Metabolic dysfunction-associated steatohepatitis (MASH): a plain-language guide

MASH is the form of fatty liver disease in which extra fat in the liver is accompanied by inflammation and injury to liver cells, which is what can lead over time to scarring, cirrhosis and liver cancer [6,11].

This page provides general information. It does not replace advice from a doctor or another qualified healthcare professional.

Key facts

  • MASH is not a separate illness from fatty liver disease. It is the part of the wider condition, MASLD, where fat is joined by inflammation and liver-cell injury [6,11].
  • The names changed in 2023. NASH became MASH, and NAFLD became MASLD. Readers will still meet the old names everywhere [1,24].
  • Two reasons drove the change. The old names described the condition by what it was not, and the words “nonalcoholic” and “fatty” were felt to be stigmatizing by most of the experts and patient advocates surveyed [1].
  • MASH is usually silent. A person can have cirrhosis caused by MASH and still feel well, and routine liver blood tests are often normal [5,7].
  • Around 5 percent of adults worldwide are estimated to have MASH, and MASLD with MASH is the second leading cause of end-stage liver disease and liver transplantation in Europe [23].
  • There is now a medicine approved specifically for MASH with moderate to advanced scarring, and a second approved in the United States. Availability differs between countries [10,11,12,21].

On this page

What is MASH?

MASH stands for metabolic dysfunction-associated steatohepatitis. It is a condition of the liver in which three things happen at once [6,11]:

  • Fat. Extra fat has built up inside liver cells.
  • Inflammation. The liver is irritated and swollen in response.
  • Liver-cell injury. Liver cells are damaged and swell, which specialists call ballooning [11].

The third element is the point. Fat alone is common and often harmless. Fat plus inflammation plus injury sets off a repair cycle that lays down scar tissue, and scarring leads to cirrhosis and liver cancer [16,22].

MASH sits inside a larger condition

The umbrella condition is MASLD, metabolic dysfunction-associated steatotic liver disease: fat in the liver in someone who also has at least one of five cardiometabolic features, once heavy alcohol use and other causes are ruled out [24]. Most people with MASLD have fat with little or no inflammation, and that form usually does not progress [6]. MASH is the smaller group where inflammation and injury are present too, and nobody can tell them apart by how they feel [6]. See also the trialport guide to fatty liver disease and MASLD.

The names changed in 2023

In June 2023 a consensus of three international liver associations, drawing on 236 panelists from 56 countries, renamed NAFLD as MASLD and NASH as MASH [1]. The old naming defined the condition by exclusion, by what it was not, and the words were felt to be stigmatizing, by 61 percent of those surveyed for “nonalcoholic” and 66 percent for “fatty” [1]. The new names describe it through the metabolic features that drive it [1,24]. Readers will still meet NASH and NAFLD in older leaflets, on results and in conversation, and they mean the same conditions. The United Kingdom’s guideline was renamed in July 2026 [2].

How common is it?

Around 32 percent of adults worldwide are estimated to have MASLD and around 5 percent to have MASH, with MASLD at 30 percent across the European Union and the United Kingdom [23]. United States government estimates put MASLD at about 24 percent of adults and MASH at 1.5 to 6.5 percent [6].

These are estimates, not counts: confirming MASH has historically needed a liver biopsy, which cannot be done across a population, so figures vary and many go undiagnosed [5,19].

Rates run far higher in some groups: MASH is estimated at 33.5 percent among people living with overweight or obesity and 31.6 percent among people with type 2 diabetes [23]. More than a third of Australians are thought to have fatty liver disease [26], and in a Dubai study of 94,754 adults, half screened positive for MASLD risk factors [25].

MASLD including MASH is now the second leading cause of end-stage liver disease and liver transplantation in Europe [23].

What causes it?

MASH begins with a problem in metabolism, the way the body takes and stores energy from food. Fat builds up inside liver cells, damages and inflames them, and the repeated repair that follows lays down scar tissue [16].

The metabolic conditions involved are type 2 diabetes or prediabetes, overweight or obesity, high blood pressure and abnormal blood fats. Doctors use the term metabolic syndrome for any three of a large waist, high triglycerides, low HDL cholesterol, high blood pressure and raised blood glucose [7]. Genes, meaning small differences in the instructions inside cells, also matter and may help explain why rates differ between ethnic groups [6,7]. Risk rises with age, is higher in men, and increases after menopause in women [16].

