A cross-sectional study on self-reported physical and mental health-related quality of life in rheumatoid arthritis and the role of illness perception

Rheumatoid arthritis (RA) is a chronic systemic disabling condition with a global prevalence of an estimated 0.2–1.0% [1] that can lead to impairment in activities of daily living and work productivity and compromise the overall well-being of RA patients [2]. In RA, the presentation and course of the disease are individual for every patient. The severity of the disease can be confined to mild articular affection or manifested as severe, multisystem disease. Also, individuals’ perceptions of single symptoms differ and have been attributed to individual differences in adaptation to rheumatoid arthritis [3, 4]. Despite significant improvements in the medical management, treatment and prognosis of RA, it is common for patients to experience deficits in physical and mental health functioning [5, 6]. The burden of disease in RA depends on both emotional and physical components and the respective impact on overall well-being may vary in individual patients. As specific RA therapy usually targets specific outcomes (e.g. disease activity), the evaluation of its success is mostly seen from the clinical view and rarely includes a patient’s overall health-related quality of life (HRQoL) [7, 8]. Therapeutic interests thus increasingly shift from merely symptomatic treatment to restoring, or at least improving, HRQoL [8].

Despite similar levels of disease activity and severity, rheumatologists have observed individual variations in HRQoL. Therefore, more and more emphasis is put on other factors in addition to a strict medical/symptom-related model. Social support, for example, has a substantial effect on QoL [9] and previous research has shown that social support has beneficial effects on RA patients [10, 11].

Also, psychosocial models were discussed as a framework to explain these individual differences in HRQoL and daily functioning in chronically ill patients [5, 12]. An individual’s reaction and adaptation to a health threat such as a chronic disease depends on the individual’s cognitive and emotional representation of this threat in their mind [13]. This psychological factor, which is considered to be an important determinant of perception [14].

In the Common-Sense Model (CSM) of Howard Leventhal and colleagues, illness perception is the key construct that suggests that people have personal beliefs about their illness that often do not match medical views but that nevertheless determine, to a large extent, how people respond to their illness. [15] Illness perception is not only based on symptoms, but also on illness related consequences, past experiences of illness and associated anxiety. [16] Research suggests, that patients cluster their ideas about an illness around five coherent themes or components. These components together make up the patient’s perception of their illness. The components provide a framework for patients to make sense of their symptoms, assess health risk, and direct action and coping. Each of these components holds a perception about one aspect of the illness and together they provide the individual’s coherent view of an illness. The components include the timeline of the disease, the ability to control the disease and the extent to which the treatment helps in controlling the disease, the understanding of the cause, and the consequences and the emotional response to them. It also includes the perception of symptoms and the labels attributed to the disease (identity) [15, 17, 18].

Illness perception has a significant implication for adaptation to illness and has been shown to outweigh the impact of medical disease status on depression, physical function and pain and play an important role in the explanation of distress outcome in chronic illness including rheumatic disease [19‐21]. It influences how anxious or depressed a patient becomes and these effects may be moderated by other factors such as levels of social support and the presence of additional co-morbidities [22]. In earlier studies, patients’ beliefs about their RA have been related to outcomes such as disability, psychiatric morbidity and pain when clinical measures have not [23]. In chronic disease, cognitive therapies are partly directed at influencing illness beliefs, they are thus amenable to interventions [24].

We assume that, in RA patients, specific beliefs in the timeline of the disease, the ability to control the treatment, the consequences, the comprehensibility of the disease and the emotional response are related to physical and mental HRQoL. Thus, in the present study, we aimed to analyse the association of these illness perceptions with physical and mental HRQoL in patients with RA.

RA has a substantial effect on HRQoL [35], and routine assessment of the disease’s impact on a patient’s life, including assessment of fatigue and HRQoL, has been recommended in recent guidelines [36]. In the present study, we assessed physical and mental HRQoL in an outpatient population of RA patients with stable disease course and examined illness perception and symptoms attributable to RA and their contribution to physical and mental HRQoL (SF-36).

The main finding of this study was, that in multivariate analysis, only two aspects of illness perception (consequences and cyclical timeline) explained 63% variance in physical HRQoL and only one aspect of illness perception (emotional representation) and fatigue explained 58% variance in mental HRQoL.

Our study supports the CSM, which states that people’s beliefs about their illness are associated with their HRQoL. Although there are studies showing that the relation between illness perception and illness outcomes, including overall well-being, are mediated by coping with illness [37], there is evidence, that in chronic disease, illness perception has a stronger influence on HRQoL than coping strategies [38, 39].

In our study perceived little impact on daily life (consequences) and a weaker belief in the recurrence of RA (timeline cyclical) was associated with a higher score in physical HRQoL. In a qualitative study on fears and beliefs in rheumatoid arthritis the unpredictability of the disease course was a common source of anxiety, however, these fears were lower in remission but when exacerbations occurred, or a treatment stopped working initial fears were reactivated. The variability in the course was in itself a major source of uncertainty and worries. Also, no longer being able to manage activities of daily living was a common fear on the impact of the disease. This covered all aspects of daily living from getting up to driving or climbing stairs [40].

Our finding that patients with a weaker emotional response to their disease is associated with a better mental HRQoL is in line with previous studies on RA [41] and other chronic diseases [42].

