Early use of donepezil against psychosis and cognitive decline in Parkinson's disease: a randomised controlled trial for 2 years.

OBJECTIVES: Brain acetylcholine is decreased even in patients with cognitively preserved Parkinson's disease (PD). We investigated whether early and long-term use of donepezil prevents psychosis in non-demented PD patients.
METHODS: A double-blinded, placebo-controlled trial was conducted. A total of 145 non-demented PD patients were randomly assigned to receive 5 mg/day donepezil (n=72) or placebo (n=73) for 96 weeks. Medications for PD were not restricted, but antipsychotic drugs were not permitted throughout the study. The primary outcome measure was survival time to psychosis that was predefined by Parkinson's Psychosis Questionnaire (PPQ) B score ≥2 or C score ≥2. Secondary outcome measures included psychosis developing within 48 weeks, total PPQ score, Mini-Mental State Examination (MMSE), Wechsler Memory Scale (WMS) and subgroup analysis by apolipoprotein ε4 genotyping.
RESULTS: Kaplan-Meier curves for psychosis development were very similar between the two groups, and the Cox proportional hazard model revealed an adjusted HR of 0.87 (95%CI 0.48 to 1.60). The changes in MMSE and WMS-1 (auditory memory) were significantly better with donepezil than in placebo. In the subgroup analysis, donepezil provided an HR of 0.31 (0.11-0.86) against psychosis in 48 weeks for apolipoprotein ε4 non-carriers.
CONCLUSIONS: Although donepezil provided beneficial effects on PPQ, MMSE and auditory WMS score changes in 2 years, it had no prophylactic effect on development of psychosis in PD. Apolipoprotein ε4 may suppress the antipsychotic effect of donepezil. TRIAL REGISTRATION NUMBER: UMIN000005403. © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

RCT Entities:   Population Interventions Outcomes

Introduction

Prophylaxis against psychosis and cognitive decline is an unmet need in Parkinson’s disease (PD). During long-term medical treatment of motor symptoms and signs, patients with PD often develop psychosis, with a reported prevalence of about 10%–40%,1–3 and psychosis is one of the most common non-motor symptoms.4 5 While motor symptoms and signs develop gradually and usually progress steadily, psychosis often occurs unexpectedly, even in early stages of the disease or in non-demented patients.6 Cognitive decline is also an important issue in long-term treatment, and most patients suffer from it in advanced stages.

Antagonists to dopaminergic receptors are efficacious against current psychosis in PD, but they are known to worsen motor symptoms and signs.7 Clozapine, a dopamine antagonist with a partial antagonistic activity to the serotonin 5HT-2A receptor, improves psychosis without worsening extrapyramidal signs, but its clinical use is restricted owing to potential agranulocytosis.8 9 In placebo-controlled randomised trials, other antidopaminergic drugs such as quetiapine and olanzapine, which are structurally similar to clozapine, have not proved efficacious against psychosis. Olanzapine improves psychosis, but its effectiveness is not superior to placebo and, in addition, it significantly worsens PD motor symptoms.10 Although quetiapine has been reported to be efficacious against PD psychosis in some case reports, randomised controlled trials show that it provides no significant benefits compared with placebo.11–13 Another drug, risperidone, improves psychosis, but it worsens motor symptoms.14 In addition to dopamine, serotonin is also associated with psychosis in PD. A serotonin 5HT-3 receptor antagonist, ondansetron, can improve psychotic symptoms,15 and pimavanserin, a 5HT-2 inverse agonist, improves psychosis16 17; however, it is uncertain whether these drugs provide prophylaxis against PD psychosis.

Previous studies demonstrated degeneration of cholinergic neurons in PD brains, in addition to degeneration of dopaminergic neurons,18 19 and cholinergic neuronal degeneration is associated with the development of psychosis and cognitive disturbance.20 21 In addition, the use of central anticholinergic drugs is strongly associated with the development of psychosis and cognitive disturbance.22 23 The main hypothesis of the present study was that pharmacological reinforcement of cholinergic neuronal transmission would provide prophylaxis against psychosis, and in addition, beneficial effects on cognitive function in non-demented PD patients.

