ArticlePloS one2012
Population physiology: leveraging electronic health record data to understand human endocrine dynamics.
Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03911687 (Communicating Narrative Concerns Entered by RNs), which is not on this map. Cited by 18 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Communicating Narrative Concerns Entered by RNs (CONCERN) Clinical Decision Support (CDS) System
Who cites it
18 citing papers in PubMed, 25 citations in OpenAlex.
- A multiobjective optimization approach to data assimilation for complex biological systems with sparse data.Mathematical biosciences · 2026Article
- A simple modeling framework for prediction in the human glucose-insulin system.Chaos (Woodbury, N.Y.) · 2023Article
- Incorporating real-world evidence into the development of patient blood glucose prediction algorithms for the ICU.Journal of the American Medical Informatics Association : JAMIA · 2021Article
- Delay-induced uncertainty for a paradigmatic glucose-insulin model.Chaos (Woodbury, N.Y.) · 2021Article
- The parameter Houlihan: A solution to high-throughput identifiability indeterminacy for brutally ill-posed problems.Mathematical biosciences · 2019Article
- Methodological variations in lagged regression for detecting physiologic drug effects in EHR data.Journal of biomedical informatics · 2018Article
- Mechanistic machine learning: how data assimilation leverages physiologic knowledge using Bayesian inference to forecast the future, infer the present, and phenotype.Journal of the American Medical Informatics Association : JAMIA · 2018Article
- When to re-order laboratory tests? Learning laboratory test shelf-life.Journal of biomedical informatics · 2018Article
- High-fidelity phenotyping: richness and freedom from bias.Journal of the American Medical Informatics Association : JAMIA · 2018Article
- Estimating summary statistics for electronic health record laboratory data for use in high-throughput phenotyping algorithms.Journal of biomedical informatics · 2018Article
- Prognostic burden of heart failure recorded in primary care, acute hospital admissions, or both: a population-based linked electronic health record cohort study in 2.1 million people.European journal of heart failure · 2017Article
- Comparing lagged linear correlation, lagged regression, Granger causality, and vector autoregression for uncovering associations in EHR data.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2016Article
- Predictability Bounds of Electronic Health Records.Scientific reports · 2015Article
- Parameterizing time in electronic health record studies.Journal of the American Medical Informatics Association : JAMIA · 2015Article
- Identifying and mitigating biases in EHR laboratory tests.Journal of biomedical informatics · 2014Article
- Dynamical phenotyping: using temporal analysis of clinically collected physiologic data to stratify populations.PloS one · 2014Article
- Defining a comprehensive verotype using electronic health records for personalized medicine.Journal of the American Medical Informatics Association : JAMIA · 2013Article
- Data assimilation of glucose dynamics for use in the intensive care unit.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference · 2012Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
Studying physiology and pathophysiology over a broad population for long periods of time is difficult primarily because collecting human physiologic data can be intrusive, dangerous, and expensive. One solution is to use data that have been collected for a different purpose. Electronic health record (EHR) data promise to support the development and testing of mechanistic physiologic models on diverse populations and allow correlation with clinical outcomes, but limitations in the data have thus far thwarted such use. For example, using uncontrolled population-scale EHR data to verify the outcome of time dependent behavior of mechanistic, constructive models can be difficult because: (i) aggregation of the population can obscure or generate a signal, (ii) there is often no control population with a well understood health state, and (iii) diversity in how the population is measured can make the data difficult to fit into conventional analysis techniques. This paper shows that it is possible to use EHR data to test a physiological model for a population and over long time scales. Specifically, a methodology is developed and demonstrated for testing a mechanistic, time-dependent, physiological model of serum glucose dynamics with uncontrolled, population-scale, physiological patient data extracted from an EHR repository. It is shown that there is no observable daily variation the normalized mean glucose for any EHR subpopulations. In contrast, a derived value, daily variation in nonlinear correlation quantified by the time-delayed mutual information (TDMI), did reveal the intuitively expected diurnal variation in glucose levels amongst a random population of humans. Moreover, in a population of continuously (tube) fed patients, there was no observable TDMI-based diurnal signal. These TDMI-based signals, via a glucose insulin model, were then connected with human feeding patterns. In particular, a constructive physiological model was shown to correctly predict the difference between the general uncontrolled population and a subpopulation whose feeding was controlled.
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Registered trials
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.