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Artykuł oryginalny

Subjective sleep disturbances at the time of diagnosis in patients with polymyalgia rheumatica and in patients with seronegative elderly-onset rheumatoid arthritis. A pilot study

Ciro Manzo
1
,
Alberto Castagna
2

1.
Internal and Geriatric Medicine Department, Azienda Sanitaria Locale Napoli 3 Sud, Rheumatologic Outpatient Clinic Hospital “Mariano Lauro”, Sant’Angello, Italy
2.
Geriatric Medicine Department Azienda Sanitaria Provinciale Catanzaro, Fragility Outpatient Clinic, Casa della Salute di Chiaravalle Centrale, Catanzaro, Italy
Data publikacji online: 2020/08/31
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Introduction

Polymyalgia rheumatica (PMR) and seronegative elderly-onset rheumatoid arthritis (SEORA) are two of older adults’ most common inflammatory rheumatic diseases [1, 2]. At their first presentation, there are many similarities between PMR and SEORA so that they were considered the same disease or as two different aspects of the same nosographic entity [3]. Moreover, it should not be ruled out in clinical practice that patients initially diagnosed with PMR might be reclassified as having a different disease during their follow-ups [4].

In addition to the involvement of the shoulder girdle, common findings are morning stiffness longer than 45 minutes, raised erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) concentrations, and a good response to low doses of glucocorticoids (GCs) [57]. Nevertheless, in patients with PMR, GCs are used for several months and in some cases throughout life. In contrast, in patients with SEORA, short-term treatment should be considered only when initiating or changing disease-modifying anti-rheumatic drugs, followed by prednisone tapering [8].

In PMR, sleep disorders have rarely been assessed, even if patients report them [911].

In patients with RA, correlations between sleep disorders and pain, mood disorders and GC therapy have been investigated more frequently than the relationship between sleep quality and disease activity (which is still controversial) [1217]. However, in patients with SEORA data are very scarce and these correlations are much less clear.

To our best knowledge, no data are available in the literature about the usefulness of the assessment of subjective sleep disturbances in the differential diagnosis between PMR and SEORA patients at the time of diagnosis.

Material and methods

Study design

It is an observational case-case study.

Objectives

To evaluate whether the assessment of subjective sleep disorders shows differences between patients with PMR and those with SEORA, at the time of diagnosis and in the absence of GC therapy.

To assess whether these differences relate to some factors such as CRP concentrations, co-morbidities, morning stiffness duration, and mood disorders such as depression and anxiety.

Setting and participants

We approached all the patients consecutively referred to two bi-centric outpatient clinics from January to June 2018, with clinical, laboratory and instrumental findings consistent with a diagnosis of PMR or SEORA.

Polymyalgia rheumatica was diagnosed according to 2012 European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) [11]. Seronegative elderly-onset rheumatoid arthritis was diagnosed in patients older than 60 years without rheumatoid factor (FR) and/or anti-citrullinated peptide antibodies (ACPA) according to the criteria proposed by the American Rheumatism Association (ARA) in 1987 [18].

Exclusion criteria were:

  • malignancy,

  • body mass index (BMI) > 30 kg/m2,

  • intake in the previous month of GCs and/or of drugs used to treat sleep disturbance or that could favor sleep disturbances [19, 20] .

Routine laboratory tests such as blood urea nitrogen, complete blood count; liver function tests, creatinine, ESR, CRP concentrations, fecal immunochemical occult blood test and measurement of fecal calprotectin were assessed. The patients with abnormal values were evaluated for further ,more in-depth diagnostic investigations.

After informed consent, we asked the patients to fill out a questionnaire including the Medical Outcomes Study – Sleep Scale (MOS-SS), pain Visual Analogic Scale (VAS), Cumulative Illness Rating Scale (CIRS), Neuropsychiatric Inventory (NPI), and duration (minutes) of morning stiffness (MS). Some socio-demographic data, such as age and sex, were also included in the questionnaire. After the first visit (T0), all patients began therapy with a standardized dose (12.5–15 mg/day) of prednisone, and were submitted to a new clinical and laboratory evaluation after one month (T1) and after 12 months (T2). On those occasions, all patients re-filled in the same questionnaire. Patients who changed the first diagnosis during follow-ups were excluded.

