Evidence map›Paper›PMID 34151592›Full record

ArticleAmerican journal of physiology. Renal physiology2021

FGF21 prevents low-protein diet-induced renal inflammation in aged mice.

Han Fang, Sujoy Ghosh, Landon C Sims, Kirsten P Stone, Cristal M Hill, Denisha Spires, Daria V Ilatovskaya, Christopher D Morrison, Thomas W Gettys, Krisztian Stadler

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Gut microbes · 2026
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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

10 authors at 2 institutions in 2 countries.

Han FangLaboratory of Nutrient Sensing and Adipocyte Signaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Sujoy GhoshLaboratory of Computational Biology, Pennington Biomedical Research Center, Baton Rouge, Louisiana.ORCID 0000-0002-7601-165X
Landon C SimsLaboratory of Nutrient Sensing and Adipocyte Signaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Kirsten P StoneLaboratory of Nutrient Sensing and Adipocyte Signaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Cristal M HillLaboratory of Neurosignaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Denisha SpiresDivision of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Daria V IlatovskayaDivision of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Christopher D MorrisonLaboratory of Neurosignaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Thomas W GettysLaboratory of Nutrient Sensing and Adipocyte Signaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Krisztian StadlerOxidative Stress and Disease Laboratory, Pennington Biomedical Research Center, Baton Rouge, Louisiana.ORCID 0000-0003-3187-5793
Pennington Biomedical Research Center · USMedical University of South Carolina · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Leanne Maree Redman · 2005 to 2026
$26.5M
Mitochondria-Mediated Effects and Therapeutic Potential of Atrial Natriuretic Peptide in Salt-Sensitive Hypertension Diversity SupplementR01HL148114 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ILATOVSKAYA, DARIA · 2020 to 2024
$2.8M
MECHANISMS OF METABOLIC REGULATION BY DIETARY METHIONINE RESTRICTIONR01DK096311 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2020
$2.7M
Mitochondrial overload and proximal tubular cell atrophyR01DK115749 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI STADLER, KRISZTIAN · 2018 to 2021
$1.8M
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restrictionR01DK121370 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2020 to 2023
$1.5M
FGF21 is an endocrine signal of protein restrictionR01DK105032 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2016 to 2019
$1.4M
Neuronal FGF21 Signaling in the Detection of Dietary Protein RestrictionF32DK115137 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI HILL, CRISTAL MONIQUE · 2017 to 2019
$185k
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL148114HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK096311HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK105032,DK121370HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK115137HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK115749HHS | NIH | National Institute of General Medical Sciences (NIGMS) GM104940NHLBI NIH HHS R01 HL148114NIDDK NIH HHS F32 DK115137NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK096311NIDDK NIH HHS R01 DK105032NIDDK NIH HHS R01 DK115749NIDDK NIH HHS R01 DK121370NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

Low-protein (LP) diets extend lifespan through a comprehensive improvement in metabolic health across multiple tissues and organs. Many of these metabolic responses to protein restriction are secondary to transcriptional activation and release of FGF21 from the liver. However, the effects of an LP diet on the kidney in the context of aging has not been examined. Therefore, the goal of the current study was to investigate the impact of chronic consumption of an LP diet on the kidney in aging mice lacking FGF21. Wild-type (WT; C57BL/6J) and FGF21 knockout (KO) mice were fed a normal protein diet (20% casein) or an LP (5% casein) diet ad libitum from 3 to 22 mo of age. The LP diet led to a decrease in kidney weight and urinary albumin-to-creatinine ratio in both WT and FGF21 KO mice. Although the LP diet produced only mild fibrosis and infiltration of leukocytes in WT kidneys, the effects were significantly exacerbated by the absence of FGF21. Accordingly, transcriptomic analysis showed that inflammation-related pathways were significantly enriched and upregulated in response to LP diet in FGF21 KO mice but not WT mice. Collectively, these data demonstrate that the LP diet negatively affected the kidney during aging, but in the absence of FGF21, the LP diet-induced renal damage and inflammation were significantly worse, indicating a protective role of FGF21 in the kidney.

Indexed as

AgingAnimalsDiet, Protein-RestrictedEnergy MetabolismFibroblast Growth FactorsInflammationKidneyLiverMiceMice, Inbred C57BLMice, KnockoutNephritisfibroblast growth factor 21Fibroblast Growth FactorsagingFGF21inflammationkidneylow-protein diet

Identifiers

PMID34151592
PMCPMC8530754
OpenAlexW3176514196

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.