Donepezil is reported to ameliorate psychotic symptoms in dementia with Lewy bodies (DLB),24 but it is unclear whether donepezil would provide beneficial effects in non-demented PD patients. PD and DLB have commonality in their pathological changes and cholinergic neuronal destruction, and the activity of brain acetylcholinesterase is relatively preserved in non-demented PD patients compared with patients with PD dementia or DLB.25 In this context, larger pharmacological responses to cholinesterase inhibitors were expected in patients without dementia than those with dementia, and it was thought that early and long-term use may provide beneficial effects against psychosis development and cognitive decline in PD.

Methods

Study design

The efficacy of donepezil against psychosis in PD Efficacy of Donepezil Against Psychosis (EDAP) study was a double-blinded, placebo-controlled, parallel-armed, randomised trial that was performed as a physician-initiated study for approval based on the Pharmaceutical Affairs Law, between May 2011 and November 2013, at eight hospitals of the National Hospital Organization, Japan. The core of the study protocol was published previously.26 To investigate the efficacy of donepezil for prevention of psychosis, the time-to-event (development of psychosis) was compared between patients treated with donepezil hydrochloride and those treated with placebo, because survival time analysis is a suitable approach for this purpose. Focusing on hallucinations, illusions and delusions, psychosis was monitored by a Parkinson’s Psychosis Questionnaire (PPQ) every 4 weeks, and the diagnosis of psychosis was based on the criteria predefined by the PPQ scores. PPQ consists of four categories: early symptoms/sleep disturbances (PPQ-A), hallucinations/illusions (PPQ-B), delusions (PPQ-C) and orientation (PPQ-D). The range of each category is 0–9 points, and the total score ranges from 0 to 36 points.27 Decline of cognitive function was investigated by the Mini-Mental State Examination (MMSE) and Wechsler Memory Scale (WMS). Daytime sleepiness was evaluated using the Epworth Sleepiness Scale (ESS),28 which is a suitable measure in PD.29

Eligibility

Patients with PD who were 20–80 years old (inclusive) at the time of signing the consent and that met the PD diagnostic criteria according to steps 1 and 2 of the UK Brain Bank Parkinson’s Disease Criteria, with modified Hoehn-Yahr (mH-Y) stage from 2.5 to 4 (during the ON period if patients suffered from motor fluctuations), and with an MMSE score of 24 or more were invited to participate in the trial. Because risk of psychosis is elevated in patients with mH-Y 4, those patients without dementia were also invited to participate. Other inclusion criteria included lack of psychosis at study entry, and PPQ-B (hallucinations/illusions) and PPQ-C (delusions) scores of zero for at least 8 weeks before study enrolment. If PPQ-B and PPQ-C scores were zero for at least 8 weeks before study entry, patients who had had psychosis were also included. The inclusion criteria did not take into consideration the scores of PPQ-A (early features/sleep disorders) or PPQ-D (orientation/recent memory).

The study excluded patients who had been treated with donepezil or anticholinergic drugs in the preceding 4 weeks, with antipsychotic drugs in the preceding 12 weeks, or fulfilled the criteria of probable DLB according to the third report of the DLB consortium.30 Patients who had been diagnosed with schizophrenia or undergone stereotactic brain surgery were also excluded. Those with allergy to piperidine derivatives, severe hepatic or renal dysfunction, sick sinus syndrome or cardiac conduction block in the atrium, sinoatrial block or atrioventricular block of 2° or more or had severe bronchial asthma, severe peptic ulcers or severe obstructive pulmonary disorders were also excluded. Patients with a heart rate less than 45/min or QT time >460 ms on an ECG were also excluded at screening, as were pregnant women or patients with malignancy. The purpose and methods were explained, and signed consent was obtained.

