A Population-Based and Clinical Cohort Validation of the Novel Consensus Definition of Metabolic Hyperferritinemia

• Published in: The journal of clinical endocrinology and metabolism Vol. 109; no. 6; pp. 1540 - 1549
• Main Authors: Liu, Wen-Yue, Lian, Li-You, Zhang, Huai, Chen, Sui-Dan, Jin, Xin-Zhe, Zhang, Ni, Ye, Chen-Hui, Chen, Wen-Ying, Bee, George Goh Boon, Wang, Fu-Di, Miele, Luca, Corradini, Elena, Valenti, Luca, Zheng, Ming-Hua
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 01.06.2024
• Subjects: Albumin; Biopsy; Cardiovascular diseases; China; Clinical; Clinical outcomes; Comorbidity; Comparative analysis; Creatinine; Fatty liver; Ferritin; Fibrosis; Liver; Liver diseases; Metabolism; Mortality; Sarcopenia; Steatosis; Type 2 diabetes; China; metabolic syndrome; metabolic dysfunction–associated fatty liver disease; iron overload; metabolic hyperferritinemia; Iron overload; Metabolic hyperferritinemia; Metabolic syndrome; Metabolic dysfunction-associated fatty liver disease
• ISSN: 0021-972X; 1945-7197; 1945-7197
• DOI: 10.1210/clinem/dgad749

Abstract Context There is limited data on the clinical significance of metabolic hyperferritinemia (MHF) based on the most recent consensus. Objective We aimed to validate the clinical outcomes of MHF in the general population and patients with biopsy-proven metabolic dysfunction–associated fatty liver disease (MAFLD). Methods The NHANES database and PERSONS cohort were included. MHF was defined as elevated serum ferritin with metabolic dysfunction (MD) and stratified into different grades according to ferritin (grade 1: 200 [females]/300 [males]—550 ng/mL; grade 2: 550-1000 ng/mL; grade 3: >1000 ng/mL). The clinical outcomes, including all-cause death, comorbidities, and liver histology, were compared between non-MHF and MHF in adjusted models. Results In NHANES, compared with non-MHF with MD, MHF was related to higher risks of advanced fibrosis (P = .036), elevated albumin–creatinine ratio (UACR, P = .001), and sarcopenia (P = .013). Although the association between all grades of MHF and mortality was insignificant (P = .122), grades 2/3 was associated with increased mortality (P = .029). When comparing with non-MHF without MD, the harmful effects of MHF were more significant in mortality (P < .001), elevated UACR (P < .001), cardiovascular disease (P = .028), and sarcopenia (P < .001). In the PERSONS cohort, MHF was associated with more advanced grades of steatosis (P < .001), lobular inflammation (P < .001), advanced fibrosis (P = .017), and more severe hepatocellular iron deposition (P < .001). Conclusion Both in the general population and in at-risk individuals with MAFLD, MHF was related with poorer clinical outcomes.