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| ID | Type | Description | Link |
|---|---|---|---|
| R01AI121383 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| University of Minnesota | OTHER |
| University of Pennsylvania | OTHER |
| National Institute of Allergy and Infectious Diseases (NIAID) | NIH |
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This cross-disciplinary study will assemble and longitudinally follow a large, diverse birth cohort to determine the relationships between early life antibiotic exposure, microbiome development, growth, antibodies, and immunostimulation.
Perinatal and infant antibiotic exposures are common and have been linked to changes in the gut microbiome, which plays a central role in health and disease. Childhood obesity is an epidemic and animal models have linked antibiotic induced changes in the microbiome with increased adiposity. Infants become colonized with trillions of bacteria in the first few hours of life. During this time period, their nascent immune system develops tolerance to commensal microbes
The primary objectives are to measure the impact of common perinatal and early childhood antibiotic exposures on the structure and function of the developing gut microbiome. To determine the association between common perinatal and early childhood antibiotic exposures and weight/adiposity gain in a large birth cohort of children. To determine mechanisms for the association between microbiome changes over time and the rate of weight/adiposity gain in a large birth cohort of children. To determine the normal developmental pattern by which healthy children develop antibodies in their blood against the microbes that naturally colonize their intestines. To determine the association between immunostimulation and protection from persistent colonization in humans.
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| Measure | Description | Time Frame |
|---|---|---|
| cumulative microbial diversity | 24 months | |
| weight trajectory adjusted for time varying length | 24 months |
| Measure | Description | Time Frame |
|---|---|---|
| total number of individual bacterial taxa | 24 months | |
| expression levels of bacterial gene categories | 24 months | |
| fat stores in the upper arm/extremity |
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Inclusion Criteria (if not specified, applies to child):
Exclusion Criteria (if not specified, applies to child):
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Our study population will be comprised of children born at Pennsylvania Hospital between 2016-2018 and subsequently, followed in the Children's Hospital of Philadelphia (CHOP) Care Network or one of four other local primary care pediatric practices.
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| Name | Affiliation | Role |
|---|---|---|
| Jeffrey S Gerber, MD, PhD | Children's Hospital of Philadelphia | Principal Investigator |
| Dan Knights, PhD | University of Minnesota | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104 | United States |
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| Label | URL |
|---|---|
| Official study website | View source |
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De-identified individual participant data will be shared with collaborators at the Knights Lab at the University of Minnesota.
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| ID | Term |
|---|---|
| D063766 | Pediatric Obesity |
| ID | Term |
|---|---|
| D009765 | Obesity |
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
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Stool samples Saliva samples nasal swab skin swabs blood draw cord blood heel stick
Skinfolds at the triceps are measured (0.1 mm) with a skinfold caliper |
| 24 months |
| fat stores in the upper back/trunk | Skinfolds at the superiliac and subscapular sites are measured (0.1 mm) with a skinfold caliper | 24 months |
| supine length trajectory | 24 months |
| determine the association between immunostimulation and protection from persistent colonization in humans | 24 months |
| Use autologous serum antibodies to "tag" fecal microbes | 24 months |
| D009750 |
| Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |