Prevalence of steatotic liver disease associated with metabolic dysfunction (MASLD) in patients with type 2 diabetes mellitus. A multicenter Argentine cross-sectional study

Authors

  • Javier Giunta Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina
  • Guillermo Alzueta Private practice, Balcarce, Buenos Aires Province, Argentina
  • Cecilia Araya La Trinidad Sanatorium, Ramos Mejía, Province of Buenos Aires, Argentina
  • María Aubone Dr. Guillermo Rawson Decentralized Public Hospital, San Juan, Argentina
  • María Basbus Comprehensive Center for Diabetes, Endocrinology and Nutrition (CIDEN), Jujuy, Argentina
  • Santiago Bruzzone Institute of Metabolic Research (IDIM), City of Buenos Aires, Argentina
  • Ramón Carulla Albarracín Medical Offices, Bariloche, Río Negro, Argentina
  • Alejandra Cicchitti University Hospital Mendoza, Mendoza, Argentina
  • Patricia Cuart Diagnostic Center, Corrientes, Argentina
  • Guillermo Dieuzeide Comprehensive Care Center for Diabetes, Endocrinology and Metabolism, Chacabuco, Chacabuco, Province of Buenos Aires, Argentina
  • Olga Escobar Dr. Mario Víctor Stivala Hospital, La Cocha, Tucumán, Argentina
  • Karina Fuentes Private Hospital of Córdoba, Córdoba, Argentina
  • Susana Fuentes El Cruce Néstor Kirchner Hospital, Florencio Varela, Buenos Aires Province, Argentina
  • Teresita García Comprehensive Medical Center (CMIC), Tucumán, Argentina
  • Joaquín González Institute of Clinical Medicine and Diabetes, Mendoza, Argentina
  • Luciana Grilli Lucio Molas/Favaloro Hospital Complex, Santa Rosa, La Pampa, Argentina
  • Mercedes Gutiérrez Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina
  • Hugo Ibáñez Social Welfare Organization for Public Employees (OSEP), Mendoza, Argentina
  • Arturo López San Carlos Sanatorium, Bariloche, Río Negro, Argentina
  • Patricia Mascaró Medical Office Diagnosis, Comodoro Rivadavia, Chubut, Argentina
  • Sebastián Marciano Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina
  • Carolina Miglianelli Lucio Molas/Favaloro Hospital Complex, Santa Rosa, La Pampa, Argentina
  • Fernando Morana Bariloche Zonal Hospital, Dr. Ramón Carrillo, San Carlos, Bariloche, Río Negro, Argentina
  • José Morando Dr. Guillermo Rawson Decentralized Public Hospital, San Juan, Argentina
  • Marisol Olivares Lucio Molas/Favaloro Hospital Complex, Santa Rosa, La Pampa, Argentina
  • Cristina Oviedo Private practice, City of Buenos Aires, Argentina
  • Lucas Romero Social Welfare Organization for Public Employees (OSEP), Mendoza, Argentina
  • Martín Rodríguez Institute of Clinical Medicine and Diabetes, Mendoza, Argentina
  • Sergio Rueda Dr. Guillermo Rawson Decentralized Public Hospital, San Juan, Argentina
  • Natalia Segura Dr. A. Maggio Municipal Diabetes Center, Los Polvorines, Malvinas Argentinas, Province of Buenos Aires, Argentina
  • Amira Sleiman Santa Clara de Asís Private Hospital, Salta, Argentina
  • Olguita Vera Private practice, Río Gallegos, Santa Cruz, Argentina
  • Dong Woo Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina
  • Adriana Álvarez Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina

DOI:

https://doi.org/10.47196/diab.v60i1.1316

Keywords:

steatotic liver disease associated with metabolic dysfunction, MASLD, type 2 diabetes mellitus, hepatic steatosis, prevalence

Abstract

Introduction: steatotic liver disease associated with metabolic dysfunction (MASLD) is highly prevalent in people with type 2 diabetes mellitus (T2DM), but there are still no reported data in the Argentine population. The redefined MASLD was used because it emphasizes the associated metabolic dysfunction and allows for a broader diagnostic approach.