Data sources and methods of assessment

The MOS-SS is a 12-item questionnaire evaluating sleep quality and quantity, with a score between 12 and 71. No formal cut-off scores are provided. It is divided into 6 dimensions evaluating “sleep disturbance”, “snoring”, “sleep awakening short of breath or with headache”, “sleep adequacy”, “somnolence”, and “quantity of sleep/optimal sleep”. A sleep problems index summarizes information across the 9-item MOS-SS. Higher scores indicate greater sleep impairment [21]. The MOS-SS psychometric properties have been evaluated in patients with a variety of conditions characterized by pain; in particular, it is considered the best choice in assessing sleep impairment due to pain [22, 23]. Additionally, it showed good validity, reliability and sensitivity to change in two studies involving RA patients [14, 24].

The VAS was used for assessing pain, with 0 points standing for no pain and 10 points for maximum pain.

Depression and anxiety were assessed using the NPI, with 0 points for absent and 3 points for severe [25]. Although the NPI was developed to assess dementia-related behavioral and psychological disturbances, it was also validated in the assessment of psychological changes in non-dementia patients [26].

The CIRS quantifies the burden of disease in elderly patients, through 14 blocks of organ involvement, with a score between zero (no problem) and three (marked problem). High scores indicate higher severity. Its maximum score is 56 points [27].

The classification criteria proposed by the ARA in 1987 were preferred to the 2010 ACR/EULAR classification criteria. As several researchers highlighted, 2010 ACR/EULAR classification criteria have a specificity lower than 1987 ACR criteria, classifying about 50% of patients (especially if older than 60 years) with non-RA diagnoses as having RA [28, 29]. Taking into account that SEORA is the most frequent PMR-mimicking disease, the low specificity of 2010 EULAR/ACR criteria could have been misleading.

Study size

Based on our unpublished data, it was calculated that 20 patients affected by PMR and 33 patients affected by SEORA had to be recruited to have 95% power with a 5% type 1 error level to detect a minimum clinically significant difference.

Statistical analysis

Descriptive statistics were recorded for each variable, with the quantitative variables shown as mean values and standard deviation. In the population, we considered the variables showing a normal distribution. Indeed, the asymmetry in the evaluated variables was between –2 and +2, and the median practically coincided with the mean. The Anderson-Darling test also confirmed the data (possibly normal; α 0.05). Differences between groups were calculated with the t-test. All p-values were two-sided and a p-value < 0.05 was considered as statistically significant. Data analysis was performed using SPSS Statistics for Windows version 23 software (SPSS Inc., Chicago, IL, USA).

Ethical approval

The study was approved by the local Ethical Committee (number: 05.2018) and carried out in accordance with the Helsinki Declaration, revised in 2013.

Results

The main demographic data and medical records of enrolled patients are listed in Table I. In Table II, we reported MOS-SS total points, CIRS scores, pain VAS, NPI scores, CRP concentrations and MS duration at T0, T1 and T2. The MOS-SS scores and MS were the only variables to show at T0 a significant difference between the two cohorts. In particular, MOS-SS scores were 47.6 ±8.4 in the PMR cohort and 28.26 ±12.4 in the SEORA one, with p-values = 0.000. Morning stiffness duration was 90 ±9.9 minutes in PMR and 45 ±5.5 minutes in SEORA, with p-value = 0.000. At T1 and T2, MOS-SS scores and MS duration decreased in the two groups, and we did not find significant differences at the end of the study.

Table I

Demographic and medical data of our 53 enrolled patients

CharacteristicsValue
Demographics
Female/Male, n35/18
Age at first diagnosis, years61–100
Medical record
CRP concentration, median23.39 ±6.83
CIRS, median27.9 ±4.9
NPI, median6.0 ±5.3

[i] CRP – C-reactive protein, CIRS – Cumulative Illness Rating Scale, NPI – Neuropsychiatric Inventory.

Table II

MOS-SS, CIRS, NPI, pain VAS, CRP concentrations and MS duration in PMR and in SEORA patients, at the time of first diagnosis (T0), after 1 month (T1) and after 12 months (T2) of prednisone therapy (12.5–15 mg/day, gradually decreasing)

