HC 8 Flashcards

1
Q

What is NIRS?

A

Near infrared spectroscopy.

The principle of optical tomography is that an object can be reconstructed by gathering light transmitted through it.

The requirement is that the object transmits at least partially light. The use of near infrared light is between 650 and 1000nm.

Skin, tissue and bone are largely transparent to near infrared light.
It is a not so massive and cheaper machine than MRI.

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2
Q

How does NIRS work?

A

Light on the skull and then measure the reflection of light. Reflectance provides information about the activity in the brain. Light is directed to the skull by a set of small photo emitters. Reflectance is picked up by a set of photo detectors.

Penetration of the depth of light is proportional to source-detector distance.

Oxyhemoglobin (HbO2) and deoxyhemoglobin (HbR) are strong absorbers of light, but differ in their absorption spectra. Smaller than 800nm, HbR absorbs better and more than 800nm, HbO2 absorbs better. Use light with different wavelengths.

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3
Q

What is fNIRS?

A

Functional near infrared spectroscopy.

Concentration of HbO2 and HbR change due to neural activity. This causes the reflection of light to change.

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4
Q

How does fNIRS work?

A

Reconstruct the object with the light that shines through it. Different light absorbtion depending on how far the detectors are from the source. It is cheaper than MRI.

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5
Q

How does fNIRS relate to fMRI?

A

It picks up the same BOLD contrast, oxyhemoglobin and HRF that is the basis of fMRI.

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6
Q

How can fNIRS be applied?

A

It can be used with infants and children, since it is less sensitive to motion.

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7
Q

How does fNIRS compare to fMRI?

A

Advantage:
+Portable, cheaper, silent, more practical and less intrusive. Good tolerance to motion artefacts.
+Measures both oxygenated and deoxygenated hemoglobin levels
+Better temporal resolution. Higher sampling rate

Disadvantage:
-No fine spatial localization. The main cause is because bones scatter light (both the transmitted and reflected.)
-Measures only superficial activity. No reflectance from within sulci or deeper structures

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8
Q

What is PET?

A

Positron Emission Tomography. It is an imaging technique that helps visualize metabolic processes in the body, providing valuable information for diagnosing and managing various diseases. It is much more expensive than MRS.

It is an unique contribution relative to fMRI, measuring metabolism and can detect biomarkers and neurotransmitter concentrations.

Positron emission involves injection of radioactive tracers. It is not an injection of the isolated isotope, but attached to a molecule with specific biological action. Molecule and site injection determines spread of the tracer.

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9
Q

What are the principles of PET?

A
  1. Radiotracer injection: a small amount of a radioactive substance called a radiotracer is injected into the patient’s bloodstream.
  2. Radiotracer uptake: the radiotracer circulates through the body and accumulates in tissues with high metabolic activity.
  3. Positron Emission: The radioactive isotope in the tracer decays by emitting a positron which is the antimatter counterpart of an electron.
  4. Annihilation event: when a positron encounters an electron in the body, they annihilate each other.
  5. Detection: the PET scannen consists of a ring of detectors that surround the patient. They pick up the gamma photons produced by annihilation events.
  6. Image reconstruction: the PET system uses the timing and location of the detected gamma photons to reconstruct a three-dimensional image of the tracer distribution in the body. This process involves complex algorithms that compute likelihood of where annihilation events occured.
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10
Q

What are the steps of a PET-Scan procedure?

A
  1. Preparation: The patient may be asked to fast to ensure low blood sugar levels, which helps accuracy of the test.
  2. Radiotracer administration: the radiotracer is injected and the patient typically waits to allow the tracer to distribute and accumulate in the target tissues.
  3. Scanning: the patient lies on a table that moves through the PET scannen, which captures the gamma photons emitted from the body.
  4. Data processing: The collected data is processed by a computer to generate detailed images of the tracer concentration in different tissues.
  5. Interpretation: interpret images to identify areas of abnormal metabolic activity.
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11
Q

What are coincidence events?

A

Fundamental to the operation of PET scannes, enabling the accurate localization of metabolic activity within the body and generation of high-resolution images.

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12
Q

What are half-lifes in PET?

A

The half-life of a radioisotope in PET is a key parameter that influences the timing, logistics and clinical utility of the imaging procedure. It determines how long the radiotracer remains active in the body, affecting both the quality of the imaging data and the radiation exposure to the patient.

Because they are short, conditions in blocks also need to be short. Different transmitters have different half-lifes.

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13
Q

How is oxygen-15 used to measure neural activity?

A

Short half-life of 2 minutes. The distribution is a linear relationshop to incoming blood volume. The total amount of oxygen in a brain region is an indication of local neural activity, because of the over-supply of oxygenated blood following neural acitivty.

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14
Q

How does a typical PET experiment look like?

A

-Low number of conditions (4-8)
-Conditions are typically tested in blocks of around 1 minute
-Often only 2 blocks per condition
-In between blocks short waiting period with new injection

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15
Q

What are some unique contributions of PET?

A

Measures metabolism. The tracer fluorine-18 is attached to glucose. This is called fluerodeoxyglucose (FDG). This can be used to diagnose cancer and brain diseases.