Objectives: primary: to estimate the prevalence of MASLD in people with type 2 diabetes in Argentina. Secondary: to explore its association with anthropometric factors, cardiovascular risk, and liver fibrosis; to evaluate fibrosis in centers with access to elastography.

Materials and methods: an observational, cross-sectional, multicenter study was conducted between April and December 2023 in 21 specialized DM care centers. Adults with a confirmed diagnosis of T2DM were included. The diagnosis of MASLD was based on the presence of hepatic steatosis by ultrasound along with metabolic criteria. FIB-4 and Hearts scores were calculated in the Americas. Fibroscan elastography was performed in centers where fibroscan was available.

Results: a total of 579 individuals were included (median age: 60 years; 67% obese). The prevalence of MASLD was 81.2% (95% CI: 77.8–84.3), with regional variations ranging from 77.9% to 90.3%. A strong association was found between MASLD and higher body mass index (OR for obesity: 8.9; 95% CI: 4.1–19.6; p<0.001) and waist circumference. No significant associations were observed between MASLD and estimated cardiovascular risk or between FIB-4 and Hearts scores. Fibroscan elastography was performed in 63 patients, with a median of 5.7 kPa (4.7–9.5).

Conclusions: eight out of 10 individuals with T2DM presented MASLD, with a significant association with excess weight. These findings reinforce the need to implement systematic strategies for screening for liver damage and comprehensively address obesity in this population.

Author Biographies

Javier Giunta, Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina

Italian Hospital of Buenos Aires

Guillermo Alzueta, Private practice, Balcarce, Buenos Aires Province, Argentina

Private practice

Cecilia Araya, La Trinidad Sanatorium, Ramos Mejía, Province of Buenos Aires, Argentina

La Trinidad Sanatorium

María Aubone, Dr. Guillermo Rawson Decentralized Public Hospital, San Juan, Argentina

Dr. Guillermo Rawson Decentralized Public Hospital

María Basbus, Comprehensive Center for Diabetes, Endocrinology and Nutrition (CIDEN), Jujuy, Argentina

Comprehensive Center for Diabetes, Endocrinology and Nutrition (CIDEN)

Santiago Bruzzone, Institute of Metabolic Research (IDIM), City of Buenos Aires, Argentina

Institute of Metabolic Research (IDIM)

Ramón Carulla, Albarracín Medical Offices, Bariloche, Río Negro, Argentina

Albarracín Medical Offices

Alejandra Cicchitti, University Hospital Mendoza, Mendoza, Argentina

University Hospital Mendoza

Patricia Cuart, Diagnostic Center, Corrientes, Argentina

Diagnostic Center

Guillermo Dieuzeide, Comprehensive Care Center for Diabetes, Endocrinology and Metabolism, Chacabuco, Chacabuco, Province of Buenos Aires, Argentina

Comprehensive Care Center for Diabetes, Endocrinology and Metabolism

Olga Escobar, Dr. Mario Víctor Stivala Hospital, La Cocha, Tucumán, Argentina

Dr. Mario Víctor Stivala Hospital

Karina Fuentes, Private Hospital of Córdoba, Córdoba, Argentina

Private Hospital of Córdoba

Susana Fuentes, El Cruce Néstor Kirchner Hospital, Florencio Varela, Buenos Aires Province, Argentina

El Cruce Néstor Kirchner Hospital

Teresita García, Comprehensive Medical Center (CMIC), Tucumán, Argentina

Comprehensive Medical Center (CMIC)

Joaquín González, Institute of Clinical Medicine and Diabetes, Mendoza, Argentina

Institute of Clinical Medicine and Diabetes

Luciana Grilli, Lucio Molas/Favaloro Hospital Complex, Santa Rosa, La Pampa, Argentina

