AzTrials
AzTrials

Non-Alcoholic Fatty Liver DiseaseNCT05194553

Identification and Characterization of NAFLD in Turkey

An observational study of Non-Alcoholic Fatty Liver Disease and Liver Diseases, run by Maastricht University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Non-alcoholic fatty liver disease (NAFLD) is with 25% the most prevalent liver disorder in Western society and is associated with overweight, obesity, metabolic syndrome (MetS), type 2 diabetes mellitus (T2DM) and cardiovascular diseases (CVD). Read more about this study

Who is it for?
Ages 18 to 80 years
How many people
450 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Feb 2022to 15 Jun 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: 500 male and female participants aged between 18-80, who can sign the informed consent and are eligible to participate.

Who may be able to join

  • Able to understand and sign the informed consent
  • Able to speak Turkish
  • Between 18-80 years
  • BMI >25 kg/m²
  • Having one of the following conditions: 1)Insulin resistance 2)Impaired glucose tolerence 3)type 2 diabetes mellitus, 4)hypertension 5)dyslipidemia 6)cardiovascular diseases (atherosclerosis, angina pectoris, ischaemic heart condition, cerebrovascular condition)

Who cannot join

  • Excessive alcohol use (more than 20 g/day for women and 30g/day for men= >2 glasses alcohol/day for women and >3 glasses for men)
  • Other liver diseases: Hepatitis B virus, Hepatitis C virus, autoimmune hepatitis, primary biliary cirrhosis, hemochromatosis, Wilson's disease, Alpha 1 antitrypsin deficiency
  • Secondary causes for steatosis: disorders of lipid metabolism, HCV Genotype 3, total parental nutrition, severe surgical weight loss, medications (amiodarone, tamoxifen, methotrexate, corticosteroids and HAART), lean steatosis, Celiac disease, environmental toxicity
  • Pregnancy and breastfeeding.
  • A history of bariatric surgery.
  • Diagnosis of liver cirrhosis and/or hepatocellular carcinoma.
  • Current diagnosis of extrahepatic malignancy(s) or prior diagnosis within last 5 years.
  • Individuals about to undergo a surgery or otherwise medical procedure that will interfere with data collection and analyses planned within the current cohort, will initially be excluded from participation, but are offered the opportunity to participate at a later moment in time (e.g., after 3 months are myocardial infarction patients are eligible for participation).

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Pax Clinic

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Identification and Characterization of Non-alcoholic Fatty Liver Disease Among Risk Groups in Turkey

Non-alcoholic fatty liver disease (NAFLD) is with 25% the most prevalent liver disorder in Western society and is associated with overweight, obesity, metabolic syndrome (MetS), type 2 diabetes mellitus (T2DM) and cardiovascular diseases (CVD). NAFLD is defined by a hepatic fat accumulation of more than 5% in the absence of classical causes of steatogenesis (e.g. alcohol and steatogenic drugs). It represents a broad spectrum of clinical entities from steatosis to advanced liver disease with hepatic failure. Most of the patients have simple steatosis, however in about 15-30% non-alcoholic steatohepatitis (NASH) develops, which leads to an overall increase in morbidity and mortality due to the progression to fibrosis, cirrhosis and hepatocellular carcinoma (HCC). Patients with NAFLD have no or few, mainly specific symptoms; and generally there is a silent progression of simple steatosis to NASH and in the end liver-related morbidity and mortality. Despite the clinical importance and the potential impact on healthcare resources, the majority of NAFLD patients are currently not detected due to the lack of non-invasive methods to diagnose NAFLD. To date, the prevalance of NAFLD in Turkey among subjects at risk, and its relation to common comorbidities such as obesity, T2DM and CVD is not clear. Therefore, identification of NAFLD patients in this cohort will give information on the prevalence in the group of uncomplicated overweight and obesity and those with concomitant cardiometabolic diseases. By early detecting these patients at risk to develop progressive liver diseases and extrahepatic manifestations, it will be possible to intervene and improve health. Within this context, this study aims to detect prevalence of NAFLD among risk groups. Also, the risk factors related to NAFLD etiology and progression, such as overweight, obesity, T2DM, CVD, diet and physical activity will be studied to have a better understanding of their presumed causal relationship with NAFLD.

