Literature DB >> 24194641

Cognitive functioning correlates of self-esteem and health locus of control in schizophrenia.

Chien-Shu Wang1, Jo Yung-Wei Wu, Wei-Chung Chang, Shu-Ping Chuang.   

Abstract

AIM: The study aimed to investigate the relationship among sociodemographic factors, neurocognitive factors, self-esteem, and health locus of control in patients diagnosed with schizophrenia. We examined the self-esteem, internal health locus of control, and external health locus of control through sociodemographic and neurocognitive factors.
METHODS: Forty-six schizophrenic patients and 31 healthy residents from the community or hospital were recruited as the control group. All subjects participated in the self-esteem questionnaire, health locus of control questionnaire, and a series of neuropychological measures.
RESULTS: Multiple regression analysis revealed that inhibition of attention and external health locus of control were predictors for self-esteem (r=-0.30, P<0.05; r=0.41, P<0.01); inhibition of attention and external health locus of control were contributors for internal health locus of control (r=-0.43, P<0.01; r=0.61, P<0.001); and education was related to external health locus of control (r=-0.31, P<0.05).
CONCLUSION: The current study integrated background characteristics and cognitive function to better understand the impact of self-esteem and health locus of control in schizophrenia. The findings indicated that inhibition of attention, external health locus of control, and education contributed to self-esteem, internal health locus of control and external health locus of control. However, the overall predicted variance accounted for by these predictors was small; thus, further research is necessary to examine imperative variables related with self-esteem and health locus of control in schizophrenia.

Entities:  

Keywords:  cognitive functioning; external health locus of control; internal health locus of control; schizophrenia; self-esteem

Year:  2013        PMID: 24194641      PMCID: PMC3814929          DOI: 10.2147/NDT.S51682

Source DB:  PubMed          Journal:  Neuropsychiatr Dis Treat        ISSN: 1176-6328            Impact factor:   2.570


Introduction

Schizophrenia patients may experience alterations in self concept and thus face difficulties in dealing with self-esteem.1–3 In recent decades, self-esteem has emerged as an essential concept possibly related to the psychopathology and treatment of patients with severe psychiatric illness.1,4–6 Brown et al7 found that there was a strong negative association between self-evaluation and interpersonal relationship, including parents, children, and close friends. Further studies have demonstrated that schizophrenia patients with lower self-esteem experienced a higher risk of suicidal ideation, more depression, and poor psychosocial functioning.8–10 Accordingly, negative evaluations of the self have been correlated with mental health problems.11,12 On the other hand, people with higher self-esteem and internal health locus of control usually have a positive self-concept and maintain a better mood.13–17 Several studies have found higher self-esteem in relation to better medication compliance and treatment adherence.18,19 Health locus of control is essential for maintaining a healthy life environment, and assesses the extent to which individuals believe that their health is related to their own behaviors (internal health locus of control) or to some external consequences (external health locus of control).20 A person with a high internal locus of control may feel more empowered to convert to healthy behaviors, while on the other hand, high external locus of control is often correlated with psychosocial maladjustment.21,22 People with schizophrenia-spectrum disorders and bipolar disorder were found to be more likely to have a health locus of control determined by powerful others and chance when compared to people with nonpsychotic mental illness.23 Neurocognitive variables, such as executive functioning have not been associated with the self-esteem of schizophrenia;24 however, researchers have found that schizophrenia patients with intact executive functioning have a higher level of self-esteem.25 Previous studies indicated that patients, diagnosed under the schizophrenia spectrum disorder, who have poor attention tend to score lower in self-esteem and have a greater acceptance of stigma.24,26 Additional neurocognitive variables of schizophrenia or schizoaffective disorder have also been examined, showing deficits in immediate memory, language, delayed memory, verbal ability, processing speed, visual working memory, and verbal memory when compared with healthy samples.27,28 In sum, self-esteem and health locus of control during the long-term rehabilitation process of schizophrenia are important in understanding their experiences and in implicating further treatment. The present study aimed at identifying correlates of these self-concepts and health locus of control from a broad range of sociodemographic and neuropsychological factors.

