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. 2025 May 6;9(5):e0704. doi: 10.1097/HC9.0000000000000704

Awareness of metabolic dysfunction–associated steatotic liver disease (MASLD) in 4 major cities in the United States

Jeffrey V Lazarus 1,2,, Trenton M White 1,2, Alina M Allen 3, Silvana Pannain 4, Naim Alkhouri 5, Meena B Bansal 6, Michael Charlton 7, Brett E Fortune 8, Yehuda Handelsman 9, Scott Isaacs 10, Ira M Jacobson 11, Sonal Kumar 12, Melina I Manolas 13, Mazen Noureddin 14, Mary E Rinella 15, Norah Terrault 16, Ayman El-Mohandes 1
PMCID: PMC12055070  PMID: 40331869

Abstract

graphic file with name hc9-9-e0704-g001.jpg

Keywords: diabetes, MASH, MASLD, noncommunicable diseases, prevention, risk factors, urban health policy

INTRODUCTION

Metabolic dysfunction–associated steatotic liver disease (MASLD), known until mid-2023 as NAFLD, 1 and its more severe form, metabolic dysfunction–associated steatohepatitis (MASH), are characterized by liver fat accumulation, often comorbid with obesity, type 2 diabetes, hypertension, and dyslipidemia—conditions associated with insulin resistance and related metabolic risk factors. 2 MASLD, part of the spectrum of fatty liver diseases (now collectively called steatotic liver disease), is the most common chronic liver disease globally, affecting ~30% of adults and over 10% of children—a 50% increase in prevalence over 3 decades. 3

Despite this high and increasing prevalence, public awareness remains low, which led to awareness being selected as 1 of 6 priority areas in the global MASLD/MASH research agenda. 4 In 2016, an estimated 6.3% of individuals with MASLD in the United States were aware of their condition, even lower among younger adults and non-Hispanic Black populations. 5 Many remain unaware as MASLD is often asymptomatic until progressing to advanced stages (eg, MASH with liver fibrosis, cirrhosis). 6

Given the importance of early diagnosis and recent changes in the nomenclature of this disease, this study aims to estimate the level of awareness of the disease among the general public, people with diabetes, and primary care providers (PCPs).

METHODS

The survey for this study consisted of two sections: sociodemographic questions and items assessing awareness of MASLD and fatty liver disease (Supplemental Materials and Methods, http://links.lww.com/HC9/B970).

We recruited 5408 participants from the four largest cities in the United States: New York City, NY; Los Angeles, CA; Chicago, IL; and Houston, TX, respectively, 7 via river sampling, telephone recruitment, direct mail invitations, and opt-in options. Weighting resulted in samples of adults in the general population (n=4000, n=1000 per city), self-reporting a diabetes diagnosis (n=1000, n=250 per city), and PCPs (n=800, n=200 per city). Data were collected on 5–13 September 2024 through online panels provided by Consensus Strategies.

Descriptive statistics summarize sample demographic characteristics, including age, gender, education level, and race/ethnicity. Frequency distributions and percentages estimate awareness of MASLD and fatty liver disease. Chi-square tests evaluate differences between groups. The Emerson College (USA) institutional review board approved this study in August 2024 (protocol 25-003-F-E-8/21). Written, informed consent was obtained from each participant before enrollment.

RESULTS

Awareness of MASLD

In the general population sample (n=4000), 18.7% reported having heard of the term “MASLD” (Table 1). Among cities, residents of New York showed the highest awareness at 21.2%, followed by Chicago (20.2%), Los Angeles (17.0%), and Houston (16.2%). Among individuals with diabetes, 37.8% reported familiarity with MASLD (Supplemental Table S1, http://links.lww.com/HC9/B970). Among PCPs, 54.7% reported awareness (Supplemental Table S2, http://links.lww.com/HC9/B970). Overall, ethnicity was not associated with awareness: 18.6% and 18.7% of Black/African American and Hispanic/Latino respondents, respectively, were aware of MASLD (70.4% and 67.0% unaware, respectively), compared with 19.8% of White/Caucasian respondents. Among those with less than a high school education, 4.7% were aware, 79.1% were not, and 16.2% were unsure. By insurance status, 23.6% of those with private insurance were aware, compared with 17.7% on Medicare and 4.4% of those without health insurance. Those aged 60+ years reported 9.7% awareness, compared with 27.9% in the 30–39 age group (Table 1).

TABLE 1.

