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A study to determine the ability of plasma B-type Natriuretic Peptide signal peptide (BNP-SP) concentrations to act as a specific and early clinical biomarker of Acute Myocardial Infarction

A study to determine the ability of plasma B-type Natriuretic Peptide signal peptide (BNP-SP) concentrations to act as a specific and early clinical biomarker of Acute Myocardial Infarction in patients with chest pain.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12609000040268
Acronym
BNP Signal Peptide measurement in Acute Myocardial Infaction “SP-AMI”
Enrollment
80
Registered
2009-01-19
Start date
2007-07-22
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Early clinical detection of acute coronary syndromes (ACS) can be difficult. In particular, distinction between cardiac and non-cardiac events may entail 12-36 hours of delay whilst serial biomarker results are awaited and/or subsequent tests (such as exercise electrocardiography) are performed. We have achieved the first ever identification of a signal peptide in the circulation (B-type Natriuretic Peptide signal peptide (BNP-SP)) and show that it has potential to specifically and rapidly identify cardiac ischemia. We will measure serial BNP-SP concentrations in patients with clear documented myocardial infarction. This research has the potential to speed up diagnosis and ultimately improve outcomes for patients with acute coronary events. 50 patients presenting to the coronary care unit of Christchurch Hospital with typical chest pains (=4 hours from onset), clear evidence of ST-elevation on ECG together with a rise and fall of plasma troponin levels will be studied. Venous blood samples will be drawn at baseline (0), 0.5, 1, 2, 4, 8, 12, 24, 48 and 72 hours. For each blood sample, we will also measure standard plasma biomarkers of myocardial injury.

Interventions

We will measure serial BNP-SP concentrations in patients admitted to hospital within 4 hours of symptom onset and with clear documented myocardial infarction to determine if temporal plasma concentrations of BNP-Signal Peptide (BNP-SP) achieve peak values within 1-3 hours of onset of infarction. Blood samples will be collected at 0, 0.5, 1. 2. 4, 8, 12, 24, 48 and 72 hours post admission. The study will continue until recruitment and blood sampling is complete for 50 people with acute myocardi

We will measure serial BNP-SP concentrations in patients admitted to hospital within 4 hours of symptom onset and with clear documented myocardial infarction to determine if temporal plasma concentrations of BNP-Signal Peptide (BNP-SP) achieve peak values within 1-3 hours of onset of infarction. Blood samples will be collected at 0, 0.5, 1. 2. 4, 8, 12, 24, 48 and 72 hours post admission. The study will continue until recruitment and blood sampling is complete for 50 people with acute myocardial infarction, 10 with chronic renal failure on maintenance haemodialysis, 5 patients with hypothyroidism, 5 patients with thyrotoxicosis and 10 patients presenting to the emergency department with acute heart failure not secondary to Acute Myocardial Infarction.

Sponsors

Health Research Council of New Zealand
Lead SponsorGovernment body

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

50 males or females 18 years of age or older Admitted to the coronary care unit of Christchurch Hospital with typical chest pains (<4 hours from onset), clear evidence of "ST" segment elevation on Electrocardiograph together with a rise and fall of plasma Troponin levels and 10 patients with chronic renal failure on maintenance haemodialysis 5 patients with hypothyroidism and 5 patients with thyrotoxicosis 10 patients presenting to the emergency department with acute heart failure not secondary to Acute Myocardial Infarction

Exclusion criteria

Unable to give informed consent Unable to comply with study requirements

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 31, 2026