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Positron emission tomography

Image:ECAT-Exact-HR--PET-Scanner.jpg

Positron emission tomography (PET) is a nuclear medicinemedical imagingtechnique which produces a three dimensional image or map of functional processes in the body.


Inhaltsverzeichnis

  • 1 Description
  • 2 Applications
  • 3 PET scans safety
  • 4 See also
  • 5 References
  • 6 External links

Description

Image:PET-image.jpg Image:PET-schema.png Image:PET-detectorsystem.png

A short-lived radioactivetracer isotopewhich decays by emitting a positron, chemically incorporated into a metabolically active molecule, is injected into the living subject (usually into blood circulation). There is a waiting period while the metabolically active molecule (usually a sugar) becomes concentrated in tissues of interest, then the subject is placed in the imaging scanner. The short-lived isotope decays, emitting a positron. After travelling up to a few millimetersthe positron annihilates with an electron, producing a pair of annihilationphotons (similar to gamma rays) moving in opposite directions. These are detected when they reach a scintillatormaterial in the scanning device, creating a burst of light which is detected by photomultiplier tubes. The technique depends on simultaneous or coincident detection of the pair of photons: photons which do not arrive in pairs (i.e., within a few nanoseconds) are ignored. By measuring where the annihilation photons end up, their origin in the body can be plotted, allowing the chemical uptake or activity of certain parts of the body to be determined. The scanner uses the pair-detection events to map the density of the isotope in the body, in the form of slice images separated by about 5 mm. The resulting map shows the tissues in which the molecular probe has become concentrated, and is read by a nuclear medicine physician or radiologist, to interpret the result in terms of the patient's diagnosis and treatment. PET scans are increasingly read alongside CT scans or MRI scans, the combination giving both anatomic and metabolic information (what the structure is, and what it is doing). PET is used heavily in clinical oncology (medical imagingof tumors and the search for metastases) and in human brainand heart research.

Alternative methods of scanning include x-ray computed tomography(CT), magnetic resonance imaging(MRI) and functional magnetic resonance imaging(fMRI), ultrasoundand single photon emission computed tomography(SPECT).

However, while other imaging scans such as CTand MRI, isolate organic anatomic changes in the body, PET scanners are capable of detecting areas of molecular biologydetail (even prior to anatomic change) via the use of radiolabelled molecular probes that have different rates of uptake depending on the type of tissue involved. The changing of regional blood flow in various anatomic structures (as a measure of the injected positron emitter) can be visualized and relatively quantified with a PET scan.

Radionuclides used in PET scanning are typically isotopeswith short half livessuch as 11C(~20 min), 13N(~10 min), 15O(~2 min), and 18F(~110 min). Due to their short half lives, the radionuclides must be produced in a cyclotronat or near the site of the PET scanner. These radionuclides are incorporated into compounds normally used by the body such as glucose, wateror ammoniaand then injected into the body to trace where they become distributed. Such labelled compounds are known as radiotracers.

PET as a technique for scientific investigation in humans is limited by the need for clearance by ethics committees to inject radioactive material into participants, and also by the fact that it is not advisable to subject any one participant to too many scans. In neurological research, this limitation can be partly overcome by the use of short-lived radionuclides that result in a lower radiation dose. PET also has an expanding role in the assessment of response to therapy, and in particular cancer therapy (e.g. Young et al. 1999).

PET is also used in pre-clinical studies using animals, where it allows repeated investigations into the same subjects. This is particularly valuable in cancer research, as it results in an increase in the statistical quality of the data (subjects can act as their own control) and very substantially reduces the numbers of animals required for a given study. A further limitation arises from the high costs of cyclotrons needed to produce the short-lived radionuclides for PET scanning (for example 18F). Few hospitals and universities are capable of maintaining such systems, and most clinical PET is supported by third-party suppliers of radio-tracers which can supply many sites simultaneously. This limitation restricts clinical PET primarily to the use of tracers labelled with 18F, which has a half life of 110 minutes and can be transported a reasonable distance before use, or to 82Rubidium, which can be created in a portable generator and is used for myocardial perfusion studies.

