Williams-Gray Caroline H, Goris An, Saiki Misuzu, Foltynie Thomas, Compston D Alastair S, Sawcer Stephen J, Barker Roger A
Cambridge Centre for Brain Repair, Dept. of Clinical Neurosciences, University of Cambridge, Forvie Site, Robinson Way, Cambridge, CB2 2PY, UK.
J Neurol. 2009 Mar;256(3):493-8. doi: 10.1007/s00415-009-0119-8. Epub 2009 Mar 18.
Further to the well-established association between apolipoprotein E (APOE) and Alzheimer's disease, this gene has also been implicated in both susceptibility to, and dementia in, Parkinson's disease (PD). However studies to date have produced contradictory findings. We conducted a case-control study in a population of 528 PD patients and 512 healthy controls and found no significant difference in allele or genotype distribution of APOE between the two groups. An updated meta-analysis showed a modest increase of APOE-epsilon2 carriers amongst PD patients compared to controls [P = 0.017, OR = 1.16 (95 % CI 1.03-1.31)]. 107 of our patients were incident cases participating in a population-based epidemiological study. Longitudinal follow-up of this cohort over a mean of 5.0 +/- 0.7 years from diagnosis revealed no significant impact of APOE-epsilon4 carrier status on risk of dementia or rate of cognitive decline. An updated meta-analysis indicated an over-representation of APOE-epsilon4 carriers amongst PD dementia compared to non dementia cases [OR 1.74 (1.36-2.23), P = 1 x 10(-4)], although small sample sizes, heterogeneity of odds ratios and publication bias may have confounded this finding. In conclusion, our study does not support previously reported associations between APOE genotype and susceptibility to, or cognitive decline in, PD. An updated meta-analysis indicates any association with PD susceptibility is at most modest, an observation with important implications for further study of this issue. Large scale longitudinal studies would be best placed to further evaluate any impact of APOE genotype on cognitive decline in PD.
除了载脂蛋白E(APOE)与阿尔茨海默病之间已确立的关联外,该基因还与帕金森病(PD)的易感性和痴呆有关。然而,迄今为止的研究结果相互矛盾。我们在528名PD患者和512名健康对照人群中进行了一项病例对照研究,发现两组之间APOE的等位基因或基因型分布没有显著差异。一项更新的荟萃分析显示,与对照组相比,PD患者中APOE-ε2携带者略有增加[P = 0.017,OR = 1.16(95%CI 1.03 - 1.31)]。我们的107名患者是参与基于人群的流行病学研究的新发病例。从诊断开始对该队列进行平均5.0±0.7年的纵向随访发现,APOE-ε4携带者状态对痴呆风险或认知衰退率没有显著影响。一项更新的荟萃分析表明,与非痴呆病例相比,PD痴呆患者中APOE-ε4携带者的比例过高[OR 1.74(1.36 - 2.23),P = 1×10⁻⁴],尽管样本量小、比值比的异质性和发表偏倚可能混淆了这一发现。总之,我们的研究不支持先前报道的APOE基因型与PD易感性或认知衰退之间的关联。一项更新的荟萃分析表明,与PD易感性的任何关联至多是适度的,这一观察结果对该问题的进一步研究具有重要意义。大规模纵向研究最适合进一步评估APOE基因型对PD认知衰退的任何影响。