PET targets specific neurotransmitter systems. Tracer is attached to a molecule with concentration related to activity of one specific neurotransmitter.

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16
Q

What are some important neurotransmitters?

A

Amino acids: GABA, glutamate, glycine
Monoamines: Dopamine, noradrenaline, serotonin

17
Q

What is the norepinephrine/noradrenaline system for?

A

-Arousal, vigilance, attention
-Processing of salient events
-Memory formation

18
Q

What is the serotonin system for?

A

-Mood, emotion
-Reward processing
-Impulsivity

19
Q

What is the dopamine system for?

A

-Reward processing
-Cognitive control
-Memory formation

20
Q

What is transmitter-specific PET?

A

It refers to the use of PET to target and visualize specific neurotransmitter systems in the brain. This is a specialized application of PET and crucial in neuroscience to research and do clinical diagnostics to understand the brain function, studying neuropsychiatric disorders and developing treatments.

21
Q

What is the basis of transmitter-specific PET?

A

-Neurotransmitters are chemical messengers in the brain that transmit signals across synapses between neurons.

-Transmitter-specific PET uses radiotracers designed to bind selectively to specific neurotransmitter receptors, transporters or enzymes involved in neurotransmitter syntheses or metabolism. These radiotracers are labeled with positron-emitting isotopes.

-By binding to specific targets, these radiotracers allow the visualization and quantification of neurotransmitter systems in different regions of the brain. This helps in assessing the density, distribution and activity of receptors and transporters.

22
Q

Which diseases can be studied with the dopamine system?

A

Parkinson’s, shizophrenia and addiction.

23
Q

Which diseases can be studied with the serotonin system?

A

Depression, anxiety and other mood disorders.

24
Q

Which diseases can be studied with the glutamate system?

A

Schizophrenia, neurodegenerative diseases and cognitive functions.

25
Q

Which diseases can be studied with the GABA system?

A

Epilepsy, anxiety disorders.

26
Q

How does transmitter-specific PET imaging work?

A
  1. The readiotracer specific to the neurotransmitter of interest is injected in the bloodstream.
  2. The radiotracer travels to the brain and binds to its specific targets. The distribution and binding of radiotracer reflects the activity and density of the target sites.
  3. The patient undergoes a PET scan. The scanner detects the gamma photons emitted from the positron annhiliation events which occur as the radiotracer decays.
  4. The collected data is processed to create images showing the concentration and distribution of the radiotracer in the brain. These images represent the activity of the specific neurotransmitter being studied.
  5. Quantitative analysis can be performed to measure receptor density, binding potential or transporter availability. This data helps in understanding the functioning and abnormalities in neurotransmitter systems.
27
Q

How should the amount of binding be interpreted in PET?

A

It is tracer vs transmitter to bind to a receptor, enzyme or transporter. They compete. The tracer binds to a receptor that is available. The more dopamine there is, the less receptors there are for the tracer to bind to.

So, the level of tracer binding is inversely proportional to the level of transmitter binding. The higher the tracer binding, the lower the transmitter binding.

This is only in transmitter-specific PET, so the output of the PET-scan needs to be interpreted with caution, because the stronger the signal or activation, the less neurotransmitters there are.

28
Q

What is SPECT?

A

Single-Photon Emission Computed Tomography.

It is a simpler form of PET. It uses readily avaible, stable radioligands (no cyclotron required). Gamma photon is emitted by the radioisotope and detected by simple gamma camera.

29
Q

How is SPECT different from PET?

A

-Longer tracer half-life. Images are processed over longer time. There is a limit on the number of test conditions, but production and transport is an advantage.

-Lower spatial resolution, because of the small set of sensors instead of a ring). The picture is less precise and has lower clarity.

30
Q

What are the principles of SPECT?

A

-A small amount of radiotracer is administered through injection.

-The radiotracer circulates through the body and accumulates in specifc organs or tissue depending on its chemical properties and physiological processes being studied.

-The radioactive decay of the radiotracer emits gamma photons, which are high-energy photons.

-A gamma camera detects the emitted gamma photons.

-The gamma camera rotates around the patient, acquiring multiple two-dimensional images from different angles.

-Computer algorithms reconstruct the acquired projections into a three-dimensional image of radiotracers distribution within the body.

31
Q

When is SPECT better and when is PET better to use?

A

It depends on the research question and availbility.

If you want something that costs less and much more available to use, than SPECT is better than PET. SPECT is also much less sensitive to use than PET, so it may be better to use with certain groups of people that have difficulty with staying still.

PET is better in terms of spatial and temporal resolution and has a better variaty of ligands and signal to noise ratio (high is good).

32
Q

How does PET and SPECT compare to fMRI?

A

+PET and SPECT target synaptic neurotransmission directly
+Ability to measure blood volume quantitavily
+Confronted with less unknown parameters when we try to relate measured signal to neural acitivty.

-Temportal and spatial resolution poorer than fMRI
-More invasive. Exposure to radiation
-Expensive. PET tracers cannot be transported and need a cyclotron on site for radioisotope production
-Tracers are often limited to specific regions or unspecific in their distribution.