Prognostic Implication of High Sensitivity C-Reactive Protein in Acute Coronary Syndrome Patients
Prognostic Implication of High Sensitivity C-Reactive Protein in Acute Coronary Syndrome Patients
Prognostic Implication of High Sensitivity C-Reactive Protein in Acute Coronary Syndrome Patients
11(03), 236-244
Article DOI:10.21474/IJAR01/16413
DOI URL: http://dx.doi.org/10.21474/IJAR01/16413
RESEARCH ARTICLE
PROGNOSTIC IMPLICATION OF HIGH SENSITIVITY C-REACTIVE PROTEIN IN ACUTE
CORONARY SYNDROME PATIENTS
A scientific statement issued by Centre for Disease Control (CDC) and American Heart Asso-ciation (AHA) has
mentioned hs-CRP as the only inflammatory marker that can be used for risk prediction both for primary and
secondary prevention of cardiovascular events.[2]
CRP has become the most effective and sensitive marker for inflammation and unremarkable predictor of
cardiovascular risk.CRP’s predictive power for vascular risk detection resides between 0.1 to 0.5 mg/dl, a level
which is present in most of the healthy individuals without inflammation. Hence, a high sensitive assay is required
which has very low detection values.[3].
Methodology:-
An observational cross sectional study was carried out for one year at the department of Medicine in SMBT medical
college,Igatpuri.The study comprised of a total of 48 patients above 18 yrs of age with confirmed acute coronary
syndrome.The ethical and scientific committee approval was taken.After taking informed consent,detailed history
was taken from the patients or relatives.The technique and risks of the procedure were discussed with all the
patients.
The blood sample of patients was collected on admission and levels of hs-CRP was evaluated as follows,
According to American Heart Association and Centres for Disease control and prevention states that,
Hs- CRP - risk
Less than 1 - lower vascular risk
1 to 3 - moderate vascular risk
More than 3 - higher vascular risk
Inclusion Criteria
1.All consecutive patients with ACS including unstable angina(UA) ,non-ST elevation myocardial
infarction(NSTEMI) and ST elevation myocardial infarction(STEMI) were included in the study.
2.Patients above the age of 18 years.
Exclusion Criteria
1.Patients not willing for consent.
2.Patients with stable coronary artery
3.Patients with ischemic stroke.
4.Patients with valvular heart disease.
5.Patients with acute or chronic kidney disease.
6.Patients with acute or chronic liver disease.
7.Collagen vascular disease and rheumatological disorders.
8.Febrile disorders.
9.Malignancy.
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Results:-
Out of the 48 acute coronary syndrome patients; 36 patients were diagnosed as ST elevation MI (STEMI) and 12
patients as non ST elevation MI (NSTEMI). Out of 36 STEMI patients; 20 patients were males and 16 patients were
females. Out of 12 NSTEMI patients; 6 patients were males and 6 patients were females.
In male patients with STEMI, the mean of peak value of Hs-CRP measured between 36-48 hours was 1.03 mg/dl. In
female patients with STEMI, the mean of peak value of Hs-CRP measured between 36-48 hours was 1.37 mg/dl.
In male patients with NSTEMI, the mean of peak value of Hs-CRP measured between 36-48 hours was 0.99 mg/dl.
In female patients with NSTEMI, the mean of peak value of Hs-CRP measured between 36-48 hours was 0.95
mg/dl.
Among male patients with STEMI; 85% of patients had modifiable risk factor of smoking, alcohol and non-
modifiable risk factor of Diabetes mellitus or Systemic Hypertension and 15% of patients had no associated risk
factor.
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Among female patients with STEMI; 81% of patients had risk factor of Diabetes mellitus or Systemic Hypertension
and 19% of patients had no associated risk factor.
Among male patients with NSTEMI; 83% of patients had modifiable risk factor of smoking, alcoholic and non-
modifiable risk factor of Diabetes mellitus or Systemic Hypertension and 17% of patients had no associated risk
factor.
Among female patients with NSTEMI; 60% of patients had non-modifiable risk factor of Diabetes mellitus or
Systemic Hypertension and 40% of patients had no associated risk factor.
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Among STEMI patients, the highest level of peak value of Hs-CRP is seen in extensive AWMI with a mean value of
1.77mg/dl and 1.29mg/dl for females and males, respectively. Among NSTEMI patients, the mean values (peak) Hs-
CRP are 0.99 and 0.950 for males and females, respectively.
The mean of baseline values of Hs-CRP for anterior wall myocardial infarction (AWMI), extensive AWMI, inferior
wall myocardial infarction (IWMI), antero-septal myocardial infarction (ASMI) and combined IWMI/PWMI
(posterior wall myocardial infarction) were found to be 0.480 mg/dl, 0.825 mg/dl, 0.375 mg/dl, 0.685 mg/dl and
0.404 mg/dl, respectively in our study. So the highest baseline level of Hs-CRP was recorded for patients with
extensive AWMI (0.825mg/dl).
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In patients with STEMI; 8% of patients had normal EF; 25% of patients had moderate EF; 50% of patients had low
EF and 17% of patients had very low Ejection fraction.
In patients with NSTEMI; 9% of patients had normal EF; 83% of patients had moderate EF; 8% of patients had low
EF and no patients had very low Ejection fraction.