Body weight is part of the picture and not the whole picture: up to 1 in 5 people with MASLD have a body mass index in the healthy range [16]. Nobody chooses to develop this condition, and weight is shaped by far more than personal choices [16]. Experts still do not know why some people with liver fat develop MASH and others never do [6].

What are the symptoms?

This is the most important thing on the page. MASH is usually silent. A person can have cirrhosis caused by MASH and have no symptoms at all [7].

Early symptoms, where they appear, are vague: tiredness, and discomfort in the upper right of the abdomen where the liver sits [7,17]. Neither is specific to the liver, and many people with MASH feel well [17], so asking a doctor about tests beats waiting for a symptom.

When to seek urgent help. Symptoms of advanced liver disease are the exception, and most people with MASH will never experience them. Tell a doctor straight away, or seek urgent care, if any of these appear: yellowing of the skin or the whites of the eyes, which is harder to see on black or brown skin; vomiting blood; black, tarry stools; confusion or unusual changes in mood; swelling of the abdomen, legs or feet; bruising very easily; dark urine; or losing weight without trying [17,26].

How is it diagnosed?

No single test diagnoses MASH, part of why it is missed [19]. Diagnosis starts with a family doctor, who asks about other conditions, medicines and alcohol intake to rule out alcohol-related liver disease, and moves to a liver specialist, called a hepatologist, if results suggest advanced scarring [2,19].

Blood tests, with an important caveat. Raised liver enzymes can be a clue [8]. Normal ones prove nothing. More than 80 percent of people with MASLD have normal routine liver blood tests, and United Kingdom guidance says plainly that those tests should not be used to rule MASLD out or to check for advanced scarring [2,5].

Fibrosis scores combine several results into one number. FIB-4 uses age, two liver enzymes and the platelet count, and a result below about 1.3 is usually low risk and above 2.67 high risk [19,25]. United Kingdom guidance suggests the enhanced liver fibrosis test, treating a score of 10.51 or above as advanced fibrosis [2].

Scans. Ultrasound shows fat but not inflammation or scarring. Transient elastography, often called FibroScan, is a quick painless scan of liver stiffness, which reflects scarring [8,19].

Liver biopsy remains the only test that can prove MASH, and its role is shrinking [8]. Guidelines now use blood scores first and imaging second, keeping biopsy for unclear or high-risk cases, and the newest MASH medicine can be prescribed on either route [8,14,24].

How is it treated?

Treatment has two aims: to stop the condition getting worse, and to let the liver repair what it can [20]. Damage can be slowed and sometimes partly reversed, especially at earlier stages [18,20].

Everyday changes. Reducing liver fat addresses the root cause, and research shows that reducing body weight lowers liver fat, with larger reductions also lowering inflammation and scarring [9]. Weight loss should be gradual, since rapid loss can make liver disease worse [9]. It is genuinely hard, and a doctor can refer someone to a dietitian or local program [20]. Physical activity helps on its own terms, reducing liver fat even when body weight does not change, with the clearest effect at around 150 minutes of brisk walking a week [9,24].

Resmetirom is the first medicine approved specifically for MASH. It is a daily tablet that activates a receptor in liver cells to increase fat breakdown, reducing inflammation and scarring [11]. United States regulators approved it in March 2024 and European regulators in August 2025, both conditionally, for adults with non-cirrhotic MASH and moderate to advanced fibrosis [10,11]. What it does not do is also on the record. There is no evidence yet that it reduces liver transplants or improves survival, long-term studies are still running, and it is not for people with decompensated cirrhosis [10,11]. The most common side effects are diarrhea and nausea [10]. It is under review and not yet available in the United Kingdom [21].

GLP-1 receptor agonists copy a natural hormone that helps control blood sugar and appetite [21]. In August 2025 United States regulators gave semaglutide accelerated approval for the same group [12]. In the European Union its authorized indication covers weight management, not MASH [13], and in the United Kingdom it is under review [21].