Procedures

Screening for eligibility was performed, and written informed consent was obtained from candidate participants at the first study visit (V1), and eligibility was confirmed at the second study visit (V2). Participants were randomly assigned to receive donepezil hydrochloride or placebo, and observation began at V2. Randomisation was performed by a centralised web-based service with a dynamic allocation for sites, mH-Y stage (2.5–3 vs 4), sex, and history of psychosis. The investigational drug (3 mg/day donepezil) or placebo was started at V3 (2 weeks from the start of observation), and the dose was escalated to 5 mg/day at V4 (4 weeks from the start of the observation), according to the standard dosages approved for Alzheimer’s disease by the Pharmaceuticals and Medical Devices Agency in Japan. Donepezil or placebo was prescribed in the morning. The allocation was generated by a computer and concealed by a key-code holder (KK). The tablets of both donepezil and placebo were manufactured by Eisai Pharmaceutical Company, Japan, and were physically indistinguishable, as confirmed by KK, who did not have any other roles in the study.

Evaluation and definition of psychosis

To detect the development of psychosis including hallucinations, illusions and delusions, patients or their caregivers kept a psychosis diary that had been pre-prepared by the investigators. Every 4 weeks, the PPQ was performed, the psychosis diary was checked and the participants and caregivers were interviewed. The development of psychosis was defined as PPQ-B (hallucinations or illusions) ≥2 points or PPQ-C (delusions) ≥2 points, because psychosis with these scores was considered clinically relevant. When the scores of PPQ-B or PPQ-C were ≥2 points, the onset of symptoms was determined by checking the diary and by interviewing patients and caregivers. In case of inconsistency between the diary and interviews, the earlier date was considered the onset date.

Outcome measures

The primary outcome measure, which was the time to the first development of psychosis from randomisation, that is, the beginning of study observation (V2), was compared between the donepezil and placebo groups. The secondary outcome measures included changes in total PPQ scores and cognitive function, which was evaluated by MMSE, WMS and the Frontal Assessment Battery (FAB).

PPQ was performed every 4 weeks, while mH-Y, Unified Parkinson's Disease Rating Scale Part 3 (UPDRS-III) and ESS were conducted every 8 weeks. MMSE and WMS were conducted at V1 and V2, respectively, while FAB was performed in the period between V2 and V3. MMSE, WMS and FAB were repeated at V9 (24 weeks), V15 (48 weeks), V21 (72 weeks) and V27 (96 weeks).

Apolipoprotein E subgroup analysis

Because the response to donepezil is modified by apolipoprotein E genotypes in Alzheimer disease,31 we analysed outcome measures in subgroups according to the ε4 allele.

Sample size calculation

In our previous study that followed 258 patients with PD over 2 years, 51 (19.7%) patients had psychosis requiring antipsychotic medication.23 We reanalysed the rate of psychosis requiring antipsychotic medication from our previous study according to the eligibility criteria described above, and we assumed that the cumulative occurrence of psychosis was 45% in the placebo group, which was reduced to 22.5% in the donepezil group. The sample size was calculated with the conditions: α=0.05 (bilateral), power=0.8 and using the log-rank test.

We assumed that 48 events were required and calculated a sample size of 142 (71 in each group) patients to provide 80% power with a 5% significance level for a log-rank test.26

Statistical analysis

The primary outcome measure, time from randomisation to the development of psychosis, was compared between the two treatment groups by a Cox proportional hazard model that incorporated possible confounding factors. To identify confounding factors, Kaplan-Meier curves were drawn, dividing patients into two groups by factors such as age, sex, PD duration, PD severity, daytime sleepiness and psychosis history, and the effect size of interventions was estimated as an HR after adjustment of the identified confounding factors. If no confounding factors were identified, the difference was compared by a log-rank test. Missing data were regarded as censored but not supplemented in survival analysis.

Secondary outcome measures, changes in PPQ, MMSE, WMS and FAB scores at V9, V15, V21 and V27 from baseline were compared. The data were statistically tested, and the effect size was estimated using a generalised estimating equation (GEE) with an M-based working matrix because they were measured repeatedly every 24 weeks. Generalised linear models assume that individual data in a group are independent from one another; however, in cluster analysis, this assumption often fails. In contrast to generalised linear models, GEE is a statistical method to deal with longitudinal and clustered (non-independent) data.32 Missing data were not supplemented in GEE. Data were analysed using IBM SPSS V.21.

