Evidence map›Paper›PMID 40202975›Full record

ArticlePLOS digital health2025

Chronobiologically-informed features from CGM data provide unique information for XGBoost prediction of longer-term glycemic dysregulation in 8,000 individuals with type-2 diabetes.

Jamison H Burks, Leslie Joe, Karina Kanjaria, Carlos Monsivais, Kate O'laughlin, Benjamin L Smarr

Abstract read
In one paragraph

Article in PLOS digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jamison H BurksShiu Chen - Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California, United States of America.ORCID https://orcid.org/0000-0003-4816-5704
Leslie JoeHalicioğlu Data Science Institute, University of California San Diego, La Jolla, California, United States of America.
Karina KanjariaHalicioğlu Data Science Institute, University of California San Diego, La Jolla, California, United States of America.
Carlos MonsivaisHalicioğlu Data Science Institute, University of California San Diego, La Jolla, California, United States of America.
Kate O'laughlinHalicioğlu Data Science Institute, University of California San Diego, La Jolla, California, United States of America.
Benjamin L SmarrShiu Chen - Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California, United States of America.ORCID https://orcid.org/0000-0003-4442-3956

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 Diabetes causes dysregulation of blood glucose, which leads to long-term, multi-tissue damage. Continuous glucose monitoring devices are commercially available and used to track glucose at high temporal resolution so that individuals can make informed decisions about their metabolic health. Algorithms processing these continuous data have also been developed that can predict glycemic excursion in the near future. These data might also support prediction of glycemic stability over longer time horizons. In this work, we leverage longitudinal Dexcom continuous glucose monitoring data to test the hypothesis that additional information about glycemic stability comes from chronobiologically-informed features. We develop a computationally efficient multi-timescale complexity index, and find that inclusion of time-of-day complexity features increases the performance of an out-of-the-box XGBoost model in predicting the change in glucose across days. These findings support the use of chronobiologically-inspired and explainable features to improve glucose prediction algorithms with relatively long time-horizons.

Identifiers

PMID40202975
PMCPMC11981153

What OpenQuestion holds

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Registered trials

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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.