Optimizing the preclinical Alzheimer's cognitive composite with semantic processing: The PACC5

Kathryn V. Papp1,2, Dorene M. Rentz1,2, Irina Orlovsky1,2, Reisa A. Sperling1,2, Elizabeth C. Mormino2,3
1Center for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA
2Department of Neurology, Massachusetts General Hospital, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA
3Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA, USA

Tóm tắt

AbstractIntroductionAmyloid‐related decline in semantic memory was recently shown to be observable in the preclinical period of Alzheimer's disease. Cognitive composites designed to be sensitive to cognitive change in preclinical Alzheimer's disease (e.g., preclinical Alzheimer's cognitive composite [PACC]) and currently used in secondary prevention trials do not currently integrate measures of semantic processing. Our objective was to determine whether a standard semantic measure (i.e., category fluency [CAT] to animals, fruits, and vegetables) adds independent information above and beyond Aβ‐related decline captured by the PACC.MethodsClinically normal older adults from the Harvard Aging Brain Study were identified at baseline as Aβ+ (n = 70) or Aβ− (n = 209) using Pittsburgh compound B–positron emission tomography imaging and followed annually with neuropsychological testing for 3.87 ± 1.09 years. The relationships between PACC, CAT, and variations of the PACC including/excluding CAT were examined using linear mixed models controlling for age, sex, and education. We additionally examined decline on CAT by further grouping Aβ+ participants into preclinical stage 1 and stage 2 on the basis of neurodegeneration markers.ResultsCAT explained unique variance in amyloid‐related decline, with Aβ+'s continuing to decline relative to Aβ−'s in CAT even after controlling for overall PACC decline. In addition, removal of CAT from the PACC resulted in a longitudinal Aβ+/− effect size reduction of 20% at 3‐year follow‐up and 12% at 5‐year follow‐up. Finally, both stage 1 and stage 2 participants declined on CAT in comparison with stage 0, suggesting CAT declines early within the preclinical trajectory.ConclusionAddition of CAT to the PACC provides unique information about early cognitive decline not currently captured by the episodic memory, executive function, and global cognition components and may therefore improve detection of early Aβ‐related cognitive decline.

Tài liệu tham khảo

10.1016/S1474-4422(12)70291-0 10.1002/1531-8249(199903)45:3<358::AID-ANA12>3.0.CO;2-X 10.1126/scitranslmed.3007941 Sperling R.A., 2011, Testing the Right Target and Right Drug at the Right Stage, Sci Transl Med, 3, 10.1126/scitranslmed.3002609 Rentz D.M., 2013, Promising developments in neuropsychological approaches for the detection of preclinical Alzheimer's disease: a selective review, Alzheimers Res Ther, 5, 1, 10.1186/alzrt222 U. Food D. Administration.Guidance for Industry. Alzheimer's Disease: Developing Drugs for the Treatment of Early Stage Disease Draft Guidance. Federal Register: Center for Drug Evaluation and Research2013 Available at:https://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm338287.pdf. Accessed November 21 2017 10.1001/jamaneurol.2014.803 10.1016/j.dadm.2015.11.003 10.1016/0022-3956(75)90026-6 Wechsler D., 1987, Wechsler Memory Scale‐revised Wechsler D., 1981, WAIS‐R Manual: Wechsler Adult Intelligence Scale‐Revised Grober E., 2009, The free and cued selective reminding test: evidence of psychometric adequacy, Psychol Sci Q, 51, 266 10.1016/j.jalz.2017.01.018 10.1080/01688638708410764 10.1016/j.neuropsychologia.2009.11.019 10.1002/ana.21509 10.1016/j.jalz.2014.02.002 10.1037/neu0000246 10.1212/WNL.0b013e31828c2fc8 10.1016/j.neuropsychologia.2004.06.022 10.1016/j.jalz.2011.03.003 10.1212/WNL.46.3.700 10.1001/jama.1993.03500180078038 10.1016/S0896-6273(02)00569-X 10.1001/jamaneurol.2014.2031 10.1021/jm030026b 10.1002/ana.20009 10.1016/j.neurobiolaging.2009.07.002 10.1212/WNL.0000000000000431 10.1002/ana.22628 10.1001/archneur.1992.00530360051017 10.1016/j.neuroimage.2015.02.011 Venneri A., 2016, Paradigm shift: semantic memory decline as a biomarker of preclinical Alzheimer's disease, Biomark Med, 10, 5, 10.2217/bmm.15.53 Eastman J.A., 2013, Cortical thickness and semantic fluency in Alzheimer's disease and mild cognitive impairment, Am J Alzheimers Dis (Columbia), 1, 81 10.1093/arclin/14.6.481 10.1016/j.trci.2016.12.001