ClinicalTrials.gg
Status unknownNCT03979261Updated Jun 14, 2019

Predisposition to Infectious Endocarditis

An observational study in Infective Endocarditis, sponsored by Assistance Publique Hopitaux De Marseille. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-06-14.

Sponsored by Assistance Publique Hopitaux De Marseille · Observational

The sponsor has not verified this record recently (last verified Jun 2019), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
450
Ages
18 Years and older
Sex
All
01

Study summary

To evaluate the gender-related elements, a first step will be to analyze the impact of sex ratio on different parameters such as age in endocarditis and the type of underlying valvulopathy and other associated comorbidities.

Read the detailed description

Numerous epidemiological studies have made it possible to highlight the impact of the genus on the occurrence and natural evolution of numerous valvulopathies. Severe valve leakage occurs more frequently in men. This association is also observed in patients with aortic bicuspid infarction where infective endocarditis (IE) is 3 times more common in men with a sex ratio of 9 to 2 to 1. Male sex is also a risk factor of AEs in the admission score used in initial patient management used to stratify the risk of AE and start probabilistic antibiotic therapy. Several hypotheses were evoked and none made it possible to understand the impact of sex on the risk of IE. The transcriptome study of IE patients revealed 2 potential biomarkers. S100A11 (S100 calcium binding protein A11) is a diagnostic marker and AQP9 (Aquaporin 9 gene) a poor prognostic factor in patients with AE. Coxiella burnetii AE is more common and more severe in humans. A study in the C57 / BL6 mouse demonstrated the role of 17 beta-estradiol in decreasing bacterial load and granuloma formation in female mice. The hypothesis formulated is that sex hormones play a role in the natural history of IS. This hypothesis was confirmed at the transcriptome level in mice and allowed to identify transcriptomic signatures according to sex; male mice with a more marked inflammatory response to C. burnetii. In order to evaluate the gender-related elements, an initial work will be to analyze the impact of sex ratio on different parameters such as age in endocarditis and the type of underlying valvulopathy and other associated comorbidities.

The second part of the project will study (i) the transcriptional profile of the native valves removed in patients with endocarditis-free valvulopathy in male and female subjects (ii) the transcriptional profile of native valves removed during endocarditis in matching sex underlying valvulopathy and microorganism. This will evaluate a possible difference in susceptibility to endocardial fixation. (iii) the transcriptional profile of PBMCs (circulating mononuclear cells) in this same patient, which will make it possible to study the transcriptional profile of the circulating genes and to evaluate the possible difference in predisposition to endocardial fixation.

Finally, the third part will focus on the histological analysis of the valves collected to study the differences between man and woman (local inflammatory reaction, cell type found).

02

Conditions studied

  • Infective Endocarditis

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03

In context

Endocarditis

174 studies on the registry are indexed under Endocarditis; 52 are open to participants now.

This study's planned enrollment of 450 is above the median of 256 across 84 observational studies indexed under Endocarditis.

Browse Endocarditis studies →

Lead sponsor

Assistance Publique Hopitaux De Marseille is the lead sponsor of 700 studies on the registry; 144 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Probability sample

Study population

Patient with valvulopathy or infective endocarditis requiring cardiac surgery as part of routine care.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient with infectious endocarditis
  • Patient with valvulopathy or infective endocarditis requiring cardiac surgery as part of routine care.
  • Major patient
  • Patient informed of the study and having expressed no opposition to participate in the study.
  • Patient affiliated to a social security scheme.

Exclusion criteria

Exclusion Criteria:

  • Minor patient
  • Pregnant or nursing patient.
  • Patient deprived of liberty or under judicial decision.
  • Major patient under tutorship or curatorship.
  • Patient not agreeing to participate
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
450 participants (estimated)
Patient registry
No

Groups and cohorts

  • sex ratio evaluation

    Valvular surgery is performed in 30-40% of cases. The Cardiology and Cardiac Surgery De la Timone services 1000 patients as part of their valvulopathy and 450 benefit from cardiac surgery. On the other hand, transcriptomic analysis by microarray will only be done on 40 patients because the analysis costs 150 € / patients.

    Diagnostic Test: evolution of sex ratio according to age

Interventions

  • Diagnostic testevolution of sex ratio according to age

    Histological study of the collected valves to study the differences according to the sex of the inflammatory reaction and the cellular type found.

06

What researchers measure

Primary outcomes

  1. Evolution of sex ratio as a function of age and underlying pathologies (comorbidities and valvulopathies)

    Time frame: 36 months

Secondary outcomes

  1. transcriptional profile by microarray

    rate of indigenous valves removed in patients with valvulopathy without endocarditis by gender

    Time frame: 36 months

07

Study locations

1 site
  • Laboratoires d'immunologie et d'infectiologie
    Marseille, Cedex 5 13354, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 14, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03979261
Responsible party
Sponsor
First posted
Jun 7, 2019
Start date
Jul 1, 2019 (estimated)
Primary completion
Jul 1, 2022 (estimated)
Completion
Jul 1, 2022 (estimated)
Last update
Jun 14, 2019

Study contacts

Didier RAOULT, IP
Contact
didier.raoult@ap-hm.fr
04 13 73 20 5
Jean-Olivier ARNAUD
study director · AP HM

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

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