Apathy Reflects Extra-Striatal Dopaminergic Degeneration in de novo Parkinson's Disease


Por: Sampedro, F, Martinez-Horta, S, Marin-Lahoz, J, Pagonabarraga, J, Kulisevsky, J

Publicada: 1 ene 2022
Resumen:
Background: Apathy represents a core neuropsychiatric symptom in Parkinson's disease (PD). As there is currently no established effective treatment for apathy in PD, further investigating the biological origin of this symptom is needed to design novel therapeutic strategies. Among the multiple neurotransmitter alterations that have been associated with apathy, the involvement of extra-striatal dopaminergic degeneration remains to be fully explored. Objective: To investigate whether apathy in PD reflects increased dopaminergic degeneration extending beyond striatal regions. Methods: In the de novo PD cohort of the Parkinson's Progression Markers Initiative (PPMI), we performed whole-brain I-123-Ioflupane Single Photon Emission Computed Tomography (DAT-SPECT) analyses to characterize cross-sectional and longitudinal differences in DAT uptake associated with the presence of apathy. We also assessed the relationship between apathy and cognition in this sample, as apathy has been suggested to herald cognitive decline. Results: Apathetic PD patients (N= 70) had similar sociodemographic, clinical, and biomarker profiles compared to the non-apathetic group (N=333) at baseline. However, apathy was associated with an increased risk of developing cognitive impairment after a four-year follow-up period (p = 0.006). Compared to non-apathetic patients, apathetic patients showed a widespread reduction of extra-striatal DAT uptake at baseline as well as an increased longitudinal loss of DAT uptake (corrected p < 0.05). Conclusion: Isolated apathy in PD is associated with extra-striatal dopaminergic degeneration. As this abnormal dopamine depletion was in turn related to cognitive performance, this might explain, at least partially, the increased risk of apathetic PD patients to develop cognitive impairment or dementia.

Filiaciones:
Sampedro, F:
 Hosp Santa Creu & Sant Pau, Movement Disorders Unit, Neurol Dept, Mas Casanovas 90, Barcelona 08041, Spain

 Biomed Res Inst IIB St Pau, Barcelona, Spain

 Ctr Invest Red Enfermedades Neurodegenerat CIBERN, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Radiol Dept, Barcelona, Spain

Martinez-Horta, S:
 Hosp Santa Creu & Sant Pau, Movement Disorders Unit, Neurol Dept, Mas Casanovas 90, Barcelona 08041, Spain

 Biomed Res Inst IIB St Pau, Barcelona, Spain

 Ctr Invest Red Enfermedades Neurodegenerat CIBERN, Barcelona, Spain

Marin-Lahoz, J:
 Hosp Santa Creu & Sant Pau, Movement Disorders Unit, Neurol Dept, Mas Casanovas 90, Barcelona 08041, Spain

 Biomed Res Inst IIB St Pau, Barcelona, Spain

 Ctr Invest Red Enfermedades Neurodegenerat CIBERN, Barcelona, Spain

Pagonabarraga, J:
 Hosp Santa Creu & Sant Pau, Movement Disorders Unit, Neurol Dept, Mas Casanovas 90, Barcelona 08041, Spain

 Biomed Res Inst IIB St Pau, Barcelona, Spain

 Ctr Invest Red Enfermedades Neurodegenerat CIBERN, Barcelona, Spain

Kulisevsky, J:
 Hosp Santa Creu & Sant Pau, Movement Disorders Unit, Neurol Dept, Mas Casanovas 90, Barcelona 08041, Spain

 Biomed Res Inst IIB St Pau, Barcelona, Spain

 Ctr Invest Red Enfermedades Neurodegenerat CIBERN, Barcelona, Spain
ISSN: 18777171
Editorial
IOS PRESS, NIEUWE HEMWEG 6B, 1013 BG AMSTERDAM, NETHERLANDS, Países Bajos
Tipo de documento: Article
Volumen: 12 Número: 5
Páginas: 1567-1574
WOS Id: 000826217800015
ID de PubMed: 35491803

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