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Is there a linear relationship between the Brief Psychiatric Rating Scale and the Clinical Global Impression-Schizophrenia scale? A retrospective analysis
© Sawamura et al; licensee BioMed Central Ltd. 2010
Received: 21 May 2010
Accepted: 7 December 2010
Published: 7 December 2010
Although the Brief Psychiatric Rating Scale (BPRS) is widely used for evaluating patients with schizophrenia, it has limited value in estimating the clinical weight of individual symptoms. The aim of this study was 4-fold: 1) to investigate the relationship of the BPRS to the Clinical Global Impression-Schizophrenia Scale (CGI-SCH), 2) to express this relationship in mathematical form, 3) to seek significant symptoms, and 4) to consider a possible modified BPRS subscale.
We evaluated 150 schizophrenia patients using the BPRS and the CGI-SCH, then examined the scatter plot distribution of the two scales and expressed it in a mathematical equation. Next, backward stepwise regression was performed to select BPRS items that were highly associated with the CGI-SCH. Multivariate regression was conducted to allocate marks to individual items, proportional to their respective magnitude. We assessed the influence of modifications to the BPRS in terms of Pearson's r correlation coefficient and r-squared to evaluate the relationship between the two scales. Utilizing symptom weighting, we assumed a possible BPRS subscale.
By plotting the scores for the two scales, a logarithmic curve was obtained. By performing a logarithmic transformation of the BPRS total score, the curve was modified to a linear distribution, described by [CGI-SCH] = 7.1497 × log10[18-item BPRS] - 6.7705 (p < 0.001). Pearson's r for the relationship between the scales was 0.7926 and r-squared was 0.7560 (both p < 0.001). Applying backward stepwise regression using small sets of items, eight symptoms were positively correlated with the CGI-SCH (p < 0.005) and the subset gave Pearson's r of 0.8185 and r-squared of 0.7198. Further selection at the multivariate regression yielded Pearson's r of 0.8315 and r-squared of 0.7036. Then, modification of point allocation provided Pearson's r of 0.8339 and r-squared of 0.7036 (all these p < 0.001). A possible modified BPRS subscale, "the modified seven-item BPRS", was designed.
Limited within our data, a logarithmic relationship was assumed between the two scales, and not only individual items of the BPRS but also their weightings were considered important for a linear relationship and improvement of the BPRS for evaluating schizophrenia.
Schizophrenia is a serious mental disorder characterized by a number of symptoms. To evaluate the effects of treatment for schizophrenia, it is important to assign quantitative values to the symptoms. Many rating scales have been used to evaluate various symptomatic domains in schizophrenia . This has led to confusion regarding the suitability of the different scales available, not only in relation to evaluation and treatment of the disease but also in research and clinical studies of the effects of medication. Currently, consensus is lacking about which rating scales are appropriate to evaluate schizophrenia. Evaluation scales that are relevant, quick, user-friendly, graduated at equal intervals and with high linearity are needed to facilitate measurement-based treatment of schizophrenia. The Brief Psychiatric Rating Scale  is one of the standard instruments used most frequently in daily practice for evaluating the severity of schizophrenia. Also popular are the Clinical Global Impression-Schizophrenia Scale , the Positive and Negative Syndrome Scale , the Scale for Assessment of Positive Symptoms  and the Scale for Assessment of Negative Symptoms . Although the BPRS includes 18 items and the allocation of marks is defined clearly, as all items have the same range of marks (i.e., 1-7), it is not unusual to find that scores for the BPRS differ widely from those for the CGI-SCH.
Ideally, scores from one scale could be mapped directly onto the other, making it possible to compare individuals evaluated with one scale or the other. We decided to investigate this divergence analytically, looking at the clinical weight of respective symptoms (the relative magnitudes of symptoms in schizophrenia) and the issue of scale nonlinearity. In the present study, we investigated whether there was a linear relationship between the scores of the two scales, to observe whether linearity of the BPRS to the CGI-SCH could be influenced by changing point allocation of the BPRS through devising an example of a possible modified BPRS subscale.
