Evidence map›Paper›PMID 35408967›Full record

ReviewInternational journal of molecular sciences2022

Iron Metabolism in Aging and Age-Related Diseases.

Yao Tian, Yuanliangzi Tian, Zhixiao Yuan, Yutian Zeng, Shuai Wang, Xiaolan Fan, Deying Yang, Mingyao Yang

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 67 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 2 pooled it
14.6field-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

67 citing papers in PubMed, 2 syntheses or guidelines pooled it, 96 citations in OpenAlex.

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  13. Oxidative Stress andInternational journal of molecular sciences · 2026
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7 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 1 institution in 1 country.

Yao TianInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.
Yuanliangzi TianInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.ORCID 0000-0002-8448-0245
Zhixiao YuanInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.
Yutian ZengInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.
Shuai WangInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.
Xiaolan FanInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.ORCID 0000-0003-0968-6734
Deying YangInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.
Mingyao YangInstitute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu 611130, China.ORCID 0000-0001-6508-2738
Sichuan Agricultural University · CN

Funding

National Natural Science Foundation of China 31771338
6 · The paper itself

Abstract

Iron is a trace metal element necessary to maintain life and is also involved in a variety of biological processes. Aging refers to the natural life process in which the physiological functions of the various systems, organs, and tissues decline, affected by genetic and environmental factors. Therefore, it is imperative to investigate the relationship between iron metabolism and aging-related diseases, including neurodegenerative diseases. During aging, the accumulation of nonheme iron destroys the stability of the intracellular environment. The destruction of iron homeostasis can induce cell damage by producing hydroxyl free radicals, leading to mitochondrial dysfunction, brain aging, and even organismal aging. In this review, we have briefly summarized the role of the metabolic process of iron in the body, then discussed recent developments of iron metabolism in aging and age-related neurodegenerative diseases, and finally, explored some iron chelators as treatment strategies for those disorders. Understanding the roles of iron metabolism in aging and neurodegenerative diseases will fill the knowledge gap in the field. This review could provide new insights into the research on iron metabolism and age-related neurodegenerative diseases.

Indexed as

AgingNeurodegenerative DiseasesHomeostasisHumansIronIron Chelating AgentsIronIron Chelating Agentsagingiron chelatoriron metabolismmitochondrianeurodegenerative diseases

Identifiers

PMID35408967
PMCPMC8998315
OpenAlexW4220838505

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.