Evidence map›Paper›PMID 29894202›Full record

Trial reportAmerican journal of physiology. Endocrinology and metabolism2018

Insulin resistance is a significant determinant of sarcopenia in advanced kidney disease.

Serpil M Deger, Jennifer R Hewlett, Jorge Gamboa, Charles D Ellis, Adriana M Hung, Edward D Siew, Cindy Mamnungu, Feng Sha, Aihua Bian, Thomas G Stewart and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of physiology. Endocrinology and metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Serpil M DegerDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Jennifer R HewlettDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Jorge GamboaDepartment of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center , Nashville, Tennessee.
Charles D EllisDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Adriana M HungDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Edward D SiewDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Cindy MamnunguDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Feng ShaDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Aihua BianVanderbilt Center for Kidney Diseases, Vanderbilt University Medical Center , Nashville, Tennessee.
Thomas G StewartVanderbilt Center for Kidney Diseases, Vanderbilt University Medical Center , Nashville, Tennessee.
Naji N AbumradDepartment of Surgery, Vanderbilt University Medical Center , Nashville, Tennessee.ORCID 0000-0002-6874-6306
T Alp IkizlerDepartment of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center , Nashville, Tennessee.
Vanderbilt University Medical Center · USVA Tennessee Valley Healthcare System · USFlorida Atlantic University · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Structural Biology Facility CoreP30ES000267 · NIEHS · VANDERBILT UNIVERSITY · PI GUENGERICH, F PETER · 1985 to 2014
$20.3M
VANDERBILT NEPHROLOGY TRAINING PROGRAMT32DK007569 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARRIS, RAYMOND C., IKIZLER, TALAT ALP · 1988 to 2024
$5.8M
Vanderbilt O'Brien Mouse Kidney Physiology and Disease CenterP30DK079341 · NIDDK · VANDERBILT UNIVERSITY · PI HARRIS, RAYMOND C. · 2008 to 2013
$4.4M
Nutrition and Metabolism in Dialysis PatientsK24DK062849 · NIDDK · VANDERBILT UNIVERSITY · PI IKIZLER, TALAT ALP · 2003 to 2012
$1.6M
Mitochondrial Dysfunction in Chronic Kidney DiseaseK23DK100533 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GAMBOA, JORGE LUIS · 2013 to 2017
$763k
National Center for Advancing Translational Sciences UL1 TR000445National Institute of Diabetes and Digestive and Kidney Diseases K23 DK100533National Institute of Diabetes and Digestive and Kidney Diseases K24 DK062849National Institute of Diabetes and Digestive and Kidney Diseases P30 DK020593National Institute of Diabetes and Digestive and Kidney Diseases P30 DK079341National Institute of Diabetes and Digestive and Kidney Diseases T32 DK007569National Institute of Environmental Health Sciences P30 ES000267NIDDK NIH HHS K23 DK100533
6 · The paper itself

Abstract

Maintenance hemodialysis (MHD) patients display significant nutritional abnormalities. Insulin is an anabolic hormone with direct effects on skeletal muscle (SM). We examined the anabolic actions of insulin, whole-body (WB), and SM protein turnover in 33 MHD patients and 17 participants without kidney disease using hyperinsulinemic-euglycemic-euaminoacidemic (dual) clamp. Gluteal muscle biopsies were obtained before and after the dual clamp. At baseline, WB protein synthesis and breakdown rates were similar in MHD patients. During dual clamp, controls had a higher increase in WB protein synthesis and a higher suppression of WB protein breakdown compared with MHD patients, resulting in statistically significantly more positive WB protein net balance [2.02 (interquartile range [IQR]: 1.79 and 2.36) vs. 1.68 (IQR: 1.46 and 1.91) mg·kg fat-free mass

Indexed as

AdultBody CompositionCross-Sectional StudiesFemaleGlucoseGlucose Clamp TechniqueHumansInsulinInsulin ResistanceMaleMiddle AgedMuscle, SkeletalPhosphorylationRenal DialysisRenal Insufficiency, ChronicSarcopeniaGlucoseInsulinhemodialysismetabolismmusclenutrition

Identifiers

PMID29894202
PMCPMC6336962
OpenAlexW2807764515

What OpenQuestion holds

Textmetadata
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.