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Updated: Nov 18, 2025

Human Circadian Phenotyping and Diurnal Performance Testing in the Real World
Published on: April 7, 2020
Circadian Misalignment Rather Than Sleep Duration is Associated with MAFLD: A Population-Based Propensity
Zhiyuan Weng1, Weijie Ou2, Jiaofeng Huang2
1Cardiology Department, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 350001, People's Republic of China.
Circadian misalignment (CM) is linked to metabolic (dysfunction) associated fatty liver disease (MAFLD). This study found CM independently associated with MAFLD, independent of sleep duration.
Area of Science:
- Metabolic health
- Sleep science
- Hepatology
Background:
- Circadian misalignment (CM) is a known contributor to metabolic disorders.
- Metabolic (dysfunction) associated fatty liver disease (MAFLD) is a recently defined condition requiring metabolic dysfunction.
- The relationship between CM and MAFLD is not well understood.
Purpose of the Study:
- To investigate the association between circadian misalignment (CM) and metabolic (dysfunction) associated fatty liver disease (MAFLD).
Main Methods:
- Utilized the NHANES 2017-2018 database.
- Diagnosed liver steatosis and fibrosis using Fibroscan®.
- Defined CM by mistimed, late, or irregular sleep patterns.
- Employed propensity score matching (PSM) for age and gender.
Main Results:
- A higher prevalence of MAFLD was observed in the CM group (45.41% vs 28.48%).
- Circadian misalignment (CM) more than doubled the risk of MAFLD.
- Short sleep duration (<6 hours) was not an independent risk factor for MAFLD or liver fibrosis when CM was considered.
Conclusions:
- Circadian misalignment (CM) is an independent risk factor for metabolic (dysfunction) associated fatty liver disease (MAFLD).
- Short sleep duration alone is not an independent predictor of MAFLD or liver fibrosis when controlling for CM.
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