Status:

RECRUITING

Association of HsCAR with MAFLD and Liver Fibrosis: a Cross-sectional Study

Lead Sponsor:

Chongqing Medical University

Conditions:

Metabolic Dysfunction-associated Fatty Liver Disease

Hepatic Steatosis

Eligibility:

All Genders

18-90 years

Brief Summary

The goal of this observational study is to investigate the associations between a novel inflammatory marker, high sensitivity C-reactiveprotein to albumin ratio (hsCAR), and steatosis and fibrosis of ...

Detailed Description

Background Inflammation is related to the occurrence and development of fatty liver. Our research aimed to investigate the link between an inflammatory indicator, high-sensitivity C-reactive protein t...

Eligibility Criteria

Inclusion

  • Total participants from NHANES 2017-2020
  • Participants diagnosed with MAFLD. Metabolic dysfunction-associated fatty liver disease (MAFLD) is the term used to describe hepatic steatosis in the presence of metabolic abnormalities, excess weight, obesity, or type 2 diabetic mellitus.
  • Diagnosis of diabetes mellitus: (1) taking glucose-lowering drugs; (2) HbA1c ≥ 6.5% (48 mmol/mol); (3) fasting plasma glucose ≥ 7.0 mmol/L (126 mg/dL); (4) 2-hour plasma glucose (2hPG) ≥ 11.1 mmol/L (200 mg/dL).
  • Overweight or obesity: defined as BMI≥25 kg/m2 in Caucasians or BMI≥23 kg/m2 in Asians
  • If presence of at least two metabolic risk abnormalities:
  • Waist circumference≥102/88 cm in Caucasian men and women (or≥90/80 cm in Asian men and women)
  • Blood pressure≥130/85 mmHg or specific drug treatment
  • Plasma triglycerides≥150 mg/dl (≥1.70 mmol/L) or specific drug treatment
  • Plasma HDL-cholesterol \<40 mg/dl (\<1.0 mmol/L) for men and \<50 mg/dl (\<1.3 mmol/L) for women or specific drug treatment
  • Prediabetes (i.e., fasting glucose levels 100 to 125 mg/dl \[5.6 to 6.9 mmol/L\], or 2-hour post-load glucose levels 140 to 199 mg/dl \[7.8 to 11.0 mmol\] or HbA1c 5.7% to 6.4% \[39 to 47 mmol/mol\])
  • Homeostasis model assessment of insulin resistance score≥2.5
  • Plasma high-sensitivity C-reactive protein level \>2 mg/L

Exclusion

  • Liver ultrasound data not available
  • participants without complete clinical data
  • participants under 18 years old
  • participants with cancer.

Key Trial Info

Start Date :

July 18 2023

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

December 28 2026

Estimated Enrollment :

7000 Patients enrolled

Trial Details

Trial ID

NCT05974904

Start Date

July 18 2023

End Date

December 28 2026

Last Update

February 12 2025

Active Locations (1)

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1

The Second Affiliated Hospital of Chongqing Medical University

Chongqing, Chongqing Municipality, China, 400000