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Fiska Rosita
Universitas Sebelas Maret, RSUD Dr. Moewardi Surakarta, Jawa Tengah, Indonesia

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Astaxantin Topikal Sebagai Terapi Adjuvan terhadap Kadar Serum Interleukin 8 pada Akne Vulgaris Fiska Rosita; Putti Fatiharani Dewi; Muhammad Eko Irawanto; Rina Sidharta
Jurnal Health Sains Vol. 2 No. 9 (2021): Jurnal Health Sains
Publisher : Syntax Corporation Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.46799/jhs.v2i9.269

Abstract

Acne vulgaris (AV) is a chronic inflammatory disease of the pilosebasea unit associated with the sebum glands. Reactive oxygen species play a role in av pathophysiology. Astaxantin has an anti-inflammatory effect so administration of this topical ASX is expected to cause improvement of lesions in AV. The purpose of the study was to find out that topical astaxantin can lower serum levels of interleukin-1(. This study is a clinical experimental study using the pre and post control design group design double-blind randomized controlled trial with 2 groups, namely the treatment group given standard AV therapy drugs in the form of gel containing tretinoin 0.025% + clindamycin phosphate 1.2% and astaxantin gel 5% and control group given the same standard AV therapy drug and placebo gel. Acne vulgaris (AV) is a chronic inflammatory disease of the pilosebasea unit associated with the sebum glands. Reactive oxygen species play a role in av pathophysiology. Astaxantin has an anti-inflammatory effect so administration of this topical ASX is expected to cause improvement of lesions in AV. The purpose of the study was to find out that topical astaxantin can lower serum levels of interleukin-1(. This study is a clinical experimental study using the pre and post control design group design double-blind randomized controlled trial with 2 groups, namely the treatment group given standard AV therapy drugs in the form of gel containing tretinoin 0.025% + clindamycin phosphate 1.2% and astaxantin gel 5% and control group given the same standard AV therapy drug and placebo gel. Serum IL-8 levels were assessed at weeks 0 and VIII as an in vitro study. The paired difference between the serum IL-8 pretest and postest levels in the treatment group was p=0.751 and the control group was p=0.837. The unpaired test of il-8 level examination between the treatment group and the control group on the pretest was p=0.607 and the posttest was p=0.297 showed no significant difference. The addition of topical astaxantin as an AV supplemental therapy has not been shown to lower serum IL-8 levels.
Pengaruh Terapi Layering Krim Cysteamine 5% dan Asam Traneksamat 3% terhadap Skor Masi Pasien Melasma Putti Fatiharani Dewi; Ummi Rinandari; Fiska Rosita; Arie Kusumawardani; Nugrohoaji Dharmawan
Jurnal Health Sains Vol. 2 No. 9 (2021): Jurnal Health Sains
Publisher : Syntax Corporation Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.46799/jhs.v2i9.277

Abstract

Melasma is a hypermelanosis disorder that arises typical of areas of the skin that are often exposed to sunlight. Melasma therapy is relatively difficult because there is often chronicity in melasma. Until now therapy with Kligman formula is still an option, but kligman formula has some side effects, especially for long-term use. Cysteamine works by inhibiting the enzyme tyrosinase. Traneksamat acid works by inhibiting the activity of plasmin in keratinocytes known as stimulators of tyrosinase activity The purpose of the study proved and analyzed the effectiveness of cysteamine cream layering therapy 5% and tranexilic acid 3% compared to kligman formula modification in melasma sufferers to improve MASI score. Experimental research method, pre and post control group design double-blind randomied controlled trial with 28 samples of melasma patients namely group A using layering cysteamine cream 5% and traneksamat acid 3% compared to the group of patients melasma i.e. group A using layering cysteamine cream 5% and traneksamat acid 3% compared to the group of patients. Assessment and measurement of the effectiveness of therapy is carried out during weeks 0, 2, 4 and 8, with an assessment of MASI score. The analysis used is the t-pair test and the Wilcoxon test. Statistical tests are considered meaningful if p<0.05. The results of the study decreased the difference in MASI score in group A obtained in week 4 and week 8, while group B in week 8. The difference in the difference in MASI score change between group A and group B in weeks 4 and 8 indicates a significant difference (p=0.025 and p=0.003). Conclusion of 5% layering cysteamine therapy and 3% tranex acid indicates a decrease in the difference in MASI score earlier than modified Kligman cream therapy.