Objectives To investigate the impact of sleep disturbances on Parkinson’s disease (PD) clinical motor subtypes and disease-related disability in a multicentre setting.
Methods We report a cross-sectional relationship between sleep-related symptoms and clinical motor subtypes (tremor dominant (TD); intermediate; postural instability and gait disturbances (PIGDs)) identified in a multicentre study, including 436 patients with PD and 401 age-matched controls. PD-related sleep problems (PD-SP), excessive daytime sleepiness (EDS) and probable REM sleep behaviour disorder (pRBD) were evaluated using the PD sleep scale (PDSS)-2, Epworth Sleepiness Scale (ESS) and RBD screening questionnaire-Japanese version (RBDSQ-J), respectively.
Results PD-SP (PDSS-2 ≥18; 35.1% vs 7.0%), EDS (ESS ≥10; 37.8% vs 15.5%) and pRBD (RBDSQ-J ≥5; 35.1% vs 7.7%) were more common in patients with PD than in controls. The prevalence of restless legs syndrome did not differ between patients with PD and controls (3.4% vs 2.7%). After adjusting for age, sex, disease duration and Movement Disorder Society-Unified PD Rating Scale (MDS-UPDRS) part III score, the PIGD group had higher PDSS-2 and ESS scores than the TD group. The RBDSQ-J scores did not differ among the TD, intermediate and PIGD groups. A stepwise regression model predicting the MDS-UPDRS part II score identified the Hoehn and Yahr stage, followed by the number of sleep-related symptoms (PD-SP, EDS and pRBD), disease duration, MDS-UPDRS part III score, PIGD subtype, depression and MDS-UPDRS part IV score as significant predictors.
Conclusion Our study found a significant relationship between sleep disturbances and clinical motor subtypes. An increased number of sleep-related symptoms had an impact on disease-related disability.
- Parkinson’s disease
- sleep disorders
- excessive daytime sleepiness
- clinical motor phenotype
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Parkinson’s disease (PD) is a clinical entity that includes the following remarkably heterogeneous clinical presentations: tremor dominant, postural instability and gait difficulty (PIGD); several previous studies1 2 have suggested that early disease onset and rapid disease progression are also clinical presentations that may represent the underlying pathophysiological differences between individual patients.3 A recent review has related non-motor symptoms, such as sleep disturbances, olfactory disturbances and psychiatric symptoms, to specific clinical subtypes of PD, including the brainstem-dominant phenotype, limbic-dominant phenotype and cognitive-dominant phenotype.4 In PD, differences in the pathological progression patterns, such as bottom-up, top-down or the olfactory to limbic route, and in the severity of the Lewy-related pathology may have an impact on clinical presentations5 6; thus, clinical subtyping may be useful to indicate the underlying aetiology, prognosis or treatment response.
In PD, sleep disturbances and excessive daytime sleepiness (EDS) are multifactorial, complex problems attributed to disease pathology involving the brainstem/hypothalamus and are also secondarily due to motor/non-motor symptoms, as well as comorbid primary sleep disorders. Sleep disorders include restless legs syndrome (RLS) and REM sleep behaviour disorder (RBD); PD-related motor and non-motor symptoms can also cause nocturnal problems. These sleep problems are frequently observed and become prevalent in the late stage of the disease. In contrast, in addition to RBD, other sleep disorders and EDS can emerge in the premotor and early stages of PD, possibly reflecting the disease-related pathology responsible for sleep-wake disturbances.7 Because the pathophysiology of these sleep disorders involves both dopaminergic and non-dopaminergic mechanisms during the disease course, different types of sleep disorders may have different effects on the disease course, possibly constituting distinct phenotypes of PD. The relationship between RBD and the clinical subtypes akinetic-rigid and gait-freezing has been reported8 9; however, this finding remains controversial.10 11 Moreover, few studies have investigated the effect of non-motor symptoms on the clinical motor subtypes,12 and thus whether the presence of different non-motor symptoms can predict the specific clinical motor subtype remains an open question.
In this multicentre study, we aimed to characterise the clinical motor subtype related to the type and number of sleep-related symptoms in patients with PD and investigate the impact of sleep-related symptoms on disease-related disability.
Patients and methods
We performed a multicentre study to assess the non-motor symptoms (NMS) of patients with PD between September 2014 and April 2016, including eight university hospitals in the Kanto region of Japan. The Kanto region consists of 7 prefectures, including the capital, Tokyo, and is called the Greater Tokyo Area, which has a population of approximately 42.6 million that accounts for one-third of the entire Japanese population, according to 2010 Population Census of Japan, Preliminary Counts of the Population and Households.