Applications

PET is a valuable technique for some diseases and disorders, because it is possible to target the radio-chemicals used for particular bodily functions.

  1. Oncology: PET scanning with the tracer (18F) fluorodeoxyglucose(FDG, FDG-PET) is widely used in clinical oncology. This tracer is a glucose analog and is taken up by cells, phosphorylated by hexokinase(whose mitochondrialform is greatly elevated in rapidly-growing malignant tumours), and retained by tissues with high metabolic activity, such as the brain, the liver, and most types of malignant tumours. As a result FDG-PET can be used for diagnosis, staging, and monitoring treatment of cancers, particularly in Hodgkin's disease, non Hodgkin's lymphoma, and lung cancer. However because individual scans are more expensive than conventional imaging with CTand MRI, expansion of FDG-PET in cost-constrained health services will depend on proper Health Technology Assessment. Oncology scans using FDG make up over 90% of all PET scans in current practice.
  2. Neurology: PET neuroimagingis based on an assumption that areas of high radioactivity are associated with brain activity. What is actually measured indirectly is the flow of blood to different parts of the brain, which is generally believed to be correlated, and usually measured using the tracer oxygen (15O). Research continues into the use of radiolabelled F-DOPA and FDDNP as more specific probes.
  3. Cardiology: In clinical cardiology FDG-PET can identify so-called "hibernating myocardium", but its cost-effectivenessin this role versus SPECTis unclear.
  4. Neuropsychology/ Cognitive neuroscience: To examine links between specific psychological processes or disorders and brain activity.
  5. Pharmacology: In pre-clinical trials, it is possible to radio-label a new drug and inject it into animals. The uptake of the drug, the tissues in which it concentrates, and its eventual elimination, can be monitored far more quickly and cost effectively than the older technique of killing and dissecting the animals to discover the same information. PET scanners for rats and apes are marketed for this purpose.

PET scans safety

PET scanning is invasive, in that radioactive material is injected into the subject. However the total dose of radiation is small, usually around 7 mSv. This can be compared to 2.2 mSv average annual background radiation in the UK, 0.02 mSv for a chest X-Ray, up to 8 mSv for a CT scan of the chest, 2-6 mSv per annum for aircrew, and 7.8 mSv per annum background exposure in Cornwall(Data from UK National Radiological Protection Board).

Because the half-life of 18F is about two hours, the prepared doses decay significantly during the working day. If the FDGis delivered to the scanning suite in the morning, the specific activity falls during the day, and a relatively larger volume of radiopharmaceutical must be injected in later patients to deliver the same radioactive dose.

See also

  • antimatter
  • functional neuroimaging
  • neuroimaging
  • SPECT(Single Photon Emission Computed Tomography)
  • statistical parametric mapping

References

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External links

  • How PET Works- Online educational resource about PET for teachers and students. Includes downloadable teaching material and worksheets.
  • Let's Play PET- Very good illustrated introduction to PET
  • Imaging Atlas of PET-CT
  • Introduction to PET Physics
  • GE HealthCare, Philips, Siemens- Major manufacturers of PET scanners
  • Thompson Cancer Survival Research Center info on PET
  • What is PET?da:Positronemissionstomografi

de:Positronen-Emissions-Tomographie es:Tomografía por emisión de positrones eo:Pozitrona Emisia Tomografio fr:Tomographie à émission de positon is:PET-skanni he:PET nl:Positronemissietomografie ja:???????? no:PET pl:Pozytonowa emisyjna tomografia komputerowa pt:PET (exame médico)

Retrieved from "http://en.wikipedia.org/Positron_emission_tomography"



This article is licensed under the GNU Free Documentation License.
It uses material from the http://en.wikipedia.org/wiki/Positron+emission+tomography Wikipedia article Positron emission tomography.

 
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