Evidence map›Paper›PMID 38977950›Full record

ArticleBMC gastroenterology2024

The prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD)-related advanced fibrosis and cirrhosis in the United States population utilizing AGILE 3 + and AGILE 4 scores: analysis of the NHANES 2017-2018 cycle.

Naim Alkhouri, Ashraf Almomani, Phuc Le, Julia Y Payne, Imad Asaad, Prido Polanco, Phillip Leff, Prabhat Kumar, Mazen Noureddin

Abstract read
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Article in BMC gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Naim Alkhouri *Hepatology and Liver Transplantation, Arizona Liver Health, Chandler, 20201 W Fairview St, AZ, 85224, USA. nalkhouri@azliver.com.
Ashraf Almomani *Cleveland Clinic Florida, Florida, USA.
Phuc LeCleveland Clinic Florida, Florida, USA.
Julia Y PayneCleveland Clinic Florida, Florida, USA.
Imad AsaadCleveland Clinic Florida, Florida, USA.
Prido PolancoHepatology and Liver Transplantation, Arizona Liver Health, Chandler, 20201 W Fairview St, AZ, 85224, USA.
Phillip LeffHepatology and Liver Transplantation, Arizona Liver Health, Chandler, 20201 W Fairview St, AZ, 85224, USA.
Prabhat KumarCleveland Clinic Foundation, Ohio, USA.
Mazen NoureddinCedar Sinai Medical Center, Los Angeles, CA, USA.

Funding

AHRQ HHS R01 HS026937
6 · The paper itself

Abstract

backgroundStudies attempted to estimate MASLD-related advanced fibrosis (AF) and cirrhosis (MC) prevalence utilized tests with low positive predictive value (PPV) which overestimates prevalence. AGILE3 + and 4 scores were developed to increase the PPV of both; respectively. In this study, we used these scores to assess the prevalence of AF and MC.

methodsParticipants aged ≥ 18 years with VCTE exam in the NHANES 2017-2018 cycle were included. We excluded pregnant women, patients with excessive alcohol intake, hepatitis B/C, and ALT or AST > 500 IU/L. MASLD was defined with CAP score > 248 dB/m. MASLD subjects with AGILE 3 + score of ≥ 0.68 and AGILE 4 score of ≥ 0.57 were considered to have advanced fibrosis and cirrhosis; respectively. AGILE 3 + of 0.45-0.67 and AGILE 4 of 0.25-0.57 were grey zone, whereas AGILE 3 + < 0.45 and AGILE 4 < 0.25 were considered a rule-out.

results1244 subjects were included in the final analysis. The Median age was 53 (51.4-54.6) years, 55.6% were male, median BMI was 33.8 kg/m2 and 41.1% had T2DM. Based on AGILE 3+, 80.3% of the MASLD population were at low risk for AF and 11.5% were in grey zone. The prevalence of AF due to MASLD was 8.1% corresponding to 4.5 million Americans. Based on AGILE 4 score, 96.5% of the MASLD population were at low risk for cirrhosis and 2.4% were in the grey zone. The prevalence of MASLD-cirrhosis was 1.1% corresponding to 610,000 Americans.

conclusionOur results suggest that approximately 4.5 million people in the U.S. have AF and 0.6 million have cirrhosis due to MASLD.

Indexed as

Liver CirrhosisNutrition SurveysAdultFatty LiverFemaleHumansMaleMiddle AgedPredictive Value of TestsPrevalenceSeverity of Illness IndexUnited StatesAdvanced fibrosisAGILECirrhosisElastographyMASLDNHANES

Identifiers

PMID38977950
PMCPMC11229262

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.