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Clinical and clinical-pharmacogenetic models for prediction of the most common psychiatric complications due to dopamingeric treatment in Parkinson's disease
ID
Redenšek Trampuž, Sara
(
Author
),
ID
Jenko Bizjan, Barbara
(
Author
),
ID
Trošt, Maja
(
Author
),
ID
Dolžan, Vita
(
Author
)
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https://academic.oup.com/ijnp/article/23/8/496/5876239
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Abstract
Background: The most common psychiatric complications due to dopaminergic treatment in Parkinson's disease are visual hallucinations and impulse control disorders. Their development depends on clinical and genetic factors. Methods: We evaluated the simultaneous effect of 16 clinical and 34 genetic variables on the occurrence of visual hallucinations and impulse control disorders. Altogether, 214 Parkinson's disease patients were enrolled. Their demographic, clinical, and genotype data were obtained. Clinical and clinical-pharmacogenetic models were built by The Least Absolute Shrinkage and Selection Operator penalized logistic regression. The predictive capacity was evaluated with the cross-validated area under the receiver operating characteristic curve (AUC). Results: The clinical-pharmacogenetic index for prediction of visual hallucinations encompassed age at diagnosis (OR = 0.99), rapid eye movement (REM) sleep behavior disorder (OR = 2.27), depression (OR = 1.0002), IL6 rs1800795 (OR = 0.99), GPX1s1050450 (OR = 1.07), COMT rs165815 (OR = 0.69), MAOB rs1799836 (OR = 0.97), DRD3 rs6280 (OR = 1.32), and BIRC5 rs8073069 (OR = 0.94). The clinical-pharmacogenetic index for prediction of impulse control disorders encompassed age at diagnosis (OR = 0.95), depression (OR = 1.75), beta-blockers (OR = 0.99), coffee consumption (OR = 0.97), NOS1 rs2682826 (OR = 1.15), SLC6A3rs393795 (OR = 1.27), SLC22A1 rs628031 (OR = 1.19), DRD2 rs1799732 (OR = 0.88), DRD3 rs6280 (OR = 0.88), and NRG1 rs3924999 (OR = 0.96). The cross-validated AUCs of clinical and clinical-pharmacogenetic models for visual hallucinations were 0.60 and 0.59, respectively. The AUCs of clinical and clinical-pharmacogenetic models for impulse control disorders were 0.72 and 0.71, respectively. The AUCs show that the addition of selected genetic variables to the analysis does not contribute to better prediction of visual hallucinations and impulse control disorders. Conclusions: Models could be improved by a larger cohort and by addition of other types of Parkinson's disease biomarkers to the analysis.
Language:
English
Keywords:
Parkinson's disease
,
polymorphism
,
pharmacogenetics
,
impulse control disorders
,
predictive model
,
psychiatric complications
,
visual hallucinations
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2020
Number of pages:
Str. 496-504
Numbering:
Vol. 23, iss. 8
PID:
20.500.12556/RUL-144749
UDC:
616.8
ISSN on article:
1461-1457
DOI:
10.1093/ijnp/pyaa028
COBISS.SI-ID:
12969219
Publication date in RUL:
10.03.2023
Views:
676
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85
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Record is a part of a journal
Title:
The international journal of neuropsychopharmacology
Shortened title:
Int. j. neuropsychopharmacol.
Publisher:
Oxford University Press, CINP
ISSN:
1461-1457
COBISS.SI-ID:
1197541
Licences
License:
CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:
http://creativecommons.org/licenses/by-nc/4.0/
Description:
A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.
Secondary language
Language:
Slovenian
Keywords:
Parkinsonova bolezen
,
polimorfizem
,
farmakogenetika
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0170
Name:
Molekulski mehanizmi uravnavanja celičnih procesov v povezavi z nekaterimi boleznimi pri človeku
Funder:
ARRS - Slovenian Research Agency
Funding programme:
Young researchers
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