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Cardiac function
test
By : zalak , jemisha , namrta , priyanka ,
kalyani , dipika
Introduction
o Cardiac function tests used to determine
whether there has been any cardiac tissue
damage.
o This tests performed to help diagnose a
cardiac disease.
o Myocardial infarction
o Coronary artery disease
o Atherosclerosis
Cardiac function tests include
1. CK (Creatine kinase)
2. CK-MB
3. LDH (Lactate Dehydrogenase)
4. SGOT
5. Troponin
6. Myoglobin
7. Lipid Profile :
1. Cholesterol
2. Triglyceride
3. HDL-cholesterol
4. LDL-cholesterol
5. VLDL-cholesterol
8. LDL/HDL ratio
9. LDL/Total cholesterol
10. Apolipoprotein – A1
11. Apolipoprotein - B
1. CK (CREATINE KINASE)
Principle:
Method : Increasing Kinetic
Biological reference range :- 25-120 U/L
Clinical Significance:
 CPK ( Creatine phosphokinase ) activity is
increase in
 Brain (CK-BB = 1%)
 Cerebro-vascular stroke
 heart muscle (CK-MB = 5-10%)
 Myocardial infarction
 Acute coroary syndrome
 skeletal muscle. (CK-MM= 85%)
 Crush injury
 Myopathy
 Polymyositis
2. CK-MB
Principle:
 measurement of CK activity in the presence of an
antibody to CK-M monomer.
 This antibody completely inhibits the activity of CK-MM
& half of the activity of CK-MB while not affecting the B
subunit activity of CK-MB &CK-BB.
Method :
• Increasing Kinetic UV method
Biological reference range :-0 - 25 IU/L
Significance:
• CK-MB present only in cardiac tissue
• So…Specific for diagnosis of cardiac
disease
CK-2 & CK-3 in normal subject &
After 24 hours of Myocardial Infarction
Creatine Kinase isoenzymes in blood
3. LDH (lactate dehydrogenase)
Principle:
 Lactate dehydrogenase catalyses the conversion of
pyruvate to lactate.
Lactate dehydrogenase
Lactate + NAD+ ---------------- Pyruvate + NADH + H+
The rate of NADH+ formation is measured by 340nm
filter.
It is direactly propotional to serum LDH activity.
Method :
• IFCC method (Lactate to Pyruvate method )
• Increasing kinetic
Biological reference range :- 70-240 IU/L
Clinical significance :
 RBC
 Malaria
 Sickle cell anemia
 hemolytic disorder
 Liver
 Viral Hepatitis
 Liver malgnancy
 Alcoholic liver disease
 Cardiac tissue
 Myocardial infarction
 Skeletal muscle
 Muscular distrophy
 Crush injury
LDH Iso-enzyme
4. GOT ( AST )
Principle:
L-Aspartate+α Ketoglutarate
GOT(with P5P)
Oxaloacetate + LGlutamate
Oxaloacetate + NADH + H+
MDH
Malate + NAD+
AST = Aspartate Transaminase
GOT = Glutamic Oxalate Transaminase
The rate of NADH to NAD is measured as a decrease in absorbance at 340
nm.
 Method:
 IFCC method with / without Pyridoxal 5 phosphate
(P5P)
 Decrease UV - kinetic
 Biological reference range:
 15 – 45 IU/L
 Clinical significance:
1. Acute hepatocellular damage
2. Myocardial infarction
3. Congestive heart failure.
4. Biliary tract obstruction
5. Cholicyctisis
5. Cardiac Troponin – I &
Cardiac Troponin - T
 The troponin complex consists of 3 components;
 Troponin C(calcium binding)
 Troponin I(actomysin ATPase inhibitary element)
 Troponin T(tropomyosin binding element).
 Measured by
 ELISA or RIA techniques.
 Immunoturbidometry
 Immuno-diffusion method
 Serum level of troponin T increases within 6 hrs of
myocardial infarction.
 Troponin I is released into the blood within 4 hrs after
the onset of cardiac symtoms.
