Evidence map›Paper›PMID 33710398›Full record

ReviewDiabetologia2021

'Smart' insulin-delivery technologies and intrinsic glucose-responsive insulin analogues.

Mark A Jarosinski, Balamurugan Dhayalan, Nischay Rege, Deepak Chatterjee, Michael A Weiss

Open access · hybridAbstract readReview
In one paragraph

Review in Diabetologia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
12.8field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
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  8. Applications and prospects of biomaterials in diabetes management.Frontiers in bioengineering and biotechnology · 2025
    Review
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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

5 authors at 3 institutions in 1 country.

Mark A JarosinskiDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID https://orcid.org/0000-0002-2814-8643
Balamurugan DhayalanDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID https://orcid.org/0000-0001-6002-1207
Nischay RegeDepartment of Medicine, Yale University School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0002-3858-9530
Deepak ChatterjeeDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID https://orcid.org/0000-0002-6441-2974
Michael A WeissDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA. weissma@iu.edu.ORCID https://orcid.org/0000-0003-1325-1610
Indiana University School of MedicinePurdue University West Lafayette · USYale University · US

Funding

Non-Standard Protein Design in Molecular Endocrinology: Insulin and GlucagonR01DK040949 · NIDDK · UNIVERSITY OF CHICAGO · PI CHERRINGTON, ALAN D, GEORGIADIS, MILLIE M · 1989 to 2024
$8.4M
Therapeutic Protein Engineering of Single-Chain Insulin AnalogsR01DK118536 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI CHERRINGTON, ALAN D, ISMAIL-BEIGI, FARAMARZ · 2018 to 2022
$2.7M
Molecular engineering of complementary glucose-responsive conformational switches in insulin and glucagonR01DK127761 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI ISMAIL-BEIGI, FARAMARZ, LAWRENCE, MICHAEL COLIN · 2020 to 2022
$1.7M
NIDDK NIH HHS R01 DK040949NIDDK NIH HHS R01 DK118536NIDDK NIH HHS R01 DK127761
6 · The paper itself

Abstract

Insulin replacement therapy for diabetes mellitus seeks to minimise excursions in blood glucose concentration above or below the therapeutic range (hyper- or hypoglycaemia). To mitigate acute and chronic risks of such excursions, glucose-responsive insulin-delivery technologies have long been sought for clinical application in type 1 and long-standing type 2 diabetes mellitus. Such 'smart' systems or insulin analogues seek to provide hormonal activity proportional to blood glucose levels without external monitoring. This review highlights three broad strategies to co-optimise mean glycaemic control and time in range: (1) coupling of continuous glucose monitoring (CGM) to delivery devices (algorithm-based 'closed-loop' systems); (2) glucose-responsive polymer encapsulation of insulin; and (3) mechanism-based hormone modifications. Innovations span control algorithms for CGM-based insulin-delivery systems, glucose-responsive polymer matrices, bio-inspired design based on insulin's conformational switch mechanism upon insulin receptor engagement, and glucose-responsive modifications of new insulin analogues. In each case, innovations in insulin chemistry and formulation may enhance clinical outcomes. Prospects are discussed for intrinsic glucose-responsive insulin analogues containing a reversible switch (regulating bioavailability or conformation) that can be activated by glucose at high concentrations.

Indexed as

Insulin Infusion SystemsBlood GlucoseBlood Glucose Self-MonitoringDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2GlucoseHumansInsulinInventionsPancreas, ArtificialBlood GlucoseGlucoseInsulinArtificial pancreasGlucose-responsive insulinGlucose-responsive polymersGlucose sensorHormone-receptor recognitionReview

Identifiers

PMID33710398
PMCPMC8158166
OpenAlexW3134775417

What OpenQuestion holds

Textmetadata
LicenceTDM
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.