Awareness of MASLD and fatty liver disease among the general population

Heard of MASLD Heard of fatty liver disease
Yes No Unsure p Yes No Unsure p
Sample (n=4000) 18.7 68.6 12.7 78.1 17.2 4.7
City 0.312 0.424
 Chicago 20.2 68.7 11.1 80.1 15.4 4.5
 Houston 16.2 69.3 14.5 78.9 17.4 3.8
 Los Angeles 17.0 69.4 13.6 74.7 19.0 6.4
 New York City 21.2 67.1 11.7 78.6 17.1 4.3
Gender 0.000 0.000
 Man 20.1 68.3 11.5 76.6 19.2 4.2
 Woman 17.3 69.4 13.2 79.8 15.5 4.6
 Other/Prefer not to say 14.3 34.7 51.0 53.0 5.1 41.9
Ethnicity 0.426 0.000
 Hispanic or Latino of any race 18.7 67.0 14.4 77.0 18.1 5.0
 White or Caucasian 19.8 69.7 10.6 85.7 10.8 3.5
 Black or African American 18.6 70.4 11.0 69.1 26.1 4.8
 Asian 17.5 69.0 13.5 79.5 12.8 7.7
 Other or multiple races 13.4 67.6 19.0 73.0 24.3 2.8
Education 0.000 0.000
 Less than High School 4.7 79.1 16.2 62.5 34.0 3.5
 High School or General Educational Development (GED) Diploma 13.5 70.7 15.8 68.6 24.9 6.5
 Some College 9.1 77.6 13.4 78.4 15.5 6.2
 Associate or Vocational Degree 18.3 67.9 13.8 85.3 11.7 3.0
 Bachelor Degree 19.3 69.6 11.1 83.0 12.1 4.9
 Post-Graduate Degree (eg, Masters, Lawyer, Doctor) 45.7 46.9 7.4 88.5 9.4 2.1
Age 0.000 0.020
 18–29 20.7 67.4 12.0 70.0 23.9 6.0
 30–39 27.9 62.5 9.6 77.1 18.7 4.2
 40–49 21.9 62.7 15.4 81.0 14.5 4.5
 50–59 13.7 74.2 12.1 81.9 13.0 5.0
 60+ 9.7 75.7 14.7 82.2 13.9 3.9
Insurance status 0.000 0.000
 Private health insurance (eg, employer-based, Affordable Care Act (ACA) State Marketplaces) 23.6 65.4 11.1 86.6 10.7 2.7
 Medicare 17.7 71.2 11.0 81.7 14.5 3.8
 Medicaid 19.3 66.8 14.0 71.5 21.7 6.8
 Other health insurance 14.2 68.5 17.3 72.5 22.7 4.8
 None 4.4 81.7 13.9 62.1 29.4 8.5

Awareness of fatty liver disease

Awareness of the term “fatty liver disease” was significantly higher across all groups as compared to awareness of MASLD. In the general population, 78.1% had heard of fatty liver disease, with the highest awareness in Chicago (80.1%), followed by New York City (78.6%), Houston (78.9%), and Los Angeles (74.7%) (Table 1). Among people with diabetes, 85.4% reported awareness of fatty liver disease, with New York City showing the highest awareness (89.6%), followed by Chicago (84.7%), Houston (84.3%), and Los Angeles (83.0%) (Supplemental Table S1, http://links.lww.com/HC9/B970). Among PCPs, 86.6% were aware of fatty liver disease, with awareness levels ranging from 89.4% in Chicago to 88.3% in New York City, 86.3% in Houston, and 82.6% in Los Angeles (Supplemental Table S2, http://links.lww.com/HC9/B970). Among those with less than a high school education, 78.5% were aware, compared with 88.0% of those with an Associate or Vocational Degree. By insurance status, 86.6% of those with private health insurance were aware, compared with 81.7% of those on Medicare and 75.7% of those without health insurance. Those aged 60+ years reported 82.2% awareness, compared with 77.1% in the 30–39 age group (Table 1).

DISCUSSION

The study findings highlight the limited awareness of the 2023 nomenclature change from NAFLD to MASLD, with fewer than one-fifth of the general population, approximately one-third of adults with diabetes, and only about half of PCPs having heard of the new term MASLD. 1 In sharp contrast, awareness of the umbrella term “fatty liver disease,” which now encompasses MASLD through to alcohol-associated liver disease and has been used for over 4 decades, but previously excluded alcohol-associated liver disease, was high. Over three-quarters of respondents in the general population were aware of the disease, and even more among those with diabetes and PCPs. The relatively low awareness of the term MASLD among PCPs is concerning, given their role in identifying at-risk individuals, managing early-stage MASLD, and referring to specialists when necessary. 8

The contrast in terminology awareness reflects the challenges of transitioning to new nomenclature, especially when the older term has been embedded in public and professional discourse for decades, often minimized as “just fatty liver.” Effective dissemination of MASLD will require coordinated efforts among healthcare organizations, policymakers, and the media to ensure that patients, at-risk groups, and providers understand the implications of MASLD, its risk factors, and its management strategies. These efforts should emphasize that the nomenclature shift aims to provide greater clarity regarding the disease’s metabolic origins while reducing the stigma associated with both the terms “fatty” and “nonalcoholic,” thereby supporting a more nuanced and targeted approach to prevention and care. Strengthening MASLD-related training and resources for PCPs could enhance their capacity to address the disease effectively within primary care settings.