Read the detailed description

Non-alcoholic fatty liver disease (NAFLD), characterized with more than 5% intrahepatic fat accumulation in the absence of classical causes of steatogenesis, is considered as a growing epidemic with a global prevalence estimated around 25%. NAFLD usually manifests as simple steatosis, however in about 15-30% cases it can progress to its inflammatory type of NASH, which may in turn lead to fibrosis, cirrhosis, and hepatocellular carcinoma (HCC). Given that patients typically have no or few symptoms, it is fundamental to detect and treat NAFLD at the earliest stage to decrease liver-related morbidity and mortality.

NAFLD is known to be the hepatic manifestation of the metabolic syndrome (MetS), a cluster of metabolic disorders including abdominal obesity, type 2 diabetes mellitus (T2DM), and cardiovascular diseases (CVD). It has been reported that NAFLD risk increases with obesity, diabetes mellitus, and dyslipidemia. In line with this, the highest prevalence of NAFLD is reported from South America and the Middle East, where MetS is also widespread, making it a major public health issue in these regions. Similarly, the clinical significance of NAFLD has progressively increased in Turkey lately. With an obesity rate of 32% according to latest WHO reports, and T2DM rate of 15%, Turkey can be considered a risky region in terms of NAFLD burden. Despite the increasing burden of NAFLD in Turkey, few studies have been undertaken to identify its prevalence showing conflicting results due to excessive heterogeneity in design. 8 studies that were undertaken in the past 15 years reported a prevalence between 10,6% and 60%. One study that included subjects with MetS reported as high as 94.3%. It is critically important to develop new evidence regarding NAFLD prevalence among this patient group in Turkey and the association between MetS comorbidities and NAFLD severity so as to establish NAFLD risk groups and develop effective population screening and public health policies targeting this patient group.

The optimal screening method to detect hepatic steatosis in the general population remains to be established. The reference standard is liver biopsy; however, it is problematic to conduct studies that involve liver biopsy due to its invasiveness, high cost and patient discomfort. Therefore, ultrasonographic imaging (USG) is usually favored as the first-line modality in most clinical practices. However, USG has limited sensitivity and does not reliably detect steatosis when <20% or in individuals with BMI>40 kg/m2. Controlled attenuation parameter (CAP) measured with transient elastography (TE), on the other hands, has recently emerged as a reliable imaging tool for the screening and diagnosis of NAFLD on a population scale. It is suggested to have high sensitivity in identifying mild steatosis and yields a good correlation with steatosis grades. Therefore, CAP can enable early and noninvasive detection of NAFLD at the subclinical level. It is important to detect NAFLD at the earliest possible stage because once it is established hepatic insulin resistance increases, which, in turn, may trigger, in 30-40% of cases, NAFLD progression to its inflammatory phenotype Non-alcoholic Steatohepatitis (NASH) and eventually, hepatocarcinoma, cirrhosis, and liver failure.

As of today, treatment of NAFLD is only possible through lifestyle modifications such as following a healthy balanced diet and doing regular physical activity, given that no pharmacological treatment has been approved yet for NAFLD. Weight loss of 7-10% BW seems to have proven efficacy especially in overweight subjects. Different dietetic approaches have been proposed to reach the weight loss goal; however, no consensus has been reached yet on the type of medical nutrition therapy to be offered to NAFLD patients. Having said that, in the recent EASL-EASD-EASO Clinical Practice Guidelines, Mediterranean diet (MED DIET) was recommended as the diet of choice for the treatment of NAFLD together with weight loss initiatives. Indeed, a growing body of evidence suggest that MED DIET exerts health benefits even without accompanying weight reduction, which is the main obstacle in lifestyle interventions.

Higher adherence to the MED DIET has shown to have beneficial effects on the progression of hepatic steatosis in observational studies and clinical trials (n<90 followed up for<6 months) in patients with existing hepatic steatosis. These findings are confirmed in The Swiss CoLaus and UK Fenland cohorts which reported lower risk of hepatic steatosis with higher adherence to MED DIET.

