Oral Statin Therapy in <scp>KRT16</scp> ‐ and <scp>KRT17</scp> ‐Associated Palmoplantar Epidermal Differentiation Disorder (Pachyonychia Congenita)

Palmoplantar epidermal differentiation disorder associated with pachyonychia congenita (pEDD-PC) is a rare autosomal dominant skin disorder caused by pathogenic variants in keratin genes, including KRT6A, KRT6B, KRT6C, KRT16, and KRT17. While statins have been reported to alleviate symptoms in KRT6A-pEDD-PC, their efficacy in other subtypes remains unclear. We report six adult patients, including four with KRT17 variants and two with KRT16 variants, who underwent off-label oral statin therapy. Statins were administered for at least 6 months following dose stabilization. Although the treatment was well tolerated in most cases, no significant clinical improvement in plantar calluses or pain was observed. All patients discontinued therapy due to insufficient efficacy. Our findings indicate that oral statin therapy may offer limited benefit in KRT16/KRT17-pEDD-PC and suggest the potential importance of early intervention and genotype-specific therapeutic strategies.

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Publication Details

Journal
The Journal of Dermatology
Published
2025-08-12
DOI
https://doi.org/10.1111/1346-8138.17900
Primary Topic
Skin and Cellular Biology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Oral Statin Therapy in KRT16 ‐ and KRT17 ‐Associated Palmoplantar Epidermal Differentiation Disorder (Pachyonychia Congenita)

Mika Watanabe, Ken Natsuga, Chao‐Kai Hsu, Chih‐Yu Chang et al.
The Journal of Dermatology
Skin and Cellular Biology Research
article

Oral Statin Therapy in KRT16 ‐ and KRT17 ‐Associated Palmoplantar Epidermal Differentiation Disorder (Pachyonychia Congenita)

Mika Watanabe, Ken Natsuga, Chao‐Kai Hsu, Chih‐Yu Chang, Sota Itamoto, Hideyuki Ujiie, Wei‐Ting Tu
article en

Abstract

Palmoplantar epidermal differentiation disorder associated with pachyonychia congenita (pEDD-PC) is a rare autosomal dominant skin disorder caused by pathogenic variants in keratin genes, including KRT6A, KRT6B, KRT6C, KRT16, and KRT17. While statins have been reported to alleviate symptoms in KRT6A-pEDD-PC, their efficacy in other subtypes remains unclear. We report six adult patients, including four with KRT17 variants and two with KRT16 variants, who underwent off-label oral statin therapy. Statins were administered for at least 6 months following dose stabilization. Although the treatment was well tolerated in most cases, no significant clinical improvement in plantar calluses or pain was observed. All patients discontinued therapy due to insufficient efficacy. Our findings indicate that oral statin therapy may offer limited benefit in KRT16/KRT17-pEDD-PC and suggest the potential importance of early intervention and genotype-specific therapeutic strategies.

The Journal of DermatologyVol. 52(10)
Hokkaido University (JP), National Cheng Kung University Hospital (TW), National Cheng Kung University (TW)
National Cheng Kung University Hospital, National Cheng Kung University
Good health and well-being
Openalex Percentile: Top 78%
Skin and Cellular Biology Research
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Oral Statin Therapy in <scp>KRT16</scp> ‐ and <scp>KRT17</scp> ‐Associated Palmoplantar Epidermal Differentiation Disorder (Pachyonychia Congenita) — Mika Watanabe, Ken Natsuga, et al. · The Journal of Dermatology (2025) | TGRS Research Map | TGRS