Predisposition and Transition Mechanisms From Arterial Hypertension to Heart Failure (Hypercare)

April 27, 2015 updated by: Central Hospital, Nancy, France

Genetics and Genomics of Hypertension Associated With Microinflammation, Oxydative Stress, Chronic Renal Disease and Heart Failure (A2-B2-B3)

This project aims at investigating the genetic, genomic and proteomic basis of hypertension and susceptibility to hypertension-related end organ damage (renal damage and heart failure). It will include cross sectional as well as follow-up studies with a large number of subjects and variety of phenotypes, to explore the pathophysiology of hypertension and hypertension-related disease.

Study Overview

Status

Completed

Conditions

Detailed Description

In all index patients and recruited family members, recorded data will include the following :

  • Past medical history, drug history and family history
  • Physical examination
  • Height, weight, waist and hip circumference
  • Cardiac examination
  • Vascular examination
  • Blood pressure
  • Plasma and urine samples
  • Body composition (DEXA)
  • Tissue Doppler imaging

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alsace
      • Strasbourg, Alsace, France, 67000
        • Centre D'Investigation Clinique de Strasbourg
    • Lorraine
      • Nancy, Lorraine, France, 54000
        • Hopital Brabois Adulte

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • index patient :

    • Caucasian patients of either sex who were diagnosed to have essential hypertension (as defined below) before the age of 50 y.
    • The index patient should not be older than 60 years at the time of enrolment.
    • Definition of hypertension for the index patient:

      • If untreated: Systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 95 mmHg.
      • If already on treatment: Treatment with more of 2 different antihypertensive drugs at the time of enrolment.
    • At least three first degree relatives of whom at least one should be affected and at least one be from a different generation (parents or offspring aged 18 years or above) must be willing to participate in the family study. For definition of hypertension in relatives of the index patient see below.
    • Written informed consent
  • family

    • at least three other first degree relatives must be willing to participate in the family study:
    • at least one first-degree relative must be affected with diagnosis of hypertension made before age of 50 years AND
    • at least one first degree relative must be from a different generation (offspring or parents).

Exclusion Criteria:

  • index patient :

    • Any known form of secondary hypertension, including sleep apnoea syndrome
    • Any known previous clinical complications of hypertension (angina, MI, stroke, TIA, peripheral artery disease) at any time
    • Any known renal disease, including GFR < 60 mL/min as estimated by the abbreviated MDRD formula, or kidney stones
    • Kidney or other organ transplantation
    • Type 1 diabetes mellitus
    • Heart failure stage D (AHA/ACC criteria)
    • Any malignant concomitant diseases or history of malignant diseases within the last five years, with exception of treated squamous skin cancer or basalioma
    • Clinical or laboratory signs of acute infection, especially urinary tract infection
    • Systemic inflammatory diseases, such as autoimmune diseases, connective tissue diseases or collagenoses.
    • Steroids or any other immunosuppressive drug
    • Severe known liver disease (ALT or gamma-GT above three-fold of upper normal limit)
    • Current alcohol consume of more than 21 drinks/week (1 drink = a bottle (0,33 l) beer, a glass (0,2 l) of wine, or 4 cl = 40 ml of spirit (40%)) or drug abuse such as cocaine
  • family

    • any organ transplantation
    • any malignant concomitant disease
    • acute infection
    • systemic inflammatory disease
    • severe liver disease
    • current alcohol or drug abuse

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: NOE
multicentric family-based cohort. prospective and transversal study
blood and urine sample

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
genetic biomarkers
Time Frame: time point 1 : first day ; Time point
time point 1 : first day ; Time point

Secondary Outcome Measures

Outcome Measure
Time Frame
oxidative stress markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
microinflammation markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
renal function and damage markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
cardiac and large artery growth, remodelling dysfunction and failure markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: faiez ZANNAD, Pr, Central Hospital, Nancy, France

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2008

Primary Completion (Actual)

February 1, 2015

Study Completion (Actual)

February 1, 2015

Study Registration Dates

First Submitted

February 5, 2010

First Submitted That Met QC Criteria

April 27, 2015

First Posted (Estimate)

April 30, 2015

Study Record Updates

Last Update Posted (Estimate)

April 30, 2015

Last Update Submitted That Met QC Criteria

April 27, 2015

Last Verified

February 1, 2010

More Information

Terms related to this study

Other Study ID Numbers

  • HYPERCARE(english v. 1.0)JRPB3
  • Cpp : 07.11.11
  • Dgs: 2007-0537

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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