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Psychological Medicine (2010), 40, 20692077. f Cambridge University Press 2010 doi:10.

1017/S0033291710000164

O R I G I N A L AR T I C LE

Impact of severity and type of depression on quality of life in cases identied in the community
R. Nuevo1,2, C. Leighton1, G. Dunn3, C. Dowrick4, V. Lehtinen5, O. S. Dalgard6, P. Casey7, zquez-Barquero2,8 and J. L. Ayuso-Mateos1,2* J. L. Va
1 2

noma de Madrid, Madrid, Spain Department of Psychiatry, Hospital Universitario de la Princesa, Universidad Auto n Biome dica en Red de Salud Mental, CIBERSAM, Spain Instituto de Salud Carlos III, Centro de Investigacio 3 Biostatistics, School of Community-Based Medicine, University of Manchester, UK 4 Division of Primary Care, University of Liverpool, UK 5 National Research and Development Centre for Welfare and Health, Turku, Finland 6 National Institute of Public Health, Oslo, Norway 7 Department of Psychiatry, University College Dublin, Mater Misericordiae Hospital, Dublin, Ireland 8 s de Valdecilla, Santander, Spain Department of Psychiatry, Universidad de Cantabria, Hospital Universitario Marque

Background. The impact of dierent levels of depression severity on quality of life (QoL) is not well studied, particularly regarding ICD-10 criteria. The ICD classication of depressive episodes in three levels of severity is also controversial and the less severe category, mild, has been considered as unnecessary and not clearly distinguishable from non-clinical states. The present work aimed to test the relationship between depression severity according to ICD-10 criteria and several dimensions of functioning as assessed by Medical Outcome Study (MOS) 36-item Short Form general health survey (SF-36) at the population level. Method. A sample of 551 participants from the second phase of the Outcome of Depression International Network (ODIN) study (228 controls without depression and 313 persons fullling ICD criteria for depressive episode) was selected for a further assessment of several variables, including QoL related to physical and mental health as measured with the SF-36. Results. Statistically signicant dierences between controls and the depression group were found in both physical and mental markers of health, regardless of the level of depression severity ; however, there were very few dierences in QoL between levels of depression as dened by ICD-10. Regardless of the presence of depression, disability, widowed status, being a woman and older age were associated with worse QoL in a structural equation analysis with covariates. Likewise, there were no dierences according to the type of depression (single-episode versus recurrent). Conclusions. These results cast doubt on the adequacy of the current ICD classication of depression in three levels of severity. Received 14 January 2009 ; Revised 7 January 2010 ; Accepted 7 January 2010 ; First published online 11 February 2010 Key words : Depressive episode, disability, quality of life, severity, SF-36.

Introduction Depressive disorders are an important public health problem because they are highly prevalent and adversely aect quality of life (QoL) and levels of disability (Kessler et al. 1994 ; Oord et al. 1996 ; Bijl et al. 1998 ; Ayuso-Mateos et al. 2001). It has been projected that in the future they will be the second most frequent cause of years lost to disability in the world (WHO, 2001). The impact of depression on patients

* Address for correspondence : Dr J. L. Ayuso-Mateos, Hospital a, C/ Diego Universitario de La Princesa, Servicio de Psiquiatr n 62, 28006 Madrid, Spain. de Leo (Email : joseluis.ayuso@uam.es)

well-being and QoL has been shown to be equal to, or greater than, that of several other major chronic medical conditions (Wells & Sherbourne, 1999 ; Sprangers et al. 2000 ; Bonicatto et al. 2001). Cases of depression are classied into subgroups according to the criteria of the International Classication of Disorders (ICD), to facilitate treatment planning in the clinical situation. The ICD-10 (WHO, 1992) categorizes episodes of depressive disorder into two types : single and recurrent . Each episode is, in turn, classied according to level of severity : mild , moderate , severe , severe with psychotic features and unspecied severity . The level of severity is dened according to the ICD-10 by the number of depressive symptoms. The sum of these symptoms,

