| Literature DB >> 31778407 |
Daiane Oliveira Vale San Gomes1, Mauro Batista de Morais1.
Abstract
OBJECTIVE: To perform a systematic review of literature data on gut microbiota and the efficacy of probiotics for the treatment of constipation in children and adolescents. DATA SOURCE: The research was performed in the PubMed, the Scientific Electronic Library Online (SciELO) and the Latin American and Caribbean Health Sciences Literature (LILACS) databases in English, Portuguese and Spanish. All original articles that mentioned the evaluation of the gut microbiota or the use of probiotics in children with constipation in their title and abstract were selected. DATA SYNTHESIS: 559 articles were found, 47 of which were selected for reading. From these, 12 articles were included; they studied children and adolescents divided into two categories: a gut microbiota evaluation (n=4) and an evaluation of the use of probiotics in constipation therapy (n=8). The four papers that analyzed fecal microbiota used different laboratory methodologies. No typical pattern of gut microbiota was found. Regarding treatment, eight clinical trials with heterogeneous methodologies were found. Fifteen strains of probiotics were evaluated and only one was analyzed in more than one article. Irregular beneficial effects of probiotics have been demonstrated in some manifestations of constipation (bowel frequency or consistency of stool or abdominal pain or pain during a bowel movement or flatulence). In one clinical trial, a complete control of constipation without the use of laxatives was obtained.Entities:
Mesh:
Year: 2019 PMID: 31778407 PMCID: PMC6909257 DOI: 10.1590/1984-0462/2020/38/2018123
Source DB: PubMed Journal: Rev Paul Pediatr ISSN: 0103-0582
Figure 1Study flowchart.
Characteristics of studies evaluating the gut microbiota of children and adolescents with constipation.
| Authors, year, reference, location |
n (age) division of groups | Definition of constipation | Analysis of fecal microbiota | Results of children with constipation compared to controls |
|---|---|---|---|---|
|
Zoppi et al., 1998 Italy |
42 (5-14 years old) 28 with constipation 14 healthy controls | Bowel movement frequency: <1 every 48 hours and hard stools |
Material analyzed: a stool sample. Culture in selective and non-selective media supplemented by biochemical assay |
- Similar anaerobic total count in individuals with and without constipation. In those with constipation, we observed: - a higher number of anaerobes of the genera - a greater number of - a greater number of In the control group, the counts of |
|
Zhu et al., 2014 United States |
22 (10-13 years old) eight obese patients with constipation 14 obese controls without constipation | NASPGHAN Guideline (2006): | Material analyzed: a stool sample. Pyrosequencing of the 16S rRNA gene |
In those with constipation, we observed: - a decrease in the filament - an increase in Constipation was not associated with a decrease in |
|
Meij et al., 2016 Holland |
137 (4-18 years old) 76 with constipation 61 healthy controls | Rome III Criterion (2006) for functional constipation |
Material analyzed: a stool sample. Microbiota profile based on IS-pro multiplex PCR method |
- No differences were found in phyla and bacterial diversity according to Shannon’s index. In those with constipation, the following were found: - an increase in - a decrease in |
|
Moraes et al., 2016 Brazil |
79 (3-36 months) 39 with constipation 40 healthy controls | Rome III Criterion (2006) for functional constipation |
Material analyzed: a stool sample. Total Bacterial Count, |
- No difference was observed in the counts for total bacterial and bifidobacterium. - In those with constipation, a lower (p = 0.022) concentration of |
NASPGHAN: North American Society for Pediatric Gastroenterology, Hepatology and Nutrition.
