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Laske, Christoph

0009-0009-3434-936X

Mayo Clinic

German Center for Neurodegenerative Diseases

Citations 28

Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease
Brown, Belinda M. , Sohrabi, Hamid R. , Taddei, Kevin , Gardener, Samantha L. , Rainey‐Smith, Stephanie R. , Peiffer, Jeremiah J. , Xiong, Chengjie , Fagan, Anne M. , Benzinger, Tammie L.S. , Buckles, Virginia, Erickson, Kirk I. , Clarnette, Roger, Shah, Tejal , Masters, Colin L. , Weiner, Michael W. , Cairns, Nigel J., Rossor, Martin N. , Graff‐Radford, Neill R. , Salloway, Stephen , Vöglein, Jonathan , Laske, Christoph , Noble, James M. , Schofield, Peter R. , Bateman, Randall J. , Morris, John C. , Martins, Ralph N. , Schofield, Peter R , Bateman, Randall J , Masters, Colin L , Vöglein, Jonathan , Benzinger, Tammie L S , Morris, John C , Noble, James M

Alzheimer's & Dementia | May 11, 2017 | Volume: 13 | Issue: 11 | Pages: 1197-1206

10.1016/j.jalz.2017.03.008 Get It

AbstractIntroductionThe objective of this study was to evaluate the relationship between self‐reported exercise levels and Alzheimer's disease (AD) biomarkers, in a cohort of autosomal dominant AD mutation carriers.MethodsIn 139 presymptomatic mutation carriers from the Dominantly Inherited Alzheimer Network, the relationship between self‐reported exercise levels and brain amyloid load, cerebrospinal fluid (CSF) Aβ42, and CSF tau levels was evaluated using linear regression.ResultsNo differences in brain amyloid load, CSF Aβ42, or CSF tau were observed between low and high exercise groups. Nevertheless, when examining only those already accumulating AD pathology (i.e., amyloid positive), low exercisers had higher mean levels of brain amyloid than high exercisers. Furthermore, the interaction between exercise and estimated years from expected symptom onset was a significant predictor of brain amyloid levels.DiscussionOur findings indicate a relationship exists between self‐reported exercise levels and brain amyloid in autosomal dominant AD mutation carriers.
F5‐02‐03: BDNF VAL66MET Moderates Cognitive Impairment, Neuronal Dysfunction and TAU in Preclinical Autosomal Dominant Alzheimer's Disease
Fagan, Anne M. , Benzinger, Tammie Lee Smith, Ricardo, Allegri, Chhatwal, Jasmeer P. , Farlow, Martin R. , Graff‐Radford, Neill R. , Laske, Christoph , Ringman, John M. , Salloway, Stephen , Lim, Yen Ying , Hassenstab, Jason , Cruchaga, Carlos , Goate, Alison , Benzinger, Tammie L.S. , Maruff, Paul , Snyder, Peter J. , Masters, Colin L. , Allegri, Ricardo , Xiong, Chengjie , McDade, Eric , Rossor, Martin N. , Schofield, Peter William , Holtzman, David M. , Morris, John C. , Bateman, Randall J.

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_7 | Pages: No page available

10.1016/j.jalz.2016.06.689 Get It

O2‐03‐02: are White Matter Hyperintensities a Core Feature of Alzheimer’s Disease or Just a Reflection of Amyloid Angiopathy? Evidence From the Dominantly Inherited Alzheimer Network (DIAN)
Zimmerman, Molly E. , Viqar, Fawad, Narkhede, Atul, Benzinger, Tammie Lee Smith, Marcus, Daniel S., Cairns, Nigel J. , Buckles, Virginia, Saykin, Andy J., Ringman, John M. , Ryan, Natalie S. , Förster, Stefan , Laske, Christoph , Salloway, Stephen , Correia, Stephen , Weiner, Michael W. , Mayeux, Richard , Lee, Seonjoo , Tosto, Giuseppe , Goate, Alison , Fox, Nick C. , Holtzman, David M. , Ghetti, Bernardino , McDade, Eric , Martins, Ralph N. , Saykin, Andy J., Masters, Colin L. , Schofield, Peter R. , Sperling, Reisa Anne , Bateman, Randall J. , Morris, John C. , Jack, Clifford R. , Brickman, Adam M.

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_4 | Pages: No page available

10.1016/j.jalz.2016.06.406 Get It

White matter hyperintensities are a core feature of Alzheimer's disease: Evidence from the dominantly inherited Alzheimer network
Lee, Seonjoo , Viqar, Fawad, Zimmerman, Molly E. , Narkhede, Atul, Benzinger, Tammie L.S. , Marcus, Daniel S. , Fagan, Anne M. , Goate, Alison , Fox, Nick C. , Cairns, Nigel J., Buckles, Virginia, Martins, Ralph N. , Saykin, Andrew J. , Masters, Colin L. , Ringman, John M. , Ryan, Natalie S. , Förster, Stefan , Laske, Christoph , Schofield, Peter R. , Salloway, Stephen , Correia, Stephen , Jack, Clifford R. , Weiner, Michael W. , Bateman, Randall J. , Morris, John C. , Mayeux, Richard , Network, for the Dominantly Inherited Alzheimer, Tosto, Giuseppe , Holtzman, David M. , Ghetti, Bernardino , McDade, Eric , Sperling, Reisa Anne , Brickman, Adam M. , Network, for the Dominantly Inherited Alzheimer, Jack, Clifford R , Saykin, Andrew J , Schofield, Peter R , Bateman, Randall J , Masters, Colin L , Benzinger, Tammie L S , Fox, Nick C , Morris, John C , Goate, Alison M

