Welcome to the AD/PD™ 2022 Interactive Program

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Displaying One Session

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132

PROGRESSION OF SELF-PERCIEVED SPEECH AND SWALLOWING IMPAIRMENT IN NON-ADVANCED STAGES OF PARKINSON’S DISEASE

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132
Lecture Time
05:15 PM - 05:30 PM

Abstract

Aims

To assess changes in patient perceptions of speech and swallowing impairments associated with Parkinson’s disease across the first six years post-diagnosis.

Methods

Data from the Unified Parkinson’s Disease Rating Scale (UPDRS) was obtained for 269 newly diagnosed people with PD across the first six years post-diagnosis (baseline, and then annual assessments through year six). Data from UPDRS scale items associated with “speech” and “swallowing” were collated across each assessment time point. The rate of change over time was assessed using parametric and non-parametric statistical analyses.

Results

Self-perceived speech and swallowing impairments were identified as mild at the time of initial diagnosis and progressed within the mild range of impairment across six years. The rate of change over time was significant for perceived speech impairment ([F(5.5, 1158.8) = 21.1, p <.001) and perceived swallowing impairment ([F(5.2, 1082.6) = 8.6, p <.001). There were no effects of age at diagnosis or motor phenotype on the rate of change for either speech or swallowing.

Conclusions

Self-perceptions of speech and swallowing impairment changed significantly over time in newly diagnosed PWPD. The presence of self-perceived mild speech and swallowing impairments in the initial years post-diagnosis may support the need for intervention to improve and or sustain function over time.

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FRONTOPARIETAL CONTROL NETWORK CHANGES MAINTAINED 1 YEAR AFTER COGNITIVE TRAINING IN HEALTHY OLDER ADULTS

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132
Lecture Time
05:30 PM - 05:45 PM

Abstract

Aims

Cognitive training may reduce dementia risk and mitigate cognitive aging. Prior research shows the connectivity of higher-order resting-state networks (RSN) of inter-network modulation (frontoparietal control network; FPCN) and executive functioning (cingulo-opercular network; CON) may improve acutely after cognitive training. It is unknown whether RSN changes maintain after cognitive training ends. This study examined FPCN and CON connectivity 1-year after cognitive training healthy older adults.

Methods

58 healthy older adults (mean age=71.2) were randomized into a cognitive training (CT; n=30) or an educational control (ET; n=28) group. Over 12-weeks, CT underwent 40-hours of 4 attention/speed-of-processing and 4 working memory tasks, and ET watched 40-hours of educational videos. Participants randomly received sham or active transcranial direct current stimulation, although this was not a variable of interest in this study. Participants underwent resting-state functional magnetic resonance imaging at baseline, 3-month, and 1-year time points. Mixed linear models assessed group differences/change in FPCN and CON connectivity from 3-month to 1-year timepoints, controlling for baseline connectivity, age, sex, education, scanner, and tDCS. There were no group differences in baseline FPCN or CON.

Results

FPCN group main effect showed higher CT 3-month connectivity maintains at 1-year timepoint [beta=-.039;p=.010;95%CI:-.070--.009). CON group main effect or group by time interactions were not significant.

Conclusions

Increased FPCN connectivity maintains at least 1-year post cognitive training, although power analysis recommends a larger sample size. The FPCN may be a neural target to strengthen cognitive training response and could be involved in reduced dementia risk. Future studies should assess this effect in a larger group.

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THE MEDIATING ROLES OF NEURO-BIOMARKERS IN THE RELATIONSHIP BETWEEN EDUCATION AND LATER-LIFE COGNITION.

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132
Lecture Time
05:45 PM - 06:00 PM

Abstract

Aims

Background: Increased education has been associated with reduced risk of Alzheimer’s disease and related dementias (ADRD). The role of neuropathies and neurovascular damage in the education-cognition relationship are poorly understood and may differ by sex.

Objective: To determine: 1) whether ADRD biomarkers mediate the relationship between education and cognitive function and 2) whether these mediating relationships differ by sex.

Methods

Methods: Participants included 537 adults (ages 55-94 years, mean=73) from the Alzheimer’s Disease Neuroimaging Initiative - 3 (ADNI 3) with complete data on education (years), cognition (episodic memory (EM), executive functioning (EF), language (LANG) composites), and neuroimaging. Neuroimaging mediators included hippocampal (HV), cortical grey matter (CGMV), and white matter hyperintensity (WMH) volumes and meta-temporal tau PET standard uptake value ratio. We performed causal mediation analyses with education as the exposure, HV, CGMV, WMH, and meta-temporal tau as separate mediating factors, and each cognitive domain score as separate outcomes, adjusting for age, race, sex, cardiovascular history, BMI, depression, and APOE4 status. Secondary analyses analyzed sex-stratified mediation models.

Results

Results: Across domains, HV mediated the largest percent of the relationship between education and cognition (EM: 15.7%, EF: 14.5%, LANG: 11.4%) compared to CGMV, WMH, and tau PET. In sex-stratified models, HV mediated education’s associations with EM and EF among women (EM: 20.2%, p=0.03; EF: 19.8%, p=0.05) but not men.

Conclusions

Conclusions: HV mediated the largest percent of the relationship between education and cognition. The neurobiological mechanisms (e.g., hippocampal and chronic vascular risk pathways) through which education impacts later-life cognition may vary between men and women.

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EEG AS A MARKER OF PSYCHIATRIC AND COGNITIVE SYMPTOMS IN PRODROMAL DEMENTIA WITH LEWY BODIES

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132
Lecture Time
06:00 PM - 06:15 PM

Abstract

Abstract Body

Background: Electrophysiological markers of prodromal dementia with Lewy bodies
were described in the spectral domain. The sub-second temporal resolution may provide additional information.
Objective: 1. To evaluate electroencephalography (EEG) microstates in patients with mild cognitive impairment with Lewy bodies (MCI-LB) and to assess the association between their temporal dynamics and the spectral marker, 2. To assess EEG microstate changes with the disease progression at 1year follow-up visit and the association with psychiatric and cognitive symptoms.
Methods: Temporal parameters of EEG microstates were compared between 21 patients with MCI-LB and 21 healthy controls. The dominant alpha frequency was correlated with microstate parameters. Changes in EEG microstates were assessed in the MCI-LB at 1-year follow-up visit and correlated with depressive symptoms and cognitive outcomes.
Results: Microstates A-D showed higher occurrence in the patient group. Microstate B which is attributed to the visual network revealed shorter mean duration and increased time coverage; its occurrence correlated with the dominant alpha frequency in the patient group. At one-year follow-up, MCI-LB subjects demonstrated higher time coverage, occurrence and duration of microstate D (which is attributed to the he frontoparietal network) as compared to the baseline visit. The changes in microstate D parameters were related to psychiatric symptoms changes and cognitive decline in the MCI-LB group.
Conclusions: Temporal dynamics of all EEG microstates were altered in medication-naïve subjects with prodromal dementia with Lewy bodies. Longitudinal
follow-up revealed changes in the microstate engaged in attention and executive function that correlated with both cognitive and affective symptoms of MCI-LB.

The study was supported by the AZV grant of the Czech Ministry of Health NU20-04-00294 and European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 734718 (CoBeN).
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TBA

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132
Lecture Time
06:15 PM - 06:30 PM

DISCUSSION

Session Type
SYMPOSIUM
Date
Thu, 17.03.2022
Session Time
05:15 PM - 06:45 PM
Room
ONSITE: 131-132
Lecture Time
06:30 PM - 06:45 PM