Evidence map›Paper›PMID 36743698›Full record

ArticleOxidative medicine and cellular longevity2023

Mitochondrial Dysfunction and Increased DNA Damage in Vascular Smooth Muscle Cells of Abdominal Aortic Aneurysm (AAA-SMC).

Bengi S Tavris, Andreas S Peters, Dittmar Böckler, Susanne Dihlmann

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.7field-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

22 citing papers in PubMed, 22 citations in OpenAlex.

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  7. Aging-AssociatedJournal of the American Heart Association · 2026
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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

4 authors at 1 institution in 1 country.

Bengi S TavrisKlinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinik Heidelberg, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.ORCID https://orcid.org/0000-0002-1901-4555
Andreas S PetersKlinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinik Heidelberg, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.ORCID https://orcid.org/0000-0002-1347-7575
Dittmar BöcklerKlinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinik Heidelberg, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.ORCID https://orcid.org/0000-0003-2421-2019
Susanne DihlmannKlinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinik Heidelberg, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.ORCID https://orcid.org/0000-0002-3737-7755
Heidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is increasing evidence for enhanced oxidative stress in the vascular wall of abdominal aortic aneurysms (AAA). Mitochondrial damage and dysfunction are hypothesized to be actors in altered production of reactive oxygen species (ROS) and oxidative stress. However, the role of mitochondria and oxidative stress in vascular remodelling and progression of AAA remains uncertain. We here addressed whether mitochondrial dysfunction is persistently increased in vascular smooth muscle cells (VSMCs) isolated from AAA compared to healthy VSMC. AAA-derived VSMC cultures (AAA-SMC,

Indexed as

Aortic Aneurysm, AbdominalMuscle, Smooth, VascularAngiotensin IIAorta, AbdominalDNA DamageHumansMitochondriaMyocytes, Smooth MuscleNADPReactive Oxygen SpeciesAngiotensin IINADPReactive Oxygen Species

Identifiers

PMID36743698
PMCPMC9891816
OpenAlexW4318033600

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.