Department of Neurology and Alzheimer Center, VU University Medical Center, Amsterdam, the Netherlands.
Neurology. 2012 Aug 21;79(8):763-9. doi: 10.1212/WNL.0b013e3182661f91. Epub 2012 Aug 8.
To investigate the relationship between brain microbleeds (MBs) and the rate of cognitive decline in Alzheimer disease (AD).
In this cohort study, we studied 221 patients with AD with available baseline MRI scans (1.0 or 1.5 T) and at least 2 Mini-Mental State Examinations (MMSE) scores obtained more than 1 year apart from our memory clinic. Mean ± SD follow-up time was 3 ± 1 years, and patients had a median of 4 MMSE scores (range 2-17). We used linear mixed models with sex and age as covariates to investigate whether MBs influenced the rate of cognitive decline.
Mean age was 68 ± 9 years, 109 (49%) patients were female, and the baseline MMSE score was 22 ± 4. There were 39 patients (18%) with MBs (median 2, range 1-27) and 182 without. Linear mixed models showed that overall patients declined 2 MMSE points per year. We found no association of the presence of MBs with baseline MMSE or change in MMSE. Adjustment for atrophy, white matter hyperintensities, lacunes, and vascular risk factors did not change the results nor did stratification for MB location, APOE ε4 carriership, or age at onset (≤65 years vs >65 years). Repeating the analyses with number of MBs as predictor rendered similar results.
MBs did not influence the rate of cognitive decline in patients with AD. The formerly reported increased risk of mortality in patients with MBs seems not to be attributable to a steeper rate of decline per se but might be due to vascular events, including (hemorrhagic) stroke.
探讨脑微出血(MBs)与阿尔茨海默病(AD)认知下降速度的关系。
在这项队列研究中,我们研究了 221 例 AD 患者,这些患者基线 MRI 扫描(1.0 或 1.5T),且在我们的记忆诊所至少有 2 次 MMSE 评分,两次评分时间间隔超过 1 年。平均随访时间为 3 ± 1 年,患者的 MMSE 评分中位数为 4 分(范围 2-17)。我们使用线性混合模型,以性别和年龄为协变量,来研究 MBs 是否影响认知下降的速度。
患者平均年龄为 68 ± 9 岁,109 例(49%)为女性,基线 MMSE 评分为 22 ± 4。39 例(18%)患者存在 MBs(中位数 2 个,范围 1-27),182 例患者不存在 MBs。线性混合模型显示,所有患者每年 MMSE 评分下降 2 分。我们发现 MBs 的存在与基线 MMSE 或 MMSE 变化均无关联。调整萎缩、脑白质高信号、腔隙和血管危险因素、MB 位置、APOE ε4 携带状态或发病年龄(≤65 岁与>65 岁)后,结果未发生改变,分层分析也未改变结果。以 MB 数量为预测因子重复分析得到了相似的结果。
MBs 并未影响 AD 患者的认知下降速度。以前报道的 MBs 患者死亡率增加的原因似乎不是下降速度本身的增加,而可能是由于血管事件,包括(出血)性卒中。