Lucio Molas/Favaloro Hospital Complex

Mercedes Gutiérrez, Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina

Italian Hospital of Buenos Aires

Hugo Ibáñez, Social Welfare Organization for Public Employees (OSEP), Mendoza, Argentina

Social Welfare Organization for Public Employees (OSEP)

Arturo López, San Carlos Sanatorium, Bariloche, Río Negro, Argentina

San Carlos Sanatorium

Patricia Mascaró, Medical Office Diagnosis, Comodoro Rivadavia, Chubut, Argentina

Medical Office Diagnosis

Sebastián Marciano, Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina

Italian Hospital of Buenos Aires

Carolina Miglianelli, Lucio Molas/Favaloro Hospital Complex, Santa Rosa, La Pampa, Argentina

Lucio Molas/Favaloro Hospital Complex

Fernando Morana, Bariloche Zonal Hospital, Dr. Ramón Carrillo, San Carlos, Bariloche, Río Negro, Argentina

Bariloche Zonal Hospital

José Morando, Dr. Guillermo Rawson Decentralized Public Hospital, San Juan, Argentina

Dr. Guillermo Rawson Decentralized Public Hospital

Marisol Olivares, Lucio Molas/Favaloro Hospital Complex, Santa Rosa, La Pampa, Argentina

Lucio Molas/Favaloro Hospital Complex

Cristina Oviedo, Private practice, City of Buenos Aires, Argentina

Private practice

Lucas Romero, Social Welfare Organization for Public Employees (OSEP), Mendoza, Argentina

Social Welfare Organization for Public Employees (OSEP)

Martín Rodríguez, Institute of Clinical Medicine and Diabetes, Mendoza, Argentina

Institute of Clinical Medicine and Diabetes

Sergio Rueda, Dr. Guillermo Rawson Decentralized Public Hospital, San Juan, Argentina

Dr. Guillermo Rawson Decentralized Public Hospital

Natalia Segura, Dr. A. Maggio Municipal Diabetes Center, Los Polvorines, Malvinas Argentinas, Province of Buenos Aires, Argentina

Dr. A. Maggio Municipal Diabetes Center

Amira Sleiman, Santa Clara de Asís Private Hospital, Salta, Argentina

Santa Clara de Asís Private Hospital

Olguita Vera, Private practice, Río Gallegos, Santa Cruz, Argentina

Private practice

Dong Woo, Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina

Italian Hospital of Buenos Aires

Adriana Álvarez, Italian Hospital of Buenos Aires, City of Buenos Aires, Argentina

Italian Hospital of Buenos Aires

References

I. European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD), European Association for the Study of Obesity (EASO). EASL-EASD-EASO. Clinical practice guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). J Hepatol. 2024;81:492-542.

II. 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. Ann Hepatol. 2024;29: 101133.

III. En Li Cho E, Ang CZ, Quek J, Fu CE, Lim LKE, Heng ZEQ, et al. Global prevalence of non-alcoholic fatty liver disease in type 2 diabetes mellitus: an updated systematic review and meta-analysis. Gut. 2023;72: 2138-2148.

IV. Eslam M, Newsome PN, Sarin SK, Anstee QM, Targher G, Romero-Gómez M, et al. A new definition for metabolic dysfunction-associated fatty liver disease: An international expert consensus statement. J Hepatol. 2020;73:202-209.

V. European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD), European Association for the Study of Obesity (EASO). EASL-EASD-EASO Clinical Practice Guidelines for the management of non-alcoholic fatty liver disease. J Hepatol. 2016;64:1388-1402.

VI. Omaña-Guzmán I, Rosas-Diaz M, Martínez-López YE, Pérez-Navarro LM, Diaz-Badillo A, Alanis A, et al. Strategic interventions in clinical randomized trials for metabolic dysfunction-associated steatotic liver disease (MASLD) and obesity in the pediatric population: a systematic review with meta-analysis and bibliometric analysis. BMC Med. 2024;22: 548.

