ArticleOdontology2025
LncRNA HOTTIP as a potential biomarker of chronic periodontitis and its role in inflammatory responses.
Article in Odontology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Chronic periodontitis (CP) is a prevalent oral condition that can elicit a broad spectrum of inflammatory responses. This study investigates the impact of lncRNA HOTTIP on inflammatory responses of CP via targeting and regulating miR-205-5p. This study involved 117 CP patients and 101 controls. The expression levels of HOTTIP and miR-101-3p in the gingival crevicular fluid (GCF) of CP patients were quantified using qPCR. The levels of inflammatory factors IL-1β, IL-6, IL-10, and TNF-α, were measured through ELISA. ROC analysis was conducted to evaluate the diagnostic efficacy. The LPS-induced hPDLFs injury model was established to investigate the effects of HOTTIP silencing, as well as the concurrent inhibition of HOTTIP and miR-101-3p expression, on cellular functionality and inflammatory responses. HOTTIP was elevated in the GCF of CP patients, whereas miR-101-3p was reduced (P < 0.001). HOTTIP exhibited a positive correlation with inflammatory markers and periodontal indicators (r > 0, P < 0.01). HOTTIP possessed the potential to serve a specific biomarker for the auxiliary diagnosis of CP (AUC = 0.967, P < 0.001), as well as a critical parameter for assessing the periodontal condition of patients. In LPS-induced hPDLFs model, the silencing of HOTTIP was found to enhance cell proliferation (P < 0.01), reduce apoptosis (P < 0.001), and the release of inflammatory factors (P < 0.05). However, the simultaneous inhibition of both HOTTIP and miR-101-3p, this inhibitory effect on inflammatory response was counteracted (P < 0.05). HOTTIP regulated cellular function and the release of inflammatory factors via miR-101-3p, thereby exacerbating the inflammatory response with CP patients. HOTTIP is anticipated to emerge as a promising biomarker for the diagnosis of CP.
Indexed as
Identifiers
40146466What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.