Annals of Neurology | March 26, 2016 | Volume: 79 | Issue: 6 | Pages: 929-939

10.1002/ana.24647 Get It

ObjectiveWhite matter hyperintensities (WMHs) are areas of increased signal on T2‐weighted magnetic resonance imaging (MRI) scans that most commonly reflect small vessel cerebrovascular disease. Increased WMH volume is associated with risk and progression of Alzheimer's disease (AD). These observations are typically interpreted as evidence that vascular abnormalities play an additive, independent role contributing to symptom presentation, but not core features of AD. We examined the severity and distribution of WMH in presymptomatic PSEN1, PSEN2, and APP mutation carriers to determine the extent to which WMH manifest in individuals genetically determined to develop AD.MethodsThe study comprised participants (n = 299; age = 39.03 ± 10.13) from the Dominantly Inherited Alzheimer Network, including 184 (61.5%) with a mutation that results in AD and 115 (38.5%) first‐degree relatives who were noncarrier controls. We calculated the estimated years from expected symptom onset (EYO) by subtracting the affected parent's symptom onset age from the participant's age. Baseline MRI data were analyzed for total and regional WMH. Mixed‐effects piece‐wise linear regression was used to examine WMH differences between carriers and noncarriers with respect to EYO.ResultsMutation carriers had greater total WMH volumes, which appeared to increase approximately 6 years before expected symptom onset. Effects were most prominent for the parietal and occipital lobe, which showed divergent effects as early as 22 years before estimated onset.InterpretationAutosomal‐dominant AD is associated with increased WMH well before expected symptom onset. The findings suggest the possibility that WMHs are a core feature of AD, a potential therapeutic target, and a factor that should be integrated into pathogenic models of the disease. Ann Neurol 2016;79:929–939
Guidelines for the standardization of preanalytic variables for blood‐based biomarker studies in Alzheimer's disease research
O’Bryant, Sid E. , Gupta, Veer Bala , Henriksen, Kim , Jeromin, Andreas, Lista, Simone , Bazenet, Chantal, Soares, Holly , Lovestone, Simon , Hampel, Harald , Montine, Thomas J. , Blennow, Kaj , Foroud, Tatiana, Carrillo, María C. , Graff‐Radford, Neill R. , Laske, Christoph , Breteler, Monique M.B. , Shaw, Leslie M. , Trojanowski, John Q. , Schupf, Nicole , Fagan, Anne M. , Oberoi, Pankaj, Umek, Robert M., Weiner, Michael W. , Grammas, Paula , Posner, Holly, Martins, Ralph N. , groups, STAR-B and BBBIG working, Edwards, Melissa , Rissman, Robert A. , groups, STAR-B and BBBIG working, O'Bryant, Sid

Alzheimer's & Dementia | October 1, 2014 | Volume: 11 | Issue: 5 | Pages: 549-560

10.1016/j.jalz.2014.08.099 Get It

Abstract The lack of readily available biomarkers is a significant hindrance toward progressing to effective therapeutic and preventative strategies for Alzheimer's disease (AD). Blood‐based biomarkers have potential to overcome access and cost barriers and greatly facilitate advanced neuroimaging and cerebrospinal fluid biomarker approaches. Despite the fact that preanalytical processing is the largest source of variability in laboratory testing, there are no currently available standardized preanalytical guidelines. The current international working group provides the initial starting point for such guidelines for standardized operating procedures (SOPs). It is anticipated that these guidelines will be updated as additional research findings become available. The statement provides (1) a synopsis of selected preanalytical methods utilized in many international AD cohort studies, (2) initial draft guidelines/SOPs for preanalytical methods, and (3) a list of required methodological information and protocols to be made available for publications in the field to foster cross‐validation across cohorts and laboratories.
P1–229: sTNF‐R1 as a biomarker of Alzheimer's disease varies by APOE‐ε4 status
Edwards, Melissa, Como, Tori, Hall, James , Laske, Christoph , Graff‐Radford, Neill R. , Devous, Michael D. , Johnson, Leigh , Barber, Robert C. , O’Bryant, Sid E.

Alzheimer's & Dementia | October 9, 2013 | Volume: 9 | Issue: 4S_Part_6 | Pages: No page available

10.1016/j.jalz.2013.05.453 Get It

Biomarkers in Alzheimer's Disease and Lewy Body Disorders with Dementia
Leyhe, Thomas, Darreh‐Shori, Taher , Laske, Christoph , Mielke, Michelle M. , Maetzler, Walter , Mielke, Michelle M

International Journal of Alzheimer's Disease | January 9, 2013 | Volume: 2013 | Issue: No issue available | Pages: 1-2

10.1155/2013/473181 Get It