Evidence map›Paper›PMID 24937037›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2014

Biomarkers in type 1 diabetes: application to the clinical trial setting.

James E Tooley, Kevan C Herold

Abstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Prioritizing Early Disease Intervention.Therapeutic innovation & regulatory science · 2023
    Article
  4. Review
  5. Immune cell trafficking to the islets during type 1 diabetes.Clinical and experimental immunology · 2019
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. 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

2 authors.

James E TooleyDepartment of Immunobiology and Internal Medicine, Yale University, New Haven, Connecticut, USA.
Kevan C Herold

Funding

YALE UNIVERSITY CLINICAL AND TRANSLATIONAL SCIENCE AWARD PROGRAMUL1RR024139 · NCRR · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2006 to 2011
$56.8M
Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Richard A Flavell · 1993 to 2026
$44.0M
Phase II Trial of HOKT3gamma 1 (ALA-ALA) in Type 1 DiabetesR01DK057846 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold · 2000 to 2026
$11.1M
The role of the innate immune system on Treg reprogramming in human autoimmune diU01AI102011 · NIAID · YALE UNIVERSITY · PI HAFLER, DAVID A., HEROLD, KEVAN C · 2012 to 2016
$3.8M
Measurement of Beta Cell Death in DiabetesR42DK095639 · NIDDK · L2 DIAGNOSTICS, LLC · PI HEROLD, KEVAN C · 2014 to 2015
$1.3M
Analysis of beta cell death in Type 1 diabetesDP3DK101122 · NIDDK · YALE UNIVERSITY · PI HEROLD, KEVAN C · 2013 to 2013
$807k
Measurement of Beta Cell Death in DiabetesR41DK095639 · NIDDK · L2 DIAGNOSTICS, LLC · PI HEROLD, KEVAN C · 2012 to 2012
$285k
Howard Hughes Medical InstituteNCRR NIH HHS RR024139NCRR NIH HHS UL1 RR024139NIAID NIH HHS AI102011NIAID NIH HHS U01 AI102011NIDDK NIH HHS DK045735NIDDK NIH HHS DK057846NIDDK NIH HHS DK095639NIDDK NIH HHS DP3 DK101122NIDDK NIH HHS DP3DK101122NIDDK NIH HHS P30 DK045735NIDDK NIH HHS R01 DK057846NIDDK NIH HHS R41 DK095639NIDDK NIH HHS R42 DK095639
6 · The paper itself

Abstract

purpose of reviewBiomarkers of type 1 diabetes (T1D) are important for assessing risk of developing disease, monitoring disease progression, and determining responses to clinical treatments. Here we review recent advances in the development of biomarkers of T1D with a focus on their utility in clinical trials. RECENT

findingsMeasurements of autoantibodies and metabolic outcomes have been the foundation of monitoring T1D for the past 20 years. Recent advancements have led to improvements in T-cell-specific assays that have been used in large-scale clinical trials to measure antigen-specific T cell responses. Additionally, new tools are being developed for the measurement of β cell mass and death that will allow for more direct measurement of disease activity. Lastly, recent studies have used both immunologic and nonimmunologic biomarkers to identify responders to treatments in clinical trials. SUMMARY: Use of biomarkers in the study of T1D has largely not changed over the past 20 years; however, recent advancements in the field are establishing new techniques that allow for more precise monitoring of disease progression. These new tools will ultimately lead to an improvement in understanding of disease and will be utilized in clinical trials.

Indexed as

Disease ProgressionAutoantibodiesAutoantigensBiomarkersDiabetes Mellitus, Type 1Flow CytometryHumansImmunoblottingInsulin-Secreting CellsInterleukin-18T-LymphocytesAutoantibodiesAutoantigensBiomarkersInterleukin-18

Identifiers

PMID24937037
PMCPMC4163003

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.