DRD3 Predicts Cognitive Impairment and Anxiety in Parkinson's Disease: Susceptibility and Protective Effects

被引:0
|
作者
Goncalves, Alexandra [1 ,2 ]
Mendes, Alexandre [3 ,4 ]
Damasio, Joana [3 ,4 ]
Vila-Cha, Nuno [5 ]
Boleixa, Daniela
Leal, Barbara [5 ,6 ]
Cavaco, Sara [1 ,5 ,6 ]
机构
[1] Ctr Hosp Univ Santo Antonio, Neuropsychol Serv, Porto, Portugal
[2] Univ Porto, Fac Med, Porto, Portugal
[3] Ctr Hosp Univ Santo Antonio, Neurol Dept, Porto, Portugal
[4] Univ Porto, Inst Ciencias Biomed Abel Salazar ICBAS, Unit Multidisciplinary Res Biomed UMIB, Porto, Portugal
[5] ITR Lab Integrat & Translat Res Populat Hlth, Porto, Portugal
[6] Univ Porto, Inst Ciencias Biomed Abel Salazar ICBAS, Immunogenet Lab, Dept Patol & Imunol Mol, Porto, Portugal
关键词
Parkinson's disease; dopamine D3 receptor; cognition; anxiety; DEMENTIA RATING-SCALE; RECEPTOR; ASSOCIATION; DEPRESSION; VALIDITY; ONSET; D-3; POLYMORPHISM; PRAMIPEXOLE; PROGRESSION;
D O I
10.3233/JPD-230292
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: A possible genetic contribution of dopamine D3 receptor (DRD3) to cognitive impairment in Parkinson's disease (PD) has yet to be investigated. Objective: To explore the effects of rs6280 (Ser9Gly) genotype on PD patients' cognitive performance and to clarify possible interactions with psychopathology. Methods: Two hundred and fifty-three consecutive PD patients underwent neurological and neuropsychological evaluations, which included: Unified Parkinson's Disease Rating Scale (UPDRS), Hoehn & Yahr scale (H&Y), Dementia Rating Scale-2 (DRS-2), and Hospital Anxiety and Depression Scale (HADS). rs6280 polymorphism was genotyped for all PD patients and for 270 ethnically matched healthy volunteers (HC). Non-parametric group comparisons and logistic regressions were used for data analyses. Results: rs6280 genotype did not differ between PD and HC groups. PD patients with rs6280 CC genotype had more impaired cognitive performance (i.e., <1st percentile of demographically adjusted norms) on DRS-2 subscales Initiation/Perseveration and Construction than those with TT genotype. These associations remained statistically significant when other covariates (e.g., demographic features, disease duration, severity of motor symptoms in OFF and ON states, anti-parkinsonian medication, and psychopathology symptoms) were taken into consideration. PD patients with rs6280 TC had less anxiety (i.e., HADS Anxiety >= 11) than those with TT (p = 0.012). This association was also independent of other covariates. Conclusions: Study findings suggest that rs6280 CC genotype predisposes to executive dysfunction and visuoconstructional deficits, whereas the heterozygous genotype protects from anxiety in PD. These effects do not appear to be dependent of one another. rs6280 is not a genotypic susceptibility factor for PD.
引用
收藏
页码:313 / 324
页数:12
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