The Impact of Nicotinamide Mononucleotide Sustained-release Tablets on Immunosenescence and Metablism in Middle-aged and Elderly Individuals With Metabolic Disorders.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-70
SponsorQing Su

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • NMN

    Dietary supplement

    NMN SR tablets(1000mg/tablets) , 1 tablet daily before breakfast

  • Placebo

    Dietary supplement

    Matching Placebo (tablets) once daily before breakfast

Treatment groups

126 Participants
are divided into 2 treatment groups
Group A: NMN ArmExperimental treatment 1 intervention
Group B: Placebo ArmPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

CD3+CD8+CD27-CD28- T cells as a percentage of CD3+CD8+ T cells, expressed in %, evaluated by flow cytometry

Time frame
26 weeks

Secondary outcomes

1

Body composition analysis, expressed in kg, %, and g/cm², evaluated by dual-energy X-ray absorptiometry

Time frame
26 weeks
2

Determination of fasting blood glucose and OGTT 2-hour blood glucose, expressed in mmol/L, evaluated by glucose oxidase method

Time frame
26 weeks
3

CD3+CD8+CD27- T cells as a percentage of total CD3+CD8+ T cells, expressed in %, evaluated by flow cytometry

Time frame
26 weeks
4

CD3+CD8+CD28- T cells as a percentage of total CD3+CD8+ T cells, expressed in %, evaluated by flow cytometry

Time frame
26 weeks

Other outcomes

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