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Serum Adiponectin in Chinese Population and Its Correlation to Cardiovascular and Cerebrovascular Diseases

Serum Adiponectin Concentration, Activity and Isoforms in Chinese Population and Its Correlation to Cardiovascular and Cerebrovascular Diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01372800
Enrollment
30000
Registered
2011-06-14
Start date
2011-05-01
Completion date
2036-10-01
Last updated
2025-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Infarction, Myocardial Infarction

Keywords

adiponectin, cardiovascular diseases, cerebrovascular diseases

Brief summary

Adiponectin (Ad) is an abundant protein in human body, and reports have shown that it act as a novel risk factor for brain and heart ischemia injury. This 5 years follow-up study will focus on serum adiponectin concentration, activity and isoforms in Chinese population and its correlation to these diseases.

Detailed description

Adiponectin (Ad) is an abundant protein hormone regulatory of numerous metabolic processes, anti-inflammatory, vascular protective, and anti-ischemic properties. Since its 1995 discovery, Ad has garnered considerable attention for its role in diabetic and cardiovascular pathology. Clinical observations have demonstrated the association of hypoadiponectinemia in patients with obesity, cardiovascular disease, and insulin resistance. There is growing evidence supporting Ad can act as a novel risk factor for cardiovascular and cerebrovascular injury. This 5 years follow-up study will focus on serum adiponectin concentration, activity and isoforms in Chinese population and its correlation to cardiovascular and cerebrovascular diseases.

Interventions

None listed

Sponsors

Xijing Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* available for 5 years of follow-up study

Exclusion criteria

* Death caused other than cardiovascular and cerebralvascular diseases till the study ends * Floating Population * Pregnancy, lactation, or child bearing women * Tumor * Active hepatic disease or hepatic dysfunction, or AST/ALT \> 1.5UNL * Severe renal dysfunction(Scr \> 3 mg/dl or 264μmol/L) * Patients with any condition which, in the investigator's judgment, might increase the risk to the subject for any adverse event or abnormal laboratory finding

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants with major adverse events5 yearsMajor adverse events included but were not limited to death during the study caused by cardiovascular events or cerebrovascular events.

Secondary

MeasureTime frameDescription
blood routine, glucose and lipid profile; ECG;5 yearsthe tests mentioned above will be taken once per year
serum adiponectin concentration, activity and isoforms5 yearsserum adiponectin concentration, activity and isoforms will be monitored once per year.

Countries

China

Contacts

Primary ContactLing Tao, M.D Ph.D
lingtao2006@gmail.com+86-15002955798

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026