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Int J Psychiatry Clin Pract 2015; 19: 246252. 2015 Informa Healthcare
ISSN 1365-1501 print/ISSN 1471-1788 online. DOI: 10.3109/13651501.2015.1084328
ORIGINAL ARTICLE
informahealthcare.com/ijpcp
Sung-Jin Kim1, Joo-Cheol Shim2, Bo-Geum Kong1, Je-Wook Kang1, Jung-Joon Moon1,
Dong-Wook Jeon1, Young-Soo Seo3, Min-Kyung Oh4 & Do-Un Jung1
Department of Psychiatry, Busan Paik Hospital, Inje University, Busan, Korea, 2Shim Joo Cheol Psychiatry
Clinic, Busan, Korea, 3Department of Psychiatry, Sharing and Happiness Hospital, Busan, Korea, and
4
Department of Clinical Pharmacology, Busan Paik Hospital, Inje University, Busan, Korea
Abstract
Objectives. Cognitive dysfunction is a core feature of schizophrenia; deficits often manifest prior to diagnosis and persist throughout the course of the illness. This study was performed to assess the difference
in cognitive function and daily living skills between the early- and late-stage schizophrenia. Methods.
Fifty-five clinically stable patients with schizophrenia were recruited (25 with 5-year and 30 with
5-year disease durations). We evaluated subjects clinical states, cognitive function, and psychosocial
factors. The Korean versions of MATRICS Consensus Cognitive Battery and UCSD Performance-based
Skills Assessment were used for evaluating cognitive function and daily living skills. Chi-square, Wilcoxon rank sum, and t-tests were used to analyze the data. Results. The two groups did not differ for most
demographic variables. No significant differences between groups were found for clinical symptoms,
psychosocial factors, or non-social cognitive domains. However, the early-stage group had higher social
cognition domain scores than the late-stage group (p 0.01). Early-stage patients scored significantly
higher than those in the late-stage group did in the communication and comprehension/planning domains (p 0.037 and 0.027, respectively), and total score (p 0.003) of the Performance-based Skills
Assessment. Conclusions. We observed significant differences between patients with early- and late-stage
illness with regard to social cognition and performance-based skills.
Key words: Cognition, psychosocial factors, schizophrenia
(Received 12 January 2015; accepted 13 August 2015)
Introduction
Schizophrenia is a chronic psychiatric disorder that causes
long-lasting disabilities in major domains of the patients
daily life (Wiersma et al. 2000). Patients with schizophrenia
typically manifest symptoms in early adulthood and experience difficulties in social and occupational functions and
independent living thereafter (McGlashan 1988). Many
chronic patients with schizophrenia live in assisted living
facilities and long-stay institutions (Cohen et al. 2000). Less
than 15% patients with schizophrenia are engaged in paid
employment (Slade and Salkever 2001).
Cognitive dysfunction is one of the core symptoms of
schizophrenia, and is closely related to everyday functioning, prognosis, and quality of life (Green et al. 2004).
Patients with schizophrenia exhibit deficits in most cognitive domains, showing significant differences compared with
control subjects with regard to attention, memory, and executive function (Sharma and Antonova 2003). Approximately
90% of patients with schizophrenia have a deficit at least in
one cognitive domain, and 75% suffer from deficiencies in
two or more cognitive domains (Palmer et al. 1997). Cognitive deficits are prominent in the first schizophrenic episode, but they are more conspicuous in patients with an early
Correspondence: Do-Un Jung, Department of Psychiatry, Busan Paik
Hospital, Inje University, 75, Bokji-ro, Busanjin-Gu, Busan, Republic
of Korea, 614735. Tel: 82-51-890-6189. Fax: 82-51-894-2532.
E-mail: gabriel.jdu@gmail.com
DOI: 10.3109/13651501.2015.1084328
capacities in the understanding of others minds and decentration during prolonged psychoses (Vohs et al. 2014). In that
study, social cognition did not differ between two groups.
Functional impairments have worsened over the disease
course in interpersonal functioning, vocational functioning,
and everyday functioning (Reichenberg et al. 2014).
While positive schizophrenia symptoms are relatively
well controlled with drug treatment, cognitive functions
show constant degradation in the early stages of disease, and
social, occupational, and other everyday functions continue
to decrease. These deficits can lead to recurrent episodes
(Lauriello et al. 1999), and failure during psychosocial rehabilitation programs (Green et al. 2000). Therefore, one of
the goals of schizophrenia treatment is to improve everyday
functions rather than the symptoms themselves. Studies have
been conducted to assess these functions (Harvey 2013).