Study limitations may include recall bias from self-reported data, selection bias favoring health-conscious or diagnosed individuals, and variability in awareness levels in cities with differing healthcare and information access, warranting further research.

Supplementary Material

hc9-9-e0704-s001.pdf (301.1KB, pdf)

Acknowledgments

ACKNOWLEDGMENTS

Jeffrey V. Lazarus and Trenton M. White acknowledge institutional support to ISGlobal from the grant CEX2023-0001290-S funded by MCIN/AEI/10.13039/501100011033 and support from the Generalitat de Catalunya through the CERCA Program.

FUNDING INFORMATION

This study was funded by the CUNY Graduate School of Public Health and Health Policy, New York City, NY, USA.

CONFLICTS OF INTEREST

Jeffrey V. Lazarus reports speaker fees from Echosens, Gilead Sciences, Moderna, Novo Nordisk, Novovax, Pfizer, and ViiV; and grants from Echosens, Boehringer Ingelheim, Gilead Sciences, GSK, Madrigal Pharmaceuticals, Novo Nordisk, and Roche Diagnostics, outside the submitted work. Yehuda Handelsman received research grants, consultant fees, and speaker honoraria from 89Bio, Amgen, Applied Therapeutic, AstraZeneca, Bayer, Boehringer Ingelheim, Corcept, Endogenex, Esperion, Ionis, Lilly, Mankind, Merck, Merck-Pfizer, Novartis, Novo Nordisk, Regeneron, and Sanofi. Brett E. Fortune reports consultant fees from WL Gore, BD Medical, and Novo Nordisk. Melina Manolas has received payments from Doximity for advertising its services for physicians via her social media platforms. Silvana Pannain has received grants from Novo Nordisk for an investigator-initiated trial with payments made to her institution. She has also served as a speaker and advisor for Novo Nordisk and Lilly and owns stock or stock options in Lilly, Novo Nordisk, and Viking. Mary E. Rinella has served on the scientific executive committee for Akero, Novo Nordisk, Lilly, and Madrigal Pharmaceuticals; provided scientific consulting for 89Bio, Akero, Novo Nordisk, Lilly, Madrigal, NGM, Histoindex, Intercept, Sonic Incytes, and GSK; and received honoraria for CME symposia from GSK, Madrigal, and Novo Nordisk and support to attend meetings from Novo Nordisk and Boehringer Ingelheim. Meena B. Bansal has received grants from NIH, CDC/NIOSH, Pfizer, The Kinetix Group, Histoindex, and Siemens, consulting fees from The Kinetix Group, Madrigal, Pfizer, Fibronostics, Novo Nordisk, GSK, Boston Pharma, Merck, Boehringer Ingelheim, and CurveBio; and has served on advisory boards for Surrozen, Madrigal, GSK, Novo Nordisk, and Boehringer Ingelheim. Alina M. Allen has received grants from the National Institutes of Health, Novo Nordisk, Pfizer, Target Pharma, Oncoustics, Escopics, and Siemens; and consulting fees from Madrigal, Boehringer Ingelheim, Novo Nordisk, and GSK. Naim Alkhouri has received grants from 89bio, Akero, Arbutus Biopharma, AstraZeneca, BioAge, Boehringer Ingelheim, Bristol Myers Squibb, Corcept Therapeutics, CymaBay, DSM, Galectin Therapeutics, Genentech, Genfit, Gilead, Healio, Hepagene, Intercept, Inventiva, Ionis, Ipsen, Lilly, Madrigal, Merck, NGM Biopharma, Noom, NorthSea, Novo Nordisk, Perspectum, Pfizer, PharmaIN, Poxel, Viking, and Zydus; consulting fees from 89bio, Akero, Boehringer Ingelheim, Echosens, Fibronostics, Gilead, Intercept, Ipsen, Madrigal, NorthSea, Novo Nordisk, Perspectum, and Pfizer; and honoraria from AbbVie, AstraZeneca, Echosens, Gilead, Intercept, Ipsen, Madrigal, and Perspectum. Norah Terrault has received grants from the National Institutes of Health (NIH), GSK, Genentech-Roche, Helio Health, Durect Corp, Eiger Pharmaceuticals, and ImmunoCore for institutional support for clinical trials; royalties from Elsevier; and honoraria for lectures from CASL, EASL, PSSLD, APASL, GUILD, ILTS, and several academic institutions; as well as travel support for lectures from AASLD, INASL, and EASL. Michael Charlton consults for and receives grants from Gilead, Intercept, NGM Bio, Genfit, Conatus, and Novartis. Mazen Noureddin has received research support from Allergan, Akero, BMS, Gilead, Galmed, Galectin, Genfit, Conatus, Enanta, Madrigal, Novartis, Pfizer, Shire, Viking, and Zydus; he is a shareholder or has stocks in Anaetos, ChronWell, CytoDyn, Ciema, Rivus Pharma, and Viking. Ira M. Jacobson has received grant and research support from Gilead and Genfit and has served as a consultant or advisor for AbbVie, Bristol Myers Squibb, Intercept, Gilead, Merck, Trek, Janssen, Springbank, and Assembly Biosciences. Sonal Kumar consults for and has received speaking fees from Novo Nordisk, Ipsen, Intercept, Gilead, Madrigal, and GSK; she has received research support from Kinetix Group. The remaining authors have no conflicts to report.

