The role of arterial pulsatility and white matter microstructure in age-related cognitive decline

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THE PRIORITY RESEACE CENTRE FOR TRANSLATIONAL NEUROSCIENCE AND MENTAL HEALTH The role of arterial pulsatility and white matter microstructure in age-related cognitive decline T.Jolly, P.Michie, G.Bateman R.Fulham P.Cooper, C.Levi, M.Parsons & F.Karayanidis. Functional Neuroimaging Laboratory

Age-related cognitive decline Ageing population (population aged >65 yo expected to double over the next 20 years) Loss of independence Poorer outcomes for elderly Increase risk of late life depression Places increased demand on carers Increased burden on health care system

Trajectories in cognitive decline with age Goh et al., (2012). Psychol Aging 27(3), 707-719

Considerable variability in some trajectories Goh et al., (2012). Psychol Aging 27(3), 707-719

Trajectories in cognitive decline with age Variable trajectory (one size does not fit all) Some adults maintain high functioning well into later life (Super agers) Age-related decline more noticeable for certain functions Understanding what drives these differences is important for being able to detect early stages of cognitive decline

White matter and age-related cognitive decline Considerable research on the topic Partial support for the view that age-related cognitive decline is mediated by changes within cerebral white matter Some dispute as to which cognitive functions are influenced by white matter changes (memory vs executive function vs processing speed deficits) Strongest findings detected in studies that have measured microstructural properties of white matter vs macrostructural changes

Task switching paradigm Use of contextual cues to flexibly alternate between tasksets Single task block Continued performance of one task in isolation Mixed task block Switching between two alternative tasks as indicated by contextual cues For review see: Karayanidis, Jamadar, Ruge, Phillips, Heathcote, Forstmann, 2010 Mixing cost = repeat trials in mixed-task block vs single-task block Influenced by level of target interference

Task switching in ageing Variability in proactive and reactive cognitive control processes across the adult lifespan Frini Karayanidis *, Lisa R. Whitson, Andrew Heathcote and Patricia T. Michie Frontiers in Psychology 2011 Task practice differentially modulates task-switching performance across the adult lifespan Lisa R. Whitson, Frini Karayanidis *, Patricia T. Michie Acta Psychologica 139 (2012) 124-136 Consistent finding of increased mixing-cost in older adults -Increased demands placed on working memory -Greater task ambiguity -Failure to fully disengage alternative task

Fronto-parietal involvement in task switching Cerebral white matter integrity and cognitive aging: Contributions from diffusion tensor imaging. Madden D, Bennett H, and Song A. Neuropsychol Rev 2009 Age-related slowing of task switching is associated with decreased integrity of frontoparietal white matter. Gold B, Powell D, Liang X, Jicha G and Smith C. Neurobiology of aging Demonstrated importance of frontoparietal white matter in task-switching However, did not investigate the influence of diffuse white matter changes in task switching and whether these effects were regionally specific or whether they can be just as easily accounted for by gross changes

Current Study Is the degree in which age related decline in cognitive control related to changes in structural integrity of white matter Participants Healthy older adults Mild ischaemic attack Neuropsych measures WASI, MoCA WMS LM Digit Span, choice RT CANTAB (IED, SWM, SOC, SSP, PRM) Expt tasks with ERPs Cued-trials task-switching Stop-signal Functional Measures Functional Assessment Questionnaire Geriatric Depression Scale SF-36 DASS-42 Imaging Siemens 3T Verio T1 structural (MPRAGE) Fluid Attenuated Inversion Recovery (FLAIR) Diffusion Weighted Imaging (DWI) sequence Test Re-test @ 20-24mo

70 participants Sample characteristics 35 recruited from HMRI volunteer register 35 recruited from neurology clinic Measure Mean (SD) Range Age (yrs) 66.79 (9.54) 43-87 years FSIQ 111.64 (14.60) 81-141 MoCA 25.97 (3.11) 17-30 Clinical profile Yes No Vascular risk factors present 39 (56%) 31 (44%) Hypertension 27 (39%) Hypercholesterolemia 21 (30%) Atrial fibrillation 11 (16%) Multiple vascular risk factors 24 (34%)

Cognitive domains Working memory Digit span (WAIS-IV) Spatial span (CANTAB) Spatial working (CANTAB) Executive Function Stockings of Cambridge (CANTAB) Intra-extra dimensional set shift (CANTAB) Episodic memory Logical memory (WMS-IV) Pattern Recognition memory (CANTAB) Processing speed Choice RT Letter classification task Number classification task

Cue-target interval = 1000ms Response-cue interval = 600ms Task switching Outcome measures: Error mixing-cost RT mixing-cost For both neutral and incongruent target types

White matter tractography White matter connections estimated using high b-value diffusion weighted MRI (b = 3000, 64 directions on Siemens 3T Verio with 32 channel head coil) Probabilistic whole brain tractography was performed using MRTrix software to derive tractogram Tractogram was then filtered into 18 separate white matter pathways using constraint ROI s derived from a DTI tract atlas from John Hopkins University (JHU).

Measure of WM disruption Macroscopic changes White matter hyperintensities Microscopic environment Mean FA Mean Diffusivity Axial Diffusivity Radial Diffusivity Hua et al., (2008). Neuroimage, 39(1), 336-347.