Other options. Bariatric surgery is not a direct MASH treatment, and it can improve the liver in some people with MASLD and obesity [14,20]. Where advanced fibrosis is present, United Kingdom specialists may also consider pioglitazone or vitamin E [3]. Availability differs by country.

Treating what sits alongside it. Managing type 2 diabetes, blood pressure and cholesterol is central, since the greatest risk to overall health here is often heart attack and stroke [18,20]. People taking statins should keep taking them [4]. Guidance asks clinicians to explain staying within national low-risk alcohol limits, and to advise stopping completely where advanced fibrosis or cirrhosis is present [2,20].

Where cirrhosis has developed, scans for liver cancer are usually offered every six months, and European guidance also recommends monitoring for raised pressure in the liver’s blood supply [14,22]. A transplant may be considered if the liver cannot recover [14].

Living with MASH

Monitoring continues even when nothing feels wrong, with retesting every few years at low risk and again after starting treatment [2,3]. No complementary or alternative medicine has been shown to treat this condition and some can harm the liver. Smoking speeds liver disease up, so stopping helps [20]. A diagnosis carrying assumptions about weight and drinking can be hard to talk about, and liver charities run free helplines [1,20].

Thinking about a clinical trial?

Clinical trials test whether a treatment works and is safe. Deciding whether to look into one is personal, and it helps to take it in steps.

1. Understand what the study is asking

It is worth being clear on what a study involves:

  • what the researchers are trying to learn
  • what is being studied, and what it is compared with
  • how long it lasts, and whether there is follow-up afterward
  • what visits and tests are involved, including whether a liver biopsy is needed
  • how far you would travel, and how often
  • the possible benefits, the known and unknown risks, and what happens at the end

MASH studies often run a year or longer, because liver changes are slow, and many involve fasting blood tests, scans and a record of activity or food between visits.

2. Consider possible medical suitability

Every trial has rules about who can take part, called eligibility criteria. For a MASH study they might include MASH confirmed on a recent liver biopsy or by validated non-invasive tests, a fibrosis stage inside a set range with cirrhosis excluded, a FIB-4 or liver stiffness reading between set limits, stable body weight beforehand, blood sugar inside a stated range for people with type 2 diabetes, alcohol below a stated limit, no other cause of liver disease, and staying on a steady dose of current medicines.

trialport’s medifit helps people consider information related to possible medical suitability. It does not diagnose a condition, confirm eligibility or replace formal screening by the study team.

Explore MASH clinical trials through trialport

3. Consider whether participation fits your life

A study can look right on paper and still be hard in practice. Worth thinking through:

  • the time each visit takes, and how many there are in total
  • how fasting visits and scans would fit around work, school or caring for other people
  • travel, distance and who would come with you
  • how you would feel about being weighed and asked about food, activity and alcohol at every visit
  • who supports you, and whether you understand the study well enough to decide

trialport’s readifit helps people reflect on their understanding, motivation, time, routines, support, emotions and practical arrangements.

4. Ask questions before deciding

Useful questions to put to a research team:

  • Why is this study being carried out, and what is already known?
  • What would I need to do, and for how long?
  • What are the known risks and side effects, and what is still unknown?
  • Could I receive a placebo? A placebo is a dummy treatment with no active medicine, used so researchers can compare results fairly. Would I still receive usual care alongside it?
  • Would I need a liver biopsy, how many, and when?
  • Would my current medicines be changed, paused or kept as they are?
  • What would I be told about alcohol, and what if I find that hard?
  • Can I leave after joining, and what happens to my care if I do?
  • Could I keep receiving the treatment afterward, and are travel costs covered?

Taking part is voluntary. A person can ask questions, speak with people they trust and choose not to participate.

Search for clinical trials at app.trialport.com.

Current research

  • Approved medicines, still being studied. Both were approved on changes in the liver rather than long-term outcomes, and longer studies are testing whether they reduce cirrhosis, transplant and death [10,11,12,24].
  • New drug classes. Several treatments are in late-stage testing and none is approved, among them lanifibranor, efruxifermin, pegozafermin and survodutide [24].
  • Better tests and earlier detection, including non-invasive ways to identify MASH itself rather than only the scarring it causes, called an urgent gap by the United Kingdom guideline committee, and ways to find people at risk from routine blood results [5,23,24,25].

