Evidence map›Paper›PMID 38124275›Full record

ArticleThe Journal of clinical endocrinology and metabolism2024

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

Wen-Yue Liu, Li-You Lian, Huai Zhang, Sui-Dan Chen, Xin-Zhe Jin, Ni Zhang, Chen-Hui Ye, Wen-Ying Chen, George Goh Boon Bee, Fu-Di Wang and 4 more

Abstract readValidation Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Wen-Yue LiuDepartment of Endocrinology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Li-You LianMAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Huai ZhangBiostatistics and Medical Quality Management Office, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Sui-Dan ChenDepartment of Pathology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Xin-Zhe JinDepartment of Laboratory, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Ni ZhangMAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Chen-Hui YeMAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Wen-Ying ChenMAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
George Goh Boon BeeDepartment of Gastroenterology and Hepatology, Singapore General Hospital, Singapore 169608, Singapore.
Fu-Di WangThe Fourth Affiliated Hospital, School of Public Health, Zhejiang University School of Medicine, Hangzhou 310000, China.
Luca MieleDepartment of Internal Medicine Medical and Surgical Sciences, Fondazione Policlinico A. Gemelli IRCCS, Università Cattolica di Roma, Rome 00168, Italy.
Elena CorradiniDepartment of Medical and Surgical Sciences, Università degli Studi di Modena e Reggio Emilia, Modena 41100, Italy.
Luca ValentiDepartment of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan 20121, Italy.ORCID 0000-0001-8909-0345
Ming-Hua ZhengMAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.ORCID 0000-0003-4984-2631

Funding

National Natural Science Foundation of China 82070588
6 · The paper itself

Abstract

contextThere is limited data on the clinical significance of metabolic hyperferritinemia (MHF) based on the most recent consensus.

objectiveWe aimed to validate the clinical outcomes of MHF in the general population and patients with biopsy-proven metabolic dysfunction-associated fatty liver disease (MAFLD).

methodsThe 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.

resultsIn 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).

conclusionBoth in the general population and in at-risk individuals with MAFLD, MHF was related with poorer clinical outcomes.

Indexed as

FerritinsHyperferritinemiaAdultAgedCohort StudiesConsensusConsensus Statements as TopicFemaleHumansMaleMiddle AgedNutrition SurveysPrognosisFerritinsiron overloadmetabolic dysfunction–associated fatty liver diseasemetabolic hyperferritinemiametabolic syndrome

Identifiers

PMID38124275
PMCPMC11099479

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Registered trials

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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.