Methods

Participants

Forty-six schizophrenia outpatients were interviewed using the Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM-IV) Diagnoses29 from the department of psychiatry at the Zuoying Branch of Kaohsiung Armed Forces General Hospital in Taiwan. Two psychiatrists made the diagnoses independently. When an inconsistent diagnosis occurred between the original two psychiatrists, an assessment made by a third psychiatrist was incorporated to reach a consensus. All participants were receiving ongoing medical treatment. Participants who were experiencing acute psychotic symptoms (including mood disorders) or had a history of mental retardation or who had participated in substance abuse or who had shown any neurological disorder in the preceding 6 months were excluded from the study. Clinical stability was defined as no acute hospitalizations or changes in medication in the previous month. Thirty-one healthy adults were selected from a pool of participants who voluntarily participated in the neuropsychological assessment and questionnaire through several sources including word-of-mouth and advertisements in the community or in the hospital. None of them had any history of neurological or psychiatric disease, and none was taking any medication known to affect the central nervous system at the time of the study. Prior to receiving assessments, all participants gave written consent to participate in the study. Twenty-three schizophrenic patients were being prescribed atypical antipsychotic medication at baseline and the other 23 schizophrenic patients were given typical antipsychotic medication. The 46 schizophrenic patients in the study had a mean age of 41.3 years (standard deviation [SD] =8.9 years) and a mean of 16.3 years duration of illness (SD =8.5 years). The onset age of illness was 25.2 years (SD =7.4 years). There were more males than females (60.9%) in the patient group (however, this condition was inversed in the healthy control group). No significant differences were found between the genders on most sociodemographic and clinical characteristics, except for immediate face recognition memory, number of errors of crossmodal integration, and number of omission of inhibition (go/no-go 1–2) in the patient group. No significant gender differences were found on most socio-demographic and clinical characteristics among the healthy control group.

Measurement

Rosenberg self-esteem scale (RSES)

The Rosenberg self-esteem scale is a 10-item rating scale used to assess a person’s overall evaluation of his or her worthiness as a human being.30 Responses are coded on a 4-point scale ranging from 1 (strongly disagree) to 4 (strongly agree). Items with negative statements are reverse scored and higher scores indicate higher self-esteem.

Health locus of control questionnaire

The health locus of control questionnaire consists of 13 items divided into two subscales.31 Internal health locus of control assesses one’s belief in their ability to influence an event. External health locus of control measures one’s belief that their health status is the result of external factors. All items are scored on a Likert scale, ranging from 1 (completely disagree) to 4 (completely agree). The inter-rater reliability was 0.98.

Wisconsin Card Sorting Test

The Wisconsin Card Sorting Test was originally developed to assess planning capacity, capacity of shifting cognitive strategies, and control of impulsive responses in reaction to environmental changes.32 Participants have to match a target card with one of four category cards according to different principles (eg, matched by color, form, and number in proper order). After each trial, a correct or incorrect feedback is given to the participant, indicating if they have matched the card appropriately. As the test progresses, there are unannounced shifts in the sorting principle which require the participant to change his or her approach. The test ends when the participant has completed six categories or 128 trials.

Subtests of the Wechsler Memory Scale-Third Edition Manual

The Wechsler Memory Scale–Third Edition Manual has been used widely for the evaluation of memory in adults.33 Faces Memory (I): This test presents 24 picture faces to the participant and requires them to memorize all of the faces and distinguish these faces in a 48-face item list. Verbal Paired Associations Memory (I): This test requires the participant to memorize eight verbal paired associations and provide the correct verbal word pair. Digit Span: Used to measure working memory, participants are presented with a series of digits (eg, digit span forward and backward) and immediate reiteration is required. Spatial Span: It has been viewed as an indicator of working memory and visuospatial processing, and as a nonverbal version of Digit Span.

