Topical Estrogen Accelerates Cutaneous Wound Healing in Aged Humans Associated with an Altered Inflammatory Response
Open accessAbstract
The effects of intrinsic aging on the cutaneous wound healing process are profound, and the resulting acute and chronic wound morbidity imposes a substantial burden on health services. We have investigated the effects of topical estrogen on cutaneous wound healing in healthy elderly men and women, and related these effects to the inflammatory response and local elastase levels, an enzyme known to be up-regulated in impaired wound healing states. Eighteen health status-defined females (mean age, 74.4 years) and eighteen males (mean age, 70.7 years) were randomized in a double-blind study to either active estrogen patch or identical placebo patch attached for 24 hours to the upper inner arm, through which two 4-mm punch biopsies were made. The wounds were excised at either day 7 or day 80 post-wounding. Compared to placebo, estrogen treatment increased the extent of wound healing in both males and females with a decrease in wound size at day 7, increased collagen levels at both days 7 and 80, and increased day 7 fibronectin levels. In addition, estrogen enhanced the strength of day 80 wounds. Estrogen treatment was associated with a decrease in wound elastase levels secondary to reduced neutrophil numbers, and decreased fibronectin degradation. In vitro studies using isolated human neutrophils indicate that one mechanism underlying the altered inflammatory response involves both a direct inhibition of neutrophil chemotaxis by estrogen and an altered expression of neutrophil adhesion molecules. These data demonstrate that delays in wound healing in the elderly can be significantly diminished by topical estrogen in both male and female subjects.
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Topical application of estrogens or ER agonists in aged females and males can improve healing, partially due to reduced MIF and activation of keratinocytes.
“Topical application of estrogens or ER agonists in both aged females and males can improve healing, which may be partially due to the reduced expression of macrophage migration inhibitory factor (MIF) and activation of keratinocytes [145–147].”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [145]
The Effect of Estrogen on Wound Healing (page not available) reports improved healing with topical estrogen in elderly women and men. This paper does not establish the claimed effects of ER agonists or attribute the improvement to reduced MIF expression or keratinocyte activation; its inflammatory findings instead concern neutrophils and elastase. (LLM, conf=0.88)
Experimental — accuracy not yet measuredEstrogen is a positive effector in wound healing.
“estrogen has been demonstrated as a positive effector in wound healing.”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [145]
Age-related changes can be reversed by systemic hormone replacement therapy or topical estrogen in both male and female subjects.
“Furthermore, age-related changes can be reversed by the systemic administration of hormone replacement therapy (175) or by topical estrogen in both male and female subjects (176).”
From Wound repair and regeneration: Mechanisms, signaling, and translation (2014) · cites this paper as [176]
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References 36 · Cited by 420
Research works printed but not linked: 3
- McDonald JA, Kelley DG: Degradation of fibronectin by human leu- cocyte elastase. J Biol Chem 1980, 255:8848 -8858
- Herron G, Banda M, Clark E, Gavnilovic J, Werb Z: Secretion of metalloproteinases by stimulated capillary endothelial cells. J Biol Chem 1986, 261:2814 -2818
- Nakajima K, Powers J, Ashe B, Zimmerman M: Mapping the extended substrate site of Cathepsin G and human leucocyte elastase. J Biol Chem 1979, 254:4027-4032
- Authors
- Ashcroft, G. S., Greenwell-Wild, T., Horan, M. A., Wahl, S. M., & Ferguson, M. W. J.
- Affiliations
- National Institutes of Health (US)
- Salford Royal Hospital (GB)
- Corresponding author
- Ashcroft, Gillian S.
- ORCID
- Ferguson, Mark W.J.
- Venue
- The American Journal of Pathology
- Publisher
- Elsevier BV
- Published
- 1999-10
- Volume
- 155
- Issue
- 4
- Pages
- 1137-1146
- ISSN
- 0002-9440 (ISSN-L)
- PMC
- PMC1867002
- OpenAlex
- W1982912850
- Cited by
- 420
- References
- 36
- Citations by year
- 2026: 7 · 2025: 12 · 2024: 9 · 2023: 5 · 2022: 18 · 2021: 10 · 2020: 16 · 2019: 16 · 2018: 13 · 2017: 13 · 2016: 20 · 2015: 11 · 2014: 30 · 2013: 16 · 2012: 21
- FWCI
- 10.62
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- American Journal Of Pathology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion)
- Funders
- Janssen Pharmaceuticals
- Topics
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Health Sciences › Medicine › Dermatology › Dermatologic Treatments and Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Keywords
- topical estrogen, skin wound healing, aging, older adults, inflammation, neutrophils, elastase, fibronectin degradation, collagen, wound strength, neutrophil chemotaxis, neutrophil adhesion molecules, chronic wounds
- MeSH terms
- Aged, Cell Count, Collagen, Double-Blind Method, Estradiol, Female, Fibronectins, Flow Cytometry, Humans, Inflammation, Male, Neutrophils, Receptors, Estrogen, Skin, Wound Healing, Blotting, Western, Cell Adhesion Molecules, Lewis X Antigen, Leukocyte Elastase
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