Evidence map›Paper›PMID 39582871›Full record

ReviewFrontiers in immunology2024

Exploring mechanisms of skin aging: insights for clinical treatment.

Meiqi Zhang, Yumeng Lin, Zhongyu Han, Xuewen Huang, Shuwei Zhou, Siyu Wang, Yan Zhou, Xuan Han, Haoran Chen

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Trial
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  6. Review
  7. Valorization ofPlants (Basel, Switzerland) · 2026
    Article
  8. Review
  9. Review
  10. Review
  11. Activity ofFrontiers in pharmacology · 2026
    Article
  12. Article
  13. Antibiotics (Basel, Switzerland) · 2025
    Review
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  17. Review
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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

9 authors.

Meiqi Zhang *School of Medical and Life Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Yumeng Lin *Health Management Center, Nanjing Tongren Hospital, School of Medicine, Southeast University, Nanjing, China.
Zhongyu Han *School of Medical and Life Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Xuewen HuangSchool of Medical and Life Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Shuwei ZhouJiangsu Key Laboratory of Molecular and Functional Imaging, Department of Radiology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Siyu WangScience and Education Department, Chengdu Xinhua Hospital Affiliated to North Sichuan Medical College, Chengdu, China.
Yan ZhouScience and Education Department, Chengdu Xinhua Hospital Affiliated to North Sichuan Medical College, Chengdu, China.
Xuan HanScience and Education Department, Chengdu Xinhua Hospital Affiliated to North Sichuan Medical College, Chengdu, China.
Haoran ChenScience and Education Department, Chengdu Xinhua Hospital Affiliated to North Sichuan Medical College, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The skin is the largest organ in the human body and is made up of various cells and structures. Over time, the skin will age, which is not only influenced by internal factors, but also by external environmental factors, especially ultraviolet radiation. Aging causes immune system weakening in the elderly, which makes them more susceptible to dermatosis, such as type 2 inflammatory mediated pruritus. The immune response in this condition is marked by senescent cells consistently releasing low amounts of pro-inflammatory cytokines through a senescence-associated secretory phenotype (SASP). This continuous inflammation may accelerate immune system aging and establish a connection between immune aging and type 2 inflammatory skin diseases. In addition, two chronic pigmentation disorders, vitiligo and chloasma, are also associated with skin aging. Aged cells escape the immune system and accumulate in tissues, forming a microenvironment that promotes cancer. At the same time, "photoaging" caused by excessive exposure to ultraviolet radiation is also an important cause of skin cancer. This manuscript describes the possible links between skin aging and type 2 inflammation, chronic pigmentation disorders, and skin cancer and suggests some treatment options.

Indexed as

Skin AgingAnimalsCellular SenescenceHumansSenescence-Associated Secretory PhenotypeSkinSkin NeoplasmsUltraviolet Raysagingchronic pigmentary disordersskinskin cancertype 2 inflammatory

Identifiers

PMID39582871
PMCPMC11581952

What Socratic 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 Socratic graph.