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The Role of the Vitamin D Receptor Gene Polymorphisms in Hepatocarcinogenesis

Primary Purpose

Liver Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
The VDR genotype
Sponsored by
Sherief Abd-Elsalam
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Liver Cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Hcv cirrhotic patient with and without Hcc

Exclusion Criteria:

  • Malignancy other than HCC
  • Co-infection with Hepatitis B virus (HBV) and Human immunodeficiency virus (HIV)
  • Cirrhosis is due to causes other than chronic hepatitis C

Sites / Locations

  • Tanta university - faculty of medicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

Hepatocellular carcinoma (HCC)

Liver cirrhosis

Control group

Arm Description

The VDR genotype in 20 HCV cirrhotic patient with HCC

The VDR genotype in 20 HCV cirrhotic patient without HCC

The The VDR genotype in 10 healthy individuals as control

Outcomes

Primary Outcome Measures

number of HCC patients with abnormal (APAL) VDR polymorphism

Secondary Outcome Measures

Full Information

First Posted
May 31, 2015
Last Updated
December 30, 2017
Sponsor
Sherief Abd-Elsalam
Collaborators
Tanta University
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1. Study Identification

Unique Protocol Identification Number
NCT02461979
Brief Title
The Role of the Vitamin D Receptor Gene Polymorphisms in Hepatocarcinogenesis
Official Title
The Role of the Vitamin D Receptor Gene Polymorphisms in Hepatocarcinogenesis in Cirrhotic Patients Infected With Chronic Hepatitis C Virus
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sherief Abd-Elsalam
Collaborators
Tanta University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Previous data have suggested that vitamin D levels may influence cancer development. In particular, several single nucleotide polymorphisms have been described in the Vitamin D receptor( VDR gene), and some polymorphisms are associated with tumor occurrence. For instance, VDR polymorphisms have been related to cancers of the breast, prostate, skin, colon-rectum, bladder and kidney, although with conflicting observations . VDR polymorphisms have also been investigated in the context of some chronic liver diseases, such as chronic hepatitis B, primary biliary cirrhosis and autoimmune hepatitis . In a recent published study, VDR polymorphism may be used as a molecular marker to predict the risk and to evaluate the disease severity of HCC in patients with chronic hepatitis B. A significant association of VDR (ApaI) polymorphism with the development of HCC in chronic HCV infection may help to identify those who are at high risk of developing HCC.
Detailed Description
Hepatitis C virus (HCV) infection is one of the major public health problems worldwide . Chronic HCV infection is characterized by a high rate of progression to fibrosis, chronic hepatitis, leading to cirrhosis and ultimately to hepatocellular carcinoma (HCC). Early detection is critically important because the most effective treatment for HCC is surgical resection or ablation therapy when the tumour is small. On the other hand, genetic factors can also contribute, particularly gene polymorphisms of inflammatory cytokines and growth factor ligands and receptors . Vitamin D is involved in the metabolism of skeleton as a systemic hormone but also has important roles in the regulation of host immune responses, fibrogenesis and development of cancer through vitamin D receptor (VDR). Previous data have suggested that vitamin D levels may influence cancer development. In particular, several single nucleotide polymorphisms have been described in the VDR gene, and some polymorphisms are associated with tumor occurrence. For instance, VDR polymorphisms have been related to cancers of the breast, prostate, skin, colon-rectum, bladder and kidney, although with conflicting observations. VDR polymorphisms have also been investigated in the context of some chronic liver diseases, such as chronic hepatitis B, primary biliary cirrhosis and autoimmune hepatitis . In a recent published study, VDR polymorphism may be used as a molecular marker to predict the risk and to evaluate the disease severity of HCC in patients with chronic hepatitis B. A significant association of VDR ApaI polymorphism with the development of HCC in chronic HCV infection may help to identify those who are at high risk of developing HCC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cancer

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hepatocellular carcinoma (HCC)
Arm Type
Other
Arm Description
The VDR genotype in 20 HCV cirrhotic patient with HCC
Arm Title
Liver cirrhosis
Arm Type
Other
Arm Description
The VDR genotype in 20 HCV cirrhotic patient without HCC
Arm Title
Control group
Arm Type
Other
Arm Description
The The VDR genotype in 10 healthy individuals as control
Intervention Type
Other
Intervention Name(s)
The VDR genotype
Intervention Description
The VDR genotype will determined by polymerase chain reaction (PCR) amplication and restriction length fragment polymorphisms.
Primary Outcome Measure Information:
Title
number of HCC patients with abnormal (APAL) VDR polymorphism
Time Frame
6 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Hcv cirrhotic patient with and without Hcc Exclusion Criteria: Malignancy other than HCC Co-infection with Hepatitis B virus (HBV) and Human immunodeficiency virus (HIV) Cirrhosis is due to causes other than chronic hepatitis C
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sherief Abd-elsalam, lecturer
Phone
00201095159522
Email
Sheriefabdelsalam@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Sherief Abd-elsalam, lecturer
Phone
00201095159522
Email
sherif_tropical@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fathia Asal, Prof
Organizational Affiliation
hepatology dept-Tanta
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Amal El Bendary, Professor
Organizational Affiliation
Clinicalpathology dept-Tanta
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
WALAA Elkhalawany, lecturer
Organizational Affiliation
hepatology dept-Tanta
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sherief abd-elsalm, lecturer
Organizational Affiliation
hepatology dept-Tanta
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Basma Shetaa, physician
Organizational Affiliation
Tanta University
Official's Role
Study Chair
Facility Information:
Facility Name
Tanta university - faculty of medicine
City
Tanta
State/Province
Elgharbia
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sherief Abdelsalam, lecturer
Phone
00201095159522
Email
Sheriefabdelsalam@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Role of the Vitamin D Receptor Gene Polymorphisms in Hepatocarcinogenesis

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