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用于阿尔茨海默病痴呆预测的五年生物标志物进展变异性:一种复杂的日常生活活动标志物能否填补空白?

Five-year biomarker progression variability for Alzheimer's disease dementia prediction: Can a complex instrumental activities of daily living marker fill in the gaps?

作者信息

Tarnanas Ioannis, Tsolaki Anthoula, Wiederhold Mark, Wiederhold Brenda, Tsolaki Magda

机构信息

Health-IS Lab, Department of Management, Technology and Economics, ETH Zurich, Zurich, Switzerland; Piaget Research Foundation, Nürnberg, Germany.

3rd Department of Neurology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.

出版信息

Alzheimers Dement (Amst). 2015 Nov 14;1(4):521-32. doi: 10.1016/j.dadm.2015.10.005. eCollection 2015 Dec.

Abstract

INTRODUCTION

Biomarker progressions explain higher variability in cognitive decline than baseline values alone. This study examines progressions of established biomarkers along with a novel marker in a longitudinal cognitive decline.

METHODS

A total of 215 subjects were used with a diagnosis of normal, mild cognitive impairment (MCI) or Alzheimer's disease (AD) at baseline. We calculated standardized biomarker progression rates and used them as predictors of outcome within 5 years.

RESULTS

Early cognitive declines were more strongly explained by fluorodeoxyglucose-positron emission tomography, precuneus and medial temporal cortical thickness, and the complex instrumental activities of daily living (iADL) marker progressions. Using Cox proportional hazards model, we found that these progressions were a significant risk factor for conversion from both MCI to AD (adjusted hazard ratio 1.45; 95% confidence interval 1.20-1.93; P = 1.23 × 10(-5)) and cognitively normal to MCI (adjusted hazard ratio 1.76; 95% confidence interval 1.32-2.34; P = 1.55 × 10(-5)).

DISCUSSION

Compared with standard biological biomarkers, complex functional iADL markers could also provide predictive information for cognitive decline during the presymptomatic stage. This has important implications for clinical trials focusing on prevention in asymptomatic individuals.

摘要

引言

生物标志物进展比单独的基线值能更好地解释认知衰退的更高变异性。本研究在纵向认知衰退中考察了既定生物标志物以及一种新型标志物的进展情况。

方法

共有215名受试者在基线时被诊断为正常、轻度认知障碍(MCI)或阿尔茨海默病(AD)。我们计算了标准化生物标志物进展率,并将其用作5年内结果的预测指标。

结果

早期认知衰退更能由氟脱氧葡萄糖正电子发射断层扫描、楔前叶和内侧颞叶皮质厚度以及复杂的日常生活工具性活动(iADL)标志物进展来解释。使用Cox比例风险模型,我们发现这些进展是从MCI转化为AD(调整后风险比1.45;95%置信区间1.20 - 1.93;P = 1.23×10⁻⁵)以及从认知正常转化为MCI(调整后风险比1.76;95%置信区间1.32 - 2.34;P = 1.55×10⁻⁵)的显著风险因素。

讨论

与标准生物标志物相比,复杂的功能性iADL标志物也可为症状前阶段的认知衰退提供预测信息。这对于针对无症状个体预防的临床试验具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/badb/4879487/95072f23a830/gr1.jpg

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