Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Dec 5:2:2059513116676828.
doi: 10.1177/2059513116676828. eCollection 2016 Jan-Dec.

The effects of advanced glycation end products (AGEs) on dermal wound healing and scar formation: a systematic review

Affiliations
Review

The effects of advanced glycation end products (AGEs) on dermal wound healing and scar formation: a systematic review

Lennert Van Putte et al. Scars Burn Heal. .

Abstract

Introduction: With ageing, the skin gradually loses its youthful appearance and functions like wound healing and scar formation. The pathophysiological theory of Advanced Glycation End products (AGEs) has gained traction during the last decade. This review aims to document the influence of AGEs on the mechanical and physiologic properties of the skin, how they affect dermal wound healing and scar formation in high-AGE populations like elderly patients and diabetics, and potential therapeutic strategies.

Methods: This systematic literature study involved a structured search in Pubmed and Web of Science with qualitative analysis of 14 articles after a three-staged selection process with the use of in- and exclusion criteria.

Results: Overall, AGEs cause shortened, thinned, and disorganized collagen fibrils, consequently reducing elasticity and skin/scar thickness with increased contraction and delayed wound closure. Documented therapeutic strategies include dietary AGE restriction, sRAGE decoy receptors, aminoguanidine, RAGE-blocking antibodies, targeted therapy, thymosin β4, anti-oxidant agents and gold nanoparticles, ethyl pyruvate, Gal-3 manipulation and metformin.

Discussion: With lack of evidence concerning scars, no definitive conclusions can yet be made about the role of AGEs on possible appearance or function of scar tissue. However, all results suggest that scars tend to be more rigid and contractile with persistent redness and reduced tendency towards hypertrophy as AGEs accumulate.

Conclusion: Abundant evidence supports the pathologic role of AGEs in ageing and dermal wound healing and the effectiveness of possible therapeutic agents. More research is required to conclude its role in scar formation and scar therapy.

Keywords: Advanced glycosylation end products (AGEs); cicatrix; connective tissue; dermal wound healing; fibrosis; photoageing; scarring; skin ageing.

PubMed Disclaimer

Conflict of interest statement

Declaration of conflicting interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Methodological flowchart.
Figure 2.
Figure 2.
Dermal effects of Advanced Glycation End Products.

References

    1. Viña J, Borrás C, Miquel J. Theories of ageing. IUBMB Life 2007; 59: 249–254. - PubMed
    1. Paul RG, Bailey AJ. Glycation of collagen: the basis of its central role in the late complications of ageing and diabetes. Int J Biochem Cell Biol 1996; 28: 1297–1310. - PubMed
    1. Tortora GJ, Grabowski SR. Principles of Anatomy and Physiology. New York, NY: HarperCollins College Publishers, 1993.
    1. Adam J, Singer M, Richard AF, et al. Cutaneous wound healing. N Engl J Med 1999; 341: 738–746. - PubMed
    1. Fore J. A review of skin and the effects of ageing on skin structure and function. Ostomy Wound Manage 2006; 52: 24–35. - PubMed

How to cite this article

    1. Van Putte L, De Schrijver S, Moortgat P. The effects of Advanced Glycation End Products (AGEs) on dermal wound healing and scar formation: a systematic review. Scars, Burns & Healing, 2016. DOI: 10.1177/2059513116676828. - DOI - PMC - PubMed

LinkOut - more resources