MRI Made Easy
MRI Made Easy
Fig. 1: Protons possess a positive charge. Like the earth, they are constantly
turning around an axis and have their own magnetic field.
Fig. 2: Normally, protons are aligned in a random fashion. This, however, changes when
they are exposed to a strong external magnetic field. Then they are aligned in only two
ways, either parallel or anti-parallel to the external magnetic field.
8 MRI made easy The proton
Naturally, the preferred state of align- of the applied magnetic ield. To get a
ment is the one that needs less energy. rough idea: for about 10 million pro-
So more protons are on the lower ener- tons “walking on their hands”, there
gy level, parallel to the external mag- are about 10,000,007 “walking on their
netic ield, walking on their feet, so to feet”. The difference “007” is probably
speak. A smaller number is on the high- easy to remember, isn’t it?
er energy level, anti-parallel, “walking It may be obvious at this point al-
on their hands”. ready that for MRI the mobile protons
The difference in number is, however, are important (which are a subset of all
very small and depends on the strength protons that are in the body).
The proton MRI made easy 9
It is possible and necessary to precise- and anti-parallel. The state that needs
ly calculate this frequency. This is done less energy is preferred, and so there are
by using an equation called the Larmor a few more protons “walking on their
equation: feet” than “on their hands” (igure 3).
B0 is the strength of the external mag- culated by the Larmor equation, and is
netic ield, which is given in Tesla (T) higher in stronger magnetic ields. Why
(see page 94), and is this precession frequency important?
γ is the so-called gyro-magnetic ratio. It has something to do with the “reso-
nance” in magnetic resonance imaging.
The equation states that the precession But to understand this will take a few
frequency becomes higher when the more minutes.
magnetic ield strength increases. The After the break you should go over
exact relationship is determined by the this last summary again, and then con-
gyro-magnetic ratio γ. This gyro-mag- tinue . . .
netic ratio is different for different ma-
terials (e.g. the value for hydrogen pro-
tons is 42.5 MHz/T).
It can be compared to an exchange
Introducing the
rate, which is different for different coordinate system
currencies. To make communication (and drawing
of illustrations) easier, let us start using
a coordinate system like the one used
Time to take a break at school (igure 5). As you can see, the
However, let us briely re- z-axis runs in the direction of the mag-
view what we have learned netic ield lines, and thus can represent
up to now: them. So we can stop drawing the ex-
7 Protons have a positive ternal magnet in all other illustrations.
electrical charge, which is constantly From here on we will also illustrate
moving, because the protons possess a the protons as vectors, as little arrows.
spin. Maybe you remember: a vector rep-
7 This moving electrical charge is resents a certain force (by its size) that
nothing more than an electrical cur- acts in a certain direction (direction of
rent, and the latter always induces a the arrow). The force that is represent-
magnetic ield. ed by vectors in our illustrations, is the
7 So every proton has its own little magnetic force.
magnetic ield, and can thus be seen as
a little bar magnet.
7 When we put a patient in the MR
Fig. 5: Using
a coordinate
system makes
the description
of proton motion
in the magnetic
field easier, and
we can also stop
drawing the ex-
ternal magnet.
12 MRI made easy Precession
Fig. 6: The five protons, which “point” down, cancel out the magnetic effects of the same number of protons,
which “point” up (A). So in effect it is sufficient to look only at the four unopposed protons (B).
Now, let us look at igure 6. Here we tons in your body precessing this fast.
have 9 protons pointing up, precessing It is easy to imagine that at a certain
parallel to the external magnetic ield moment, there may be one proton (A in
lines, and 5 protons pointing down, the illustration) pointing in one direc-
precessing anti-parallel to the external tion, and another proton (A’) pointing
magnetic ield. exactly in the opposite direction. The
What we see in the igure is just a pic- result is very important; the magnetic
ture taken at a speciic point in time. A forces in the opposing directions cancel
picture taken just a little later would each other out, like two persons pulling
show the protons in different posi- at the opposite ends of a rope. Finally,
tions, because they precess. The preces- for every proton pointing down, there
sion actually goes very fast, the preces- is one pointing up, cancelling its mag-
sion frequency for hydrogen protons is netic effect. But as we have learned:
somewhere around 42 MHz in a mag- there are more protons pointing up
netic ield strength of 1 Tesla (see page than down, and the magnetic forces of
94); this means that the protons pre- these protons are not cancelled by oth-
cess around the “ice cream cone” more ers. So we are left – in effect – with some
than 42 million times per second. Now protons (4 in our example) pointing up
there are millions and millions of pro- (igure 6).
Precession MRI made easy 13
Fig. 10:
Energy exchange is The “speed” of protons and resonance
possible when protons
and the radio frequency
pulse have the same
frequency.
What speed, or better,
what frequency did the
protons have?
They had their precession frequency
which can be calculated by the Larmor
equation (see page 10). So the Larmor
equation gives us the necessary fre-
quency of the RF pulse to send in. On-
ly when the RF pulse and the protons
have the same frequency, can protons
pick up some energy from the radio
wave, a phenomenon called resonance
– this is where the “resonance” in mag-
netic resonance comes from.
The term resonance can be illustrated
by the use of tuning forks. Imagine that
you are in a room with different kinds
of tuning forks, tuned e.g. to a, e, and d.
Somebody enters the room with a tun-
ing fork with “a”-frequency that was
struck to emit sound. Of all the tun-
ing forks in the room, all of a sudden
the other “a”-forks, and only those, pick
up energy, start to vibrate and to emit
sound, they show a phenomenon called
resonance.
