Hoyt Brian D, Massman Paul J, Schatschneider Christopher, Cooke Norma, Doody Rachelle S
Department of Psychology, University of Houston, Houston, Tex, USA.
Arch Neurol. 2005 Mar;62(3):454-9. doi: 10.1001/archneur.62.3.454.
The apolipoprotein E epsilon4 (APOE epsilon4) allele is associated with an increased risk of developing Alzheimer disease (AD). However, findings regarding an association between the APOE epsilon4 allele and the rate of decline in AD have been mixed.
To examine the relationship between the APOE epsilon4 allele and the rate of cognitive and functional decline in AD using individual growth curve analyses.
Longitudinal cohort study.
Alzheimer Disease Research Center at Baylor College of Medicine.
A total of 189 patients meeting NINCDS-ADRDA (National Institute of Neurological and Communicative Disorders and Stroke-Alzheimer's Disease and Related Disorders Association) criteria for probable AD at baseline who underwent annual follow-up evaluations for at least 2 years.
Individual growth curve parameters derived from baseline and follow-up performance on global and specific measures of cognitive and functional abilities.
Patients with 2 APOE epsilon4 alleles exhibited a slower rate of decline on measures of global cognitive functioning and functional abilities. No significant association was detected between the APOE epsilon4 allele and the rate of decline on measures of specific cognitive functions.
Although the APOE epsilon4 allele is associated with an increased risk of developing AD, it seems that having 2 APOE epsilon4 alleles is associated with a slower clinical course. These findings are consistent with hypotheses that the biological processes contributing to the onset of AD are different from those involved in determining its clinical course.
载脂蛋白Eε4(APOEε4)等位基因与患阿尔茨海默病(AD)风险增加相关。然而,关于APOEε4等位基因与AD病情衰退速率之间关联的研究结果并不一致。
采用个体生长曲线分析来研究APOEε4等位基因与AD患者认知及功能衰退速率之间的关系。
纵向队列研究。
贝勒医学院阿尔茨海默病研究中心。
共有189例患者,在基线时符合美国国立神经疾病与中风研究所-阿尔茨海默病及相关疾病协会(NINCDS-ADRDA)可能患AD的标准,且接受了至少2年的年度随访评估。
从认知和功能能力的整体及特定指标的基线和随访表现得出的个体生长曲线参数。
携带两个APOEε4等位基因的患者在整体认知功能和功能能力指标上的衰退速率较慢。未检测到APOEε4等位基因与特定认知功能指标衰退速率之间存在显著关联。
虽然APOEε4等位基因与患AD风险增加相关,但似乎携带两个APOEε4等位基因与较慢的临床病程相关。这些发现与以下假设一致,即导致AD发病的生物学过程与决定其临床病程的过程不同。