About this trial
The ageing of our country is increasing and the ageing of the population has led to a significant increase in aging related diseases. During the aging process of the organism, cellular senescence can occur in all systems of the body, of which the senescence of the immune system is called immunosenescence. Some studies have shown that metabolic disorders can also trigger aging. This study investigated the effect of nicotinamide mononucleotide (NMN) supplementation on immunosenescence in middle-aged and elderly people through a placebo-controlled long-range clinical trail, aiming to provide a new method to improve immunosenescence. The effects of NMN supplementation on glucose and lipid metabolic indexes, body composition and telomere length of peripheral blood cells are also investigated, which may open up new ideas for the prevention and treatment of glucose and lipid metabolic diseases.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 50-70 years with overweight or obesity (BMI 24kg/m2);
At least one of the following three: metabolism-related fatty liver disease (diagnosed by ultrasound); pre-diabetes; type 2 diabetes mellitus with HbA1c <7% without glucose-lowering drug therapy;
Agreed to participate in the trial and could adhere to the follow-up and visit the hospital on their own; signed the informed consent form.
Disqualifiers
Patients with tumours;
Patients with autoimmune diseases (excluding Hashimoto's thyroiditis);
Severe cardiovascular disease or cardiac insufficiency;
Systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg;
Trial design
Parallel
Treatments tested in this trial
NMN
Dietary supplementNMN SR tablets(1000mg/tablets) , 1 tablet daily before breakfast
Placebo
Dietary supplementMatching Placebo (tablets) once daily before breakfast
Treatment groups
Trial outcomes
Primary outcomes
CD3+CD8+CD27-CD28- T cells as a percentage of CD3+CD8+ T cells, expressed in %, evaluated by flow cytometry
Secondary outcomes
Body composition analysis, expressed in kg, %, and g/cm², evaluated by dual-energy X-ray absorptiometry
Determination of fasting blood glucose and OGTT 2-hour blood glucose, expressed in mmol/L, evaluated by glucose oxidase method
CD3+CD8+CD27- T cells as a percentage of total CD3+CD8+ T cells, expressed in %, evaluated by flow cytometry
CD3+CD8+CD28- T cells as a percentage of total CD3+CD8+ T cells, expressed in %, evaluated by flow cytometry
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Qing Su
Lead sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Sponsor institution