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The correlation coefficient of peak values of Hs- CRP (36-48 hrs) to ejection fraction in STEMI and NSTEMI cases
are -0.65 and -0.54.
There is a statistically significant correlation between peak values of Hs- CRP (36-48 hrs) to ejection fraction in
STEMI patients with a p value of 0.006.
Among NSTEMI cases, the correlation between baseline and peak values of Hs-CRP and ejection fraction is
statistically insignificant with p-value of 0.5 and 0.07, respectively.
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Discussion:-
1. Out of the 48 acute coronary syndrome patients who participated in our study; 36 patients were diagnosed as ST
elevation MI (STEMI) and 12 patients as non ST elevation MI (NSTEMI). Out of 36 STEMI patients; 20
patients were males and 16 patients were females. Out of 12 NSTEMI patients; 6 patients were males and 6
patients were females.
2. Among male patients with STEMI; 85% of patients had risk factor of smoking, alcohol, Diabetes mellitus or
Systemic Hypertension and 15% of patients had no associated risk factor. Among female patients with STEMI;
81% of patients had risk factor of Diabetes mellitus or Systemic Hypertension and 15% of patients had no
associated risk factor.
3. Among male patients with NSTEMI; 83% of patients had risk factor of smoking, alcoholic, Diabetes mellitus or
Systemic Hypertension and 17% of patients had no associated risk factor. Among female patients with
NSTEMI; 60% of patients had risk factor of Diabetes mellitus or Systemic Hypertension and 40% of patients
had no associated risk factor.
4. In our study, in STEMI cases the mean value of Hs-CRP measured within 6 hours (baseline value) was 0.52
mg/dl and the mean of peak value measured between 36-48 hours was 1.82 mg/dl. In NSTEMI cases, the mean
value of Hs-CRP measured within 6 hours (baseline value)) and the mean of peak value of Hs-CRP (measured
between 36-48 hours) were 0.29 mg/dl and 0.97 mg/dl, respectively. For the controls, the mean value of Hs-
CRP for males was 0.12 mg/dl and for females it was 0.19mg/dl. (Normal range of Hs-CRP <0.2mg/dl)
5. The mean of peak values of Hs-CRP in males for anterior wall myocardial infarction (AWMI), extensive
AWMI, inferior wall myocardial infarction (IWMI), antero-septal myocardial infarction (ASMI) and combined
IWMI/PWMI (posterior wall myocardial infarction) were found to be 1.12 mg/dl, 1.29 mg/dl, 0.94 mg/dl, 0.96
mg/dl and 0.96 mg/dl, respectively in our study. So, for males the highest level of Hs-CRP was recorded for
patients with extensive AWMI (1.29mg/dl).
6. In females, the mean of peak value of Hs-CRP with anterior wall myocardial infarction (AWMI), extensive
AWMI, inferior wall myocardial infarction (IWMI), antero-septal myocardial infarction ASMI and combined
IWMI (inferior wall myocardial infarction)/PWMI (posterior wall myocardial infarction) was found to be 1.38
mg/dl, 1.77 mg/dl, 1.37 mg/dl, 1.34 mg/dl and 1.20 mg/dl, respectively. The highest level of Hs-CRP was
recorded for patients with extensive AWMI (1.77mg/dl) among females also.
7. In patients with STEMI; 8% of patients had normal EF; 25% of patients had moderate EF; 50% of patients had
low EF and 17% of patients had very low EF. In patients with NSTEMI; 9% of patients had normal EF; 83% of
patients had moderate EF; 8% of patients had low EF and no patients had very low EF.
8. Higher values of baseline and peak values of Hs-CRP were seen in patients who had ST – elevation MI
(STEMI) than in Non ST – elevation MI (NSTEMI).
9. The patients with higher peak values of Hs-CRP had a poor Ejection fraction and the association between them
was statistically significant in our study.
Conclusion:-
1. The levels of Hs-CRP correlate with several cardiovascular risk factors such as smoking,diabetes mellitus and
hypertension.
2. Higher level of baseline Hs-CRP along with extensive myocardial infarction in the Electrocardiogram is
associated with a extensive myocardial infarction.
3. Elevated levels of Hs-CRP is related to the presence of plaque rupture ,which provokes acute coronary
syndrome.Therefore, in a resource limited country like India, evaluation of Hs-CRP would be considered as a
modality where optical coherence tomography and coronary intravascular ultrasound is not available.
4. So, the assessment of Hs-CRP levels may enable the physician in detecting the severity of acute coronary
syndrome patients and in planning a more prompt and effective reperfusion therapy.
References:-
1.Harrison’s principles of internal medicine
2. Relationship of high-sensitive C-reactive protein withcardiovascular risk factors, clinical presentation
andangiographic profile in patients with acute coronarysyndrome: An Indian perspective;IntJCardiol. 2010 Dec
3;145:553
3. Evaluation of hs-CRP levels in acute coronary syndromes; R. S. PushpaKumari, Priya John, V. A. Vipula.
Evaluation of hs-CRP levels in acute coronary syndromes. IAIM, 2016;3(6): 77-81
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4. Relationship between coronary arterial remodeling, fibrous cap thickness and high-sensitivity C-reactive protein
levels in patients with acute coronary syndrome ;Circ J .2009 Jul;73(7):1291-5. doi: 10.1253/circj.cj-08-0968. Epub
2009 May 12.
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