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Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice

We conducted a research study to create the groundwork for personalized solutions within a skin aging segment. This test utilizes genetic and general laboratory data to predict individual susceptibility to weak skin characteristics, leveraging the research on genetic polymorphisms related to skin fu...

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Autores principales: Sepetiene, Ramune, Patamsyte, Vaiva, Valiukevicius, Paulius, Gecyte, Emilija, Skipskis, Vilius, Gecys, Dovydas, Stanioniene, Zita, Barakauskas, Svajunas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532532/
https://www.ncbi.nlm.nih.gov/pubmed/37763073
http://dx.doi.org/10.3390/jpm13091305
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author Sepetiene, Ramune
Patamsyte, Vaiva
Valiukevicius, Paulius
Gecyte, Emilija
Skipskis, Vilius
Gecys, Dovydas
Stanioniene, Zita
Barakauskas, Svajunas
author_facet Sepetiene, Ramune
Patamsyte, Vaiva
Valiukevicius, Paulius
Gecyte, Emilija
Skipskis, Vilius
Gecys, Dovydas
Stanioniene, Zita
Barakauskas, Svajunas
author_sort Sepetiene, Ramune
collection PubMed
description We conducted a research study to create the groundwork for personalized solutions within a skin aging segment. This test utilizes genetic and general laboratory data to predict individual susceptibility to weak skin characteristics, leveraging the research on genetic polymorphisms related to skin functional properties. A cross-sectional study was conducted in a collaboration between the Private Clinic Medicina Practica Laboratory (Vilnius, Lithuania) and the Public Institution Lithuanian University of Health Sciences (Kaunas, Lithuania). A total of 370 participants agreed to participate in the project. The median age of the respondents was 40, with a range of 19 to 74 years. After the literature search, we selected 15 polymorphisms of the genes related to skin aging, which were subsequently categorized in terms of different skin functions: SOD2 (rs4880), GPX1 (rs1050450), NQO1 (rs1800566), CAT (rs1001179), TYR (rs1126809), SLC45A2 (rs26722), SLC45A2 (rs16891982), MMP1 (rs1799750), ELN (rs7787362), COL1A1 (rs1800012), AHR (rs2066853), IL6 (rs1800795), IL1Beta (rs1143634), TNF-α (rs1800629), and AQP3 (rs17553719). RT genotyping, blood count, and immunochemistry results were analyzed using statistical methods. The obtained results show significant associations between genotyping models and routine blood screens. These findings demonstrate the personalized medicine approach for the aging segment and further add to the growing literature. Further investigation is warranted to fully understand the complex interplay between genetic factors, environmental influences, and skin aging.
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spelling pubmed-105325322023-09-28 Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice Sepetiene, Ramune Patamsyte, Vaiva Valiukevicius, Paulius Gecyte, Emilija Skipskis, Vilius Gecys, Dovydas Stanioniene, Zita Barakauskas, Svajunas J Pers Med Article We conducted a research study to create the groundwork for personalized solutions within a skin aging segment. This test utilizes genetic and general laboratory data to predict individual susceptibility to weak skin characteristics, leveraging the research on genetic polymorphisms related to skin functional properties. A cross-sectional study was conducted in a collaboration between the Private Clinic Medicina Practica Laboratory (Vilnius, Lithuania) and the Public Institution Lithuanian University of Health Sciences (Kaunas, Lithuania). A total of 370 participants agreed to participate in the project. The median age of the respondents was 40, with a range of 19 to 74 years. After the literature search, we selected 15 polymorphisms of the genes related to skin aging, which were subsequently categorized in terms of different skin functions: SOD2 (rs4880), GPX1 (rs1050450), NQO1 (rs1800566), CAT (rs1001179), TYR (rs1126809), SLC45A2 (rs26722), SLC45A2 (rs16891982), MMP1 (rs1799750), ELN (rs7787362), COL1A1 (rs1800012), AHR (rs2066853), IL6 (rs1800795), IL1Beta (rs1143634), TNF-α (rs1800629), and AQP3 (rs17553719). RT genotyping, blood count, and immunochemistry results were analyzed using statistical methods. The obtained results show significant associations between genotyping models and routine blood screens. These findings demonstrate the personalized medicine approach for the aging segment and further add to the growing literature. Further investigation is warranted to fully understand the complex interplay between genetic factors, environmental influences, and skin aging. MDPI 2023-08-25 /pmc/articles/PMC10532532/ /pubmed/37763073 http://dx.doi.org/10.3390/jpm13091305 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sepetiene, Ramune
Patamsyte, Vaiva
Valiukevicius, Paulius
Gecyte, Emilija
Skipskis, Vilius
Gecys, Dovydas
Stanioniene, Zita
Barakauskas, Svajunas
Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice
title Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice
title_full Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice
title_fullStr Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice
title_full_unstemmed Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice
title_short Genetical Signature—An Example of a Personalized Skin Aging Investigation with Possible Implementation in Clinical Practice
title_sort genetical signature—an example of a personalized skin aging investigation with possible implementation in clinical practice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532532/
https://www.ncbi.nlm.nih.gov/pubmed/37763073
http://dx.doi.org/10.3390/jpm13091305
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