Biological reference range:-
Troponin I : 0.04 – 40 ng/ml.
Troponin T : 0.01 – 25 ng/ml.
Significance:
For diagnosis of myocardial damage.
 Most sensitive
 Specific test
 Early detectable.
 It used mainly in the diagnosis of chest-pain
patients when ECG is normal.
Cardiac Marker
Cardiac Marker
Plasma Enzymes Changes
After Myocardial Infarction
6. myoglobin
 O2 binding protein in skeletal and cardiac muscles
 Released mailnly from skeletal muscle damaged
tissues.
 Its level rises more rapidly than C-troponin and CK-
MB.
Principle:
 RIA (Radio-Immuno Assay )
 ELISA (Enzyme Link Immuno-Sorbant Assay)
 Chemiluminescence.
Biological reference range:-
25 – 72 ng/ml
Significance:
• Major skeletal muscular injury
• Crush injury
• Burns
7. Lipid profile:
1. Total Cholesterol
2. Triglyceride
3. HDL-cholesterol ( High Density Lipoprotein )
4. LDL-cholesterol ( Low Density Lipoprotein )
5. VLDL-cholesterol ( Very Low Density Liporotein )
 Cholesterol
Principle:
 Absorbance of quinoneimine dye is measured at
500nm.
Method:
• Enzymatic method
Biological reference range:-
Less than 199 mg /dL (Normal)
200 – 239 mg/dl (borderline)
More than 240 mg/dl (high)
Clinical significance : -
Increase cholesterol suggestive of increase probability of
following
• Atherosclerosis
• Coronary artery disease
• Ischemic heart disease
• Cerebro-Vascular Stroke
• Hypertension
• Xanthoma
Decrease cholesterol suggestive of increase probability of
following
• Depression
 Triglyceride
Principle:
 Absorption of quinoneimine dye (red color) is
measured at 510nm.
Method :
 GPO – POD Method
 End point method
Biological reference range:-
<150mg/dl
Clinical significance:
• 150 to 400 mg/dl is consider borderline
hypertriglyceridemia.
• More than 400 mg/dl only, increase risk of
pancreatitis
HDL , LDL , VLDL
 HDL(High Density Lipoprotine)
Principle:
 Precipitates of all lipoprotein other than HDL (LDL
& VLDL lipoproteins)
 Precipitation done by
 Dextran Sulfate
 phosphotungsate acid
 Polyethyl glycol
 HDL left in the supernatant is tested using
cholesterol assay.
Method: Precipitation reaction
Biological reference range :- 40-60 mg/dl
HDL less than 40mg/dl means high risk of heart
disease.
Significance:
 HDL transport cholesterol from peripheral tissues
to liver by reverse cholesterol transport.
 HDL also helps in the removal of macrophages
from the arterial walls.
 LDL(Low Density Lipoprotien)
Principle:
 Direct method: (selective precipitation)
 Indirect method: (fridewald equation)
LDL = [Total Cholesterol – HDL] – Plasma TG
(mg/dl)
5
Biological reference range:- 130-160 mg/dl
LDL more than 160mg/dl means high risk of heart
disease.
Significance:
 LDL tarnsport cholesterol from liver to peripheral
cells.
 VLDL(very low density
lipoprotien)
Friedewald’s equation:
VLDL = Triglyceride/5 (mg/dl)
Limitation :
Can not useful in case of TG > 400 mg%
Biological reference range:- 2-30 mg/dl
Ratio of Cholesterol
DETERMINATION OF
APOLIPOPROTIEN- A1 & B
METHOD:- Turbidimetric immunoassays (TIA)
PRINCIPLE:-
 An insoluble TIA is formed by the reaction
between the apo A-I antigen in human serum &
the specific antibody in the antibody reagent. By
using the activactor reagent,maximum exposure
of antigenic sites achieved.
 The turbidity is measured at 340nm.
Biological reference range:-
 Apolipoprotein A:-
 More than 50mg/dl is desirable.
