Clinical, Biochemical and Body Composition Analysis in Assessment of Steatosis in Non Alcoholic Fatty Liver Disease
Role of Clinical, Biochemical and Body Composition Analysis in Assessment of Steatosis in Patients With Non Alcoholic Fatty Liver Disease
Non-alcoholic fatty liver disease (NAFLD) includes a spectrum of liver disorders characterized by accumulation of hepatic fat in absence of significant alcohol consumption (<20 gm/day) and other causes of liver diseases. It is the most common cause of asymptomatic elevation of liver enzymes worldwide (Marchesini et al., 2003).
Unfortunately, to date, existing non- or minimally invasive biomarkers are inadequate. While a number of non- or minimally invasive tests are able to rule out fibrosis or cirrhosis, no single test to identify steatosis, to early diagnose NASH, or to predict the disease progression is available. Moreover, specialized, combined tests are required to assess treatment response in clinical trials on emerging compounds (Piazzolla and Mangia, 2020).
Among minimally invasive tools, plasma biomarkers and composite scores defined as "wet biomarkers" are commonly used. For example, fasting insulin level and its use in measurement of insulin resistance, Lipid Accumulation Product (LAP) score (Bedogni et al., 2010), the NAFLD Liver Fat Score (NLFS) (Kontronen et al., 2009), Hepatic Steatosis Index (HSI) (Lee et al., 2010), controlled attenuation parameter (CAP) measurement by fibroscan (Piazzolla and Mangia, 2020). Recent studies have shown that CAP significantly correlates with the percentage of steatosis and steatosis grade and that median CAP is higher among patients with significant steatosis (Sasso et al., 2012 & Karlas et al., 2017).
The prevalence of NAFLD is 80-90% in obese, 30-50% in patients with diabetes and up to 90% in patients with hyperlipidemia (Abenavoli et al., 2014)
Central obesity or visceral fat (VF) (determined by waist circumference (WC)) is defined as the presence of excess fat in the abdomen, and this type of obesity is often associated with the development and progression of NAFLD or more advanced forms of liver disease (Abenavoli et al., 2016). Thus, measurement of body composition rather than BMI may be helpful in the prediction of NAFLD (Milić et al., 2014 and Abenavoli et al., 2016)
There is a growing need to assess the steatosis in NAFLD patients using minimally invasive tools.
研究概览
地位
条件
研究类型
注册 (预期的)
联系人和位置
学习联系方式
- 姓名:Wafaa G Mohamed, Master
- 电话号码:01111390732
- 邮箱:wafaa_gamal_post@med.sohag.edu.eg
研究联系人备份
- 姓名:Ghada M Kamal, Professor
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
Patients: A total of 80 adult subjects will be included.
Inclusion criteria:
Adult subjects with bright liver by abdominal ultrasound will be recruited for the study. The diagnosis will be based on CAP score result measured by Fibroscan.
描述
Inclusion criteria:
- Adult subjects with bright liver by abdominal ultrasound will be recruited.
- The diagnosis will be based on CAP score result measured by Fibroscan.
Exclusion criteria:
- Alcohol consumption.
- Patients with other liver diseases as acute and chronic viral hepatitis, autoimmune hepatitis, primary biliary cirrhosis, drug-induced hepatitis.
- Decompensated liver disease.
- Other end organ failure.
- Pregnancy.
- Patients on statins or fenofibrate.
学习计划
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设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
studying anthropometric measurements of NAFLD cases.
大体时间:2 years
|
-study anthropometric measurements.
|
2 years
|
|
measurement of steatosis by fibroscan examination
大体时间:2 years
|
Fibroscan examination measuring control attenuation parameter "CAP score"
|
2 years
|
|
body muscle percentage
大体时间:2 years
|
measurement of body muscle percentage
|
2 years
|
|
body fat percentage.
大体时间:2 years
|
measurement of body fat percentage
|
2 years
|
|
measurement of body water percentage.
大体时间:2 years
|
measurement of body water percentage.
|
2 years
|
|
measuring serum cholesterol
大体时间:2 years.
|
measuring serum cholesterol by mg/ dl.
|
2 years.
|
|
measuring serum triglycerides.
大体时间:2 years.
|
measuring serum triglycerides by mg/ dl.
|
2 years.
|
|
measuring serum insulin level.
大体时间:2 years.
|
measuring of serum insulin level using ELISA kits
|
2 years.
|
合作者和调查者
出版物和有用的链接
一般刊物
- Abenavoli L, Di Renzo L, De Lorenzo A. Body Composition and Non-alcoholic Fatty Liver Disease. J Lifestyle Med. 2016 Mar;6(1):47-8. doi: 10.15280/jlm.2016.6.1.47. Epub 2016 Mar 31. No abstract available.
- Abenavoli L, Milic N, Peta V, Alfieri F, De Lorenzo A, Bellentani S. Alimentary regimen in non-alcoholic fatty liver disease: Mediterranean diet. World J Gastroenterol. 2014 Dec 7;20(45):16831-40. doi: 10.3748/wjg.v20.i45.16831.
- Amato MC, Giordano C, Galia M, Criscimanna A, Vitabile S, Midiri M, Galluzzo A; AlkaMeSy Study Group. Visceral Adiposity Index: a reliable indicator of visceral fat function associated with cardiometabolic risk. Diabetes Care. 2010 Apr;33(4):920-2. doi: 10.2337/dc09-1825. Epub 2010 Jan 12.
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初级完成 (预期的)
研究完成 (预期的)
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其他研究编号
- Soh-Med-21-06-13
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