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APOE ε4 is associated with exacerbation of cognitive decline in patients with multiple sclerosis
Jiong Shi1, Jiang-Long Tu, Shawn D Gale
1Division of Neurology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, USA. jiong.shi@chw.edu
Background:
: In previous studies we and others have demonstrated an association with apolipoprotein (APOE) ε4 genotype and the presence of cognitive deficits in multiple sclerosis (MS). In this follow-up study, we have assessed whether APOE ε4 status exacerbates progression of cognitive deficits in MS.
Methods:
: A total of 197 patients with MS were assessed for APOE genotype, and baseline cognitive performance was measured using a standardized battery of tests. One hundred seventy patients (86.3%) were clinically followed up for 1 year and were assessed for progression of cognitive deficits.
Results:
: The APOE ε4 allele was present in 24.7% of patients. During 1-year follow-up, significant progression of cognitive deficits was found in APOE ε4 carriers (P=0.001) after logistic regression analysis controlling for sex, ethnicity, age, education, disease duration, severity, and subtype.
Conclusions:
: APOE ε4 carriers with MS have worsening progression of cognitive deficits than noncarriers. APOE ε4 carrier status predicts cognitive decline in verbal learning and memory.
Insights
Apolipoprotein E ε4 carriers with multiple sclerosis (MS) experience accelerated cognitive decline. This genetic factor specifically predicts worsening verbal learning and memory deficits over one year.
Area of Science:
- Neuroimmunology
- Genetics
- Cognitive Neuroscience
Background:
- Previous research links Apolipoprotein E (APOE) ε4 genotype to cognitive deficits in multiple sclerosis (MS).
- The APOE ε4 allele is a known genetic risk factor for various neurological conditions.
Purpose of the Study:
- To investigate if APOE ε4 genotype exacerbates the progression of cognitive deficits in patients with MS.
- To determine the predictive value of APOE ε4 status on cognitive decline in MS.
Main Methods:
- Assessed APOE genotype in 197 MS patients.
- Measured baseline cognitive performance using standardized tests.
- Followed 170 MS patients for 1 year to assess cognitive progression.
Main Results:
- APOE ε4 allele was present in 24.7% of the MS cohort.
- Significant progression of cognitive deficits observed in APOE ε4 carriers over 1 year (P=0.001).
- Logistic regression controlled for demographic and clinical factors.
Conclusions:
- APOE ε4 carriers with MS exhibit a worse progression of cognitive deficits compared to non-carriers.
- APOE ε4 carrier status is a significant predictor of cognitive decline, particularly in verbal learning and memory.
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