Evidence map›Paper›PMID 36582744›Full record

ArticleFood chemistry. Molecular sciences2023

Dietary polyphenols and their relationship to the modulation of non-communicable chronic diseases and epigenetic mechanisms: A mini-review.

Felipe Tecchio Borsoi, Iramaia Angélica Neri-Numa, Williara Queiroz de Oliveira, Fabio Fernandes de Araújo, Glaucia Maria Pastore

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Food chemistry. Molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
11.6field-weighted citation impact, top 1% 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

43 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review
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

5 authors at 1 institution in 1 country.

Felipe Tecchio BorsoiLaboratory of Bioflavors and Bioactive Compounds, Department of Food Science and Nutrition, Faculty of Food Engineering, University of Campinas, 13083-862 Campinas, SP, Brazil.
Iramaia Angélica Neri-NumaLaboratory of Bioflavors and Bioactive Compounds, Department of Food Science and Nutrition, Faculty of Food Engineering, University of Campinas, 13083-862 Campinas, SP, Brazil.
Williara Queiroz de OliveiraLaboratory of Bioflavors and Bioactive Compounds, Department of Food Science and Nutrition, Faculty of Food Engineering, University of Campinas, 13083-862 Campinas, SP, Brazil.
Fabio Fernandes de AraújoLaboratory of Bioflavors and Bioactive Compounds, Department of Food Science and Nutrition, Faculty of Food Engineering, University of Campinas, 13083-862 Campinas, SP, Brazil.
Glaucia Maria PastoreLaboratory of Bioflavors and Bioactive Compounds, Department of Food Science and Nutrition, Faculty of Food Engineering, University of Campinas, 13083-862 Campinas, SP, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic Non-Communicable Diseases (NCDs) have been considered a global health problem, characterized as diseases of multiple factors, which are developed throughout life, and regardless of genetics as a risk factor of important relevance, the increase in mortality attributed to the disease to environmental factors and the lifestyle one leads. Although the reactive species (ROS/RNS) are necessary for several physiological processes, their overproduction is directly related to the pathogenesis and aggravation of NCDs. In contrast, dietary polyphenols have been widely associated with minimizing oxidative stress and inflammation. In addition to their antioxidant power, polyphenols have also drawn attention for being able to modulate both gene expression and modify epigenetic alterations, suggesting an essential involvement in the prevention and/or development of some pathologies. Therefore, this review briefly explained the mechanisms in the development of some NCDs, followed by a summary of some evidence related to the interaction of polyphenols in oxidative stress, as well as the modulation of epigenetic mechanisms involved in the management of NCDs.

Indexed as

8-oxodG, 8-oxo-2́deosyguanosineABCG, ATP Binding Cassette Subfamily G MemberADAM10, α-secretaseADRB3, adrenoceptor Beta 3APP, amyloid-β precursor proteinARF, auxin response factorARHGAP24, Rho GTPase Activating Protein 24ARH-I, aplysia ras homology member IATF6, activating transcription factor 6ATP2A3, ATPase Sarcoplasmic/Endoplasmic Reticulum Ca2+ Transporting 3BCL2L14, apoptosis facilitator Bcl-2-like protein 14Bioactive compoundsCDH1, cadherin-1CDKN, cyclin dependent kinase inhibitorCPT, carnitine palmitoyltransferaseCREBH, cyclic AMP-responsive element-binding protein HDANT2, DXZ4 associated non-noding transcript 2, distalDAPK1, death-associated protein kinase 1DNA methylationDNMT, DNA methyltransferaseDOT1L, disruptor of telomeric silencing 1-likeEWASs, epigenome-wide association studiesEZH2, Enhancer of zeste homolog 2FAS, Fas cell Surface Death ReceptorGDNF, glial cell line-derived neurotrophic factorGFAP, glial fibrillary acid proteinGSTP1, Glutathione S-transferases P1Gut microbiota modulationHAT, histone acetylasesHDAC, histone deacetylasesHistone modificationsHSD11B2, 11 beta-hydroxysteroid dehydrogenase type 2IGFBP3, insulin-like growth factor-binding protein 3IGT, impaired glucose toleranceKCNK3, potassium two pore domain channel subfamily K Member 3lncRNA, long non-coding RNAMBD4, methyl-CpG binding domain 4MGMT, O-6-methylguanine-DNA methyltransferaseNAFLD, Non-alcoholic fatty liver diseasencRNA, non-coding RNAoAβ-induced-LTP, oligomeric amyloid-beta induced long term potentiationOCT1, Organic cation transporter 1OGG1, 8-Oxoguanine DNA GlycosylaseOxidative stressPAI-1, plasminogen activator inhibitor 1Personalized nutritionPHOSPHO1, Phosphoethanolamine/Phosphocholine Phosphatase 1PLIN1, perilipin 1POE3A, RNA polymerase IIIPPARGC1A, PPARG coactivator 1 alphaPPAR, peroxisome proliferator-activated receptorPRKCA, Protein kinase C alphaPTEN, phosphatase and tensin homologueRASSF1A, Ras association domain family member 1SAH, S -adenosyl-l-homocysteineSAM, S-adenosyl-methionineSD, sleep deprivationSOCS3, suppressor of cytokine signaling 3SREBP-1C, sterol-regulatory element binding protein-1CTBX2, t-box transcription factor 2TCF7L2, transcription factor 7 like 2TET, ten-eleven translocation proteinsTNNT2, cardiac muscle troponin TTPA, 12-O-tetradecanoylphorbol-13-acetate

Identifiers

PMID36582744
PMCPMC9793217
OpenAlexW4312084667

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.