Subtests of the test of attentional performance

The tests of attention used in this study were developed and validated for the assessment of attentional deficits in children and adults with cerebral lesions.34 Participants are orally instructed to perform the computerized tasks. Tests were only performed when participants made no errors during the practice trials. The alertness tasks: participants respond by pressing a button when a visual stimulus appeared on a computer screen. A total of 80 trials were undertaken. The task was constructed according to an A-B-B-A design in order to compensate for effects of fatigue; that is, the examination consists of four blocks (each with 20 target stimuli) in the sequence: (a) Run: without warning tone (b) Run: with warning tone (c) Run: with warning tone (d) Run: without warning tone. The test of crossmodal integration: arrows directing up or down and high or low sounds are presented simultaneously. The participant is asked to press a response button as quickly as possible when a target stimulus occurs (eg, when the pitch of the tone and the direction of the arrow are in agreement). The task measures selective attention as the capacity to integrate sensory information of different modalities. The flexibility task: the “set shifting” task requires the participant to place each hand on a separate response button while viewing a computer screen, on which a letter and a number are displayed simultaneously. The participant has to press the left or right button according to whether the target stimulus (eg, letter or number) appears to the left or the right of the center of the monitor. The inhibition task: the task assesses the capacity to perform an appropriate reaction under time pressure and to simultaneously inhibit an inappropriate behavior response. Two forms of this test were administrated. 1) Test form “1 of 2:” an upright cross (+) and a diagonal cross (×) are presented in an altering sequence on the screen. The participant has to press the button as quickly as possible whenever the diagonal cross appears. 2) Test form “2 of 5:” a sequence of five squares with different patterns appears on the screen and two of these squares are defined as target stimulus, upon the appearance of which the participant presses the button as quickly as possible. The incompatibility task: arrows pointing to the left or the right are presented briefly on the left or right side of the fixation point in the center of the monitor. The participants are required to press a response button as quickly as possible on the side indicated by the direction of the arrow. A compatible condition occurs when the side of arrow in the visual field and the side of the responding hand correspond. Incompatibility occurs when the side of arrow and the direction in which it points do not correspond.

Statistical analysis

All statistical analyses were carried out using SPSS version 12.0 (IBM Corporation, Armonk, NY, USA). We performed Pearson correlation tests among sociodemographic characteristics, neuropsychological variables, self-esteem, internal health locus of control, and external health locus of control. Comparisons of age, education, and marital status between the patient and control groups were performed using two sample t-tests or chi-square statistics as appropriate. Comparisons of clinical measures between patient and control groups were performed using one-way analysis of covariance, controlling age and education as covariates. Corrections for multiple testing were used according to the Bonferroni method. Significance at an alpha level of 0.05 was applied. Only significant variables were shown in the table. Stepwise regression analyses were performed to explore the relative contribution of each significant variable between self-esteem and health locus of control measures.

Results

Sample demographics were as follows: the mean age of the patient group and the healthy control group were 41.3 years (SD =8.9 years) and 48.7 years (SD =15.7 years), respectively. The education level of the majority (65.2%) of the patient group consisted of senior high school and 69.6% were single; 64.5% of the healthy control group had a university degree and 74.2% were married. Clinical characteristics of the patient and control groups are shown in Table 1. Correlations of sociodemographic variables, neuropsychological variables, self-esteem, internal health locus of control, and external health locus of control are presented in Table 2. For all patients, the equivalent dosage of typical and atypical antipsychotic medication converted to chlorpromazine was 336 mg (SD =66.19 mg). The medication dosage was not correlated with any sociodemographic or neuropsychological variables. The onset of illness was not correlated with gender, education, neuropsychological variables, or clinical measures. Only significant variables are shown in Table 2.
Table 1

Sociodemographic and clinical characteristics of patient group and healthy control group

