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The Multiple Sclerosis Severity Allele rs10191329A and Cognitive Function: A UK Biobank Study
Ioanna Zimianiti1,2, Sheena Waters1, Adil Harroud3,4,5
1Centre for Preventive Neurology, Wolfson Institute of Population Health, Queen Mary University of London, UK.
The genetic variant rs10191329A is linked to worse cognitive function in healthy individuals. This finding suggests a potential role for this variant in neurological disease outcomes, including Multiple Sclerosis.
Area of Science:
- Neurogenetics
- Cognitive Neuroscience
Background:
- A genome-wide association study identified the genetic variant rs10191329A associated with Multiple Sclerosis severity and long-term disability.
- Brain resilience was implicated as a key factor influencing outcomes in Multiple Sclerosis.
Purpose of the Study:
- To investigate the potential influence of the rs10191329A genetic variant on cognitive function.
- To explore the association of rs10191329A with cognition in healthy controls and patients with neurological diseases.
Main Methods:
- Utilized the UK Biobank dataset for the study.
- Assessed cognitive performance using tests for reaction time, fluid intelligence, and prospective memory.
Main Results:
- Observed a weak but consistent association between the rs10191329A variant and poorer cognitive function in healthy controls.
- Identified similar, albeit non-significant, trends of impaired cognition associated with rs10191329A in Multiple Sclerosis, Parkinson's disease, and dementia cohorts.
Conclusions:
- The findings support the hypothesis that the rs10191329A genetic variant may impact cognitive function.
- Results suggest rs10191329A could influence neurological disease outcomes, potentially through effects on brain health and resilience.
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