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The Exploratory Study on the Baseline Level of NAD+/NADH in Peripheral Blood Samples of Different Gender and Age Groups of Healthy Adults.

Not yet recruiting
Conditions
NAD+/NADH in Peripheral Blood Monitoring
Interventions
Other: Detection of NAD+/NADH concentration of Peripheral Blood Samples
Registration Number
NCT05997628
Lead Sponsor
Shanghai Cell Therapy Group Co.,Ltd
Brief Summary

This study investigates the concentration levels of NAD+/NADH in peripheral blood samples and immune cells of healthy adults of different age groups under daily physiological and lifestyle conditions, in order to determine the baseline levels of NAD+/NADH in adult populations of different age groups and genders. Simultaneously examining the biological status and function of human immune cells, blood biochemistry, biological age levels, to explore the biological function and mechanism of NAD+/NADH in the aging process of the human body.

Detailed Description

In this study, 60 subjects will be enrolled in three groups according to the age range of 20-40, 41-60 and 61-80. Each group has 20 subjects, and the sex ratio of each group is 1:1. After each participant is enrolled, peripheral blood samples are taken before breakfast and before lunch to detect NAD+/NADH levels in peripheral blood and determine the physiological baseline levels of NAD+/NADH in different age groups. At the same time, the subjects tested Hematology, blood biochemical indicators, as well as the expression of subsets of peripheral blood immune cells and SIRT1 level at the same time point, to study the change trend of NAD+/NADH level in different age groups, and the correlation between this trend and Hematology age, immune indicators.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
    1. Male/females of 18 to 85 years of age.

    2. Able to provide written Informed Consent.

    3. Body Mass Index ranging from 18 to 25 kg/m2(bounds included), with a stable weight over the last 2 months (±2.5 kg).

    4. Able to follow verbal and written study directions.

    5. Must not be taking or be willing to take any supplements containing any form of niacin for seven days prior to baseline and for the duration of the study.

    6.Able to maintain consistent diet and lifestyle habits according to the study

Exclusion Criteria
    1. Male/females of 18 to 85 years of age.

    2. Able to provide written Informed Consent.

    3. Body Mass Index ranging from 18 to 25 kg/m2(bounds included), with a stable weight over the last 2 months (±2.5 kg).

    4. Able to follow verbal and written study directions.

    5. Must not be taking or be willing to take any supplements containing any form of niacin for seven days prior to baseline and for the duration of the study.

    6. Able to maintain consistent diet and lifestyle habits according to the study.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
18-40 yearsDetection of NAD+/NADH concentration of Peripheral Blood SamplesEach group has 20 subjects, and the sex ratio of 18-40 years group is 1:1. After each participant is enrolled, peripheral blood samples are taken before breakfast and before lunch to detect NAD+/NADH levels in peripheral blood and determine the physiological baseline levels of NAD+/NADH in different age groups
41-60 yearsDetection of NAD+/NADH concentration of Peripheral Blood SamplesEach group has 20 subjects, and the sex ratio of 41-60 years group is 1:1. After each participant is enrolled, peripheral blood samples are taken before breakfast and before lunch to detect NAD+/NADH levels in peripheral blood and determine the physiological baseline levels of NAD+/NADH in different age groups
61-80 yearsDetection of NAD+/NADH concentration of Peripheral Blood SamplesEach group has 20 subjects, and the sex ratio of 61-80 years group is 1:1. After each participant is enrolled, peripheral blood samples are taken before breakfast and before lunch to detect NAD+/NADH levels in peripheral blood and determine the physiological baseline levels of NAD+/NADH in different age groups
Primary Outcome Measures
NameTimeMethod
The baseline in NAD+ and NADH concentrations in whole blood of healthy adults.Fasting at 0 hour, 4 hour on the day of the trial

Monitor

Counting of blood cell indicators such as red blood cells, white blood cells, and platelets in healthy adultsFasting at 0 hour on the day of the trial

Monitor

Blood biochemical indicators of the healthy adults monitoring including liver function; lood lipids; blood sugar; renal function; uric acid; lactate dehydrogenase; creatine kinase, etcFasting at 0 hour on the day of the trial

Monitor

Peripheral blood immune cell phenotype of the healthy adults monitoring including NK cells, B lymphocytes, eosinophils, T lymphocytes, platelet neutrophils, basophils, and monocytes, etcFasting at 0 hour on the day of the trial

Monitor

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Shanghai Mengchao Cancer Hospital

🇨🇳

Shanghai, Shanghai, China

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