Shaw Leslie M, Korecka Magdalena, Lee Edward B, Cousins Katheryn A Q, Vanderstichele Hugo, Schindler Suzanne E, Tosun Duygu, DeMarco Mari L, Brylska Magdalena, Wan Yang, Burnham Samantha, Sciulli Alexandria, Vulaj Amberley, Tropea Thomas F, Chen-Plotkin Alice, Wolk David A
Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Neurology Department, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Alzheimers Dement. 2025 Jan;21(1):e14264. doi: 10.1002/alz.14264. Epub 2024 Nov 30.
We describe the Alzheimer's Disease Neuroimaging Initiative (ADNI) Biomarker Core major activities from October 2004 to March 2024, including biobanking ADNI cerebrospinal fluid (CSF), plasma, and serum biofluid samples, biofluid analyses for Alzheimer's disease (AD) biomarkers in the Biomarker Core and various non-ADNI laboratories, and continuous assessments of pre-analytics.
Validated immunoassay and mass spectrometry-based assays were performed in CSF with a shift to plasma, a more accessible biofluid, as qualified assays became available. Performance comparisons across different CSF and plasma AD biomarker measurement platforms have enriched substantially the ADNI participant database enabling method performance determinations for AD pathology detection and longitudinal assessments of disease progression.
Close collaboration with academic and industrial partners in the validation and implementation of AD biomarkers for early detection of disease pathology in treatment trials and ultimately in clinical practice is a key factor for the success of the work done in the Biomarker Core.
Describe ADNI Biomarker Core biobanking and sample distribution from 2007 to 2024. Discuss validated mass spectrometry and immunoassay methods for ADNI biofluid analyses. Review collaborations with academic and industrial partners to detect AD and progression. Discuss major challenges, and progress to date, for co-pathology detection. Implementation in the ATN scheme: co-pathology and modeling disease progression.
我们描述了2004年10月至2024年3月期间阿尔茨海默病神经影像倡议(ADNI)生物标志物核心的主要活动,包括对ADNI脑脊液(CSF)、血浆和血清生物流体样本进行生物样本库建设,在生物标志物核心和各个非ADNI实验室对阿尔茨海默病(AD)生物标志物进行生物流体分析,以及对分析前因素进行持续评估。
随着合格检测方法的出现,在脑脊液中进行了经过验证的免疫测定和基于质谱的检测,并转向了更容易获取的生物流体血浆。对不同脑脊液和血浆AD生物标志物测量平台的性能比较极大地丰富了ADNI参与者数据库,从而能够确定AD病理检测的方法性能和疾病进展的纵向评估。
在治疗试验以及最终在临床实践中,与学术和行业合作伙伴在AD生物标志物的验证和实施方面密切合作,以早期检测疾病病理,这是生物标志物核心工作取得成功的关键因素。
描述2007年至2024年ADNI生物标志物核心的生物样本库建设和样本分发情况。讨论用于ADNI生物流体分析的经过验证的质谱和免疫测定方法。回顾与学术和行业合作伙伴在检测AD及其进展方面的合作。讨论共病病理检测的主要挑战和迄今取得的进展。在ATN方案中的实施:共病病理和疾病进展建模。