Improved cognitive function is one of the major goals of
schizophrenia treatment. In related studies, assessment tools
have played important roles. The National Institute of Mental
Health (NIMH) announced a standardized tool for evaluating cognitive functions and potential treatment response in
patients with schizophrenia called the MATRICS Consensus Cognitive Battery (MCCB) (Nuechterlein et al. 2008).
The MCCB is a sensitive tool for the detailed evaluation of
patients cognitive functions. For evaluating the everyday
functioning of patients with schizophrenia, assessments have
been proposed that involve observing the patients actual
living situation or assessing the patients functions through
role-playing. The University of California San Diego (UCSD)
Performance-based Skills Assessment (UPSA) is a widely
used role-playing tool for evaluating the everyday functions
of patients with schizophrenia (Patterson et al. 2001). It is
easy to apply, and its validity and reliability are supported
by various reports (Figueira and Brissos 2011; Mausbach
et al. 2008; Mausbach et al. 2011). Thus, the UPSA is a leading measure for studies of cognition in schizophrenia. The
MCCB composite scores have substantial association with
the UPSA composite score (Keefe et al. 2011), and as reported
by Burton et al (2013), the MCCB three-factor model shows
an association with the UPSA composite score.
Numerous studies have been conducted to assess differences in cognitive functions in subjects with different stages
of schizophrenia. However, these investigations only evaluated basic cognitive functions. The objective of this study
was to examine cognitive functions across different stages of
schizophrenia by evaluating basic cognitive functions with
the MCCB and daily living skills with the UPSA.
Methods
Subjects
This study included patients diagnosed with schizophrenia
based on the Diagnostic and Statistical Manual of Mental
Disorders 4th edition (DSM-IV) (APA 1994), who satisfied the following conditions: 1) age between 18 and 65
years, 2) outpatients with a stable condition for the previous
3 months, 3) no changes in medications for the past 3
months, and 4) willing to provide informed consent and participate in the study. The exclusion criteria were as follows: 1)
Results
Demographic data
A total of 55 subjects participated, with 25 and 30 subjects in
the early- and late-stage groups, respectively. The early-stage
group included 16 males (64%) and 9 females (36%), and the
late-stage group consisted of 18 males (60%) and 12 females
(40%). The average age of subjects in the late-stage group was
41.97 6.67, which was significantly higher than the average
age in the early-stage group (29.08 7.10, p 0.001). Subjects in the early-stage group received a mean 13.64 2.23
years of education, compared with 12.40 2.30 years in the
late-stage group (p 0.041). The average illness durations
were 33.52 19.46 and 224.43 69.92 months for the earlyand late-stage groups, respectively (p 0.001). The number
of hospitalizations was also significantly different between the
two groups: 2.00 1.29 and 6.24 5.34 hospitalizations for
the early- and late-stage groups, respectively (p 0.001). The
late-stage group was more involved in vocational/psychosocial rehabilitation (p 0.006). The chlorpromazine equivalent doses were 501.89 250.15 mg and 542.23 347.56 mg
for the early- and late-stage groups, respectively (p 0.05).
There were 22 (88%) subjects in the early-stage group who
took antiparkinsonian medications, compared with 19 (63%)
subjects in the late-stage group (p 0.037). There were 6
smokers (24%) and 19 non-smokers (76%) in the early-stage
group, compared with 14 smokers (46.67%) and 16 nonsmokers (53.33%) in the late-stage group (Table I).
Clinical symptoms
The total PANSS scores did not reveal a significant difference
between the two groups; the early- and late-stage group scores
were 70.32 12.86 and 69.40 12.96 points, respectively.
However, there was a significant difference (p 0.048) in the
positive symptom subscale (early-stage group: 16.60 4.56
and late-stage group: 19.13 4.69) but not the other subscales. There was no significant difference between the two
groups on the CGI-SCH (Table I).
Psychosocial factor characteristics
PSP, SQLS, and ISP results were not significantly different
between the two groups (Table I).
Cognitive function characteristics
Assessment of basic cognitive functions using the Korean
version of MCCB showed no significant difference between
the two groups in terms of the total score and most subscale
items. However, the early-stage group social cognition domain
score was 30.92 9.07, which was significantly higher than
the score of the late-stage group (24.14 9.28, p 0.010).
The early-stage group also scored significantly higher in the
assessment of everyday functions using the Korean version
of UPSA. Specifically, the total score was significantly higher
for the early-stage group (75.59 12.54) compared with the
late-stage group (65.19 14.00, p 0.003). Specifically, the
early-stage group scored significantly higher than the latestage group in the communication domain (13.61 3.10 vs.
11.55 3.78, respectively, p 0.037) and comprehension/
DOI: 10.3109/13651501.2015.1084328
Table I. Demographic and clinical characteristics of early- and late-stage patients with schizophrenia.
