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Genetic-specific Effects of Fructose on Liver Lipogenesis

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

NAFLD

Treatments

Other: Sugar drink

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03783195
17-3348
P30DK056336-16S1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The primary goal of this study is to identify a set of genotypes that increase the risk for nonalcoholic fatty liver disease (NAFLD) and predispose individuals to increased de novo lipogenesis (DNL) and liver fat accumulation when exposed to fructose intake. The proposed goal will be achieved through the completion of following aims:

  1. To determine the impact of prolonged exposure of fructose on hepatic lipid accumulation in Caucasian individuals with high and low genetic risk for NAFLD,
  2. to determine the impact of acute exposure of fructose on hepatic DNL, and
  3. to determine the relationship between markers of DNL, liver fat accumulation and serum concentrations of lipids, uric acid and liver function markers before and after the fructose challenge.

Full description

BACKGROUND AND RATIONALE Non-alcoholic fatty liver disease (NAFLD) is characterized by fat accumulation in liver cells not caused by alcohol. A leading cause of chronic liver disease in the US, NAFLD represents a group of disorders including steatosis, nonalcoholic steatohepatitis with fibrosis. It has substantially risen in prevalence over the last two decades with the estimated prevalence being 20% among US adults and 25% in young adults (18-39 years). Over 64 million individuals are believed to have NAFLD with annual medical costs rising to more $100 billion. More common in individuals who are obese or diabetic and/or have metabolic syndrome, NAFLD has been associated with increased cirrhosis, liver-related mortality and hepatocellular carcinoma.

Both genetic and environmental, including nutritional, factors contribute to the onset and progression of NAFLD. Increased consumption of sugar-sweetened, fructose-rich beverages has been linked to NAFLD. Fructose, commonly found in soft drinks, fruit juices and energy drinks, affects many metabolic processes, foremost being an increase in fat accumulation in the liver and hence, NAFLD. Genome-wide and candidate gene studies have identified several genes associated with NAFLD. However, none of these studies have shown the cumulative effects of single nucleotide polymorphisms (SNPs) on changes in liver fat when exposed to fructose. The results from this study can be extrapolated to larger cohorts and other ethnicities and are therefore, expected to lay the foundation for developing personalized nutritional plans.

Enrollment

15 patients

Sex

All

Ages

12 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Subjects 12 - 40 years
  2. No history of alcohol abuse (> 7 drinks per week)
  3. History of fructose intake of < 14 drinks per week
  4. Caucasian ethnicity
  5. BMI > 25kg/m² - 32kg/m² or 85th -99th percentile but otherwise healthy

Exclusion criteria

  1. ages < 12 and > 40 years
  2. Pregnant/lactating
  3. known alcohol abuse or fructose intake > 14 drinks per week
  4. not of Caucasian ethnicity
  5. glucose levels > 100 mg/dL if fasting, > 140mg/dL if within 2 hours post meal and > 200 mg/dL if random sample
  6. taking anti-hypertensive, anti-diabetic, uric acid and/or lipid-lowering medications
  7. known diagnosis of diabetes, fructose intolerance, chronic kidney disease, NAFLD or any liver-related disease, hypertriglyceridemia, polycystic ovary syndrome, hypothyroidism, obstructive sleep apnea, hypopituitarism and hypogonadism
  8. BMI < 25kg/m² or > 32 kg/m² or < 85th or > 99th percentile
  9. Liver fat fraction >5% as per baseline MRI scan

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

15 participants in 2 patient groups

High GRS group
Experimental group
Description:
This group consists of individuals who are in the highest quartile of the genetic risk score (GRS) and will ingest one sugar drink (equal to 2 soft drinks) per day for 3 weeks. The GRS is computed by adding the number of alleles that increase the risk for liver lipogenesis or fatty liver.
Treatment:
Other: Sugar drink
Low GRS group
Experimental group
Description:
This groups consists of individuals who are in the lowest quartile of the genetic risk score (GRS) and will ingest one sugar drink (equal to 2 soft drinks) per day for 3 weeks. The GRS is computed by adding the number of alleles that increase the risk for liver lipogenesis or fatty liver.
Treatment:
Other: Sugar drink

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Brea Nance; Saroja Voruganti, PhD

Data sourced from clinicaltrials.gov

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