Evidence map›Paper›PMID 26341131›Full record

ArticleDiabetes care2015

Effect of Repeated Glucagon Doses on Hepatic Glycogen in Type 1 Diabetes: Implications for a Bihormonal Closed-Loop System.

Jessica R Castle, Joseph El Youssef, Parkash A Bakhtiani, Yu Cai, Jade M Stobbe, Deborah Branigan, Katrina Ramsey, Peter Jacobs, Ravi Reddy, Mark Woods and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes care, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
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  3. Review
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Adjunctive Therapies to Optimize Closed-loop Glucose Control.Journal of diabetes science and technology · 2021
    Article
  10. Review
  11. Article
  12. Role of Glucagon in Automated Insulin Delivery.Endocrinology and metabolism clinics of North America · 2020
    Review
  13. Insulin-and-Glucagon Artificial Pancreas Versus Insulin-Alone Artificial Pancreas: A Short Review.Diabetes spectrum : a publication of the American Diabetes Association · 2019
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
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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

11 authors at 3 institutions in 1 country.

Jessica R CastleDepartment of Medicine, Division of Endocrinology, Harold Schnitzer Diabetes Health Center Oregon Health & Science University, Portland, OR castleje@ohsu.edu.
Joseph El YoussefDepartment of Medicine, Division of Endocrinology, Harold Schnitzer Diabetes Health Center Oregon Health & Science University, Portland, OR.
Parkash A BakhtianiDepartment of Medicine, Division of Endocrinology, Harold Schnitzer Diabetes Health Center Oregon Health & Science University, Portland, OR.
Yu CaiAdvanced Imaging Research Center, Oregon Health & Science University, Portland, OR.
Jade M StobbeAdvanced Imaging Research Center, Oregon Health & Science University, Portland, OR.
Deborah BraniganDepartment of Medicine, Division of Endocrinology, Harold Schnitzer Diabetes Health Center Oregon Health & Science University, Portland, OR.
Katrina RamseyOregon Clinical and Translational Research Institute Biostatistics & Design Program, Oregon Health & Science University, Portland, OR.
Peter JacobsDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR.
Ravi ReddyDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR.
Mark WoodsAdvanced Imaging Research Center, Oregon Health & Science University, Portland, OR Portland State University, Portland, OR.
W Kenneth WardDepartment of Medicine, Division of Endocrinology, Harold Schnitzer Diabetes Health Center Oregon Health & Science University, Portland, OR.
Oregon Health & Science University · USAdvanced Imaging Research (United States) · USPortland State University · US

Funding

Oregon Clinical and Translational Research InstituteUL1TR000128 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ELLISON, DAVID H · 2012 to 2015
$28.7M
TRAINING IN ENDOCRINOLOGY, DIABETES, NUTRITIONT32DK007674 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI KLEIN, ROBERT FREDERICK · 1993 to 2013
$3.1M
Mitigating risk in a closed loop system by exercise detection and miniaturizationDP3DK101044 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI CASTLE, JESSICA R, JACOBS, PETER G · 2013 to 2013
$2.9M
Optimization of an Adaptive Dual-Hormone External Endocrine Pancreas.K23DK090133 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI EL YOUSSEF, JOSEPH · 2011 to 2015
$863k
NCATS NIH HHS UL1 TR000128NCATS NIH HHS UL1-TR-000128NIDDK NIH HHS DP3 DK101044NIDDK NIH HHS K23 DK090133NIDDK NIH HHS T32 DK007674NIDDK NIH HHS T32-DK-007674
6 · The paper itself

Abstract

objectiveTo evaluate subjects with type 1 diabetes for hepatic glycogen depletion after repeated doses of glucagon, simulating delivery in a bihormonal closed-loop system. RESEARCH DESIGN AND

methodsEleven adult subjects with type 1 diabetes participated. Subjects underwent estimation of hepatic glycogen using (13)C MRS. MRS was performed at the following four time points: fasting and after a meal at baseline, and fasting and after a meal after eight doses of subcutaneously administered glucagon at a dose of 2 µg/kg, for a total mean dose of 1,126 µg over 16 h. The primary and secondary end points were, respectively, estimated hepatic glycogen by MRS and incremental area under the glucose curve for a 90-min interval after glucagon administration.

resultsIn the eight subjects with complete data sets, estimated glycogen stores were similar at baseline and after repeated glucagon doses. In the fasting state, glycogen averaged 21 ± 3 g/L before glucagon administration and 25 ± 4 g/L after glucagon administration (mean ± SEM) (P = NS). In the fed state, glycogen averaged 40 ± 2 g/L before glucagon administration and 34 ± 4 g/L after glucagon administration (P = NS). With the use of an insulin action model, the rise in glucose after the last dose of glucagon was comparable to the rise after the first dose, as measured by the 90-min incremental area under the glucose curve.

conclusionsIn adult subjects with well-controlled type 1 diabetes (mean A1C 7.2%), glycogen stores and the hyperglycemic response to glucagon administration are maintained even after receiving multiple doses of glucagon. This finding supports the safety of repeated glucagon delivery in the setting of a bihormonal closed-loop system.

Indexed as

AdultBlood GlucoseDiabetes Mellitus, Type 1Feedback, PhysiologicalFemaleGlucagonHormonesHumansHypoglycemiaInsulinLiver GlycogenMaleBlood GlucoseGlucagonHormonesInsulinLiver Glycogen

Identifiers

PMID26341131
PMCPMC4613914
OpenAlexW1864933933

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.