Apolipoprotein B:-
 less than 80mg/dl is desirable.

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cardiac_function_test_2018.ppt

  • 1. Cardiac function test By : zalak , jemisha , namrta , priyanka , kalyani , dipika
  • 2. Introduction o Cardiac function tests used to determine whether there has been any cardiac tissue damage. o This tests performed to help diagnose a cardiac disease. o Myocardial infarction o Coronary artery disease o Atherosclerosis
  • 3. Cardiac function tests include 1. CK (Creatine kinase) 2. CK-MB 3. LDH (Lactate Dehydrogenase) 4. SGOT 5. Troponin 6. Myoglobin 7. Lipid Profile : 1. Cholesterol 2. Triglyceride 3. HDL-cholesterol 4. LDL-cholesterol 5. VLDL-cholesterol 8. LDL/HDL ratio 9. LDL/Total cholesterol 10. Apolipoprotein – A1 11. Apolipoprotein - B
  • 4. 1. CK (CREATINE KINASE) Principle:
  • 5. Method : Increasing Kinetic Biological reference range :- 25-120 U/L Clinical Significance:  CPK ( Creatine phosphokinase ) activity is increase in  Brain (CK-BB = 1%)  Cerebro-vascular stroke  heart muscle (CK-MB = 5-10%)  Myocardial infarction  Acute coroary syndrome  skeletal muscle. (CK-MM= 85%)  Crush injury  Myopathy  Polymyositis
  • 6. 2. CK-MB Principle:  measurement of CK activity in the presence of an antibody to CK-M monomer.  This antibody completely inhibits the activity of CK-MM & half of the activity of CK-MB while not affecting the B subunit activity of CK-MB &CK-BB. Method : • Increasing Kinetic UV method
  • 7. Biological reference range :-0 - 25 IU/L Significance: • CK-MB present only in cardiac tissue • So…Specific for diagnosis of cardiac disease
  • 8.
  • 9. CK-2 & CK-3 in normal subject & After 24 hours of Myocardial Infarction Creatine Kinase isoenzymes in blood
  • 10. 3. LDH (lactate dehydrogenase) Principle:  Lactate dehydrogenase catalyses the conversion of pyruvate to lactate. Lactate dehydrogenase Lactate + NAD+ ---------------- Pyruvate + NADH + H+ The rate of NADH+ formation is measured by 340nm filter. It is direactly propotional to serum LDH activity.
  • 11. Method : • IFCC method (Lactate to Pyruvate method ) • Increasing kinetic Biological reference range :- 70-240 IU/L Clinical significance :  RBC  Malaria  Sickle cell anemia  hemolytic disorder  Liver  Viral Hepatitis  Liver malgnancy  Alcoholic liver disease  Cardiac tissue  Myocardial infarction  Skeletal muscle  Muscular distrophy  Crush injury
  • 13. 4. GOT ( AST ) Principle: L-Aspartate+α Ketoglutarate GOT(with P5P) Oxaloacetate + LGlutamate Oxaloacetate + NADH + H+ MDH Malate + NAD+ AST = Aspartate Transaminase GOT = Glutamic Oxalate Transaminase The rate of NADH to NAD is measured as a decrease in absorbance at 340 nm.  Method:  IFCC method with / without Pyridoxal 5 phosphate (P5P)  Decrease UV - kinetic
  • 14.  Biological reference range:  15 – 45 IU/L  Clinical significance: 1. Acute hepatocellular damage 2. Myocardial infarction 3. Congestive heart failure. 4. Biliary tract obstruction 5. Cholicyctisis
  • 15. 5. Cardiac Troponin – I & Cardiac Troponin - T  The troponin complex consists of 3 components;  Troponin C(calcium binding)  Troponin I(actomysin ATPase inhibitary element)  Troponin T(tropomyosin binding element).  Measured by  ELISA or RIA techniques.  Immunoturbidometry  Immuno-diffusion method  Serum level of troponin T increases within 6 hrs of myocardial infarction.  Troponin I is released into the blood within 4 hrs after the onset of cardiac symtoms.
