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益生菌CMU改善口臭的随机对照试验。

Improvement of halitosis by probiotic bacterium CMU: A randomized controlled trial.

作者信息

Han Hee-Seung, Yum Haeji, Cho Young-Dan, Kim Sungtae

机构信息

Department of Periodontology, School of Dentistry and Dental Research Institute, Seoul National University and Seoul National University Dental Hospital, Seoul, Republic of Korea.

出版信息

Front Microbiol. 2023 Jan 17;14:1108762. doi: 10.3389/fmicb.2023.1108762. eCollection 2023.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03ff/9886871/cad435ba98e2/fmicb-14-1108762-g001.jpg

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