Relationship between regional 18F-fluorodeoxyglucose and 13N ammonia uptake in normal myocardium assessed by positron emission tomography: Patterns of mismatch and effects of aging

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Increased regional myocardial 18F fluorodeoxyglucose (18FDG) uptake in relation to 13N ammonia (13NH3) uptake - i.e. glucose metabolism-blood flow 'mismatch' - appears to be a strong indicator of myocardial viability in patients with ischemic heart disease (IHD) and regionally reduced contractile function. Reference values of regional 18FDG and 13NH3 uptake have not been determined in healthy subjects with the target age for the development of IHD. We therefore studied healthy middle-aged and old men using positron emission tomography (PET). Twenty-three healthy men aged 51 to 83 years of age were studied. 18FDG and 13NH3 uptake was quantified in 16 myocardial segments with PET and circumferential profile analysis. The relative 18FDG/13NH3 uptake was considerably heterogeneous with 18FDG uptake consistently higher than 13NH3 uptake in the left lateral ventricular wall. This regional 'mismatch' pattern was observed in all subjects, but was most prominent in middle-aged men. The observed age-dependency was the result of a progressive increased in 13NH3 uptake with advancing age in the left ventricular lateral wall. Age-matched reference values of myocardial 18FDG and 13NH3 uptake appears to be important for the discrimination between physiological and pathological glucose metabolism-blood flow mismatch assessed by PET and circumferential profile analysis.

OriginalsprogEngelsk
TidsskriftInternational Journal of Cardiovascular Imaging
Vol/bind17
Udgave nummer5
Sider (fra-til)361-370
Antal sider10
ISSN0167-9899
DOI
StatusUdgivet - 2001
Eksternt udgivetJa

Bibliografisk note

Funding Information:
We are grateful for the collaboration with Merete Appleyard, The Copenhagen City Heart Study. The assistance of Drs Liselotte Hùjgård, Lars Friberg, Markus Nowak, Sùren Holm and Mikael Jensen, The Cyclotron & PET-unit, Department of Clinical Physiology and Nuclear Medicine, Rigs-hospitalet is highly appreciated. Helle Jung Lar-sen, Käte Petersen, Brita Dondera and Bitten Vindberg are thanked for excellent technical assistance. This study was supported by the Danish Heart Foundation, The Research Council of Rigshospitalet, Novo's Foundation, the Foundation of Mr and Mrs Nyegaard and The Birthe and John Meyer foundation.

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