Evidence map›Paper›PMID 29125070›Full record

ReviewRejuvenation research2018

Circulating Mitochondrial DNA at the Crossroads of Mitochondrial Dysfunction and Inflammation During Aging and Muscle Wasting Disorders.

Anna Picca, Angela Maria Serena Lezza, Christiaan Leeuwenburgh, Vito Pesce, Riccardo Calvani, Maurizio Bossola, Ester Manes-Gravina, Francesco Landi, Roberto Bernabei, Emanuele Marzetti

Open access · greenAbstract readReview
In one paragraph

Review in Rejuvenation research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
6.5field-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.

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

85 citing papers in PubMed, 142 citations in OpenAlex.

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25 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 2 countries.

Anna Picca1 Department of Geriatrics, Neuroscience and Orthopedics, Teaching Hospital "Agostino Gemelli," Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Angela Maria Serena Lezza2 Department of Biosciences, Biotechnology and Biopharmaceutics, University of Bari , Bari, Italy .
Christiaan Leeuwenburgh3 Division of Biology of Aging, Department of Aging and Geriatric Research, Institute on Aging, University of Florida , Gainesville, Florida.
Vito Pesce2 Department of Biosciences, Biotechnology and Biopharmaceutics, University of Bari , Bari, Italy .
Riccardo Calvani1 Department of Geriatrics, Neuroscience and Orthopedics, Teaching Hospital "Agostino Gemelli," Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Maurizio Bossola4 Department of Surgery, Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Ester Manes-Gravina1 Department of Geriatrics, Neuroscience and Orthopedics, Teaching Hospital "Agostino Gemelli," Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Francesco Landi1 Department of Geriatrics, Neuroscience and Orthopedics, Teaching Hospital "Agostino Gemelli," Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Roberto Bernabei1 Department of Geriatrics, Neuroscience and Orthopedics, Teaching Hospital "Agostino Gemelli," Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Emanuele Marzetti1 Department of Geriatrics, Neuroscience and Orthopedics, Teaching Hospital "Agostino Gemelli," Catholic University of the Sacred Heart School of Medicine , Rome, Italy .
Università Cattolica del Sacro Cuore · ITUniversity of Bari Aldo Moro · ITUniversity of Florida · US

Funding

University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTIAAN LEEUWENBURGH · 2007 to 2026
$22.8M
NIA NIH HHS P30 AG028740
6 · The paper itself

Abstract

Mitochondrial structural and functional integrity is maintained through the coordination of several processes (e.g., biogenesis, dynamics, mitophagy), collectively referred to as mitochondrial quality control (MQC). Dysfunctional MQC and inflammation are hallmarks of aging and are involved in the pathogenesis of muscle wasting disorders, including sarcopenia and cachexia. One of the consequences of failing MQC is the release of mitochondria-derived damage-associated molecular patterns (DAMPs). By virtue of their bacterial ancestry, these molecules can trigger an inflammatory response by interacting with receptors similar to those involved in pathogen-associated responses. Mitochondria-derived DAMPs, especially cell-free mitochondrial DNA, have recently been associated with conditions characterized by chronic inflammation, such as aging and degenerative diseases. Yet, their actual implication in the aging process and muscle wasting disorders is at an early stage of investigation. Here, we review the contribution of mitochondria-derived DAMPs to age-related systemic inflammation. We also provide arguments in support of the exploitation of such signaling pathways for the management of muscle wasting conditions.

Indexed as

AgingAnimalsDNA, MitochondrialHumansInflammationMitochondriaOxidative StressSarcopeniaDNA, MitochondrialautophagycachexiaDAMPsmitochondrial biogenesismitochondrial quality controlsarcopenia

Identifiers

PMID29125070
PMCPMC6103247
OpenAlexW2767746559

What OpenQuestion holds

Textmetadata
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.