18 MRI made easy RF pulse
on page 13). Due to the RF pulse, the add up in this direction. This results
protons do not point in random direc- in a magnetic vector pointing to the
tions any more, but move in step, in side to which the precessing protons
synch – they are “in phase”. They now point, and this is in a transverse direc-
point in the same direction at the same tion (figure 13). This is why it is called
time, and thus their magnetic vectors transversal magnetization.
20 MRI made easy RF pulse
Fig. 15: In a strong external magnetic field, a new magnetic vector along the external field is
established in the patient (A). Sending in an RF pulse causes a new transversal magnetiza-
tion while longitudinal magnetization decreases (B). Depending on the RF pulse, longitudinal
magnetization may even totally disappear (C).
22 MRI made easy The MR signal
Fig. 17: After the RF pulse is switched off, protons go back from their higher to the lower state of energy, i.e. point up again.
This is illustrated “one-by-one”. The effect is that longitudinal magnetization increases and grows back to its original value. Note that for
simplicity the protons were not depicted as being in phase: this subject is covered in more detail in figures 20 and 26.
After the RF pulse is switched off, pro- And this is why this process is not
tons go back to the lower state of ener- only called longitudinal relaxation, but
gy, i.e. point up again, but not all pro- also spin-lattice relaxation.
tons do this at exactly the same time. By going back on their feet, pointing
Instead it is a continuous process, as if upwards again, these protons no longer
one proton after the other goes back to cancel out the magnetic vectors of the
its original state. This is illustrated in same number of protons pointing up, as
figure 17 for a group of protons. The ef- they did before. So, the magnetization
fect is that longitudinal magnetization in this direction, the longitudinal mag-
increases and grows back to its original netization increases, and finally goes
value. back to its original value (figure 17).
What happens to the energy which If you plot the longitudinal mag
they had picked up from the RF pulse? netization vs. time after the RF pulse is
This energy is just handed over to switched off, you get a curve like figure
their surroundings, the so-called lat- 18. It increases with time. This curve is
tice. also called a T1-curve.
Longitudinal magnetization MRI made easy 25
About T2
Fig. 19: T1 is the longitudinal relaxation time
that has something to do with the exchange of
thermal energy. Enough about the longitu-
dinal magnetization – what
Reminding you also that it describes happens with the trans-
the spin-“1”attice relaxation.
But there are more hidden hints to versal magnetization?
this: the “1” also looks like a match. Let us assume that this is the situation just
And this match should remind you of before the RF pulse is switched off.
something, which we also have men- When the RF pulse is switched off, the
tioned already: longitudinal relaxation protons get out of step, out of phase again,
has something to do with exchange of as nobody is telling then to stay in step.
energy, thermal energy, which the pro- For the sake of simplicity, this has been
tons emit to the surrounding lattice illustrated for a group of protons which
while returning to their lower state of all “point up” in figure 20. We heard ear-
energy. lier that protons precess with a frequency
Transversal magnetization MRI made easy 27
Fig. 20: After the RF pulse is switched off, protons lose phase coherence, they get out of step. When you look at these
dephasing proton ensembles from the top (which is illustrated in the lower part of the figure), it becomes obvious, how they
fan out. Fanning out, they point less and less in the same direction, and thus transversal magnetization decreases.
T 2 is T x 2 is TT is Tt
and this means, it describes the “T
transversal”, thus the relaxation of
the transversal magnetization. The
resulting curve in figure 21 thus is one is the T1- and which the T2 -curve?
called a T2 -curve. Another term for Just put both curves together. You can
transversal relaxation is spin-spin- see something like a mountain with a
relaxation, reminding us of the un- ski slope. You first have to climb to the
derlying mechanism, a spin-spin in- top – T1-curve –, before you ski down –
teraction. How to remember, which T2 -curve (figure 22).
larger molecules do not move around ences in the surroundings (the mag-
as fast, so their local magnetic fields netic field variations) influence you
do not cancel each other out as much. considerably. When you drive very fast
These larger differences in local mag- (which is the same as if the surround-
netic fields consequently cause larger ings move very fast), you do not feel
differences in precessing frequencies, each single pot hole anymore. Before
thus protons get out of phase faster, T2 they have a major effect on you, you
is shorter. are already back at normal street lev-
This can be illustrated by the follow- el; thus their effect is averaged out, you
ing example: imagine that you drive are much less influenced by differences
down a street with many pot holes. in the surroundings (the variations in
When you drive slowly (which is equal magnetic field strength).
to the surroundings moving slowly What does all this have to do with
and you are standing still), you will be what we want to know? All these proc-
bumping up and down in your car as esses influence how your MR picture
it drives over each pot hole. The differ- will finally look!
Well, in this
case we’ve got
a problem.
36 MRI made easy Relaxation
7
is longer than T2 .
T1 varies with the mag-
Now let us perform an
netic field strength; in experiment
stronger magnetic fields it Look at figure 25, where you can see
is longer. two protons, precessing around the z-
7 Water has a long T1, fat has a short T1. axis. I hope you recall that the z-axis
7 T2 of water is longer than the T2 of im- indicates the direction of a magnetic
pure liquids containing larger mole- field line (see page 9). Instead of on-
cules. ly these two protons, in reality there
may be 8 pointing up and 6 pointing
down, or 82 up and 80 down – there
shall only be two more protons point- will decrease, in our example to zero
ing up. (one pointing up is neutralized by one
As we know, these are the ones that pointing down). But: as both protons
have a net magnetic effect because are in phase, there is now a transver-
their effects are not cancelled out. sal magnetization which had not been
Now let us send in an RF pulse, there before.
