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早期阿尔茨海默病的骨密度和脑萎缩。

Bone density and brain atrophy in early Alzheimer's disease.

机构信息

Department of Physical Therapy and Rehabilitation Sciences, University of Kansas School of Allied Health, Kansas City, KS, USA.

出版信息

J Alzheimers Dis. 2009;18(4):777-85. doi: 10.3233/JAD-2009-1185.

Abstract

Studies suggest a link between bone loss and Alzheimer's disease. To examine bone mineral density (BMD) in early Alzheimer's disease (AD) and its relationship to brain structure and cognition, we evaluated 71 patients with early stage AD (Clinical Dementia Rating (CDR) 0.5 and 1) and 69 non-demented elderly control participants (CDR 0). Measures included whole body BMD by dual energy x-ray absorptiometry (DXA) and normalized whole brain volumes computed from structural MRI scans. Cognition was assessed with a standard neuropsychological test battery. Mean BMD was lower in the early AD group (1.11 +/- 0.13) compared to the non-demented control group (1.16 +/- 0.12, p = 0.02), independent of age, gender, habitual physical activity, smoking, depression, estrogen replacement, and apolipoprotein E4 carrier status. In the early AD group, BMD was related to whole brain volume (b = 0.18, p = 0.03). BMD was also associated with cognitive performance, primarily in tests of memory (logical memory [b = 0.15, p = 0.04], delayed logical memory [b = 0.16, p = 0.02], and the selective reminding task - free recall [b = 0.18, p = 0.009]). BMD is reduced in the earliest clinical stages of AD and associated with brain atrophy and memory decline, suggesting that central mechanisms may contribute to bone loss in early AD.

摘要

研究表明,骨质疏松症与阿尔茨海默病之间存在关联。为了研究早期阿尔茨海默病(AD)中的骨矿物质密度(BMD)及其与大脑结构和认知的关系,我们评估了 71 名早期 AD 患者(临床痴呆评定量表(CDR)为 0.5 和 1)和 69 名非痴呆老年对照组参与者(CDR 为 0)。评估方法包括使用双能 X 射线吸收法(DXA)测量全身 BMD 以及从结构磁共振扫描计算出的归一化全脑体积。认知功能使用标准神经心理学测试量表进行评估。早期 AD 组的平均 BMD(1.11 +/- 0.13)低于非痴呆对照组(1.16 +/- 0.12,p = 0.02),独立于年龄、性别、习惯性体力活动、吸烟、抑郁、雌激素替代治疗和载脂蛋白 E4 状态。在早期 AD 组中,BMD 与全脑体积呈正相关(b = 0.18,p = 0.03)。BMD 还与认知表现相关,主要与记忆测试有关(逻辑记忆 [b = 0.15,p = 0.04],延迟逻辑记忆 [b = 0.16,p = 0.02],以及选择性提醒任务 - 自由回忆 [b = 0.18,p = 0.009])。AD 的最早临床阶段的 BMD 降低,与脑萎缩和记忆下降有关,这表明中枢机制可能导致早期 AD 中的骨丢失。

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