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NORMAL MYELINATION OF BRAIN
Dr.Chandra sekharDR.DUONG
What is myelin ? Myelin is an electrically insulating phospholipid
layer that surrounds the axons of many neurons.
Myelin is produced by specialized cells:
Oligodendrocytes in the central nervous system Schwann cells in the peripheral nervous system.
Composition of myelin
Myelin is composed of about 80% lipid fat and about 20% protein.
Myelinisation
Myelin sheaths wrap themselves around
axons. Each oligodendrocyte can myelinate several
axons (up to 40), so the destruction of even only
a few oligodendrocytes can have an extensive demyelination effect.
Function of myelin layer The main consequence of a myelin layer is an
increase in the speed at which impulses propagate along the myelinated fiber.
Myelination also helps prevent the electrical current from leaving the axon.
Axons with normal myelin Demyelinated axons: Nerve impulse conduction slows or stops completely
Normal Myelination pattern of the pediatric brain
Myelination causes changes in the signal intensity of the brain.
Myelination starts during the 5th fetal month with myelination of the cranial nerves and continues throughout life.
Myelination progress is from:
caudal to cephalad
dorsal to ventral
central to periphery.
•Starts in the 2nd trimester and continous into adulthood
•Evolves in predictable sequential fashion over the first 2 postnatal years
•Functional significance and psychomotor development of brain
•Beginning with PNS > Spinal cord > Brain stem > Supratentorial brain
Brainstem first > Cerebellum > Internal capsule > Basal ganglia > Corpus callosum > Cerebral hemispheresOptic tract in occipital lobe 1st > parietal + frontal
MR imaging is the most sensitive
Imaging approaches
MR is the only imaging technique that assesses myelination.
T1WI show myelination as increasing hyperintensity.
T2WI show myelination as increasing hypointensity.
Diffusion imaging shows myelnation as decreasing diffusivity.
Assessment of myelination
Many ways to assess myelination by MR
Qualitative method: Assess milestones when changes of myelination appear on T1,T2 weighted images.
Quantitative methods: Assess changes in diffusivity,FA,MT and compare with values of age-matched patients.
Basic principles of myelination on MRI
Myelinated WM appears hyper intense on T1W and hypointense on T2W images.
Unmyelinated white matter appears hypointense on T1W and hyper intense on T2W images.
Increase in signal intensity on T1W images precede the decrease in signal intensity on T2W images.
T1WI:
Most sensitive in children less than 1 year of age 1 Hyper-intense
T2WI:
Most sensitive in children between the age of 1 and 2
Gradual shift from hyper- to hypo-intense ralative to GM
Because T2 of the immature brain have relatively poor grey/white matter distinction due to high water content of the unmyelinated matter.
FLAIR:Follows the same pattern as T2 but somewhat lags behind PD WIUseful in distinguishing gliosis fromDWI:In acute setting more sensitive than T1 or T2
MR SpectroscopyIncreased Myo-Inostol and Choline in neonatesNAA increased with myelination (1st yr)
Normal Myelination
Birth (full term)
Brainstem Cerebellum Posterior limb of internal capsule
One month
Deep cerebellar white matter
Corticospinal tracts
Pre/ postcentral gyri
Optic nerves, tracts
3 Months
Brachium pontis, cerebellar follia Ventral brainstem Optic radiations Anterior limb of internal capsule Occipital subcortical U fibres Corpus callosum splenium
6 Months
Corpus callosum genu Paracentral subcortical U fibres Centrum semiovale (partial)
8 Months
Centrum semiovale (complete except for some fronto temporal areas)
Subcortical U fibres (complete except for most rostral frontal areas)
12 Months
Peripheral
extension into the subcortical WM begins at about 1 year and is essentially complete by 22-24 months except in the “terminal zones”
18 Months
Progressive myelination in the IC, CC, forceps minor, forceps major and central and subcortical white matter
24 Months
Myelination milestones
Term birth : Brainstem, cerebellum, posterior limb of the IC
1 months : Deep cerebellar WM
3 months : Anterior limb of the IC, splenium of the CC
6 months : Genu of the CC
8 months: Centrum semiovale
12 months: Peripheral extension into the subcortical WM
18-24 months: Like adult
Terminal zones
These are areas of known slow myelination within the brain and should not be mistaken for areas of ischemia.
They are seen from about age 16 months until age 10 years.
Terminal zones
Persistent signal intensity in lateral, superior, and posterior to the lateral ventricles, particularly in the region of trigones.
Perivascular spaces
Curvilinear periventricular areas that are iso intense to CSF on all imaging sequences.
Anatomic Region
T1WI T2WI
Superior cerebellar peduncle
28 gest wks 27 gest wks
Median longitudinal fasciculus
25 gest wks 29 gest wks
Medial lemnisci 27 gest wks 30 gest wks
Lateral lemnisci 26 gest wks 27 gets wks
Myelination Patterns on MRI
High signal Low signalAnatomic Region: Brain T1 T2Cerebellar peduncle, middle 0 0-2 months
Cerebral White matter 0-4 months 3-5 months
Posterior limb internal capsule Anterior Portion Posterior Portion
1 month0
4-7 months0-2 months
Anterior limb internal capsule 2-3 months 7-11 months
Corpus callosum, genu 4-6 months 5-8 months
Corpus callosum, splenium 3-4 months 4-6 months
Occipital white matter Central Peripheral
3-5 months4-7 months
9-14 months11-15 months
Frontal white matter Central Peripheral
3-6 months7-11 months
11-16 months14-18 months
Centrum semiovale 2-4 months 7-11 months
Myelination Patterns on MRI
Thank you