Patient group n=46Healthy control group n=31P-value
Neurocognitive performances
Executive functioning
General performance measures
 Total correct responses61.4 (25.1)73.1 (10.1)0.017
 Total response errors46.5 (21.2)29.8 (19.0)0.000*
 Total categories completed3.0 (2.29)5.3 (1.3)0.000*
Perseveration
 Perseverative responses30.3 (23.1)15.3 (9.7)0.000*
 Perseverative errors28.3 (20.9)13.7 (8.4)0.000*
Conceptual ability
 Trials to complete first category24.9 (22.7)17.1 (9.1)0.084
 Conceptual level responses41.5 (23.7)66.9 (17.8)0.000*
Immediate face recognition memory7.8 (3.3)11.2 (3.1)0.001*
Verbal paired associations memory5.6 (3.3)9.9 (2.7)0.000*
Digit span
 Forward10.0 (2.7)11.7 (2.2)0.052
 Backward8.1 (3.3)10.8 (3.2)0.051
 Total9.3 (3.0)11.5 (3.1)0.197
Spatial span
 Forward9.0 (3.3)9.9 (2.7)0.969
 Backward7.3 (3.0)8.4 (2.4)0.931
 Total7.5 (3.3)9.2 (2.5)0.447
Alertness
Without warning
 Median of reaction time (in ms)422.4 (274.9)368.3 (163.5)0.073
 Variability of reaction time (in ms)106.6 (102.3)83.5 (74.8)0.140
With warning
 Median of reaction time (in ms)361.9 (198.6)334.5 (125.9)0.201
 Variability of reaction time (in ms)79.6 (78.1)58.0 (39.7)0.036
Crossmodal integration
 Number of errors4.2 (5.3)0.6 (1.1)0.001*
 Number of omission2.0 (2.8)0.8 (1.1)0.012
Flexibility
Letter
 Number of correct46.9 (3.44)48.9 (1.5)0.007
 Number of errors1.4 (1.6)0.5 (0.7)0.008
  Median of reaction time (in ms)625.9 (226.4)520.9 (121.2)0.000*
Number
 Number of correct47.6 (3.5)49.6 (0.7)0.003*
 Number of errors1.1 (1.7)0.1 (0.3)0.004
  Median of reaction time (in ms)663.7 (228.7)508.2 (87.0)0.000*
Go/no-go 1–2
 Number of errors5.0 (4.3)2.1 (1.7)0.005
 Number of omission1.3 (1.8)0.7 (1.0)0.125
  Median of reaction time (in ms)419.3 (139.3)377.5 (80.4)0.007
  Variability of reaction time (in ms)101.7 (59.1)77.5 (26.5)0.016
Go/no-go 2–5
 Number of errors6.3 (7.2)2.3 (3.9)0.094
 Number of omission3.8 (5.1)2.6 (4.4)0.217
  Median of reaction time (in ms)637.9 (134.9)600.9 (87.5)0.033
  Variability of reaction time (in ms)155.9 (84.9)118.6 (53.5)0.047
Incompatibility
 Number of errors7.7 (8.5)4.1 (5.8)0.183
F (visual field)3.5 (3.8)4.1 (5.9)0.544
F (hand)2.1 (3.12)2.5 (2.9)0.684
F (visual field × hand)12.5 (14.4)19.1 (20.3)0.371
Clinical characteristics
Self-esteem22.8 (3.8)24.0 (2.5)0.519
Internal health locus of control20.6 (3.8)23.0 (2.4)0.004
External health locus of control15.2 (3.4)13.1 (2.3)0.060

Note:

P<0.003 (Bonferroni corrected).

Abbreviation: ms, milliseconds.

Table 2

Correlations among sociodemographic variables, neuropsychological variables, self-esteem, internal health locus of control, and external health locus of control (n=46)

Variables
Illness of durationPRPESSBAMOAMWAVOAOWFLMFNMG1MG2M
1. Age0.62**0.40**0.36**0.39**0.43**0.33*0.44**0.30*0.45**0.38**0.42**0.43**
DSBDSSSBSSAMOAMWAVOG1M
2. Illness of duration0.34*0.35*0.33*0.31*0.30*0.31**0.45*0.30*
EHLC
3. Education−0.31*
TCCG1VIHLCEHLC
4. SE0.30*−0.30*0.49**0.41**
G1VEHLC
5. IHLC0.43**0.62**
EducationSSB
6. EHLC−0.31*−0.31*

Notes:

P<0.05;

P<0.01.

Abbreviations: AMO, median of reaction time of alertness (without warning); AMW, median of reaction time of alertness (with warning); AOW, variability of reaction time of alertness (with warning); AVO, variability of reaction time of alertness (without warning); DS, digit span; DSB, digit span backward; EHLC, external health locus of control; FLM, median of reaction time of flexibility (letter); FNM, median of reaction time of flexibility (number); G1M, median of reaction time of inhibition of attention (go/no-go 1–2); G1V, variability of reaction time of inhibition of attention (go/no-go 1–2); G2M, median of reaction time of inhibition of attention (go/no-go 2–5); IHLC, internal health locus of control; PR, perseverative responses; PE, perseverative errors; SE, self-esteem; SS, spatial span; SSB, spatial span backward; TCC, total categories completed.

