Evidence map›Paper›PMID 28853981›Full record

ArticleAutophagy2017

Intermittent fasting preserves beta-cell mass in obesity-induced diabetes via the autophagy-lysosome pathway.

Haiyan Liu, Ali Javaheri, Rebecca J Godar, John Murphy, Xiucui Ma, Nidhi Rohatgi, Jana Mahadevan, Krzysztof Hyrc, Paul Saftig, Connie Marshall and 5 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 101 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 1 pooled it
9.3field-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.

NCT03940482 naunknown statusnot on this mapstarted 2019, after this paper: background citation

Time Restricted Eating As Treatment (TREAT) for Diabetes Mellitus: A Pre-Post 12 Week Study on the Effectiveness of Intermittent Fasting in Asians With Type 2 Diabetes Mellitus

TypeinterventionalSponsorSingapore General HospitalRan2019 to 2023Enrolled50ConditionsType 2 Diabetes MellitusArmsTime Restricted Eating As Treatment (TREAT) for Diabetes.
NCT05031429 nacompletednot on this mapstarted 2022, after this paper: background citation

Time Limited Eating in New-Onset Type 1 Diabetes: Feasibility, Acceptability, and Effect on β-cell Function

TypeinterventionalSponsorChildren's Hospital Los AngelesRan2022 to 2023Enrolled12ConditionsType 1 DiabetesArmsTime Limited Eating
3 · Its place in the literature

Who cites it

101 citing papers in PubMed, 1 synthesis or guideline pooled it, 188 citations in OpenAlex.

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41 more citing papers are in PubMed but not listed here.

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

15 authors at 3 institutions in 2 countries.

Haiyan Liua Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
Ali Javaheria Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
Rebecca J Godara Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
John Murphya Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
Xiucui Maa Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
Nidhi Rohatgic Department of Pathology and Immunology , Washington University School of Medicine , St. Louis , MO , USA.
Jana Mahadevand Division of Endocrinology , Department of Internal Medicine , Washington University School of Medicine , St. Louis , MO , USA.
Krzysztof Hyrce Department of Neurology , Washington University School of Medicine , St. Louis , MO , USA.
Paul Saftigf Institut für Biochemie, Christian-Albrechts-Universität zu Kiel , Kiel , Germany.
Connie Marshallc Department of Pathology and Immunology , Washington University School of Medicine , St. Louis , MO , USA.
Michael L McDanielc Department of Pathology and Immunology , Washington University School of Medicine , St. Louis , MO , USA.
Maria S Remedid Division of Endocrinology , Department of Internal Medicine , Washington University School of Medicine , St. Louis , MO , USA.
Babak Razania Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
Fumihiko Uranod Division of Endocrinology , Department of Internal Medicine , Washington University School of Medicine , St. Louis , MO , USA.
Abhinav Diwana Center for Cardiovascular Research and Division of Cardiology , Washington University School of Medicine , St. Louis , MO , USA.
Washington University in St. Louis · USJohn Cochran VA Medical Center · USKiel University · DE

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI James Alexander Fitzpatrick · 2013 to 2026
$27.1M
PRINCIPLES IN CARDIVASCULAR RESEARCH TRAINING PROGRAMT32HL007081 · NHLBI · WASHINGTON UNIVERSITY · PI Abhinav Diwan, Karen Ellen Joynt Maddox · 1985 to 2026
$10.6M
ROLE OF AUTOPHAGIC FLUX IN CARDIAC MYOCYTE VIABILITYR01HL107594 · NHLBI · WASHINGTON UNIVERSITY · PI Abhinav Diwan · 2011 to 2026
$5.9M
THE ROLE OF MACROPHAGE LYSOSOMAL BIOGENESIS IN ATHEROSCLEROSISR01HL125838 · NHLBI · WASHINGTON UNIVERSITY · PI RAZANI, BABAK · 2015 to 2025
$4.6M
BETA-CELL EXHAUSTION AND GLUCOTOXICITY IN DIABETESR01DK098584 · NIDDK · WASHINGTON UNIVERSITY · PI REMEDI, MARIA SARA · 2013 to 2017
$1.7M
HARNESSING THE LYSOSOME MACHINERY IN MACROPHAGES TO PREVENT HEART FAILUREK08HL138262 · NHLBI · WASHINGTON UNIVERSITY · PI JAVAHERI, ALI · 2017 to 2021
$752k
WHOLE SLIDE IMAGING SYSTEM FOR TRANSLATIONAL NEUROSCIENCES10RR027552 · NCRR · WASHINGTON UNIVERSITY · PI LEE, JIN-MOO · 2010 to 2010
$275k
Enhancing Beneficial Autophagy to Prevent Heart FailureI01BX001969 · VA · ST. LOUIS VA MEDICAL CENTER · PI DIWAN, ABHINAV · 2014 to 2017
–
BLRD VA I01 BX000448BLRD VA I01 BX001969NCRR NIH HHS S10 RR027552NHLBI NIH HHS K08 HL138262NHLBI NIH HHS R01 HL107594NHLBI NIH HHS R01 HL125838NHLBI NIH HHS T32 HL007081NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK056341NIDDK NIH HHS R01 DK098584
6 · The paper itself

Abstract

Obesity-induced diabetes is characterized by hyperglycemia, insulin resistance, and progressive beta cell failure. In islets of mice with obesity-induced diabetes, we observe increased beta cell death and impaired autophagic flux. We hypothesized that intermittent fasting, a clinically sustainable therapeutic strategy, stimulates autophagic flux to ameliorate obesity-induced diabetes. Our data show that despite continued high-fat intake, intermittent fasting restores autophagic flux in islets and improves glucose tolerance by enhancing glucose-stimulated insulin secretion, beta cell survival, and nuclear expression of NEUROG3, a marker of pancreatic regeneration. In contrast, intermittent fasting does not rescue beta-cell death or induce NEUROG3 expression in obese mice with lysosomal dysfunction secondary to deficiency of the lysosomal membrane protein, LAMP2 or haplo-insufficiency of BECN1/Beclin 1, a protein critical for autophagosome formation. Moreover, intermittent fasting is sufficient to provoke beta cell death in nonobese lamp2 null mice, attesting to a critical role for lysosome function in beta cell homeostasis under fasting conditions. Beta cells in intermittently-fasted LAMP2- or BECN1-deficient mice exhibit markers of autophagic failure with accumulation of damaged mitochondria and upregulation of oxidative stress. Thus, intermittent fasting preserves organelle quality via the autophagy-lysosome pathway to enhance beta cell survival and stimulates markers of regeneration in obesity-induced diabetes.

Indexed as

AutophagyFastingAnimalsBasic Helix-Loop-Helix ProteinsBeclin-1Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2InsulinInsulin-Secreting CellsLysosomal-Associated Membrane Protein 2LysosomesMiceMice, Mutant StrainsMitochondriaNerve Tissue ProteinsObesityBasic Helix-Loop-Helix ProteinsBeclin-1Becn1 protein, mouseInsulinLysosomal-Associated Membrane Protein 2Nerve Tissue ProteinsNeurog3 protein, mouseautophagybeta cellsdiabetesintermittent fastinglysosomes

Identifiers

PMID28853981
PMCPMC5788488
OpenAlexW2751088406

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.