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Does Alzheimer's disease with early onset progress faster than with late onset? A case-control study of clinical progression and cerebrospinal fluid biomarkers

机译:早发性阿尔茨海默氏病的进展是否快于晚发?临床进展和脑脊液生物标志物的病例对照研究

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Background: Early-onset Alzheimer's disease (EOAD) is generally thought to have a more rapid course compared to late-onset Alzheimer's disease (LOAD). The faster progression of EOAD observed in some studies has also been thought to correlate with cerebrospinal fluid (CSF) biomarkers. Our clinical experience has not been suggestive of any difference in disease progression; therefore, we decided to investigate whether differences in clinical progression and CSF biomarkers between EOAD and LOAD could be demonstrated. Methods: Case-control study with 42 patients, 21 EOAD and 21 matched LOAD patients. Rates of progression were calculated and these, as well as CSF biomarker levels, were statistically compared. Results: There were no statistically significant differences in clinical progression between the EOAD group and the LOAD group. There was no significant difference in the absolute values of CSF biomarkers, but a tendency towards lower levels of β-amyloid in patients with EOAD was observed. Conclusions: Our findings did not converge with results from the majority of previous studies, which have been suggestive of a faster clinical progression in EOAD. Possibly, the very strict algorithm by which our patients were matched explains our findings. However, the findings should be repeated in a larger study population.
机译:背景:一般认为早发性阿尔茨海默氏病(EOAD)与晚发性阿尔茨海默氏病(LOAD)相比病程更快。在某些研究中观察到的EOAD的更快进展也被认为与脑脊液(CSF)生物标志物相关。我们的临床经验并未提示疾病进展有任何差异。因此,我们决定调查是否可以证明EOAD和LOAD之间的临床进展和CSF生物标志物的差异。方法:病例对照研究包括42例患者,21例EOAD和21例相匹配的LOAD患者。计算进展速度,并对这些以及CSF生物标志物水平进行统计学比较。结果:EOAD组和LOAD组之间的临床进展无统计学差异。 CSF生物标志物的绝对值无显着差异,但观察到EOAD患者的β-淀粉样蛋白水平降低。结论:我们的发现与大多数以前的研究结果不一致,这表明EOAD的临床进展更快。可能,匹配患者的非常严格的算法解释了我们的发现。但是,应在更大的研究人群中重复这些发现。

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