The aim was to understand the extent to which sociodemographic and neuropsychological factors were independently related to self-esteem, internal health locus of control, and external health locus of control. Two or three stepwise multiple regression analyses were performed, as shown in Table 1, allowing significant variables that are related to the dependent variables to enter the assessment to predict self-esteem, internal health locus of control, and external health locus of control. As summarized in Table 3, inhibition of attention and external health locus of control emerged to contribute significantly as predictors of subjects’ self-esteem (adjusted R=0.22, P<0.01). Inhibition of attention and external health locus of control emerged as significant contributors to internal health locus of control (adjusted R=0.54, P<0.001). For external health locus of control, only education was a significant predictor (adjusted R=0.08, P<0.05). Table 3 presents the details of the beta weights of each contributing variable.
Table 3

Multiple regressions predicting self-esteem, internal health locus of control, and external health locus of control scores from sociodemographic and neuropsychological variables (n=46)

MeasureContributing sociodemographic and neuropsychological variablesBetatΔR2Fchange
Self-esteemInhibition of attention (go/no-go 1–2)−0.30−2.090.094.59*
External health locus of control0.413.130.169.85**
Internal health locus of controlInhibition of attention (go/no-go 1–2)−0.43−3.210.1910.35**
External health locus of control0.616.060.3736.80***
External health locus of controlEducation−0.31−2.210.104.90*

Notes:

P<0.05;

P<0.01;

P<0.001.

Discussion

Although the associations among various factors in this study had small effect sizes, background characteristics and main neuropsychological variables showed several significant relationships. The findings of this study provide evidence that inhibition of attention and external locus of control were associated with self-esteem in schizophrenia. Schizophrenia and poor attention were significantly associated with poor self-esteem, which is consistent with previous studies.24,26 With regard to health locus of control, previous research suggested that people with external control orientations demonstrated poor adjustment to illness and were less likely to find available resources to cope with problems.35–40 Within the sociodemographic factors, education was inversely related to external health locus of control, indicating that schizophrenia patients with higher education held less belief that their health status was the result of external factors (lower scores in external locus of control). Internal health locus of control was found to correlate negatively with inhibition of attention (variability of reaction time), suggesting that schizophrenic patients with higher internal health locus of control had a lower rate of impulse control. We also found that schizophrenia with better self-esteem was associated with higher external locus of control, implying their healthy behaviors were determined by powerful others and chance. The above findings were not consistent with the research of Goodman et al,41 who found that lower self-esteem scores were significantly correlated with higher levels of external control among female schizophrenics. It is probable that the discrepancies between findings may be because a majority of the sample group recruited in Goodman et al’s41 study had an education level less than a senior high school degree, and the average age was younger, which may influence their self-esteem level. The present study also found that internal health locus of control was strongly associated with external health locus of control, which accounted for 37% of the variance of internal health locus of control. In contrast, self-esteem in the healthy control group was positively correlated with internal health locus of control and negatively correlated with external health locus of control. This discrepancy and the higher correlation between the internal health locus of control and external health locus of control may have resulted from the illness attribution biases provided by the patients or their relatives. For example, it is probable that patients or relatives may explain the occurrence of their illness as an accident and not of their own responsibility, or accept medical assistance and religion to help provide them with normal functioning and to maintain self-esteem; all of which correlate with internal health locus of control. The present study investigated self-esteem and health locus of control with respect to sociodemographic characteristics and neuropsychological variables, and found that only inhibition of attention, external health locus of control, and education were associated with self-esteem, internal health locus of control, and external health locus of control. The predicted variance accounted for by inhibition of attention and education on self-esteem and external health locus of control was small (ΔR2 =0.09, ΔR2 =0.10), respectively. It is probable that additional factors not included in this study may better relate to self-esteem and external health locus of control. Research findings thus suggest that individuals with a high sense of mastery, better health, emotional stability, extraversion, and conscientiousness experience higher self-esteem.42 Compared to the healthy control group, schizophrenic patients in this study showed more deficits on some neuropsychological variables. This result was consistent with previous reports of schizophrenia exhibiting cognitive impairment.27,28 In accordance with Bentall et al’s1 findings, the results of the present study also showed that schizophrenic patients did not differ in their level of self-esteem when compared to the healthy control group. Although previous research showed that lower self-esteem correlated with mental suffering among patients under the schizophrenia spectrum disorder,8–10 few of these studies made comparisons between the self-esteem scores of a patient group to a healthy control group. Although we did not separate the schizophrenic patients into subtypes, most of the patients recruited were in the remitted paranoid stage. Possible explanations in the different maintenance of self-esteem can be referred to several theories of paranoia, psychological models of symptom development, relatives’ reactions, and self-reference effect.24,42–44 Gender differences in the neurocognitive functioning of the schizophrenic patients were observed only in immediate face recognition memory and attention, including number of errors of crossmodal integration and number of omissions of inhibition. Females displayed better performance in immediate face recognition memory, poor scores in number of errors of crossmodal integration and lower scores in number of omissions of inhibition. Consistently, Han et al27 also found that male schizophrenic patients had more serious cognitive deficits than females in immediate and delayed memory. Results by Bozikas et al45 found that female schizophrenics outperformed men only in verbal learning and memory, while the genders were consistent in ability on other cognitive domains (including inhibition, executive function, visual memory, visuospatial skills, and psychomotor speed). The cross-sectional nature of our study did not allow us to test the causal effect of socio-demographic characteristics or neuropsychological variables with self-esteem and health locus of control in schizophrenia; thus, prospective longitudinal study designs and larger samples are required to replicate findings. In the present study, inhibition of attention and external health locus of control explained the variance of self-esteem. Inhibition of attention and external health locus of control were significant predictors of internal health locus of control, and education was negatively associated with external health locus of control. These findings also have implications for psychosocial interventions and cognitive training in schizophrenia. Given the impact of inhibition of attention, external health locus of control, and education on self-esteem, internal health locus of control, and external health locus of control, increasing importance should be placed on developing effective treatments or psychoeducation on the improvement of self-esteem and health locus of control among schizophrenic patients.46
  37 in total

