Evidence map›Paper›PMID 38960895›Full record

ArticlePhysiological reports2024

Intermuscular adipose tissue accumulation is associated with higher tissue sodium in healthy individuals.

Lale A Ertuglu, Melis Sahinoz, Aseel Alsouqi, Serpil Muge Deger, Andrew Guide, Mindy Pike, Cassianne Robinson-Cohen, Elvis Akwo, Michael Pridmore, Rachelle Crescenzi and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Physiological reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04067752 (Nutrition, Inflammation and Insulin Resistance in End-Stage Renal Disease), which is not on this map. Cited by 4 papers.

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

NCT04067752 nacompletednot on this map

Nutrition, Inflammation and Insulin Resistance in End-Stage Renal Disease

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2022 to 2024Enrolled18ConditionsEnd-stage Renal DiseaseArmshigh dialysate sodium concentration (138 mEq/L), Low dialysate sodium concentration
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Intramuscular adipose tissue: from progenitor to pathology.American journal of physiology. Cell physiology · 2025
    Review
  4. 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

17 authors.

Lale A ErtugluDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Melis SahinozDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Aseel AlsouqiNow with Division of Hematology and Oncology, Department of Medicine, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Serpil Muge DegerDivision of Nephrology, Department of Medicine, Dokuz Eylul University, Izmir, Turkey.
Andrew GuideDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Mindy PikeDivision of Epidemiology, Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
Cassianne Robinson-CohenDivision of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Elvis AkwoDivision of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Michael PridmoreDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Rachelle CrescenziDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Meena S MadhurDivision of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Annet KiraboDivision of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0001-8580-9359
David G HarrisonDivision of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Friedrich C LuftExperimental and Clinical Research Center, MDC/Charité, Berlin, Germany.
Jens TitzeProgram in Cardiovascular and Metabolic Disorders, Duke NUS Medical School, Bukit Merah, Singapore.
T Alp IkizlerDivision of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Jorge L GamboaDivision of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-4204-7670

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 O'Brien Kidney Center - Core D - Clinical and Translational CoreP30DK114809 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DE CAESTECKER, MARK P. · 2017 to 2021
$5.9M
Role of Mitochondrial Dysfunction in the Response to Exercise in Patients with Advanced Kidney DiseaseR01DK125794 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GAMBOA, JORGE LUIS, IKIZLER, TALAT ALP · 2021 to 2025
$3.3M
American Heart Association (AHA) 14SFRN20770008CSRD VA I01 CX001755HHS | NIH | National Center for Advancing Translational Sciences (NCATS) UL1-TR000445HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) P30-DK114809HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) R01DK125794NCATS NIH HHS UL1 TR000445NIDDK NIH HHS P30 DK114809NIDDK NIH HHS R01 DK125794U.S. Department of Veterans Affairs (VA) 5I01CX001755
6 · The paper itself

Abstract

BACKGROUND AND

aimsHigh tissue sodium accumulation and intermuscular adipose tissue (IMAT) are associated with aging, type 2 diabetes, and chronic kidney disease. In this study, we aim to investigate whether high lower-extremity tissue sodium accumulation relates to IMAT quantity and whether systemic inflammatory mediators and adipocytokines contribute to such association.

methodsTissue sodium content and IMAT accumulation (percentage of IMAT area to muscle area) were measured in 83 healthy individuals using sodium imaging (

resultsMedian (interquartile range) muscle and skin sodium contents were 16.6 (14.9, 19.0) and 12.6 (10.9, 16.7) mmol/L, respectively. Median IMAT was 3.69 (2.80, 5.37) %. In models adjusted for age, sex, BMI, GDR, adiponectin, and high-sensitivity C-reactive protein, increasing tissue sodium content was significantly associated with higher IMAT quantity (p = 0.018 and 0.032 for muscle and skin tissue sodium, respectively). In subgroup analysis stratified by sex, skin sodium was significantly associated with IMAT only among men. In interaction analysis, the association between skin sodium and IMAT was greater with increasing levels of high-sensitivity C-reactive protein and interleukin-6 (p for interaction = 0.022 and 0.006, respectively).

conclusionsLeg muscle and skin sodium are associated with IMAT quantity among healthy individuals. The relationship between skin sodium and IMAT may be mediated by systemic inflammation.

Indexed as

Adipose TissueMuscle, SkeletalSodiumAdultFemaleHumansInsulin ResistanceMagnetic Resonance ImagingMaleMiddle AgedSkinSodiuminflammationintermuscular adipose tissuetissue sodium accumulation

Identifiers

PMID38960895
PMCPMC11222016

What Socratic holds

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Registered trials

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 Socratic graph.