Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy

作者：van der Walt A^*; Stankovich J; Bahlo M; Taylor B V; van der Mei I A F; Foote S J; Kilpatrick T J; Rubio J P; Butzkueven H

来源：Neurology, 2009, 73(13): 1018-1025.

DOI：10.1212/WNL.0b013e3181b9c85e

Background: The influence of APOE allelic heterogeneity on multiple sclerosis (MS) disease severity has been reported in multiple datasets with conflicting results. Several studies have reported an unfavorable association of APOE epsilon 4 with more severe clinical disease course while, in contrast, APOE epsilon 2 has been associated with a more benign disease course. In this study, we examine the influence of heterogeneity of the APOE gene on disease severity in a large, Australian, population-based MS cohort.
Methods: Associations between APOE allele status, 2 promoter region single nucleotide polymorphisms (- 219 G/T and 113 C/G), and 4 measures of disease severity were tested in 1,006 patients with relapsing-remitting MS and secondary progressive MS: 1) Multiple Sclerosis Severity Score; 2) Progression Index (Expanded Disability Status Scale/disease duration); 3) age at first symptom; and 4) interval between the first and second attack. The Symbol Digit Modalities Test was used as a single cognitive marker in 889 patients. Brain atrophy was measured in 792 patients using the intercaudate ratio. APOE epsilon 4 and epsilon 3 carriers were stratified by - 219 G/T or 113 C/G to investigate haplotypic heterogeneity in the APOE gene region.
Results: In this MS study, neither APOE allele status nor promoter region heterogeneity at positions - 219 G/T or 113 C/G influenced the clinical disease severity, cognition, or cerebral atrophy.
Conclusions: Allelic and haplotypic heterogeneity of the APOE gene region does not influence multiple sclerosis disease course in this well-defined Australian multiple sclerosis cohort. Neurology (R) 2009;73:1018-1025

• 出版日期2009-9-29
• 单位河北医科大学