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Urinary tract infections are very common in pediatrics. Urinary antibiotic prophylaxis is commonly used in children with malformative uropathies. Long-term, low-dose antibiotic prophylaxis with trimethoprim-sulfamethoxazole has been associated with a decrease in the number of urinary tract infections in susceptible children, but not systematically with a decrease in the risk of renal scarring (depending of uropathy stage).
Long-term antibiotic prophylaxis has implications for the acquisition of antibiotic resistance. A child receiving antibiotic prophylaxis for urinary tract infection is around 6 times more likely to develop a multidrug-resistant infection. In the general population, the microbiota of children treated with curative antibiotics is less diverse in terms of species and strains. In addition, short-term compositional changes are observed between consecutive samples of children treated with antibiotics.
The gut microbiota modulates the immune system, in particular via metabolites (SCFA, polysaccharide A) produced by bacteria that modify the expansion and function of regulatory T-cells. The disturbances of the intestinal microbiota play a role in the medium and long term on the acquisition of pathologies, such as atopy.
The study authors wish to describe the intestinal microbiota of children with vesico-ureteral reflux treated long-term with trimethoprim-sulfamethoxazole and compared it those not receiving antibiotic prophylaxis and to healthy children.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cases | Children aged 1 to 3 years with vesico ureteral reflux of grade 3 or higher, under antibiotic prophylaxis |
| |
| Controls | Children aged 1 to 3 years with uropathy, without antibiotic prophylaxis |
| |
| Healthy Controls | Healthy children aged 1 to 3 years. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Stool sampling | Other | Stool sample taken at home 24 hours before hospital visit |
|
| Measure | Description | Time Frame |
|---|---|---|
| α-diversity of the gut microbiota between groups | N index of a stool sample measured by the Shannon index (H^') which incorporates the total number of different Operational Taxonomic Units and the relative proportions of these Operational Taxonomic Units. | Day 0 |
| Measure | Description | Time Frame |
|---|---|---|
| The β-diversity of the gut microbiota between groups | Operational Taxonomic Units measured by Bray Curtis Index | Day 0 |
| The number of bacterial genera present in the gut microbiota between groups |
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Inclusion Criteria:
The patient must be a member or beneficiary of a health insurance plan
Patient with no objection to participation in the study from the parent or guardian
Child with a diversified diet.
o Specific inclusion criteria for group 1 (cases):
Child with grade 3 or higher vesicoureteral reflux.
Child on trimethoprim-sulfamethoxazole therapy for at least 5 months.
o Specific inclusion criteria for group 2 (controls):
Child with uropathy and without long-term trimethoprim-sulfamethoxazole treatment.
o Specific inclusion criteria for group 3 (healthy controls):
Child without uropathy or long-term trimethoprim-sulfamethoxazole treatment.
Exclusion Criteria:
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For the purpose of the study three groups of children will be constituted:
Children aged 1 to 3 years with vesico ureteral reflux of grade 3 or higher, under antibiotic prophylaxis; Children aged 1 to 3 years with uropathy, without antibiotic prophylaxis; Controls: Healthy children aged 1 to 3 years.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Anne Filleron | Contact | 04.66.68.32.86 | anne.filleron@chu-nimes.fr |
| Name | Affiliation | Role |
|---|---|---|
| Anne Filleron | CHU de Nimes | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Montpellier | Recruiting | Montpellier | France |
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Stool samples
Relative abundance Operational Taxonomic Units present
| Day 0 |
| The prevalence of multi-resistant bacteria | % of isolated bacteria producing extended spectrum betalactamase, carbapenemase-producing Enterococcus faecium and glycopeptide-resistant Enterococcus faecium and bacteria resistant to trimethoprim-sulfamethoxazole | Day 0 |
| CHU de Nîmes | Recruiting | Nîmes | France |
|