Evidence map›Paper›PMID 41032001›Full record

ReviewMayo Clinic proceedings2025

Skinspan

Saranya P Wyles, Hasina S Maredia, Ryeim B Ansaf, Moudar R Dweydari, Ryan T Hurt, Sara L Bonnes, Sundeep Khosla, Nathan K LeBrasseur, Zoe Diana Draelos, Mark D P Davis

Abstract readReview
In one paragraph

Review in Mayo Clinic proceedings, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

10 authors.

Saranya P WylesDepartment of Dermatology, Mayo Clinic, Rochester, MN, USA. Electronic address: wyles.saranya@mayo.edu.
Hasina S MarediaDepartment of Dermatology, Mayo Clinic, Rochester, MN, USA.
Ryeim B AnsafDepartment of Biomedical Sciences, University of Connecticut, Farmington, CT, USA; Young Innovative Investigator Program, Cato T. Laurencin Institute for Regenerative Engineering, University of Connecticut Health Center, Farmington, CT.
Moudar R DweydariUniversity of Illinois at Urbana-Champaign, Champaign, IL; Georgetown University School of Medicine, Washington, D.C.
Ryan T HurtDepartment of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Sara L BonnesDepartment of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Sundeep KhoslaDepartment of Internal Medicine, Mayo Clinic, Rochester, MN, USA; Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.
Nathan K LeBrasseurRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.
Zoe Diana DraelosDermatology Consulting Services, PLLC, High Point, NC, USA.
Mark D P DavisDepartment of Dermatology, Mayo Clinic, Rochester, MN, USA.

Funding

Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
Defining the interactions of senescent immune cells and skeletal cellsR01AG076515 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, David G Monroe · 2022 to 2026
$2.4M
Characterization of senescent cell populations in skeletal agingR01AG086085 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, David G Monroe · 2024 to 2026
$1.6M
Topical Senolytics for Chronic Wound HealingR03AG082919 · NIA · MAYO CLINIC ROCHESTER · PI WYLES, SARANYA PURUSHOTHAMAN · 2023 to 2023
$323k
NIA NIH HHS P01 AG062413NIA NIH HHS R01 AG076515NIA NIH HHS R01 AG086085NIA NIH HHS R03 AG082919
6 · The paper itself

Abstract

Skin aging is an inherent biological component of human aging. As the global population ages, the incidence of age-related skin conditions has become increasingly prevalent. Both intrinsic and extrinsic factors, collectively known as the skin "exposome," contribute to visible and physiological changes. The skin's layers, including the epidermis, dermis, and hypodermis, function both independently and interdependently in these aging processes. Intrinsic factors such as hormonal fluctuations, genetic predispositions, and cellular senescence, defined as an irreversible cell cycle arrest, drive physiological age-related skin changes. These changes are underpinned by several interconnected hallmarks of aging, including genomic instability, telomere attrition, epigenetic alterations, and loss of proteostasis, all of which impair cell renewal and dermal structure. Stem cell exhaustion and mitochondrial dysfunction reduce the skin's capacity to regenerate and adapt to stress, whereas altered intercellular communication and chronic low-grade inflammation ("inflammaging") further accelerate aging phenotypes such as loss of elasticity, epidermal thinning, and delayed wound healing. Extrinsic factors, including ultraviolet radiation, air pollution, smoking, and poor nutrition, compound these effects by increasing oxidative stress, DNA damage, and activating senescence-associated secretory phenotypes. Lifelong sun protection, nutritious dietary habits, regular physical activity, and topical interventions such as sunscreen and moisturizers help maintain a resilient skin microenvironment. This review highlights the urgent need to recognize, prevent, and treat skin aging. Emerging therapies targeting root-cause mechanisms may revolutionize dermatologic care and extend skin healthspan - now known as skinspan.

Indexed as

Healthy AgingLongevitySkin AgingHumansSkin

Identifiers

PMID41032001
PMCPMC12702499

What OpenQuestion holds

Textmetadata
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.