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1.
Annals of Dermatology ; : 761-761, 2018.
Article in English | WPRIM | ID: wpr-718756

ABSTRACT

The authors would like to change the corresponding author of the article.

2.
Annals of Dermatology ; : 432-440, 2018.
Article in English | WPRIM | ID: wpr-716503

ABSTRACT

BACKGROUND: Skin hydration is a common problem both in elderly and young people as dry skin may cause irritation, dermatological disorders, and wrinkles. While both genetic and environmental factors seem to influence skin hydration, thorough genetic studies on skin hydration have not yet been conducted. OBJECTIVE: We used a genome-wide association study (GWAS) to explore the genetic elements underlying skin hydration by regulating epidermal differentiation and skin barrier function. METHODS: A GWAS was conducted to investigate the genetic factors influencing skin hydration in 100 Korean females along with molecular studies of genes in human epidermal keratinocytes for functional study in vitro. RESULTS: Among several single nucleotide polymorphisms identified in GWAS, we focused on Single Stranded DNA Binding Protein 3 (SSBP3) which is associated with DNA replication and DNA damage repair. To better understand the role of SSBP3 in skin cells, we introduced a calcium-induced differentiation keratinocyte culture system model and found that SSBP3 was upregulated in keratinocytes in a differentiation dependent manner. When SSBP3 was overexpressed using a recombinant adenovirus, the expression of differentiation-related genes such as loricrin and involucrin was markedly increased. CONCLUSION: Taken together, our results suggest that genetic variants in the intronic region of SSBP3 could be determinants in skin hydration of Korean females. SSBP3 represents a new candidate gene to evaluate the molecular basis of the hydration ability in individuals.


Subject(s)
Aged , Female , Humans , Adenoviridae , Cell Differentiation , DNA Damage , DNA Replication , DNA, Single-Stranded , DNA-Binding Proteins , Genome-Wide Association Study , In Vitro Techniques , Introns , Keratinocytes , Polymorphism, Single Nucleotide , Skin
3.
Annals of Dermatology ; : 394-396, 2018.
Article in English | WPRIM | ID: wpr-715088

ABSTRACT

No abstract available.


Subject(s)
Humans , Sebum
4.
Korean Journal of Dermatology ; : 376-378, 2017.
Article in Korean | WPRIM | ID: wpr-136688

ABSTRACT

No abstract available.


Subject(s)
Pigmentation
5.
Korean Journal of Dermatology ; : 376-378, 2017.
Article in Korean | WPRIM | ID: wpr-136685

ABSTRACT

No abstract available.


Subject(s)
Pigmentation
6.
Annals of Dermatology ; : 263-267, 2017.
Article in English | WPRIM | ID: wpr-45445

ABSTRACT

BACKGROUND: Alopecia areata (AA) is an autoimmune skin disease difficult to manage and treat. The pathogenesis of AA features a T-cell-associated autoimmune process, and systemic immunosuppressive therapy is prescribed widely for AA. OBJECTIVE: To evaluate the efficacy and tolerance of systemic low-dose methotrexate (LD-MTX) therapy in treatment of recalcitrant AA multiplex. METHODS: In a retrospective, non-controlled study, we evaluated 29 patients with recalcitrant AA treated with LD-MTX and assessed the therapeutic response according to severity of disease, disease duration, cumulative dose of MTX, and drug safety. RESULTS: MTX was administered twice weekly, and the mean maximum weekly dose was 14.48 mg. The response was A5 (regrowth=100.0%) in 14 (48.3%) patients and A4 (regrowth of 75%~90%) in 12 (41.4%) patients. Three patients had poor response to LD-MTX treatment (A2: n=2 [6.9%], A1: n=1 [3.4%]). All three of the patients showing a poor response had disease durations exceeding 24 months. Relapse was observed in 31% of patients with more than 75% regrowth. Common side-effects were elevated liver enzyme levels and gastrointestinal discomfort. CONCLUSION: LD-MTX appears to be an effective and well-tolerated treatment for recalcitrant AA multiplex.


Subject(s)
Humans , Alopecia Areata , Alopecia , Liver , Methotrexate , Recurrence , Retrospective Studies , Skin Diseases
7.
Annals of Dermatology ; : 187-193, 2017.
Article in English | WPRIM | ID: wpr-25587

ABSTRACT

BACKGROUND: Micro-needle patches have been recently used to increase skin permeability, which improves drug delivery, and for cosmetic purposes. However, these patches may often have limited efficacy due to insufficient skin penetration and reduced compliance caused by discomfort. OBJECTIVE: We evaluated the efficacy and the safety of soluble micro-spicule containing epidermal growth factor (MS-EGF) for the treatment of periocular wrinkles. METHODS: Twenty healthy volunteers aged 33 to 54 years were enrolled in a randomized, controlled, split-face study. For 4 weeks, a periocular wrinkle was treated daily with either a soluble MS-EGF cream or a cream containing EGF alone. All subjects underwent 8 weeks of follow-up. Efficacy was assessed using an ultrasonic measurement of dermal depth and density, digital skin image analysis, 5-point photonumeric scale for periocular wrinkles and subjective satisfaction. RESULTS: MS-EGF group showed statistically significant increase of dermal depth and density compared to EGF alone group after 4 and 8 weeks. In addition, there was a marked improvement shown in clinical and 3-dimensional skin image in MS-EGF group. The treatments were well-tolerated; no significant side-effect was noted. CONCLUSION: The MS-EGF formulation may represent an effective and biocompatible advance in the treatment of periocular wrinkles.


Subject(s)
Compliance , Epidermal Growth Factor , Follow-Up Studies , Healthy Volunteers , Permeability , Skin , Ultrasonics
8.
Annals of Dermatology ; : 828-828, 2017.
Article in English | WPRIM | ID: wpr-25200

ABSTRACT

The authors note that the units on page 188 were reported incorrectly.

9.
Korean Journal of Dermatology ; : 213-215, 2017.
Article in Korean | WPRIM | ID: wpr-53852

ABSTRACT

No abstract available.


Subject(s)
Carcinoma, Squamous Cell , Epithelial Cells , Porokeratosis
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