Longitudinal data with incomplete entries pose a significant challenge for clinical score regression over multiple time points. Although many methods primarily estimate longitudinal scores with complete baseline features (i.e., features collected at the initial time point), such snapshot features may overlook beneficial latent longitudinal traits for generalization. Alternatively, certain completion approaches (e.g., tensor decomposition technology) have been proposed to impute incomplete longitudinal data before score estimation, most of which, however, are transductive and cannot utilize label semantics. This work presents a tensor coupled learning (TCL) paradigm of incomplete longitudinal features and labels for clinical score regression. The TCL enjoys three advantages: 1) It drives semantic-aware factor matrices and collaboratively deals with incomplete longitudinal entries (of features and labels), during which a dynamic regularizer is designed for adaptive attribute selection. 2) It establishes a closed loop connecting baseline features and the coupled factor matrices, which enables inductive inference of longitudinal scores relying on only baseline features. 3) It reinforces the information encoding of baseline data by preserving the local manifold of longitudinal feature space and detecting the temporal alteration across multiple time points. Extensive experiments demonstrate the remarkable performance improvement of our method on clinical score regression with incomplete longitudinal data.
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http://dx.doi.org/10.1109/TPAMI.2024.3471800 | DOI Listing |
Stat Med
February 2025
Clinical Epidemiology & Biostatistics (CEBU), Murdoch Children's Research Institute, Parkville, Australia.
Longitudinal studies are frequently used in medical research and involve collecting repeated measures on individuals over time. Observations from the same individual are invariably correlated and thus an analytic approach that accounts for this clustering by individual is required. While almost all research suffers from missing data, this can be particularly problematic in longitudinal studies as participation often becomes harder to maintain over time.
View Article and Find Full Text PDFJ Biomed Sci
January 2025
Neurosciences, Biomedical Research Institute, Hasselt University, Agoralaan Building C, 3590, Diepenbeek, Belgium.
Background: Deficient DNA repair and excessive DNA damage contribute to neurodegenerative disease. However, the role of DNA damage and repair in spinal cord injury (SCI) is unclear. SCI, a debilitating disruption of the structural and biological network of the spinal cord, is characterized by oxidative stress.
View Article and Find Full Text PDFClin Orthop Relat Res
January 2025
Department of Orthopaedic Surgery, Mayo Clinic, Phoenix, AZ, USA.
Background: Resilience refers to the ability to adapt or recover from stress. There is increasing appreciation that it plays an important role in wholistic patient-centered care and may affect patient outcomes, including those of orthopaedic surgery. Despite being a focus of the current orthopaedic evidence, there is no strong understanding yet of whether resilience is a stable patient quality or a dynamic one that may be modified perioperatively to improve patient-reported outcome scores.
View Article and Find Full Text PDFJ Vet Intern Med
January 2025
Department of Small Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Background: The pathophysiology of polyuria and polydipsia secondary to exogenous glucocorticoid excess is incompletely understood.
Objective: Investigate plasma AVP (pAVP) and serum CoP (sCoP) concentrations in healthy dogs before, during, and after abrupt discontinuation of a long-term course of orally administered prednisolone.
Animals: Eight healthy neutered young adult research Beagles.
The long-term effects of repeated COVID-19 vaccinations on adaptive immunity remain incompletely understood. Here, we conducted a comprehensive three-year longitudinal study examining T cell and antibody responses in 78 vaccinated individuals without reported symptomatic infections. We observed distinct dynamics in Spike-specific humoral and cellular immune responses across multiple vaccine doses.
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