Characteristics of placebo-controlled randomized trials of probiotics / comparison in constipation in children and adolescents.
| Study, year, reference | Patients | Probiotic | Comparison (n)/presentation | Duration | Allocation concealment/blind analysis/intention to treat/follow-up losses | ||
|---|---|---|---|---|---|---|---|
| n (age) | Definition of constipation | Genus, species and strain (n) | Dose/presentation | ||||
| Banaszkiewicz et al., 2005 |
(2-16 years old) | Less than three bowel movements/wk. for at least 12 weeks |
| 2x/day 10 9 CFU/capsules | placebo + lactulose (n = 41)/capsules | 26 weeks (12 weeks of treatment) | yes/yes/yes/yes |
| Bu et al., 2007 |
45 (1-4 years old) | Less than three bowel movements/wk. for more than two months and anal fissure with bleeding or faecal leak or hard/large stools |
| 2x/day 8 × 108 CFU/capsules | MgO (n = 18) Placebo (n = 9)/capsules | 4 weeks | yes/yes/yes/yes |
| Coccorullo et al., 2010 |
44 (5-10 months old) | Rome III Criterion (2006) for functional constipation |
| 1x/day 108 CFU/oily suspension in drops | Placebo (n = 22)/oily suspension in drops | eight weeks | yes/yes/yes/yes |
| Tabbers et al., 2011 |
148 (3-16 years old) | Rome III Criterion (2006) for functional constipation |
| 2x/day 4.25 x 109 CFU/fermented milk | Placebo (n=74)/Low lactose non-fermented dairy | five weeks (three weeks of treatment) | yes/yes/yes/yes |
| Guerra et al., 2011 |
59 (5-15 years old) | Rome III Criterion (2006) for functional constipation |
| 1x/day 109 CFU/goat yogurt | Placebo (n = 30)/goat yogurt | ten weeks (crossover after five weeks) | yes/yes/yes/yes |
| Sadeghzadeh et al., 2014 |
48 (4-12 years old) | Rome III Criterion (2006) for functional constipation | Protexin* (n = 24) | 1x/day 109 CFU + lactulose/sachet | placebo + lactulose (n = 24)/sachet | four weeks | yes/yes/yes/yes |
| Russo et al., 2017 |
55 (4-12 years old) | Rome III Criterion (2006) for functional constipation | Probiotic Mix** + PEG 4000 (n = 27) | 1 sachet/day | PEG 4000 (n = 28)/sachet | eight weeks | yes/no/yes/yes |
| Wojtyniak et al., 2017 |
81 (1-4 years old) | Rome III Criterion (2006) for functional constipation |
| 2x/day 8 × 10 8 CFU/capsules | Placebo (n = 48)/capsules | four weeks | yes/yes/yes/yes |
CFU: colony forming units; PEG: polyethylene glycol (0.4 to 0.8 g/kg/day); MgO: magnesium oxide (50 mg/kg/day); lactulose (1 mL/kg/day); *Protexin®: Lactobacillus casei PXN 37, Lactobacillus rhamnosus PXN 54, Streptococcus thermophiles PXN 66, Brief bifidobacterium PXN 25, Lactobacillus acidophilus PXN 35, Bifidobacterium infantis PXN 27 and Lactobacillus bulgaricus PXN 39; **probiotic mix: Brief bifidobacterium M-16 V®, Infant Bifidobacterium M-63® and Bifidobacterium longum BB536®.
Results summary of studies evaluating the role of probiotics in the treatment of constipation in children and adolescents.