We consecutively recruited 490 patients with PD (age 69.4±8.0 years; 225 males (M)) from outpatient clinics at the participating facilities. Bedridden patients or patients who were unable to answer the questionnaire were initially excluded from this study. After excluding dementia, which was defined as a Mini-Mental Status Examination (MMSE) score lower than 24, and missing data, 436 patients with PD (age 69.3±7.8 years; 197 M) were included in this study. Age-matched and sex-matched control subjects with no history of any neurological or psychiatric diseases (n=401; age 69.2±8.6 years; 187 M) were recruited from the medical staff and their friends and family.
A diagnosis of PD was confirmed according to the UK Brain Bank Clinical Diagnostic Criteria,13 which defines the core motor features as bradykinesia and at least one of the following symptoms: rigidity, resting tremors or postural instability. All the patients were assessed by board-certified neurologists who were experienced in movement disorders; the patients also underwent brain imaging to exclude atypical parkinsonian syndrome or vascular parkinsonism. Drug-induced parkinsonism was excluded based on the clinical history. Disease severity was rated by Hoehn and Yahr (HY) staging. All the patients with PD completed the Japanese version of the MDS-UPDRS part II (motor experiences of daily living), MDS-UPDRS part III (motor examination) and MDS-UPDRS part IV (motor complications).14 Disease-related disability was assessed using the MDS-UPDRS part II.15 The clinical motor subtypes were defined using the MDS-UPDRS parts II and III, including the tremor-dominant subtype (ratio ≥1.5), PIGD subtype (ratio ≤1) and indeterminate subtype (ratios >1.0 and<1.5), as previously described.16 Early disease onset, defined as disease onset below 55 years of age, was also assessed.2
All the participants completed questionnaires regarding their habits, education and sleep status. The presence of visual hallucinations and falls during the past year were determined during interviews. The PD sleep scale (PDSS)-2, comprising 15 individual items for assessing nocturnal non-motor and motor problems, was used to evaluate PD-related sleep problems.17 The following three domain scores of the PDSS-2 were also evaluated: ‘disturbed sleep’ (items 1–3, 8 and 14); ‘motor symptoms at night’ (items 4–6, 12 and 13) and ‘PD symptoms at night’ (items 7, 9–11 and 15).18 PDSS-2 scores ≥18 were defined as clinically relevant PD-related sleep problems (PD-SP).19 The Japanese version of the Epworth Sleepiness Scale (ESS) was used, and excessive daytime sleepiness (EDS) was defined as an ESS score of 10 or greater.20 The RBD screening questionnaire-Japanese version (RBDSQ-J), was used, and an RBDSQ-J score of 5 or greater was defined as probable RBD (pRBD).21 RLS was diagnosed based on four essential features on the questionnaire after excluding RLS mimics such as positional discomfort, muscle cramp, venous stasis, vascular claudication and peripheral neuropathy and confirmed by the neurologists.22 The semi-structured Mini International Neuropsychiatric Interview based on the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, was administered to the participants to assess depression (both minor and major depression).23 The levodopa equivalent dose (LED) was calculated based on the previously reported conversion factors.24
This study was conducted in accordance with the Declaration of Helsinki. The study was approved by the institutional review boards of the participating facilities, and written informed consent was obtained from all participants enrolled in the study.
Mann-Whitney U test or Student’s t-test were used where appropriate to compare the continuous variables, and Χ2 or Fisher’s exact tests were used to compare the categorical variables between the patients with PD and controls. The demographic characteristics of the tremor-dominant, intermediate and PIGD groups were compared using a one-way analysis of variance for continuous variables and Χ2 test for categorical variables. When comparing the prevalence of sleep disorders among the patients with clinical subtypes of PD, differences were adjusted by age, sex, disease duration and MDS-UPDRS part III score using a binary logistic regression model. To predict PIGD, we performed a logistic regression analysis that included age, sex, disease duration, HY stage and LED as covariates. The correlation between MDS-UPDRS part II with other variables was analysed using Spearman's rank correlation coefficients. A logistic regression analysis of PD-SP, EDS or pRBD as a dependent variable was performed, with age, sex, disease duration, HY stage, MDS-UPDRS parts II, III and IV, visual hallucinations, falls during the past year, depression, dopamine agonist use and levodopa use as the independent variables. A stepwise regression analysis was conducted to predict disease-related disability (MDS-UPDRS part II), which included age, sex, HY stage, disease duration, MMSE, MDS-UPDRS part III, MDS-UPDRS part IV, number of sleep-related symptoms (0–3; PDSS-2, pRBD or EDS), depression, tremor-dominant/PIGD score ratio, dopamine agonist use and levodopa use as the independent variables. Two-tailed p values of <0.05 were considered statistically significant. IBM SPSS software V.24.0 (IBM SPSS, Tokyo, Japan) was used for the statistical analyses, and GraphPad Prism for Windows (V.5.01; GraphPad Software, San Diego, California, USA) was used to generate the figure.