Correlation table Measure Age White matter RaD Working memory -.365*** -.367*** Episodic memory -.265* -.411*** Executive function -.430*** -.468*** Processing speed -.494*** -.676*** *p<.05, **p<.01, ***p<.001 Both increasing age and white matter disruption associated with poorer performance across multiple cognitive domains

Correlations with age controlling for white matter radial diffusivity Measure Working memory Episodic memory Executive function Processing speed Age 72% attenuated 99% attenuated 77% attenuated 93% attenuated White matter RaD Nearly all age related variance in episodic memory and processing speed can be accounted for by variability in white matter radial diffusivity All correlations with age removed after controlling for variability associated with white matter radial diffusivity

Correlations with white matter radial diffusivity controlling for age Measure Working memory Episodic memory Executive function Processing speed Age White matter RaD 71% attenuated 37% attenuated 62% attenuated 35% attenuated Association between white matter radial diffusivity with episodic memory, executive function and processing speed occurs independently of age Correlations between white matter RaD and episodic memory, executive function and processing speed remained significant after controlling for variability associated with age

Executive Function (Z-score) Processing speed (Z-score) Working Memory (Z-score) Episodic Memory (Z-score) 2.5 Working memory 2.5 Episodic memory 1.5 1.5 0.5 0.5-0.5-0.5-1.5-1.5-2.5-2.5 R² = 0.1347-3.5 0.38 0.43 0.48 0.53 R² = 0.1686-3.5 0.38 0.43 0.48 0.53 White matter RaD White matter RaD Executive function Processing speed 2.5 2.5 1.5 1.5 0.5 0.5-0.5-0.5-1.5-1.5-2.5-2.5-3.5 R² = 0.2189-3.5 R² = 0.4573 0.38 0.43 0.48 0.53 0.38 0.43 0.48 0.53 White matter RaD White matter RaD

Mixing cost (RT) Mixing cost (errors) Mixing costs increase as a function of white matter microstructure 50 40 30 20 10 0 R² = 0.2533-10 0.38 0.43 0.48 0.53 White matter RaD Error mixing cost with white matter microstructure more obvious with high target interference 1500 1300 1100 900 700 500 300 100-100 0.38 0.43 0.48 0.53 White matter RaD R² = 0.1704 RT mixing cost with white matter microstructure more obvious with low target interference

Influence of diffuse vs regional white matter changes on mixing-cost Trial Overall white matter IFOL ILFL SLFL Error mixing cost (incongruent).503***.520***.534***.523*** Error mixing cost (neutral).351**.350**.343**.336** RT mixing cost (incongruent).290**.339**.365**.341** RT mixing cost (neutral).415***.470***.489***.466*** IFOL = Inferior fronto-occipital fasciculus left ILFL = Inferior longitudinal fasciculus left SLFL = Superior longitudinal fasciculus left All of the remaining 15 white matter tracts demonstrated weaker correlations compared to overall white matter.

Influence of diffuse vs regional white matter changes on mixing-cost Trial Overall white matter IFOL ILFL SLFL Error mixing cost (incongruent).503***.520***.534***.523*** Error mixing cost (neutral).351**.350**.343**.336** RT mixing cost (incongruent).290**.339**.365**.341** RT mixing cost (neutral).415***.470***.489***.466*** Remained significant even after controlling for variability associated with overall white matter

anterior IFOL posterior Large degree of spatial overlap between three white matter tracts Provides support for previous studies that highlighted the importance of frontoparietal networks in task switching. ILFL Disruption to task specific networks leads to a decrease in efficiency in task switching, as demonstrated by delayed RT, but does not specifically impact accuracy SLFL

Arterial Pulsatility Index Arterial Pulsatility Index Arterial Pulsatility Index Early detection of microstructural white matter changes associated with arterial pulsatility Todd A.D. Jolly, Grant A. Bateman, Christopher R. Levi, Mark W. Parsons, Patricia T. Michie, Frini Karayanidis* Frontiers in Human Neuroscience 1.7 1.5 1.7 1.5 CVRF absent CVRF present 1.3 1.1 0.9 R² = 0.2323 1.3 1.1 0.9 R² = 0.0159 0.7 0.7 R² = 0.3765 0.5 0.35 0.37 0.39 0.41 0.43 0.45 Mean FA 0.5 0.35 0.37 0.39 0.41 0.43 0.45 Mean FA 1.7 1.5 1.3 1.1 0.9 R² = 0.2201 0.7 0.5 0.39 0.42 0.45 0.48 0.51 0.54 Radial Diffusivity This study demonstrated that increased arterial pulsatility is associated with microstructural changes in the white matter. We postulated that increased arterial pulsatility may increase shear stress to perivascular oligodendrocytes,resulting in demyelination.

We have established Age-related decline in many aspects of cognitive functioning are mediated by changes in white matter microstructure White matter microstructural changes are associated with a decrease in a number of different cognitive domains Cognitive control deficits are associated with disruption to fronto-parietal white matter regions White matter microstructural disruption increases as a function of elevated arterial pulsatility

We did investigate the potential role of arterial pulsatility mediating the relationship between white matter microstructure and cognitive decline. However, the addition of arterial pulsatility as a covariate had little impact on the strength of the association between white matter microstructure and cognitive function. This suggests that while arterial pulsatility is related to changes in white matter microstructure, it does not appear to explain the cognitive decline that associated with microstructural disruption within the white matter.

Research Team Investigators Prof Chris Levi, Neurology A/Prof Mark Parsons, Neurology A/Prof Frini Karayanidis, Psychology Em. Prof Pat Michie, Psychology Dr Grant Bateman, MRI Unit A/Prof Peter Schofield, Neuropsychiatry Dr Ross Fulham, Psychology RHD Todd Jolly Patrick Cooper Clinical Professional Doctorate Syarifah Wan Ahmadul Badwi Undergraduate students Jaime Rennie Programming Tony Kemp In-house software (EEGDisplay) Dr Ross Fulham This project is funded by Hunter Medical Research Institute (HMRI) Project Award to FK as well as APA Scholarship and HMRI RHD Top-Up Award to TJ PRIORITY RESEARCH CENTRE FOR TRANSLATIONAL NEUROSCIENCE AND MENTAL HEALTH