Neuropsychiatric symptoms in Serbian patients with Parkinson's disease
Mirjana Petrovic
a
, Elka Stefanova
b,c
, Ljubomir Ziropadja
d
, Tanja Stojkovic
b,c
, Vladimir S. Kostic
b,c,
⁎
a
Clinic of Neurology, Clinical Center Kragujevac, Serbia
b
Faculty of Medicine, University of Belgrade, Serbia
c
Clinic of Neurology, CCS, Serbia
d
Faculty of Philology, University of Belgrade, Serbia
abstract article info
Article history:
Received 14 January 2016
Received in revised form 12 May 2016
Accepted 10 June 2016
Available online 13 June 2016
Background: Parkinson's disease [PD] is associated with wide variety of neuropsychiatric symptoms, although it is
primarily considered as a movement disorder.
Objective: To examine whether PD patients can be meaningfully classified into subgroups according to their neu-
ropsychiatric symptoms, reported by their caregivers.
Methods: Three hundred and sixty PD patients [mean age = 63.5, SD = 10.3] from the academic clinical setting
were assessed with the 12-subscale Neuropsychiatric Inventory Questionnaire [NPI]. A two-stage cluster analysis
was used to identify the subgroups groups of patients with specific neuropsychiatric profile.
Results: Three hundred and twenty-one PD patients [89%] showed at least one psychiatric symptom. The most
common symptoms were anxiety [73.1%], depression [64.7%], and apathy [51.7%], and nighttime disturbance
[51.3%], whereas the least common were euphoria [0.3%], and delusions [1.7%]. The mean [SD] total NPI compos-
ite score was 16.9 [17.4]. Two hundred eight PD subjects [58%] of the total sample had at least one symptom with
a score ≥ 4. Three clusters were identified: a] Cluster 1, with no or few NPI symptoms [n = 200; 55.6%]; b] Cluster
2, with mild to moderate symptoms on depression, anxiety and apathy scales [n = 140; 38.9%]; and c] Cluster 3
with high agitation, disinhibition and irritability scores [n = 20 patients; 5.6%]. PD subjects with clinically signif-
icant neuropsychiatric symptoms were older with more severe motor and cognitive impairment.
Conclusions: This study emphasizes the high prevalence and importance of neuropsychiatric symptoms in PD pa-
tients; therefore clinicians should also focus on treating in parallel with motor symptoms.
© 2016 Elsevier B.V. All rights reserved.
Keywords:
Neuropsychiatric inventory
Caregiver
Cluster analysis
1. Introduction
Prevalence of neuropsychiatric co-morbidities in Parkinson's disease
[PD] varies widely among reported series due to increasing age of pa-
tients, duration of the disease, cognitive impairment and assessment
tools [1–6]. Also, cultural, social and family structure might be responsi-
ble for differences [7–12].
Growing evidence indicated existence of PD subtypes based on asso-
ciated neuropsychiatric and behavioral problems [5,6,13], either in the
cohorts of the early stage “de novo” PD patients [14], or in those with
dementia [13]. Neuropsychiatric symptoms (NPS) are part of the non-
motor manifestation of PD, and have a significant impact on the quality
of life [QoL] of PD patients, and on a caregiver burden and distress [pres-
ence of NPS apart from dementia is associated with caregiver distress]
[8,15,16,17].
Therefore, in the present study we administered the Neuropsychiat-
ric Inventory [NPI] [18], to evaluate the frequency of neuropsychiatric
symptoms and accompanied caregiver distress in a representative sam-
ple of Serbian patients with PD, recruited at the academic tertiary clini-
cal center. The NPI uses a screening strategy to minimize administration
time, examining and scoring only those behavioral domains with posi-
tive responses to screening questions. Both the frequency and the sever-
ity of each behavior are determined. Information for the NPI is obtained
from a caregiver familiar with the patient's behavior [18]. We expected
Journal of the Neurological Sciences 367 (2016) 342–346
⁎ Corresponding author at: Institute of Neurology, CCS, Dr Subotica 6, 11000 Belgrade,
Serbia.
E-mail address: vladimir.s.kostic@gmail.com (V.S. Kostic).
http://dx.doi.org/10.1016/j.jns.2016.06.027
0022-510X/© 2016 Elsevier B.V. All rights reserved.
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