The aim of the present study is 4-fold: 1) to investigate the linearity of the BPRS in relation to its items and mark allocation by examining the reasons for the incongruity between BPRS scores and clinicians' impressions of symptom severity in schizophrenic patients; 2) to determine a mathematical expression that represents the relationship between the BPRS and the CGI-SCH more precisely; 3) to seek which symptoms are important from a clinical standpoint; and 4) if possible, to construct an example of a possible modified BPRS subscale that is expected to have improved correlation with the CGI-SCH scores compared with the full BPRS within the limitations of the data obtained in this trial.
This was a retrospective study of outpatients and inpatients treated at the Tokyo Women's Medical University, Miyazaki Hospital and Depression Prevention Medical Center, Kyoto Jujo Rehabilitation Hospital, Japan, who met the DSM-IV-TR  criteria for schizophrenia. A total of 150 patients (74 males, 76 females) with a mean age of 44.5 years (range, 17-83) were included in this study. Fifty patients were suffering their first episode of schizophrenia or attending for initial treatment (Group A) and 100 were randomly selected during either the acute or chronic phase of schizophrenia (Group B). The study involved a retrospective chart review and was approved by the ethics committee of our institution.
All patients were evaluated and rated from their medical records using the BPRS and the CGI-SCH during the same session, but at initial consultation for Group A and at a random treatment session for Group B. In this study, we utilized the CGI-SCH as a scale that substituted for the evaluation made by the patients' psychiatrists under the tentative assumption that the CGI-SCH had perfect linearity and that it represented the precise clinical global impression of the treating psychiatrists.
If the linearity of the BPRS to the CGI-SCH was not initially apparent, we aimed to derive a mathematical equation to represent more precisely the relationship between the scales, clarifying which symptoms were important in evaluating schizophrenia and how we could improve the correlation between the BPRS and the CGI-SCH. Two experienced psychiatrists shared their evaluations, and the scores for the BPRS and the CGI-SCH were presented graphically, making it possible to examine whether the two demonstrated a linear relationship. At this stage, we examined the distribution on the scatter plot of the two scales and expressed the relationship in a precise mathematical equation. Next, backward stepwise regression was performed, with the CGI-SCH as a dependent variable and with all 18 items of the BPRS as independent variables. An F-value of less than 2.000 was used to identify variables for removal. In addition, backward stepwise regression with F-value at the same condition was performed using three small sets of variables based on derived scores. These independent variable groups were: positive symptoms (conceptual disorganization, grandiosity, hostility, suspiciousness, hallucinations, and excitement); negative symptoms (emotional withdrawal and blunted affect); and general psychopathological symptoms (somatic concern, anxiety, guilt, tension, bizarre behavior, depressed mood, motor retardation, uncooperativeness, unusual thought content, and disorientation) with reference to three domains of the PANSS. Variables showing a positive association with the CGI-SCH were derived from these three domains, and multivariate regression analysis was performed using the selected items as independent variables and the CGI-SCH as a dependent variable. By convention in stepwise regression, even if p values exceed 0.05, it is permissible to adopt the variables if those symptoms are judged as clinically important, as long as the p values do not exceed 0.20. However, we selected the variables positively associated with the CGI-SCH within the condition that p values were less than 0.05. In the stepwise and multivariate regression analyses, we often obtained variables inversely associated with the CGI-SCH. In this study, we adopted a way to remove them. Furthermore, utilizing the results of multivariate regression, we allocated marks in proportion to the magnitude of the multiple regression coefficient of each variable so that each symptom was allocated different marks proportional to the positive multiple regression coefficient.