Characteristics
Gender
Male, n (%)
Female, n (%)
Age (years)
Education (years)
Duration of illness (months)
Number of hospitalization
Vocational/psychosocial rehabilitation, n (%)
Antipsychotic medication
Monotherapy, n (%)
Polytherapy, n (%)
Antiparkinsonian medication, n (%)
Benzodiazepine medication, n (%)
Average daily neuroleptic dose (mg, CPZE)
Smoking
Smoker, n (%)
Non-smoker, n (%)
PANSS
Positive subscale
Negative subscale
General psychopathology subscale
Total score
CGI-SCH
Positive symptoms
Negative symptoms
Depressive symptoms
Cognitive symptoms
PSP
SQLS
ISP
Early stage
(n 25,
mean SD)
Late stage
(n 30,
mean SD)
16 (64)
9 (36)
29.08 7.10
13.64 2.23
33.52 19.46
2.00 1.29
11 (44)
18 (60)
12 (40)
41.97 6.67
12.40 2.30
224.43 69.92
6.24 5.34
24 (80)
15 (60)
10 (40)
22 (88)
16 (64)
501.89 250.15
15 (50)
15 (50)
19 (63)
18 (60)
542.23 347.56
6 (24)
19 (76)
14 (46.67)
16 (53.33)
0.082
16.60 4.56
18.80 3.94
34.37 6.72
70.32 12.86
19.13 4.69
17.10 4.33
33.17 6.29
69.40 12.96
0.048
0.137
0.513
0.793
3.16 1.25
3.00 1.04
2.24 0.78
2.72 1.02
60.92 11.24
42.52 16.26
14.28 5.17
3.53 1.33
2.73 0.74
2.33 0.71
2.60 0.76
60.23 10.42
39.17 20.36
13.90 5.73
0.292
0.273
0.645
0.604
0.822
0.509
0.653
p value
0.761
0.001
0.041
0.001
0.001
0.006
0.458
0.037
0.761
0.872
CGI-SCH, Clinical Global Impression-Schizophrenia scale; CPZE, chlorpromazine equivalent; ISP, Insight Scale for
Psychosis; K-WAIS, Short-form of Korean-Wechsler Adult Intelligence Scale; PANSS, Positive and Negative Syndrome
Scale; PSP, Personal and Social Performance Scale; SD, standard deviation; SOFAS, Social and Occupational Functioning
Assessment Scale; SQLS, Schizophrenia Quality of Life Scale.
MCCB
Speed of processing
Attention/Vigilance
Working memory
Verbal learning
Visual learning
Reasoning and
problem-solving
Social cognition
Composite score
UPSA
Finance
Communication
Comprehension/Planning
Transportation
Household skills
Total score
Early stage
(N 25,
mean SD)
Late stage
(N 30,
mean SD)
p value
33.80 11.83
36.29 10.85
32.68 11.29
34.20 7.48
40.76 14.23
42.32 10.51
34.34 11.89
38.69 10.35
31.76 10.82
31.52 5.99
35.69 13.83
39.11 6.68
0.867
0.449
0.761
0.149
0.191
0.309
30.92 9.07
26.70 12.07
24.14 9.28
24.12 8.61
0.010
0.408
17.20 2.89
13.61 3.10
12.56 3.01
14.72 2.52
17.50 5.11
75.59 12.54
16.74 2.93
11.55 3.78
10.44 3.64
13.18 2.84
13.28 8.37
65.19 14.00
0.467
0.037
0.027
0.059
0.052
0.003
contained in others facial expressions and voices. Understanding and managing emotions is involved in the higherlevel process. The second is social perception: decoding and
interpreting social cues in others. The third is ToM/mental
state attribution, which involves recognizing certain intentions or behaviors that may affect his/her behaviors and those
of others. The fourth is attributional style/bias, which is the
way of determining positive or negative reasons for a certain
life event. On the managing emotions part of the MSCEIT
in the MCCBs social cognition domain, it was about how
effective the actions might be in managing their emotions
or others emotions. Thus, the social cognition domain in
the MCCB seems to have a relationship mainly with emotion processing. One study found that social cognition in
patients with schizophrenia are closely related with everyday functions and interpersonal and social/occupational
skills (Couture et al. 2006). This was classified as an important prognostic factor and a treatment goal for patients with
schizophrenia (Kee et al. 2003).
In the assessment of everyday functions using the UPSA,
the early-stage group scored higher than the late-stage
group in communication, comprehension/planning, and
total scores. Many patients with schizophrenia have difficulties communicating with and comprehending conversations with other people; some of them even have difficulties
understanding basic phrases and jokes (Brune et al. 2007).