The mean onset age and disease duration of the patients with PD were 61.9±9.5 and 7.4±5.3 years, respectively. The mean HY stage was 2.3±0.7 (HY stage 1, n=41; HY stage 2, n=254; HY stage 3, n=120; HY stage 4, n=20; HY stage 5, n=1). The MDS-UPDRS part II, III and IV scores were 12.6±8.9, 28.6±13.3 and 2.0±3.3, respectively. Eighty-five patients (19.5%) had early disease onset. Thirty-four patients (7.8%) were drug naïve, and 227 (52.1%) and 365 (83.7%) patients were taking dopamine agonists or levodopa, respectively. Sixty (13.8%) patients were taking entacapone, 116 (26.6%) selegiline, 84 (19.3%) pramipexole, 57 (13.1%) ropinirole, 36 (8.3%) rotigotine, 35 (8.0%) pergolide, 10 (2.3%) cabergoline, 31 (7.1%) amantadine and 73 (16.7%) zonisamide. Eight patients (1.8%) were treated with deep brain stimulation. The demographic data of the patients with PD and the controls are shown in table 1. Compared with the controls, the patients with PD used less alcohol and tobacco. Regarding the sleep assessments, PD-SP, EDS and pRBD were significantly more common in the patients with PD than in the controls (table 1). However, the prevalence of RLS did not differ between the patients with PD and the controls (3.4% vs 2.7%, p=0.69).
The patients with PD were categorised into the following three groups according to their motor subtypes: tremor dominant (n=157, 36.0%), intermediate (n=45, 10.3%) and PIGD (n=234, 53.7%). The characteristics of the patients with PD according to the motor subtypes are shown in table 2. The PIGD phenotype was characterised by an older age, longer disease duration and higher scores on the MDS-UPDRS parts II, III and IV than the other subtypes. In the PIGD subtype, LED and the prevalence of hallucinations and falls during the past year were higher than in the other subtypes.
Table 3 shows the characteristics of the patients with PD according to the presence of sleep-related symptoms (PD-SP, EDS and pRBD). A mild male predominance was associated with EDS and pRBD. Compared with the patients without the above-mentioned sleep problems, the PD-SP and pRBD groups had longer disease durations, higher MDS-UPDRS part II, III and IV scores and LEDs and higher rates of depression, whereas the EDS group had higher MDS-UPDRS part II and IV scores and a higher rate of early disease onset. A specific clinical motor subtype, that is, an increased rate of PIGD was significantly related to the presence of PD-SP and EDS but not pRBD.
There was a significant overlap of various sleep-related symptoms in the patients with PD. The prevalence of two out of three coexisting sleep-related symptoms (EDS, PD-SP and pRBD) was approximately 20%. The coexistence of all three symptoms (EDS, PD-SP and pRBD) was 12.2% (figure 1). The logistic regression analysis of EDS, pRBD and PD-SP using a likelihood ratio forward selection showed that male sex, the MDS-UPDRS part III score, hallucinations and the MDS-UPDRS part II score were contributing factors to EDS; male sex, hallucinations, the MDS-UPDRS part II score were contributing factors to pRBD and disease duration, depression and MDS-UPDRS part II score were contributing factors to PD-SP (table 4). Male sex (OR 1.821; 95% CI 1.135 to 2.921, p=0.013), HY stage (OR 3.818; 95% CI 2.460 to 5.926, p<0.0001), LED (OR 1.001; 95% CI 1.000 to 1.002, p=0.0014) and EDS (OR 1.8; 95% CI 1.130 to 3.039, p=0.014) were the significant predictors of the PIGD subtype in the logistic regression analysis.
Figure 2 shows the comparison of the PDSS-2, ESS and RBDSQ-J scores among the tremor-dominant (TD), intermediate and PIGD groups. After adjusting for age, sex, disease duration and MDS-UPDRS part III, the PIGD group had a higher PDSS-2 total score than the tremor-dominant group and a higher PDSS-2 domain ‘PD symptoms at night’ score than the TD and intermediate groups. The ESS score was higher in the PIGD than in the TD group. The RBDSQ-J score did not significantly differ among the groups.