With regard to linearity, we then examined the distribution on the scatter plot of the BPRS and the CGI-SCH scores. We obtained the Pearson's r coefficient as an indication of the degree of linearity of the relationship between the two scales, r-squared being one of values used to estimate how much the fit of model shrinks (by observing how r-squared decreased), before and after exclusion of the various items and modification of the mark allocation. Furthermore, we examined whether the selection of specific items and/or changing the distribution of the marks enhanced the correlation of the BPRS with the CGI-SCH and how much the r-squared decreased. On the basis of the results, we constructed an example of a possible modified BPRS subscale, "the modified seven-item BPRS", which would be expected to have a higher correlation with the CGI-SCH within the limitations of the applicability for our data at this stage. We used SPSS for Windows, version 14  for the stepwise regression analysis, Stata Release 10.0  for the multivariate regression analysis, and Microsoft Excel 2003  for plotting the graph.
Results of stepwise regression 1.
95% Confidence Interval
-0.407828 - -0.099222
0.251002 - 0.575332
-0.561719 - -0.140454
0.221771 - 0.495195
-0.364195 - -0.014304
-0.038676 - 0.372666
-0.333861 - 0.028287
0.048346 - 0.276605
0.079527 - 0.437178
0.045524 - 0.480081
Unusual thought content
0.003277 - 0.292296
-0.018534 - 0.296652
0.632328 - 1.644886
Results of stepwise regression 2.
Positive symptoms (conceptual disorganization, grandiosity, hostility, suspiciousness, hallucinations and excitement)
95% Confidence Interval
0.296437 - 0.542909
0.116685 - 0.378984
0.194333 - 0.382877
1.262703 - 1.910059
Negative symptoms (emotional withdrawal and blunted affect)
95% Confidence Interval
0.530592 - 0.807089
2.292775 - 2.956368
General psychopathological symptoms (somatic concern, anxiety, guilt, tension, bizarre behavior, depressed mood, motor retardation, uncooperativeness, unusual thought content and disorientation)
95% Confidence Interval
-0.384830 - -0.056837
0.119856 - 0.383734
0.148916 - 0.458278
0.073381 - 0.374041
Unusual thought content
0.227160 - 0.474829
-0.088087 - 0.577979
0.967587 - 1.892939
Results of multivariate regression.
Multiple Regression Coefficient
95% Confidence Interval
0.185228 - 0.466563
-0.056024 - 0.262592
0.022258 - 0.255944
-0.529734 - -0.096182
0.100363 - 0.370158
0.126424 - 0.468118
0.079897 - 0.520976
Unusual thought content
-0.046852 - 0.238266
0.710298 - 1.477155
The BPRS is one of the most frequently used instruments for evaluating the psychopathology of patients with schizophrenia. Although its psychometric properties in terms of reliability, validity and sensitivity have been extensively examined , patients are examined by clinicians with different observer ratings using different criteria. On the other hand, assessment with the CGI-SCH is based on a score of 1-7, making it simple and relevant. The CGI-SCH may be as sensitive as the BPRS in detecting efficacy differences between antipsychotic drugs , but it is necessary that treatment response be interpreted in the context of patient characteristics . However, patients with different characteristics but with similar scores are often treated similarly in clinical trials. Therefore, training is required for performing a standardized evaluation . Other user-friendly assessments include the Revised Global Outcome Assessment of Life in Schizophrenia (Revised GOALS) , the Investigator's Assessment Questionnaire (IAQ)  and the Targeted Inventory on Problems in Schizophrenia (TIP-Sz) , although they have some limitations in terms of methodology. We also believe that other important aspects of illness management should be supplemented with appropriate subjective scales as necessary . Nonetheless, there is no consensus among clinicians regarding the most suitable scale. To address this perplexing issue, more advanced investigations are necessary to devise rating scales using some form of statistical method.
Leaving aside the debate over whether psychopathological severity or state can be expressed in evaluation scales such as the BPRS or the CGI-SCH and accepting the need and utility of such instruments, we focused here on improving the BPRS scale. We examined whether the more detailed assessment afforded by its items and individual point allocations could be made proportional to the simpler and more global CGI-SCH scale.
