Evidence map›Paper›PMID 34116618›Full record

ArticleJournal of diabetes science and technology2022

The Effects of Additional Local-Mixing Compartments in the DISST Model-Based Assessment of Insulin Sensitivity.

Nicholas Lam, Rua Murray, Paul D Docherty, Lisa Te Morenga, J Geoffrey Chase

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Article in Journal of diabetes science and technology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Nicholas LamDepartment of Mechanical Engineering, University of Canterbury, Christchurch, New Zealand.
Rua MurraySchool of Mathematics and Statistics, University of Canterbury, Christchurch, New Zealand.ORCID 0000-0001-5563-1721
Paul D DochertyDepartment of Mechanical Engineering, University of Canterbury, Christchurch, New Zealand.ORCID 0000-0003-1661-2573
Lisa Te MorengaFaculty of Health, Victoria University of Wellington, New Zealand.
J Geoffrey ChaseDepartment of Mechanical Engineering, University of Canterbury, Christchurch, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe identification of insulin sensitivity in glycemic modelling can be heavily obstructed by the presence of outlying data or unmodelled effects. The effect of data indicative of local mixing is especially problematic with models assuming rapid mixing of compartments. Methods such as manual removal of data and outlier detection methods have been used to improve parameter ID in these cases, but modelling data with more compartments is another potential approach.

methodsThis research compares a mixing model with local depot site compartments with an existing, clinically validated insulin sensitivity test model. The Levenberg-Marquardt (LM) parameter identification method was implemented alongside a modified version (aLM) capable of operator-independent omission of outlier data in accordance with the 3 standard deviation rule. Three cases were tested: LM where data points suspected to be affected by incomplete mixing at the depot site were removed, aLM, and LM with the more complex mixing model.

resultsWhile insulin parameters identified in the mixing model differed greatly from those in the DISST model, there were strong Spearman correlations of approximately 0.93 for the insulin sensitivity values identified across all 3 methods. The 2 models also showed comparable identification stability in insulin sensitivity estimation through a Monte Carlo analysis. However, the mixing model required modifications to the identification process to improve convergence, and still failed to converge to feasible parameters on 5 of the 212 trials.

conclusionsThe mixing compartment model effectively captured the dynamics of mixing behavior, but with no significant improvement in insulin sensitivity identification.

Indexed as

Insulin ResistanceBlood GlucoseHumansInsulinMonte Carlo MethodBlood GlucoseInsulinglycemic modellingleast squares estimationnumerical optimizationoutlier data

Identifiers

PMID34116618
PMCPMC9445349

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