which has just the correct strength The RF pulse seemingly “tilts” the
and duration, so that one of the two longitudinal magnetic vector 90° to
protons picks up energy to go into the side.
a higher state of energy, i.e. points Such an RF pulse is called a 90°
down/walks on its hands. pulse. Naturally, other RF pulses are
What will happen? The longitudi- also possible, and are named accord-
nal magnetization (up to now result- ingly, e.g. 180° pulse.
ing from two protons pointing up)
38 MRI made easy Relaxation
To really understand this, let us look to their lower state of energy, and
at another example. In figure 26A, we they lose phase coherence.
have 6 protons pointing up; we send in It is important to note that both
an RF pulse, which lifts 3 of them onto processes occur simultaneously and
a higher energy level (B). independently. For the sake of sim-
The result: we no longer have a lon- plicity, let us look at what happens
gitudinal, but a transversal magneti- step by step, and first focus on the lon-
zation (again having used a 90° pulse). gitudinal magnetization:
What happens, when the RF pulse is 7 After the RF pulse is switched off
ing in 4 protons pointing up, and two You surely have already noticed that
pointing down. The net effect: we the transversal magnetization de-
now have a longitudinal magnetiza- creases at the same time (figure 26C-
tion of “2”. E). Why? You should be able to answer
7 Then the next proton goes back up; this: After the RF pulse is switched off,
now 5 protons are pointing up, and one the precessing protons lose phase co-
down, resulting in a net longitudinal herence.
magnetization of “4” (figure 26D). In figure 26B, all protons point in the
7 After the next proton goes up, longi- same direction, but then increasingly
tudinal magnetization equals “6” (fig- get out of phase, and thus kind of fan
ure 26E). out (figure 26C-E).
In figure 27, only the longitudinal and of force in the original directions. If we
transversal magnetic vectors are de- do the same with the longitudinal and
picted at corresponding times as in fig- the transversal vector, we get the sum
ure 26. These magnetic vectors add up vector.
to a sum vector ( J). This sum vector is very important,
As you remember, vectors represent as it represents the total magnetic mo-
forces of a certain size and a certain di- ment of a tissue in general, and thus
rection. If you add up vectors pointing can be used instead of the two single
to different directions, you will come vectors, representing longitudinal and
up with a direction that is somewhere transversal magnetization separately.
in between, depending on the amount Our magnetic sum vector during relax-
Relaxation MRI made easy 41
I hope that you recall that a changing mag- magnetic vector as having some kind of a
netic force/moment can induce an electric sound-emitting device like a steam pipe
current, which is the signal that we receive at its tip. The further the vector goes
and use in MR. away from the microphone, the less
So if we put up an antenna somewhere loud the sound. The frequency of the
(figure 28), we will get a signal as illustrat- sound, however, remains the same be-
ed. This is easy to imagine, if you think of cause the sum vector spins with the
the antenna as a microphone, and the sum precessing frequency (figure 29). So the
signal from our experiment disappears inducing electrical currents in the an-
with time, however, it has a constant tenna. Instead of the terms “longitudi-
frequency. nal” or “transversal magnetization”, we
This type of signal is called a free in- can also use the term “signal or signal
duction decay signal, or FID signal. intensity” at the axis of our T1- and T2 -
By now it should be obvious that the curves.
magnetic vector directly determines This will hopefully become clearer, as
the MRI signal and signal intensity by you continue reading.
Fig. 30A
When you use more than one RF pulse – a The resulting image is called a T1-weight-
succession of RF pulses – you use a so-called ed image. This means that the difference
pulse sequence. As you can use different of signal intensity between tissues in that
pulses, e.g. 90° or 180° pulses, and the time image, the tissue contrast, is mainly due
intervals between successive pulses can be to their difference in T1. However, there is
different, there can be many different pulse always more than one parameter influenc-
sequences. As we saw in our experiment, ing the tissue contrast; in our example, T1 is
the choice of a pulse sequence will deter- just the most outstanding one.
mine, what kind of signal you get out of a
tissue. So it is necessary to carefully choose What is a short, what is a long TR?
and also describe the pulse sequence for a A TR of less than 500 msec is considered to
specific study. be short, a TR greater than 1,500 msec to be
The pulse sequence that we used was long. As you may imagine or know already,
made up of one type of pulse only, the 90° we cannot only create T1-weighted images,
pulse. This was repeated after a certain but also T2 -weighted images, and so-called
time, which is called TR = time to repeat. proton density (-weighted) images.
This proton density, which is also called
How did TR influence the signal in our spin density, influences tissue contrast and
experiment? can be explained quite simply: where there
With a long TR we got similar signals from are many protons, we will have “lots” of
both tissues, both would appear the same signals. Where there are no protons, there
on an MR picture, since the transversal will be no signal. We will read more about
magnetization was the same for both tis- this later. The point is that by using certain
sues. Using a shorter TR, there was a dif- pulse sequences, we can make certain tis-
ference in signal intensity between the tis- sue characteristics to be more or less im-
sues, determined by their difference in T1. portant in the resulting image.
Fig. 30B
How do we obtain a
T2-weighted image?
This is a little more difficult to under-
stand. Let us perform another experi-
ment, which is a little different from
the ones before. First, we use a 90°
pulse. The longitudinal magnetiza-
tion is tilted, we get a transversal
magnetization. What happens after
this pulse, when we wait a short
time?
You can surely answer this question
without difficulty – if not, go back to
page 27 before you continue to read.
After the pulse is switched off, lon-
gitudinal magnetization starts to re-
appear, the transversal magnetiza-
tion, however, starts to disappear.
