Characterizing heterogeneity in Alzheimer’s disease progression: a semiparametric model

The progression of Alzheimer's disease (AD), a leading cause of dementia worldwide, is known for its variability and complexity, challenging the conventional methods of monitoring and predicting disease trajectories. This study introduces a semiparametric modeling approach to analyze longitudinal cognitive and imaging data. We studied two different outcome variables from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database: the Alzheimer's Disease Assessment Scale-Cognitive Subscale 13 (ADAS13) scores and ventricular volumes [Formula: see text]. Unlike traditional linear mixed effects models, semiparametric models do not assume a linear AD progression over time. Semiparametric models offer the advantage of capturing the non-linear features of AD progression, such as cognitive decline and neurodegeneration, represented by changes in ADAS13 scores and ventricular enlargement, respectively. By integrating regression splines and mixed modeling techniques, we provide a nuanced understanding of AD progression that captures the heterogeneity of disease trajectories. Our analysis reveals variations in the timing and degree of cognitive decline and neurodegeneration among AD patients, underlining the need for personalized approaches for monitoring and managing AD. This study's findings contribute to the modeling of AD progression and offer potential implications for interventions and prognostic assessments in clinical and research settings.

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Publication Details

Journal
Scientific Reports
Published
2025-03-05
DOI
https://doi.org/10.1038/s41598-025-92540-5
Citations
5
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
7.36
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article

Characterizing heterogeneity in Alzheimer’s disease progression: a semiparametric model

Christopher G. Kevil, Mohammad Alfrad Nobel Bhuiyan, John A. Vanchiere, Emrah Gecili et al.
5 citations
Scientific Reports
Dementia and Cognitive Impairment Research
7.36
article

Characterizing heterogeneity in Alzheimer’s disease progression: a semiparametric model

Christopher G. Kevil, Mohammad Alfrad Nobel Bhuiyan, John A. Vanchiere, Emrah Gecili, Elizabeth A. Disbrow, Steven A. Conrad, Md. Shenuarin Bhuiyan, Fatih Gelir, Suneel Babu Chatla
article en
5 citations

Abstract

The progression of Alzheimer's disease (AD), a leading cause of dementia worldwide, is known for its variability and complexity, challenging the conventional methods of monitoring and predicting disease trajectories. This study introduces a semiparametric modeling approach to analyze longitudinal cognitive and imaging data. We studied two different outcome variables from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database: the Alzheimer's Disease Assessment Scale-Cognitive Subscale 13 (ADAS13) scores and ventricular volumes [Formula: see text]. Unlike traditional linear mixed effects models, semiparametric models do not assume a linear AD progression over time. Semiparametric models offer the advantage of capturing the non-linear features of AD progression, such as cognitive decline and neurodegeneration, represented by changes in ADAS13 scores and ventricular enlargement, respectively. By integrating regression splines and mixed modeling techniques, we provide a nuanced understanding of AD progression that captures the heterogeneity of disease trajectories. Our analysis reveals variations in the timing and degree of cognitive decline and neurodegeneration among AD patients, underlining the need for personalized approaches for monitoring and managing AD. This study's findings contribute to the modeling of AD progression and offer potential implications for interventions and prognostic assessments in clinical and research settings.

Scientific ReportsVol. 15(1)
Cincinnati Children's Hospital Medical Center (US), The University of Texas at El Paso (US), University of Cincinnati (US), Louisiana State University Health Sciences Center Shreveport (US)
Openalex Percentile: Top 3%
Dementia and Cognitive Impairment Research
7.36
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