Genetic Susceptibility to Rheumatic Heart Disease in the Pacific Region

NCT ID: NCT02188862

Last Updated: 2014-07-15

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

Total Enrollment

2372 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-09-30

Study Completion Date

2013-12-31

Brief Summary

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The purpose of this study is to investigate whether there are genetic differences between patients with rheumatic heart disease and members of the general population.

Detailed Description

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The investigators will micro-array genotype approximately 300,000 single nucleotide polymorphisms (SNP) using DNA samples from patients with rheumatic heart disease (cases) from New Caledonia and Fiji, and members of the general population (controls) from New Caledonia, Vanuatu and Fiji. The investigators will perform standard quality control checks on the SNP data using measures such as call rate, heterozygosity, duplication and relatedness, and exclude variants on the basis of deviation from Hardy-Weinberg equilibrium and minor allele frequency. We will also impute variants not present on the micro-array with reference to the latest release of 1000 Genomes data and whole-genome sequence data from sixty Melanesian individuals from New Caledonia from the phenotypic extremes in this study.

The investigators will conduct a discovery analysis in using a genome-wide association study approach focusing on Oceanic cases and controls from the Francophone nations of New Caledonia and Vanuatu. This analysis will be corrected for bias due to population stratification using the Linear Mixed Model (LMM) and consider additive, dominant and recessive genetic models. The investigators will then perform LMM association testing for variants with P-value in the discovery analysis less than 1x10\^-5 in Oceanic cases and controls from Fiji and combine the association statistics by fixed-effects meta-analysis. The investigators will consider variants with significant effects in the same direction in discovery and replication analyses with combined P-value less than 1x10\^-8 to have replicated. Unless there is clear evidence that associated variants are specific to Oceanic populations, further replication analyses for associated variants in cases and controls of Indian Descent from Fiji, as well as individuals of other and admixed ethnicities from both Fiji and New Caledonia.

Recruitment completed in December 2013. After receipt of funding from the British Heart Foundation, genotyping and analysis will begin in July 2014.

Conditions

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Rheumatic Heart Disease Mitral Stenosis

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Rheumatic heart disease cases

Patients with rheumatic heart disease as defined in the case criteria

No interventions assigned to this group

Population controls

Individuals from the general population divided into new controls (recruited specifically for this study) and existing controls (recruited to previous population genetics studies in the region)

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of rheumatic heart disease based on one of:

* World Heart Federation definite echocardiographic criteria
* World Heart Federation borderline echocardiographic criteria and history of acute rheumatic fever
* Mitral stenosis with valve area less than 2.0 cm2
* Previous surgery for rheumatic heart disease

* Healthy individual living in a community where cases were identified

Exclusion Criteria

* Age less than five years
* Inability to give consent
2. New Controls


* Past medical history or systems suggestive of rheumatic heart disease, acute rheumatic fever or other valvular heart disease
* Age less than five years
* Inability to give consent
Minimum Eligible Age

5 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ministry of Health, Fiji

OTHER_GOV

Sponsor Role collaborator

Fiji National University

OTHER

Sponsor Role collaborator

Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role collaborator

Institut Necker Enfants Malades

OTHER

Sponsor Role collaborator

Centre Hospitalier Territorial de Nouvelle-Calédonie

OTHER

Sponsor Role collaborator

University of Melbourne

OTHER

Sponsor Role collaborator

University of Oxford

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tom Parks, MRCP DTM&H

Role: PRINCIPAL_INVESTIGATOR

University of Oxford

Mariana Mirabel, MD

Role: PRINCIPAL_INVESTIGATOR

Institut National de la Santé Et de la Recherche Médicale, France

Andrew C Steer, FRACP PhD

Role: PRINCIPAL_INVESTIGATOR

University of Melbourne

Adrian VS Hill, DPhil DM

Role: STUDY_CHAIR

University of Oxford

Locations

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Colonial War Memorial Hospital

Suva, , Fiji

Site Status

Centre Hospitalier Territorial de Nouvelle Caledonie

Noumea, , New Caledonia

Site Status

Wellcome Trust Centre for Human Genetics, University of Oxford

Oxford, , United Kingdom

Site Status

Countries

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Fiji New Caledonia United Kingdom

Related Links

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Other Identifiers

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PACIFICRHDGEN

Identifier Type: -

Identifier Source: org_study_id

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