VII. Ali SMJ, Lai M. Metabolic dysfunction-associated steatotic liver disease. Ann Intern Med. 2025;178: ITC1-ITC16.

VIII. Machado MV. MASLD treatment-a shift in the paradigm is imminent. Front Med (Lausanne). 2023;10: 1316284.

IX. Li Y, Yang P, Ye J. et al. Updated mechanisms of MASLD pathogenesis. Lipids Health Dis. 2024;23(1):117. doi: 10.1186/s12944-024-02108-x

X. Stefan N, Yki-Järvinen H, Neuschwander-Tetri BA. Metabolic dysfunction-associated steatotic liver disease: heterogeneous pathomechanisms and effectiveness of metabolism-based treatment. Lancet Diabetes Endocrinol. 2025;13:134-148.

XI. Dulai PS, Singh S, Patel J, Soni M, Prokop LJ, Younossi Z, et al. Increased risk of mortality by fibrosis stage in nonalcoholic fatty liver disease: Systematic review and meta-analysis. Hepatology. 2017;65:1557-1565.

XII. Chalasani N, Younossi Z, Lavine JE, Charlton M, Cusi K, Rinella M, et al. The diagnosis and management of nonalcoholic fatty liver disease. Practice guidance from the American Association for the Study of Liver Diseases. Hepatology. 2018;67(1):328-357. doi: 10.1002/hep.29367.

XIII. Angulo P, Kleiner DE, Dam-Larsen S, Adams LA, Bjornsson ES, Charatcharoenwitthaya P, et al. Liver fibrosis, but no other histologic features, is associated with long-term outcomes of patients with nonalcoholic fatty liver disease. Gastroenterology. 2015;149: 389-97.e10.

XIV. Younossi ZM, Golabi P, Paik JM, Henry A, Van Dongen C, Henry L. The global epidemiology of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH): a systematic review. Hepatology. 2023;77:1335-1347.

XV. Younossi ZM, Golabi P, de Avila L, Paik JM, Srishord M, Fukui N, et al. The global epidemiology of NAFLD and NASH in patients with type 2 diabetes. A systematic review and meta-analysis. J Hepatol. 2019;71:793-801.

XVI. Lonardo A, Nascimbeni F, Mantovani A, Targher G. Hypertension, diabetes, atherosclerosis and NASH: cause or consequence? Journal of Hepatology. 2018;68(2):335-352. doi: 10.1016/j.jhep.2017.09.021.

XVII. Stefan N, Cusi K. A global view of the interplay between non-alcoholic fatty liver disease and diabetes. Lancet Diabetes Endocrinol. 2022;10:284-296.

XVIII. Lomonaco R, Godinez Leiva E, Bril F, Shrestha S, Mansour L, Budd J, et al. Advanced liver fibrosis is common in patients with type 2 diabetes followed in the outpatient setting. The need for systematic screening. Diabetes Care. 2021;44: 399-406.

XIX. Kasper P, Martin A, Lang S, Kütting F, Goeser T, Demir M, et al. NAFLD and cardiovascular diseases: a clinical review. Clinical Research in Cardiology. 2021; 110(7):921-937. doi: 10.1007/s00392-020-01709-7.

XX. Byrne CD, Targher G. Non‐alcoholic fatty liver disease‐related risk of cardiovascular disease and other cardiac complications. Diabetes, Obesity and Metabolism. 2022;(supp 2):28-43. doi: 10.1111/dom.14484.

XXI. Byrne CD, Targher G. NAFLD: a multisystem disease. Journal of Hepatology. 2015:S47-S64. doi: 10.1016/j.jhep.2014.12.012.

XXII. Wild SH, Morling JR, McAllister DA, Kerssens J, Fischbacher C, Parkes J, et al. Type 2 diabetes and risk of hospital admission or death for chronic liver diseases. Journal of Hepatology. 2016;1358-1364. doi: 10.1016/j.jhep.2016.01.014.