Why does the transversal magnetiza-
tion disappear? It is because the pro-
Time to echo MRI made easy 49
ter a certain time (which we call TE/2, er ones. If we wait another time TE/2,
half of TE, for reasons you will under- the faster ones will have caught up
stand in a few minutes), we will send with the slower ones (see figure 33F).
in a 180° pulse. What happens? At this point in time, the protons
The 180° pulse acts like a rub- are nearly in phase again, which re-
ber wall; it makes the protons turn sults in a stronger transversal mag-
around, so that they precess in ex- netization, and thus in a stronger
actly the opposite direction, which is signal again. A little later, however,
clockwise. the faster precessing protons will be
The result is that the faster precess- ahead again, with the signal decreas-
ing protons are now behind the slow- ing again.
50 MRI made easy The echo
To illustrate this: think about a race be- bounce back, like a mountain reflecting
tween a tortoise and a hare starting at sound waves as echoes. This is why the
the same line (figure 34). After a certain resulting strong signal is also called an
time (TE/2), the hare is ahead of the tor- echo, or spin echo.
toise. When you make the competitors After we have our signal, our spin
run in the opposite direction for the echo, the protons lose phase coherence
same length of time, they will both be again, the faster ones getting ahead, as
back at the starting line at exactly the we have seen.
same time (assuming, that they run at We naturally can perform the experi-
constant speed). ment again with another 180° pulse,
and another and another . . .
In our experiment, the 180° pulse acts If we now plot time vs. signal intensi-
like a wall, from which the protons ty, we get a curve like in figure 35.
Fig. 35: The 180° pulse refocuses the dephasing protons, which results in a stronger signal,
the spin echo after the time TE. The protons then dephase again and can be refocused anoth-
er time by a 180° pulse, and so on. Thus it is possible to obtain more than one signal, more
than one spin echo. The spin echoes, however, differ in intensity due to so-called T2-effects.
A curve connecting the spin echo intensities is the T2-curve. If we did not use the 180° pulse,
the signal intensity would decay much faster. A curve describing the signal intensity in that
case is the T2*-(T2 star) curve, which is described in a little more detail on page 52.
52 MRI made easy The echo
From this curve we can see that the spin same speed also for the time TE/2. After
echo, the resulting signal, decreases with 2 x TE/2 = TE, the buses will be back at
time. Responsible for this is the fact that the starting line. The signal intensity that
our 180° pulse only “neutralizes” effects you record with your microphone then
that influence the protons in a constant depends only on inherent properties, i.e.
manner, and these are the constant inho- how tired the crowds have become.
mogeneities of the external magnetic field. Let us have a look at our curve, when
Inconstant inhomogeneities from lo- we plotted time vs. signal intensity send-
cal magnetic fields inside the tissue can- ing in several 180° pulses (see figure 35).
not be “evened out”, as they may influence If you do not use a 180° pulse to neutral-
some protons before the 180° pulse differ- ize constant external inhomogeneities,
ently than after the 180° pulse. So some of the protons will experience larger differ-
the protons may still be behind or in front ences in magnetic field strength, when
of the majority of the protons that will the RF pulse is switched off. Due to this,
reach the starting line at the same time. they will be out of phase faster, the trans-
So from echo to echo, the intensity of the versal relaxation time will be shorter.
signal goes down due to so-called T2-ef- A curve describing the signal intensity
fects. A curve connecting the spin echo in that case is the T2*- (T2 star) curve. The
intensities is the T2-curve. star distinguishes this shorter transver-
May be we should illustrate this by an sal relaxation time from the T2 after the
example: imagine two buses full of peo- 180° pulse, which we have already talk-
ple, e.g. after a soccer or football game. ed about.
They are standing at a starting line (fig- The corresponding effects are named
ure 36). With two microphones, you re- T2*-effects. These T2*-effects are impor-
cord the signal (e.g. the singing from the tant with the so-called fast imaging se-
crowd) that is coming from each bus. The quences; we will hear about them later,
buses leave in the same direction. and cover them in more detail in the book
Listening to the singing of the crowds, on “MR Buzzology”.
i.e. recording the signal, you may recog- In our example with the buses this
nize that one signal disappears faster would mean that we just record the sig-
than the other. nals, as the buses drive away. The signals
This can have two different causes: The vanish due to extrinsic (bus speed) and
difference in signal intensities, the differ- intrinsic (exhaustion of the passengers)
ence in singing, may be due to differences properties under these circumstances
in inherent properties of the two groups (see figure 36).
(internal inhomogeneities); may be in The type of pulse sequence that we used
one bus, there are only the “party ani- in our experiment, is called a spin echo
mals”, who did not become tired as fast as sequence, consisting of a 90° pulse and a
the people in the other crowd. 180° pulse (causing the echo). This pulse
Or . . . may be one bus is driving faster sequence is very important in MR im-
than the other (loss of signal would thus aging, as it is the workhorse among the
be due to external influences, the external pulse sequences, which can be used for
magnetic field inhomogeneities). many things. It is important to realize
To figure out what is actually the reason that with a spin echo sequence, we can-
for the signal disappearing, you can make not only produce T2-, but also T1- and pro-
the buses turn around after a certain time ton density-weighted images. We will get
TE/2, and have them drive back with the to that a little later.
The echo MRI made easy 53
Fig. 37: T2-curves for two tissues with different transversal relaxation times; tissue A has a shorter T2
than tissue B, thus loses transversal magnetization faster. With a short TE (TEshort), the difference in signal
intensity is less pronounced than after a longer TE (TElong).