| Author, year, reference and place | Probiotic | Results of children with constipation compared to control group |
|---|---|---|
|
Banaszkiewicz et al., 2005 Poland |
|
Treatment successa was similar (p> 0.05) at the 12th week (experimental group=72% and control group=68%) and at the 24th week (experimental group =64% and control group=65%). There was no difference between the groups regarding weekly number of bowel movements, the force of the bowel movement, fecal escape and the number of required doses of laxatives. |
|
Bu et al., 2007 Taiwan |
|
Greater (p=0.01) treatment successa in the magnesium oxide (72.2%) and probiotic (77.8%) groups compared to the placebo (11.1%). The magnesium oxide and probiotic groups presented a higher (p = 0.03) frequency of bowel movement, a lower (p = 0.01) frequency of hardened stools and a lower (p = 0.04) frequency of glycerin enema use in comparison to the placebo. Episodes of abdominal pain were less frequent (p = 0.03) in the probiotic group compared to the magnesium oxide and placebo groups. There was an increase in the percentage of lactobacilli in anaerobic microbiota after probiotic treatment (p = 0.03) and when compared to the magnesium oxide and placebo groups (p = 0.02), there was no correlation with bowel movement frequency. There was no difference between the groups regarding the frequency of lactulose use, bowel movement episodes and appetite alteration. |
|
Coccorullo et al., 2010 Italy |
|
No definition of therapeutic success. Higher frequency of probiotic bowel movements in the second (p = 0.042), fourth (p = 0.008) and eighth (p = 0.027) weeks of treatment versus the control. There was no difference between groups with regard to stool consistency. There was an increase (p = 0.02) of inconsolable crying episodes in the probiotic group. In the control group, an increase in inconsolable crying was also observed, however, it did not reach statistical significance (p = 0.08). |
|
Tabbers et al., 2011 Holland and Poland |
|
Treatment successb was higher in the probiotic group (38%) compared to the placebo group (24%), but there was no significant difference (p=0.06). In the probiotic group, a reduction (p = 0.02) in flatulence frequency was observed. There was no difference between the probiotic and control groups regarding bowel movement frequency, stool consistency, fecal incontinence, pain during bowel movements, abdominal pain and bisacodil use. Higher bisacodil intake was observed in the control group (p=0.0069). |
|
Guerra et al., 2011 Brazil |
|
They do not present total data obtained in the two intervention periods with probiotic or control. They mention that in the probiotic group, considering all the results, there was a significant difference in the frequency of bowel movements, pain in bowel movements and abdominal pain. |
|
Sadeghzadeh et al., 2014 Iran | Protexin® |
No definition of therapeutic success. At the end of the fourth week it was found that the probiotic group had a higher (p = 0.042) bowel movement frequency and an improvement (p = 0.049) in stool consistency when compared to the placebo group. In the first week of intervention, a lower (p=0.030) frequency of fecal incontinence, a lower frequency (p=0.017) of abdominal pain and a greater weight gain (p=0.002) was found. These variables were similar in the fourth week of the study. |
|
Russo et al., 2017 Italy |
Brief bifidobacterium M-16 V® , Infant Bifidobacterium M-63® and Bifidobacterium longum BB536®.
|
In the second week of the study, treatment successc was higher with PEG (72%) compared to the PEG + probiotic mixture group (59%) (p=0.02). After one month (the fourth week), there was no difference in treatment success between the PEG group (88%) and the PEG + probiotic mixture group (81.8%). There was no difference between groups regarding bowel movement frequency, stool consistency, abdominal pain, fecal incontinence and rectal bleeding after two months (eighth week) of study. One month after the end of the study (12nd week), a clinical remission rate was observed in the PEG + probiotic mixture group in 64% of patients and 52% in the PEG-only group (p=0.28). |
|
Wojtyniak et al., 2017 Poland |
Lcr35 |
There was no difference in treatment successa between the groups. In the probiotic group, there was a lower (p = 0.005) bowel movement frequency in allof the studied weeks compared to the placebo group. Comparing from the baseline to the fourth week of study, there was an increase (p<0.001) in bowel movement frequency and an improvement (p<0.001) in stool consistency in both groups. |
PEG: polyethylene glycol; atreatment success defined as> 3 spontaneous bowel movements per week without fecal leaks; btreatment success defined as >3 bowel movements/week, <1 episode of fecal incontinence in the last two weeks of product consumption; ctreatment success defined as ≥3 bowel movements per week; stool consistency ≥ type 3 according to the Bristol scale; and no episodes of abdominal pain, fecal incontinence, painful bowel movement or rectal bleeding.