Ethnic background and distribution of clinical phenotypes in patients with probable progressive supranuclear palsy

被引:5
作者
Couto, Blas [1 ,2 ,3 ]
Di Luca, Daniel G. [2 ]
Antwi, Jeffrey [1 ,2 ]
Bhakta, Puja [1 ,2 ]
Fox, Susan [1 ,2 ]
Tartaglia, Maria Carmela [4 ,5 ]
Kovacs, Gabor G. [1 ,2 ,5 ,6 ,7 ,8 ,9 ]
Lang, Anthony E. [1 ,2 ,5 ,10 ,11 ]
机构
[1] Toronto Western Hosp, Edmond J Safra Program Parkinsons Dis, Rossy Program PSP Res, Toronto, ON M5T 2S8, Canada
[2] Toronto Western Hosp, Morton & Gloria Shulman Movement Disorders Clin, Toronto, ON M5T 2S8, Canada
[3] Inst Neurociencia Cognit & Traslac INCyT, INECO CONICET Favaloro, Buenos Aires, Argentina
[4] Toronto Western Hosp, Memory Clin, Toronto, ON, Canada
[5] Univ Toronto, Tanz Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[6] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[7] Univ Toronto, Dept Med, Toronto, ON, Canada
[8] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
[9] Univ Hlth Network, Krembil Brain Inst, Toronto, ON, Canada
[10] Univ Hlth Network, Dept Med, Div Neurol, Toronto, ON, Canada
[11] Univ Toronto, Toronto, ON, Canada
关键词
Progressive supranuclear palsy; Diversity; Ethnic; Race; Epidemiology; ATYPICAL PARKINSONISM; IMMIGRANTS; CLUSTER; DISEASE;
D O I
10.1016/j.parkreldis.2024.106955
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Progressive Supranuclear Palsy (PSP) is a sporadic neurodegenerative disease without a clear geographic prevalence. Cohorts studied in the UK and India showed no higher prevalence of atypical parkinsonism in South Asian patients. We describe the ethnic and racial background of PSP patients in the Greater Toronto Area (GTA), Canada. Methods: A prospective observational study of patients with clinically probable PSP evaluated at the dedicated Rossy PSP program. Demographic and clinical data were collected at baseline including PSP phenotype. Results were compared with the latest demographic information from the greater Toronto area. Results: Of the 197 patients screened, 135 had probable PSP and resided within the GTA. The mean age at visit was 71.1 years, disease duration 4.4 years, and disease severity moderate. Compared to our catchment area, there was a higher proportion of patients with a South Asian origin and a lower proportion of patients from East and Southeastern Asia and Africa. A secondary analysis using population census data limited to individuals greater than 65 confirmed the significantly higher representation of South Asians in our clinic but found no differences for other racial and ethnic origins. Conclusion: Evaluation of this Toronto cohort found a greater than expected proportion of affected individuals with South Asian ethnic and racial origin. Despite limitations, our results suggest the possibility of a racial and ethnic predisposition to PSP. Further studies are needed to confirm and to address potential associated risk factors, and genome-environmental interactions.
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