The echo MRI made easy 55
Let us have a look at two different tis- heavily T2 -weighted. But (and there is
sues. Tissue B (water or CSF) has a longer always a “but”) if we wait longer, the
T2 than tissue A (brain). total signal intensity becomes small-
Both T2 -curves in this example start er and smaller. The signal-to-noise ra-
at the same point. If we only wait a tio becomes smaller, the image appears
short TE, TEshort, the difference in signal grainy.
intensity between tissue A and tissue B An example to illustrate this signal-
is very small, both tissues may hardly to-noise problem: when you receive a
be distinguished, as there is hardly any local radio station in your radio, this
contrast (which is the difference in sig- gives you a good signal, e.g. loud music
nal intensity of tissues). and only little static noise.
Consequence: with a short TE, differ- When you drive out of town, the sig-
ences in T2 do not influence tissue con- nal intensity of the radio station be-
trast very much. comes weaker, and you will hear more
As both T2 -curves diverge with a static noise; and when you drive even
longer TE, TElong, the difference in T2 - further away, you may not be able to
curves, and thus the difference in sig- discern the music from the background
nal intensity meaning contrast, is noise. And this is the same for the MR
more pronounced in our example. So it signal: there is always some noise in
might be reasonable to wait a very long the system, however, when the signal
TE; the resulting image should be very is strong, this does not matter much.
However, the smaller the signal, the
harder it is to differentiate it from the
background noise.
We’ll be able to
determine if you have a
brain in just a
moment…
56 MRI made easy The echo
Let us review some facts TR. A TR of less than 500 msec is con-
sidered to be short, a TR of more than
We have learned: 1,500 msec to be long (just to give you
7 The spin echo sequence a rough idea). A short TE is one that is
consists of a 90° and a as short as possible, a long TE also is
180° pulse. more than 3 times as long.
7 After the 90° pulse, protons de- A TE of less than 20 msec is con-
phase due to external and internal sidered to be short, a TE more than
magnetic field inhomogeneities. 80 msec to be long.
7 The 180° pulse rephases the de-
Fig. 39: It is possible to determine signal intensity for a tissue using a spin echo
sequence by combining the T1- and the T2-curve for that tissue. The longitudinal mag-
netization after the time TR is equal to the amount of transversal magnetization we start
out with, as it is “tilted” 90 degrees. This transversal magnetization immediately starts
to disappear by a rate which is determined by the transversal relaxation time, and thus
by the T2-curve. The signal intensity of the tissue after a time TE can then be inferred
from the T2-curve at this time TE (which starts after TR!).
Fig. 40: By combining T1- and T2-curves, signal intensity of certain tissues can be determined for a
pulse sequence using TR and TE as illustrated, and as explained in figure 39. What happens, when we
choose a long TR, as illustrated? With a long TR, differences in T1, in longitudinal magnetization time
are not very important any more, as all tissues have regained their full longitudinal magnetization.
When we only wait a very short TE, then differences in signal intensity due to differences in T2 have
not yet had time to become pronounced. The resulting image is thus neither T1- nor T2-weighted, but
mostly determined by the proton density of the tissues (for this, ideally TE should be zero).
also depends on TE, the time that we as enough time has passed by to allow
wait after the 90° pulse. So we now even tissues with a long T1 to relax to-
only have to look for the signal inten- tally. So when we choose a long TR, as
sity at the time TE on the T2 -curve. we just said, then differences in T1 do
not really matter.
What image do we get, when we When we also use a short TE, differ-
choose a long TR and a short TE? ences in signal intensity due to differ-
This is illustrated in figure 40. Here ences in T2 have not had enough time
are the T1- and T2 -curves for two dif- to become pronounced yet.
ferent tissues. The signal that we get, is thus nei-
As we heard earlier, with a very long ther T1- nor T2 -weighted, but mainly
TR, all tissues will have totally recov- influenced by differences in proton or
ered their longitudinal magnetiza- spin density.
tion; differences in T1 of the tissues ex- The more protons, the more signal,
amined will not influence the signal, if you look at it simply (figure 40).
60 MRI made easy Spin echo sequence
Fig. 41: When we wait a long TR and a long TE, differences in T2 have had
time enough to become pronounced, the resulting picture is T2-weighted.
Fig. 42: When we wait a shorter time TR, differences in T1 influence tissue contrast to a
larger extent, the picture is T1-weighted, especially when we also wait a short TE (when
signal differences due to differing T2s have not had time to become pronounced).
If you have not been And what do you see in figure 44? The
same couple is having tea. Now, hav-
concentrating ing tea which is usually served hot, al-
for the last few minutes, you ways takes a long time. And in the illus-
are probably thinking about tration the long TEa makes two people
giving up right now. How to happy. This should remind you that a
remember this – even if you long TE gives a T2 -weighted image.
do not understand all of it (which hope-
fully is not the case)?
Try looking at figure 43. What can
you see? A man with short TRousers.
And considering the weather condi-
tions, this makes only one person in the
picture happy.
This should remind you that a short
TR (TRousers) gives a T1-weighted im-
age (only 1 is happy).
B
Image interpretation MRI made easy 65
Fig. 46: T2-curves of different tissues can intersect. The signal intensity
of the tissues is reversed choosing a TE beyond the crossing point (TEC ):
before this crossing point (e.g. at TE1), tissue A has a higher signal inten-
sity than tissue B. This means that image contrast is still determined by
differences in T1: the tissue A with the shorter T1 has the stronger signal
intensity. At TEC , both tissues have the same signal intensity, and thus
cannot be differentiated. After this crossing point (e.g. at TE2 ), the rela-
tive signal intensities are reversed, and tissue B has the stronger signal.
