Cognitive Impairment in Parkinson's Disease: An Updated Overview Focusing on Emerging Pharmaceutical Treatment Approaches

被引:23
作者
Degirmenci, Yildiz [1 ,2 ]
Angelopoulou, Efthalia [3 ]
Georgakopoulou, Vasiliki Epameinondas [4 ]
Bougea, Anastasia [3 ]
机构
[1] Istanbul Hlth & Technol Univ, Sch Med, Dept Neurol, TR-34093 Istanbul, Turkiye
[2] Sisli Kolan Int Hosp, Neurol Clin, Parkinsons Dis & Movement Disorders Unit, TR-34384 Istanbul, Turkiye
[3] Natl & Kapodistrian Univ Athens, Eginit Hosp, Med Sch, Dept Neurol 1, Athens 11528, Greece
[4] Laikon Gen Hosp, Dept Infect Dis, COVID 19 Unit, Athens 11527, Greece
来源
MEDICINA-LITHUANIA | 2023年 / 59卷 / 10期
关键词
Parkinson's disease; cognition; dementia; cognitive decline; cognitive impairment; pharmacological treatments; BEHAVIORAL DEFICITS; NONMOTOR FEATURES; DEMENTIA; MODEL; MOTOR; PD; NEUROPROTECTION; CEFTRIAXONE; ATOMOXETINE; DYSFUNCTION;
D O I
10.3390/medicina59101756
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cognitive impairment in patients with Parkinson's disease (PD) is one of the commonest and most disabling non-motor manifestations during the course of the disease. The clinical spectrum of PD-related cognitive impairment includes subjective cognitive decline (SCD), mild cognitive impairment (MCI) and PD dementia (PDD). As the disease progresses, cognitive decline creates a significant burden for the family members and/or caregivers of patients with PD, and has a great impact on quality of life. Current pharmacological treatments have demonstrated partial efficacy and failed to halt disease progression, and novel, effective, and safe therapeutic strategies are required. Accumulating preclinical and clinical evidence shows that several agents may provide beneficial effects on patients with PD and cognitive impairment, including ceftriaxone, ambroxol, intranasal insulin, nilotinib, atomoxetine, mevidalen, blarcamesine, prasinezumab, SYN120, ENT-01, NYX-458, GRF6021, fosgonimeton, INT-777, Neuropeptide S, silibinin, osmotin, cordycepin, huperzine A, fibroblast growth factor 21, Poloxamer 188, ginsenoside Rb1, thioredoxin-1, tangeretin, istradefylline and Eugenia uniflora. Potential underlying mechanisms include the inhibition of a-synuclein aggregation, the improvement of mitochondrial function, the regulation of synaptic plasticity, an impact on the gut-brain axis, the modulation of neuroinflammation and the upregulation of neurotrophic factors, as well as cholinergic, dopaminergic, serotoninergic and norepinephrine neurotransmission. In this updated overview, we aim to cover the clinical aspects of the spectrum of PD-related cognitive impairment and discuss recent evidence on emerging treatment approaches that are under investigation at a preclinical and clinical level. Finally, we aim to provide additional insights and propose new ideas for investigation that may be feasible and effective for the spectrum of PD-related cognitive impairment.
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页数:17
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