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临床试验/CTRI/2025/06/089591
CTRI/2025/06/089591尚未招募不适用

The Relationship Between YKL-40, IL-6, and NFI in MAFLD-Related Liver Fibrosis: A Clinical Perspective

Jamia Hamdard1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2025年10月7日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
Jamia Hamdard
入组人数
150
试验地点
1
主要终点
To assess the correlation between serum levels of YKL-40 and IL-6 with liver fibrosis stages using the Novel Fibrosis Index (NFI) in MAFLD patients.

研究概览

简要总结

Metabolic dysfunction-associated fatty liver disease (MAFLD) is the most common chronic liver condition globally, closely linked to type 2 diabetes mellitus (T2DM), obesity, and metabolic syndrome. Non-invasive tools are increasingly being used to evaluate liver fibrosis in MAFLD, as liver biopsy is invasive and not practical for routine diagnosis. The Novel Fibrosis Index (NFI) is an emerging non-invasive score that combines clinical and metabolic parameters to assess fibrosis stages. Additionally, serum biomarkers like YKL-40 and inflammatory cytokines like IL-6 are known to be elevated in liver inflammation and fibrosis. This single-center, cross-sectional, hospital-based study aims to evaluate the serum levels of YKL-40 and IL-6 in MAFLD patients and correlate them with the stages of liver fibrosis as determined by NFI. The study also includes a healthy control group for comparative biomarker analysis. Blood samples will be analyzed using ELISA kits, and fibrosis staging will be done using non-invasive methods like FibroScan and NFI calculation. The study is being conducted at HAHC Hospital, Jamia Hamdard, New Delhi, and aims to include 150 participants (75 MAFLD patients and 75 healthy controls) over a period of 6 months. The outcomes may help establish YKL-40 and IL-6 as potential non-invasive biomarkers for liver fibrosis assessment in MAFLD.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Participants aged 18 to 65 years old Participants with a diagnosis of Metabolic dysfunction-associated fatty liver disease (MAFLD) confirmed by ultrasound and Fibroscan.
  • Presence of at least one metabolic risk factor, such as type 2 diabetes mellitus (T2DM), obesity, or metabolic dysregulation.
  • Willingness and ability to provide written informed consent.
  • Healthy human volunteers for controls.

排除标准

  • History of significant alcohol consumption exceeding established thresholds for men and women.
  • Presence of coexisting chronic liver diseases or history of hepatotoxic drug use.
  • Advanced systemic illnesses or malignancies.
  • Patients having any other inflammatory diseases like arthritis, IBS Patients undergone any liver surgery or transplantation.
  • Patients having history of head injury, neurocognitive disorder, or any other neuronal disease.
  • Individuals with TB , any form of malignancies present or history of HIV-AIDS or any disease that could impair the biomarkers levels.
  • Individuals currently taking medications that significantly impact glucose metabolism or biomarker levels (e.g.corticosteroids, certain antipsychotics).
  • Individual with acute infection or inflammatory conditions at the time of recruitment.
  • Pregnant individuals or those planning to become pregnant during study period will be excluded due to potential confounding effects on biomarkers.

结局指标

主要结局

To assess the correlation between serum levels of YKL-40 and IL-6 with liver fibrosis stages using the Novel Fibrosis Index (NFI) in MAFLD patients.

时间窗: Single Time Point

次要结局

  • To validate the Novel Fibrosis Index (NFI) against Fibroscan & APRI(To assess the relationship between IL-6 & YKL-40 levels in MAFLD patients To compare YKL-40 levels with age, gender, BMI, & diet in MAFLD patients)

研究者

发起方
Jamia Hamdard
申办方类型
Research institution and hospital

研究点 (1)

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