Trajectories of pain over 6 years in early Parkinson’s disease: ICICLE-PD

Pain is a common, under recognised symptom in people with Parkinson’s disease (PD) [1] with up to 85% of people with PD reporting pain [2, 3]. Pain influences quality of life and is ranked by people with PD as one of the most troublesome early non-motor symptoms [7]. There have been a number of cross-sectional studies evidencing a significantly higher prevalence of pain in people with PD compared to age-matched controls [4‐6]. Currently, the largest study of pain (n = 1957) [2], a cross-sectional study, focused on a sample of early stage PD, but to date there have been few longitudinal studies of early PD or with matched controls to explore changes of pain over time. To date, management options are limited, and there is a need for high-quality studies to enhance our understanding to direct therapies to manage pain in PD [8].

To date, no longitudinal studies have focused primarily on pain in PD; however, some measured pain as a small component alongside other non-motor symptoms [10‐13] or quality of life [14, 15]. Three studies followed individuals over 2 years and found the presence of pain to be one of the most common symptoms at baseline [10], which could remain relatively stable [13] to significantly worsen with those in the early stages of PD (< 2 years), irrespective of dopaminergic therapy [11]. Within these studies only one measure of pain was collected. Three studies performed a 4-year follow-up and found the presence [15] and frequency of pain to significantly increase [12] and that the increase of pain has a direct impact on cost on disease expenditure over time [14]. However, the stability of pain over time in people with PD was not explored, and pain formed a very limited focus of each of the studies. One study [10] had a control group, but did not measure unexplained pain. Unexplained pain has been highlighted as a problem in PD [16] and warrants further investigation over time to understand how pain evolves. We hypothesised that pain in PD would be more prevalent than age-matched controls over time and that the frequency of pain in PD would increase.

The study was approved by the Newcastle and North Tyneside 1 Research Ethics Committee and performed according to the Declaration of Helsinki. All participants provided written informed consent. Recently, diagnosed people with PD were recruited from the community and outpatient clinics in Newcastle upon Tyne and Gateshead from June 1, 2009 to December 31, 2011 as part of the Incidence of Cognitive Impairment in Cohorts with Longitudinal Evaluation in PD (ICICLE-PD) study [17]. Full inclusion criteria have been detailed elsewhere [17]; in brief, newly diagnosed people with PD diagnosed by a movement disorders expert according to the UK Brain Bank criteria were included. Participants returned at 18-month intervals for follow-up evaluation. Age- and sex-matched healthy control subjects were recruited from the local community and underwent a similar assessment schedule as PD participants.

One hundred and fifty-four newly diagnosed participants with PD and 99 age-matched controls completed baseline assessments and the NMSQ. Figure 1 presents a flowchart of the number of individuals at each time point. Baseline comparisons of both groups are presented in Table 1. PD participants scored significantly lower for global cognition and significantly higher for depression. No other significant differences between the groups were found (p > 0.05 for all).

We have shown that unexplained pain is common across the early stages of PD and occurs more frequently than in age-matched controls. To our knowledge, this is the first study to explore the presence, frequency, and trajectory of pain in PD over 72 months.

Whilst it is known from cross-sectional studies that pain often occurs more frequently in people with PD than age-matched control group [4], few longitudinal studies that capture pain have included a comparator. One longitudinal study exploring non-motor symptoms over 2 years reported that the severity of ‘pain and other sensations,’ measured by a single item on the MDS-UPDRS, was significantly more severe in the PD compared to age-matched controls [10]. The current study enhances our understanding of the presence of unexplained pain specifically being significantly higher in the PD group over time, as well as consideration of a longer time period. This is an important finding, as it has been identified that people with PD are uncertain about raising the problem of unexplained pain to healthcare professionals due to uncertainty regarding the link to PD and uncertainty surrounding treatment despite facing daily challenges with this symptom [24].

