A Clinical Study of Association Between Postoperative Dyslipidemia and Organ Rejection in Transplant Patients
Recruiting now
Conditions studied: Heart Transplant Failure and Rejection
In brief
Abnormal lipid metabolism is a common complication after organ transplantation, with pathological changes in lipid parameters occurring in approximately 60-80% of cardiac transplant recipients receiving triple immunotherapy with cyclosporine, imid azathioprine, and methylprednisolone. With the significant increase in long-term survival and increasing age of transplant patients, atherosclerotic cardiovascular diseases, such as those caused by dyslipidemia, have become a major cause of transplant organ failure and recipient death. However, the causes of dyslipidemia after organ transplantation, as well as the effects and mechanisms of dyslipidemia on transplant rejection, are unknown. Previous studies have found that 1. increased lipid levels occur in recipients after heart transplantation; 2. during rejection, hepatic PCSK9 expression is increased in recipients; 3. a high-fat environment increases the immunoreactivity of human peripheral blood lymphocytes. It is suggested that PCSK9-lipid disorder-immune cell interactions may be associated with the development of transplant rejection. In this project, we propose to (1) establish a long-term follow-up system for postoperative cardiac transplantation patients in our department to track the characteristics of lipid changes in transplantation patients, to clarify the link between dyslipidemia and rejection, and to provide a strong evidence-based medical basis for the management of lipids during the perioperative period and in the postoperative period; (2) expand the dimensions of lipid-related assays under the support of the above system, and to incorporate transcriptomic, proteomic, and metabolomic research methods to elucidate transplantation rejection in a multidimensional manner. (ii) Expanding the dimensions of lipid-related assays to include transcriptomic, proteomic, and metabolomic studies to elucidate the relationship between PCSK9 and dyslipidemia in transplant patients; (iii) Adopting single-cell sequencing technology to deeply reveal the potential mechanism by which changes in lipids affect T-cell-mediated rejection of cardiac transplants. The mechanism of T-cell-mediated cardiac transplantation rejection is revealed by single-cell sequencing.
Key facts
- Study ID
- NCT05994274
- Run by
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
- People needed
- 80
- Starts
- 2023-12-01
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2023-08-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- After heart transplantation
- Age ≥ 18
- Disease duration: symptomatic heart failure ≥ 6 months prior to screening date
- The patient's informed consent
You may not qualify if…
- Refusal of the patient to provide consent
- Suspected poor capability to follow instructions and cooperate
- Another life-threatening disease with poor prognosis (survival less than 2 years)
- Participation in any other clinical study within less than 30 days prior to screening date
Where it is running
- Wuhan Union Hospital — Wuhan, China (enrolling)
Full record on ClinicalTrials.gov
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