The MDS-UPDRS part II score was positively correlated with the disease duration (r=0.47, p<0.0001), HY stage (r=0.46, p<0.0001) and the MDS-UPDRS part III (r=0.42, p<0.0001), MDS-UPDRS part IV (r=0.34, p<0.0001), PDSS-2 (r=0.53, p<0.0001), ESS (r=0.36, p<0.0001) and RBDSQ-J (r=0.24, p<0.0001) scores. The MDS-UPDRS part II score was negatively correlated with the TD/PIGD ratio (r=−0.38, p<0.0001). A significant correlation was also obtained with the PDSS-2 three domain scores: ‘disturbed sleep’ (r=0.42, p<0.0001), ‘motor symptoms at night’ (r=0.44, p<0.0001) and ‘PD symptoms at night’ (r=0.51, p<0.0001).
To determine the predictors for disease-related disability in the patients with PD, we performed a stepwise regression analysis. In the stepwise regression model of disease-related disability (MDS-UPDRS part II), the final model showed that the HY stage, followed by an increased number of sleep-related symptoms (0–3; PD-SP, EDS and pRBD), disease duration, MDS-UPDRS part III score, PIGD subtype, depression and MDS-UPDRS part IV score were significant predictors (table 5).
In this cross-sectional multicentre study, we confirmed a significantly higher prevalence of sleep-related symptoms, such as PD-SP, EDS and pRBD, in the patients with PD than in the age-matched and sex-matched controls; these results are similar to those of previous cross-sectional studies.25–28 Prospective studies have also shown that the prevalence of EDS increases during the disease course29–31; however, the prevalence of pRBD32 33 or insomnia has been observed to fluctuate34 35 during follow-ups. Gjerstad et al34 have reported that the prevalence of insomnia in patients with PD fluctuates from 54% to 60% over an 8-year period; meanwhile in a 5-year-prospective study, the prevalence of insomnia was 27% at baseline, and among the patients without insomnia at baseline, 33% developed insomnia at some point during the follow-up.35 In addition, we found a significant overlap in three sleep-related symptoms (EDS, PD-SP and pRBD). The prevalence of two and three coexisting sleep-related symptoms was one-fifth and one-eighth, respectively (figure 1). In our study, the prevalence of RLS was low in our total cohort and was similar between the patients with PD and controls (3.4% vs 2.7%), although an increased prevalence of RLS has been reported in Japanese patients with PD compared with that in controls (12% vs 2.3%).36
When categorising the patients with PD based on the presence or absence of specific sleep problems (PD-SP, EDS or pRBD), we found relationships between the sleep-related symptoms and specific clinical parameters. Compared with the patients with PD without sleep-related symptoms, the PD-SP and pRBD groups had longer disease durations, higher MDS-UPDRD part II, III and IV scores and greater rates of depression, while the EDS group had higher MDS-UPDRS part II and IV scores and a higher rate of early disease onset. These findings suggest that motor impairments and depression are associated with PD-SP and pRBD. Notably, we found a significant link between the clinical motor subtypes and sleep-related symptoms (PD-SP, EDS and pRBD) by observing that (1) the PIGD subtype was the predominant clinical motor subtype in the PD-SP and EDS groups but not in the pRBD group (table 3) and (2) the PIGD group had significantly higher PDSS-2 and ESS scores than the TD group after correcting for age, sex, disease duration and MDS-UPDRS III (figure 2). Our study is the first attempt to cross-sectionally correlate the clinical motor subtypes and several sleep-related symptoms, such as PD-SP, EDS and pRBD, in patients with PD. Although, in our study, the ESS and PDSS-2 total scores remained higher in the PIGD group than in the TD groups in the general linear model after controlling for the confounding factors, because the PIGD subtype showed severe motor symptoms and disease severity compared with the TD phenotype, the disease progression might have influenced PD-SP and EDS. Furthermore, pRBD was not associated with a specific motor subtype.
