Effects on the Skin Microbiome by a Moisturizer Formulated for Eczema-Prone and Sensitive Skin

March 2025 | Volume 24 | Issue 3 | 275 | Copyright © March 2025


Published online February 28, 2025

doi:10.36849/JDD.8707

Cleo Whiting BAa, Sara Abdel Azim MSa, Nicolas Joly-Tonetti PhDb, Nadège Lachmann MSb, Adam Friedman MD FAADa

aDepartment of Dermatology, George Washington University School of Medicine and Health Sciences, Washington, DC
bGlobal Sensitive Skincare Faculty, Galderma, Lausanne, Switzerland

Abstract
Background: Cutaneous dysbiosis contributes to the pathophysiology of atopic dermatitis and potentially that of sensitive skin; regulation of the bacterial communities through skincare products is an emerging management strategy. Previous studies have highlighted the utility of ingredients that function as prebiotics, are anti-inflammatory, and have barrier-repairing properties to help shift species richness and composition toward more eubiotic states.
Methods: In a single-site open-label study, a moisturizer containing colloidal oatmeal, Ophiopogon japonicus root extract (AD-Resyl®, SILAB, France), and a patented filaggrin protein byproduct was evaluated for its effect on the bacterial communities of eczema-prone and sensitive skin (n=12). Skin swab samples from participants' cheeks were collected before and after applying the moisturizer twice daily for 21 days. Measures of alpha diversity (richness, Shannon diversity index) and beta diversity were calculated using paired, comparative analyses of sampled bacterial loads.
Results: Bacterial species richness was significantly increased in 10 participants (P<0.05) without dysbiotic shifts in overall microbial composition.
Conclusion: These results support the use of a moisturizer containing anti-inflammatory and skin barrier-repairing ingredients for managing atopic dermatitis and add to our knowledge of the skin microbiome in sensitive skin.

J Drugs Dermatol. 2025;24(3):275-280. doi:10.36849/JDD.8707

INTRODUCTION

Atopic dermatitis (AD) is a common, chronic inflammatory skin disease for which cutaneous dysbiosis is a core component of disease pathophysiology.1,2 AD-associated dysbiotic changes in the skin microbiome composition include an increased abundance of Staphylococcus aureus (S. aureus), S. epidermidis, and S. haemolyticus, decreased bacterial species diversity, and reduced colonization of the fungal genus Malassezia.3 Regulation of the skin microbiota is an emerging strategy for managing AD, and monitoring could be a biomarker for disease activity and treatment success.4-6 Cosmetic skin care products may be tools for microbial manipulation through barrier restoration and foundational support for diverse cutaneous flora. Even simpler, anti-inflammatory ingredients could theoretically augment the microbiota through this mechanism alone and enhance AD treatment and management.

Colloidal oatmeal is an often used ingredient in skin care products for AD for its anti-inflammatory, anti-pruritic, and barrier repair properties and is listed in the US Food and Administration monograph as a skin barrier protectant and irritation-relieving ingredient for skin irritation due to eczema; notably, colloidal oat also acts as a prebiotic, encouraging the balanced growth of commensal bacteria.7-10 Additionally, extracts from the plant Ophiopogon japonicus have demonstrated immunoregulatory activity in an AD mouse model11 and clinically improved AD symptoms and patient’s quality of life compared to placebo.12 Finally, filaggrin, an essential protein for maintenance of the epidermal barrier, is reduced in atopic skin.13 Reduced levels of filaggrin metabolic byproducts such as pyrrolidone carboxylic acid (PCA) correlate with disease severity,14 thus topical replenishment of PCA may improve the defective skin barrier in AD. Despite these findings, the impact of these combined ingredients on improving dysbiosis has not been well elucidated to date.

Sensitive skin syndrome (SSS) is a condition of increased skin reactivity to innocuous exposures and is associated with an impaired skin barrier like AD. Although the skin microbiome of sensitive skin is not well understood, it is suspected that this impaired skin barrier contributes to the abnormal neurosensory responses of this condition.15-17