Genetic Factors and Immunological Determinism of Persistent Consequences of Chikungunya

NCT ID: NCT03690648

Last Updated: 2022-08-30

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 600 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-08-01
• Study Completion Date: 2021-12-31

Brief Summary

Chikungunya virus (CHIKV) infection has become a threat to public health worldwide. Reunion Island, due to the 2005-2006 epidemic, has acquired unique expertise and remains at the forefront of global research on this disease. The idea of genetic determinism of the clinical expression of infectious diseases has been supported by many epidemiological arguments over the past fifty years. The identification of genetic variants, associated with a disease, often allows a better understanding of the molecular mechanisms involved with consequent significant benefits such as the development of specific biomarkers for new preventive (vaccination) and / or therapeutic (drug design) approaches. In the absence of well-documented hypotheses about the genes potentially involved in the occurrence or evolution of a disease, genome-wide association studies (GWAS), whole genome, of nucleotide polymorphisms (SNPs) and the principle of linkage disequilibrium, under the commonly accepted hypothesis that the expression of a common disease is based on a small number of alleles commonly found in the population (frequency of minor allele greater than 1-5%), have become a method of choice, free of hypothesis, to specify the part of heritability of a complex disease and to identify its genetic determinants. Several epidemiological arguments support a significant proportion of genetic determinism in the explanation of the evolutionary pattern of Chikungunya, whose proportion of chronic forms can reach 40-60% in population-based studies conducted in the two years following an epidemic:

• There are few risk factors associated with chronic forms and these appear to be unclear (age, comorbidities with several elements of the metabolic syndrome) or inconsistent (immune burden) in population studies;
• The incidence of severe or atypical forms is rare in the order of 1% of infections;
• In contrast to the acute phase (J1-J21) for which there seems to be a role of the viral load intensity and a consensual pro-inflammatory immune signature according to a recent meta-analysis]; The role of the intensity of the viral load in the pathogenesis of chronic arthralgia (> J90) and their immune signature remain to be determined, the latter being rather nonspecific, according to studies conducted in Reunion, Italy or Singapore.

These elements justify the interest of a GWAS in the Chikungunya to identify new avenues and mechanistic hypotheses likely to explain the chronic arthralgia characteristic of the disease.

Conditions

Chikungunya Fever

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Saliva collection

• Clinical examination;
• Quality of life survey;
• Saliva collection for genetical analysis

Quality of life survey

Intervention Type: OTHER

Administration of scales: SF-12v2, EQ-5D, QCD, DN4, EIMIR, MFIS-5 et EHAD

Saliva collection

Intervention Type: GENETIC

Collection of 20 ml of saliva with a kit of saliva collection

Saliva and Blood collection

• Clinical examination;
• Quality of life survey;
• Saliva and blood collection for genetical analysis

Quality of life survey

Intervention Type: OTHER

Administration of scales: SF-12v2, EQ-5D, QCD, DN4, EIMIR, MFIS-5 et EHAD

Saliva collection

Intervention Type: GENETIC

Collection of 20 ml of saliva with a kit of saliva collection

Blood collection

Intervention Type: GENETIC

Collection of 20 ml of blood with kit of blood collection

Interventions

Quality of life survey

Administration of scales: SF-12v2, EQ-5D, QCD, DN4, EIMIR, MFIS-5 et EHAD

Intervention Type: OTHER

Saliva collection

Collection of 20 ml of saliva with a kit of saliva collection

Intervention Type: GENETIC

Blood collection

Collection of 20 ml of blood with kit of blood collection

Intervention Type: GENETIC

Eligibility Criteria

Inclusion Criteria

• -Subject of the seroprevalence survey or neighbor living in the same neighborhood likely to confirm an exposure status or known;
• Exposure status established by specific IgG serology, collected between March 1st, 2005 and December 31st, 2006;
• Affiliated to a social security scheme;
• Age between 18 and 75 years old;
• Paternal and maternal 1st and 2nd degree ascendants (parents and grandparents) and at least 3 generations of the family present on the island (grandparents born on the island of Réunion);
• Able to spit

Exclusion Criteria

• Exposure status unknown;
• Absence of social security;
• Age <18 years and> 75 years;
• Physical inability to spit;
• Pregnant women;
• Protected person (tutorship or curatorship).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Conservatoire national des Arts et Métiers

OTHER

Sponsor Role: collaborator

Centre Hospitalier Universitaire de la Réunion

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CHU de La Réunion

Saint-Pierre, , Reunion

Countries

Reunion

Other Identifiers

2016/CHU/12

Identifier Type: -

Identifier Source: org_study_id