Many previous attempts have been made to evaluate the adequacy of the BPRS from the viewpoint of which items should be selected because of their relevance. However, no study has approached this issue by addressing how the degree of linearity of the BPRS can be changed by modifying not only its constituent items but also their weighting, using stepwise regression and multivariate regression analysis. In the present study, we first examined whether the BPRS and the CGI-SCH showed a mutual linear relationship. By plotting the BPRS scores and the CGI-SCH scores in the form of a graph, we compared their respective distributions. The scatter plot of the 18-item BPRS and the CGI-SCH yielded a curve with upper convexity, thus demonstrating that the relationship between the two scales was not linear (see Figure 1). Because the shape of the curve had upper convexity similar to a logarithmic curve, we performed a common logarithmic transformation on the 18-item BPRS score. Then, we were able to obtain a possibly more precise equation as a logarithmic form shown in Figure 2. From this result, we presumed that there was a possibility that an increase in the logarithm of the total score for all symptoms might be roughly proportional to the global increase in symptom severity observed clinically in schizophrenic patients. We recognize, however, that this model has applicability to only this trial at this stage. We inferred that the logarithmic relationship between the single score scale, the CGI-SCH, and the plural score scale, the BPRS, might be an important tool in our determination of the severity of illness. We then investigated whether modifying the constituent items and/or allocation of marks could affect the linearity of the BPRS, at least, within this trial itself, looking at the correlation of the BPRS with the CGI-SCH in terms of Pearson's r and r-squared, which express one of the degrees of the fit between the two scales. To evaluate the clinical severity of schizophrenia, we substituted the CGI-SCH score for the clinical impression.
Partly because the values of Pearson's r were slightly higher between "the seven-item BPRS" (constructed by selection of specific items) and the CGI-SCH than between the 18-item BPRS and the CGI-SCH without considerable decreases of r-squared, the shape of the scatter plot between the two scales became more linear than that before the selection. We inferred that there was a possibility that the selection of these items from 18 items is related to the linearity of the BPRS. The clinical weights might be related to the heightened values of Pearson's r between "the modified seven-item BPRS" (constructed by changing the allocation of marks) and the CGI-SCH, as the shape of the scatter plot between the two scales became more linear than before. We presumed that there was a possibility that the weighting was also associated with the linearity of the BPRS.
Furthermore, by assigning different weights to each item proportional to the respective regression coefficients, we were able to compose a possible modified BPRS subscale, "the modified seven-item BPRS", by assuming that the magnitude of each regression coefficient represented the respective clinical weight of each item. This scale is only an example of a possible modified BPRS subscale that we are able to assume within our data, and the number of items decreased from 18 to 7.
Historically, a widely used algorithm employing a stepwise method was first proposed by Efroymson , and supplementary articles were later reported by Hocking  and others. In the field of psychiatry, stepwise methods have been used for predicting the quality of life of schizophrenic patients by reference to schizophrenia symptoms , for estimating predictive values of neurocognition in schizophrenic patients , and for estimation of the relationship between executive functions and positive symptoms in schizophrenia .
However, some problems with stepwise and multivariate regression analysis have been reported. To compare the relative magnitudes of variables, the partial regression coefficients are often normalized using their respective standard deviations. However, the predictor variable is at least partially redundant with other predictors and the regression coefficient is influenced by the range of the predictor variable . In addition, the relative importance of predictor variables is a tenuous concept, and comparison of the importance of predictors is not always the best approach in multiple regression. As the individual items of the BPRS had the same range of marks (1-7), we considered that there would not be crucial differences in the sizes of standard deviations for predictor variables in this study. With this assumption, we considered that, for practical purposes, the magnitudes of the standardized and unstandardized β might be regarded as almost equivalent. For these reasons, we utilized the magnitude of the unstandardized β (multiple regression coefficient) to modify the distribution of marks of the BPRS and to design a tentative BPRS subscale. If supplemented with this adjustment, the scatter plot representing the relationship between "the modified seven-item BPRS" and the CGI-SCH showed a distribution proportional to the scatter plot connecting the score of "the seven-item BPRS" multiplied by the unstandardized β (multiple regression coefficient) for each item and the score of the CGI-SCH. This is because both have almost the same significance on the graph. Additional improvements in fit may be possible.
