Perfusion and Permeability Imaging Flashcards

1
Q

What is the basic principle of MR contrast agents?

A

MR contrast agents are paramagnetic molecules
Presence of the contrast agent alters the magnetic environment and therefore alters the signal
T1 and T2 are both shortened in the presence of gadolinium based contrast agents

T1 weighted images exhibit increased signal
T2 weighted images exhibit decreased signal

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2
Q

What is perfusion imaging?

A

Perfusion describes the local blood flow through a region of brain tissue
Perfusion imaging uses an injected dye in order to see blood flow through tissues

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3
Q

What 3 techniques are used to derive the perfusion values?

A
  1. Dynamic susceptibility contrast
  2. Dynamic contrast enhanced
  3. Arterial spin labelling
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4
Q

What are the measurable parameters of interest in perfusion imaging?

A

CBF - cerebral blood flow
CBV - cerebral blood volume
MTT - mean transit time

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5
Q

What is mean transit time?

A

How fast the agent is moving around the body

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6
Q

What type of imaging is most commonly used for perfusion imaging, specifically dynamic susceptibility contrast?

A

Often uses T2* weighted imaging in perfusion imaging as it is more sensitive to intravascular contrast

Generally gradient-echo echo-planar T2* weighted

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7
Q

Describe the methodology of perfusion imaging

A
  1. Acquire baseline pre-contrast images
  2. Inject a contrast agent ‘bolus’
  3. Observe signal change during first passage of bolus through the brain
  4. T2* weighted sequence is sensitive to intravascular contrast agent
  5. Requires high temporal resolution multi-slice imaging

Gadolinium contrast agent (Gd) is injected (usually intravenously) and a time series of fast T2-weighted images is acquired. As Gadolinium passes through the tissues, it induces a reduction of T2 in the nearby water protons; the corresponding decrease in signal intensity observed depends on the local Gd concentration, which may be considered a proxy for perfusion. The acquired time series data are then postprocessed to obtain perfusion maps with different parameters, such as BV (blood volume), BF (blood flow), MTT (mean transit time)

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8
Q

What do the properties of the contrast agent uptake curve tell us?

A

Perfusion measurements
Area under curve = amount of contrast = CBV
Curve width (FWHM) = first moment = MTT
CBF = CBV/MTT

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9
Q

What is FWHM?

A

Full width at maximum half

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10
Q

What is a clinical application of MTT perfusion imaging?

A

Can be used to predict tissue at risk from stroke - if lots of tissue at risk from stroke patient will receive thrombolysis

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11
Q

Why is it important to have both measures of blood flow and mean transit time?

A

Often, blood flow can over compensate for a previous flow deficit (hyperemia) and therefore mean transit time is important

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12
Q

What is another method of measuring perfusion?

A

Arterial spin labelling
ASL is an MRI technique that measures perfusion without using an exogenous contrast agent
Instead, blood is magnetically labelled in the. neck as it flows into the brain
The labelled blood acts as an endogenous contrast agent
The difference in signal between labelled and non-labelled images is proportional to the cerebral blood flow

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13
Q

What types of tissue can ASL measure?

A

Good technique for grey matter (enough signal to measure strokes or tumours reliably)
Lower blood flow in the white matter so harder to image

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14
Q

What is the structure and function of the blood brain barrier?

A

Endothelial cells form tight junctions creating a blood brain barrier
This barrier allows access to essential molecules, such as glucose, while keeping out toxins
Unfortunately it also severely impedes drug delivery
Breakdown of the blood brain barrier can occur in various disease states e.g., tumours, multiple sclerosis, small vessel disease

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15
Q

What is permeability imaging?

A

Permeability imaging attempts to quantify the permeability of the blood vessel endothelial wall
In normal subjects blood vessel integrity is maintained and no leakage occurs
Imperfections in the vessel wall can occur in various disease states e.g., tumours, small vessel disease

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16
Q

What technique does permeability imaging use?

A

Dynamic Contrast Enhanced Magnetic Resonance Imaging

17
Q

What type of image does permeability imaging acquire?

A

T1-weighted MR images following injection of a contrast agent such as gadolinium

18
Q

What does permeability imaging exploit in order to detect what?

A

DCE-MRI exploits this T1 enhancement in order to detect and evaluate regions of BBB disruption

The repeated acquisition of T1-weighted images provides measurements of signal enhancement as a function of time, which differ between healthy and pathologic tissue

19
Q

What are the measurable parameters of interest in permeability imaging?

A

Ktrans = volume transfer constant (reflects the efflux rate of gadolinium contrast from blood plasma into the tissue)

Ktrans depends on three factors: plasma blood flow (F), vascular permeability (P), and capillary surface area (S) per unit mass

ve = volume fraction of the extravascular extracellular space in tissue

20
Q

What is EES?

A

Extravascular extracellular space

21
Q

What is the methodology of permeability imaging?

A
  1. Acquire baseline pre-contrast images
  2. Inject a contrast agent ‘bolus’
  3. Observe signal change for a period up to 30 mins after injection
  4. Convert signal change into contrast agent concentration
  5. T1 weighted sequence is sensitive to leakage of contrast agent into the extravascular extracellular space (EES)
22
Q

What does a single post-contrast image represent?

A

A single post-contrast image provides information on the ‘amount’ of leakage at a specific time

23
Q

What does permeability imaging require?

A

Measuring permeability requires dynamic information

24
Q

What are the clinical applications of permeability imaging?

A

Diagnosing malignant tumours, benign tumours or assessing normal tissue

25
Q

What are the typical trends of different pathologies in permeability imaging?

A

Malignant tumour = large and fast contrast uptake with washout

Benign tumour = large but more progressive contrast uptake

Normal tissue = minimal contrast uptake

26
Q

What is the relationship between signal enhancement and contrast agent concentration?

A

Signal enhancement is not linearly related to contrast agent concentration

Increasing the concentration of contrast agent too much leads to a decrease in the signal intensity

27
Q

What does signal enhancement depend on?

A

It exhibits a high dependency on the pre-contrast tissue T1 (T10)

28
Q

How is contrast agent concentration calculated?

A

T10 must be measured to enable contrast agent concentration to be calculated from the signal enhancement measurements

29
Q

How is permeability linked to tumours?

A

Without a blood supply, tumours are limited to about 1–2 mm in diameter

In order to grow, cancer cells send out signalling molecules that stimulate new blood vessel formation. This process is called ‘angiogenesis’

The new vessels are often formed imperfectly and without tight endothelial junctions. The degree of impairment to the BBB can then be measured using MR permeability imaging

Higher grade, more aggressive tumours tend to be more vascular and faster growing. The aggressiveness of tumours may therefore be observed using MR permeability imaging

30
Q

How do tumour microvessels compare to healthy endothelial cells?

A

Vessels formed during angiogenesis are imperfect

The ‘pore’ size can be up to 2000nm in diameter

In contrast, standard endothelial pore size is ~ 4nm

31
Q

What else can permeability imaging be used to assess?

A

Treatment response e.g., tumour steroid response