Olichney J M, Hansen L A, Hofstetter C R, Grundman M, Katzman R, Thal L J
Alzheimer's Disease Research Center, University of California-San Diego, La Jolla, USA.
Arch Neurol. 1995 Jul;52(7):702-8. doi: 10.1001/archneur.1995.00540310076019.
To determine if severe cerebral amyloid angiopathy (AA) in patients with Alzheimer's disease (AD) is associated with an increased prevalence of cerebral infarction diagnosed at autopsy. Amyloid angiopathy is increasingly recognized as a cause of ischemic infarcts, as well as cerebral hemorrhages. However, the relationship of AA to cerebral infarction in patients with AD is uncertain.
Retrospective clinicopathological study of autopsy-confirmed cases of AD.
One hundred forty-five deceased patients with AD confirmed at autopsy.
Semiquantitative scores of AA severity were done in four brain regions: midfrontal, inferior parietal, superior temporal, and hippocampal. The finding of cerebral infarction at autopsy was modeled as a function of AA severity, hypertension, age at death, AD severity, and sex in chi 2 and multiple logistic regression analyses.
Severe AA was significantly associated with cerebral infarction at autopsy in patients with AD (odds ratio [OR], 3.5; 95% confidence interval [CI], 1.4 to 8.9). None of the other independent variables in the multiple logistic regression analysis were significant predictors. While hypertension was equally common in the severe and mild AA subgroups, the combination of both severe AA and hypertension interacted to increase the risk of infarction (OR, 14.2; 95% CI, 3.2 to 63.4) beyond that observed with hypertension (OR, 1.1; 95% CI, 0.4 to 3.2) or severe AA (OR, 1.3; 95% CI, 0.3 to 5.3) alone.
Severe AA is associated with an increased frequency of cerebral infarction in patients with AD. This appears to be largely due to an interaction between severe AA and hypertension that may produce multiplicative injuries on the vasculature. Further study with regard as to how AA may cause ischemia and its role in the neuropathologic and clinical progression of AD is needed.
确定阿尔茨海默病(AD)患者的严重脑淀粉样血管病(AA)是否与尸检时诊断出的脑梗死患病率增加相关。淀粉样血管病日益被认为是缺血性梗死以及脑出血的一个病因。然而,AD患者中AA与脑梗死的关系尚不确定。
对尸检确诊的AD病例进行回顾性临床病理研究。
145例经尸检确诊的已故AD患者。
在四个脑区(额中回、顶下小叶、颞上回和海马体)对AA严重程度进行半定量评分。在卡方检验和多元逻辑回归分析中,将尸检时脑梗死的发现作为AA严重程度、高血压、死亡年龄、AD严重程度和性别的函数进行建模。
AD患者中,严重AA与尸检时的脑梗死显著相关(优势比[OR]为3.5;95%置信区间[CI]为1.4至8.9)。多元逻辑回归分析中的其他独立变量均不是显著的预测因素。虽然高血压在严重AA和轻度AA亚组中同样常见,但严重AA和高血压共同作用会增加梗死风险(OR为14.2;95%CI为3.2至63.4),高于单独高血压(OR为1.1;95%CI为0.4至3.2)或严重AA(OR为1.3;95%CI为0.3至5.3)时观察到的风险。
严重AA与AD患者脑梗死发生率增加相关。这似乎主要是由于严重AA与高血压之间的相互作用,可能对血管系统造成多重损伤。需要进一步研究AA如何导致缺血及其在AD神经病理学和临床进展中的作用。