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Basic MRI Spect Xiaojuan Li PhD

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    Basic MR Imaging(MRI) and MR

    spectroscopy (MRS)

    Basic MR Imaging(MRI) and MR

    spectroscopy (MRS)

    Xiaojuan Li, PhD

    Dept of Radiology, UCSF

    PT210, March 1st, 2005

    Xiaojuan Li, PhD

    Dept of Radiology, UCSF

    PT210, March 1st, 2005

    MRI OverviewMRI Overview

    QuestionsQuestions

    ow do we get MR signals?

    ow do we reconstruct MR images?

    ow do we interpret MR images?

    ow do we get MR signals?

    ow do we reconstruct MR images?

    ow do we interpret MR images?

    Protons constantly spins around an axis

    The positive charge attached with proto

    also moves

    Electrical current magnetic field

    Protons constantly spins around an axis

    The positive charge attached with proto

    also moves

    Electrical current magnetic field

    SpinsSpins

    MR Signals -- SpinsMR Signals -- Spins

    N

    S

    N

    S

    N

    S

    PrecessionPrecession

    0 = B 0Larmor frequency

    N

    S

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    R Signals -- Magnetic VectorsR Signals -- Magnetic Vectors

    m Status

    d with B0

    y

    M0

    Signal released

    during relaxation

    M0 back to Equ.

    status

    x y

    zM

    0

    Apply B1| B0

    M0 titled to xy

    plane

    x y

    zM

    0

    B1

    Relaxation -- T1Relaxation -- T1

    T1 relaxation

    (longitudinal relaxation)T1 relaxation

    (longitudinal relaxation)

    t=T1

    M0

    0.63M0

    Spin-lattice relaxation

    x y

    zM

    0

    Energy change btw spi

    surroundings;

    T1 time depends on tiss

    composition, structure a

    surroundings

    Relaxation -- T2Relaxation -- T2

    axation (transverse

    relaxation)axation (transverse

    relaxation)

    t=T2

    Spin-spin relaxation

    x y

    zM

    0

    Loss of phase coherence due to:

    1) Molecular interactions;

    2) Inhomogeneity of B0

    1/T2* = 1/T2 + 1/T2inhomo

    Spin EchoSpin Echo

    In Phase Out of Phase

    after time due to different

    rotating freq

    Spins flip 1800

    around y axis

    In ph

    again

    time

    1800 RF pulse

    LocalizationLocalization

    ice selection

    hase encoding

    equency encoding

    ice selection

    hase encoding

    equency encoding

    Slice SelectionSlice Selection

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    Phase encodingPhase encoding

    Turn the gradient on for a period of time then off

    Frequency EncodingFrequency Encoding

    Spins with the sam

    phase have differe

    frequencies

    Spins with the sam

    frequencies have

    different phases

    Spins with the sam

    phase have differe

    frequencies

    Spins with the sam

    frequencies have

    different phases

    The gradient is on during

    data acquisition

    Image ReconstructionImage Reconstruction

    Spatial

    Decoding

    K-space Spatial domain

    Pulse SequencePulse Sequence

    RF

    Gz

    Gx

    Gy

    DA

    TE

    TR

    Echo

    TE: time of echo; TR: time of repetition

    900 1800

    Image Contrast - T1 weightImage Contrast - T1 weight

    1B T1A

    TRTR

    rt TR give T1 weight. Tissues with short T1 are brighter

    T2B

    M0

    0.37M0

    T2A

    Image Contrast - T2 weightImage Contrast - T2 weight

    TE TE

    Long TE gives T2 weight. Tissues with long T2 are br

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    Image ContrastImage Contrast

    T2ProtonDensityong TR

    T1, T2T1hort TR

    Long TEShort TE

    normally have longest T1 and T2, so it appears darker

    weighted images and brighter in T2-weighted images.

    reful to images with fluid suppression though!)

    Factors affecting MR signalsFactors affecting MR signals

    PD: Proton density at location (x,y,z)

    T1: Longitudinal relaxation time

    T2: Transverse relaxation time

    TR: Time of RepetitionTE: Time of Echo

    TI: Time of Inversion

    FA: Flip angle

    Pulse sequence, flow, contrast medium etc

    Contrast agentContrast agent

    Post-contrast T1-weighted imagentrast T1-weighted image

    contrast c

    cc

    c ccc c

    c c

    cc

    c

    cc

    cc

    c

    cc

    c c

    c c

    c

    c

    c

    c

    cc

    c

    c

    c

    c

    Blood-Brain-Barrier

    Normal Tissues

    Tumors

    MR SpectroscopyMR Spectroscopy

    MRS is a powerful, non-invasive, non-

    destructive tool to study chemical compositio

    and metabolic processes.

    Proton MRS detects signal from protons from

    metabolites other than water.

    MRS is a powerful, non-invasive, non-

    destructive tool to study chemical compositio

    and metabolic processes.

    Proton MRS detects signal from protons from

    metabolites other than water.

    Chemical ShiftChemical Shift

    0

    0 = B 0

    i = B0(1i)

    In presence of B0, the electrons

    surrounding atoms will also

    interact with the field.

    The I depends on molecularenvironment a spin experiences.

    To get rid of B0 dependency,

    this chemical shift is defined as

    parts per million (ppm):

    = i ref

    ref10

    6

    1-H MRS for brain tissue1-H MRS for brain tissue

    5.0 4.0 3.0 2.0 1.0

    ppm

    CholineCreatine

    N-acetyl aspartate

    (lactate/

    lipid)

    water

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    MR spectroscopic imagingMR spectroscopic imaging

    Tumor

    Cho

    Necrosis

    Normal

    NAA

    Crt

    R spectroscopy provides a unique biochemicaldow to study cellular metabolism non-invasively,ch helps to improve the sensitivity and specificity forecting active tumor.

    R spectroscopy provides a unique biochemicaldow to study cellular metabolism non-invasively,ch helps to improve the sensitivity and specificity forecting active tumor.

    Comparison with MRIComparison with MRI

    No frequency encoding during acquisitio

    Long acquisition time

    Low SNR and low resolution due to low

    concentration of metabolites of interest Provides metabolic or functional

    information that may help to improve

    diagnosis and treatment monitoring

    No frequency encoding during acquisitio

    Long acquisition time

    Low SNR and low resolution due to low

    concentration of metabolites of interest

    Provides metabolic or functional

    information that may help to improve

    diagnosis and treatment monitoring

    Grade 3

    Grade 4

    +Lip

    Lac+Lip

    17

    e 4 vs. Grade 3 of brain tumorse 4 vs. Grade 3 of brain tumors

    ReferencesReferences

    MR Made Easy, GE and BERLEX

    http://www.cis.rit.edu/htbooks/mri/

    http://www.cis.rit.edu/htbooks/nmr/

    MR Made Easy, GE and BERLEX

    http://www.cis.rit.edu/htbooks/mri/

    http://www.cis.rit.edu/htbooks/nmr/


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