Ana Eliza Castanho Garrini Dos Santos, Fátima Antonia Aparecida Zanin, Dacio Antônio Pantano Junior, Tamiris Silva, Karen Muller Ramalho, Maria Fernanda Setúbal Dextro Rodrigues, Lara Jansiski Motta, Sandra Kalil Bussadori, Aldo Brugnera Junior, Anna Carolina Ratto Tempestini Horliana
{"title":"Evaluation of Gingival Inflammation after Tooth Whitening In-Office with Violet LED: A Randomized Controlled Clinical Trial with a Split-Mouth Design.","authors":"Ana Eliza Castanho Garrini Dos Santos, Fátima Antonia Aparecida Zanin, Dacio Antônio Pantano Junior, Tamiris Silva, Karen Muller Ramalho, Maria Fernanda Setúbal Dextro Rodrigues, Lara Jansiski Motta, Sandra Kalil Bussadori, Aldo Brugnera Junior, Anna Carolina Ratto Tempestini Horliana","doi":"10.1177/25785478251380384","DOIUrl":null,"url":null,"abstract":"<p><p>This split-mouth randomized study evaluated the effect of in-office tooth whitening with violet Light-Emitting Diode (LED) on gingival inflammation, assessed by gingival crevicular fluid (GCF) interleukin-6 (IL-6) level, histomorphology, and immunohistochemical analysis of Tumor Necrosis Factor (TNF-α) and Cluster of Differentiation 8 (CD8) expression, with and without gingival barrier protection. Thirteen volunteers requiring gingivoplasty were included. The whitening procedure was performed with parameters of 400 nm, 134J/cm<sup>2</sup>, and 20 cycles of 30 sec with 60 sec of standby. Gingival surgery was performed 48 h post-whitening for histomorphology analysis, while GCF IL-6 levels were quantified using an Enzyme-Linked Immunosorbent Assay (ELISA). We also attempted immunohistochemical analysis of TNF-α and CD8 expression; however, the small gingival specimens, which were primarily epithelial tissue, limited the reliability of the results. No statistically significant differences were observed between sides for histomorphology or GCF IL-6. These findings suggest that LED whitening without a gingival barrier may not induce gingival inflammation. However, further studies with larger and gender-balanced samples, extended time points, and additional cytokine markers are needed to confirm these results.</p>","PeriodicalId":94169,"journal":{"name":"Photobiomodulation, photomedicine, and laser surgery","volume":" ","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Photobiomodulation, photomedicine, and laser surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/25785478251380384","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0
Abstract
This split-mouth randomized study evaluated the effect of in-office tooth whitening with violet Light-Emitting Diode (LED) on gingival inflammation, assessed by gingival crevicular fluid (GCF) interleukin-6 (IL-6) level, histomorphology, and immunohistochemical analysis of Tumor Necrosis Factor (TNF-α) and Cluster of Differentiation 8 (CD8) expression, with and without gingival barrier protection. Thirteen volunteers requiring gingivoplasty were included. The whitening procedure was performed with parameters of 400 nm, 134J/cm2, and 20 cycles of 30 sec with 60 sec of standby. Gingival surgery was performed 48 h post-whitening for histomorphology analysis, while GCF IL-6 levels were quantified using an Enzyme-Linked Immunosorbent Assay (ELISA). We also attempted immunohistochemical analysis of TNF-α and CD8 expression; however, the small gingival specimens, which were primarily epithelial tissue, limited the reliability of the results. No statistically significant differences were observed between sides for histomorphology or GCF IL-6. These findings suggest that LED whitening without a gingival barrier may not induce gingival inflammation. However, further studies with larger and gender-balanced samples, extended time points, and additional cytokine markers are needed to confirm these results.