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Fructose is a Metabolic and Inflammatory Pathogenic Factor in Metabolic Dysfunction-associated Steatohepatitis (MASH)

RecruitingNAAges 45 Years - 65 YearsAllQueen Mary University of London
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In plain words

What the trial is, and whether it could suit you

MASLD (Metabolic dysfunction-associated steatotic liver disease) is a condition where fat builds up in the liver. It is the most common cause of liver disease worldwide. In some people, the fat can irritate the liver (inflammation) and cause damage. This is a more serious condition called MASH (Metabolic dysfunction-associated steatohepatitis). People with MASH more at risk of liver cirrhosis (advanced scarring in the liver) and liver cancer. It is not fully understood why MASLD becomes MASH, or why this happens in some people but not in others. However, it is known that our diet plays a role. Research shows a diet high in a type of sugar called fructose might make MASLD worse. Fructose is found in fruit, honey and table sugar, and lots of processed food and drinks. The body deals with fructose differently to other sugars, which is why fructose may be a problem. Although scientists have

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📋 Eligibility rules (as published)
Inclusion Criteria: * Able and willing to give written informed consent * Age 45-65 at consent * HbA1c \< 48 mmol/mol * Overweight and stage I obesity using BMI thresholds adjusted for ethnicity: * 23.0kg/m2 - 32.4kg/m2 in South Asian, Chinese, other Asian, Middle Eastern, Black African or African-Caribbean populations * 25kg/m2 - 34.9kg/m2 in White populations MASH Patients: Clinical diagnosis of MASH and F2 - F3 fibrosis: Either: Liver biopsy within 12 months of baseline Or: • History of histologically-diagnosed MASH with current evidence of fatty liver, AST\>20 and Fibroscan CAP≥248 dB/m and stiffness 9.5kPa -14kPa Or: • FAST score \>0.67 Patients with steatosis: • defined by Fibroscan CAP≥248dB/m and stiffness \<7.9kPa. Healthy controls: • defined by Fibroscan CAP\<248dB/m and stiffness \<7.9kPa. Exclusion Criteria: * Unwilling or unable to give consent * Age \<45 or \>65 * Any form of diabetes mellitus * Currently pregnant * Known fructose intolerance or food allergy * Diagnosis of cirrhosis or Fibroscan stiffness \>14kPa * Current Child-Pugh B/C or episode of decompensation in last year * Non-MASLD liver disease known to participant (including viral hepatitis, auto-immune hepatitis, primary sclerosing cholangitis, primary biliary cholangitis, haemochromatosis, sarcoidosis, cystic fibrosis, sickle cell disease) * Regular alcohol intake \> 14 units a week for females and \>21 units a week for males (participant-reported) * Smoking, vaping or use of nicotine-containing products within the last month * Taking prohibited medication: * Probiotic or antibiotic use within last 4 weeks (Note: participants will be considered eligible if they have undergone a 4-week washout from probiotics or 4-weeks after discontinuing antibiotic use) * any oral steroids within the last 6 weeks * current, or within 3 months, use of immunosuppressive medication * Amiodarone, nitrofurantoin, or anti-fungals within 3 months * Use of anti-obesity medication - orlistat or GLP-1 receptor agonist-containing treatments within 6 months * Use of vitamin E, pioglitazone or other medication for MASH including current or within 3 months enrolment in clinical trial unless documented to have been on placebo * History of malignancy (except basal cell carcinoma), or medication for malignancy within the last 2 years * Any major organ transplant (excluding corneal or hair) * Clinical diagnosis of chronic kidney disease 3 or above, or of heart failure (NYHA 3 or 4) * COPD requiring home oxygen * Known eating disorder (e.g. anorexia nervosa) or severe mental illness (e.g. schizophrenia) * Investigator opinion that study is unsuitable for patient
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What it tests

  • fructose
  • glucose
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Where

2 sites
Royal London Hospital
London, United Kingdom
Blizard Institute, Faculty of Medicine and Dentistry, Queen Mary University of London
London, United Kingdom
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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