Evidence map›Paper›PMID 36629330›Full record

Trial reportJournal of diabetes science and technology2024

Estimation of a Machine Learning-Based Decision Rule to Reduce Hypoglycemia Among Older Adults With Type 1 Diabetes: A Post Hoc Analysis of Continuous Glucose Monitoring in the WISDM Study.

Anna R Kahkoska, Kushal S Shah, Michael R Kosorok, Kellee M Miller, Michael Rickels, Ruth S Weinstock, Laura A Young, Richard E Pratley

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of diabetes science and technology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
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

8 authors at 5 institutions in 1 country.

Anna R KahkoskaDepartment of Nutrition, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0003-2701-101X
Kushal S ShahDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Michael R KosorokDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Kellee M MillerJaeb Center for Health Research, Tampa, FL, USA.
Michael RickelsRodebaugh Diabetes Center, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Ruth S WeinstockDivision of Endocrinology, Diabetes, and Metabolism, SUNY Upstate Medical University, Syracuse, NY, USA.ORCID 0000-0001-5859-5666
Laura A YoungDivision of Endocrinology and Metabolism, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Richard E PratleyAdventHealth Translational Research Institute, Orlando, FL, USA.
University of North Carolina at Chapel Hill · USJaeb Center for Health Research · USSUNY Upstate Medical University · USTranslational Research Institute for Metabolism and Diabetes · USUniversity of Pennsylvania · US

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
North Carolina Translational and Clinical Science Institute (NC TraCS) KL2KL2TR002490 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEINBERGER, MORRIS · 2018 to 2022
$11.0M
NCATS NIH HHS KL2 TR002490NCATS NIH HHS UL1 TR001878
6 · The paper itself

Abstract

backgroundThe Wireless Innovation for Seniors with Diabetes Mellitus (WISDM) study demonstrated continuous glucose monitoring (CGM) reduced hypoglycemia over 6 months among older adults with type 1 diabetes (T1D) compared with blood glucose monitoring (BGM). We explored heterogeneous treatment effects of CGM on hypoglycemia by formulating a data-driven decision rule that selects an intervention (ie, CGM vs BGM) to minimize percentage of time <70 mg/dL for each individual WISDM participant.

methodThe precision medicine analyses used data from participants with complete data (n = 194 older adults, including those who received CGM [n = 100] and BGM [n = 94] in the trial). Policy tree and decision list algorithms were fit with 14 baseline demographic, clinical, and laboratory measures. The primary outcome was CGM-measured percentage of time spent in hypoglycemic range (<70 mg/dL), and the decision rule assigned participants to a subgroup reflecting the treatment estimated to minimize this outcome across all follow-up visits.

resultsThe optimal decision rule was found to be a decision list with 3 steps. The first step moved WISDM participants with baseline time-below range >1.35% and no detectable C-peptide levels to the CGM subgroup (n = 139), and the second step moved WISDM participants with a baseline time-below range of >6.45% to the CGM subgroup (n = 18). The remaining participants (n = 37) were left in the BGM subgroup. Compared with the BGM subgroup (n = 37; 19%), the group for whom CGM minimized hypoglycemia (n = 157; 81%) had more baseline hypoglycemia, a lower proportion of detectable C-peptide, higher glycemic variability, longer disease duration, and higher proportion of insulin pump use.

conclusionsThe decision rule underscores the benefits of CGM for older adults to reduce hypoglycemia. Diagnostic CGM and laboratory markers may inform decision-making surrounding therapeutic CGM and identify older adults for whom CGM may be a critical intervention to reduce hypoglycemia.

Indexed as

Blood GlucoseBlood Glucose Self-MonitoringDiabetes Mellitus, Type 1HypoglycemiaMachine LearningAgedAged, 80 and overClinical Decision RulesContinuous Glucose MonitoringFemaleHumansHypoglycemic AgentsMaleMiddle AgedBlood GlucoseHypoglycemic Agentscontinuous glucose monitoringheterogeneous treatment effectshypoglycemiaolder adultsprecision medicinetype 1 diabetes

Identifiers

PMID36629330
PMCPMC11418529
OpenAlexW4315619580

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.