98%
921
2 minutes
20
Longitudinal studies are commonly used to examine possible causal factors associated with human health and disease. However, the statistical models, such as two-way ANOVA, often applied in these studies do not appropriately model the experimental design, resulting in biased and imprecise results. Here, we describe the linear mixed effects (LME) model and how to use it for longitudinal studies. We re-analyze a dataset published by Blanton et al. in 2016 that modeled growth trajectories in mice after microbiome implantation from nourished or malnourished children. We compare the fit and stability of different parameterizations of ANOVA and LME models; most models found that the nourished versus malnourished growth trajectories differed significantly. We show through simulation that the results from the two-way ANOVA and LME models are not always consistent. Incorrectly modeling correlated data can result in increased rates of false positives or false negatives, supporting the need to model correlated data correctly. We provide an interactive Shiny App to enable accessible and appropriate analysis of longitudinal data using LME models.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092652 | PMC |
http://dx.doi.org/10.1242/dmm.048025 | DOI Listing |
Epilepsy Behav
September 2025
Department of Neurology, Washington University School of Medicine, 660 Euclid Ave., Campus Box 8111, St. Louis, MO, USA; Institute of Public Health, Washington University in St. Louis, 600 S Taylor Ave, St. Louis, MO 63110, USA.
Objectives: Insufficient data exist for driving risk for people with epilepsy (PWE). This longitudinal, retrospective case-control study examines the differences in driving behaviors among older adults with/without epilepsy history using a novel naturalistic driving datalogger.
Methodology: Eligible participants were cognitively normal ([CDR] = 0) or had mild cognitive impairment (MCI) ([CDR] = 0.
J Affect Disord
August 2025
College of Artificial Intelligence, Southwest University, Chongqing 400715, China. Electronic address:
Introduction: Chronic pain and depression are closely related among older adults. However, little is known about gender differences in the comorbidity of chronic pain and depression, as well as the underlying mechanisms.
Method: Using data from the China Health and Retirement Longitudinal Study (CHARLS, N = 13,712), this study combined cross-sectional network analysis and longitudinal linear mixed-effects models (LME) to investigate gender-specific patterns in the pain-depression interaction across three waves (2011-2015).
Alzheimers Dement
August 2025
Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, California, USA.
Tauopathies are neurodegenerative diseases characterized by pathological tau protein inclusions and dementia. Tauopathy mouse models with MAPT mutations replicate tau-related pathologies and are widely used for therapeutic research. This scoping review examines 409 treatment evaluations in MAPT mouse models.
View Article and Find Full Text PDFAnal Chim Acta
October 2025
Department of Pharmacy, University of Oslo, P.O Box 1068, Blindern, 0316, Oslo, Norway; Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark. Electronic address:
Background: Three-phase liquid membrane extraction (LME) of acids involves mass transfer from an acidified sample, through an organic liquid membrane into an alkaline aqueous acceptor. However, this approach presents challenges for acids with pK > 9-10, as their efficient extraction often requires extreme pH conditions in the acceptor, which can compromise chemical stability and compatibility with chromatographic analysis. Alternatively, a polar organic solvent can be used as acceptor, but this may challenge the stability of the liquid membrane and the integrity of the extraction system.
View Article and Find Full Text PDFJ Alzheimers Dis
August 2025
Department of Neurology, Washington University School of Medicine, St Louis, MO, USA.
BackgroundIdentifying predictive biomarkers of cognitive decline is critical for timely intervention in early Alzheimer's disease and related dementia. Biomarkers such as cerebrospinal fluid (CSF) neurofilament light (NfL), and MRI-based hippocampal atrophy are potential indicators of neurodegeneration, but their long-term predictive value remains unclear.ObjectiveThis study examined 20-year longitudinal associations between CSF NfL, MRI-based hippocampal atrophy, and cognitive decline in cognitively normal older adults.
View Article and Find Full Text PDF