XXIII. Amer J, Alnees M, Salameh M, Daraghmeh A, Kabha A, AlHabil Y, et al. The diagnostic utility of FIB-4 as a non-invasive tool for liver fibrosis scoring among NAFLD patients: a retrospective cross-sectional study. Eur Rev Med Pharmacol Sci. 2024;28: 3104-3111.

XXIV. Strajhar P, Berzigotti A, Nilius H, Nagler M, Dufour J-F. Estimating the prevalence of adults at risk for advanced hepatic fibrosis using FIB-4 in a Swiss tertiary care hospital. PLoS One. 2025;20:e0317629.

XXV. WHO CVD Risk Chart Working Group. World Health Organization cardiovascular disease risk charts: revised models to estimate risk in 21 global regions. Lancet Glob Health. 2019;7:e1332-e1345.

XXVI. American Diabetes Association Professional Practice Committee. 2. Classification and diagnosis of diabetes. Standards of Medical Care in Diabetes 2022. Diabetes Care. 2022;45:S17-S38.

XXVII. Kanwal F, Shubrook JH, Younossi Z, Natarajan Y, Bugianesi E, Rinella ME, et al. Preparing for the NASH epidemic. A call to action. Diabetes Care. 2021;44:2162-2172.

XXVIII. Sterling RK, Lissen E, Clumeck N, Sola R, Correa MC, Montaner J, et al. Development of a simple noninvasive index to predict significant fibrosis in patients with HIV/HCV coinfection. Hepatology. 2006;43(6):1317-1325. doi: 10.1002/hep.21178.

XXIX. Younossi Z, Anstee QM, Marietti M, Hardy T, Henry L, Eslam M, et al. Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention. Nat Rev Gastroenterol Hepatol. 2018;15:11-20.

XXX. Hernaez R, Lazo M, Bonekamp S, Kamel I, Brancati FL, Guallar E, et al. Diagnostic accuracy and reliability of ultrasonography for the detection of fatty liver: a meta-analysis. Hepatology 2011;54:1082-1090.

XXXI. Lee C-M, Kim M, Kang B-K, Jun DW, Yoon EL. Discordance diagnosis between B-mode ultrasonography and MRI proton density fat fraction for fatty liver. Sci Rep. 2023;13: 15557.

XXXII. Moon S, Chung GE, Joo SK, Park JH, Chang MS, Yoon JW, et al. A PNPLA3 Polymorphism confers lower susceptibility to incident diabetes mellitus in subjects with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol. 2022;20:682-691.

XXXIII. Zhang X, Chen K, Yin S, Qian M, Liu C. Association of leisure sedentary behavior and physical activity with the risk of nonalcoholic fatty liver disease: a two-sample Mendelian randomization study. Front Nutr. 2023;10:1158810.

XXXIV. Lazarus JV, Mark HE, Anstee QM, Arab JP, Batterham RL, Castera L, et al. Advancing the global public health agenda for NAFLD: a consensus statement. Nat Rev Gastroenterol Hepatol. 2022;19:60-78.

XXXV. Gancheva S, Roden M, Castera L. Diabetes as a risk factor for MASH progression. Diabetes Res Clin Pract. 2024;217:111846.

XXXVI. Bril F, Cusi K. Management of nonalcoholic fatty liver disease in patients with type 2 diabetes. A call to action. Diabetes Care. 2017;40: 419-430.

XXXVII. Méndez-Sánchez N, Qi X. Metabolic dysfunction-associated steatotic liver disease: prevalence, research insights and the future directions. Springer Nature;2024.

XXXVIII. Park CC, Nguyen P, Hernández C, Bettencourt R, Ramírez K, Fortney L, et al. Magnetic resonance elastography vs transient elastography in detection of fibrosis and noninvasive measurement of steatosis in patients with biopsy-proven nonalcoholic fatty liver disease. Gastroenterology. 2017;152:598-607.e2.

Published

2026-03-20

Issue

Section

Original article