Association between Apolipoprotein E genotype and functional outcome in acute ischemic stroke
Xiaoming Rong1, Jingjuan Chen2, Dong Pan1
1Department of Neurology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.
APOE ε4 carriers have a significantly higher risk of poor functional outcomes after acute ischemic stroke (AIS). The APOE genotype may also influence the association between inflammation markers, like neutrophil-to-lymphocyte ratio (NLR), and stroke disability.
Area of Science:
- Neurology
- Genetics
- Immunology
Background:
- The apolipoprotein E (APOE) gene is implicated in various neurological conditions.
- Understanding APOE's role in acute ischemic stroke (AIS) can refine prognostic assessments.
- Inflammation plays a critical role in stroke pathophysiology and recovery.
Purpose of the Study:
- To investigate the impact of APOE alleles on functional outcomes in AIS patients.
- To determine if APOE genotype modifies the relationship between inflammation and stroke-related disability.
Main Methods:
- Retrospective analysis of demographic and clinical data from 1929 AIS patients.
- Assessment of functional outcome at 3 months using the modified Rankin scale (mRS) score (2-6 for dependence or death).
- Evaluation of APOE ε4 carrier status and neutrophil-to-lymphocyte ratio (NLR) in relation to outcomes.
Main Results:
- APOE ε4 carriers (17.73%) had a significantly increased probability of poor functional outcome (adjusted OR 4.62, P < 0.001).
- Among APOE ε4 carriers, high NLR was associated with stroke-related disability (Ptrend = 0.035), but not in non-ε4 carriers.
- Poor functional outcome (mRS 2-6) was observed in 20.43% of all patients.
Conclusions:
- APOE ε4 carriage is a significant risk factor for worse functional outcomes following AIS.
- APOE genotype may modulate the association between inflammatory markers (NLR) and long-term stroke-related disability.
- These findings highlight the importance of genetic factors in predicting stroke recovery.
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