{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,1]],"date-time":"2026-11-01T08:24:52Z","timestamp":1793521492008,"version":"4.5.0"},"reference-count":64,"publisher":"American Medical Association (AMA)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi241536-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Metabolic dysfunction\u2013associated steatotic liver disease (MASLD) is the most common cause of chronic liver disease and is projected to become the leading indication for liver transplant (LT) in the US. Understanding its clinical burden can help to identify opportunities for prevention and treatment.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi241536-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To project the burden of MASLD in US adults from 2020 to 2050.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi241536-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This decision analytical modeling study used an agent-based state transition model that simulates the natural history of MASLD progression among adults 18 years of age or older. Primary data sources for model inputs were the published literature.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi241536-7\">\n                    <jats:title>Exposure<\/jats:title>\n                    <jats:p>Natural history of MASLD.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi241536-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Cases of MASLD, metabolic dysfunction\u2013associated steatohepatitis (MASH), fibrosis, hepatocellular carcinoma (HCC), LT, and liver-related death.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi241536-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>The model simulated 2\u202f821\u202f624 individuals (mean age. 35.8 years; 50.9% female). The model predicted a steady increase in the prevalence of MASLD from 33.7% (86.3 million people) in 2020 to 41.4% (121.9 million people) by 2050. Cases of MASH would increase from 14.9 million (5.8% of US adults) in 2020 to 23.2 million (7.9% of US adults) by 2050. The number of cases of MASH and clinically significant fibrosis (ie, F\u2265F2, centrilobular and periportal fibrosis or more severe disease) were estimated to increase from 6.7 million to 11.7 million. By 2046 to 2050, MASLD would cause 22\u202f440 new cases of HCC and 6720 new cases of LT per year compared with 11\u202f483 new cases of HCC and 1717 new cases of LT in 2020 to 2025. Liver-related mortality was estimated to increase from 30\u202f500 deaths (1.0% of all-cause deaths in adults) in 2020 to 95\u202f300 deaths (2.4%) in 2050.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi241536-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this decision analytical modeling study, the model forecast a substantial increase in clinical burden of MASLD over the next 3 decades in the absence of effective treatments. These results suggest that health systems should plan for large increases in the number of HCC cases and in the need for LT.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2024.54707","type":"journal-article","created":{"date-parts":[[2025,1,17]],"date-time":"2025-01-17T11:31:14Z","timestamp":1737113474000},"page":"e2454707","source":"Crossref","is-referenced-by-count":273,"title":["Estimated Burden of Metabolic Dysfunction\u2013Associated Steatotic Liver Disease in US Adults, 2020 to 2050"],"prefix":"10.1001","volume":"8","author":[{"given":"Phuc","family":"Le","sequence":"first","affiliation":[{"name":"Center for Value-Based Care Research, Cleveland Clinic, Cleveland, Ohio"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Moosa","family":"Tatar","sequence":"additional","affiliation":[{"name":"Center for Value-Based Care Research, Cleveland Clinic, Cleveland, Ohio"},{"name":"University of Houston School of Pharmacy, Houston, 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