Evidence mapPaperPMID 40880508Full record

ReviewDiabetes care2026

Advancing Type 1 Diabetes Management: Integrating Novel Therapies, Technologies, and Adjunctive Approaches.

Jennifer R Snaith, Phoom Narongkiatikhun, Petter Bjornstad, Jerry R Greenfield, Kalie L Tommerdahl

Abstract readReview
In one paragraph

Review in Diabetes care, 2026. 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. Trial
  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

5 authors.

Jennifer R SnaithDiabetes and Metabolism, Garvan Institute of Medical Research, Sydney, New South Wales, Australia.ORCID 0000-0001-8559-8387
Phoom NarongkiatikhunDivision of Endocrinology, Metabolism, and Nutrition, Department of Medicine, University of Washington School of Medicine, Seattle, WA.
Petter BjornstadDivision of Endocrinology, Metabolism, and Nutrition, Department of Medicine, University of Washington School of Medicine, Seattle, WA.ORCID 0000-0002-5160-2947
Jerry R GreenfieldDiabetes and Metabolism, Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
Kalie L TommerdahlDivision of Endocrinology, Metabolism, and Nutrition, Department of Medicine, University of Washington School of Medicine, Seattle, WA.

Funding

Immunometabolism and the Cardio-Renal Axis in T1D-associated Atherosclerosis: Insights from the CaRe T1D BiobankU01DK142249 · UNIVERSITY OF WASHINGTON · 2025 to 2025
$1.0M
Advancing ADPKD Treatment with GLP-1RA: A Study of Glucagon-Like Peptide-1 Receptor Agonists' Efficacy, Safety, and MechanismR01DK138915 · UNIVERSITY OF COLORADO DENVER · 2025 to 2025
$678k
Pathogenesis of kidney disease in type 1 diabetes: a modern kidney biopsy cohortR01DK132399 · UNIVERSITY OF WASHINGTON · 2025 to 2025
$607k
Type 1 Diabetes Impacts of Semaglutide on Cardiovascular Outcomes (T1-DISCO)R01HL165433 · UNIVERSITY OF COLORADO DENVER · 2025 to 2025
$599k
Efficacy and Mechanisms of Dapagliflozin in Promoting Kidney Function and Cardiovascular Health in Kidney Transplant RecipientsR01DK137844 · UNIVERSITY OF COLORADO DENVER · 2025 to 2025
$589k
Puberty, diabetes, and the kidneys, when eustress becomes distressR01DK129211 · SEATTLE CHILDREN'S HOSPITAL · 2025 to 2025
$510k
MANATEE-T1D: Metformin ANd AutomaTEd insulin delivery system Effects on renal vascular resistance, insulin sensitivity, and cardiometabolic function in youth with Type 1 DiabetesK23HL159292 · SEATTLE CHILDREN'S HOSPITAL · 2025 to 2025
$182k
American Diabetes Association 11-23-ICTST2DYAmerican Diabetes Association 7-23-ICTST2DY-01American Diabetes Association 7-23-ICTST2DY-08American Heart Association 20IPA35260142Boettcher FoundationBreakthrough T1D Australia (Formally JDRF) Grant# 3-SRA-2023-1296-M-NJuvenile Diabetes Research Foundation International 3-SRA-2022-1097-M-BJuvenile Diabetes Research Foundation International 3-SRA-2022-1230-M-BJuvenile Diabetes Research Foundation International 3-SRA-2022-1243-M-BJuvenile Diabetes Research Foundation International 3-SRA-2023-1373-M-BKPMP Glue GrantLudeman Family Centre for Women's Health Research at the University of Colorado Anschutz Medical CampusNHLBI NIH HHS HL159292NHLBI NIH HHS K23 HL159292NHLBI NIH HHS L40 HL159798NHLBI NIH HHS R01 HL165433NIDDK NIH HHS R01 DK129211NIDDK NIH HHS R01 DK132399NIDDK NIH HHS R01 DK137844NIDDK NIH HHS R01 DK138915NIDDK NIH HHS U01 DK142249Seattle Children's Research InstituteUW Medicine Diabetes Institute
6 · The paper itself

Abstract

In type 1 diabetes, a condition that necessitates lifelong exogenous insulin replacement, there is heavy reliance on technology-assisted insulin delivery and glucose monitoring. Yet, people living with type 1 diabetes still face dysglycemia, weight gain, vascular complications, ketoacidosis and severe hypoglycemia, and psychological distress. Cardiovascular and kidney disease remain the leading causes of morbidity and mortality, yet traditional risk factors (smoking, hypertension, hyperlipidemia, obesity, hyperglycemia) incompletely explain this excess burden. Emerging evidence highlights the role of insulin resistance, inflammation, and endothelial dysfunction exacerbated by current subcutaneous insulin therapies in type 1 diabetes, independent of overweight/obesity status. This has fueled interest in addressing metabolic challenges in type 1 diabetes through novel insulin analogs, adjunctive noninsulin therapies, and integrated technologies. Our review explores the potential synergy between technologies and adjunctive therapeutics to address unique physiologic drivers of metabolic dysfunction in type 1 diabetes. Innovations such as multihormonal systems, dynamic glucose and ketone monitoring, and automated insulin titration hold promise. However, leveraging emerging insights from nutrient-stimulated hormone-based therapies and other drug classes such as insulin-sensitizing agents and sodium-glucose cotransporter 2 inhibitors could pave the way for designing combination type 1 diabetes-specific therapies. Large, placebo-controlled trials are needed to progress the field toward use of combination therapies that reduce metabolic and vascular complications and ease patient burden in type 1 diabetes.

Indexed as

Diabetes Mellitus, Type 1Hypoglycemic AgentsHumansInsulinInsulin Infusion SystemsHypoglycemic AgentsInsulin

Identifiers

PMID40880508
PMCPMC13053879

What Socratic 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 Socratic graph.