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Impact of Donor and Recipient ST2 / IL-33 Pathway After Heart Transplantation (ISIDORE)

G

Groupe Hospitalier Pitie-Salpetriere

Status

Unknown

Conditions

Heart Transplant Failure and Rejection

Study type

Observational

Funder types

Other

Identifiers

NCT03050892
CIC-1421-16-01

Details and patient eligibility

About

Evaluate the association between donor soluble protein ST2 (sST2) serum levels and 30-day recipient mortality in order to improve graft screening.

Full description

Soluble protein sST2 has recently become a prognostic biomarker in the context of acute myocardial infarction and chronic heart failure, and recent studies also show that sST2 is involved in acute rejection of the cardiac graft in recipients. Experimental studies confirm that the ST2 / IL-33 pathway is involved in the process leading to cardiac transplant rejection in animals. In particular, administration of IL-33 would have a positive effect on pre-clinical cardiac graft survival. No study have looked at the level of ST2 / IL-33 of the donor, with the purpose that it might reflect the condition of the transplanted heart and its initial level of Immune tolerance and maybe predict the risk of subsequent dysfunction.

In this non-interventional study, several blood samples will be taken on donors before organ procurement and on recipients prior to grafting, on day 7 and at the time of each myocardial biopsy (approximately 16 myocardial biopsies the first year). Serum level of sST2 and IL-33 will then be determined according to the ELISA method on each blood sample.

Fifty consecutive couple donors/ recipients will be included in the study. This number of subjects is calculated to detect a doubling of the donor sST2 level between the two recipient groups with 30-day mortality and without mortality (potency: 90%, alpha risk: 0.05, bilateral).

Enrollment

50 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Consenting recipients
  • Consenting donors to organ/tissue donation for the purpose of scientific research

Exclusion criteria

  • Non consenting recipients
  • Non consenting donors to organ/tissue donation for the purpose of scientific research
  • Multi-organ transplantation

Trial contacts and locations

1

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Central trial contact

Antonella Galeone, MD, PhD

Data sourced from clinicaltrials.gov

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