Evidence map›Paper›PMID 31908037›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

Late-onset renal hypertrophy and dysfunction in mice lacking CTRP1.

Susana Rodriguez, Hannah C Little, Parnaz Daneshpajouhnejad, Blythe D Shepard, Stefanie Y Tan, Andrew Wolfe, Muhammad Umar Cheema, Sandeep Jandu, Owen M Woodward, C Conover Talbot and 4 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. SGLT2 Inhibition Attenuates Renal Tubular Senescence by Suppressing CTRP1-Mediated Glucotoxic Stress in Diabetic Kidney Disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. CTRP10 is required for optimal motor function.The Journal of biological chemistry · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. CTRP11 contributes modestly to systemic metabolism and energy balance.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  7. Aging and chronic high-fat feeding negatively affect kidney size, function, and gene expression in CTRP1-deficient mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  8. Article
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

14 authors at 3 institutions in 1 country.

Susana RodriguezDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Hannah C LittleDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Parnaz DaneshpajouhnejadDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Blythe D ShepardDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Stefanie Y TanDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Andrew WolfeDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Muhammad Umar CheemaDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Sandeep JanduDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Owen M WoodwardDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland.
C Conover TalbotInstitute for Basic Biomedical Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Dan E BerkowitzDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Avi Z RosenbergDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jennifer L PluznickDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
G William WongDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Johns Hopkins University · USJohns Hopkins Medicine · USUniversity of Maryland, Baltimore · US

Funding

CTRP and Metabolic ControlR01DK084171 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Guang William Wong · 2010 to 2026
$8.0M
Microbial Short Chain Fatty Acids and Blood Pressure RegulationR01HL128512 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI PLUZNICK, JENNIFER L · 2016 to 2020
$2.0M
Uncovering the Functional Role of Olfr78 in Blood Pressure RegulationR01DK107726 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PLUZNICK, JENNIFER L · 2016 to 2020
$1.8M
Molecular Mechanisms of Uric Acid HomeostasisR01DK114091 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WOODWARD, OWEN M · 2017 to 2020
$1.4M
Short Chain Fatty Acids (SCFAs) and SCFA G-protein Coupled Receptors in HypertensionR56DK107726 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PLUZNICK, JENNIFER L · 2021 to 2021
$100k
Elucidation of the role of myonectin in regulating lipid partitioning and metabolismF31DK116537 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI LITTLE, HANNAH · 2017 to 2018
$84k
NHLBI NIH HHS R01 HL128512NIDDK NIH HHS F31 DK116537NIDDK NIH HHS R01 DK084171NIDDK NIH HHS R01 DK107726NIDDK NIH HHS R01 DK114091NIDDK NIH HHS R56 DK107726
6 · The paper itself

Abstract

Local and systemic factors that influence renal structure and function in aging are not well understood. The secretory protein C1q/TNF-related protein 1 (CTRP1) regulates systemic metabolism and cardiovascular function. We provide evidence here that CTRP1 also modulates renal physiology in an age- and sex-dependent manner. In mice lacking CTRP1, we observed significantly increased kidney weight and glomerular hypertrophy in aged male but not female or young mice. Although glomerular filtration rate, plasma renin and aldosterone levels, and renal response to water restriction did not differ between genotypes, CTRP1-deficient male mice had elevated blood pressure. Echocardiogram and pulse wave velocity measurements indicated normal heart function and vascular stiffness in CTRP1-deficient animals, and increased blood pressure was not due to greater salt retention. Paradoxically, CTRP1-deficient mice had elevated urinary sodium and potassium excretion, partially resulting from reduced expression of genes involved in renal sodium and potassium reabsorption. Despite renal hypertrophy, markers of inflammation, fibrosis, and oxidative stress were reduced in CTRP1-deficient mice. RNA sequencing revealed alterations and enrichments of genes in metabolic processes in CTRP1-deficient animals. These results highlight novel contributions of CTRP1 to aging-associated changes in renal physiology.

Indexed as

AdipokinesAnimalsBlood PressureHypertensionHypertrophyInflammationKidneyMice, KnockoutSignal TransductionAdipokinesCTRP1 protein, mouseaging-associated renal physiologyC1q/TNF-related protein 1kidney function

Identifiers

PMID31908037
PMCPMC7739198
OpenAlexW2997958405

What OpenQuestion holds

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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.