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Serotonin-related functional genetic variants affect the occurrence of psychiatric and motor adverse events of dopaminergic treatment in Parkinson’s disease : a retrospective cohort study
ID
Redenšek Trampuž, Sara
(
Avtor
),
ID
Blagus, Tanja
(
Avtor
),
ID
Trošt, Maja
(
Avtor
),
ID
Dolžan, Vita
(
Avtor
)
PDF - Predstavitvena datoteka,
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MD5: C1C69CB8921B93E54DFA9619D5F05F1B
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/2075-4426/12/2/266
Galerija slik
Izvleček
The serotonergic system is important in Parkinson’s disease (PD) pathogenesis as it can take over dopamine production after a large portion of dopaminergic neurons is lost through neurodegeneration. The aim of this study was to evaluate the effect of genetic variability of serotonergic genes on the occurrence of motor complications and psychiatric adverse events (AE) due to dopaminergic treatment. We enrolled 231 patients and their clinical data were collected. Genotyping was performed for eight genetic variants. Logistic regression was used for analysis. Carriers of the HTR1A rs6295 GC genotype (OR = 2.58; 95% CI = 1.15–5.78; p = 0.021), TPH2 rs4290270 AA genotype (OR = 2.78; 95% CI = 1.08–7.03; p = 0.034), and at least one TPH2 rs4570625 T allele (OR = 1.86; 95% CI = 1.00–3.44; p = 0.047) had increased risk for visual hallucinations (VH). Additionally, carriers of at least one SLC6A4 5-HTTPLR rs25531 S (OR = 0.52; 95% CI = 0.28–0.96; p = 0.037) or at least one L$_G$ allele (OR = 0.37; 95% CI = 0.14–0.97; p = 0.044) had a decreased chance for VH. Constructed haplotypes of the TPH2 showed increased risk for VH (OR = 1.94; 95% CI = 1.06–3.55; p = 0.032) and impulse control disorders (OR = 5.20; 95% CI = 1.86–14.50; p = 0.002). Finally, individual gene–gene interactions showed decreased odds for the development of motor AE. Our findings suggest that the serotonergic pathway may play an important role in the development of AE resulting from dopaminergic treatment.
Jezik:
Angleški jezik
Ključne besede:
Parkinson’s disease
,
motor complications
,
visual hallucinations
,
impulse control disorders
,
dyskinesia
,
polymorphism
,
serotonin
,
adverse event
,
pharmacogenomics
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2022
Št. strani:
13 str.
Številčenje:
Vol. 12, iss. 2, art. 266
PID:
20.500.12556/RUL-137342
UDK:
616.8
ISSN pri članku:
2075-4426
DOI:
10.3390/jpm12020266
COBISS.SI-ID:
97247491
Datum objave v RUL:
13.06.2022
Število ogledov:
860
Število prenosov:
112
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Journal of personalized medicine
Skrajšan naslov:
J. pers. med.
Založnik:
MDPI
ISSN:
2075-4426
COBISS.SI-ID:
31207641
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:
11.02.2022
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
Parkinsonova bolezen
,
motorični zapleti
,
vizualne halucinacije
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P1-0170
Naslov:
Molekulski mehanizmi uravnavanja celičnih procesov v povezavi z nekaterimi boleznimi pri človeku
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
J7-2600
Naslov:
Presnovne možganske spremembe nevrodegenerativnih demenc in njihove korelacije s histopatološkimi spremembami v možganih
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