Evidence map›Paper›PMID 40939730›Full record

ArticleMolecular metabolism2025

Dietary isoleucine content modulates the metabolic and molecular response to a Western diet in mice.

Michaela E Trautman, Cara L Green, Michael R MacArthur, Krittisak Chaiyakul, Yasmine H Alam, Chung-Yang Yeh, Reji Babygirija, Isabella James, Michael Gilpin, Esther Zelenovskiy and 10 more

Abstract read
In one paragraph

Article in Molecular metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Michaela E TrautmanDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA; Nutrition and Metabolism Graduate Program, University of Wisconsin-Madison, Madison, WI, USA.
Cara L GreenDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Michael R MacArthurLewis-Sigler Institute of Integrative Genomics, Princeton University, Princeton, NJ 08540, USA.
Krittisak ChaiyakulDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, WI 53705, USA.
Yasmine H AlamDepartment of Biological Chemistry, University of California, Irvine, Irvine, CA 92697, USA.
Chung-Yang YehDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Reji BabygirijaDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA; Cell and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI, USA.
Isabella JamesDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA.
Michael GilpinDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA.
Esther ZelenovskiyDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Madelyn GreenDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Ryan N MarshallDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Alexander RaskinDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Michelle M SonsallaDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA; Howard Hughes Medical Institute, University of Wisconsin-Madison, Madison, WI 53706, USA.
Victoria FloresDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA; Nutrition and Metabolism Graduate Program, University of Wisconsin-Madison, Madison, WI, USA.
Judith A SimcoxDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA; Howard Hughes Medical Institute, University of Wisconsin-Madison, Madison, WI 53706, USA; Wisconsin Nathan Shock Center of Excellence in the Biology of Aging, Madison, WI 53705, USA.
Irene M OngDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, WI 53705, USA.
Kristen C MaleckiDepartment of Population Health Sciences, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53726, USA.
Cholsoon JangDepartment of Biological Chemistry, University of California, Irvine, Irvine, CA 92697, USA.
Dudley W LammingDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA; Nutrition and Metabolism Graduate Program, University of Wisconsin-Madison, Madison, WI, USA; Cell and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI, USA; Wisconsin Nathan Shock Center of Excellence in the Biology of Aging, Madison, WI 53705, USA; Comparative Biomedical Sciences Graduate Program, University of Wisconsin-Madison, Madison, WI, USA; University of Wisconsin Carbone Comprehensive Cancer Center, University of Wisconsin, Madison, WI 53705, USA; University of Wisconsin-Madison Comprehensive Diabetes Center, Madison, WI 53705, USA. Electronic address: dlamming@medicine.wisc.edu.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Pamela K Kreeger · 1985 to 2026
$142.6M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Role of Beta-Catenin in Urinary DysfunctionU54DK104310 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI STRAND, DOUGLAS WILLIAM, VEZINA, CHAD M. · 2014 to 2023
$12.8M
Project 3: Modulation of the head and neck tumor immune microenvironment by targeting the TAM family of receptorsP50CA278595 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Susan Lynn Thibeault · 2022 to 2026
$12.5M
Project 4: Role of Receptor Tyrosine Kinase AXL in HNSCC Therapy ResistanceP50DE026787 · NIDCR · UNIVERSITY OF WISCONSIN-MADISON · PI WHEELER, DERIC L · 2016 to 2020
$10.8M
Biology of Aging and Age-Related Diseases Training GrantT32AG000213 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Rozalyn M. Anderson, Sanjay Asthana · 1991 to 2026
$9.9M
Wisconsin Nathan Shock CenterP30AG092586 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI RICKI J COLMAN · 2025 to 2026
$3.8M
Translational analysis of a novel intervention to promote healthy aging.R01AG085898 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI RICKI J COLMAN, Dudley William Lamming · 2024 to 2026
$3.2M
The regulation of health and longevity by branched-chain amino acidsR01AG056771 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Dudley William Lamming · 2018 to 2026
$3.1M
The regulation of cancer and aging by methionineR01AG084156 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI VINCENT L. CRYNS, JOHN M DENU · 2023 to 2026
$2.5M
Elucidating hallmarks of aging in the development of lower urinary tract dysfunction (LUTD)R01DK131175 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI RICKE, WILLIAM A · 2021 to 2024
$2.3M
The regulation of health and longevity by branched-chain amino acidsRF1AG056771 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI LAMMING, DUDLEY WILLIAM · 2023 to 2023
$2.1M
BLRD VA I01 BX004031BLRD VA IS1 BX005524NCI NIH HHS P30 CA014520NCI NIH HHS P50 CA278595NIAAA NIH HHS R01 AA029124NIA NIH HHS F31 AG081115NIA NIH HHS F32 AG077916NIA NIH HHS F99 AG083290NIA NIH HHS K00 AG083290NIA NIH HHS K99 AG084921NIA NIH HHS P30 AG092586NIA NIH HHS R01 AG056771NIA NIH HHS R01 AG084156NIA NIH HHS R01 AG085898NIA NIH HHS R01 AG094153NIA NIH HHS R56 AG056771NIA NIH HHS RF1 AG056771NIA NIH HHS T32 AG000213NIA NIH HHS U01 AG081482NIDCR NIH HHS P50 DE026787NIDDK NIH HHS P30 DK020579NIDDK NIH HHS R01 DK125859NIDDK NIH HHS R01 DK131175NIDDK NIH HHS R01 DK133479NIDDK NIH HHS U54 DK104310
6 · The paper itself

Abstract

The amino acid composition of the diet has recently emerged as a critical regulator of metabolic health. Consumption of the branched-chain amino acid isoleucine is positively correlated with body mass index in humans, and reducing dietary levels of isoleucine rapidly improves the metabolic health of diet-induced obese male C57BL/6J mice. However, there are some reports that dietary supplementation with extra BCAAs has health benefits. Further, the interactions between sex, genetic background, and dietary isoleucine levels in response to a Western Diet (WD) remain incompletely understood. Here, we find that although the magnitude of the effect varies by sex and strain, reducing dietary levels of isoleucine protects C57BL/6J and DBA/2J mice of both sexes from the deleterious metabolic effects of a WD, while increasing dietary levels of isoleucine impairs aspects of metabolic health. Despite broadly positive responses across all sexes and strains to reduced isoleucine, the molecular response of each sex and strain is highly distinctive. Using a multi-omics approach, we identify a core sex- and strain-independent molecular response to dietary isoleucine, and identify mega-clusters of differentially expressed hepatic genes, metabolites, and lipids associated with each phenotype. Intriguingly, the metabolic effects of reduced isoleucine in mice are not associated with FGF21 - and we find that in humans, plasma FGF21 levels are likewise not associated with dietary levels of isoleucine. Finally, an analysis of human NHANES data shows that isoleucine content varies widely across foods, and that individuals with higher Healthy Eating Index scores tend to consume lower amounts of isoleucine. Our results suggest that the dietary level of isoleucine is a potential mediator of the metabolic and molecular response to a WD, and imply that reducing dietary isoleucine may represent a theoretically translatable strategy to protect from the negative metabolic consequences of a WD.

Indexed as

Diet, WesternIsoleucineAmino Acids, Branched-ChainAnimalsFemaleHumansLiverMaleMiceMice, Inbred C57BLMice, Inbred DBAObesityAmino Acids, Branched-ChainIsoleucineAdiposityBranched-chain amino acidsInsulin resistanceIsoleucineMetabolic healthWestern diet

Identifiers

PMID40939730
PMCPMC12495292

What Socratic holds

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LicenceCC BY-NC-ND
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 Socratic graph.