Study status checked: 3 August 2026. Research moves quickly and what is being studied changes, so this list will date. For current information, search at app.trialport.com.

Support and further information

In the United Kingdom, Liver UK, formerly the British Liver Trust, has the clearest patient information on this condition and a free nurse-led helpline [15,20], and NICE guideline NG49 sets out what care should look like [2]. In the United States, the NIDDK pages on fatty liver disease are detailed and government-reviewed, though last reviewed in 2021 and so predating the renaming and the first approved medicine [6,9]. In Australia, the Liver Foundation runs a liver nurse line [26]. Coverage is thinner elsewhere, and a hospital liver clinic is the best starting point.

Well-known people with MASH

Dan Marino, the American football quarterback and Pro Football Hall of Fame member, revealed in September 2025 that he has MASH. He was diagnosed in 2007 after mentioning fatigue at a routine check-up, was told it could be reversible, and has since managed it with regular activity and yearly scans [27]. He had almost no symptoms, which is how most cases present.

Questions people often ask

Is MASH the same as NASH?
Yes. NASH was renamed MASH in 2023, when NAFLD became MASLD, and both names remain in use [1,15].

What is the difference between MASLD and MASH?
MASLD means fat in the liver alongside metabolic features [24]. MASH is the form where inflammation and liver-cell injury are present too, which drives scarring [6].

Do I have MASH if my liver blood tests are normal?
Normal results do not rule it out. More than 80 percent of people with MASLD have normal routine liver blood tests, and guidance says those tests should not be used to rule the condition out [2,5].

Is this caused by drinking?
No. MASH is defined by metabolic features and the definition excludes heavy alcohol use [24]. Alcohol still strains a liver already working hard, so guidance asks people to stay within national low-risk limits [2,20].

Did I bring this on myself?
No. Nobody chooses to develop this condition, weight is shaped by far more than personal choices, and up to 1 in 5 people with MASLD have a body mass index in the healthy range [16]. Stigma in the old names is one reason they changed [1].

Is there a medicine for it?
Yes, for some people. Resmetirom is approved in the United States and the European Union for adults with non-cirrhotic MASH and moderate to advanced scarring, and semaglutide in the United States [10,11,12]. Neither is approved for MASH in the United Kingdom [21].

