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Serum Concentration of lgG in Patient With Acute Coronary Syndrome

Changes in Glycopeptides of Serum Immunoglobulin G in Patients With Acute Myocardial Infarction and the Relationships Between Its Change and Prognosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03394092
Enrollment
100
Registered
2018-01-09
Start date
2018-01-15
Completion date
2019-03-01
Last updated
2019-03-19

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

Conditions

Acute Coronary Syndrome

Keywords

immunoglobulin G

Brief summary

The aim of this study is to investigate the changes in glycopeptides of serum immunoglobulin G in patients with acute myocardial infarction and the relationships between its change and prognosis.

Detailed description

Immunoglobin G (IgG), a highly abundant glycoprotein in serum, is known to participate in blood immune responses.It has been an increasing interest in the analysis of the abnormal glycosylation of human lgG in healthy and disease states, such as autoimmune diseases and cancer.However, there is few relevant studies about the changes in glycopeptides of serum immunoglobulin G in patients with acute myocardial infarction. This study was performed for the frst timeto assess the quantitative changes of serum IgG glycosylation in patients with acute myocardial infarction and the relationships between its change and prognosis.

Interventions

DIAGNOSTIC_TESTQuantitative measurements the changes of IgG glycosylation

Serum (50 each group) is obtained into ethylenediaminetetraacetic acid(EDTA) tubes from all subjects via antecubital venepuncture.Blood is obtained into ethylenediaminetetraacetic acid(EDTA) tubes from all subjects via antecubital venepuncture to assess the quantitative changes of IgG glycosylation by HPLC-MRM at 0 , 3 and 7 days after admission.

Sponsors

Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian
CollaboratorUNKNOWN
The First Affiliated Hospital of Dalian Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

\- diagnosed as STEMI. * 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 quantitative determination of lgG12 monthsQuantitative measurements the changes of serum IgG glycosylation by HPLC-MRM

Secondary

MeasureTime frameDescription
Relationship between the serum hs-CRP and the quantitative level of lgG glycopeptides in peripheral blood.12 monthscorrelation between the serum hs-CRP and lgG
MACEs during 12-month follow-up12 monthsAssociation of quantitative level of lgG with prognosis
The changes of LVEF in two groups12 monthsAssociation of quantitative level of lgG with the changes of cardiac function

Countries

China

Outcome results

None listed

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