- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07591337
SNRK & Vascular Endothelial Aging
May 12, 2026 updated by: Xintong Ge, Tianjin Medical University
The Association Between SNRK and Vascular Endothelial Aging
Cardiovascular diseases pose a serious threat to public health, and their prevalence is on the rise year by year.
Vascular aging is an independent risk factor for cardiovascular diseases, and endothelial cell senescence is an early event in vascular aging.
Its occurrence can lead to endothelium-dependent vasodilation dysfunction, reduced vascular permeability, and the release of the senescence-associated secretory phenotype (SASP).
These vascular pathological changes further damage the vascular media, leading to vascular remodeling and reduced compliance, accelerating the progression of atherosclerosis, and ultimately resulting in cardiovascular diseases such as coronary heart disease and hypertension.
Recent research of the investigators has revealed that SNRK, a new member of the AMPK family of cellular energy sensors, plays a key regulatory role in vascular development.
Based on this finding, the investigators propose the scientific hypothesis that SNRK responds to both physiological and pathological aging stimuli through differential mechanisms and regulates the process of endothelial cell senescence.
In this study, the investigators will explore the correlation between SNRKAS and carotid vascular structure and endothelial function by measuring the levels of the SNRK upstream lncRNA (SNRKAS) in participants' peripheral blood, in conjunction with carotid ultrasound examinations.
The findings will provide a solid scientific basis for elucidating new mechanisms underlying the onset and progression of vascular aging and for identifying novel therapeutic targets.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
180
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xintong Ge, M.D.
- Phone Number: 86-022-60362237
- Email: xge@tmu.edu.cn
Study Locations
-
-
Tianjin Municipality
-
Tianjin, Tianjin Municipality, China, 300052
- Recruiting
- Tianjin Medical University General Hospital
-
Contact:
- Xintong Ge, M.D.
- Email: xge@tmu.edu.cn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Estimated by statistical analysis, a total of 180 subjects were included from individuals who come for physical examinations or medical visits to the leading and collaborating administrations of this project, and meet the inclusion criteria between April 2026 and March 2029.
Description
Inclusion Criteria:
- Aged 18-80 years, with the capacity to make decisions independently or represented by an authorized legal guardian;
- Able to provide complete personal information, medical history, and lifestyle history (e.g., smoking and alcohol consumption history);
- No history of severe cardiovascular disease, and deemed eligible for inclusion by a physician.
Exclusion Criteria:
- Women who are pregnant or may become pregnant;
- Patients with a history of neurological disorders, tumors, severe cardiovascular or pulmonary disease, liver failure, kidney failure, or blood disorders;
- Patients who have undergone carotid stenting, carotid endarterectomy, or other similar procedures, or who have unilateral carotid artery occlusion due to any cause;
- Patients who have participated in another clinical trial within the past 4 weeks;
- Individuals deemed unsuitable for this clinical trial by the investigators.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
< 40 years old
Participants of < 40 years old.
|
|
|
40-60 years old
Participants of 40-60 years old.
|
|
|
> 60 years old
Participants of > 60 years old.
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum levels of SNRKAS detected by RT-PCR
Time Frame: At enrollment
|
serum levels of SNRKAS (fold change)
|
At enrollment
|
|
Degree of bilateral carotid artery stenosis detected by Doppler ultrasound
Time Frame: At enrollment
|
Intima-media thickness (mm) and lumen diameter (mm) of bilateral common carotid artery and internal carotid artery
|
At enrollment
|
|
Pulse wave velocity in both carotid arteries detected by Doppler ultrasound
Time Frame: At enrollment
|
Peak systolic velocity (cm/s) of bilateral common carotid artery and internal carotid artery
|
At enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood lipids levels detected by automated biochemical analyzer (LABOSPECT 008, Hitachi)
Time Frame: At enrollment
|
Total Cholesterol (mmol/L), Triglycerides (mmol/L), High-Density Lipoprotein (mmol/L), Low-Density Lipoprotein (mmol/L)
|
At enrollment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Minghui Zou, Ph.D., mhzou@tmu.edu.cn
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2026
Primary Completion (Estimated)
April 30, 2029
Study Completion (Estimated)
April 30, 2029
Study Registration Dates
First Submitted
May 6, 2026
First Submitted That Met QC Criteria
May 12, 2026
First Posted (Actual)
May 15, 2026
Study Record Updates
Last Update Posted (Actual)
May 15, 2026
Last Update Submitted That Met QC Criteria
May 12, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB2026-YX-172-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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