Is ChatGPT a reliable source of scientific information regarding third-molar surgery?

BACKGROUND: ChatGPT (OpenAI) is a large language model. This model uses artificial intelligence and machine learning techniques to generate humanlike language and responses, even to complex questions. The authors aimed to assess the reliability of responses provided via ChatGPT and evaluate its trustworthiness as a means of obtaining information about third-molar surgery. METHODS: The authors assessed the 10 most frequently asked questions about mandibular third-molar extraction. A validated questionnaire (Chatbot Usability Questionnaire) was used and 2 oral and maxillofacial surgeons compared the answers provided with the literature. RESULTS: Most of the responses (90.63%) provided via the ChatGPT platform were considered safe and accurate and followed what was the stated in the English-language literature. CONCLUSIONS: The ChatGPT platform offers accurate and scientifically backed answers to inquiries about third-molar surgical extraction, making it a dependable and easy-to-use resource for both patients and the general public. However, the platform should provide references with the responses to validate the information. PRACTICAL IMPLICATIONS: Patients worldwide are exposed to reliable information sources. Oral surgeons and health care providers should always advise patients to be aware of the information source and that the ChatGPT platform offers a reliable solution.

Transcription factor STAT1 gene polymorphism is associated with the development of severe forms of periodontal disease.

INTRODUCTION: Periodontal disease (PD) is one of the most common inflammatory diseases, affecting about 10 % of the world population. The establishment of PD is influenced by polymorphisms in genes involved with the inflammatory response. Signal Transducer and Activator of Transcription (STAT)-1 is a transcription factor that plays a key role in the intracellular signaling triggered by cytokines and, thus, its activation is critical in inflammatory diseases. AIM AND METHODS: We aim to evaluate the occurrence of association between STAT-1 (rs3771300) polymorphism and distinct clinical forms and severity of PD; we genotyped 180 subjects using realtime PCR. RESULTS AND CONCLUSION: We observed that the presence of the G allele for STAT-1 was associated with twice as high of a chance to develop aggressive periodontitis, and the most severe form of the disease.

Morphometric study of incisive canal and its anatomic variations in brazilian individuals.

Objective: To conduct a morphometric evaluation of the incisive canal, adjacent structures, and their anatomic variations in Brazilian individuals.Methods: A retrospective study was conducted using a sample of 157 multislice computed tomography images of adult Brazilian individuals of both sexes (20-96 years). The exam was performed with the RadiAnt DICOM Viewer 4.0.1 (64-bit) software that uses the DICOM PACS standard for visualization of medical and dental images.Results: The values for length and height of the canal, thickness of the palatine bone plate, and latero-lateral diameter of the incisive foramen were higher in men than in women (p < 0.05).Conclusion: The findings of this study demonstrated morphometric differences for the following parameters: latero-lateral diameter; width of canals at all levels measured; palatine bone plate height; canal length and palatine bone plate thickness in relation to the male and female sexes in the Brazilian population.

Prevalence and characterization of maxillary sinus septa in a brazilian population.

BACKGROUND: The aim of this study was to assess the anatomic aspects of the maxillary sinus septa, by means of computed tomography images, in a Brazilian population. The results might be of clinical significance in sinus lift surgery planning. MATERIAL AND METHODS: In the study, 123 computed tomographs obtained from a private radiology clinic were used. They were analyzed by a single, trained and calibrated observer in order to evaluate the presence, quantity, localizations, dimensions, orientations and different characteristics in dentate, partially edentulous and completely edentulous individuals of the sinus septa. RESULTS: Of the individuals analyzed, 26% had a septum in the maxillary sinus, with 59.6% being classified as complete, 44.2% showed prevalence for the middle region of the maxillary sinus. There was no statistically significant difference between the right and left sides (p>0.05). CONCLUSIONS: The majority of patients in the sample analyzed presented to septa in the maxillary sinuses, and when septa were present, a higher number of occurrence was noted in the middle region of the maxillary sinus. (This region is normally the choice of sinus lift surgery). There was no predilection relative to age, sex and type of dentition. Key words:Multislice computed tomography, maxillary antrum, anatomic variation.

Three-dimensional characteristics of submandibular salivary gland of ageing rats: an HRSEM study.

The characteristics of the submandibular glands of ageing Wistar rats were studied using light and high-resolution scanning electron microscopy (HRSEM) methods. For light microscopy, the samples were fixed in Bouin solution and embedded in paraffin. Sections were stained with hematoxilin-eosin and Azo-Carmin. For conventional scanning electron microscopy, the tissues were fixed in modified Karnovsky solution, and treated with NaOH solution for 3-4 days. The O-D-O method was used for HRSEM. The samples were fixed in 2% osmium tetroxide, macerated in diluted osmium and dehydrated in an increasing series of ethanol. The samples were dried in a critical point dryer, coated with gold-palladium and examined in a Hitachi high-resolution scanning electron microscope, S-900. The results showed that submandibular glands with lobules are separated by connective tissue septum. The acinar formations and the ducts, revealing the serous and mucous cells were observed. After fracture in liquid nitrogen and treatment with NaOH solution to remove the cellular components, the original disposition of the collagen bundles fibers were revealed corresponding to the round, oval or irregular acinar and ductal structures. In the cytoplasm, organelles such as mitochondria, rough endoplasmic reticulum, Golgi apparatus and serous and mucous secretory granules were observed localized in the apical portion in three-dimensional HRSEM images. The serous secretory granules presented different sizes and shapes showing the modifications which occurred in the ageing rats. The striated duct cells revealed the presence of the secretory cells and mitochondria in parallel disposition. The mitochondrial cristae were noted in three-dimensional aspects. The lumen presented numerous cytoplasmic microprojections. The lumen of excretor ducts are covered by polygonal epithelial cells containing numerous microplicae.

