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Study to Investigate Adipocyte Cell and Lipid Turnover in Obese Adolescents

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Yale University

Status

Completed

Conditions

Pediatric Obesity

Treatments

Other: Palmitate Diet

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT02395003
2R01HD028016 (U.S. NIH Grant/Contract)
2R01HD028016-20A1 (U.S. NIH Grant/Contract)
1503015459

Details and patient eligibility

About

Insulin Resistance is the best predictor of whether the obese adolescent will develop type 2 diabetes. The present studies will focus on determining what might cause fat to accumulate in the subcutaneous fat regions and lead to local inflammation, causing insulin resistance to develop in obese adolescents.

Full description

The purpose of this study is to test whether the reduced transcription of key lipogenic/adipogenic genes in abdominal subcutaneous adipose tissue (SAT) in obese adolescents with a High VAT/SAT (visceral adipose tissue/subcutaneous adipose tissue) ratio translates functionally into a reduced in vivo triglyceride (TG) synthesis and adipocyte proliferation, which in turn will contribute to ectopic fat accumulation and insulin resistance (IR). To test whether the storage capacity of gluteal SAT is linked to the level of VAT/SAT fat distribution in obese adolescents. To explore if changes in dietary fat intake (palmitate intake) alters ceramide concentration in both plasma and adipose tissue (AT) and the Inflammasome complex in the different fat distribution phenotypes and their associations with IR.

Enrollment

26 patients

Sex

All

Ages

12 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Overweight (85-95th% age and gender specific) or Obese (>95th% age and gender specific)
  • Ages 12-18 years
  • Absence of any endocrinopathy
  • Absence of any therapy with medication known to alter glucose metabolism (i.e.: Oral steroids, certain psychiatric medications such as Xeleca, Lithium, Paxil)
  • English Speaking subjects

Exclusion criteria

  • Any disease known to alter glucose metabolism (T2DM)
  • Diuretic Medication
  • Pregnant or breastfeeding
  • Type 1 or 2 diabetes

Trial design

26 participants in 4 patient groups

High VAT/SAT high Palmitate Diet
Description:
Subjects with a high ratio of visceral to subcutaneous fat consuming high Palmatite oil diet for 12 weeks
Treatment:
Other: Palmitate Diet
Low VAT/SAT
Description:
Subjects with a low ratio of visceral to subcutaneous fat
Treatment:
Other: Palmitate Diet
Lean Controls
Description:
Lean control
High VAT/SAT- low Palmitate Diet
Description:
Subjects with a high ratio of visceral to subcutaneous fat consuming low Palmatite oil diet for 12 weeks

Trial contacts and locations

1

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Central trial contact

Bridget Pierpont, MA; Jessica M Nouws, BS

Data sourced from clinicaltrials.gov

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