Safety analysis

For safety analysis, adverse effects in the two groups were collected. In addition, we investigated the changes in UPDRS-III and in dose of dopaminergic medications, which were statistically compared using a GEE. The dose of dopaminergic drugs was calculated according to a previous report.33

Results

Baseline features of study subjects

A total of 222 candidate patients who had been diagnosed with PD and treated in the eight hospitals of the National Hospital Organization were invited to participate in the study. Sixty-five patients refused to participate, and the remaining 157 provided written informed consent, but three patients withdrew and nine were confirmed ineligible at V2 because their PPQ-B or PPQ-C scores were not zero. The remaining 145 patients (51–80 years old) were randomised, and 72 and 73 patients were allocated to donepezil hydrochloride and placebo groups, respectively (figure 1). The baseline features of the study participants are shown in table 1. Age, sex and PD duration were almost identical between the groups. The proportion of patients with mH-Y 4 was higher in the donepezil group, although the difference was not significant. MMSE, ESS, UPDRS and WMS scores were also similar. There was a slight but significant difference in FAB score, and it was higher in the donepezil than the placebo group. The prevalence of patients on dopamine agonists or amantadine was similar. The prevalence of apolipoprotein ε4 was higher in the donepezil than in the placebo group, but it was not significantly different. There were no differences between sites in patient characteristics.

Figure 1

Flow diagram of the patient recruitment process.

Table 1

Baseline characteristics of the subjects

	Donepezilgroup(N=72)	Placebogroup(N=73)
Age, year, mean (SD)	67.2(7.3)	69.0(7.0)
Female sex, n (%)	41(57)	39(53)
PD duration, year, mean (SD)	8.2(4.8)	7.8(4.3)
Modified H-Y, n (%)
2.5	36(50)	38(52)
3	25(35)	29(40)
4	11(15)	6(8)
MMSE, mean (SD)	27.8(1.9)	27.7(2.1)
History of psychosis, n (%)	25(35)	25(34)
ESS, mean (SD)	7.0(5.0)	6.7(5.3)
UPDRS, mean (SD)
Part I	0.8(1.0)	0.6(0.9)
Part II ON	6.6(5.2)	6.2(4.8)
Part II OFF	13.7(7.0)	12.2(6.9)
Part III	21.4(11.0)	21.7(8.9)
Part IV	3.2(2.5)	2.6(2.3)
WMS, mean (SD)
Auditory	49.8(18.8)	45.0(19.2)
Visual	48.8(10.8)	46.1(12.0)
Attention	57.1(11.6)	56.3(8.5)
Delayed recall	59.0(19.2)	53.3(22.7)
FAB, mean (SD)*	14.6(2.4)	13.8(2.1)
LDED (mg/day)	640.8(244.1)	624.6(240.5)
Dopamine agonist user, n (%)	48(66.7)	52(71.2)
Amantadine user, n (%)	18(25.0)	15(20.5)
Apolipoprotein E4, n (%)†	21(34.4)	16(25.0)

*n=70(donepezil), 73 (placebo), p=0.045.

†n=61(donepezil), 64 (placebo).

ESS, Epworth Sleepiness Scale; FAB, Frontal Assessment Battery; H-Y, Hoehn-Yahr; LDED, L-Dopa equivalent dose of dopaminergic replacement therapy; MMSE, Mini-Mental State Examination; PD, Parkinson’s disease; WMS, Wechsler Memory Scale.

Primary outcome

Forty-six patients developed predefined psychosis during the study. Sample size calculation assumed 48 events, and the statistical assumption was well accepted. The survival curves of psychosis-free patients showed no difference between the donepezil and placebo groups (figure 2A). The effect of potential confounding predictors (age, sex, PD duration, PD severity, sleepiness and psychosis history) was assessed using Kaplan-Meier curves. There were no differences in survival curves according to age (using median age as the cut-off value, <68 and≥68), sex or PD duration (<8 years and ≥8 years). In contrast, patients with severe PD, high ESS scores or psychosis history were significantly more prone to develop psychosis (data not shown), and therefore, these factors were included in Cox proportional hazard models. The HR of psychosis was 0.87 (95% CI 0.48 to 1.60) with adjustment for psychosis history, PD severity and sleepiness (figure 2B). The primary outcome measure was similar between females and males (online supplementary table 1).

