A Bayesian hierarchical change point model with parameter constraints

2020 ◽  
pp. 096228022094809
Author(s):  
Hong Li ◽  
Andreana Benitez ◽  
Brian Neelon

Alzheimer’s disease is the leading cause of dementia among adults aged 65 or above. Alzheimer’s disease is characterized by a change point signaling a sudden and prolonged acceleration in cognitive decline. The timing of this change point is of clinical interest because it can be used to establish optimal treatment regimens and schedules. Here, we present a Bayesian hierarchical change point model with a parameter constraint to characterize the rate and timing of cognitive decline among Alzheimer’s disease patients. We allow each patient to have a unique random intercept, random slope before the change point, random change point time, and random slope after the change point. The difference in slope before and after a change point is constrained to be nonpositive, and its parameter space is partitioned into a null region (representing normal aging) and a rejection region (representing accelerated decline). Using the change point time, the estimated slope difference, and the threshold of the null region, we are able to (1) distinguish normal aging patients from those with accelerated cognitive decline, (2) characterize the rate and timing for patients experiencing cognitive decline, and (3) predict personalized risk of progression to dementia due to Alzheimer’s disease. We apply the approach to data from the Religious Orders Study, a national cohort study of aging Catholic nuns, priests, and lay brothers.

2016 ◽  
Vol 12 ◽  
pp. P100-P100
Author(s):  
Michelle E. Farrell ◽  
Kristen M. Kennedy ◽  
Karen M. Rodrigue ◽  
Gagan S. Wig ◽  
Gérard N. Bischof ◽  
...  

2016 ◽  
Vol 12 ◽  
pp. P938-P938 ◽  
Author(s):  
Michelle E. Farrell ◽  
Kristen M. Kennedy ◽  
Karen M. Rodrigue ◽  
Gagan S. Wig ◽  
Gérard N. Bischof ◽  
...  

2012 ◽  
Vol 39 (2) ◽  
pp. 73-83 ◽  
Author(s):  
Lei Yu ◽  
Patricia Boyle ◽  
Robert S. Wilson ◽  
Eisuke Segawa ◽  
Sue Leurgans ◽  
...  

PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0244180
Author(s):  
Amir H. Meghdadi ◽  
Marija Stevanović Karić ◽  
Marissa McConnell ◽  
Greg Rupp ◽  
Christian Richard ◽  
...  

In this paper, we explore the utility of resting-state EEG measures as potential biomarkers for the detection and assessment of cognitive decline in mild cognitive impairment (MCI) and Alzheimer’s disease (AD). Neurophysiological biomarkers of AD derived from EEG and FDG-PET, once characterized and validated, would expand the set of existing diagnostic molecular biomarkers of AD pathology with associated biomarkers of disease progression and neural dysfunction. Since symptoms of AD often begin to appear later in life, successful identification of EEG-based biomarkers must account for age-related neurophysiological changes that occur even in healthy individuals. To this end, we collected EEG data from individuals with AD (n = 26), MCI (n = 53), and cognitively normal healthy controls stratified by age into three groups: 18–40 (n = 129), 40–60 (n = 62) and 60–90 (= 55) years old. For each participant, we computed power spectral density at each channel and spectral coherence between pairs of channels. Compared to age matched controls, in the AD group, we found increases in both spectral power and coherence at the slower frequencies (Delta, Theta). A smaller but significant increase in power of slow frequencies was observed for the MCI group, localized to temporal areas. These effects on slow frequency spectral power opposed that of normal aging observed by a decrease in the power of slow frequencies in our control groups. The AD group showed a significant decrease in the spectral power and coherence in the Alpha band consistent with the same effect in normal aging. However, the MCI group did not show any significant change in the Alpha band. Overall, Theta to Alpha ratio (TAR) provided the largest and most significant differences between the AD group and controls. However, differences in the MCI group remained small and localized. We proposed a novel method to quantify these small differences between Theta and Alpha bands’ power using empirically derived distributions of spectral power across the time domain as opposed to averaging power across time. We defined Power Distribution Distance Measure (PDDM) as a distance measure between probability distribution functions (pdf) of Theta and Alpha power. Compared to average TAR, using PDDF enhanced the statistical significance, the effect size, and the spatial distribution of significant effects in the MCI group. We designed classifiers for differentiating individual MCI and AD participants from age-matched controls. The classification performance measured by the area under ROC curve after cross-validation were AUC = 0.85 and AUC = 0.6, for AD and MCI classifiers, respectively. Posterior probability of AD, TAR, and the proposed PDDM measure were all significantly correlated with MMSE score and neuropsychological tests in the AD group.


2015 ◽  
Vol 11 (7S_Part_17) ◽  
pp. P784-P784
Author(s):  
Naira Goukasian ◽  
Holly LeClair ◽  
Kristy S. Hwang ◽  
John M. Ringman ◽  
Jeffrey L. Cummings ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Karolina Kauppi ◽  
Michael Rönnlund ◽  
Annelie Nordin Adolfsson ◽  
Sara Pudas ◽  
Rolf Adolfsson

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