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Cardiac metabolic imaging
Dr.Vishnukumar R, MD Nuclear Medicine
Jawaharlal Institute of Post graduate Medical Education and Research
(JIPMER),
Puducherry, India.
Learning objectives
• Various substrates utilized for cardiac
metabolism in different suituations.
• Clinical relevance of metabolism
• Tracers available
• Clinical application.
Overview of cardiac metabolism
Glycolysis
Pyruvate
Acetyl-Co-A
Kerbs cycle and ETC
(Co2 and H20)
Lactate
Fatty acid
If less or
absent O2
O2ispresent
Glucose
S.NO METABOLIC STATE SUBSTRATE USED
1 FASTING FATTY ACIDS
2 FED STATE GLUCOSE
3 EXERCISE FATTY ACID
4 STARVATION KETONE BODIES
• Pyruvate, lactate, amino acids are also utilized.
• Substrate utilization depends on metabolic state, relative
concentration in blood, insulin levels, catecholamine
levels and oxygen.
Clinical relevance
• Hibernating tissue- substrate is Glucose (GLUT-4)
• Myocardial ischemic memory
– Decreased oxidative metabolism
– Decreased fatty acid metabolism
– Activation of GLUT-1
• Cardiomyopathy and heart failure
– Decreased expression of PPAR-α
– Decreased fatty acid uptake, oxidation and storage.
– Over dependance on glucose metabolism
– Early increase in glucose metabolism followed by late
decline.
Tracers available
• Carbohydrate metabolism
F-18 FDG
C-11 Glucose
C-11 Lactate
• Fatty acid metabolism
C-11 Palmitate
F-18 FTHA
F-18 flurothiapalmitate
• Myocardial oxygen consumption
O-15 water
C-11 acetate
Clinical applications
• Myocardial viability assessment
• Hot spot imaging for ischemia
• Heart failure
Myocardial viability
• Principle: Resting glucose utilization (GLUT-4)
• FDG injected after glucose load (oral or intravenous)
• Oral glucose:
– Administer 25-50g of glucose orally
– Measure BG at 45-60 mins
– Administer FDG when BG is between 100 and 140 mg/dl.
Prime
FBG < 140mg/dl- 6U RI
FBG > 140mg/dl- 10U RI
Mix 100 U regular insulin in
500ml of NS
Infuse @
1.2ml/kg/hr
When BG <140 mg/dl start 20D @1.8ml/kg/hr
Maintain BG at
80 to 140 mg/dl
for 30 minutes
Inject FDG and scan after
40-60 mins
Maintain infusion for 30-40
mins or till end of the
study
• Findings
– Metabolic perfusion mismatch (hibernating
myocardium)
– Normal perfusion and normal metabolism (normal
myocardium, stunned myocardium)
– Perfusion and metabolism match (scar)
– Reverse mismatch pattern (non ischemic
cardiomyopathy, diabetes)
Hot spot imaging for ischemia
• Principle: Myocardial ischemic memory
• Patient will be made to fast for 12 hours, then
subjected to stress. FDG will be injected at
peak stress.
• Findings:
– Ischemic myocardium preferentially utilizes
glucose.
– Increased FDG uptake is seen in the areas of
ischemia.
Take home points
• Fasting- fatty acids; fed- glucose; exercise-
fatty acids
• Ischemic myocyte- increased glucose
utilization at exercise.
• Hibernating myocardium- resting utilization of
glucose.
• Heart failure- early increase in glucose
followed by decline in late stages; decrease in
fatty acid metabolism.
Cardiac metabolic imaging

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Cardiac metabolic imaging

  • 1. Cardiac metabolic imaging Dr.Vishnukumar R, MD Nuclear Medicine Jawaharlal Institute of Post graduate Medical Education and Research (JIPMER), Puducherry, India.
  • 2. Learning objectives • Various substrates utilized for cardiac metabolism in different suituations. • Clinical relevance of metabolism • Tracers available • Clinical application.
  • 3. Overview of cardiac metabolism
  • 4. Glycolysis Pyruvate Acetyl-Co-A Kerbs cycle and ETC (Co2 and H20) Lactate Fatty acid If less or absent O2 O2ispresent Glucose
  • 5. S.NO METABOLIC STATE SUBSTRATE USED 1 FASTING FATTY ACIDS 2 FED STATE GLUCOSE 3 EXERCISE FATTY ACID 4 STARVATION KETONE BODIES • Pyruvate, lactate, amino acids are also utilized. • Substrate utilization depends on metabolic state, relative concentration in blood, insulin levels, catecholamine levels and oxygen.
  • 6. Clinical relevance • Hibernating tissue- substrate is Glucose (GLUT-4) • Myocardial ischemic memory – Decreased oxidative metabolism – Decreased fatty acid metabolism – Activation of GLUT-1 • Cardiomyopathy and heart failure – Decreased expression of PPAR-α – Decreased fatty acid uptake, oxidation and storage. – Over dependance on glucose metabolism – Early increase in glucose metabolism followed by late decline.
  • 7. Tracers available • Carbohydrate metabolism F-18 FDG C-11 Glucose C-11 Lactate • Fatty acid metabolism C-11 Palmitate F-18 FTHA F-18 flurothiapalmitate • Myocardial oxygen consumption O-15 water C-11 acetate
  • 8. Clinical applications • Myocardial viability assessment • Hot spot imaging for ischemia • Heart failure
  • 9. Myocardial viability • Principle: Resting glucose utilization (GLUT-4) • FDG injected after glucose load (oral or intravenous) • Oral glucose: – Administer 25-50g of glucose orally – Measure BG at 45-60 mins – Administer FDG when BG is between 100 and 140 mg/dl.
  • 10. Prime FBG < 140mg/dl- 6U RI FBG > 140mg/dl- 10U RI Mix 100 U regular insulin in 500ml of NS Infuse @ 1.2ml/kg/hr When BG <140 mg/dl start 20D @1.8ml/kg/hr Maintain BG at 80 to 140 mg/dl for 30 minutes Inject FDG and scan after 40-60 mins Maintain infusion for 30-40 mins or till end of the study
  • 11.
  • 12. • Findings – Metabolic perfusion mismatch (hibernating myocardium) – Normal perfusion and normal metabolism (normal myocardium, stunned myocardium) – Perfusion and metabolism match (scar) – Reverse mismatch pattern (non ischemic cardiomyopathy, diabetes)
  • 13.
  • 14. Hot spot imaging for ischemia • Principle: Myocardial ischemic memory • Patient will be made to fast for 12 hours, then subjected to stress. FDG will be injected at peak stress. • Findings: – Ischemic myocardium preferentially utilizes glucose. – Increased FDG uptake is seen in the areas of ischemia.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19. Take home points • Fasting- fatty acids; fed- glucose; exercise- fatty acids • Ischemic myocyte- increased glucose utilization at exercise. • Hibernating myocardium- resting utilization of glucose. • Heart failure- early increase in glucose followed by decline in late stages; decrease in fatty acid metabolism.