2017
DOI: 10.1016/j.jmii.2015.10.003
|View full text |Cite
|
Sign up to set email alerts
|

Evaluation of efficacy and safety of Lactobacillus rhamnosus in children aged 4–48 months with atopic dermatitis: An 8-week, double-blind, randomized, placebo-controlled study

Abstract: The results of this study indicated that L. rhamnosus was effective in decreasing symptoms of atopic dermatitis after an 8-week treatment by comparing the mean change of SCORAD from baseline with a placebo (p < 0.05). The reduction in SCORAD resulted from a consistent decrease in all components of SCORAD. Patients who took L. rhamnosus for 8 weeks expressed less SCORAD in the three components: area of affected skin, intensity of atopic dermatitis, and patient symptoms, with a significant decrease in the mean c… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
34
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 40 publications
(34 citation statements)
references
References 34 publications
0
34
0
Order By: Relevance
“…Eight trials [ 33 37 , 39 , 41 , 43 ] reported the drop out in both intervention group and control group, and only four trials [ 33 , 39 , 41 , 43 ] used intention-to-treat (ITT) to analyze for all outcome [ 33 , 39 , 41 ] and primary outcome [ 43 ], and the other four trials [ 34 37 ] analyzed data by per-protocol (PP) and reported the data of available participants. Besides, two trials [ 39 , 41 ] analyzed by both ITT and PP. We considered one trial [ 34 ] as high risk of incomplete data for loss to follow up without ITT analysis because of 13 withdrawals in intervention group and 16 withdrawals in control group among the 100 participants in the trial.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Eight trials [ 33 37 , 39 , 41 , 43 ] reported the drop out in both intervention group and control group, and only four trials [ 33 , 39 , 41 , 43 ] used intention-to-treat (ITT) to analyze for all outcome [ 33 , 39 , 41 ] and primary outcome [ 43 ], and the other four trials [ 34 37 ] analyzed data by per-protocol (PP) and reported the data of available participants. Besides, two trials [ 39 , 41 ] analyzed by both ITT and PP. We considered one trial [ 34 ] as high risk of incomplete data for loss to follow up without ITT analysis because of 13 withdrawals in intervention group and 16 withdrawals in control group among the 100 participants in the trial.…”
Section: Resultsmentioning
confidence: 99%
“…We considered one trial [ 34 ] as high risk of incomplete data for loss to follow up without ITT analysis because of 13 withdrawals in intervention group and 16 withdrawals in control group among the 100 participants in the trial. Four trials [ 33 , 39 , 41 , 43 ] were considered as low risk of bias and the others as unclear. Eleven trials [ 21 , 25 , 29 , 33 , 35 – 37 , 40 43 ] mentioned non-commercial funding.…”
Section: Resultsmentioning
confidence: 99%
“…Indeed, cytokine profiles in co-cultures of the probiotic bacteria with PBMCs show considerable variations between species and strains. Among probiotic species, a lot of reports indicate that even different strains of Lactobacillus have various impact on the severity of AD when were administered to children [28,29].…”
Section: Discussionmentioning
confidence: 99%
“…31 However, some effects may be strain or species specific, as probiotics with Lactobacillus rhamnosus and Lactobacillus paracasei have yielded mixed results. [32][33][34][35][36] Thus far, few studies have utilized live bacteria in topical probiotics for treatment of AD. Nakatusji et al recently demonstrated that topical application of commensal skin bacteria protects against pathogens.…”
Section: Atopic Dermatitismentioning
confidence: 99%