NAD+/NADH in Peripheral Blood Monitoring
Conditions
Keywords
NADH, NAD+
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.
Interventions
Peripheral blood samples are taken before breakfast and before lunch to detect NAD+/NADH levels, hematology, blood biochemical indicators, immune cells and SIRT1 level in peripheral blood in different age groups. This experiment monitors indicators mentioned above without any drug intervention.
Sponsors
Study design
Eligibility
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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 adults | Fasting 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, etc | Fasting 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, etc | Fasting at 0 hour on the day of the trial | Monitor |
Countries
China