Sources

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  2. National Institute for Health and Care Excellence. NICE guideline NG49, Metabolic dysfunction-associated steatotic liver disease (MASLD). Published 6 July 2016, last updated 31 July 2026. Recommendations 1.1 to 1.6 and guideline overview. https://www.nice.org.uk/guidance/ng49 Accessed 3 August 2026.
  3. National Institute for Health and Care Excellence. NICE guideline NG49, Pharmacological treatment (recommendations 1.8.1 to 1.8.9). https://www.nice.org.uk/guidance/ng49/chapter/Pharmacological-treatment Accessed 3 August 2026.
  4. National Institute for Health and Care Excellence. NICE guideline NG49, People with MASLD who are taking statins (recommendations 1.7.1 to 1.7.2). https://www.nice.org.uk/guidance/ng49/chapter/People-with-MASLD-who-are-taking-statins Accessed 3 August 2026.
  5. National Institute for Health and Care Excellence. NICE guideline NG49, Recommendations for research. https://www.nice.org.uk/guidance/ng49/chapter/Recommendations-for-research Accessed 3 August 2026.
  6. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. Definition & Facts of NAFLD & NASH. Last reviewed April 2021. https://www.niddk.nih.gov/health-information/liver-disease/nafld-nash/definition-facts Accessed 3 August 2026.
  7. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. Symptoms & Causes of NAFLD & NASH. Last reviewed April 2021. https://www.niddk.nih.gov/health-information/liver-disease/nafld-nash/symptoms-causes Accessed 3 August 2026.
  8. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. Diagnosis of NAFLD & NASH. Last reviewed April 2021. https://www.niddk.nih.gov/health-information/liver-disease/nafld-nash/diagnosis Accessed 3 August 2026.
  9. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. Treatment for NAFLD & NASH. Last reviewed April 2021. https://www.niddk.nih.gov/health-information/liver-disease/nafld-nash/treatment Accessed 3 August 2026.
  10. US Food and Drug Administration. FDA Approves First Treatment for Patients with Liver Scarring Due to Fatty Liver Disease. News release, 14 March 2024. https://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-patients-liver-scarring-due-fatty-liver-disease Accessed 3 August 2026.
  11. European Medicines Agency. Rezdiffra (resmetirom): medicine overview page. Marketing authorisation issued 18 August 2025, page last updated 27 May 2026. https://www.ema.europa.eu/en/medicines/human/EPAR/rezdiffra Accessed 3 August 2026.
  12. US Food and Drug Administration, Center for Drug Evaluation and Research. Approval letter, NDA 215256/S-024, Wegovy (semaglutide), accelerated approval for noncirrhotic MASH with moderate to advanced liver fibrosis. 15 August 2025. https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/215256Orig1s024ltr.pdf Accessed 3 August 2026.
  13. European Medicines Agency. Wegovy (semaglutide): medicine overview page, therapeutic indication. https://www.ema.europa.eu/en/medicines/human/EPAR/wegovy Accessed 3 August 2026.
  14. European Association for the Study of the Liver, European Association for the Study of Diabetes, European Association for the Study of Obesity. EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). Journal of Hepatology. 2024;81(3):492-542. doi:10.1016/j.jhep.2024.04.031. Abstract read via Europe PMC: https://europepmc.org/article/MED/38851997 Accessed 3 August 2026.
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  16. Liver UK. What causes MASLD? Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/what-causes-masld/ Accessed 3 August 2026.
  17. Liver UK. What are the symptoms of MASLD? Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/what-are-the-symptoms-of-masld/ Accessed 3 August 2026.
  18. Liver UK. What are the stages of MASLD? Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/what-are-the-stages-of-masld/ Accessed 3 August 2026.
  19. Liver UK. How is MASLD diagnosed? Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/how-is-masld-diagnosed/ Accessed 3 August 2026.
  20. Liver UK. How is MASLD treated? Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/how-is-masld-treated/ Accessed 3 August 2026.
  21. Liver UK. Future treatments for MASLD. Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/future-treatments-for-masld/ Accessed 3 August 2026.
  22. Liver UK. What happens if my MASLD is more advanced? Last reviewed July 2026. https://liveruk.org/about-liver-disease/conditions/masld/what-happens-if-my-masld-is-more-advanced/ Accessed 3 August 2026.
  23. Lazarus JV, White TM, Agirre-Garrido L, et al. Assessing Europe’s policy readiness to confront the MASLD/MASH public health threat. The Lancet Regional Health – Europe. 2026;65:101713. doi:10.1016/j.lanepe.2026.101713. https://pmc.ncbi.nlm.nih.gov/articles/PMC13245526/ Accessed 3 August 2026.
  24. Reinson T, Bilson J, Childs C, Buchanan RM, Targher G, Byrne CD. Metabolic dysfunction associated steatotic liver disease: mechanisms, diagnosis, and management in adults. BMJ Medicine. 2026;5(1):e002038. doi:10.1136/bmjmed-2025-002038. https://pmc.ncbi.nlm.nih.gov/articles/PMC13052820/ Accessed 3 August 2026.
  25. Abdelgadir E, Alawadi F, Rashid F, Bashir A, Schattenberg JM. Doubling the diagnostic rate of at-risk metabolic dysfunction-associated steatohepatitis, leave no one behind. The Lancet Regional Health – Europe. 2026;60:101572. doi:10.1016/j.lanepe.2025.101572. https://pmc.ncbi.nlm.nih.gov/articles/PMC12794228/ Accessed 3 August 2026.
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  27. Ellington A. NFL Icon Dan Marino Shares Liver Disease Diagnosis. AARP. Published 17 September 2025. https://www.aarp.org/entertainment/celebrities/dan-marino-liver-disease-diagnosis/ Accessed 3 August 2026.

Review information

Written by: trialport editorial team
Reviewed by: Keith Berelowitz, Founder and CEO, trialport
Reviewed on: 3 August 2026
Next review due: 3 August 2027
References last checked: 3 August 2026

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