Evidence map›Paper›PMID 33904399›Full record

ArticleeLife2021

Adiponectin preserves metabolic fitness during aging.

Na Li, Shangang Zhao, Zhuzhen Zhang, Yi Zhu, Christy M Gliniak, Lavanya Vishvanath, Yu A An, May-Yun Wang, Yingfeng Deng, Qingzhang Zhu and 10 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
10.4field-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.

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

70 citing papers in PubMed, 91 citations in OpenAlex.

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10 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

20 authors at 3 institutions in 2 countries.

Na Li *Touchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-0604-6312
Shangang Zhao *Touchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-9209-8206
Zhuzhen ZhangTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0001-6787-3920
Yi ZhuTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Christy M GliniakTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Lavanya VishvanathTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Yu A AnTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-9678-3382
May-Yun WangTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Yingfeng DengTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0003-1314-5105
Qingzhang ZhuTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Bo ShanTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Amber SherwoodDepartment of Radiology, University of Texas Southwestern Medical Center, Dallas, United States.
Toshiharu OnoderaTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-4439-0077
Orhan K OzDepartment of Radiology, University of Texas Southwestern Medical Center, Dallas, United States.
Ruth GordilloTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.
Rana K GuptaTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-9001-4531
Ming LiuDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China.ORCID 0000-0003-2665-4072
Tamas L HorvathDepartment of Comparative Medicine and Immunobiology, Yale School of Medicine, New Haven, United States.ORCID 0000-0002-7522-4602
Vishwa Deep DixitDepartment of Comparative Medicine and Immunobiology, Yale School of Medicine, New Haven, United States.ORCID 0000-0002-5341-6494
Philipp E SchererTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0003-0680-3392
The University of Texas Southwestern Medical Center · USTianjin Medical University General Hospital · CNYale University · US

Funding

The role of AgRP/Auga-ALK pathway in FGF21's brain action on agingP01AG051459 · NIA · YALE UNIVERSITY · PI VISHWA DEEP DIXIT · 2016 to 2026
$25.7M
Adipocyte mitochondrial distress drives the intercommunication between white and brown adipose tissuesK01DK125447 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI AN, YU · 2021 to 2023
$501k
NIA NIH HHS P01 AG051459NIDDK NIH HHS K01 DK125447
6 · The paper itself

Abstract

Adiponectin is essential for the regulation of tissue substrate utilization and systemic insulin sensitivity. Clinical studies have suggested a positive association of circulating adiponectin with healthspan and lifespan. However, the direct effects of adiponectin on promoting healthspan and lifespan remain unexplored. Here, we are using an adiponectin null mouse and a transgenic adiponectin overexpression model. We directly assessed the effects of circulating adiponectin on the aging process and found that adiponectin null mice display exacerbated age-related glucose and lipid metabolism disorders. Moreover, adiponectin null mice have a significantly shortened lifespan on both chow and high-fat diet. In contrast, a transgenic mouse model with elevated circulating adiponectin levels has a dramatically improved systemic insulin sensitivity, reduced age-related tissue inflammation and fibrosis, and a prolonged healthspan and median lifespan. These results support a role of adiponectin as an essential regulator for healthspan and lifespan.

Indexed as

AdiponectinAgingAnimalsFemaleGlucoseHomeostasisInsulin ResistanceLipid MetabolismLongevityMaleMiceMice, TransgenicAdiponectinAdipoq protein, mouseGlucoseAdiponectincell biologyfat tissuehealthspanlongevitymetabolismmouse

Identifiers

PMID33904399
PMCPMC8099426
OpenAlexW3157889036

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.