1.  A cognitive model of the positive symptoms of psychosis.

Authors:  P A Garety; E Kuipers; D Fowler; D Freeman; P E Bebbington
Journal:  Psychol Med       Date:  2001-02       Impact factor: 7.723

2.  Multidimensional health locus of control: comments on the construct and its measurement.

Authors:  Aleksandra Luszczynska; Ralf Schwarzer
Journal:  J Health Psychol       Date:  2005-09

3.  Negative symptoms and concordant impairments in attention in schizophrenia: associations with social functioning, hope, self-esteem and internalized stigma.

Authors:  Paul H Lysaker; Jenifer L Vohs; Jack Tsai
Journal:  Schizophr Res       Date:  2009-02-20       Impact factor: 4.939

4.  Low self-esteem in different psychiatric conditions.

Authors:  P H Silverstone
Journal:  Br J Clin Psychol       Date:  1991-05

5.  The relationship of locus of control to pain coping strategies and psychological distress in chronic pain patients.

Authors:  James E Crisson; Francis J Keefe
Journal:  Pain       Date:  1988-11       Impact factor: 6.961

6.  Cognitive impairments in schizophrenia and schizoaffective disorder: relationship with clinical characteristics.

Authors:  Minna Torniainen; Jaana Suvisaari; Timo Partonen; Anu E Castaneda; Annamaria Kuha; Jaana Suokas; Jonna Perälä; Samuli I Saarni; Jouko Lönnqvist; Annamari Tuulio-Henriksson
Journal:  J Nerv Ment Dis       Date:  2012-04       Impact factor: 2.254

7.  Self-concept, emotion and memory performance in schizophrenia.

Authors:  Katharina Pauly; Tilo Kircher; Jochen Weber; Frank Schneider; Ute Habel
Journal:  Psychiatry Res       Date:  2010-09-20       Impact factor: 3.222

8.  Psychosocial factors as predictors for early retirement in patients with chronic low back pain.

Authors:  K Härkäpää
Journal:  J Psychosom Res       Date:  1992-09       Impact factor: 3.006

9.  A prospective study on the relationship between self-esteem and functioning during the first year after being hospitalized for psychosis.

Authors:  David Roe
Journal:  J Nerv Ment Dis       Date:  2003-01       Impact factor: 2.254

10.  Increasing self-esteem: efficacy of a group intervention for individuals with severe mental disorders.

Authors:  L Borras; M Boucherie; S Mohr; T Lecomte; N Perroud; Ph Huguelet
Journal:  Eur Psychiatry       Date:  2009-03-25       Impact factor: 5.361

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