The fact that the curves intersect is 7 With a TE beyond the crossing point
very important: (TE2 ), tissue A will have a lower signal
7 With a TE before the crossing point than tissue B.
(TE1), tissue A will have a higher signal 7 Before this crossing point (which you
Fig. 47: Flow effects are responsible for the black appearance of flowing
blood, the signal void in blood vessels.
68 MRI made easy Flow effects
This is not the only way in which some relaxation, and there is some
f low may inf luence the image, there longitudinal magnetization again,
may be all kinds of things, e.g. also as shown by the arrows pointing
f low-related enhancement. back up. The protons in the blood
Illustration 48 shows a blood ves- vessel, however, have left the slice
sel going through a slice which is be- and been replaced by protons that
ing examined. (A) represents the sit- still have all of their longitudinal
uation before the 90° pulse and (B) magnetization.
immediately after the pulse, longitu- If we send in a second 90° pulse
dinal magnetization is “tilted” 90°. now, there will be more signal com-
If we wait some more time, before ing from the vessel than from its
we send in a second 90° pulse, like surroundings, because there is more
in (C), protons will have undergone longitudinal magnetization at this
Flow effects MRI made easy 69
Fig. 49: Paramagnetic substances like gadolinium shorten the T1 and the T2
of their surroundings. The respective T1- (fig. 49A) and T2-curves (fig. 49B)
are shifted towards the left. In effect, this means that for a certain TR there is
more, for a certain TE, however, there is less signal.
Contrast media MRI made easy 71
What about MR
contrast media?
Certain so-called paramagnetic sub-
stances have small local magnetic
fields, which cause a shortening of
the relaxation times of the protons
in their neighborhood. This effect is
named proton relaxation enhance-
ment.
The body contains such paramag-
netic substances under normal cir-
cumstances. Examples are degra-
dation products of hemoglobin, e.g.
deoxyglobin and methemoglobin,
which are found in hematomas, or al-
so molecular oxygen.
Gadolinium (Gd), a paramagnetic
substance, is used in MR contrast me-
dia, like in Magnevist® or Gadovist®.
Chemically, Gadolinium is a rare
Now don’t move earth, which, however, is toxic in its
for the next thirty free state. Because of this it is bound
minutes. If you
to “some other chemical” in a certain
way called chelation, which solves the
really have to, you may problem of toxicity. For example, in
breathe. Magnevist®, this chemical is DTPA.
The pharmacological properties of
many Gadolinium-containing contrast
media like in Gadopentetate Dimeglu-
mine or Gadolinium DTPA (Magne-
vist®) or Gadobutrol (Gadovist®) are
very similar to iodinated contrast me-
dia in conventional radiology: however,
these Gadolinium-containing contrast
media are even better tolerated.
The Gd-containing contrast media
have an effect on both the signal in-
tensity of T1- and T2 -weighted imag-
es, as they shorten the T1 and the T2 of
their surroundings (figure 49), mean-
ing that the respective curves are
shifted towards the left.
In effect, for a given TR, there is
more signal, for a given TE, there is
less signal.
72 MRI made easy Contrast media
Fig. 50: In (A), the T1-curves for tissue A and B are very close to each other,
resulting in only a small difference in signal intensity between the tissues
at TR. In (B), the T1-curve of tissue A is shifted to the left, as contrast agent
entered tissue A but not tissue B. At the same time TR, there now is a much
greater difference in signal intensity, i.e. tissue contrast.
Contrast media MRI made easy 73
In figure 50, the signal intensity for two As loss of signal is often more dif-
tissues, A and B, is illustrated. The i.v. ficult to appreciate than a signal en-
administered Gd contrast medium en- hancement, T1-weighted images are
ters tissue A, but not tissue B. the predominant imaging technique
The T1 of tissue A becomes shorter used after contrast medium injection.
and the T1-curve is shifted to the left. As the contrast media are not distrib-
The result is that the signal from tis- uted evenly throughout the body, sig-
sue A at time TR is stronger than it was nals from different tissues will be influ-
before, and the two tissues can be bet- enced differently. Vascularized tumor
ter differentiated, because there is bet- tissues are enhanced, for example. This
ter contrast. may, for example, help with differen-
What happens, when we perform a tiation between tumor tissue and sur-
T2 -weighted examination after con- rounding edema, which might other-
trast medium application, we have seen wise be indistinguishable.
in figure 49: the T2 -curve is shifted to It is also important that the Gd com-
the left, reducing the signal coming at pounds do not go through the intact,
a given TE. but only through the disrupted blood-
brain barrier.
In general, it has been shown that
the use of contrast media increases le-
ed image.
7 With long TE, the image is T2 -weight-
ed.
7 Flow effects can be variable, and
ference is in the time interval between (the protons have relaxed, are saturat-
pulses, the TR (see page 45). ed), the signal is influenced by the pro-
You can see the effect in figure 52 ton density (Do you recall the stories
with the T1-curves (going uphill!) of with the short trousers and the long
two different tissues. If we send in the teas?). With a TR short, with the partial
second pulse after a long time, TR long, saturation (protons have not relaxed),
both tissues will have regained longi- the T1 becomes important for the signal
tudinal magnetization. With a TR long , intensity, so we get T1-weighted images
with the saturation recovery sequence (figure 52).
76 MRI made easy Inversion recovery sequence
the 90° pulse. The 90° pulse “tilts” the original value. So we get a T1-weighted
magnetization into the transversal image – which is even more T1-weight-
(x-y-) plane, so it can be measured/re- ed than partial saturation recovery im-
ceived. ages.
