Evidence map›Paper›PMID 29745022›Full record

ArticleAging cell2018

Restoring mitochondrial DNA copy number preserves mitochondrial function and delays vascular aging in mice.

Kirsty Foote, Johannes Reinhold, Emma P K Yu, Nichola L Figg, Alison Finigan, Michael P Murphy, Martin R Bennett

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

78 citing papers in PubMed, 122 citations in OpenAlex.

  1. Aging-AssociatedJournal of the American Heart Association · 2026
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18 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

7 authors at 1 institution in 1 country.

Kirsty FooteDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Johannes ReinholdDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Emma P K YuDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Nichola L FiggDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Alison FiniganDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Michael P MurphyMRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK.
Martin R BennettDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
University of Cambridge · GB

Funding

FOAM COUNTERCURRENT CHROMATOGRAPHY WITH A COIL PLANET CENTRIFUGEZ01HL001469 · NHLBI · HEART, LUNG, AND BLOOD INSTITUTE · PI ITO, Y · 1989 to 1989
–
BHF Centre for Research ExcellenceBritish Heart Foundation FS/10/70/28507British Heart Foundation PG/11/57/29003British Heart Foundation PG/13/25/30014British Heart Foundation PG/14/69/31032British Heart Foundation PG/16/11/32021British Heart Foundation PG/16/63/32307British Heart Foundation RG/13/14/30314British Heart Foundation (BHF) PG/13/25/30014British Heart Foundation (BHF) PG/14/69/31032British Heart Foundation (BHF) PG/16/63/32307British Heart Foundation (BHF) RG/13/14/30314Medical Research Council MC_U105663142Medical Research Council MC_UU_00015/3Medical Research Council UK MC_U105663142National Institute for Health Research Cambridge Biomedical Research CentreThe Academy of Medical SciencesWellcome Trust 110158/Z/15/ZWellcome Trust PhD Fellowship 110159/Z/15/Z
6 · The paper itself

Abstract

Aging is the largest risk factor for cardiovascular disease, yet the molecular mechanisms underlying vascular aging remain unclear. Mitochondrial DNA (mtDNA) damage is linked to aging, but whether mtDNA damage or mitochondrial dysfunction is present and directly promotes vascular aging is unknown. Furthermore, mechanistic studies in mice are severely hampered by long study times and lack of sensitive, repeatable and reproducible parameters of arterial aging at standardized early time points. We examined the time course of multiple invasive and noninvasive arterial physiological parameters and structural changes of arterial aging in mice, how aging affects vessel mitochondrial function, and the effects of gain or loss of mitochondrial function on vascular aging. Vascular aging was first detected by 44 weeks (wk) of age, with reduced carotid compliance and distensibility, increased β-stiffness index and increased aortic pulse wave velocity (PWV). Aortic collagen content and elastin breaks also increased at 44 wk. Arterial mtDNA copy number (mtCN) and the mtCN-regulatory proteins TFAM, PGC1α and Twinkle were reduced by 44 wk, associated with reduced mitochondrial respiration. Overexpression of the mitochondrial helicase Twinkle (Tw

Indexed as

AgingAnimalsDNA Copy Number VariationsDNA, MitochondrialFemaleMaleMiceMitochondriaVascular StiffnessDNA, Mitochondrialagingmitochondriamitochondrial DNAvascular stiffness

Identifiers

PMID29745022
PMCPMC6052475
OpenAlexW2800471357

What OpenQuestion holds

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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.