Our study identified that between 29 and 45% of people with PD reported unexplained pain at each assessment. This finding is in agreement with a longitudinal study exploring the progression of non-motor symptoms over 2 years, in which unexplained pain was approximately 40% at each time point [13]. Our findings highlight the presence of unexplained pain fluctuates among individuals over a longer time frame and develops our understanding of the trajectory of this type of pain with only 2% of individuals consistently reporting this symptom at each time point. Thus, this symptom may be reported for the first time or change at various stages during the course of PD, highlighting the importance of screening for unexplained pain at routine clinical consultations [24]. A previous cross-sectional study highlighted the role of central processes in pain within early/moderate PD [2] and encouraged moving away from a focus on peripheral processes. Pain has been highlighted as one of the most bothersome non-motor symptoms in early PD [7] and, this study highlights that unexplained pain symptoms are common even in early PD. Of note, the NMSQ captured unexplained pain. Chronic pain is known to recur and should not be seen as discrete events [25]. The time of reporting may also influence the responses, and may be prone to recall bias, with the response only applying to the specific time the measure was taken. A yes/no response does not capture the individual’s history of pain, the severity or frequency of the pain, and their longer term trajectory [25]. Prognostic factors for pain, such as pain intensity and beliefs that pain will last into the future, have been associated with poor outcome in low back pain [26], but such associations have not been explored in PD. Future studies should aim to capture a wider range of factors to understand pain reporting in PD, and prognostic factors.

The presence or absence of unexplained pain was not associated with motor severity (MDS-UPDRS III), disease stage (H&Y), or LEDD, corroborating findings from a shorter longitudinal study [12]. Currently, the link between pain and motor symptoms is unclear [27] and exploration of the different descriptions of pain as captured within our study can develop understanding of reporting of symptoms at different time points.

The PDQ-39 bodily discomfort domain was used in the current study to determine self-reported frequency of pain. The different descriptions of pain through two of these questions allowed detailed exploration of their relationship with other symptoms. An increased frequency of aches and pains was associated with an increased MDS-UPDRS lll score up to 36 months, whereas ‘occasional to sometimes’ muscle spasms or cramps was associated with higher MDS-UPDRS lll scores at baseline and 54 months, but not ‘always to frequent’ symptoms. The reporting of aches and pains remained fairly consistent across the different time points, albeit with fluctuations among individual participants. However, reporting of painful muscle cramps and spasms changed; although 45% never experienced this at baseline, only 2% never experienced this over 6 years. The highest percentage (28%) of individuals experiencing muscle cramps and spasms ‘often to always’ was observed at the final time point; 72 months. How individuals describe their pain is relevant to consider during clinical consultations. Individuals may experience different types of pain at different times, and these may not be mutually exclusive [30]. During pain assessments, the different descriptions and types of pain need to be captured [27] as demonstrated in the present study.

Up to 36 months, there was a trend for individuals experiencing unexplained pain and increased frequency of aches and pains or muscle spasms and cramp to be younger. This finding is in agreement with current cross-sectional studies, highlighting individuals with pain are often of a younger age, and younger age at onset being linked with pain in PD [2, 27, 28]. Geriatric depression score followed a trend to be higher in the more frequent pain groups of the PDQ-39 at each time point, with this finding echoing current cross-sectional studies exploring the association between depression, pain and PD [2, 28].

Longitudinal studies often report only one measure of pain [10, 11, 13]. Erro et al. explored the same measures as in the present study, which focused on non-motor symptoms and quality of life over a 4-year period [12]. The bodily discomfort domain of the PDQ-39 worsened over time, indicating an increased frequency of this symptom. However, this longitudinal study [12] provided very limited detail regarding pain. The present study has provided detail of how pain is described over time by people with PD and developed understanding of the trajectory. A number of cross-sectional studies classify the type of pain experienced by people with PD, with musculoskeletal pain highlighted as the most frequent [28, 29] and documenting the different types of pain reported by people with PD [30]. Further research is required longitudinally using measures such as the Kings Parkinson’s Pain Scale [31], which capture the type of pain people with PD experience in more greater detail using consistent measuring tools and classifications to allow comparisons across the literature.

The key strength of this study is that a large cohort of patients with newly diagnosed PD and age-matched controls were recruited and followed longitudinally over 6 years. Other strengths include the use of validated instruments for the assessment of motor symptoms and NMSQ and the measures of pain being validated in a PD group. This study does have several limitations. A number of participants did not return for further assessments; these participants may have been important to the findings of this study. It is possible that these patients may have reported a higher burden of pain. However, on exploration of drop out from each of the pain groups, the trend remained the same over time for each of the pain questions (data not shown). We did not use a specific measure of pain within this study or explore the use of pain medication, which should be investigated in future studies.

In conclusion, pain in PD is prevalent in the early stages of the disease, and the type and frequency of pain people with PD experience fluctuates. People with PD should be asked about their pain at each clinical consultation and given support with describing this given the different ways this can present.