ParametersPMRSEORAp
MOS-SS T047.6 ±8.428.26 ±12.40.000
MOS-SS T117.0 ±6.217.8 ±4.2NS
MOS-SS T212.7 ±5.710.6 ±3.9NS
VAS T08.0 ±2.28.7 ±3.0NS
VAS T14.1 ±1.74.1 ±1.3NS
VAS T22.4 ±2.02.9 ±2.1NS
CIRS T027.9 ±4.927.9 ±4.9NS
CIRS T127.9 ±4.927.9 ±4.9NS
CIRS T230.2 ±5.031.9 ±5.6NS
NPI T06.0 ±5.36.0 ±5.3NS
NPI T16.0 ±5.36.0 ±5.3NS
NPI T26.0 ±5.36.0 ±5.3NS
CRP, mg/dl T026.4 ±8.224.0 ±6.0NS
CRP, mg/dl T18.0 ±2.97.9 ±2.5NS
CRP, mg/dl T22.0 ±1.81.4 ±0.5NS
MS T090.0 ±9.945.0 ±5.50.000
MS T115.0 ±7.525.0 ±5.00.000
MS T25.2 ±2.85.0 ±3.0NS

[i] MOS-SS – Medical Outcomes Study – Sleep Scale, CIRS – Cumulative Illness Rating Scale, NPI – Neuropsychiatric Inventory, VAS – Visual Analogue Scale, CRP – C-reactive protein, MS – morning stiffness, PMR – polymyalgia rheumatica, SEORA – seronegative elderly-onset rheumatoid arthritis, NS – not significant.

Discussion

Some confounding factors must be taken into account in assessing subjective sleep disorders in patients with PMR or SEORA. For instance, they have been related to mood disorders, such as depression and anxiety [5]. A higher prevalence of depressive and anxiety symptoms was evident in RA patients compared to the normal population [30, 31]. Depression is also common in patients with PMR [10]. In our study, we found no correlation between sleep disorders and anxiety or depression. Indeed, NPI scores were identical in the two groups at both T0 and T1 and T2.

Other significant confounding factors, such as intake of prednisone and/or drugs used to treat or that could favor sleep disturbances in the previous month, were exclusion criteria.

Glucocorticoids given to the patients were clinically effective. After one-month therapy with a standardized dose (12.5–15 mg/day) of prednisone, MOS-SS scores significantly improved in the two groups, focusing the attention on the relationship between sleep disturbances, immunity and inflammation. This relationship is complex and unclear in many respects [32, 33]. For instance, some researchers highlighted that in patients affected by moderately or severely active RA treated with interleukin 6 (IL-6) receptor antagonist tocilizumab, sleep quality improved significantly at first-month assessment compared to baseline. This observation could suggest that IL-6 has a relevant role in the sleep impairment of RA patients [34].

Nevertheless, other biological disease-modifying anti-rheumatic drugs that are not specifically active towards this cytokine have a similar positive impact on sleep quality in patients with RA [35, 36]. Unfortunately, we did not assess serum concentrations of IL-6. However, it is common knowledge that IL-6 plays a central role in the hepatic production of CRP, and CRP concentrations were not significantly different in our patients at T0, T1 and T2.

Morning stiffness duration is another discussion point. In PMR, MS is a generally accepted core symptom with a greater decision-making impact (two points) in comparison to RA (one point) [4, 11, 18, 37, 38]. In our study, MS was significantly longer at baseline in patients affected by PMR than in those affected by SEORA (90.9 ±9.9 vs. 45.0 ±5.5; p-value = 0.000), whereas we did not find a statistically significant difference in CRP concentrations in the two groups (26.4 ±8.2 vs. 24.0 ±6.0 mg/dl;p-value = not significant). The relationship between MS and sleep impairment is bi-directional, with inflammation as only one of the involved factors. The abrupt onset of PMR during nighttime rest that is much more frequent in PMR patients than in SEORA patients and the possible role of other, different inflammation mediators can explain the discrepancy between MS and CRP concentrations [39].

Finally, we did not find a statistically significant difference in CRP concentrations in the two groups. In Table II, we did not list ESR values. It is common knowledge that in a proportion of PMR patients – from 7 up to 22% – ESR is not raised at the time of diagnosis [40, 41]. Moreover, ESR can depend on several variables, whereas this does not happen with CRP concentrations [42]. For these reasons, we choose to assess only CRP concentrations.

Strengths and limitations

The study design seems to be its main strength. On the other hand, lack of some laboratory findings (such as IL-6 serum concentrations), and of assessment of objective sleep disorders (through polysomnography, for example) could be considered as limitations.

Conclusions

Our pilot study suggests that the assessment of subjective sleep disturbances can be useful in the differential diagnosis between newly diagnosed PMR and newly diagnosed SEORA.

To date, the reasons why PMR patients have higher MOS-SS scores at the time of diagnosis remain speculative, and should inform future appropriately designed studies.

Notes

[3] Conflicts of interest The authors declare no conflict of interest.

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Copyright: © 2020 Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
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