Angioarchitecture of the anterior and medium parts of the palatine mucosa of the gerbil, Meriones unguiculatus.

The aim of this study was to examine the microvasculature of the anterior and medium portions of the hard palatine mucosa in the adult gerbil (Meriones unguiculatus) using scanning electron microscopy. The vascular corrosion casts were obtained by injection of Mercox CL-2B synthetic resin and tissue corrosion was performed using sodium hydroxide solution. These casts revealed the presence of capillary loops in the palatine plicae and a smoother/flatter vascular network in the interplicae areas. The capillary loops consisted mainly of anteriorly oriented hair-pins and we also verified a differentiation in the shape of endothelial cell nuclei, which were elongated in arterial and circular in venous vessels.

Evaluation of IL17A expression and of IL17A, IL17F and IL23R gene polymorphisms in Brazilian individuals with periodontitis.

The IL23/Th17 axis plays an important role in the pathogenesis of cell-mediated tissue damage caused either by autoimmunity or immune responses against bacterial infection. Single nucleotide polymorphisms in the IL17A, IL17F and IL23R genes have been associated with several inflammatory diseases. However, these polymorphisms have not yet been studied in periodontitis. The aim of present study was to evaluate the expression of IL17A and occurrence of the IL17A (rs2275913), IL17F (rs763780) and IL23R (rs11209026) gene polymorphisms in different clinical forms or severity of periodontitis in a sample of Brazilian individuals. Peripheral blood was obtained from 30 non-smoker individuals and analyzed by flow cytometry to determine IL-17 expression. Genomic DNA was obtained from oral swabs in 180 individuals and analyzed by Real-time PCR. The study group was composed by individuals without periodontitis (control), with aggressive periodontitis (AP) and with chronic periodontitis (CP). Higher frequency of IL17A+CD4+ T cells was observed in control group. The A+ genotype from IL17A (rs2275913) was associated with lack of disease. No association was found considering the IL17F and IL23R polymorphisms. Our data suggest that IL17A and the presence of IL17A (rs2275913) A allele are associated with the absence of periodontal disease.

Associação entre metilação do DNA e periodontite crônica: revisão de literatura / Association between DNA methylation and chronic periodontitis: literature review

A periodontite crônica (PC) é uma doença bucal caracterizada pela presença de bactérias que promovem a inflamação dos tecidos de suporte e inserção dos dentes, como resultado de complexas interações entre patógenos periodontais e a resposta imune do hospedeiro. A PC é multifatorial e os fatores envolvidos com a regulação gênica podem interferir na predisposição ao aparecimento dos sinais e sintomas da doença. Neste contexto estão os mecanismos epigenéticos caracterizados por modificação na expressão dos genes sem afetar a sequência do DNA. As principais evidências de alterações epigenéticas na PC se relacionam à análise do perfil de metilação em genes relacionados à resposta imunoinflamatória. A metilação do DNA é um mecanismo epigenético caracterizado pela adição de um grupo metil no carbono 5' do anel de citosina, inibindo efetivamente a transcrição gênica. O objetivo do estudo foi revisar a literatura sobre a metilação do DNA na PC e avaliar sua associação com a patogênese da doença. Foi realizada uma busca na base de dados (Pubmed), sem restrição de ano e/ou idioma, utilizando os seguintes descritores: (Methylation [MeSh] OR Methylation OR DNA methylation [MeSh] OR DNA methylation) and (Chronic periodontitis [Mesh] OR Chronic periodontitis). Apesar dos estudos epigenéticos em doença periodontal ainda serem escassos, com diversos pontos a serem elucidados, os achados sugerem o envolvimento da metilação do DNA em genes da resposta imunoinflamatória na patogênese da PC. (AU)

Chronic periodontitis (CP) is an oral disease characterized by the presence of bacteria that promote inflammation of the supporting tissues of the teeth, as a result of complex interactions between periodontal pathogens and the host immune response. The CP is multifactorial and the factors involved in gene regulation may interfere with the predisposition on the appearance of the signs and symptoms of the disease. In this context it has been observed the epigenetic mechanism characterized by change ingene expression without affecting the sequence of DNA. The main evidence of epigenetic changes in CP are related to the analysis of the methylation profile in genes involved with the immune response. DNA methylation is an epigenetic mechanism characterized by the addition of a methyl group on the 5' carbon of the cytosine ring, effectively inhibiting the gene transcription. The aim of this study was to review the literature on DNA methylation in CP and evaluate its association with the pathogenesis of the disease. The search was performed in the database (Pubmed) without year or language restriction restriction, using the following key words: (Methylation [MeSh] OR Methylation OR DNA methylation [MeSh] OR DNA methylation) and (Chronic periodontitis [Mesh] OR Chronic periodontitis). Despite the epigenetic studies on periodontal disease are still scarce, with several points to be elucidated, the findings suggest the involvement of DNA methylation in immune response genes in the pathogenesis of CP (AU)