Figure 2

Primary (A and B) and secondary outcome (C–E) measures. (A) The survival curves of psychosis-free patients in the donepezil and placebo groups are shown. The number below the horizontal axis shows the number of patients at risk. Censored case is indicated as vertical lines. (B) HR of psychosis was expressed as a mean with 95% CIs. The horizontal axis has a logarithmic scale. (C) Score changes of PPQ from baseline at V9, V15, V21 and V27, secondary outcomes. Data are expressed as mean and SD. There was a statistically significant difference between donepezil and placebo (p=0.004, GEE). (D) Changes in ESS scores from baseline at V9, V15, V21 and V27, secondary outcomes, expressed as mean and SD. There was a statistically significant difference (p=0.042, GEE). (E) Changes in MMSE from baseline at V9, V15, V21 and V27, secondary outcomes, expressed as mean and SD. There was a statistically significant difference (p=0.032, GEE). (F) Changes in WMS-1 (auditory memory) at V9, V15, V21 and V27, secondary outcomes, expressed as mean and SD. There was a statistically significant difference (p=0.029, GEE). ESS, Epworth Sleepiness Scale; GEE, generalised estimating equation; mH-Y, modified Hoehn-Yahr; MMSE, Mini-Mental State Examination; PPQ, Parkinson’s Psychosis Questionnaire; WMS, Wechsler Memory Scale.

Secondary outcome

Total PPQ scores elevated gradually throughout the study period in the placebo group but were stable in the donepezil group, and the difference was statistically significant (figure 2C). As well as PPQ scores, ESS scores increased gradually in the placebo group but were stable in the donepezil group, with statistical significance (figure 2D).

The score changes in MMSE with donepezil were better than placebo, and there was statistical significance (figure 2E). Changes in WMS-1 were significantly better with donepezil (figure 2F), but visual memory (WMS-2), attention (WMS-3) and frontal lobe function (FAB) were not affected by the intervention. The effect sizes are shown in table 2. Changes in PPQ scores from baseline were significantly better in donepezil than placebo in both sexes (online supplementary tables 2 and 3), suggesting that prophylactic effect of donepezil is almost similar in females and males.

Table 2

Secondary outcome measures

	Donepezil	Placebo	Treatment effect*		P values
	Means (SEM)	Means (SEM)	Means	(95%CI)
Psychosis
Cx in total PPQ	−0.12 (0.152)	0.53 (0.166)	−0.652	(−1.095 to −0.209)	0.004
Sleepiness
Cx in ESS	0.36(0.45)	1.69(0.47)	−1.33	(−2.61to −0.05)	0.042
Cognitive function
Cx in scores of MMSE	0.02 (0.28)	−0.78 (0.25)	0.8	(0.07 to 1.54)	0.032
Cx in WMS-1 (auditory memory)	11.2 (1.48)	7.06 (1.20)	4.15	(0.43 to 7.87)	0.029
Cx in WMS-2 (visual memory)	3.85 (0.66)	3.32 (0.80)	0.53	(−1.50 to 2.56)	0.609
Cx in WMS-4 (attention)	1.02 (0.87)	0.92 (0.97)	0.1	(−2.46 to 2.66)	0.94
Cx in FAB	0.07 (0.22)	0.39 (0.23)	−0.32	(−0.94 to 0.32)	0.315

Higher scores in PPQand ESS are worse.

Higher scores in MMSE, WMS and FAB are better.

*Effect size was estimated using GEE (working matrix M-dependent).

Cx: changes; ESS, Epworth Sleep Scale; FAB, Frontal Assessment Battery; GEE, generalised estimating equation; MMSE, Mini-Mental State Examination; PPQ, Parkinson’s Psychosis Questionnaire; WMS, Wechsler Memory Scale.

Subgroup analysis by apolipoprotein E genotype

In the subgroup of ε4 non-carriers, Kaplan-Meier curves split at 48 weeks and joined at 96 weeks (figure 3A). Cox proportional hazard models demonstrated a significant prophylactic effect with a HR of 0.31 (0.11–0.86, p=0.02) against psychosis development in 48 weeks (figure 3C), although the difference was not significant against psychosis development in 96 weeks (HR was 0.63 (0.28–1.41, p=0.26)). In this subgroup, there was a significant difference between donepezil and placebo for changes in total PPQ scores (figure 3E) and changes in ESS scores (figure 3G).

