Pyrophosphate Homeostasis and Hepatic Expression of ABCC6.Pyro-TH

NCT ID: NCT03576859

Last Updated: 2023-11-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-11-06

Study Completion Date

2020-10-29

Brief Summary

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In animals, normal hepatic expression of ABCC6 (ATP-binding transporter cassette, subfamily C, member 6) determines plasma pyrophosphate (PPi) concentration. PPi prevents the formation of hydroxyapatite crystals on tissues by precipitation of calcium and inorganic phosphate (Pi). It is an endogenous compound whose deficiency causes diffuse vascular calcifications in certain rare monogenic diseases, including the elastic pseudoxanthoma caused by the mutation of ABCC6. PPi is produced by enzymatic transformation of extracellular ATP and, in animals, the liver is the main supplier of ATP and PPi (more than 90%). In humans, liver transplantation offers the possibility of correlating the plasma concentration of PPi (\[PPi\]pl) with hepatic expression of ABCC6. Liver transplantation is performed in the treatment of chronic liver failure (Child B or C) or, in the absence of liver failure, in the treatment of hepatocellular carcinoma. By measuring\[PPi\]pl before transplantation and after liver function restoration and by measuring ABCC6 in the diseased liver and healthy liver, it is possible to determine whether liver failure is associated with decreased\[PPi\]pl and decreased liver expression of ABCC6, which is the objective of our pilot study. Its interest is to establish a physiopathological link between the frequent vascular calcifications in obese patients with hepatic steatosis and the production of PPi.

prupose: Look for a deficit in\[PPi\]pl in patients before the transplant compared to the phase of restoration of liver function

Detailed Description

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Conditions

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Hepatic Failure

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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cirrhotic patients with chronic liver failure

Group Type OTHER

blood sample

Intervention Type OTHER

Peripheral venous blood is collected before liver transplantation and after restoration of liver function

cirrhotic patients without chronic liver failure

Group Type OTHER

blood sample

Intervention Type OTHER

Peripheral venous blood is collected before liver transplantation and after restoration of liver function

Interventions

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blood sample

Peripheral venous blood is collected before liver transplantation and after restoration of liver function

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Indication for liver transplantation Age greater than or equal to 18 years Patients affiliated to social security

Exclusion Criteria

Patient not affiliated to social security Non-consenting patient or unable to understand the protocol and how it works Fulminant Hepatitis
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Nice

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Untiversity Hospital of Nice

Nice, , France

Site Status

Countries

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France

Other Identifiers

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18-AOI-11

Identifier Type: -

Identifier Source: org_study_id

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