The signal that we get depends on Interestingly, when the 90° pulse is
the time between the 180°- and the 90° sent in when the longitudinal mag-
pulse, the time after the inversion by netization goes from negative to posi-
the 180° pulse; this time is thus called tive, i.e. is zero, the tissue does not give
TI = inversion time. a signal! This may be useful when we
The signal intensity in an inversion do not want a tissue to show up in the
recovery image is dependent on T1, image, e.g. when we want to suppress
which determines how fast the longi- the fat signal – but let us not go into too
tudinal magnetization goes back to its much detail here.
Fig. 54: The inversion recovery sequence uses a 180° pulse which inverts the longitudinal magnetization, fol-
lowed by a 90° pulse after the time Tl. The 90° pulse “tilts” the magnetization into the transversal (x-y-) plane,
so it can be measured/received. The tissue in the bottom row goes back to its original longitudinal magnetization
faster, thus has the shorter T1. For the time Tl which is illustrated, this results in less transversal magnetization
after the 90° pulse.
78 MRI made easy Spin echo sequence
Fig. 55: Schematic illustration of a spin echo pulse sequence. This is repeatedly
illustrated, as the spin echo sequence is so important.
Fast imaging MRI made easy 79
some time, during which it may be dif- the dephasing spins: instead of a 180°
ficult for the patient to lay completely pulse, we apply a magnetic field gradi-
still. In addition, there is always some ent. This means that an uneven mag-
unavoidable motion, like respiration netic field, a gradient field, is added/su-
and heart beat. All these movements perimposed on the existing magnetic
unfortunately decrease image quality. field.
To help with these problems, fast The magnetic field gradient is
pulse sequences were developed, switched on for a short time. This re-
which take less time. Most of these sults in even larger magnetic field in-
have strange names such as FLASH homogeneities in the examined slice.
(Fast – Low – Angle – Shot), or GRASS (The magnetic field inhomogeneities
(Gradient – Recalled – Acquisition – at that already exist at that time are due
Steady – State). These sequences are to inhomogeneities of the external
very important nowadays in daily magnetic field, and the internal mag-
practice. netic field inhomogeneities inside of
Here is just a rough outline – you the tissues, which we talked about ear-
can find more details in textbooks or lier – if you do not remember this, go
the book “MR Buzzology”. back to page 27 for a short recap).
As you may already have noticed, Due to these larger magnetic field in-
the TR is the most time consuming pa- homogeneities, transversal magneti-
rameter of an imaging sequence (see zation, and thus the signal, disappears
also pages 57 and 83). It makes sense to faster (protons dephase faster!). Then
shorten TR if we want to make imag- the magnetic gradient is switched off,
ing faster. And this is done in the fast and after a short time turned back on
imaging sequences. with the same strength, but in the op-
But with a decreasing TR, there are posite direction.
some problems: The faster moving protons now be-
7 Firstly, with a spin echo sequence come the ones that move slowly, and
we used a 180° pulse to refocus the de- vice versa (similar to what happens af-
phasing spins. Unfortunately, we can- ter a 180° pulse).
not use a 180° pulse for this purpose, This results in some rephasing, and
when we do imaging with a very short thus the signal increases again to a
TR: it requires some time to “produce” certain maximum, which is called a
and to deliver a 180° pulse, and with a gradient echo. After this echo, the sig-
very short TR, there will not be enough nal decreases again.
time for that between the 90° pulses. What to do about the second prob-
7 Secondly, with decreasing TR, lon- lem, the small amount of longitudinal
gitudinal magnetization will have re- magnetization with a short TR? The
covered less and less between pulses 90° pulse, e.g. in a spin echo sequence,
80 MRI made easy Fast imaging
weighting.
7 Longer TEs produce more T2*-weight-
ing.
7 With fast scans, intense signals of-
To illustrate this: Just imagine that you our formula: What is “N”? As you know
are sitting in a large audience, where peo- from other imaging methods (or your
ple are making a lot of noise. Someone sit- PC), pictures are made of picture ele-
ting next to you whispers something in ments, which all together make up the
your ear, but you cannot really under- image matrix, e.g. a 1,024 x 768 matrix
stand him, because there is so much back- has 768 rows of 1,024 picture elements
ground noise. What you will probably do, (pixels).
is ask him to repeat what he said once or In our equation, N is the number of
several times. You mentally add up the rows in a matrix, like rows in a letter.
information which you receive each time. The more rows you have, the more time
As this signal is always the same, it will it takes for the image.
increase by adding it up. The background Just think about this as if you were
noise, however, is not always the same. writing a letter: if you have paper with
Instead, it is random and fluctuates and 5 rows on a page, you will finish a page
does not add up the way the signal does. faster than if you have 25 rows to write.
So altogether you will have a better sig- However, you have more content, more
nal-to-noise ratio (which you would also detail on a page/picture, when you work
have if the person spoke louder). Back to with more rows.
Multislice imaging MRI made easy 83
And why does TR influ- The longer the TR, the more slices we
can excite in the meantime.
ence acquisition time? So by just adding a little extra time,
If you choose a long time TR to repeat we will examine many slices instead
your pulse sequence, to perform ad- of one, and imaging time per slice de-
ditional signal measurements, imag- creases substantially.
ing takes longer than with a short TR. We perform so-called multislice im-
However, there is a trick that can short- aging. Another way to possibly reduce
en imaging time a bit. TR, and thus imaging time, is the use
While we are waiting to repeat our of a contrast medium: as we have seen,
imaging sequence in one slice, i.e. Gadolinium-DTPA shortens T1.
while we wait for TR to go by (slice A And when T1 is shorter, the TR can al-
in figure 56), we might as well make so be shorter, without a loss in signal
measurements in one or more differ- intensity of the tissue in question (see
ent slices (slices B, C and D in figure 56). figure 49).
