Evidence mapPaperPMID 42506452Full record

ReviewMetabolites2026

Molecular Mechanisms Associated with Metabolic Dysfunction: Contributions of Nutritional Genomics.

Natália Ellen Delmicon, Nathália Dos Reis Franco, Giovanna Cavanha Corsi, Roberta Mi Kyong Kim Cho, Helen Cristina Vidal, Marcelo Macedo Rogero

Abstract readReview
In one paragraph

Review in Metabolites, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Natália Ellen DelmiconDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr. Arnaldo Avenue, Sao Paulo 01246-904, SP, Brazil.ORCID 0000-0002-7241-0231
Nathália Dos Reis FrancoDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr. Arnaldo Avenue, Sao Paulo 01246-904, SP, Brazil.ORCID 0000-0002-8648-3538
Giovanna Cavanha CorsiDepartment of Food Science and Experimental Nutrition, Faculty of Pharmaceutical Sciences, University of Sao Paulo, 580 Professor Lineu Prestes Avenue, Sao Paulo 05508-000, SP, Brazil.ORCID 0000-0001-6859-1124
Roberta Mi Kyong Kim ChoDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr. Arnaldo Avenue, Sao Paulo 01246-904, SP, Brazil.ORCID 0009-0000-2438-5644
Helen Cristina VidalDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr. Arnaldo Avenue, Sao Paulo 01246-904, SP, Brazil.
Marcelo Macedo RogeroDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr. Arnaldo Avenue, Sao Paulo 01246-904, SP, Brazil.ORCID 0000-0003-0517-1645

Funding

National Council for Scientific and Technological Development 318768/2025-9São Paulo Research Foundation 2024/07903-0São Paulo Research Foundation 2024/07904-7São Paulo Research Foundation 2025/06107-9
6 · The paper itself

Abstract

Nutritional genomics has expanded our understanding of how dietary exposures interact with genetic and epigenetic mechanisms involved in metabolic dysfunction. In this context, metabolic dysfunction associated with excessive visceral adiposity arises from a multifaceted interaction between systemic inflammation, insulin resistance, and inter-individual biological susceptibility. Obesity, particularly when driven by diets rich in saturated fatty acids, disrupts intestinal homeostasis, thereby triggering metabolic endotoxemia and contributing to low-grade systemic inflammation and adipose tissue dysfunction. Advances following the Human Genome Project have broadened our understanding of the molecular mechanisms of metabolic diseases, highlighting the role of genetic variability and epigenetic regulation in obesity-related insulin resistance. In nutritional science, the integration of genomics and proteomics has further elucidated how dietary exposures interact with the biological pathways involved in this dysfunction. From a nutrigenomic perspective, this narrative review aims to discuss how genetic variability and diet-related molecular mechanisms contribute to obesity-related metabolic dysfunction, with emphasis on single-nucleotide polymorphisms in key genes, including

Indexed as

DNA methylationendotoxemiainflammationinsulin resistancemicroRNAsnutrigenomicspolymorphismsingle nucleotide

Identifiers

PMID42506452
PMCPMC13413746

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.