  • 16. Biological reference range:- Troponin I : 0.04 – 40 ng/ml. Troponin T : 0.01 – 25 ng/ml. Significance: For diagnosis of myocardial damage.  Most sensitive  Specific test  Early detectable.  It used mainly in the diagnosis of chest-pain patients when ECG is normal.
  • 18. Cardiac Marker Plasma Enzymes Changes After Myocardial Infarction
  • 19. 6. myoglobin  O2 binding protein in skeletal and cardiac muscles  Released mailnly from skeletal muscle damaged tissues.  Its level rises more rapidly than C-troponin and CK- MB. Principle:  RIA (Radio-Immuno Assay )  ELISA (Enzyme Link Immuno-Sorbant Assay)  Chemiluminescence.
  • 20. Biological reference range:- 25 – 72 ng/ml Significance: • Major skeletal muscular injury • Crush injury • Burns
  • 21. 7. Lipid profile: 1. Total Cholesterol 2. Triglyceride 3. HDL-cholesterol ( High Density Lipoprotein ) 4. LDL-cholesterol ( Low Density Lipoprotein ) 5. VLDL-cholesterol ( Very Low Density Liporotein )
  • 22.  Cholesterol Principle:  Absorbance of quinoneimine dye is measured at 500nm. Method: • Enzymatic method
  • 23. Biological reference range:- Less than 199 mg /dL (Normal) 200 – 239 mg/dl (borderline) More than 240 mg/dl (high) Clinical significance : - Increase cholesterol suggestive of increase probability of following • Atherosclerosis • Coronary artery disease • Ischemic heart disease • Cerebro-Vascular Stroke • Hypertension • Xanthoma Decrease cholesterol suggestive of increase probability of following • Depression
  • 24.  Triglyceride Principle:  Absorption of quinoneimine dye (red color) is measured at 510nm. Method :  GPO – POD Method  End point method
  • 25. Biological reference range:- <150mg/dl Clinical significance: • 150 to 400 mg/dl is consider borderline hypertriglyceridemia. • More than 400 mg/dl only, increase risk of pancreatitis
  • 26. HDL , LDL , VLDL
  • 27.  HDL(High Density Lipoprotine) Principle:  Precipitates of all lipoprotein other than HDL (LDL & VLDL lipoproteins)  Precipitation done by  Dextran Sulfate  phosphotungsate acid  Polyethyl glycol  HDL left in the supernatant is tested using cholesterol assay. Method: Precipitation reaction
  • 28. Biological reference range :- 40-60 mg/dl HDL less than 40mg/dl means high risk of heart disease. Significance:  HDL transport cholesterol from peripheral tissues to liver by reverse cholesterol transport.  HDL also helps in the removal of macrophages from the arterial walls.
  • 29.  LDL(Low Density Lipoprotien) Principle:  Direct method: (selective precipitation)  Indirect method: (fridewald equation) LDL = [Total Cholesterol – HDL] – Plasma TG (mg/dl) 5
  • 30. Biological reference range:- 130-160 mg/dl LDL more than 160mg/dl means high risk of heart disease. Significance:  LDL tarnsport cholesterol from liver to peripheral cells.
  • 31.  VLDL(very low density lipoprotien) Friedewald’s equation: VLDL = Triglyceride/5 (mg/dl) Limitation : Can not useful in case of TG > 400 mg% Biological reference range:- 2-30 mg/dl
  • 32.
  • 34. DETERMINATION OF APOLIPOPROTIEN- A1 & B METHOD:- Turbidimetric immunoassays (TIA) PRINCIPLE:-  An insoluble TIA is formed by the reaction between the apo A-I antigen in human serum & the specific antibody in the antibody reagent. By using the activactor reagent,maximum exposure of antigenic sites achieved.  The turbidity is measured at 340nm.
  • 35. Biological reference range:-  Apolipoprotein A:-  More than 50mg/dl is desirable. Apolipoprotein B:-  less than 80mg/dl is desirable.