Figure 3

Subgroup analysis by apolipoprotein ε4 (Apo E4) allele. (A and B) Kaplan-Meier curves of psychosis-free patients (A) without ε4 and (B) with the ε4 allele. The curves separate at 48 weeks in the ε4 (−) subgroup but not in the ε4 (+) subgroup. (C and D) Cox proportional hazard models for psychosis development in 48 weeks in patients (C) without ε4 and (D) with the ε4 allele. There was a statistically significant difference between donepezil and placebo groups in the ε4 (−) subgroup (HR=0.31 (95% CI 0.11 to 0.86), p=0.02), but not in the ε4 (+) subgroup (HR=0.85 (95% CI 0.192 to 3.78), p=0.84). (E and F) Changes in total PPQ scores in patients (E) without ε4 and (F) with the ε4 allele. There was a statistically significant difference between donepezil and placebo groups in the ε4 (−) subgroup (p=0.001) but not in ε4 (+) subgroup. (G and H) Change in ESS scores in patients (G) without ε4 and (H) with the ε4 allele. There was a statistically significant difference between donepezil and placebo groups in the ε4 (−) subgroup (p=0.027) but not in ε4 (+) subgroup. ESS, Epworth Sleepiness Scale; mH-Y, modified Hoehn-Yahr; PPQ, Parkinson’s Psychosis Questionnaire.

In ε4 carriers, in contrast to the ε4 (−) subgroup, Kaplan-Meier curves were similar between donepezil and placebo (figure 3B), and the adjusted HR was 0.85 (95% CI 0.19 to 3.79, p=0.84; figure 3D) and 0.86 (95% CI 0.23 to 3.32, p=0.83) for psychosis in 48 and 96 weeks, respectively. There was no difference in PPQ and ESS changes in the subgroup (figure 3F and H). The effect sizes of donepezil in each subgroup are demonstrated in table 3.

Table 3

Subgroup analysis

Subgroup	Outcome measure	Analysis	Donepezil	Placebo	Treatment effect*		P values
			Means (errors)	Means (errors)	Means	(95%CI)
e4 (−)	Psychosis development
	HR for psychosis in 48 weeks	Cox			0.31	(0.11 to 0.86)	0.02
	HR for psychosis in 96 weeks	Cox			0.63	(0.28 to 1.41)	0.26
	Cx in total PPQ	GEE	−0.28 (0.167)	0.60 (0.209)	−0.88	(−1.41 to −0.36)	0.001
	Sleepiness
	Cx in ESS	GEE	0.45 (1.93)	1.85 (1.93)	−1.4	(−2.65 to −0.16)	0.027
e4 (+)	Psychosis development
	HR for psychosis in 48 weeks	Cox			0.85	(0.19 to 3.79)	0.84
	HR for psychosis in 96 weeks	Cox			0.86	(0.23 to 3.32)	0.83
	Cx in total PPQ	GEE	0.02 (0.30)	0.20 (0.331)	−0.18	(−1.05 to 0.70)	0.69
	Sleepiness
	Cx in ESS	GEE	1.26 (3.13)	0.51 (3.19)	0.75	(−0.85 to 2.35)	0.36

*Effect size was estimated using GEE (working matrix M-dependent), adjusted for ESS/10, mH-Y (2.5 vs 3–4) and psychosis history.

Cx, changes; ESS, Epworth Sleep Scale; GEE, generalised estimating equation; mH-Y, modified Hoehn-Yahr; PPQ, Parkinson’s Psychosis Questionnaire.

The most frequent adverse event was visual hallucinations; 39 events occurred in the donepezil group and 36 in the placebo group. In addition, other types of hallucinations and delusions were also often observed. The prevalence of hallucinations and delusions was also similar in the donepezil and placebo groups. However, auditory hallucinations were less prevalent in the donepezil than in the placebo group (table 4). Worsening Parkinsonism was observed more frequently in the donepezil (12 events) than the placebo group (six events), and motor complications were also more often observed in the donepezil group. Falls and contusion injuries were observed often in both groups. Nausea, vomiting, loss of appetite and diarrhoea were more common with donepezil than with placebo. Body weight loss was observed only in patients in the donepezil group.

