Metabolically Healthy Obesity Increases the Risks of MASLD and Hyperuricemia
2 other identifiers
observational
17,040
1 country
1
Brief Summary
Although metabolically healthy obesity (MHO) is often considered a relatively benign obesity, its association with the risk of metabolic dysfunction-associated steatotic liver disease (MASLD) and hyperuricemia remains unclear. This study examined the associations between MHO and other metabolic-obesity phenotypes with MASLD and hyperuricemia, and explored the mediating roles of metabolic indicators.This study included 11,712 and 13,846 participants from a health examination cohort at the First Affiliated Hospital of Ningbo University for MASLD and hyperuricemia analyses, respectively. Participants were classified into four metabolic-obesity phenotypes, with MHO defined as obesity without metabolic syndrome components. The outcomes were MASLD and hyperuricemia. Cox regression and mediation analyses were conducted to assess associations and mediating effects.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2025
CompletedFirst Submitted
Initial submission to the registry
May 25, 2025
CompletedFirst Posted
Study publicly available on registry
June 3, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedJune 3, 2025
May 1, 2025
9 months
May 25, 2025
May 25, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Incidence of MASLD and Hyperuricemia
through study completion
7 years
Study Arms (2)
MASLD cohort
participants with non-MASLD at baseline
Hyperuricemia
participants with non-Hyperuricemia at baseline
Eligibility Criteria
This cohort study included participants who underwent comprehensive health examinations at the Physical Examination Center of the First Affiliated Hospital of Ningbo University between 2017 and 2024. A total of 18,261 individuals aged 18 years or older who completed abdominal ultrasound examinations were initially considered. After excluding underweight individuals (BMI \< 18.5 kg/m²; N = 1,138) and those with missing data on height, weight, or metabolic syndrome (MetS) components (N = 83), 17,040 participants remained eligible for further analysis.For the MASLD incidence analysis, individuals with a baseline diagnosis of MASLD or other liver diseases (N = 5,328) were excluded, resulting in 11,712 participants. For the hyperuricemia incidence analysis, those with baseline hyperuricemia (N = 3,194) were further excluded, yielding 13,846 eligible participants. During a median follow-up period of up to 7 years, 3,756 incident cases of MASLD and 3,294 incident cases of hyperuricemia were
You may qualify if:
- Underwent comprehensive health examinations at the Physical Examination Center of the First Affiliated Hospital of Ningbo University between 2017 and 2024;
- Aged 18 years or older at baseline;
- Completed an abdominal ultrasound examination during the health check-up.
You may not qualify if:
- Underweight status at baseline, defined as BMI \< 18.5 kg/m² ;
- Missing data on height, weight, or components of the metabolic syndrome ;
- Baseline diagnosis of MASLD or any other liver diseases
- Baseline diagnosis of hyperuricemia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
the First Affiliated Hospital of Ningbo University Ningbo, Zhejiang, China, 315000, Ningbo, Zhejiang Province 315000 Recruiting
Ningbo, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 25, 2025
First Posted
June 3, 2025
Study Start
April 1, 2025
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
June 3, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share