CARDIOVASCULAR JOURNAL OF AFRICA • Volume 26, No 6, November/December 2015
204
AFRICA
Cardiovascular Topics
Comparison of a qualitative measurement of heart-type
fatty acid-binding protein with other cardiac markers as
an early diagnostic marker in the diagnosis of non-ST-
segment elevation myocardial infarction
Demet Menek
ş
e Gerede, Sadi Güleç, Mustafa Kılıçkap, Cansın Tulunay Kaya, Veysel Kutay Vurgun,
Özgür Ula
ş
Özcan, Hüseyin Göksülük, Çetin Erol
Abstract
Objective:
Heart-type fatty acid-binding protein (H-FABP)
is a novel cardiac marker used in the early diagnosis of acute
myocardial infarction (AMI), which shows myocyte injury.
Our study aimed to compare bedside H-FABP measurements
with routine creatine kinase-MB (CK-MB) and troponin I
(TnI) tests for the early diagnosis of non-ST-elevation MI
(NSTEMI), as well as for determining its exclusion capacity.
Methods:
A total of 48 patients admitted to the emergency
room within the first 12 hours of onset of ischaemic-type
chest pain lasting more than 30 minutes and who did not have
ST-segment elevation on electrocardiography (ECG) were
included in the study. Definite diagnoses of NSTEMI were
made in 24 patients as a result of 24-hour follow up, and the
remaining 24 patients did not develop MI.
Results:
When various subgroups were analysed according to
admission times, H-FABP was found to be a better diagnostic
marker compared to CK-MB and TnI (accuracy index 85%),
with a high sensitivity (79%) and specificity (93%) for early
diagnosis (
≤
six hours). The respective sensitivities of bedside
H-FABP and TnI tests were 89 vs 33% (
p
<
0.05) for patients
presenting within three hours of onset of symptoms.
Conclusion:
Bedside H-FABP measurements may contribute
to correct early diagnoses, as its levels are elevated soon
following MI, and measurement is easy, with a rapid result.
Keywords:
acute coronary syndrome, non-ST-elevation myocar-
dial infarction, H-FABP, CK-MB, troponin
Submitted 26/11/14, accepted 16/3/15
Published online 14/7/15
Cardiovasc J Afr
2015;
26
: 204–209
www.cvja.co.zaDOI: 10.5830/CVJA-2015-028
Acute coronary syndrome (ACS) defines the clinical conditions
that develop as a result of an abrupt reduction in coronary
blood flow. Unstable angina pectoris (UAP), ST-elevation
acute myocardial infarction (STEMI), and non-ST-elevation
acute myocardial infarction (NSTEMI) are points on this
clinical spectrum. All these clinical syndromes should be rapidly
diagnosed and treated.
1,2
Chest pain contributes to 50% of emergency room admissions
and approximately 25% of these patients are hospitalised.
3
Patients with ACS are usually admitted with chest pain. Studies
have shown that the final diagnoses of patients admitted with
chest pain are acute myocardial infarction (AMI) in one-third
of patients, UAP in one-third, and non-cardiac chest pain in
one-third.
4
Early diagnosis of acute chest pain is especially important
and difficult in patients without persistent ST-segment elevation.
Electrocardiography (ECG) is a valuable and commonly used
test for the detection of ACS. The initial ECG is normal
or non-diagnostic in 50% of patients with ACS.
5
STEMI is
readily diagnosed with culprit ECG findings but NSTEMI/
UAP diagnoses are more challenging. Inadequate and delayed
diagnoses may lead to inappropriate treatment and delays in the
initiation of life-saving therapy.
Diagnostic criteriaof AMIwere reformedafter the introduction
of more sensitive and specific markers for cardiac injury (cardiac
troponins, CK-MB mass) and after a better understanding of
the diagnostic and prognostic importance of these markers. In
the 2012 report of the European Society of Cardiology (ESC)/
American College of Cardiology (ACC), the essential criterion
for MI was defined as elevated cardiac markers.
6
Heart-type fatty acid-binding protein (H-FABP) is a recently
discovered cardiac biomarker. It is specific to cardiomyocytes
and low-molecular weight (15 kDa) cytosolic proteins, which
represent five to 15% of the cytosolic proteins of cardiac
myocytes.
7
H-FABP plays an important role in intracellular
transport for
β
-oxidation of fatty acids in the mitochondria.
8,9
Department of Cardiology, Ankara University School of
Medicine, Ankara, Turkey
Demet Menek
ş
e Gerede, MD,
drmeneksegerede@yahoo.comSadi Güleç, MD
Mustafa Kılıçkap, MD
Cansın Tulunay Kaya, MD
Veysel Kutay Vurgun, MD
Özgür Ula
ş
Özcan, MD
Hüseyin Göksülük, MD
Çetin Erol, MD