Evidence map›Paper›PMID 38195568›Full record

Trial reportJournal of translational medicine2024

Dietary sulfur amino acid restriction in humans with overweight and obesity: a translational randomized controlled trial.

Thomas Olsen, Emma Stolt, Bente Øvrebø, Amany Elshorbagy, Elena C Tore, Sindre Lee-Ødegård, Hannibal Troensegaard, Hanna Johannessen, Beate Doeland, Anna A D Vo and 10 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04701346 (Dietary Sulfur Amino Acid Restriction, Energy Metabolism and Obesity), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.0field-weighted citation impact, top 2% 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.

NCT04701346 nacompletednot on this map

Dietary Sulfur Amino Acid Restriction, Energy Metabolism and Obesity

TypeinterventionalSponsorUniversity of OsloRan2021 to 2022Enrolled61ConditionsOverweight and ObesityArmsLow SAA diet, High SAA diet
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
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  4. Methionine restriction and mimetics to ameliorate human aging and disease.Trends in endocrinology and metabolism: TEM · 2026
    Review
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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

20 authors at 7 institutions in 6 countries.

Thomas Olsen *Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway. thomas.olsen@medisin.uio.no.ORCID 0000-0003-1805-5221
Emma Stolt *Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Bente ØvrebøDepartment of Food Safety, Norwegian Institute of Public Health, Oslo, Norway.
Amany ElshorbagyDepartment of Physiology, Faculty of Medicine, University of Alexandria, Alexandria, Egypt.
Elena C ToreDepartment of Internal Medicine and CARIM School of Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.
Sindre Lee-ØdegårdDepartment of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Hannibal TroensegaardDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Hanna JohannessenDepartment of Paedriatic Surgery, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Beate DoelandDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Anna A D VoDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Anja F DahlDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Karianne SvendsenDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Magne ThoresenDepartment of Biostatistics, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Helga RefsumDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Russell RisingD&S Consulting Services, Inc, New York, USA.
Kristýna BarvíkováDepartment of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
Marleen van GreevenbroekDepartment of Internal Medicine and CARIM School of Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.
Viktor KožichDepartment of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
Kjetil RetterstølDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Kathrine J VinknesDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
University of Oslo · NOOslo University Hospital · NOCharles University · CZMaastricht University · NLGad Consulting Services (United States) · USNorwegian Institute of Public Health · NOUniversity of Oxford · GB

Funding

Joint Programming Initiative A healthy diet for a healthy life 727565Ministerstvo Školství, Mládeže a Tělovýchovy STAY 8F20013Ministerstvo Zdravotnictví Ceské Republiky VFN64165Norges Forskningsråd 310475
6 · The paper itself

Abstract

backgroundDietary sulfur amino acid restriction (SAAR) improves metabolic health in animals. In this study, we investigated the effect of dietary SAAR on body weight, body composition, resting metabolic rate, gene expression profiles in white adipose tissue (WAT), and an extensive blood biomarker profile in humans with overweight or obesity.

methodsN = 59 participants with overweight or obesity (73% women) were randomized stratified by sex to an 8-week plant-based dietary intervention low (~ 2 g/day, SAAR) or high (~ 5.6 g/day, control group) in sulfur amino acids. The diets were provided in full to the participants, and both investigators and participants were blinded to the intervention. Outcome analyses were performed using linear mixed model regression adjusted for baseline values of the outcome and sex.

resultsSAAR led to a ~ 20% greater weight loss compared to controls (β 95% CI - 1.14 (- 2.04, - 0.25) kg, p = 0.013). Despite greater weight loss, resting metabolic rate remained similar between groups. Furthermore, SAAR decreased serum leptin, and increased ketone bodies compared to controls. In WAT, 20 genes were upregulated whereas 24 genes were downregulated (FDR < 5%) in the SAAR group compared to controls. Generally applicable gene set enrichment analyses revealed that processes associated with ribosomes were upregulated, whereas processes related to structural components were downregulated.

conclusionOur study shows that SAAR leads to greater weight loss, decreased leptin and increased ketone bodies compared to controls. Further research on SAAR is needed to investigate the therapeutic potential for metabolic conditions in humans.

trial registrationClinicalTrials.gov identifier: NCT04701346, registered Jan 8th 2021, https://www. CLINICALTRIALS: gov/study/NCT04701346.

Indexed as

Amino Acids, SulfurOverweightFemaleHumansKetone BodiesLeptinMaleObesityWeight LossAmino Acids, SulfurKetone BodiesLeptinCysteineDietary interventionLeptinMethionine restrictionObesityOverweightRandomized controlled trialSulfur amino acid restrictionWeight loss

Identifiers

PMID38195568
PMCPMC10775517
OpenAlexW4390779230

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.