VDR SNPs & 25OHD Correlated With Dyslipidemia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

1987 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-07-01

Study Completion Date

2016-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The project was aimed to explore the associations of single nucleotide polymorphisms (SNPs) of vitamin D receptor gene with specific circulating lipids in adult Chinese. The circulating 25-hydroxyvitamin D concentration was also tested to explore its interactions with SNPs in the associations.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Correlation of Vitamin D Levels in Early Pregnancy With Gestational Diabetes and Pregnancy Outcomes

NCT05212519

GDM

UNKNOWN

Vitamin D Intervention Trial in Healthy Chinese

NCT01817036

Vitamin D Deficiency

COMPLETED PHASE1

The Relationship Between VDR Gene Polymorphism and Children's Physical and Intellectual Development

NCT03742310

Development, Child

UNKNOWN NA

Effect of vitaminD3 or 25(OH)D3 Fortified Dairy on Vitmain D Status and CVD Risk Markers

NCT02535910

Hypovitaminosis D Cardiovascular Diseases

UNKNOWN NA

Efficacy Study of Vitamin D and Statins to Treat Hypercholesterolemia

NCT02009787

Primary Hypercholesterolemia

UNKNOWN NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dyslipidemias Single Nucleotide Polymorphism

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

CROSS_SECTIONAL

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

No intervention.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 1\) ≥ 20 years old Han Chinese;
* 2\) living in Shenzhen for \> 2 years;
* 3\) free of liver diseases, renal diseases, and any cancers in the past 6 months; and
* 4\) not in pregnancy for women.

Exclusion Criteria

* 1\) had severe organic diseases,
* 2\) had acute infection symptoms, allergic diseases, and malignant tumors,
* 3\) had a family history of genetic diseases,
* 4\) took VD supplements in the past 6 months,
* 5\) took medicines to control lipid levels within 12 hours, or
* 6\) took diuretics, did strenuous exercise, or overate within 24 hours before the test.

Minimum Eligible Age

20 Years

Maximum Eligible Age

81 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes