Evidence map›Paper›PMID 33947721›Full record

ReviewDiabetes2021

Altered β-Cell Prohormone Processing and Secretion in Type 1 Diabetes.

Teresa Rodriguez-Calvo, Yi-Chun Chen, C Bruce Verchere, Leena Haataja, Peter Arvan, Pia Leete, Sarah J Richardson, Noel G Morgan, Wei-Jun Qian, Alberto Pugliese and 3 more

Abstract readReview
In one paragraph

Review in Diabetes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

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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

13 authors.

Teresa Rodriguez-CalvoInstitute of Diabetes Research, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health, Munich-Neuherberg, Germany.ORCID 0000-0003-1531-8583
Yi-Chun ChenDepartment of Surgery, University of British Columbia and BC Children's Hospital Research Institute, Vancouver, Canada.
C Bruce VerchereDepartments of Surgery and Pathology and Laboratory Medicine, University of British Columbia, Centre for Molecular Medicine and Therapeutics, and BC Children's Hospital Research Institute, Vancouver, Canada.
Leena HaatajaDivision of Metabolism, Endocrinology & Diabetes, University of Michigan Medical Center, Ann Arbor, MI.
Peter ArvanDivision of Metabolism, Endocrinology & Diabetes, University of Michigan Medical Center, Ann Arbor, MI.
Pia LeeteExeter Centre of Excellence for Diabetes, Institute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, U.K.
Sarah J RichardsonExeter Centre of Excellence for Diabetes, Institute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, U.K.ORCID 0000-0002-1160-6062
Noel G MorganExeter Centre of Excellence for Diabetes, Institute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, U.K.ORCID 0000-0003-1537-8113
Wei-Jun QianBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA.
Alberto PuglieseDiabetes Research Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL.ORCID 0000-0002-7211-0319
Mark AtkinsonDepartments of Pathology and Pediatrics, Diabetes Institute, University of Florida, Gainesville, FL.
Carmella Evans-MolinaCenter for Diabetes and Metabolic Diseases, Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN.ORCID 0000-0001-7764-8663
Emily K SimsCenter for Diabetes and Metabolic Diseases, Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN eksims@iu.edu.ORCID 0000-0002-4393-954X

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
Proinsulin Trafficking for Insulin BiosynthesisR01DK048280 · NIDDK · YESHIVA UNIVERSITY · PI ARVAN, PETER · 1994 to 2024
$10.5M
The Integrated Stress Response in Human Islets During Early T1DU01DK127786 · NIDDK · UNIVERSITY OF CHICAGO · PI EVANS-MOLINA, CARMELLA, MIRMIRA, RAGHAVENDRA G · 2020 to 2025
$7.1M
Mechanisms of Beta Cell Function in Health and DiseaseR01DK093954 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EVANS-MOLINA, CARMELLA · 2011 to 2019
$3.5M
Beta cell extracellular vesicles in health and diseaseR01DK121929 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI SIMS, EMILY K · 2020 to 2024
$2.0M
Defining the Generation and Cargo of Extracellular Vesicles During the Evolution of Type 1 DiabetesR03DK117253 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI SIMS, EMILY K · 2019 to 2020
$380k
BLRD VA I01 BX001733NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK097512NIDDK NIH HHS R01 DK048280NIDDK NIH HHS R01 DK093954NIDDK NIH HHS R01 DK121929NIDDK NIH HHS R03 DK117253NIDDK NIH HHS U01 DK127786
6 · The paper itself

Abstract

Analysis of data from clinical cohorts, and more recently from human pancreatic tissue, indicates that reduced prohormone processing is an early and persistent finding in type 1 diabetes. In this article, we review the current state of knowledge regarding alterations in islet prohormone expression and processing in type 1 diabetes and consider the clinical impact of these findings. Lingering questions, including pathologic etiologies and consequences of altered prohormone expression and secretion in type 1 diabetes, and the natural history of circulating prohormone production in health and disease, are considered. Finally, key next steps required to move forward in this area are outlined, including longitudinal testing of relevant clinical populations, studies that probe the genetics of altered prohormone processing, the need for combined functional and histologic testing of human pancreatic tissues, continued interrogation of the intersection between prohormone processing and autoimmunity, and optimal approaches for analysis. Successful resolution of these questions may offer the potential to use altered prohormone processing as a biomarker to inform therapeutic strategies aimed at personalized intervention during the natural history of type 1 diabetes and as a pathogenic anchor for identification of potential disease-specific endotypes.

Indexed as

AnimalsDiabetes Mellitus, Type 1HumansInsulin-Secreting CellsIslets of LangerhansProinsulinProinsulin

Identifiers

PMID33947721
PMCPMC8173804

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.