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Completed

NCT Number: NCT04644887

Liver, Diet and Genetic Background

PNPLA3 rs738409 (I148M) variant is associated with hepatic liver accumulation and chronic liver diseases including non-alcoholic fatty liver disease. It has been shown that obesity augments genetic risk but studies investigating the interaction of PNPLA3 rs738409 risk variant and diet are scarce. The aim is to investigate the effect of dietary fat quality modification in participants with different variants of the PNPLA3 gene (rs738409). The primary outcome is the change in liver fat measured by magnetic resonance imaging in the randomized controlled 12-week dietary intervention trial.

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Key information

Age range

60 year–75 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Public Health and Clinical Nutriton

Kuopio, Finland

About this study

Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease worldwide. The composition of the diet, especially quality of dietary fat, contributes to the susceptibility to hepatic lipid accumulation. Saturated fatty acids (SFA), but not polyunsaturated fatty acids (PUFA) increases intrahepatic triglycerides with and without concomitant weight gain. Therefore, the modification of dietary fat quality is the key dietary approach for the prevention of NAFLD.

PNPLA3 rs738409 (I148M) variant is associated with hepatic liver accumulation and chronic liver diseases including NAFLD. It has been shown that obesity augments genetic risk but studies investigating the interaction of PNPLA3 rs738409 risk variant and diet are scarce. Therefore, the aim is to investigate the effect of dietary fat quality modification (high unsaturated fat vs. high SFA) on liver fat and lipid and glucose metabolism in participants with different variants (CC or GG) of the PNPLA3 gene.

The investigators will conduct the randomized controlled 12-week dietary intervention trial in participants with different homozygous PNPLA3 variants (CC or GG). The primary outcome of the intervention is in the amount of liver fat measured by nuclear magnetic resonance imaging (MRI). Altogether 140 homozygous participants (PNPLA3 rs738409 CC and GG) will be recruited from the Metabolic Syndrome in Men (METSIM) study. The inclusion criteria include BMI < 35 kg/m2 and age < 75 years. The main exclusion criteria include diabetes, acute illness, or current evidence of acute or chronic inflammatory or infective diseases.

Dietary guidance in the intervention group is based on the Nordic and Finnish nutrition recommendations with an emphasis on the quality of dietary fat. The aims for the intake of fatty acids will be SFA < 10 % of energy intake (E%) and mono- and polyunsaturated fatty acids (UFA) >2/3 of the total fat intake.

The diet of the control group corresponds to the average nutrient intake in the Nordic countries, i.e. the intake of SFA about 15 E% and the proportion of UFA about 50 % of total fat intake.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • PNPLA3 rs738409, CC or GG
  • Body mass index (BMI) < 35 kg/m2
  • Total cholesterol < 8 mmol/l
  • LDL cholesterol < 5 mmol/l
  • Fasting plasma glucose < 7 mmol/l
  • Plasma alanine aminotransferase (ALT) < 100 U/l
  • Age 60-75 y

Exclusion criteria

The main exclusion criteria include acute illness or current evidence of acute or chronic inflammatory or infective diseases. No patients with hepatitis B and/or C, autoimmune hepatitis, Wilsons disease/alpha-1-antitrypsin deficiency, hemochromatosis, chronic kidney disease, unstable hypothyroidism or lipoatrophy will be accepted. No subjects with diagnosed diabetes (any type) are accepted. In addition to that, no diagnosed depression or any mental illness rendering the patients unable to understand the nature, scope and possible sequences of the study will be accepted. Alcohol abuse (daily consumption ≥ 30 g for men and ≥ 20 g for women) is also exclusion criteria.

Treatment and study plan

Dietary intervention: Healthy diet

Other

Dietary guidance in the intervention group is based on the Nordic and Finnish nutrition recommendations with an emphasis on the quality of dietary fat. The aims for the intake of fatty acids will be SFA < 10 % of energy intake (E%) and mono- and polyunsaturated fatty acids (UFA) >2/3 of the total fat intake. The key food products such as vegetable oil-based spread, liquid margarine and canola oil are provided to the participants. The participants are recommended to use fat free (e.g. milk, sourdough milk and yogurt) and low fat (e.g. cheese ≤ 17%) dairy products and low-fat meat, poultry, and fish as well as natural nuts and seeds.

Dietary intervention: Control diet

Other

The control diet corresponds to the average nutrient intake in the Nordic countries, i.e. the intake of SFA about 15 E% and the proportion of UFA about 50 % of total fat intake. The participants of the control group will get butter-based spread for bread and cooking. They are recommended to use semi-skimmed milk (1,5 %), normal fat yogurt (~2%), normal fat cheese (~24-35 %) and avoid consumption of vegetable oils. They are allowed to eat a portion of fish and nuts once a week.

Primary outcomes

  1. Liver fat

    Time frame: 12 weeks

    The primary outcome is the change in liver fat measured by magnetic resonance imaging

Secondary outcomes

  1. Hepatic condition monitored by ultrasound

    Time frame: 12 weeks

    The hepatic condition will be monitored by ultrasound

  2. Hepatic condition monitored by elastography

    Time frame: 12 weeks

    The hepatic condition will be monitored by elastography

  3. Hepatic condition monitored by calculated indexes

    Time frame: 12 weeks

    The hepatic condition will be monitored by calculating and comparing Fibrosis-4 index, NAFLD Fibrosis Score, hepatic steatosis index, the fatty liver index and NAFLD liver fat score.

  4. Glucose metabolism

    Time frame: 12 weeks

    Changes in glucose metabolism (oral glucose tolerance test, 0, 30 min and 2 h samples)

  5. Serum lipid profile

    Time frame: 12 weeks

    Concentrations of total cholesterol, LDL cholesterol, HDL cholesterol and triglycerides

  6. Inflammatory markers

    Time frame: 12 weeks

    Serum circulating concentrations of high-sensitivity C-reactive protein

  7. Plasma metabolomic profile

    Time frame: 12 weeks

    Mass spectrometry based metabolomics analysis

  8. Plasma lipidomic profile

    Time frame: 12 weeks

    Mass spectrometry based lipidomics analysis

  9. Gut microbiota

    Time frame: 12 weeks

    The DNA/RNA of gut microbiota will be extracted and collected for high throughput metagenomics and metatranscriptomics to observe changes in type and composition of gut microbiota.

  10. Fatty acid composition of plasma lipid fractions

    Time frame: 12 weeks

    Fatty acid composition of plasma phospholipids, cholesteryl esters and triglycerides

Sponsors and collaborators

Lead sponsor

University of Eastern Finland

Other

Collaborators

  • Kuopio University Hospital

Registry information

Official study title

The Effect of Dietary Fat Quality Modification for Liver Fat Content in Participants With Different Variants in PNPLA3 Gene - Liver, Diet and Genetic Background (LIDIGE STUDY)

Acronym: LIDIGE

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Nov 25, 2020
Registry last updated
May 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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