Maintenance Notice

Due to necessary scheduled maintenance, the JMIR Publications website will be unavailable from Wednesday, July 01, 2020 at 8:00 PM to 10:00 PM EST. We apologize in advance for any inconvenience this may cause you.

Who will be affected?

Accepted for/Published in: JMIR Research Protocols

Date Submitted: Nov 22, 2022
Open Peer Review Period: Nov 13, 2022 - Jan 8, 2023
Date Accepted: Feb 26, 2023
(closed for review but you can still tweet)

The final, peer-reviewed published version of this preprint can be found here:

The Fatty Liver, Cirrhosis, and Liver Cancer Study (TENDENCY): Protocol for a Multicenter Case-Control Study

Hussain Y, Bannaga A, Fisher N, Krishnamoorthy A, Kimani P, Malik A, Truslove M, Joshi S, Hitchins M, Abbasi A, Corbett C, Brookes M, Than NN, Arasaradnam R

The Fatty Liver, Cirrhosis, and Liver Cancer Study (TENDENCY): Protocol for a Multicenter Case-Control Study

JMIR Res Protoc 2023;12:e44264

DOI: 10.2196/44264

PMID: 37256650

PMCID: 10267778

THE FATTY LIVER, CIRRHOSIS & LIVER CANCER STUDY - TENDENCY (PROTOCOL)

  • Yaqza Hussain; 
  • Ayman Bannaga; 
  • Neil Fisher; 
  • Ashwin Krishnamoorthy; 
  • Peter Kimani; 
  • Ahmad Malik; 
  • Maria Truslove; 
  • Shivam Joshi; 
  • Megan Hitchins; 
  • Abdullah Abbasi; 
  • Christopher Corbett; 
  • Matthew Brookes; 
  • Nwe Ni Than; 
  • Ramesh Arasaradnam

ABSTRACT

Background:

Hepatocellular cancer (HCC) is associated with high mortality and early diagnosis leads to better survival. Patients with cirrhosis especially due to Non-Alcoholic Fatty Liver disease (NAFLD) and viral hepatitis are at higher risk of developing HCC and form the main screening group. The current screening methods for HCC (6 monthly screening with serum Alpha Fetoprotein and Ultrasound liver) have low sensitivity and hence there is a need for better screening markers for HCC.

Objective:

Our study, TENDENCY, aims to validate the novel screening markers (Methylated SEPTIN9, Urinary Volatile Organic Compounds and Urinary peptides) for HCC diagnosis and study these non-invasive biomarkers in liver disease.

Methods:

This is a multicentre nested case-control study which involves comparing the plasma levels of methylated Septin9 between confirmed HCC cases and Cirrhotic patients (control group). It also includes the comparison of urine samples for the detection of HCC specific volatile organic compounds and peptides. Based on the findings of a pilot study carried out at UHCW, we have estimated our sample size to be 308 (88 HCC and 220 cirrhotic patients). Urine and plasma samples will be collected from all the participants and will be frozen at -80°C till the end of recruitment. Gas Chromatography-mass spectrometry (GC-MS) will be used for urinary volatile organic compounds detection and Capillary electrophoresis-mass spectrometry (CE-MS) will be utilised for urinary peptide identification. Real-time polymerase chain reaction will be used for the qualitative detection of plasma methylated Septin9(mSEPT9). The study will be monitored by the Research and Development department at UHCW.

Results:

TENDENCY study is currently in the recruitment phase. We are aiming to complete the recruitment by March 2023. The sample analysis will take place during April and May 2023.

Conclusions:

There is lack of effective screening tests for hepatocellular cancer despite higher mortality rates. The application of more sensitive plasma and urinary biomarkers for hepatocellular cancer screening in clinical practice will allow us to detect the disease at earlier stages and hence overall improve the HCC outcomes. Clinical Trial: TENDENCY has been approved by Northeast-York Ethics Committee. The IRAS number for the study is 260179 and the NIHR portfolio ID is 42438.


 Citation

Please cite as:

Hussain Y, Bannaga A, Fisher N, Krishnamoorthy A, Kimani P, Malik A, Truslove M, Joshi S, Hitchins M, Abbasi A, Corbett C, Brookes M, Than NN, Arasaradnam R

The Fatty Liver, Cirrhosis, and Liver Cancer Study (TENDENCY): Protocol for a Multicenter Case-Control Study

JMIR Res Protoc 2023;12:e44264

DOI: 10.2196/44264

PMID: 37256650

PMCID: 10267778

Download PDF


Request queued. Please wait while the file is being generated. It may take some time.

© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.

Advertisement