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利用人工智能开发牙周炎进展预测模型:一项纵向队列研究。

Developing Predictive Models for Periodontitis Progression Using Artificial Intelligence: A Longitudinal Cohort Study.

作者信息

Furquim Camila Pinheiro, Caruth Lannawill, Chandrasekaran Ganesh, Cucchiara Andrew, Kallan Michael J, Martin Lynn, Feres Magda, Bittinger Kyle, Divaris Kimon, Glessner Joseph, Kantarci Alpdogan, Giannobile William, Verma Shefali Setia, Teles Flavia

机构信息

Department of Basic & Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Department of Periodontology and Oral Implantology, Dental Research Division, University of Guarulhos, Guarulhos, São Paulo, Brazil.

出版信息

J Clin Periodontol. 2025 Oct;52(10):1478-1490. doi: 10.1111/jcpe.14194. Epub 2025 Aug 19.

DOI:10.1111/jcpe.14194
PMID:40830987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12420084/
Abstract

AIM

To construct predictive models of periodontitis progression by applying Machine Learning (ML) to baseline data from a study of periodontitis progression.

MATERIALS AND METHODS

Logistic regression (LR), multi-layer perceptron (MLP) and probabilistic graphic model (PGM) were utilised on data from a multi-centre longitudinal study in which periodontally healthy (n = 113) and periodontitis participants (n = 302) were examined bi-monthly for 12 months without treatment. Periodontal examination was performed, and salivary levels of 10 analytes were determined. Clinical and demographic parameters and analytes levels were input into the model. The performance of 14 models was compared using the area under the receiver operating characteristic curve (AUROC), and feature importance was assessed using SHapley Additive exPlanations (SHAP).

RESULTS

The PGM model (Clinical measures, saliva IL-1β, age, sex) demonstrated the best overall performance (AUROC = 0.88), compared to LR (AUROC = 0.72) and MLP (AUROC = 0.58). Although MLP had a lower Brier score (0.12), its sensitivity was 0, limiting its clinical utility. In contrast, PGM achieved a balanced sensitivity (0.55) and specificity (0.81). Feature importance analyses highlighted the number of deep periodontal pockets as a key driver of model predictions in both PGM and MLP.

CONCLUSIONS

ML models can predict periodontitis progression, supporting early detection strategies. Our integrative approach, combining clinical data with salivary biomarkers such as IL-1β, improved predictive accuracy.

摘要

目的

通过将机器学习(ML)应用于牙周炎进展研究的基线数据,构建牙周炎进展的预测模型。

材料与方法

对一项多中心纵向研究的数据使用逻辑回归(LR)、多层感知器(MLP)和概率图模型(PGM),该研究中对牙周健康者(n = 113)和牙周炎患者(n = 302)每两个月进行一次检查,为期12个月且不进行治疗。进行了牙周检查,并测定了10种分析物的唾液水平。将临床和人口统计学参数以及分析物水平输入模型。使用受试者操作特征曲线下面积(AUROC)比较14种模型的性能,并使用SHapley加性解释(SHAP)评估特征重要性。

结果

与LR(AUROC = 0.72)和MLP(AUROC = 0.58)相比,PGM模型(临床指标、唾液白细胞介素-1β、年龄、性别)表现出最佳的总体性能(AUROC = 0.88)。尽管MLP的布里尔评分较低(0.12),但其灵敏度为0,限制了其临床应用。相比之下,PGM实现了平衡的灵敏度(0.55)和特异性(0.81)。特征重要性分析突出了深牙周袋的数量是PGM和MLP中模型预测的关键驱动因素。

结论

ML模型可以预测牙周炎进展,支持早期检测策略。我们将临床数据与白细胞介素-1β等唾液生物标志物相结合的综合方法提高了预测准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/71b7ce9daf3e/JCPE-52-1478-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/5029e19a2519/JCPE-52-1478-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/9355f0e21fb4/JCPE-52-1478-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/71b7ce9daf3e/JCPE-52-1478-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/5029e19a2519/JCPE-52-1478-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/9355f0e21fb4/JCPE-52-1478-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42de/12420084/71b7ce9daf3e/JCPE-52-1478-g001.jpg

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本文引用的文献

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Multi-Centre External Validation of a Nomogram for 10-Year Periodontal Tooth Loss Prediction.用于预测10年牙周牙齿缺失的列线图的多中心外部验证
J Clin Periodontol. 2025 Jul;52(7):1044-1055. doi: 10.1111/jcpe.14143. Epub 2025 Mar 10.
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A personalized periodontitis risk based on nonimage electronic dental records by machine learning.基于机器学习的非影像电子牙科记录的个性化牙周炎风险评估
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Gingival Crevicular Fluid Biomarkers During Periodontitis Progression and After Periodontal Treatment.
牙周炎进展期及牙周治疗后龈沟液生物标志物
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Salivary and serum inflammatory biomarkers during periodontitis progression and after treatment.牙周炎进展过程中和治疗后唾液及血清中的炎症生物标志物。
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Cytokine levels in gingival tissues as an indicator to understand periodontal disease severity.牙龈组织中的细胞因子水平作为了解牙周疾病严重程度的指标。
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Development of a machine learning multiclass screening tool for periodontal health status based on non-clinical parameters and salivary biomarkers.基于非临床参数和唾液生物标志物开发用于牙周健康状况的机器学习多类别筛查工具。
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