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临床试验/NCT07389785
NCT07389785进行中(未招募)不适用

Age Related Chromatin Remodelling as a Therapeutic Target for Organ Protection in Cardiac Surgery

University of Leicester1 个研究点 分布在 1 个国家目标入组 3,055 人开始时间: 2025年9月29日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
3,055
试验地点
1
主要终点
Study 1

研究概览

简要总结

People who have multiple long-term conditions (MLTC) like kidney disease or lung disease are at higher risk of developing organ damage and poor quality of life following heart surgery. Decades of research have failed to identify drugs or treatments that prevent this.

Our research has shown that people with MLTC have changes in their heart cells before surgery that are referred to by researchers as Biological Ageing. These changes combine to make people with MLTC more susceptible to organ damage after heart surgery, have delayed recovery, and lower quality of life.

This research programme will investigate the processes linking MLTC, changes in heart cells, and organ damage.

Our previous research suggests that MLTC lead to the infiltration of white cells from the blood into the heart muscle, a process called inflammageing. This alters the DNA in heart cells, reduces their pumping function and leaves them more likely to be damaged by surgery.

We have also shown that these changes are affected by obesity. We have also shown that changes in other types of heart cells with ageing are associated with damage to the lining of blood vessels, bleeding and damage to the kidneys.

We will use existing clinical data from previous studies and molecular data from heart cells obtained at surgery to better understand the molecular changes underlying our previous observations. This includes data from previous trials of drugs and dietary modification that aimed to modify the cellular DNA changes caused by inflammageing.

Using external data, we will check whether similar results are evident in other studies. We will then select the most likely processes underlying our observations and test whether these relationships are causal using genomic analysis and the UK Biobank data. Finally, we will use established analytical methods to identify potential drugs that may target these processes.

Positive results will provide a better understanding of the heart damage that is often seen in people with MLTC as well as new treatments for evaluation on further research.

详细描述

Organ injury is common following cardiac surgery, where it contributes to excess mortality, delayed recovery, progression of LTC, poor quality of life, and increased use of healthcare resources.

People with MLTC demonstrate increased susceptibility to organ injury and its complications. Using a multi-omics approach we have shown that MLTC are associated with biological ageing in human myocardium. Using snRNAseq, we have shown that progression of MLTC are associated with acceleration of biological ageing, characterised by T cell exhaustion, dysregulated tissue resident macrophage activation, and increased susceptibility of cardiomyocytes to metabolic stress.

Genetic modification of these processes altered susceptibility to 90-day mortality following cardiac surgery in UK Biobank. Reversal of biological ageing mechanisms including mTOR activation, histone modification, disabled autophagy, or cell senescence reduces the susceptibility of myocardium to ischaemia reperfusion injury in mice. These observations lead us to hypothesise that pre-surgery reversal of biological ageing may have organ protective effects.

Cellular ageing is characterised by changes in chromatin accessibility that are determined by histone DNA interaction. The interaction between histones and DNA in the nucleosome determine the accessibility of promoters, enhancers, and transcription factors to molecular DNA and subsequently gene expression. Reversal of age-related changes in chromatin prevents cardiac ageing in mice.

In preliminary work we have shown that genetic modification underlying biological ageing in human myocardial biopsies is determined in part by changes in chromatin accessibility. We have shown associations between MLTC including obesity, genetic modification, and organ injury affecting the heart, kidney and vascular endothelium (bleeding). We now propose to comprehensively characterise the changes in chromatin accessibility, gene expression, cell secretomes and cell-cell interactions and single cell resolution that underly these observations.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients undergoing cardiac surgery with cardiopulmonary bypass (CPB) enrolled in seven clinical studies in five UK centres.

排除标准

  • Patients who did not consent to participate in the included trials, or participants who did not consent for secondary research of their data and samples.

研究组 & 干预措施

VAL-CARD

Single-centre, unblinded, randomised controlled trial (Phase 2b).

干预措施: other (Other)

MARACAS

Prospective, single-centre observational case-control study.

干预措施: other (Other)

REDWASH

A multicenter parallel-group randomized controlled trial.

干预措施: other (Other)

REVAKI-2

Phase IIB placebo-controlled randomised clinical trial.

干预措施: other (Other)

OB-CARD

Prospective, single-centre case control study.

干预措施: other (Other)

COPTIC-2

Retrospective, single-centre observational cohort trial.

干预措施: other (Other)

PRE-OP ENERGY

Single-centre, unblinded, parallel group, randomised controlled trial.

干预措施: other (Other)

结局指标

主要结局

Study 1

时间窗: 5 years

For the clinical studies, outcomes will be restricted to those measured prospectively in the individual studies. For the UK Biobank data, the primary outcome is time to death or emergency re-hospitalisation requiring overnight admission within 365 days following discharge after major surgery.

Study 2

时间窗: 5 years

The analysis will identify differentially expressed genes, gene pathways, and networks in cell types by phenotype. The data will also identify differences in promoter accessibility by cell type and phenotype

Study 3

时间窗: 5 years

These studies will provide quantitative targeted validation of genes, proteins and DNA accessibility by cell type and phenotype in human myocardial biopsies obtained at surgery in the listed studies. We will identify anonymised publicly available external data sources that have evaluated biological ageing and inflammageing in human tissues. We will duplicate our primary genomics analysis in this secondary dataset.

Study 4

时间窗: 5 years

We will quantify the effects of genetic modification of key genes and pathways identified in Studies 1-3 on mortality and freedom from hospitalisation in UK Biobank.

Study 5

时间窗: 48 hours post-operation

Clinical outcomes: Area under the troponin curve from baseline to 48 hours post-surgery.

Study 5

时间窗: 72 hours post-operation

Clinical outcomes: Area under the creatinine curve from baseline to 72 hours post-surgery.

Study 5

时间窗: 6 weeks

Process outcomes: Valproate exposure

Study 5

时间窗: 1 day (operation day)

Experimental Outcomes: Combined snRNAseq/ ATACseq in myocardial biopsies (5 per group) obtained at surgery.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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