Han Hee-Seung, Yum Haeji, Cho Young-Dan, Kim Sungtae
Department of Periodontology, School of Dentistry and Dental Research Institute, Seoul National University and Seoul National University Dental Hospital, Seoul, Republic of Korea.
Front Microbiol. 2023 Jan 17;14:1108762. doi: 10.3389/fmicb.2023.1108762. eCollection 2023.
Several and studies have evaluated the effect of probiotics on oral health; however, human clinical studies are still limited. Therefore, this study aimed to examine the effects of Chonnam Medical University (CMU)-containing tablets on halitosis. This randomized, double-blinded, placebo-controlled study included 100 adults with halitosis (age, 20-70 years). The participants were randomly assigned to the test group ( = 50) and control group ( = 50). One tablet [1 × 10 colony forming units (CFU)/tablet] was to be taken each day over 8 weeks. The concentrations of volatile sulfur compounds (VSCs), bad breath improvement scores, and oral colonization of were measured. Psychosocial indicators including depression, self-esteem, oral health-related quality of life, and subjective oral health status were evaluated. Most variables were assessed at baseline, 4, and 8 weeks, and number and safety variables were assessed at baseline and 8 weeks. Intergroup comparisons were carried out using Student's -test, Chi-square test, or Fisher's exact test on per-protocol analysis. Intragroup differences before and after intake were analyzed using the linear mixed-effect model (LMM). Per-protocol analysis was carried out in the test group ( = 45) and control group ( = 46). Total VSC was significantly lower in the probiotics group than in the placebo group at baseline (week 0, = 0.046) and at 8 weeks ( = 0.017). The sum of hydrogen sulfide and methyl mercaptan did not differ significantly between the groups at baseline; however, it was significantly lower in the probiotics group than in the placebo group at week 8 ( = 0.012). Bad breath improvement (BBI) scores were significantly reduced at week 8 ( = 0.006) in the probiotics group. Statistically significant intergroup differences were observed for changes in the level of at week 8 ( < 0.001). Psychological indicators significantly improved from baseline to week 8 in the probiotics group. No safety issues were observed in either group. The levels of was higher in patients with halitosis using CMU-containing tablets. The subjective degree of bad breath and psychological indicators were improved in patients with halitosis using CMU-containing tablets.
多项研究评估了益生菌对口腔健康的影响;然而,人体临床研究仍然有限。因此,本研究旨在探讨含全南大学(CMU)片剂对口臭的影响。这项随机、双盲、安慰剂对照研究纳入了100名患有口臭的成年人(年龄20 - 70岁)。参与者被随机分为试验组(n = 50)和对照组(n = 50)。每天服用一片[1×10菌落形成单位(CFU)/片],持续8周。测量挥发性硫化合物(VSCs)的浓度、口臭改善评分和CMU的口腔定植情况。评估包括抑郁、自尊、口腔健康相关生活质量和主观口腔健康状况在内的心理社会指标。大多数变量在基线、4周和8周时进行评估,一些数量和安全性变量在基线和8周时进行评估。在符合方案分析中,使用学生t检验、卡方检验或费舍尔精确检验进行组间比较。使用线性混合效应模型(LMM)分析摄入前后的组内差异。在试验组(n = 45)和对照组(n = 46)中进行符合方案分析。在基线(第0周,P = 0.046)和8周时(P = 0.017),益生菌组的总VSC显著低于安慰剂组。在基线时,两组之间硫化氢和甲硫醇的总和没有显著差异;然而,在第8周时,益生菌组显著低于安慰剂组(P = 0.012)。在第8周时,益生菌组的口臭改善(BBI)评分显著降低(P = 0.006)。在第8周时,观察到两组间CMU水平变化的统计学显著差异(P < 0.001)。在益生菌组中,心理指标从基线到第8周有显著改善。两组均未观察到安全问题。使用含CMU片剂的口臭患者中CMU水平较高。使用含CMU片剂的口臭患者的主观口臭程度和心理指标得到改善。