多系统故障,临界点和阿尔茨海默病的风险
Simona Merlini1,2, Edward J Bedrick3,4, Roberta Diaz Brinton1,5,6
1Center for Innovation in Brain Science, University of Arizona Health Sciences, Tucson, Arizona, USA.
概括
阿尔茨海默病 (AD) 风险因素的持续时间,如肥胖和糖尿病,显著影响发病,有时比APOEε4基因型更大. 关键的与年龄相关的临界点,特别是在62-72岁之间,揭示了AD进展的动态.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 是一个遗传学.
- 公共卫生 公共卫生
背景情况:
- 肥胖,糖尿病,高脂血症和抑郁症等医疗状况是已知的阿尔茨海默病 (AD) 的风险因素.
- 这些风险因素的持续时间以及性别和阿波利波蛋白E (APOE) 基因型等不可修改因素对阿尔茨海默病风险的影响仍然不完全理解.
研究的目的:
- 调查常见疾病持续时间对阿尔茨海默病 (AD) 风险的影响.
- 为了确定AD风险因子发病的关键年龄相关的临界点.
- 为了检查风险因素持续时间与性别和APOE基因型在AD病变发生的相互作用.
主要方法:
- 分析了来自5644名英国生物库参与者的数据.
- 利用考克斯回归建模来确定关键的临界点.
- 检查了发病年龄,危险因素持续时间,性别和APOE基因型的相互作用.
主要成果:
- 在62岁之前诊断的高血压或糖尿病比单独的APOEε4基因型具有更大的AD风险.
- 在62岁之前的肥胖增加了AD风险54%,在62-72岁之间风险几乎增加了三倍.
- 超脂血症和抑郁症的年龄独立风险增加分别为33%和69%. 在72岁以后,APOEε4成为主要的风险因素.
结论:
- 患AD风险因素的持续时间可能比APOEε4基因型对AD发作的影响更大.
- 关键的与年龄相关的临界点,特别是在62岁和72岁之间,突出了AD进展的时间性质.
- 多系统衰竭和不同的遗传轨迹 (APOEε4携带者与非携带者) 在不同性别的阿尔茨海默病发展中发挥着重要作用.
关键词:
预防AD的策略和预防策略.其他AD风险因素这是APOE基因型.阿尔茨海默病 (AD) 是一种疾病.考克斯的比例危险模型 (CPHM)英国生物银行染色体上的性别.抑郁 抑郁症 抑郁症 抑郁症 抑郁症超脂血症 (HLP) 是一种高脂血症.高血压 (HTN) 是指高血压.晚期发病的阿尔茨海默氏病 (LOAD)可以修改的风险因素.肥胖 肥胖 肥胖 肥胖 肥胖 肥胖 肥胖 肥胖第二种类型糖尿病 (T2D)不能改变的风险因素更多相关视频
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