Footnotes

Abbreviations: MASH, metabolic dysfunction–associated steatohepatitis; MASLD, metabolic dysfunction–associated steatotic liver disease; PCP, primary care provider.

Supplemental Digital Content is available for this article. Direct URL citations are provided in the HTML and PDF versions of this article on the journal's website, www.hepcommjournal.com.

Contributor Information

Jeffrey V. Lazarus, Email: jeffrey.lazarus@isglobal.org.

Trenton M. White, Email: trenton.white@isglobal.org.

Alina M. Allen, Email: allen.alina@mayo.edu.

Silvana Pannain, Email: spannain@bsd.uchicago.edu.

Naim Alkhouri, Email: nalkhouri@azliver.com.

Meena B. Bansal, Email: meena.bansal@mssm.edu.

Michael Charlton, Email: mcharlton@medicine.bsd.uchicago.edu.

Brett E. Fortune, Email: bfortune@montefiore.org.

Yehuda Handelsman, Email: yhandelsman@gmail.com.

Scott Isaacs, Email: scottisaacs@me.com.

Ira M. Jacobson, Email: ira.jacobson@nyulangone.org.

Sonal Kumar, Email: sok9028@med.cornell.edu.

Melina I. Manolas, Email: mmanolas@montefiore.org.

Mazen Noureddin, Email: NoureddinMD@houstonresearchinstitute.com.

Mary E. Rinella, Email: mrinella@bsd.uchicago.edu.

Norah Terrault, Email: terrault@usc.edu.

Ayman El-Mohandes, Email: ayman.Elmohandes@sph.cuny.edu.

REFERENCES

  • 1. Rinella ME, Lazarus JV, Ratziu V, Francque SM, Sanyal AJ, Kanwal F, et al. A multisociety Delphi consensus statement on new fatty liver disease nomenclature. Hepatology. 2023;78:1966–1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Shin S, Kim J, Lee JY, Kim J, Oh CM. Mitochondrial quality control: Its role in metabolic dysfunction-associated steatotic liver disease (MASLD). J Obes Metab Syndr. 2023;32:289–302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Riazi K, Azhari H, Charette JH, Underwood FE, King JA, Afshar EE, et al. The prevalence and incidence of NAFLD worldwide: A systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2022;7:851–861. [DOI] [PubMed] [Google Scholar]
  • 4. Lazarus JV, Mark HE, Allen AM, Arab JP, Carrieri P, Noureddin M, et al. A global research priority agenda to advance public health responses to fatty liver disease. J Hepatol. 2023;79:618–634. [DOI] [PubMed] [Google Scholar]
  • 5. Alqahtani SA, Paik JM, Biswas R, Arshad T, Henry L, Younossi ZM. Poor awareness of liver disease among adults with NAFLD in the United States. Hepatol Commun. 2021;5:1833–1847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Meagher T. Metabolic muddle. MASLD and MASH on the horizon. J Insur Med. 2023;50:147–149. [DOI] [PubMed] [Google Scholar]
  • 7. US Census Bureau . Most Populous Cities; 2024. Accessed November 15, 2024. https://www.census.gov/popclock/embed.php?component=populous
  • 8. Kanwal F, Shubrook JH, Adams LA, Pfotenhauer K, Wai-Sun Wong V, Wright E, et al. Clinical care pathway for the risk stratification and management of patients with nonalcoholic fatty liver disease. Gastroenterology. 2021;161:1657–1669. [DOI] [PMC free article] [PubMed] [Google Scholar]

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