Table 4

Treatment-related adverse events (more than 5% in either group)

	Donepezil(n=72)	Placebo(n=73)
Visual hallucinations	39(54.2)	36(49.3)
Auditory hallucinations*	8(11.1)	26(35.6)
Hallucinations, unspecified	8(11.1)	7(9.6)
Delusions	21(29.2)	19(26.0)
Cenesthopathy	2(2.8)	4(5.5)
Nasopharyngitis*	15(20.8)	20(38.4)
Parkinsonism (worsening)	12(16.7)	6(8.2)
Dyskinesias	6(8.3)	2(2.7)
Dystonia	4(5.6)	1(1.4)
Contusion	9(12.5)	8(11.0)
Fall	3(4.2)	4(5.5)
Vomiting	5(6.9)	4(5.5)
Nausea	5(6.9)	2(2.7)
Loss of appetite	6(8.3)	1(1.4)
Diarrhoea	4(5.6)	2(2.7)
Loose stool	4(5.6)	0(0)
Body weight loss	4(5.6)	0(0)
Urinary cystitis	8(11.1)	13(17.8)
Dental caries	5(6.9)	4(5.5)
Back pain	4(5.6)	7(9.6)
Limb pain	4(5.6)	2(2.7)
Headache	6(8.3)	1(1.4)
Upper respiratory tract infection	5(6.9)	4(5.5)
Aspiration pneumonia	0(0.0)	5(6.8)
Insomnia	5(6.9)	5(6.8)

The number of adverse events: number of events/patients(%).

*There were statistically significant differences in the prevalence of auditory hallucinations (p=0.00007) and nasopharyngitis (p=0.0287).

The effects on motor symptoms and signs were investigated by UPDRS-III. Since dopamine replacement therapy was not restricted, the UPDRS-III was evaluated considering the changes in dosage of dopamine replacement. In the donepezil group, the mean UPDRS-III scores increased at 16–24 weeks after randomisation but returned to the baseline at 32 weeks and remained stable thereafter. In the placebo group, the UPDRS-III scores were stable throughout the study. The mean difference in UPDRS-III was 0.45 (95% CI −1.25 to 2.15, p=0.61; figure 4A). The dose of dopaminergic replacement therapy increased steadily throughout the study in both groups, but the increase was higher in the donepezil than in the placebo group, with a mean difference of 17.6 (95% CI, −10.1 to 45.2 mg/day, p=0.213; figure 4B).

Figure 4

Changes in UPDRS-III scores and L-Dopa equivalent dose of dopaminergic replacement therapy (LDED). (A) In the donepezil group, UPDRS-III scores were transiently elevated by starting and dose escalation (3–5 mg/day) of donepezil, but then returned to baseline and remained stable. In the placebo group, the scores were stable. There were no statistically significant differences in UDPRS-III changes between donepezil and placebo groups. (B) Dopaminergic drug doses were elevated gradually in both donepezil and placebo groups and were slightly larger with donepezil than with placebo. The difference was not statistically significant. Data represent the mean with 95% CIs.

Because donepezil can enhance rapid eye movement (REM) sleep and cause nightmares,34 a lack of prophylactic effect against psychosis development may be due to nightmares caused by donepezil. In this context, we investigated PPQ-A scores (sleep disturbances including nightmares) and found no difference in PPQ-A scores between the groups; changes in PPQ-A scores were −0.20 (95% CI −0.37 to −0.03) and −0.09 (95% CI −0.28 to 0.10) in donepezil and placebo groups, respectively.

In a non-predefined subgroup analysis of MMSE <28 and MMSE ≥28, donepezil did not provide prophylactic effects against psychosis in either subgroup by survival time analysis. However, changes in PPQ from baseline were significantly better in the donepezil than in the placebo subgroup of MMSE ≥28, but not in that of MMSE <28 (online supplementary tables 4 and 5). Therefore, the effect of donepezil against psychosis may be dependent on cholinesterase activity, because it is assumed to be relatively preserved in cognitive-intact patients.

