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MASLD identifies patients with significant hepatic fibrosis and steatosis in fatty liver population
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You Denga,b,1, Wenya Chena,b,1, Wen Xiea,b,
Corresponding author
xiewen6218@163.com

Corresponding author.
a Center of Liver Diseases, Capital Medical University Affiliated to Beijing Ditan Hospital, No. 8, Jingshun East Street, Chaoyang District, Beijing 100015, China
b National Center for Infectious Diseases, Beijing 100015, China
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Received 07 October 2023. Accepted 28 January 2024
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To the editor,

We have read with interest the article by Rinella ME et al. [1], in which metabolic dysfunction-associated steatotic liver disease (MASLD) has been proposed as a novel diagnostic term that differs from non-alcoholic fatty liver disease (NAFLD). The original name change from NAFLD to metabolic dysfunction-associated fatty liver disease (MAFLD) has successfully reduced the stigma associated with the condition and emphasized its close connection with metabolic disorders [2–4]. However, the definition of MAFLD is complex, and some subitems, such as HOMA-IR and high-sensitivity C-reactive protein (hs-CRP), are not routinely measured in clinical practice across regions, which leads to underdiagnosis and delayed treatment [5,6]. The proposed name change to MASLD, which optimizes the MAFLD definition, is simplified and acceptable. MASLD is defined by inclusion rather than exclusion criteria and is diagnosed in patients with hepatic steatosis and metabolic risk factors. However, its practicality and effectiveness have not been tested and validated in real-world settings. We aimed to identify MASLD patients and compare the characteristics of MASLD and non-MASLD steatosis patients.

Our study involved 9406 patients diagnosed with fatty liver by ultrasound for analysis. Of them, 9240 (98.2%) patients were diagnosed with MAFLD and MASLD overlapping, and 95 (1.0%) patients were classified as MASLD but undiagnosed MAFLD due to the lack of hs-CRP and insulin. And 71 (0.8%) patients were identified as non-MASLD but undiagnosed MAFLD patients (Fig. 1A). In addition, MASLD patients were older, predominantly male, and exhibited a higher prevalence of metabolic disorders and elevated liver enzymes compared with non-MASLD patients. Additionally, the MASLD group displayed significant liver steatosis and fibrosis (Table S1), including elevated HSI [37.31 (34.77, 40.22) vs. 35.00 (32.35, 37.82), p<0.001], FLI [1.80 (0.81, 4.17) vs. 0.14 (0.09, 0.24), p<0.001], FIB-4 [0.97 (0.69, 1.34) vs. 0.51 (0.37, 0.78), p<0.001] and NFS [−2.06 (−2.96, −1.11) vs. −3.85 (−4.58, −3.26), p<0.001] (Fig. 1B). These findings highlight the importance of accurately identifying and treating MASLD patients to prevent further liver damage and improve outcomes.

Fig. 1.

The characteristics of MASLD patients. (A) Venn diagram in the population with fatty liver. (B) Comparison of liver steatosis scores and fibrosis scores between MASLD and Non-MASLD steatosis patients. *** p < 0.001.

(0.3MB).

In conclusion, the MASLD definition represents an improvement in identifying patients with substantial hepatic fibrosis and steatosis within the fatty liver population. The name change is necessary to reflect the underlying pathophysiology and enhance diagnostic accuracy accurately.

Authors' contributions

Wen Xie: Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Project administration, Supervision, Validation, Writing review & editing. You Deng, Wenya Chen: Formal analysis, Investigation, Methodology, Software, Validation, Visualization, Writing original draft, Writing review & editing.

Availability of data and material

Survey data will be shared upon reasonable request to the corresponding author.

Declaration of interests

None.

References
[1]
ME Rinella, JV Lazarus, V Ratziu, SM Francque, AJ Sanyal, F Kanwal, et al.
A multi-society Delphi consensus statement on new fatty liver disease nomenclature.
[2]
M Eslam, PN Newsome, SK Sarin, QM Anstee, G Targher, M Romero-Gomez, et al.
A new definition for metabolic dysfunction-associated fatty liver disease: an international expert consensus statement.
J Hepatol, 73 (2020), pp. 202-209
[3]
KI Zheng, DQ Sun, Y Jin, PW Zhu, MH Zheng.
Clinical utility of the MAFLD definition.
J Hepatol, 74 (2021), pp. 989-991
[4]
Y Fouad, I Waked, S Bollipo, A Gomaa, Y Ajlouni, D Attia.
What's in a name? Renaming ‘NAFLD’ to ‘MAFLD’.
Liver Int, 40 (2020), pp. 1254-1261
[5]
G Shiha, K Alswat, M Al Khatry, AI Sharara, N Örmeci, I Waked, et al.
Nomenclature and definition of metabolic-associated fatty liver disease: a consensus from the Middle East and North Africa.
Lancet Gastroenterol Hepatol, 6 (2021), pp. 57-64
[6]
J Xie, L Lu, Y Chen, L Xu, C Xu.
A simpler definition of MAFLD better predicts long-term all-cause mortality in American adults.
J Hepatol, 77 (2022), pp. 877-879

These authors contributed equally to the letter.

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