Fatigue had a significant impact on mental HRQoL in our fully adjusted model. A literature review [2] reported that unacceptable levels of fatigue persisted in a substantial proportion of patients with RA, despite the introduction of intensive treatments and the fact that a majority of patients with RA believed that reducing fatigue should be a key treatment aim, although fatigue-related end points were rarely reported in clinical trials.

In a study comparing the relative predictive value of disease status and illness perception, clinical variables explained some but illness perception explained the biggest part of the variance in disease-specific functioning [43]. Also, in our population in univariate regression, demographics and the clinical parameters co-morbidity, number of co-medications, disease activity, functional disability, pain and fatigue were significantly associated with physical and mental HRQoL, but when adapting these variables in the multivariate regression with illness beliefs, only fatigue remained a significant contributor to mental HRQoL.

The mean physical SF-36 score reported in this study was 38.38 and the mean mental SF-36 summary score was 46.94.

These findings are in line with a previous study and a review [6, 35], that reported similar score levels for the RA population compared to significantly higher levels in the general population.

Notably, a higher age was associated with a reduced physical HRQoL but higher mental HRQoL, supporting two previous reviews that reported positive associations between age and mental HRQoL as well as negative associations between the prevalence of depression and age in RA [35, 44].

Here the question arises, if a chronic disease like RA has a stronger impact on younger patients, as it is more difficult for them to accept the limitations caused by the disease (e.g. loss of workability).

Illness coherence was associated with mental HRQoL in univariate and multivariate regression before adjustment to social support, suggesting that people with better knowledge of their disease have a better mental HRQoL. Low health literacy was shown to be associated with functional impairments and disease severity [45] but has until now been reported in association with HRQoL in RA. The better patients knew their disease, the better they experienced mental HRQoL, presumably due to the security of knowing the disease and what to expect in the course of disease and treatment. To the best of our knowledge, the positive impact of better disease understanding on QoL has not been studied in RA patients before and might be interesting for future studies.

When interpreting this study’s results, several points should be taken into consideration.

First, a theoretical concern is the conceptual overlap between specific illness perceptions, disease parameters and HRQoL: E.g. ‘identity’ overlaps with subjectively perceived disease activity/pain (VAS scales). Here the use a standard tool to assess disease activity would cause less overlap. ‘Consequences’ overlaps with physical aspects and emotional representation with emotional aspects of quality of life scales. These overlaps have been already discussed e.g. in a study on patients with inflammatory bowel disease [46]. Also, according to cognitive behavioural theory, we hypothesized that a trigger (RA) leads to a cognitive process (illness perception) which influences emotional and behavioural factors (HRQoL). It is however possible, that in turn poor HRQoL due to other factors/circumstances leads to more negative illness perceptions.

Second, this study is limited due to its cross-sectional and monocentric character, which does not allow final conclusions to be drawn about the direction and causality of the impact of illness perception on HRQoL. The present study assesses how current illness perception is associated with the current HRQoL in RA patients. The fact that (a singular assessment of) illness perceptions only represent how the patient currently thinks, feels and understands about his/her medical condition and do not portray illness perception as an independent psychological factor, trait or process has to be taken into account [47]. Illness perception is dynamic, can change over time and is amenable to intervention [48], thus a causal relationship can only be verified through a longitudinal study potentially including psychological interventions. Illness perception-focused intervention and its effect on quality of life has been studied, for example, for patients with myocardial infarction and their spouses [49, 50] but not for RA, and is thus an interesting objective for an intervention study on RA. Third, the study population primarily consisted of female participants, reflecting the characteristic population distribution of RA patients, but also features the advantage of a balanced distribution of age and disease duration indicating a representative group of RA patients. Also, the study population was limited to participants with a stable disease course for at least 3 months, which excluded e.g. patients with acute disease flares. Patients with currently unstable disease might report other dimensions of illness perception and associations to HR QoL might differ broadly. Thus, these findings are possibly not generalizable to the entire RA population. Fourth, disease activity was assessed using a self-reported parameter and not by means of a recognized objective assessment tool such as the clinical disease activity index and may therefore not be comparable to other study results.

Despite these limitations, this study provides additional information to determinants of HRQoL in RA patients. To our knowledge multiple studies exist on the relation on illness perception on e.g. depression, subjective disease assessment or disability but only few to measure the relation of illness perception of HRoL in RA.

In RA, beliefs about the disease appear to evolve over the course of the disease [40] and illness perceptions are well defined as target to treatment in cognitive behavioural therapy[51]. A substantial finding of this study was, that in patients with stable RA illness perceptions were associated with HRQoL rather than clinical parameters. Given the low HRQoL in RA patients, beside pharmaco-, and physiotherapy, a psychological support could be added for a complete treatment approach. To our knowledge no interventional study was published on illness perception focused therapy on RA patients yet [52]. The results of this study suggest, that targeting illness perception could be tested in psychological interventions to improve HROoL, which has been shown e.g. for musculoskeletal pain [53].

This study showed that current illness perception accounts for a large part of the variance in physical and mental health-related quality of life after adjusting for demographics, clinical variables and social support. Although a longitudinal study with illness perception intervention is needed to assess the stability of beliefs and associated changes in HRQoL, the present study showed that the characterization of a patient’s illness perception is associated with his/her HRQoL. The question if HRQoL can be positively influenced by alleviating the perceived threat of their illness and strengthening positive illness beliefs would be an interesting matter for future research.