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. Author manuscript; available in PMC: 2010 Jan 27.
Published in final edited form as: Schizophr Res. 2001 Apr 15;49(1-2):1–52. doi: 10.1016/s0920-9964(01)00163-3

Table 5.

MRI Studies of progressive volume change in schizophrenia (SZ)

Study Sample N ROIs Follow-up interval Findings
Chakos et al. (1994) First episode SZ
Schizophreniform
Controls
21
8
10
caudate 18 months Increased caudate volume
with typical neuroleptics.
Volume correlated with dose;
inversely correlated with age
of onset.
Chakos et al. (1995) SZ 15 caudate 1 year Reduced caudate volume with
atypical neuroleptics.
Corson et al. (1999b) Chronic SZ 19 caudate, lenticular nucleus 2 years Typical neuroleptics increase
size of caudate/lenticular
nucleus, atypical neuroleptics
decrease size.
SPD 1
Psychosis NOS 3
Controls 0
Degreef et al. (1991) First episode SZ
Controls
13
8
cortical volume, ventricular
volume
1–2 years No difference in rate of
change for either.a
DeLisi et al. (1992) First episode SZ
Controls
50
33
temporal lobes, ventricular
volume
2 years No difference in temporal lobe
or ventricular volume. Change
in ventricular volume was
inversely correlated with
amount of time in hospital for
SZ.
(Note, some subjects
overlap with 1991
report, and some SZ
subjects were
characterized as
schizophreniform or
schizoaffective)
DeLisi et al. (1995) First episode SZ
Controls
20
5
cerebral hemispheres, medial
temporal lobe, temporal lobe,
lateral ventricles, caudate
nucleus, corpus callosum
4 years Rate of change greater in SZ
for left ventricle.a
DeLisi et al. (1997) First episode SZ
Controls
50
20
cerebral hemispheres, temporal
lobe, medial temporal lobe,
lateral ventricles, cerebellum,
caudate nucleus, corpus
callosum, Sylvian fissure
≥ 4 years Rate of change greater in SZ
for left and right hemispheres,
right cerebellum, corpus
callosum segment, and
ventricles.a
DeLisi et al. (1998) First episode SZ 50 cerebral hemispheres ventricles, 5 years Larger ventricles at baseline
correlated with poorer
premorbid functioning. Larger
ventricles at baseline also
showed less of an increase in
size at follow up compared
with smaller ventricles at
baseline.
Gur et al. (1998b) SZ patients (20 first
episode, 20 chronic)
Controls
40

17
whole brain CSF, frontal lobes,
temporal lobes
2–3 years Rate of change of frontal lobe
volume increased in SZ.a Both
subject groups showed a
reduction in temporal lobe
volume.
Jacobson et al. (1998) Childhood onset SZ
Controls
10
17
cerebral volume, superior,
anterior temporal lobe,
amygdala, hippocampus
2 years Rate of change of total
cerebral volume and temporal
lobe structures increased in
SZ.a
Keshavan et al. (1998b) First episode psychosis
Controls
17
17
cerebral volume, superior
temporal gyrus, cerebellum
1 year Volume of superior temporal
gyrus was inversely correlated
with prodrome and psychosis
duration. Rate of change of
superior temporal gyrus was
greater in patients.a Superior
temporal gyrus volume
enlarged with treatment in
some patients (i.e. reversal of
volume reduction after 1
year).
Lieberman et al. (1996) First episode SZ or
schizoaffective
Controls
62

42
qualitative measure of lateral
ventricles, third ventricle,
frontal/parietal cortex, medial
temporal
18 months Patients with poor response to
treatment showed more
ventricle enlargement and
reduced cortical volumes
compared with patients with
better response to treatment.
Nair et al. (1997) Patients with symptoms
of schizophrenia
Controls
18

5
total ventricular volume 2–3 years Rate of change greater in SZ-
like patients.a
Rapoport et al. (1997) Childhood onset SZ
Controls
16
24
ventricular volume, thalamic
area, caudate nucleus, putamen,
globus pallidus
2 years Rate of change of ventricular
volume and thalamic area
increased in SZ.a
Rapoport et al. (1999) Childhood onset SZ
Controls
15
34
gray and white matter volume
(frontal, temporal, parietal,
occipital lobes
4 years Rate of change of gray, but not
white matter in frontal,
temporal, and parietal lobes
increased in SZ.a
a

Rate of change increased in patient group means that the structure in question changed volume at a faster rate (larger volume for given period of time) than in the control group.