Bayraktutan Dunhill Medical Trust EPC Study

Ischaemic stroke develops through an interference with blood supply to the brain and continues to be one of the leading causes of morbidity and mortality in the World. Global medical statistics reveal that ~75% of all stroke patients are older than 65 years and that the stroke occurrence more than doubles every 10 years after the age of 55 in both men and women.

Although various mechanisms may alter the structure and function of the adult brain during the aging process, endothelial dysfunction is regarded as the main pathology that renders cerebral vessels susceptible to atherosclerosis and subsequent vascular events. Endothelial dysfunction also constitutes the main cause of vascular abnormality in most lacunar strokes which result from occlusion of one of the penetrating arteries deep within the brain. Cortical strokes represent another common form of ischaemic stroke and develop from an embolism from the heart or large arteries. As the endothelium maintains vascular balance through regulation of many distinct functions like vascular permeability, tone and inflammation, it is of crucial importance to preserve its integrity and function at all times to prevent age- and stroke-related vascular damage.

Recent studies show that bone marrow-derived endothelial progenitor cells (EPCs) play a key role in sustaining appropriate endothelial function by re-endothelialisation of blood vessels in adult brain and ischaemic settings. Like embryonic angioblasts, EPCs are equipped with an inherent capacity to circulate, proliferate and differentiate. Hence, the markers of endothelial maturity (KDR), immaturity (CD133) and stemness (CD34) must be simultaneously detected in relevant studies to identify all endothelial-committed and undifferentiated cells.

It is likely that environmental changes, like oxidative stress, inflammatory responses and nitric oxide availability, evoked by ischaemic injury and aging may also suppress the generation and function of EPCs. As mobilisation, recruitment and homing of EPCs to sites of vascular injury are mediated by various growth factors like the SDF-1 (stromal cell-derived factor-1), VEGF (vascular endothelial growth factor) and GCSF (granulocyte-colony stimulating factor), it is likely that the diminished expression of these factors may also negatively influence the number and function of EPCs.

Interestingly, while there is little data on functional and numerical alteration of EPCs during the chronic phase of stroke, current data regarding EPC levels during acute and subacute phases of disease are inconsistent in that stable, increased or decreased numbers have been reported as compared to healthy subjects.The time course of EPC release after acute cerebral infarction also remains inconclusive.

In light of the above, the aims of the current study are to reveal whether 1- variations in circulating EPC levels and/or their functional aspects may be used as markers to identify ischaemic stroke subtypes and predict patients' outcome; 2- differences in EPC number/function during acute, subacute or chronic phases of stroke correlate with severity and functional outcome of ischaemic stroke; 3- EPC counts and function are affected by aging process; and 4- levels or activity of key pathophysiological elements like VEGF, inflammatory cytokines and nitric oxide, known to affect EPC count and function, differ between patients with lacunar and cortical strokes and between stroke patients and healthy counterparts.

STUDY MANAGEMENT Independent outcome assessments (mRS, BI, NIHSS) will be performed on admission and days 7, 30 and 90 after stroke. The laboratory procedures will be carried out by a post-doctoral research fellow who will collate and analyse the data. The Chief Investigator has overall responsibility for the study and shall oversee all study management. The data custodian will be the Chief Investigator.

PARTICIPANT DURATION Each participant with stroke will be followed-up for 90 days from the time of recruitment. Elderly and young healthy volunteers will be seen only once.

RECRUITMENT Participants will be recruited from Nottingham University Hospitals Stroke Services. The initial approach will be from a member of the patient's usual care team (which may include the investigators) who will inform the participant or their nominated representative of all aspects pertaining to participation in the study. It will be explained to the potential participant that entry into the study is entirely voluntary and that their treatment and care will not be affected by their decision. It will also be explained that they can withdraw at any time.

PARTICIPANT WITHDRAWAL Participants may be withdrawn from study in cases of disease progression and withdrawal of consent. The participants will be made aware that this will not affect their future care.

INFORMED CONSENT No patient will be recruited into the study without obtaining their written informed consent. In cases of incapacity, the consent of an appropriate personal consultee will be sought. The Investigator will explain the details of the study and provide a Participant Information Sheet. Participants will be offered 24 hours to consider participation. However, they will be allowed to consent at an earlier time, if they prefer. In cases where stroke patients regain capacity, they will be re-consented for their ongoing participation in the study.

STATISTICS All results including subject characteristics will be reported as means±SD. Continuous variables, including age and circulating EPC level will be analysed by independent t-test among groups. Circulating EPC levels at different time points (within 48 h and on days 7, 30 and 90 post-stroke) will be compared using the repeated measures of ANOVA. Scheffe's multiple comparison will be used to analyse the intra-individual courses of parameters over time. These will then be compared among patients with lacunar and cortical strokes. Multiple logistic regression analyses will determine the independent impact of different predictive variables on functional outcome and neurological deficits.

Sample size have been calculated to allow for failures of patient attendance on days 30 and 90 (~15% for each time point) and possibility of patients illness/death during the course of the study (~5%).

ADVERSE EVENTS As this is not an interventional study, no adverse event is anticipated to develop because of it. Adverse events of venepuncture will be dealt with according to standard practice.

DATA PROTECTION The study form will only collect the minimum required information for the purposes of the study. Study forms will be held securely, in a locked room, or locked cupboard or cabinet. Access to the information will be limited to the study staff and investigators and relevant regulatory authorities. Computer held data including the study database will be held securely and password protected. All data will be stored on a secure dedicated web server. Access will be restricted by user identifiers and passwords (encrypted using a one way encryption method). Information about the study in the participant's medical records / hospital notes will be treated confidentially in the same way as all other confidential medical information. Electronic data will be backed up every 24 hours to both local and remote media in encrypted format.

STUDY DATA Monitoring of study data shall include confirmation of informed consent; source data verification; data storage and data transfer procedures; local quality control checks and procedures, back-up and disaster recovery of any local databases and validation of data manipulation. The Academic Supervisor, or where required, a nominated designee of the Sponsor, shall carry out monitoring of study data as an ongoing activity.

Entries on study forms will be verified by inspection against the source data. A sample of study forms (10% or as per the study risk assessment) will be checked on a regular basis for verification of all entries made. In addition the subsequent capture of the data on the study database will be checked. Where corrections are required these will carry a full audit trail and justification. Study data and evidence of monitoring and systems audits will be made available for inspection as/when required.