BOLD imaging
Updates to Article Attributes
Blood oxygenation level dependent (BOLD) imaging is the standard technique used to generate images in functional MRI (fMRI) studies, and relies on regional differences in cerebral blood flow to delineate regional activity.
Blood flow in the brain is highly locally controlled locally controlled in response to oxygen and carbon dioxide tension of cortical tissue. When a specific region of the cortex increases its activity in response to a task, the extraction fraction of oxygen from the local capillaries leads to an initial drop in oxygenated haemoglobin (oxyHb) and an increase in local carbon dioxide (CO2) and deoxygenated haemoglobin (deoxyHb). Following a lag of 2-6 seconds, cerebral blood flow (CBF) increases, delivering a surplus of oxygenated haemoglobin, washing away deoxyhemoglobin 1-2,2. It is this large rebound in local tissue oxygenation which is imaged.
The reason fMRI is able to detect this change is due to a fundamental difference in the paramagnetic properties of oxyHb and deoxyHb.
Deoxygenated hemoglobin is paramagnetic whereas oxygenated hemoglobin is not, and therefore the former will cause local dephasing of protons, and thus reduce the returned signal from the tissues in the immediate vicinity. Heavily T2* weighted sequences are used to detect this change, which is in the order of 1-5% 2.
There are a number of limitations of BOLD imaging (and all other techniques which image function by CBF):
- cerebral blood flow (CBF) is only an indirect marker of activity, rather than directly
visualising activevisualising active cortex - the smallest unit of brain that is able to have its blood flow individually regulated is in the order of millimeters in diameter
- CBF increasesin response to
increasedincreased activity and there is a 2-6secondsecond lag
Additionally, there are a number of limitations related to imaging sequences themselves:
- T2* sequences are susceptible to field inhomogeneity due to bone
-air-gas interface, haemosiderin/blood products, rapid flow in large veins, metal - as the change detected is small (1-5%) even small movement
artefactsartifacts can lead to poor images
-<p><strong>Blood oxygenation level dependent (BOLD) imaging</strong> is the standard technique used to generate images in <a href="/articles/functional-mri">functional MRI (fMRI) </a>studies, and relies on regional differences in cerebral blood flow to delineate regional activity. </p><p>Blood flow in the brain is highly locally controlled in response to oxygen and carbon dioxide tension of cortical tissue. When a specific region of the cortex increases its activity in response to a task, the extraction fraction of oxygen from the local capillaries leads to an initial drop in oxygenated haemoglobin (oxyHb) and an increase in local carbon dioxide (CO<sub>2</sub>) and deoxygenated haemoglobin (deoxyHb). Following a lag of 2-6 seconds, <a href="/articles/cerebral-blood-flow-cbf">cerebral blood flow (CBF)</a> increases, delivering a surplus of oxygenated haemoglobin, washing away deoxyhemoglobin <sup>1-2</sup>. It is this large rebound in local tissue oxygenation which is imaged. </p><p>The reason fMRI is able to detect this change is due to a fundamental difference in the paramagnetic properties of oxyHb and deoxyHb. </p><p>Deoxygenated hemoglobin is paramagnetic whereas oxygenated hemoglobin is not, and therefore the former will cause local dephasing of protons, and thus reduce the returned signal from the tissues in the immediate vicinity. Heavily T2* weighted sequences are used to detect this change, which is in the order of 1-5% <sup>2</sup>.</p><p>There are a number of limitations of BOLD imaging (and all other techniques which image function by CBF):</p><ul>-<li>cerebral blood flow (CBF) is only an indirect marker of activity, rather than directly visualising active cortex</li>- +<p><strong>Blood oxygenation level dependent (BOLD) imaging</strong> is the standard technique used to generate images in <a href="/articles/functional-mri">functional MRI (fMRI) </a>studies, and relies on regional differences in cerebral blood flow to delineate regional activity. </p><p>Blood flow in the brain is highly locally controlled in response to <a title="Oxygen" href="/articles/oxygen">oxygen</a> and carbon dioxide tension of cortical tissue. When a specific region of the cortex increases its activity in response to a task, the extraction fraction of oxygen from the local capillaries leads to an initial drop in oxygenated haemoglobin (oxyHb) and an increase in local carbon dioxide (CO<sub>2</sub>) and deoxygenated haemoglobin (deoxyHb). Following a lag of 2-6 seconds, <a href="/articles/cerebral-blood-flow-cbf">cerebral blood flow (CBF)</a> increases, delivering a surplus of oxygenated haemoglobin, washing away deoxyhemoglobin <sup>1,2</sup>. It is this large rebound in local tissue oxygenation which is imaged. </p><p>The reason fMRI is able to detect this change is due to a fundamental difference in the paramagnetic properties of oxyHb and deoxyHb. </p><p>Deoxygenated hemoglobin is paramagnetic whereas oxygenated hemoglobin is not, and therefore the former will cause local dephasing of protons, and thus reduce the returned signal from the tissues in the immediate vicinity. Heavily T2* weighted sequences are used to detect this change, which is in the order of 1-5% <sup>2</sup>.</p><p>There are a number of limitations of BOLD imaging (and all other techniques which image function by CBF):</p><ul>
- +<li>cerebral blood flow (CBF) is only an indirect marker of activity, rather than directly visualising active cortex</li>
-<li>CBF increases <em>in response to</em> increased activity and there is a 2-6 second lag</li>- +<li>CBF increases in response to increased activity and there is a 2-6 second lag</li>
-<li>T2* sequences are susceptible to field inhomogeneity due to bone-air interface, haemosiderin/blood products, rapid flow in large veins, metal</li>-<li>as the change detected is small (1-5%) even small movement artefacts can lead to poor images</li>- +<li>T2* sequences are susceptible to field inhomogeneity due to bone-gas interface, haemosiderin/blood products, rapid flow in large veins, metal</li>
- +<li>as the change detected is small (1-5%) even small movement artifacts can lead to poor images</li>
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