Evidence map›Paper›PMID 36555691›Full record

ReviewInternational journal of molecular sciences2022

Mitochondrial Dysfunction and Therapeutic Perspectives in Cardiovascular Diseases.

Yu Liu, Yuejia Huang, Chong Xu, Peng An, Yongting Luo, Lei Jiao, Junjie Luo, Yongzhi Li

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
10.1field-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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 127 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
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  14. Coenzyme QInternational journal of molecular sciences · 2026
    Article
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13 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

8 authors at 2 institutions in 1 country.

Yu LiuChina Astronaut Research and Training Center, Beijing 100094, China.
Yuejia HuangDepartment of Nutrition and Health, China Agricultural University, Beijing 100193, China.
Chong XuChina Astronaut Research and Training Center, Beijing 100094, China.
Peng AnDepartment of Nutrition and Health, China Agricultural University, Beijing 100193, China.ORCID 0000-0002-0421-0035
Yongting LuoDepartment of Nutrition and Health, China Agricultural University, Beijing 100193, China.ORCID 0000-0001-7834-8742
Lei JiaoChina Astronaut Research and Training Center, Beijing 100094, China.
Junjie LuoDepartment of Nutrition and Health, China Agricultural University, Beijing 100193, China.ORCID 0000-0002-8987-0533
Yongzhi LiChina Astronaut Research and Training Center, Beijing 100094, China.
China Agricultural University · CNChina Astronaut Research and Training Center · CN

Funding

the space health research foundation of Astronaut Health Center AHCC2020ZX002, 413FZ2, WSQW2001
6 · The paper itself

Abstract

High mortality rates due to cardiovascular diseases (CVDs) have attracted worldwide attention. It has been reported that mitochondrial dysfunction is one of the most important mechanisms affecting the pathogenesis of CVDs. Mitochondrial DNA (mtDNA) mutations may result in impaired oxidative phosphorylation (OXPHOS), abnormal respiratory chains, and ATP production. In dysfunctional mitochondria, the electron transport chain (ETC) is uncoupled and the energy supply is reduced, while reactive oxygen species (ROS) production is increased. Here, we discussed and analyzed the relationship between mtDNA mutations, impaired mitophagy, decreased OXPHOS, elevated ROS, and CVDs from the perspective of mitochondrial dysfunction. Furthermore, we explored current potential therapeutic strategies for CVDs by eliminating mtDNA mutations (e.g., mtDNA editing and mitochondrial replacement), enhancing mitophagy, improving OXPHOS capacity (e.g., supplement with NAD

Indexed as

Cardiovascular DiseasesMitochondrial DiseasesDNA, MitochondrialElectron TransportHumansMitochondriaReactive Oxygen SpeciesDNA, MitochondrialReactive Oxygen Speciescardiovascular diseasemitochondrial DNA mutationmitochondrial dysfunctionmitophagyoxidative phosphorylationreactive oxygen speciestherapeutic strategy

Identifiers

PMID36555691
PMCPMC9788331
OpenAlexW4312209985

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.