Among the UPSA domains, the communication and comprehension/planning categories are closely related with social
functions. Therefore, the above findings can be regarded as
supporting the results of the social cognition test using the
MCCB. Since the UPSA uses role-playing based on everyday
situations, it can be inferred that patients in the early stages
of schizophrenia are more socially functional in their everyday living compared with those in later stages. Mausbach
et al. (2008) proposed that the UPSA can be used to predict
the residential independence of patients with schizophrenia,
and another study verified a significant correlation between
UPSA results and patients occupational skills (Mausbach
et al. 2011). Taking all of these results into consideration,
it can be inferred that the constant difficulties in everyday
living and social occupational skills experienced by patients
with late-stage schizophrenia may be related to degradation
of social cognition and functions.
Some studies have also shown that everyday functions
decline throughout the lifetime in the patients with schizophrenia (Harvey et al. 2010; Reichenberg et al. 2014). All
subjects in the late-stage group were outpatients with a stable
condition, and most of them participated in the vocational/
psychosocial rehabilitation in this study. Thus, it seems that
the late-stage group experiences everyday function deficits
despite continued social stimulation.
There are several limitations of this study. First, we classified the subjects into early- and late-stage groups in a
cross-sectional study designed to compare cognitive functions across different stages of psychosis. Therefore, while
our findings are useful for assessing differences between the
two groups, it is limited in determining why there are cognitive function differences between disease stages. These limitations could be partially overcome if follow-up studies are
DOI: 10.3109/13651501.2015.1084328
Acknowledgements
The authors thank the staff of the Sharing and Happiness
Hospital for their assistance with the process of this study.
Statement of interest
The authors declare no conflict of interest with any commercial or other associations in connection with the submitted
article.
References
Addington J, Saeedi H, Addington D. 2005. The course of cognitive
functioning in rst episode psychosis: changes over time and
impact on outcome. Schizophr Res 78:3543.
APA. 1994. Diagnostic and Statistical Manual of Mental Disorder.
Washington, DC, American Psychiatric Association.
Brune M, Abdel-Hamid M, Lehmkamper C, Sonntag C. 2007. Mental
state attribution, neurocognitive functioning, and psychopathology: what predicts poor social competence in schizophrenia best?
Schizophr Res 92:151159.
Burton CZ, Vella L, Harvey PD, Patterson TL, Heaton RK,
Twamley EW. 2013. Factor structure of the MATRICS Consensus Cognitive Battery (MCCB) in schizophrenia. Schizophr Res
146:244248.
Cohen CI, Cohen GD, Blank K, Gaitz C, Katz IR, Leuchter A, et al.
2000. Schizophrenia and older adults. An overview: directions for
research and policy. Am J Geriatr Psychiatry 8:1928.
Pinkham AE, Penn DL, Green MF, Buck B, Healey K, Harvey PD. 2014.
The social cognition psychometric evaluation study: results of the
expert survey and RAND panel. Schizophr Bull 40:813823.
Rajji TK, Ismail Z, Mulsant BH. 2009. Age at onset and cognition in
schizophrenia: meta-analysis. Br J Psychiatry 195:286293.
Reichenberg A, Feo C, Prestia D, Bowie CR, Patterson TL, Harvey PD.
2014. The Course and Correlates of Everyday Functioning in
Schizophrenia. Schizophr Res Cogn 1:e47e52.
Rey MJ, Schulz P, Costa C, Dick P, Tissot R. 1989. Guidelines for the
dosage of neuroleptics. I: Chlorpromazine equivalents of orally
administered neuroleptics. Int Clin Psychopharmacol 4:95104.
Sharma T, Antonova L. 2003. Cognitive function in schizophrenia.
Decits, functional consequences, and future treatment. Psychiatr
Clin North Am 26:2540.
Slade E, Salkever D. 2001. Symptom Eects on Employment in a
Structural Model of Mental Illness and Treatment: Analysis of
Patients with Schizophrenia. J Ment Health Policy Econ 4:2534.
Sponheim SR, Jung RE, Seidman LJ, Mesholam-Gately RI, Manoach
DS, OLeary DS et al. 2010. Cognitive decits in recent-onset and
chronic schizophrenia. J Psychiatr Res 44:421428.
Vohs JL, Lysaker PH, Francis MM, Hamm J, Buck KD, Olesek K
et al. 2014. Metacognition, social cognition, and symptoms in
patients with rst episode and prolonged psychoses. Schizophr Res
153:5459.
Wiersma D, Wanderling J, Dragomirecka E, Ganev K, Harrison G,
An Der Heiden W et al. 2000. Social disability in schizophrenia:
its development and prediction over 15 years in incidence cohorts
in six European centres. Psychol Med 30:11551167.
Wilkinson G, Hesdon B, Wild D, Cookson R, Farina C, Sharma V
et al. 2000. Self-report quality of life measure for people with
schizophrenia: the SQLS. Br J Psychiatry 177:4246.