The limitations of the present study should be noted. The first was the use of the CGI-SCH as a scale that substituted for the evaluation made by the patients' psychiatrists. There is no evidence that the CGI-SCH has perfect linearity and this was merely an assumption to allow modification of the BPRS under a determinate condition. For the CGI-SCH, only a certain degree of reliability has been reported [3, 12, 13]. Nonetheless, we thought that this kind of simplification was unavoidable and the trade-off necessary, even if this assumption would sacrifice rigor to some extent in exchange for examining the degree of an abstract value such as 'linearity.'
Second, there is no evidence supporting the assumption that the BPRS score and the CGI-SCH score obtained retrospectively by coding of the symptoms reported in the clinical chart would be comparable to the data obtained from trained BPRS raters monitored for inter-rater reliability and performing standardized interviews to probe for presence and severity of a complete list of symptoms. The quality of the clinical chart is notoriously variable, so there may exist errors and distortions from missing symptoms and falsely rating symptoms as absent when reviewing a chart, because of the failure of the clinician to mention them in the chart, which would have been detected in a structured, face-to-face interview. The 0.7926 value of Pearson's r might be to some extent considered high. However, we presume that this was because the study was retrospective. Therefore, some items of the BPRS might not have been marked, thus minimizing the distribution of the BPRS score. In effect, the results of this paper may be applicable only within our own data at this stage (including the derived stepwise regression, multivariate regression and, particularly, "the modified seven-item BPRS") and there is no guarantee that the results would be comparable to prospective research. From this standpoint, our report might be regarded as one of these experimental case studies. At any rate, prospectively randomized trials are needed in future studies.
Third, through the manipulations employed here, the degree of change in Pearson's r was rather ambiguous. The increases appear slight (as a total, from 0.7926 to 0.8339; particularly, in the final manipulation, from 0.8315 to 0.8339). Moreover, it is considerably uncertain whether statistical significance exists. From another viewpoint, despite the fact that the scale was simplified, and in particular, the number of items decreased, the degree of correlation (Pearson's r) stayed at the same level or increased just slightly. Although this might indicate that a simplified subscale might be valuable in comparison with the full scale, and it might be useful to clinicians for shortening time of rating, the reproducibility of items and point allocation is quite uncertain in this model. We believe that a study of this theme in the future is desirable.
Fourth, as for r-squared, in general, the more variables we exclude from the model, the more r-squared tends to decrease. The selection of the subset for which the decrease of r-squared is smallest is preferred so that the loss of model fit would be minimal. The r-squared of our data ranged from about 0.70-0.75. The size of these numbers is not low, but they may not be sufficiently high even with the moderate degree of decrease. For example, 0.7560 for the full item BPRS; 0.7524 for the results of stepwise regression using the full items of BPRS; 0.7198 for the selected eight items from stepwise regression using three small sets; and 0.7036 for the selected seven items from multivariate regression (all p values of respective analysis of variance were less than 0.001). This means that the selection of items might have caused shrinkage of the model.
Fifth, the selection of items and modification of point allocation may have contributed some artifacts of multicollinearity. There are likely to be intercorrelations among the data. In this study, variables that were inversely correlated with the CGI-SCH score, indicating that the more severe the BPRS item, the lower the CGI-SCH score (a phenomenon which was a departure from the clinicians' experiences), were simply excluded from the model in an ad hoc procedure. This ignored the fact that the selection of the other predictors from among the list of candidates depended on the presence of the excluded variable. Additional unknown and complicated factors are predicted to exist as well, for example, that both inpatients and outpatients were evaluated by the CGI-SCH, and that the results might have been negatively influenced by differences in cognitive ability . The treatment of negative coefficients is a crucial weakness of our model.
Sixth, above all, the results are not likely to be reproducible. If we performed the same procedure on new data, it is very likely that different symptoms would be selected, and different point allocations would probably be assigned to individual items. We infer that a possible way to remedy this problem, even if partially, might be to perform a number of prospective trials in line with our method, and then summarize and calculate an average on items and point allocation. If these scales are composed as a summary, they might be less problematic than that of our trials. However, even in such scales, there would still be no assurance that they would have a greater degree of reproducibility. Therefore, the extent to which the results of this paper could be applicable may be quite limited: at the extreme, only within our present data. For this reason, future studies are necessary.
