Bad Genes or Genes Behaving Badly

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Krista Casazza, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:
NCT01041664
First received: December 30, 2009
Last updated: April 18, 2012
Last verified: April 2012

December 30, 2009
April 18, 2012
December 2009
December 2010   (final data collection date for primary outcome measure)
Evaluate the effect of diet by gene interactions on body composition measures in Hispanic American children [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01041664 on ClinicalTrials.gov Archive Site
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Bad Genes or Genes Behaving Badly
Bad Genes or Genes Behaving Badly

A key factor in the determination of body composition over the lifecourse is fat accumulation during childhood. Periods of life associated with the greatest changes in organ development and growth, i.e. early childhood, have the most significant effect on body composition, energy balance, and metabolism. Early childhood (age 3 to 7 years) represents a critical transition for the basis of adaptability in body composition, due to the rapid growth and development that occurs. Plausibly the phenotype underlying obesity and related health risk may be determined by body composition during this critical period.

Our previous research in children has consistently indicated that HA children accumulate greater amounts of fat, particularly in the intra-abdominal compartment, even at similar a BMI, and lower bone mineral content relative to EA children. The reason for these differences in body composition over the lifecourse is not clear.

Racial/ethnic differences in risk factors for health, including 'thriftiness' in body fat accumulation are often evident before the age of 7, suggesting that the racial/ethnic differences in energy utilization and subsequent fat storage may be accounted for by genetic make-up, the environment (e.g. diet), or an interaction of the two. The physiologic or behavioral process(es) that cause(s) certain children to take a trajectory towards obesity while others accrue less fat is not known. However, the economic decision of fuel utilization is a physiologic trait enabling the body to choose between shuttling 'energy' towards accrual of a particular tissue (e.g. bone vs. fat) and this trait likely has a genetic component. This genetic component may be embedded in fat storage capacity evolved from gene by environment interactions that promote thrift, particularly conserved in some populations. Although genetic background plays a role, it not known whether there is a relationship between genetic background, known candidate genes or candidate pathways and environmental contributors (e.g. diet) that impact body composition trajectory. Of central importance to our understanding of early fat mass accumulation in health disparities are the mechanisms that lead to chronic disease progression.

It is likely that variations within candidate genes may have a differential impact on individuals based on their genetic background. It is also probable that body composition is influenced by many genes, often within the same metabolic pathways, with small individual effects. These genes may not be significantly associated individually, but when examined as a unit (in a candidate pathway or gene-gene interaction framework) the association becomes significant. Further, children's early environmental exposures (e.g. diet) may interact with both genetic background and variations in candidate genes along resulting in alterations in body composition that predispose HA to excess fat accumulation throughout the lifecourse. To that end, the following specific aims will be evaluated:

Aim 1. To examine the associations between genetic admixture and body composition in children aged 3-7 years after controlling for dietary intake.

  1. Hypothesis 1.1: There is a direct association between Amerindian admixture and fat mass and in inverse association between Amerindian admixture and bone mass.
  2. Hypothesis 1.2: There is a direct association between energy intake and fat accumulation and the relationship will be particularly evident in individuals with a greater proportion of Amerindian admixture.

Aim 2. To examine the associations between genetic admixture and bone marrow fat in children aged 3-7 years after controlling for dietary intake.

  1. Hypothesis 2.1: There is a direct association between Amerindian admixture and bone marrow fat.
  2. Hypothesis 2.2: There is a direct association between energy intake and fat accumulation in bone marrow and the relationship will be particularly evident in individuals with a greater proportion of Amerindian admixture.

Aim 3. To examine the relationship between variation in candidate genes and pathways and Amerindian admixture controlling for dietary intake.

a. Hypothesis 3.1: Amerindian admixture will be associated with variations in candidate genes and pathways known to be associated with fat accumulation.

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Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
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Retention:   Samples With DNA
Description:

Samples will be labeled with the study protocol number, a unique identifier, and the date of collection.

Specimens will be obtained by the nursing staff at the PCIR. The PCIR processing lab will process the samples, which will then be stored in a locked freezer at -80oC in the restricted access CNRU Metabolism Core lab (WEBB 337).

Non-Probability Sample

Participants will be healthy children self-identifed as Hispanic American aged 3 to seven years

  • Body Composition
  • Energy Balance
  • Metabolism
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
30
June 2011
December 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Self-identified as Hispanic American
  • Healthy, not under the care of a doctor
  • Not taking medications known to affect body composition or metabolism

Exclusion Criteria:

  • Not meeting above criteria
Both
3 Years to 7 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01041664
F091006003
Yes
Krista Casazza, University of Alabama at Birmingham
University of Alabama at Birmingham
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University of Alabama at Birmingham
April 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP