AlfaAge: Cross-sectional Study for the Identification of Blood Biomarkers in Healthy Young and Old Individuals
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Concentration of B2-microglobulin
研究概览
简要总结
Ageing is clearly the most important risk factor for AD and other dementias but, despite the amount of evidence supporting this fact, the exact mechanism that link ageing and AD is still unknown and, up to now, potential therapies for AD by targeting ageing have been poorly explored. This study aims to provide a better understanding of the link between ageing and AD by means of measuring in human blood those factors that have been found to be 'pro-youthful' (GDF-11, CSF2, TIMP-2, oxytocin) or 'pro-aging' (CCL2, CCL11, CCL19, Haptoglobine, B2-microglobuline) in experimental animal models, but have not been comprehensively studied in humans.
In this proof-of-concept study these blood factors in extreme groups of age, namely young adults (18-25 yo) and old adults (≥70 yo) will be measured and the hypothesis of whether the 'pro-youthful' and 'pro-ageing' blood factors change throughout age tested. In order to include a wider range of age, human umbilical cord blood and plasma from teenagers (which is already available from a previous study) will also be included.
The ultimate goal of this study is to select the more promising blood factors and obtain data on the effect size of the differences that may allow us in the future to design a larger study.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men and women between 18 and 25 years (young adults group) or older than 70 for persons at the time of inclusion (old adults group).
- •Subjects with no subjective cognitive complaints.
- •Individuals interested in participating in the study who fully understand all the procedures that will be performed.
- •Explicit participant agreement to undergo all the study procedures, which encompass:
- •Collection of basic demographic data.
- •Collection of a blood sample.
- •Give informed consent and agree that no data resulting from the study (which is no clinically relevant) will be given to the participant
排除标准
- •No signs of subjective cognitive impairment.
- •Any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol. Including: auditive and visual impairment, renal insufficiency under hemodialysis treatment, hepatic cirrhosis, chronic pneumopathy under oxygen therapy, solid organ transplantation, fibromyalgia, active oncologic disease under treatment (excluding localized tumours).
- •Any significant major psychiatric illness (following DSM-IV diagnosis manual) o diseases that interfere with cognitive function (including major depression disorder, bipolar disorder, schizophrenia).
- •Acquired brain injury: brain traumatic injury with parenchymal or extra-axial macroscopic injury, large vessel ischemic stroke or hemorrhagic stroke, brain tumors or other conditions that may cause acquired brain injury (brain radio- or chemotherapy).
- •Parkinson's disease, epilepsy under treatment and with frequent seizures (>1 /month) in the last year, multiple sclerosis or any other neurodegenerative disease.
- •Researcher criteria: individuals that have any condition which, under researcher's view, could lead to difficulty complying with the protocol.
结局指标
主要结局
Concentration of B2-microglobulin
时间窗: at inclusion
Differences in the concentration of B2-microglobulin between age groups
Concentration of CSF2
时间窗: at inclusion
Differences in the concentration of CSF22 between age groups
Concentration of GDF11
时间窗: at inclusion
Differences in the concentration of GDF11 between age groups
Concentration of CCL11
时间窗: at inclusion
Differences in the concentration of CCL11 between age groups
Concentration of TIMP2
时间窗: at inclusion
Differences in the concentration of TIMP2 between age groups
Concentration of CCL2
时间窗: at inclusion
Differences in the concentration of CCL2 between age groups
Concentration of CCL19
时间窗: at inclusion
Differences in the concentration of CCL19 between age groups
Concentration of Haptoglobin
时间窗: at inclusion
Differences in the concentration of Haptoglobin between age groups
Concentration of oxytoxin
时间窗: at inclusion
Differences in the concentration of oxytoxin between age groups
次要结局
未报告次要终点