The true aim of this manipulation was not always to determine the best subset and/or point allocation, but to consider a specific example of a possible modified scale. Therefore, "the modified seven-item BPRS" is merely a tentative idea at this stage, to propose a new viewpoint of the importance of point allocation in the BPRS. Needless to say, the present study has many limitations, and is thus only a first step from which further studies may learn. We believe that improving evaluation scales to make them more linear could minimize distortions in evaluation for severity of illness, including over- and under-diagnosis and estimations for efficiency and effect in clinical research. We anticipate that our present results will serve as a useful reference for clinicians attempting to devise an evaluation scale, and that further research will focus on the optimal number of items, the fittest items for selection, and the allocation of marks in rigorous methodology to maximize the linearity of the BPRS.
Within the limits of our data, although there was a rough correlation, the linear relationship that had been thought to exist between the 18-item BPRS and the CGI-SCH was not apparent. Also, a roughly logarithmic relationship was assumed between the two scales. In addition, not only specific items but also their weightings were considered to be important in the realization of a linear relationship between the BPRS and the CGI-SCH and in the further improvement of the BPRS as a diagnostic scale.
The authors wish to acknowledge Katsuji Nishimura, Takao Kanai, Ken Inada and Kaoru Sakamoto for providing us with very useful advice in this study.
- Lindenmayer JP, Harvey PD, Khan A, Kirkpatrick B: Schizophrenia: measurements of psychopathology. Psychiatr Clin North Am. 2007, 30: 339-363. 10.1016/j.psc.2007.04.005.View ArticlePubMedGoogle Scholar
- Overall JE, Gorham DR: The Brief Psychiatric Rating Scale. Psychol Rep. 1962, 10: 799-812. 10.2466/PR0.10.3.799-812.View ArticleGoogle Scholar
- Haro JM, Kamath SA, Ochoa S, Novick D, Rele K, Fargas A, Rodríguez MJ, Rele R, Orta J, Kharbeng A, Araya S, Gervin M, Alonso J, Mavreas V, Lavrentzou E, Lintos N, Gregor K, Jones PB, SOHO Study Group: The Clinical Global Impression-Schizophrenia Scale: a simple instrument to measure the diversity of symptoms present in schizophrenia. Acta Psychiatr Scand. 2003, 16-23. 10.1034/j.1600-0447.107.s416.5.x. Suppl 416Google Scholar
- Kay SR, Fiszbein A, Opler LA: The Positive and Negative Syndrome Scale (PANSS) for schizophrenia. Schizophr Bull. 1987, 13: 261-276.View ArticlePubMedGoogle Scholar
- Andreasen NC: Scale for the Assessment of Positive Symptoms (SAPS). 1984, Iowa City: University of IowaGoogle Scholar
- Andreasen NC: Scale for the Assessment of Negative Symptoms (SANS). 1983, Iowa City: University of IowaGoogle Scholar
- American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision: New York. 2000View ArticleGoogle Scholar
- SPSS Inc: SPSS for Windows Version 14. 2007, Chicago, IL: SPSS IncGoogle Scholar
- Stata Corporation: Stata User's Guide, Release 10.0. 2007, College Station, Texas: Stata CorporationGoogle Scholar
- Microsoft Corporation: Microsoft Excel 2003. 2003, Microsoft Corp. Redmond, WashingtonGoogle Scholar
- Hedlund JL, Vieweg BW: The Brief Psychiatric Rating Scale (BPRS): a comprehensive review. J Oper Psychiatry. 1980, 11: 48-65.Google Scholar
