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Interethnic differences in neuroimaging markers and cognition in Asians, a population-based study

Authors :
Henri A. Vrooman
Louis Choon Kit Wong
Narayanaswamy Venketasubramanian
Mark Yu Zheng Wong
Christopher Chen
Ching-Yu Cheng
Chuen Seng Tan
Saima Hilal
Radiology & Nuclear Medicine
Department of Organisation and Personnel Management
Source :
Scientific Reports, Scientific Reports, 10. Nature Publishing Group, Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Publication Year :
2020
Publisher :
Nature Publishing Group UK, 2020.

Abstract

We examined interethnic differences in the prevalence of neuroimaging markers of cerebrovascular and neurodegenerative disease in 3 major Asian ethnicities (Chinese, Malays, and Indians), as well as their role in cognitive impairment. 3T MRI brain scans were acquired from 792 subjects (mean age: 70.0 ± 6.5years, 52.1% women) in the multi-ethnic Epidemiology of Dementia In Singapore study. Markers of cerebrovascular disease and neurodegeneration were identified. Cognitive performance was evaluated using Mini Mental State Examination (MMSE), Montreal Cognitive Assessment (MoCA), and a neuropsychological assessment. Compared to Chinese, Malays had a higher burden of intracranial stenosis (OR: 2.28. 95%CI: 1.23–4.20) and cortical atrophy (β: −0.60. 95%CI: −0.78, −0.41), while Indians had a higher burden of subcortical atrophy (β: −0.23. 95%CI: −0.40, −0.06). Moreover, Malay and Indian ethnicities were likely to be cognitively impaired (OR for Malays: 3.79. 95%CI: 2.29–6.26; OR for Indians: 2.87. 95%CI: 1.74–4.74) and showed worse performance in global cognition (β for Malays: −0.51. 95%CI: −0.66, −0.37; and Indians: −0.32. 95%CI: −0.47, −0.17). A higher burden of cerebrovascular and neurodegenerative markers were found in Malays and Indians when compared to Chinese. Further research is required to fully elucidate the factors and pathways that contribute to these observed differences.

Details

Language :
English
ISSN :
20452322
Volume :
10
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....7c8bddefe57b55b00762694a2a936a2d