Evidence map›Paper›PMID 30061536›Full record

ReviewAntioxidants (Basel, Switzerland)2018

Lipid Peroxidation-Derived Aldehydes, 4-Hydroxynonenal and Malondialdehyde in Aging-Related Disorders.

Giuseppina Barrera, Stefania Pizzimenti, Martina Daga, Chiara Dianzani, Alessia Arcaro, Giovanni Paolo Cetrangolo, Giulio Giordano, Marie Angele Cucci, Maria Graf, Fabrizio Gentile

Open access · goldAbstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed
9.9field-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

151 citing papers in PubMed, 298 citations in OpenAlex.

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91 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

10 authors at 3 institutions in 1 country.

Giuseppina BarreraDipartimento di Scienze Cliniche e Biologiche, Università di Torino, 10124 Turin, Italy. giuseppina.barrera@unito.it.
Stefania PizzimentiDipartimento di Scienze Cliniche e Biologiche, Università di Torino, 10124 Turin, Italy. stefania.pizzimenti@unito.it.
Martina DagaDipartimento di Scienze Cliniche e Biologiche, Università di Torino, 10124 Turin, Italy. martina.daga@unito.it.
Chiara DianzaniDipartimento di Scienze e Tecnologia del Farmaco, Università di Torino, 10124 Turin, Italy. chiara.dianzani@unito.it.
Alessia ArcaroDipartimento di Medicina e Scienze della Salute "V. Tiberio", Università del Molise, 86100 Campobasso, Italy. alessia.arcaro@unimol.it.
Giovanni Paolo CetrangoloDipartimento di Medicina e Scienze della Salute "V. Tiberio", Università del Molise, 86100 Campobasso, Italy. gianpaolo.cet@tiscali.it.
Giulio GiordanoPresidio Ospedaliero "A. Cardarelli", Azienda Sanitaria Regione Molise, 86100 Campobasso, Italy. giuliogiordano@hotmail.com.
Marie Angele CucciDipartimento di Scienze Cliniche e Biologiche, Università di Torino, 10124 Turin, Italy. marieangele.cucci@unito.it.
Maria GrafPresidio Ospedaliero "A. Cardarelli", Azienda Sanitaria Regione Molise, 86100 Campobasso, Italy. mariagraf@tiscali.it.
Fabrizio GentileDipartimento di Medicina e Scienze della Salute "V. Tiberio", Università del Molise, 86100 Campobasso, Italy. gentilefabrizio@unimol.it.ORCID 0000-0002-6704-3115
University of Turin · ITUniversity of Molise · ITPresidio Ospedaliero · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the various mechanisms involved in aging, it was proposed long ago that a prominent role is played by oxidative stress. A major way by which the latter can provoke structural damage to biological macromolecules, such as DNA, lipids, and proteins, is by fueling the peroxidation of membrane lipids, leading to the production of several reactive aldehydes. Lipid peroxidation-derived aldehydes can not only modify biological macromolecules, by forming covalent electrophilic addition products with them, but also act as second messengers of oxidative stress, having relatively extended lifespans. Their effects might be further enhanced with aging, as their concentrations in cells and biological fluids increase with age. Since the involvement and the role of lipid peroxidation-derived aldehydes, particularly of 4-hydroxynonenal (HNE), in neurodegenerations, inflammation, and cancer, has been discussed in several excellent recent reviews, in the present one we focus on the involvement of reactive aldehydes in other age-related disorders: osteopenia, sarcopenia, immunosenescence and myelodysplastic syndromes. In these aging-related disorders, characterized by increases of oxidative stress, both HNE and malondialdehyde (MDA) play important pathogenic roles. These aldehydes, and HNE in particular, can form adducts with circulating or cellular proteins of critical functional importance, such as the proteins involved in apoptosis in muscle cells, thus leading to their functional decay and acceleration of their molecular turnover and functionality. We suggest that a major fraction of the toxic effects observed in age-related disorders could depend on the formation of aldehyde-protein adducts. New redox proteomic approaches, pinpointing the modifications of distinct cell proteins by the aldehydes generated in the course of oxidative stress, should be extended to these age-associated disorders, to pave the way to targeted therapeutic strategies, aiming to alleviate the burden of morbidity and mortality associated with these disturbances.

Indexed as

aldehydesimmunosenescencemyelodysplastic syndromesosteopeniasarcopenia

Identifiers

PMID30061536
PMCPMC6115986
OpenAlexW2884618123

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.