- Leucht S, Engel R: The relative sensitivity of the Clinical Global Impressions Scale and the Brief Psychiatric Rating Scale in antipsychotic drug trials. Neuropsychopharmacol. 2006, 31: 406-412. 10.1038/sj.npp.1300873.View ArticleGoogle Scholar
- Leucht S, Kane JM, Kissling W, Hamann J, Etschel E, Engel R: Clinical implications of Brief Psychiatric Rating Scale scores. Br J Psychiatry. 2005, 187: 366-371. 10.1192/bjp.187.4.366.View ArticlePubMedGoogle Scholar
- Müller MJ, Rossbach W, Dannigkeit P, Müller-Siecheneder F, Szegedi A, Wetzel H: Evaluation of standardized rater training for the Positive and Negative Syndrome Scale (PANSS). Schizophr Res. 1998, 32: 151-160. 10.1016/S0920-9964(98)00051-6.View ArticlePubMedGoogle Scholar
- Naber D, Vita A: Tools for measuring clinical effectiveness. Eur Neuropsychopharmacol. 2004, 14 (Suppl 4): S435-S444. 10.1016/j.euroneuro.2004.08.002.View ArticlePubMedGoogle Scholar
- Tandon R, Devellis RF, Han J, Li H, Frangou S, Dursun S, Beuzen JN, Carson W, Corey-Lisle PK, Falissard B, Jody DN, Kujawa MJ, L'italien G, Marcus RN, McQuade RD, Ray S, Van Peborgh P, IAQ Validation Study Group: Validation of the Investigator's Assessment Questionnaire, a new clinical tool for relative assessment of response to antipsychotics in patients with schizophrenia and schizoaffective disorder. Psychiatry Res. 2005, 136: 211-221. 10.1016/j.psychres.2005.05.006.View ArticlePubMedGoogle Scholar
- Suzuki T, Uchida H, Nomura K, Takeuchi H, Nakajima S, Tanabe A, Yagi G, Watanabe K, Kashima H: Novel rating scales for schizophrenia-Targeted Inventory on Problems in Schizophrenia (TIP-Sz) and Functional Assessment for Comprehensive Treatment of Schizophrenia (FACT-Sz). Schizophr Res. 2008, 106: 328-336. 10.1016/j.schres.2008.08.013.View ArticlePubMedGoogle Scholar
- Burlingame GM, Dunn TW, Chen S, Lehman A, Axman R, Earnshaw D, Rees FM: Selection of outcome assessment instruments for inpatients with severe and persistent mental illness. Psychiatr Serv. 2005, 56: 444-451. 10.1176/appi.ps.56.4.444.View ArticlePubMedGoogle Scholar
- Efroymson MA: Multiple regression analysis. Mathematical Methods for Digital Computers. Edited by: Ralston A, Wilf HS. 1960, New York: Wiley, 191-203.Google Scholar
- Hocking RR: The analysis and selection of variables in linear regression. Biometrics. 1976, 32: 1-49. 10.2307/2529336.View ArticleGoogle Scholar
- Bow-Thomas CC, Velligan DI, Miller AL: Predicting quality of life from symptomatology in schizophrenia at exacerbation and stabilization. Psychiatr Res. 1999, 86: 131-142. 10.1016/S0165-1781(99)00023-2.View ArticleGoogle Scholar
- Milev P: Predictive values of neurocognition and negative symptoms on functional outcome in schizophrenia: a longitudinal first-episode study with 7-year follow-up. Am J Psychiatry. 2005, 162: 495-506. 10.1176/appi.ajp.162.3.495.View ArticlePubMedGoogle Scholar
- Guillem F, Rinaldi M, Pampoulova T, Stip E: The complex relationships between executive functions and positive symptoms in schizophrenia. Psychol Med. 2008, 38: 853-860. 10.1017/S0033291707002577.View ArticlePubMedGoogle Scholar
- Judd CM, McClelland GH, Ryan CS: Data Analysis: A Model Comparison Approach. 2009, New York: Routledge/Taylor and Francis, 2Google Scholar
- Brekke JS, Kohrt B, Green MF: Neuropsychological functioning as a moderator of the relationship between psychosocial functioning and the subjective experience of self and life in schizophrenia. Schizophr Bull. 2001, 27: 697-708.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-244X/10/105/prepub
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