We also determined the clinical contributors to disease-related disability, as measured by the MDS-UPDRS part II, which is the recommend tool for disability assessment.15 Disease-related disability was significantly correlated with disease severity, disease duration and the MDS-UPDRS part III and IV scores, as well as the sleep-related symptoms, such as PD-SP, pRBD and EDS. In a regression model, in addition to disease severity, an increased number of sleep-related symptoms (PD-SP, EDS and pRBD), the PIGD subtype, motor function, motor complications and depression had a significant impact on disease-related disability. Axial impairment, mood, depression and cognitive impairment have been previously reported as determinants of disability and impaired quality of life in patients with PD.37 38 PD-SP, as evaluated by the PDSS-2, has been correlated with quality of life17 18; however, this association has not been assessed in a large sample of patients with PD. Although Neikrug et al39 have reported that an increasing number of sleep disorders, such as RLS and RBD, is associated with increased non-motor symptoms. Importantly, our finding demonstrating that an increased number of sleep-related symptoms (PD-SP, EDS and pRBD) had a significant impact on disease-related disability has never been reported. Altogether, these observations may imply that these sleep disorders and related symptoms occur in association with the degree and distribution of the degeneration of brain dopaminergic/non-dopaminergic neurons, which could determine certain motor and non-motor phenotypes of PD.
A major limitation of this study is the lack of polysomnography to assess the sleep status of the patients. In our study, the incidence of RLS was much lower than that previously reported and RLS had less of an impact on disability than other sleep-related symptoms, such as PD-SP, EDS and pRBD. One possible explanation is that the range of the severity of RLS in the patients may have influenced the results. To characterise RLS in patients with PD, further studies analysing RLS and leg motor restlessness, which is reported to be more common in untreated patients with PD than in controls,40 are necessary. As another limitation, our study is a cross-sectional evaluation that included nearly an entire cohort of patients treated with dopaminergic drugs. Although we excluded dementia, defined as an MMSE score <24, we did not assess mild cognitive impairment or impulse control disorder, which may affect sleep problems, RBD and EDS. The possible effect of the use of different dopamine agonists on sleep-related symptoms was also not assessed in this study. One could argue that because the motor phenotype can change during the disease course of PD, a different motor subtype may represent only the stage of the disease. Nevertheless, our preliminary approach to correlating sleep-related symptoms with the clinical motor subtypes of a large sample of nearly all patients with PD treated with dopaminergic drugs in a multicentre study, which is close to ‘a real-world clinical setting’, is potentially meaningful. Further prospective studies are necessary to assess the relationship between clinical motor subtypes and sleep disorders and related symptoms in PD.
In conclusion, our cross-sectional survey results indicate a possible relationship between the clinical motor subtypes of PD and sleep-related symptoms and demonstrate the importance of the clinical assessment and management of sleep-related symptoms (PD-SP, EDS and pRBD), which have a significant impact on disease-related disability compared with motor symptoms in patients with PD.
The authors thank Dr Claudia Trenkwalder, Paracelsus Elena Hospital, Kassel, Germany, Department Neurosurgery, University of Göttingen, Göttingen, Germany, for her critical review of this paper. The authors also thank Dr Yuji Watanabe, Dr Hiroaki Fujita, Dr Takeo Matsubara, Dr Hirotaka Sakuramoto, Ms Sanae Tani and Ms Kaori Soma, Department of Neurology, Dokkyo Medical University, for their help with data entry.
Contributors Conceived and designed the study: KS, YO, TU, MM, NH, SK and KH. Performed the study: KS, YO, TU, MM, RS, YS, NH, SK, TY, YK, SH, TK and KH. Performed statistical analysis: KS. Wrote the paper: KS. Critical revision of the manuscript: YO, TU, MM, RS, YS, NH, SK, TY, YK, SH, TK and KH.
Competing interests None declared.
Patient consent Obtained.
Ethics approval The study was approved by the institutional review boards of the participating facilities, and written informed consent was obtained from all participants enrolled in the study.
Provenance and peer review Not commissioned; externally peer reviewed.
Collaborators Ayaka Numao, MD (Department of Neurology, Dokkyo Medical University, Tochigi, Japan), Tatsuya Yamamoto(Department of Neurology, Chiba University Graduate School of Medicine, Chiba), Taku Hatano, MD(Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan), Tomoyuki Miyamoto, MD (Department of Neurology, Dokkyo Medical University Koshigaya Hospital, Saitama, Japan), Shiho Suzuki, MD (Department of Neurology, Dokkyo Medical University, Tochigi, Japan), Yuka Watanabe, MD (Department of Neurology, Dokkyo Medical University Nikko Medical Center, Tochigi, Japan), Hideki Shimura, MD and Takao Urabe, MD (Department of Neurology, Juntendo University Urayasu Hospital, Tokyo, Japan)
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