چکیده:
Background: Apolipoprotein E (APOE) is crucial for neuronal maintenance and myelin repair. The APOE4 isoform is associated with an increased risk of neurodegeneration in multiple sclerosis patients. This study investigated the association between APOE polymorphisms and brain atrophy in multiple sclerosis patients.
Methods: The current cross-sectional study was performed on 70 relapsing-remitting multiple sclerosis (RRMS) patients, evaluating two common missense APOE polymorphisms, rs429358 and rs7412, in all participants. The FreeSurfer software measured whole-brain volume by analyzing T1-weighted Magnetic Resonance Imaging (MRI) sequences.
Diffusion tensor imaging (DTI) data were preprocessed with MRtrix3 and analyzed using FSL.
Results: Patients with APOE4 exhibited lower white matter (WM) volume than those without this isoform (274.25±32.20, vs. 307.51±36.36, p=0.02). After adjusting for confounding factors, there was a significant association between APOE4 and lower WM volume (p=0.03, partial Eta square (η²) = 0.08). Indeed, a negative independent association was found between disease duration and WM volume (p = 0.02, η² = 0.09).
DTI data were analyzed in 7 APOE4 carriers and 8 non-carriers matched for age, sex, and MS duration. FA in WM (1.75(0.13), vs. 1.83 (0.18)) and corpus callosum (2.09(0.78), vs. 2.21(0.30)) were lower in APOE4 carriers, but not significantly (p>0.05).
Conclusion: The present study suggested a potential genetic influence of APOE4 on brain WM atrophy, specifically the corpus callosum, in MS patients.
Methods: The current cross-sectional study was performed on 70 relapsing-remitting multiple sclerosis (RRMS) patients, evaluating two common missense APOE polymorphisms, rs429358 and rs7412, in all participants. The FreeSurfer software measured whole-brain volume by analyzing T1-weighted Magnetic Resonance Imaging (MRI) sequences.
Diffusion tensor imaging (DTI) data were preprocessed with MRtrix3 and analyzed using FSL.
Results: Patients with APOE4 exhibited lower white matter (WM) volume than those without this isoform (274.25±32.20, vs. 307.51±36.36, p=0.02). After adjusting for confounding factors, there was a significant association between APOE4 and lower WM volume (p=0.03, partial Eta square (η²) = 0.08). Indeed, a negative independent association was found between disease duration and WM volume (p = 0.02, η² = 0.09).
DTI data were analyzed in 7 APOE4 carriers and 8 non-carriers matched for age, sex, and MS duration. FA in WM (1.75(0.13), vs. 1.83 (0.18)) and corpus callosum (2.09(0.78), vs. 2.21(0.30)) were lower in APOE4 carriers, but not significantly (p>0.05).
Conclusion: The present study suggested a potential genetic influence of APOE4 on brain WM atrophy, specifically the corpus callosum, in MS patients.
نوع مطالعه: Original |
موضوع مقاله:
Cellular and molecular Neuroscience
دریافت: 1404/11/11 | پذیرش: 1405/3/16
دریافت: 1404/11/11 | پذیرش: 1405/3/16
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