by medical outcomes study and visual analog sleep scales. J Rheumatol. 2006;33(10):1942–1951. [PubMed] [Google Scholar]
  • 33.Nicassio PM, Ormseth SR, Custodio MK, Olmstead R, Weisman MH, Irwin MR. Confirmatory factor analysis of the Pittsburgh Sleep Quality Index in rheumatoid arthritis patients. Behav Sleep Med. 2014;12(1):1–12. doi: 10.1080/15402002.2012.720315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Moldofsky H, Lue FA, Smythe HA. Alpha EEG sleep and morning symptoms in rheumatoid arthritis. J Rheumatol. 1983;10(3):373–379. [PubMed] [Google Scholar]
  • 35.Escalante A, Del Rincon I. The disablement process in rheumatoid arthritis. Arthritis Rheum. 2002;47(3):333–342. doi: 10.1002/art.10418. [DOI] [PubMed] [Google Scholar]
  • 36.Verbrugge LM, Juarez L. Profile of arthritis disability: II. Arthritis Rheum. 2006;55(1):102–113. doi: 10.1002/art.21694. [DOI] [PubMed] [Google Scholar]
  • 37.Løppenthin K, Esbensen BA, Jennum P, Østergaard M, Christensen JF, Thomsen T, et al. Effect of intermittent aerobic exercise on sleep quality and sleep disturbances in patients with rheumatoid arthritis- design of a randomized controlled trial. BMC Musculoskelet Disord. 2014;15(1):49–57. doi: 10.1186/1471-2474-15-49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Hideki T, Norihisa T. Sleep education with self-help treatment and sleep health promotion for mental and physical wellness in Japan. Sleep Biol Rhythms. 2016;14(1):89–99. doi: 10.1007/s41105-015-0018-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Lee WH, Wee JH, Rhee CS, Yoon IY, Kim JW. Erythrocyte sedimentation rate may help predict severity of obstructive sleep apnea. Sleep Breath. 2016;20(1):419–424. doi: 10.1007/s11325-015-1245-4. [DOI] [PubMed] [Google Scholar]
  • 40.Wells G, Li T, Maxwell L, Maclean R, Tugwell P. Responsiveness of patient reported outcomes including fatigue, sleep quality, activity limitation, and quality of life following treatment with abatacept for rheumatoid arthritis. Ann Rheum Dis. 2008;67(2):260–265. doi: 10.1136/ard.2007.069690. [DOI] [PubMed] [Google Scholar]
  • 41.Katz PP, Yelin EH. Activity loss and the onset of depressive symptoms: do some activities matter more than others? Arthritis Rheum. 2001;44(5):1194–1202. doi: 10.1002/1529-0131(200105)44:5&#x0003c;1194::AID-ANR203&#x0003e;3.0.CO;2-6. [DOI] [PubMed] [Google Scholar]
  • 42.Fragiadaki K, Tektonidou MG, Konsta M, Chrousos GP, Sfikakis PP. Sleep disturbances and interleukin 6 receptor inhibition in rheumatoid arthritis. J Rheumatol. 2012;39(1):60–62. doi: 10.3899/jrheum.110617. [DOI] [PubMed] [Google Scholar]
  • 43.Picchianti-Diamanti A, Germano V, Ferlito C, Migliore A, D'Amelio R, Laganà B. Health-related quality of life and disability in patients with rheumatoid, early rheumatoid and early psoriatic arthritis treated with etanercept. Qual Life Res. 2010;19(6):821–826. doi: 10.1007/s11136-010-9651-3. [DOI] [PubMed] [Google Scholar]
  • 44.Hodkinson B, Musenge E, Ally M, Meyer PW, Anderson R, Tikly M. Functional disability and health-related quality of life in South Africans with early rheumatoid arthritis. Scand J Rheumatol. 2012;41(5):366–374. doi: 10.3109/03009742.2012.676065. [DOI] [PubMed] [Google Scholar]
  • 45.Dominick KL, Ahern FM, Gold CH, Heller DA. Health-related quality of life among older adults with arthritis. Health Qual Life Outcomes. 2004;2:5. doi: 10.1186/1477-7525-2-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Irwin MR, Olmstead R, Carrillo C, Sadeghi N, Fitzgerald JD, Ranganath VK, et al. Sleep loss exacerbates fatigue, depression, and pain in rheumatoid arthritis. Sleep. 2012;35(4):537–543. doi: 10.5665/sleep.1742. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

We have attached the databases described in the manuscript to make it available for testing by reviewers. However, we are sorry that we can’t share our data now. Because we are a team and other members of our group have been doing some further researches. Some part of the results in this manuscript is the basis of their study. However, their research is not over now and their articles have not been written or published.


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