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Serum Concentration of Wnt2 and Wnt4 in Patients With Acute Coronary Syndrome

Change of Serum Wnt2 or Wnt4 and the Relationship With Hs-CRP,cTnI and Prognosis in Patients With Acute Coronary Syndrome

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03342131
Enrollment
450
Registered
2017-11-14
Start date
2017-09-29
Completion date
2019-03-29
Last updated
2018-02-08

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

Conditions

Acute Coronary Syndrome

Keywords

Wnt signaling

Brief summary

This study aims to find the change of serum wnt effectory moleculars and the association with Hs-CRP,cTnI and Prognosis in Patients with Acute Coronary Syndrome.

Detailed description

It has been reported that wnt effecory moleculars (wnt2, wnt4, wnt11,wnt10b, DKK1, DKK2) increased in myocardium at acute phase after myocardium infarction in animal experiment. These moleculars can be detected in serum or plasma from human subjects. However, there is few relevant studies about wnt2 and wnt4 concentration in patients with acute coronary syndrome. This study valuates the serum wnt2 and wnt4 concentration in patients with acute coronary syndrome. It will possibly enable to find the relationship between serum wnt2 or wnt4 concentration and Hs-CRP, cTnI and prognosis in patients with Acute Coronary Syndrome.

Interventions

OTHERCirculating wnt 2 and wnt 4 concentration

Blood (150 each group) is obtained into ethylenediaminetetraacetic acid(EDTA) tubes from all subjects via antecubital venepuncture to explore circulating wnt 2 and wnt 4 concentration by ELISA. Continuous wnt2 and wnt4 concentration are measured in all patients with STEMI at 0 , 7days and 12 months after admission. Other patients with acute syndrome system are measured Wnt 2 and wnt4 only once within 24h after admission. Wnt2 and wnt4 concentration in Control group will be measured only once with 24h after admission.

Sponsors

Fudan University
CollaboratorOTHER
The First Affiliated Hospital of Dalian Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years

Inclusion criteria

.diagnosed as acute coronary syndrome, including STEMI and NST-ACS. * with left ventricular ejection fraction(LVEF)\>=45% * written informed consents are obtained * admitted within 24 hours after chest pain attacked

Exclusion criteria

* • complicated with rheumatic heart disease, coronary arteritis, hypertrophic cardiomyopathy or dilated cardiomyopathy * complicated with malignant tumor,the immune system diseases, blood system diseases, recently (within 2 weeks) taking glucocorticoid drugs, the use of immunosuppressive agents and cerebral infarction * with acute or chronic infection, surgery or trauma in the last month * secondary hypertension, severe liver dysfunction,severe renal insufficiency * with abnormal thyroid function or allergy to iodine agent refusal to sign the informed consent

Design outcomes

Primary

MeasureTime frameDescription
Serum wnt2 and wnt4 concentration12 monthsSerum wnt2 and wnt4 concentration in ng/ml

Secondary

MeasureTime frameDescription
Relationship between wnt2 or wnt4 and high sensitive C reaction protein (hs-CRP) concentration12 monthsCorrelation of wnt2 and wnt4 with hs-CRP concentration
Relationship between wnt2 or wnt4 and Troponin-I (Tn-I) concentration12 monthsCorrelation of wnt2 and wnt4 with Tn-I concentration
MACEs during 12-month follow-up12 monthsAssociation of wnt2 or wnt4 concentration with prognosis

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026