Basic Imaging and Contrast

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    Basic MR imaging & contrast

    Steffen Ringgaard

    Sept. 2003

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    Spatial signal encoding After excitation, signal is

    emitted from completeobject

    Linear field gradients for

    introducing spatially

    varying frequency

    Fieldgradient

    Z

    Bandwidth

    G

    Larmor frequency

    = B0

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    Definition of coordinate axes

    Fieldgradient

    Z

    Slice thickness

    Bandwidth

    G

    y, phase direction

    x, frequency direction

    z, slice direction

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    Slice excitation Simultaneous gradient

    and shaped RF-pulse Gradient induces

    linearly varying field

    Shaped RF-pulse

    excites frequency band

    Field

    gradient

    Z

    Slice thickness

    Bandwidth

    G

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    Shaped RF-pulse Rectangular slice profile

    requires sinc functionshaped pulse

    Slice thickness inversely

    proportional to pulse

    extension

    Position determined by

    frequency

    FourierTransform

    Frequency

    Time

    ( )x

    xx

    sinsinc =

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    Slice interference

    Slicegap

    Slicegap

    Halfmaximum

    height

    Halfmaximum

    height

    Slicethickness

    Slicethickness

    Interferencebetween slices

    No sliceinterference

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    Frequency encoding

    Signal from different positions has different frequency Position determined by invers Fourier Transform

    Gradient

    Higherfield

    Frequency

    Z

    Signal after Fouriertransformation

    X

    Magnetic fieldperpendicularto slice

    TimeFrequency0

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    Phase encoding With gradient applied, the

    phase of themagnetization changes

    With gradient turned off

    the frequency is again the

    same, but phases aredifferent

    When signal is read out

    (sampled) it containsmultiple frequencies and

    multiple phases

    1

    2

    3

    z z

    z z

    z z

    x x

    x x

    x x

    B0

    RF

    Gs

    ACQ

    Gp

    Gm

    Time

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    Pulse sequence

    RF

    Gs

    ACQ

    Gp

    Gm

    Excitation Phase

    encoding

    Acquisition

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    Complete pulse sequence

    Total scan time: TR*Matrix(y)

    Typical values:

    TE: 2-100 ms

    TR: 10-1000 ms

    Matrix: 128-512

    Scan time: 1-512 s

    RF

    Gs

    ACQ

    Gp

    Gm

    TRTE

    K-space

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    Contrast in MR images

    Two images with different contrast

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    Excitation of magnetization

    z

    B0

    B1

    B

    1

    x'

    y'

    z'

    x

    y

    M

    Initial

    magnetization M0

    Magnetizationafter 90 pulseo

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    Longitudinal and transversal

    components

    Transverseplane (xy)

    Transverseplane (xy)

    Longitudinalaxis (z)

    Longitudinalaxis (z)

    Mxy

    Mxy

    yy

    z z

    zM

    zM

    xx

    B0 B0

    =0

    M

    (=M)

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    Relaxation T1 relaxation:

    longitudinal relaxation

    re-growth of longitudinalmagnetization

    T2 relaxation: transverse relaxation

    disappearance oftransversal magnetization

    T2* relaxation: as T2, but taking

    inhomogeneity into account

    T2 < T1

    T2* < T2

    Time

    Longitudinal relaxation63%

    T1

    Mz

    0

    Transverse relaxation

    Time37%

    Mxy

    T2

    0

    M0

    M0

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    T1 and T2 values Tissues have different relaxation values

    Tissue T1 (ms) T2 (ms)

    Gray matter 950 100

    White matter 600 80

    Muscle 900 50

    CSF 4500 2200

    Fat 250 60Blood 1200 100-200

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    Contrast: long TRVerticalmagnetization (M )

    Signal

    +M0

    0TR

    90 pulseo

    TE

    PD weighted

    CSF, long T2

    T weighted2

    Parenchyma,short T2

    CSF, long T1

    Parenchyma,short T

    1

    z

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    Contrast: short TRVerticalmagnetization (M )

    Signal

    +M0

    0

    90 pulseo

    TE

    CSF, long T2

    T weighted1

    short T2

    CSFlong T

    1

    short T1

    Parenchyma

    Mixed influence

    z

    TR

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    Three types of weighting Proton density weighting

    TR long TE short

    T1 weighting TR short (~ T1 of tissue)

    TE short long T1 tissue is dark

    T2 weighting TR long

    TE long (~ T2 of tissue)

    long T2 tissue is bright

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    Calculating signal strengthSignal in spin echo sequence:

    Contrast between tissue A and B:

    BAABSSC =

    ( ) 211, 0T

    TT

    T

    ER

    ER

    eeTTS

    =

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    Signal and contrastSignal strength and contrast, varying TR

    0

    0.1

    0.2

    0.3

    0.4

    0.5

    0.6

    0.7

    0.8

    0.9

    1

    0 500 1000 1500 2000 2500

    Repetition time

    Signal S1

    S2

    DIFF

    Signal strength and contrast, varying TE

    0

    0.2

    0.4

    0.6

    0.8

    1

    1.2

    0 50 100 150 200 250 300

    TE, ms

    Signal S1

    S2

    DIFF

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    k y

    B C

    A

    kx0

    0

    Spin echo and gradient echo

    A

    C

    0

    k x

    ky

    90 90180

    TE

    TR

    RF

    Gz

    Gy

    G

    xsignal

    o o

    o

    Gradient echo Spin echo

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    Contrast for spin and gradient echo

    sequences

    Spin echo:

    Gradient echo:

    ( ) 211, 0T

    TT

    T

    ER

    ER

    eeTTS

    =

    ( )

    *21

    1, 0T

    T

    T

    T

    ER

    ER

    eeTTS

    =

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    MRI contrast agents Reduces T1 and T2

    Increases signal strength Improves image contrast

    Used for angiography, perfusion and myocardial

    viability Gadolinium (Gd) based contrast most common

    Gd inserted in large molecule (DTPA)

    Used in approx. 30% of clinical scans Injected intra-venously

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    Contrast agents, structure

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    Contrast agents, signal strength

    Increases signal in T1-weighted scans

    Decreases signal in T2-weighted scans

    Gd-DTPA of the kidney parenchyma

    0

    500

    1000

    1500

    2000

    2500

    0 5 10 15 20 25 30 35 40 45 50 55 60

    Time [s]

    MRIsignalintensity

    T2-weighted

    T1-weighted

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    Example of

    contrastbased

    angiography(Mobitrak)