Evidence map›Paper›PMID 32990681›Full record

ArticleJCI insight2020

Canagliflozin extends life span in genetically heterogeneous male but not female mice.

Richard A Miller, David E Harrison, David B Allison, Molly Bogue, Lucas Debarba, Vivian Diaz, Elizabeth Fernandez, Andrzej Galecki, W Timothy Garvey, Hashan Jayarathne and 13 more

Abstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 4 pooled it
–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

90 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  15. Assessing health in aging male and female mice: does cardiac function dictate frailty or physical resilience?The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
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30 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

23 authors.

Richard A MillerDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor, Michigan, USA.
David E HarrisonThe Jackson Laboratory, Bar Harbor, Maine, USA.
David B AllisonDepartment of Epidemiology and Biostatistics, Indiana University School of Public Health, Bloomington, Indiana, USA.
Molly BogueThe Jackson Laboratory, Bar Harbor, Maine, USA.
Lucas DebarbaDepartment of Biological Sciences, Integrative Biosciences Center, Wayne State University, Detroit, Michigan, USA.
Vivian DiazSam and Ann Barshop Institute for Longevity and Aging Studies and Departments of Physiology and Molecular Medicine, UT Health San Antonio, San Antonio, Texas, USA; South Texas Veterans Healthcare System, San Antonio, Texas, USA.
Elizabeth FernandezSam and Ann Barshop Institute for Longevity and Aging Studies and Departments of Physiology and Molecular Medicine, UT Health San Antonio, San Antonio, Texas, USA; South Texas Veterans Healthcare System, San Antonio, Texas, USA.
Andrzej GaleckiDepartments of Internal Medicine and Biostatistics, University of Michigan School of Medicine and School of Public Health, Ann Arbor, Michigan, USA.
W Timothy GarveyDepartment of Nutrition Sciences and Diabetes Research Center, University of Alabama at Birmingham, Birmingham, Alabama, USA; Birmingham VA Medical Center, Birmingham, Alabama, USA.
Hashan JayarathneDepartment of Biological Sciences, Integrative Biosciences Center, Wayne State University, Detroit, Michigan, USA.
Navasuja KumarDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Martin A JavorsDepartment of Psychiatry, University of Texas Health Science Center, San Antonio, Texas, USA.
Warren C LadigesDepartment of Comparative Medicine, University of Washington, Seattle, Washington, USA.
Francesca MacchiariniDivision of Aging Biology, National Institute on Aging, Bethesda, Maryland, USA.
James NelsonSam and Ann Barshop Institute for Longevity and Aging Research and Department of Cellular and Integrative Physiology, UT Health San Antonio, San Antonio, Texas, USA.
Peter ReifsnyderThe Jackson Laboratory, Bar Harbor, Maine, USA.
Nadia A RosenthalThe Jackson Laboratory, Bar Harbor, Maine, USA.
Marianna SadagurskiDepartment of Biological Sciences, Integrative Biosciences Center, Wayne State University, Detroit, Michigan, USA.
Adam B SalmonSam and Ann Barshop Institute for Longevity and Aging Studies and Departments of Physiology and Molecular Medicine, UT Health San Antonio, San Antonio, Texas, USA; South Texas Veterans Healthcare System, San Antonio, Texas, USA.
Daniel L SmithDepartment of Nutrition Sciences and Nutrition Obesity Research Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jessica M SnyderDepartment of Comparative Medicine, University of Washington, Seattle, Washington, USA.
David B LombardDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor, Michigan, USA.
Randy StrongSam and Ann Barshop Institute for Longevity and Aging Studies and Departments of Physiology and Molecular Medicine, UT Health San Antonio, San Antonio, Texas, USA; South Texas Veterans Healthcare System, San Antonio, Texas, USA.

Funding

Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI James O Hill · 2000 to 2026
$31.9M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI PETER J HORNSBY · 1995 to 2026
$30.6M
Interventions That Retard Mammalian AgingU01AG022308 · NIA · JACKSON LABORATORY · PI Ronny Korstanje · 2003 to 2026
$30.5M
Research Education CoreP30AG024824 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Neil Alexander · 2004 to 2026
$29.2M
Center for Testing Potential Anti-Aging InterventionsU01AG022307 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RANDY STRONG, Adam Salmon · 2004 to 2026
$26.3M
Laboratory for Anti-Geric Testing, Evaluation and ResearchU01AG022303 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RICHARD A MILLER · 2003 to 2026
$25.4M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joyce Lee · 2010 to 2026
$20.3M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
Sex hormones and arthritis in a long lived animal modelP30AG050886 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Jianhua Zhang · 2015 to 2026
$11.3M
Pilot Project ProgramP30ES020957 · NIEHS · WAYNE STATE UNIVERSITY · PI RUNGE-MORRIS, MELISSA A · 2014 to 2021
$10.1M
Nathan Shock Centers Coordinating CenterU24AG056053 · NIA · AMERICAN FEDERATION FOR AGING RESEARCH · PI STEVEN N. AUSTAD, Stephanie Lederman · 2017 to 2026
$6.1M
NIA NIH HHS P30 AG013319NIA NIH HHS P30 AG024824NIA NIH HHS P30 AG050886NIA NIH HHS U01 AG022303NIA NIH HHS U01 AG022307NIA NIH HHS U01 AG022308NIA NIH HHS U24 AG056053NIA NIH HHS U24 AG066346NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK056336NIDDK NIH HHS P30 DK079626NIDDK NIH HHS P30 DK089503NIEHS NIH HHS P30 ES020957NIGMS NIH HHS R01 GM101171
6 · The paper itself

Abstract

Canagliflozin (Cana) is an FDA-approved diabetes drug that protects against cardiovascular and kidney diseases. It also inhibits the sodium glucose transporter 2 by blocking renal reuptake and intestinal absorption of glucose. In the context of the mouse Interventions Testing Program, genetically heterogeneous mice were given chow containing Cana at 180 ppm at 7 months of age until their death. Cana extended median survival of male mice by 14%. Cana also increased by 9% the age for 90th percentile survival, with parallel effects seen at each of 3 test sites. Neither the distribution of inferred cause of death nor incidental pathology findings at end-of-life necropsies were altered by Cana. Moreover, although no life span benefits were seen in female mice, Cana led to lower fasting glucose and improved glucose tolerance in both sexes, diminishing fat mass in females only. Therefore, the life span benefit of Cana is likely to reflect blunting of peak glucose levels, because similar longevity effects are seen in male mice given acarbose, a diabetes drug that blocks glucose surges through a distinct mechanism, i.e., slowing breakdown of carbohydrate in the intestine. Interventions that control daily peak glucose levels deserve attention as possible preventive medicines to protect from a wide range of late-life neoplastic and degenerative diseases.

Indexed as

LongevityAnimalsBlood GlucoseCanagliflozinFemaleGlucose IntoleranceMaleMiceMice, Inbred BALB CMice, Inbred C3HMice, Inbred C57BLSex FactorsSodium-Glucose Transporter 2 InhibitorsBlood GlucoseCanagliflozinSodium-Glucose Transporter 2 InhibitorsAgingDrug therapyGlucose metabolismMouse models

Identifiers

PMID32990681
PMCPMC7710304

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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.