Fig. 57: Magnetic gradient fields are superimposed on the field of the MR magnet,
so that different cross sections of the body experience magnetic fields of differing
strength. In the illustration, the resulting magnetic field strength is increasing from 1.4
Tesla at the feet to 1.6 Tesla at the head. As magnetic field strength and precessing/
resonant frequency are directly correlated (Larmor equation), the resonant frequency
at the feet is about 60 MHz, while it is about 68 MHz at the top of the head in our
example. By selecting a certain RF pulse frequency, we determine the location of the
slice which we examine.
86 MRI made easy Slice thickness
Fig. 58: There are two ways to determine slice thickness. The first is to use an RF pulse that has not only one spe-
cific frequency, but a certain range of frequencies, a so-called bandwidth. If, for example, we send in an RF pulse,
which contains frequencies between 64 and 65 MHz, protons in slice 1 will be influenced by the RF pulse.
When the RF pulse only contains frequencies between 64 MHz and 64.5 MHz, thus has a smaller bandwidth, slice 2,
which is half as thick as slice 1, will be imaged.
When there is more difference in magnetic field strength between the level of the feet and the head, i.e. the
magnetic gradient is steeper, the resulting slice will be thinner, even though the RF pulse bandwidth is the same.
This is illustrated in (C), where the magnetic field strength varies more between the feet and the head than in (A);
the corresponding resonant frequencies are 56 to 72 MHz in (C) vs. 60 to 68 MHz in (A). Using the same RF pulse
containing frequencies from 64 to 65 MHz results in imaging of a thinner slice 3 in (C) than in (A).
88 MRI made easy Frequency encoding
Where does the signal image? The trick is similar to the slice select-
ing gradient, which is turned on only during
come from? application of the RF pulse.
Now we have selected position and After the RF pulse is sent in, all protons in
thickness of our slice. But how can we the slice precess with the same frequency.
find out, from what point of our slice a We now apply another gradient field which
certain signal is coming from – informa- – in our example – decreases from left to right.
tion that we must have to construct an So the precession frequency of the protons
will also decrease from left to right (in protons in one column will still have sig-
our example, the precession frequencies nals with the same frequency. We now
are 65, 64 and 63 MHz, respectively). can tell by the frequency from which col-
The result is that the protons in the umn a signal comes from, but still can-
different columns emit their signals not pinpoint the exact place of origin in a
with these different frequencies. The particular column. As this is not enough
gradient applied is thus called the fre- spatial information, we have to do some-
quency encoding gradient. However, all thing else.
90 MRI made easy Phase encoding
Fig. 60: To find out where in a column with the same frequency a certain signal comes from, we use an ad-
ditional gradient. In (A), the column with the precession frequency of 65 MHz from figure 59 is depicted. We now
switch on a gradient field, which is stronger at the top than at the bottom of the column for a very short time (B).
The proton at the top thus precesses faster than the one in the middle, which in turn precesses faster than the
proton at the bottom. This difference in precessing frequency only lasts for a very short time; when the gradient
is switched off, all protons experience the same magnetic field again, thus have the same 65 MHz precession
Phase encoding MRI made easy 91
Can we use all other ics, so we will only talk about the pro-
tons). Why an odd number? Just think
nuclei for imaging? about the proton as a little bar mag-
The answer is no. There are two im- net. If you have a nucleus with two
portant pre-conditions both of which (or any other even number) protons,
must be fulfilled. these little bar magnets would cling
7 Firstly, we can only use nuclei that together like any other magnets (op-
have a spin. posite poles attract).
This can be easily explained: as we The result: their magnetic moments
saw at the beginning, the protons were would cancel each other out. If we
spinning around, and thus their elec- have a nucleus with an odd number
trical charge was also spinning, mov- of protons, e.g. three, pairs of protons
ing. And the moving electrical charge will still cling together and neutralize
was the current that caused the mag- each other. However, there will always
netic field of the proton, which was be one proton left that still has a mag-
the basis for everything. If it weren’t netic moment. Nuclei with odd num-
for the spin, there would be no mag- bers of protons thus have a magnetic
netic field. moment, and can principally be used
7 Secondly, the nucleus must have an for MRI.
odd number of protons (and neutrons, Examples are: carbon-13, fluorine-19,
but this will go into too much phys- sodium-23, phosphorus-31.
What a day!
Give me a
180°-rephasing
high-frequency
impulse!
94 MRI made easy Hardware
already accustomed to
from the MR unit, the whole system
has to be shielded by a Faraday cage.
quite a bit! In addition, it has to be taken into ac-
count that larger metallic objects, es-
pecially when moving (like elevators,
cars), can influence the magnetic field
of the scanner, and should also be kept
away from the MR unit.
MR spectroscopy
MR spectroscopy has been in use for a
long time, long before MR was used for
imaging. The procedure is used as an
analytical tool, as it can identify vari-
ous chemical states of certain elements
without destruction of the sample.
Meanwhile, spectroscopy and imaging
may be combined (spectroscopic imag-
ing). This enables us to obtain in vivo
information about the chemistry and
metabolism in specific locations, like in
the brain, the liver, or even the heart.
As these measurements can be re-
peated without harm, follow-up stud-
ies of cell physiology are possible. This,
for example, can be useful in the evalu-
ation of certain diseases and the effects
of therapy.
As spectroscopy requires very ho-
mogeneous magnets with higher field
strengths, it can only be performed
with the use of MR units which have
superconducting magnets.
98 MRI made easy The final