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R. Nuevo et al. group, and 313 endorsing a diagnosis of depressive episode. Data were obtained from the Outcome of Depression International Network (ODIN) project. This project is a multi-centre epidemiological study designed to provide reliable and valid data on the prevalence, risk factors and outcome of depressive disorders within the European Union, based on an epidemiological sampling framework, and also to assess the impact of psychological interventions on the outcome of depression. A detailed description of the aims and methods of the study is provided elsewhere (Dowrick et al. 1998 ; Ayuso-Mateos et al. 2001). The study was undertaken in ve countries and nine geographical areas, and included a total sample of 8764 individuals. Each centre identied one rural and one urban setting in which to conduct its research. Community study samples were identied through census registers or lists of patients registered with primary care physicians. The dierent research teams involved made the choice on which sampling procedure to use based on their previous experience in community surveys. The overall response rate for the rst phase of the survey was 65 %, which included variations by study site, ranging from 54 % (rural Ireland) to 90 % (urban Spain). Procedure A two-phase sampling procedure (Dunn et al. 1999) was adopted in the ODIN study. The rst phase consisted of the use of mental health screening instruments and the collection of sociodemographic and medical data. This screening phase included the Beck Depression Inventory (BDI ; Beck et al. 1961), with a cut-o score >12 (Lasa et al. 2000), and the General Health Questionnaire (GHQ-12 ; Goldberg et al. 1997). The second phase included oering all of those scoring at or above the BDI threshold, and a random 5 % of responders below the threshold, a detailed interview with the Schedules for Clinical Assessment in Neuropsychiatry (SCAN) version 2.0 (WHO, 1994). The SCAN was used to generate diagnoses of depressive disorders on the basis of ICD-10 and DSM-IV categories. Health-related QoL was assessed using the 36-item short form of the Medical Outcome Study (MOS) General Health Survey (SF-36 ; Stewart et al. 1988 ; Ayuso-Mateos et al. 1999). The SF-36 has been shown to be a valid and reliable measure of QoL in depressed patients, with a high internal consistency for most subscales (ranging from 0.7 in the pain dimension to 0.9 in the physical functioning) (Ayuso-Mateos et al. 1999). The translations of the SF-36 into several dierent languages have been shown to be culturally appropriate and comparable in their content (Vilagut

which produces the total score used to determine the level of depression, does not take into consideration the type of symptoms that the patient presents. In other words, according to the current categorical system, patients who present symptoms such as plans to commit suicide, depressed mood for 2 weeks, increased fatigue and reduced concentration and attention, but who do not present disturbed sleep, diminished appetite, decreased interest and ideas of guilt and unworthiness, would have a mild level of depression. On the contrary, patients endorsing eight of the nine symptoms, but without suicidal thoughts, would have a diagnosis of severe depression. The only exception is the presence of psychotic symptoms, which changes the level of severity to severe with psychotic features regardless of the number of depressive symptoms. It is assumed that the more severe the level of the depressive episode, the greater likelihood the episode will be associated with lower QoL, even though little empirical evidence exists to support this. The distribution of QoL in the depressed population has been relatively little studied (Kruijshaar et al. 2003). Several studies have provided evidence for a continuum in the impact on QoL (e.g. Ravindran et al. 2002 ; da Silva Lima & de Almeida Fleck, 2007) as the severity of depression increases but they have generally used limited samples, considering its small size, the procedure of recruitment or the diagnostic method, and above all they have not been focused on the distinction of depression severity according to the criteria of the World Health Organization (WHO). It has been suggested that mild depression may be an unnecessary category because it is limited in time, the impact on QoL that it produces is low, and it would be diagnosed with low frequency in clinical samples compared with population samples (Keller et al. 1995 ; Dowrick et al. 1998). Hence, there is interest in studying whether subjects with mild depression constitute a dierent sample from individuals without a depressive disorder, according to the QoL that they present. The aim of this study was to analyse whether the type of depression (single or recurrent) and the different levels of severity (mild, moderate, severe), as dened by ICD-10, correlate with the impact on a persons QoL. The null hypothesis was that recurrent episodes and higher levels of severity of depression would have a greater negative impact on QoL.

