Analysis of 82Rb PET studies

Rubidium is an analogue of potassium, and [82Rb]Rb+ is actively transported into living cells by ion pumps. It is only partially extracted from blood into tissue during one capillary pass, but can still provide an estimate of tissue perfusion. Extraction of Rb+ is lower than that of K+ (Sheehan & Renkin, 1972). The main advantage of [82Rb]Rb+ over a diffusible perfusion tracer, such as [15O]H2O, is that 82Rb can be produced with a radionuclide generator without access to an on-site cyclotron.

Myocardial perfusion measurement

Positron emission tomography enables noninvasive quantification of myocardial perfusion (MBF). PET tracers that are used for assessment of MBF include diffusible tracer [15O]H2O and partially extracted tracers 82Rb and [13N]ammonia. During one capillary pass, monovalent potassium analogue 82Rb ([82Rb]Rb+) is only partially extracted by the myocardial cells via the Na+/K+ adenosine triphosphatase pump, and extraction is inversely and non-linearly proportional to perfusion. Furthermore, extraction and retention, at a given perfusion level, may be affected by drugs or severe acidosis, hypoxia, and ischemia. Normally, [82Rb]Rb+ does not leak from myocardium during the PET scan.

In 82Rb studies the scanner may be near its saturation limit, which limits the amount of tracer that can be injected. Together with the short physical halflife, this leads to a low signal-to-noise ratio. That has to be taken into account, when deciding between 2D and 3D scanning (Votaw & White, 2001). Model selection can be misguided and analysis may lead to biased results, if PET scanner is saturated or dead-time correction is not working properly. The relatively high positron energy of 82Rb leads to relatively poor image quality and reduced spatial resolution.

Consistent 82Rb administration profile can improve test-retest repeatability, especially when simplified analysis methods are used (Klein et al., 2018). Constant image quality can be achieved by administrating 82Rb activity that linearly depends on body weight (van Dijk et al., 2021).

Proton pump inhibitors (PPIs) are commonly used to reduce stomach acid production. PPIs increase gastric [82Rb]Rb+ uptake, which can affect the myocardial imaging (Alzahrani et al., 2020).

Analysis methods used in literature

Compartment models

Physiological model for 82Rb in myocardium contains three tissue compartments, capillary space, interstitial space, and intracellular space (Coxson et al., 1997). This model, and the reduced model with two tissue compartments (Huang et al., 1989), cannot be applied to noisy PET data without a priori values for some of the model parameters (Herrero et al., 1992). When recovery coefficient and distribution volume of the first tissue compartment were fixed, good repeatability can be achieved, if the signal-to-noise ratio of PET images is improved using for example wavelet-based noise reduction protocol (Lin et al., 2001; Knešaurek et al., 2009).

The further reduced one-tissue compartment model (Coxson et al., 1995; Yoshida et al., 1996; Coxson et al., 1997; Golanowski et al., 2000; Lautamäki et al., 2009) provides results with good reproducibility in rest and hyperemic conditions (Manabe et al., 2009), and is therefore better suited for clinical setting. The result of one or two tissue compartment models (K1) is dependent on both extraction and blood flow, and requires (non-linear) extraction correction, if quantitative flow estimates are needed (Lortie et al., 2007). The method was found to be in excellent concordance with [15O]H2O method in the MBF range 0.66-4.7 ml/min/g (Prior et al., 2012). Combining the one-compartmental model with clustering enhances the quality of parametric perfusion images (Mohy-ud-Din et al., 2015).

Retention model

The simplified retention model (SRM) is basically the same as the FUR method used for analysis of many tracers, mainly with irreversible uptake. In case of [82Rb]Rb+ an extraction correction function (Herrero et al., 1990; Yoshida et al., 1996; Renaud et al., 2013) is required and the result is dependent on the time of imaging the tissue concentration. Time is usually defined as the time of blood curve peak plus 1.4 min (Renaud et al., 2013; Klein et al., 2016). Scanner and image reconstruction dependent partial volume correction factor for the myocardial tissue concentration is also used. Maximum MBF that can be measured with this method is about 2-2.5 ml/(g × min) (Herrero et al., 1990).

Note that retention model accounts for the efflux from tissue to blood (k2) only by keeping the calculation time as short as possible and by applying nonlinear extraction correction. Therefore the extraction correction formula is different for different PET scan times and injection protocols, and is not the same as may be determined for K1 from compartment models. Klein et al (2016) reported that SRM was affected more by the tracer infusion protocol than the one tissue compartment model, and proposed using constant-activity-rate infusion instead of bolus administration.

El Fakhri's approach with factor analysis

El Fakhri et al. (2005) applied generalized form of least-squares factor analysis of dynamic sequences (GFADS) to generate left and right ventricular (LV and RV) TACs. A 1-tissue compartment model was used to estimate the blood flow and extraction dependent parameters k1 and k2. The contribution from both LV and RV blood to the myocardial activity was taken into account in the model as fitted parameters fiv and riv. The model was applied to TACs calculated as average of groups of voxels. Voxels were grouped with orthogonal grouping with predetermined number of groups (100).

Correction for spillover and partial volume effects

Commonly, the spillover and partial volume effects are taken into account in compartment models for 82Rb by assuming a geometrical model.


Herrero et al (1992) and Meyer et al. (2007) have published input functions for 82Rb simulation studies.

Coxson et al (1997) provide compartmental model parameters for simulations.

Suggested MBF analysis method

Our current suggestion is to apply one-tissue compartment model with geometrical model correction for spillover and partial volume effects. This method is implemented in Carimas™.

To calculate quantitative perfusion values, a nonlinear extraction correction is needed. Parameters for the correction functions may need to be determined for each institute, unless the study protocols are similar. Carimas™ implements the extraction correction function as published by Yoshida et al (1996) (Nesterov et al., 2014).

Myocardial perfusion reserve may be estimated from simple stress/rest myocardial activity ratio 2-6 min post injection (Juneau et al., 2021).

See also:

Renal blood flow measurement

[82Rb]Rb+ can be used for measurement of renal blood flow (RBF), because it is reabsorbed in the tubules of the kidney like K+, mainly in the cortex, so that the remaining activity in the urine is usually negligible. Hypokalemia is linked to increased K+/Rb+ excretion and marked urinary activity of [82Rb]Rb+, as well as some medications, such as thiazide diuretics and carbonic anhydrase inhibitor acetazolamide (Jochumsen et al., 2020). Tamaki et al (1986) and Mullani et al (1990) validated RBF measurements in dogs against microsphere method. Renal artery stenosis and catopril in dogs reduced RBF markedly (Tamaki et al., 1988).

Karlberg et al., 1982 validated [86Rb]Rb+ extraction method in rat kidneys, and used it in ischaemia-reperfusion model (Frödin et al., 1982; Karlberg et al., 1983) and UUO model (Wahlberg et al., 1984). The method has also been used in rat model of CNS-induced natriuresis (Sjöquist et al., 1986).

Human renal perfusion studies with [82Rb]Rb+ have been promising (Tahari et al., 2014; Langaa et al., 2021). The high urinary excretion of [82Rb]Rb+ in some patients may hamper the assessment of RBF (Jochumsen et al., 2020). Regadenoson increases and adenosine decreases renal perfusion as measured using [82Rb]Rb+ (Gregg et al., 2021).


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Updated at: 2023-05-10
Created at: 2009-03-17
Written by: Vesa Oikonen, Chunlei Han