Personalized oral care (Precaries): an intervention study customized according to genetic cause and risk

Anna Westerlund, Halah Khalifa, Ranna Yousif, Gustavo Silva Araujo, Evelina Lundqvist, Erica Larsson, Rakel Thrastardottir, Rebecka Akhlaghi, Victoria Granciuc, Charlotta Svanberg, Maria André, Anna Lehrkinder, Farhan Bazargani, Christina Goriel Radsjö, Caspar Carlfjord, Anke Krämer, Niels Ganzer, Isabell Hansson, Erik Frilund, Eva Josefsson, Rune Lindsten, Anders Magnusson, Brygida Grunwald, Firas Hittini, Nurije Kryeziu, Henning Looström, Mikael Sonesson, Reem Al-Taha, Hanna Surac, Seifi Esmaili, Haris Isic, Anna Tegnell, Samuel Andersson, Mai Lin Lövgren, Jenny Kallunki, Anna E Lorenzo, Elena Arezzo, Agata Jasna, Tumkur Sitaram Raviprakash, Ewa Strömqvist-Engbo, Amanda Burstedt, William Rosenbaum, Oscar öhman, Wolfgang Lohr, Ann-Charlotte Rönn, Tomas Axelsson, Lena Mårell, Lennart österman, Edward J Hollox, Ulrika Westerlind, Karina Persson, Henrik Clausen, Per Liv, Patrik Ryden, Johan Henriksson, Laura Carroll, Nongfei Sheng, Pär Larsson, Nicklas Strömberg
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Abstract

ABSTRACT Introduction Dental caries is a disease that affects billions of people, and involves high and low genetic susceptibility phenotypes and different causal subtypes. The randomized clinical trial Precaries-RCT will evaluate caries prevention in adolescents, customized according to genetic cause and risk. Here we describe the Precaries-RCT and two nested Precaries studies for cost-efficient oral healthcare and personalized dentistry. Methods and analysis Here we present a basic and adaptive protocol for the Precaries-RCT multicentre caries intervention study, customized according to genetic cause and risk. It includes prescreening for high versus low genetic caries susceptibility, through self-performed sampling by mail of up to 2000 adolescents aimed for orthodontic treatment at community clinics, of which 520 are enrolled in the RCT. The participants are allocated into two groups — a high and a low genetic caries susceptibility group — that each is assigned to intensive or standard prevention. The primary outcome is % reduction in caries increment, relative to prevention and genotype, with caries outcomes measured using tactile and visual methods, bitewing radiographs, clinical photos, and quantitative laser fluorescence. The adaptive design allows for determination of incidence and progression rates and for inclusion of additional human and microbiota biomarkers and study subjects. Biological samples (e.g. swab DNA, whole and parotid saliva, and microbiota) and questionnaire data are collected. Here we also outline the nested Precaries-adolescent sample for mining of predictor and therapeutic target genes and Precaries-birth cohort samples for implementation of our findings in childhood. Ethics and dissemination Ethical approval was obtained from the Swedish national board research ethics committee (Dnr 2020-02533). Informed consent will be obtained from each participant. The findings will be disseminated to the public through conference presentations and publication in peer-reviewed scientific journals. Trial registration number www.clinicaltrials.gov, NCT05600517
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个性化口腔护理(Precaries):根据遗传原因和风险定制的干预研究
ABSTRACTIntroduction 龋齿是一种影响数十亿人的疾病,涉及高、低遗传易感性表型和不同的致病亚型。随机临床试验 Precaries-RCT 将评估根据遗传原因和风险定制的青少年龋病预防措施。方法与分析 我们在此介绍根据遗传原因和风险定制的 Precaries-RCT 多中心龋病干预研究的基本和适应性方案。该方案包括通过自行邮寄的方式对多达 2000 名在社区诊所接受正畸治疗的青少年进行遗传性龋齿易感性高低的预筛查,并将其中的 520 人纳入 RCT。参与者被分为两组--遗传性龋齿易感性高的一组和遗传性龋齿易感性低的一组,每组都被分配到强化或标准预防组。主要结果是相对于预防和基因型的龋齿增量减少百分比,龋齿结果通过触觉和视觉方法、咬翼X光片、临床照片和定量激光荧光法进行测量。自适应设计可确定发病率和进展率,并纳入更多的人类和微生物群生物标志物和研究对象。生物样本(如拭子 DNA、全唾液和腮腺唾液以及微生物群)和问卷调查数据均已收集。在此,我们还概述了用于挖掘预测和治疗目标基因的嵌套 Precaries 青少年样本,以及用于在儿童期实施研究结果的 Precaries 出生队列样本。我们将征得每位参与者的知情同意。研究结果将通过会议演讲和在同行评审的科学杂志上发表的方式向公众传播。试验注册号 www.clinicaltrials.gov, NCT05600517
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