Evidence map›Paper›PMID 42405431›Full record

ArticleAmerican journal of human biology : the official journal of the Human Biology Council2026

A Bayesian Modeling Approach to Optimize Longitudinal Biomarker Sampling Schedules Using Hormonal Data.

Monica H Keith, Margaret Corley, Delaney J Glass, Claudia Valeggia, Melanie A Martin

Abstract read
In one paragraph

Article in American journal of human biology : the official journal of the Human Biology Council, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Monica H KeithDepartment of Anthropology, Vanderbilt University, Nashville, Tennessee, USA.
Margaret CorleyDepartment of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut, USA.
Delaney J GlassDepartment of Anthropology, University of Toronto St. George, Toronto, Ontario, USA.
Claudia ValeggiaDepartment of Anthropology, Yale University, New Haven, Connecticut, USA.
Melanie A MartinCenter for Studies in Demography and Ecology, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-0368-2791

Funding

National Science Foundation BCS-0952264NIH HHS T32 HD101442-01
6 · The paper itself

Abstract

objectivesOptimal schedules for longitudinal biomarker sampling are specific to the individual biomarkers and study aims. We present a Bayesian modeling approach for evaluating intraindividual, interindividual, and population-level biomarker variation in order to optimize precision in parameter estimates and inform biomarker sampling decisions.

methodsWe apply Bayesian linear and nonlinear mixed-effects models to estimate individual- and population-level parameters of longitudinal hormone data from 35 pubertal girls. Starting with first morning void measures of urinary testosterone and C-peptide collected across a two-year timespan, we downsample these longitudinal data systematically to evaluate precision in parameter estimates from nine sampling frequencies: annual, biannual (6-month), and quarterly (3-month) intervals with one, two, and three repeated samples per interval.

resultsStandard errors and credible intervals of individual- and population-level parameter estimates as well as the overall residual errors from our applied models indicate that specific dimensions of sampling frequency have distinct impacts on model parameters across different levels. Collectively, metrics of model fit, precision, and uncertainty indicate that more data are not always better, as we do not find parameter estimates to improve directly with increasing total sample size across models. Notably, we identify optimal sampling thresholds beyond which individual parameter estimates become less precise with additional measures.

conclusionsThe data, code, and results from these analyses provide tools for Bayesian model building, evaluation, and sampling decisions. Specific biomarker features impact precision in distinct ways, and our hormone modeling example showcases sampling analysis methods that are applicable to a broad range of biological data.

Indexed as

BiomarkersC-PeptideTestosteroneBayes TheoremFemaleHumansLongitudinal StudiesBiomarkersC-PeptideTestosteroneBayesianbiomarkermodelingoptimizationsampling

Identifiers

PMID42405431
PMCPMC13334439

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.