Evidence map›Paper›PMID 31366015›Full record

ReviewNutrients2019

The Modern Western Diet Rich in Advanced Glycation End-Products (AGEs): An Overview of Its Impact on Obesity and Early Progression of Renal Pathology.

Arianna Bettiga, Francesco Fiorio, Federico Di Marco, Francesco Trevisani, Annalisa Romani, Esteban Porrini, Andrea Salonia, Francesco Montorsi, Riccardo Vago

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 2 pooled it
9.2field-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

63 citing papers in PubMed, 2 syntheses or guidelines pooled it, 123 citations in OpenAlex.

  1. Pooled it
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  16. Toxic AGEs (TAGE) Cause Lifestyle-Related Diseases.Antioxidants (Basel, Switzerland) · 2024
    Review
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  19. Article
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3 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Arianna BettigaUrological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, 20132 Milano, Italy.
Francesco FiorioUniversità Vita-Salute San Raffaele, 20132 Milano, Italy.
Federico Di MarcoUrological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, 20132 Milano, Italy.
Francesco TrevisaniUrological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, 20132 Milano, Italy.
Annalisa RomaniPHYTOLAB (Pharmaceutical, Cosmetic, Food supplement Technology and Analysis)-DiSIA, University of Florence, 50019 Sesto Fiorentino (Florence), Italy.
Esteban PorriniUniversidad de La Laguna, Dep de Medicina Interna, ITB, Instituto de Tecnologías Biomédicas, 38320 La Laguna, Spain.
Andrea SaloniaUrological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, 20132 Milano, Italy.
Francesco MontorsiUrological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, 20132 Milano, Italy.
Riccardo VagoUrological Research Institute, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, 20132 Milano, Italy. vago.riccardo@hsr.it.ORCID 0000-0002-3781-6770
Vita-Salute San Raffaele University · ITUniversidad de La Laguna · ESUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced glycation end-products (AGEs) are an assorted group of molecules formed through covalent bonds between a reduced sugar and a free amino group of proteins, lipids, and nucleic acids. Glycation alters their structure and function, leading to impaired cell function. They can be originated by physiological processes, when not counterbalanced by detoxification mechanisms, or derive from exogenous sources such as food, cigarette smoke, and air pollution. Their accumulation increases inflammation and oxidative stress through the activation of various mechanisms mainly triggered by binding to their receptors (RAGE). So far, the pathogenic role of AGEs has been evidenced in inflammatory and chronic diseases such as chronic kidney disease, cardiovascular disease, and diabetic nephropathy. This review focuses on the AGE-induced kidney damage, by describing the molecular players involved and investigating its link to the excess of body weight and visceral fat, hallmarks of obesity. Research regarding interventions to reduce AGE accumulation has been of great interest and a nutraceutical approach that would help fighting chronic diseases could be a very useful tool for patients' everyday lives.

Indexed as

Glycation End Products, AdvancedHumansKidney DiseasesObesityGlycation End Products, Advancedadvanced glycation end-products (AGEs)carboximethyl-lysine (CML)dietobesityrenal disease

Identifiers

PMID31366015
PMCPMC6724323
OpenAlexW2965916141

What OpenQuestion 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 OpenQuestion graph.