Discussion

The subjects of this study had mild to moderate PD with a mean disease duration of 8 years, without dementia, although about one-third of them had experienced psychosis. These features were in alignment with the target of the study to investigate the hypothesis that donepezil provides prophylaxis against psychosis in non-demented PD patients. Overall, comparability between the two study groups was ensured. The number of events that occurred in the study was as expected and sufficient for proper evaluation of the efficacy of donepezil in preventing psychosis, and thus, the obtained data fitted into the statistical assumption.

Analysis using Kaplan-Meier curves indicated that donepezil does not prevent the development of psychosis. The results also implied that psychosis was associated with PD severity, sleepiness and history of psychosis, consistent with the results of previous studies.23 35 As shown in table 1, patients with mH-Y 4 were more prevalent and ESS was higher in the donepezil group than with placebo. After adjustment for these factors, the Cox proportional hazard model demonstrated an HR of 0.87, slightly smaller than 1, but the effect was not statistically significant. This finding demonstrates that donepezil does not have significant prophylactic effect against psychosis in non-demented PD patients. In contrast to the results described above, the changes in both total PPQ score and ESS were significantly better in the donepezil group than with placebo, suggesting that prevention of psychosis is a harder endpoint than score changes in total PPQ or ESS.

Because the extent of cognitive improvement with donepezil correlates with brain cholinesterase activity,36 the efficacy of donepezil was expected to be best seen in non-demented PD patients, since they are known to have preserved cholinesterase activity, rather than in patients with DLB. As expected, subgroup analysis by lower and higher baseline MMSE demonstrated that donepezil provided beneficial effects in higher MMSE group but not in lower group.

There was no significant difference in FAB scores between donepezil and placebo; however, the result is limited because of a significant difference at baseline. The present study demonstrated that donepezil was efficacious in psychological tests for cognitive function evaluated by WMS. In this regard, several previous randomised control studies showed that donepezil improves cognitive function in PD with dementia.37 38 Dubois and colleagues39 conducted a large-scale randomised control trial to investigate the effects of donepezil on cognition in PD with dementia and confirmed that donepezil improves cognitive function; however, their results showed no significant changes in psychiatric symptoms. These results suggest that while cognitive psychological test scores can be improved by donepezil, the effects on psychiatric symptoms are difficult to be detected because psychiatric symptoms can occur transiently and fluctuate. The effect size of MMSE changes in the present study was 0.80, which is clinically irrelevant, and slightly smaller than that reported previously.40 This is thought to be due to differences in clinical features of the study participants, especially differences in baseline MMSE scores. In the present study, the baseline scores were higher than in previous studies, and therefore the effect size was undervalued.

In Alzheimer’s disease, the response of cognitive dysfunction to donepezil is greater in apolipoprotein ε4 non-carriers.41 In subgroup analysis for apolipoprotein ε4, donepezil provided significant prophylactic effect against psychosis development in 48 weeks in ε4 non-carriers, but not in ε4 carriers. In addition, donepezil modulated the changes in total PPQ scores and ESS in ε4 non-carriers but not in carriers, suggesting that apolipoprotein E4 is a suppressor for psychosis prophylaxis. Apolipoprotein ε4 carriers are prone to develop dementia and the risk of hallucinations is significantly higher,42 43 although the association is controversial.44 These data suggest that apo E4 carriers may be more likely to have a comorbid amyloid burden causing cortical dysfunction that prevents donepezil from being as effective.

Previous reports showed that donepezil does not worsen extrapyramidal signs and symptoms.40 In the present study, while the UPDRS-III scores were not significantly different between donepezil and placebo, the scores of the donepezil group worsened transiently and decreased, most likely owing to increases in the dosage of dopamine replacement therapy. Thus, to maintain UPDRS-III scores, a larger dosage of dopamine replacement therapy was required in the donepezil group.

Although the effects of donepezil, at least at 5 mg/day, were weak and inadequate to provide prophylaxis against the development of psychosis in patients with PD, early use of donepezil improved the scores for PPQ, MMSE and auditory WMS significantly for 2 years in cognitive preserved patients, without worsening of motor symptoms. These results suggest that early use of donepezil may be efficacious against cognitive decline but not for prophylaxis of psychosis.