Not only the dietary pattern, but also certain micronutrient deficiencies might be related to NAFLD. New evidence suggests that also Vitamin D deficiency, which is known to associate with obesity and sedentary lifestyle, may cause NAFLD. Hypovitaminosis D is proposed to have a causative relationship with the severity and incidence of NAFLD. The association between Hypovitaminosis D and NAFLD has been examined previously. A lower serum 25(OH)D level was shown to be an independent risk factor for NAFLD. Various studies has shown a correlation between Vitamin D level and disease severity. A cross-sectional study of 6567 men concluded that participants in the lowest tertile of serum 25(OH)D levels had a significantly increased risk for NAFLD compared to those in the highest tertile. Another study found similar results. CAP was used as a tool to define hepatic steatosis in a study that showed a significant association between serum 25(OH)D levels and NAFLD.9 However, some other studies reported quite contradictory results. Collectively, the data from the published studies indicate that NAFLD subjects are more likely to be vitamin D deficient compared to controls. However, definite directionality of the results cannot be ascertained due to the limitations which include the variability in the method of diagnosis of NAFLD, clinical heterogeneity among the study groups and variability in defining vitamin D deficiency. Demonstration of a causal role of hypovitaminosis D in NAFLD progress could have important therapeutic implications. Vitamin D supplementation is easy to accomplish on a population level, hence, it can be an efficient tool to prevent NAFLD. Cochrane performed a systematic review of randomized clinical trials of Vitamin D supplementation in chronic liver diseases, 11 of which included NAFLD patients. Given the high heterogeneity of studies included, they failed to assess the beneficial and harmful effects of vitamin D supplementation in adults with chronic liver diseases. Well-designed future studies are needed to investigate this potential relation.

Keywords
NAFLD, fatty liver, NASH, non-alcoholic fatty liver disease
Medical subject headings
Non-alcoholic Fatty Liver Disease, Liver Diseases, Fatty Liver, Metabolic Syndrome, Overweight, Obesity

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. prevalence of NAFLD in risk groups in Turkey

    Measured: 1 year

Secondary outcomes (10)
  1. NAFLD's relation to risk factor: overweight

    To see if there is an effect of having a BMI between 25 and 30 kg/m² in the development of NAFLD. The physiological parameter used will be BMI.

    Measured: 1 year

  2. NAFLD's relation to risk factor: obesity

    To see if there is an effect of having a BMI more than 30 kg/m² in the development of NAFLD. The physiological parameter used will be BMI.

    Measured: 1 year

  3. NAFLD's relation to risk factor: IR

    To see if there is an effect of having a HOMA-IR more than 2.5 in the development of NAFLD. The physiological parameter used will be HOMA-IR.

    Measured: 1 year

  4. NAFLD's relation to risk factor: T2DM

    Type 2 diabetes mellitus will be assessed based on previous diagnosis and HbA1c levels.

    Measured: 1 year

  5. NAFLD's relation to risk factor: HT

    To see if there is an effect of Hypertension in the development of NAFLD. The physiological parameter used will be systolic and diastolic blood pressure.

    Measured: 1 year

  6. NAFLD's relation to risk factor: MetS

    To see if there is an effect of metabolic syndrome (defined by the criteria of the International Diabetes Federation) on the development of NAFLD.

    Measured: 1 year

  7. NAFLD's relation to risk factor: CVD

    Cardiovascular diseases will be assessed based on medical history found in the patient files.

    Measured: 1 year

  8. NAFLD's relation to risk factor: PAL

    Physical Activity Level will be determined based in IPAQ mini results

    Measured: 1 year

  9. NAFLD's relation to VDD

    To see if there is an effect of Vitamin D deficiency in the development of NAFLD. The physiological parameter used will be 25(OH)Vit D.

    Measured: 1 year

  10. NAFLD's relation to Med Diet adherence

    To see if there is an effect of Mediterranean Diet adherence in the development of NAFLD. The parameter used will be Med Diet adherence screening scale (MEDAS)

    Measured: 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Jan 2022
  2. Study start15 Feb 2022
  3. Primary completion15 May 2023
  4. Study completion15 Jun 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
450 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05194553
Sponsor's protocol ID
UMPAX-21-1
Status last verified
Jan 2024
First submitted
4 Jan 2022
Last updated
17 Jan 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Dogay Us G, Innocenti F, Koc OM, Yumuk VD, Gungor ZB, Koek GH. Prevalence of MASLD and fibrosis in Turkey: Results from a multicenter study of at-risk populations. PLoS One. 2026 Feb 12;21(2):e0341214. doi: 10.1371/journal.pone.0341214. eCollection 2026.

    PubMed 41678490

Questions about this trial

What is this clinical trial studying?

An observational study of Non-Alcoholic Fatty Liver Disease and Liver Diseases, run by Maastricht University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

prevalence of NAFLD in risk groups in Turkey (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05194553, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jan 2024.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in