Method Subjects The sample for this study comprised 551 persons : 238 without depression diagnosis constituting the control

Depression and quality of life et al. 2005). In the SF-36 higher scores indicate better QoL. Controls were the individuals who had scores <12 in the BDI, no diagnosis at the SCAN, and had completed at least six of the eight subscales on the SF-36 questionnaire (n=238). Cases were persons with an ICD-10 diagnosis of depressive disorder following the SCAN interview. These included single and recurrent depressive episodes (F 32, F 33) that were mild, moderate or severe on the SCAN (n=313), and they had completed at least six of the eight subscales of the SF36 questionnaire. The severe level included the subjects diagnosed as having severe depression with psychotic features (n=6, 1.1 % of the total sample). The nal sample sizes for the depression severity groups were : mild (n=132), moderate (n=124), and severe (n=57). Statistical analysis Statistical comparisons (x2 for categorical variables and one-way ANOVAs for continuous variables) were performed to test for dierences across groups in the main characteristics (age, gender, distribution by country, marital status, rural versus urban setting, presence versus absence of long-term illness or disability, and number of days sick during the past 6 months) of the groups of depression severity. A series of ANOVAs was then performed to study the differences between levels of severity in each of the eight when subscales on the SF-36. Post-hoc analyses (Schee homoscedasticity could be assumed, GamesHowell when it could not) were performed to test for dierences between specic groups. Eect sizes (Hedges g) were calculated for each paired comparison. These analyses (ANOVAs and post-hoc tests) were then repeated, controlling for age, gender, country, marital status, setting, presence of long-term illness or disability and number of days sick during the past 6 months, as it has been suggested that these variables aect the level of QoL and could be confounders of the eect of depression severity (Bijl & Ravelli, 2000 ; Kruijshaar et al. 2003 ; Buist-Bouwman et al. 2004 ; Jorngarden et al. 2006). Age and number of days sick were entered as covariates, and the remaining potential confounders were included as independent variables in the model, and the main eects of severity of depression were examined. To test whether the level of severity of depression was associated with a greater number of symptoms, measured by the BDI scores, a univariate ANOVA was performed comparing the four groups of severity with the BDI score as a dependent variable. Moreover, to test the interaction of BDI scores and level of depression with extent of QoL, correlation analyses were

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performed separately for each group of severity between the BDI score and each of the eight SF-36 subscales. The potential eect of dierent covariates on QoL was also analysed with a multiple-indicators multiplecauses (MIMIC) model in which a two-latent factor model of QoL (mental and physical) was assumed, with four indicators for factor, and several 01 dummy variables were introduced as covariates on the secondorder QoL latent factor : gender (women as the reference category) ; age in years ; presence of disability ; diagnosis of depression ; and marital status (dichotomizing as not widowed versus widowed and using not widowed as the reference category). These analyses were conducted in AMOS version 7.0 (Arbuckle, 2006). The asymptotically distribution-free (ADF ; Browne, 1984) estimator was used, which does not assume multivariate normality of the measured variables. According to the usual recommendations on using several indices to assess t (Reise et al. 1993), given the sensitivity to sample size shown by x2, the assessment of the model was based on multiple criteria : (a) x2, (b) the comparative t index (CFI), (c) the goodness-of-t index (GFI), (d) the TuckerLewis index (TLI), and (e) the root mean square error of approximation (RMSEA). A good t is indicated by low values for x2, values >0.90 for CFI, GFI and TLI, and values <0.06 for RMSEA (Bentler, 1990). Finally, t tests for independent samples were carried out to compare mean SF-36 scores between persons with recurrent depression and persons with a single episode. All analyses were performed with the statistical package SPSS release 14.0 (SPSS Inc., USA). Results The comparison of demographic characteristics across levels of depression severity indicated statistically signicant dierences in age [F(3, 547)=6.6, p<0.001], marital status [x2(9)=56.3, p<0.001], distribution across countries [x2(12)=127.9, p<0.001] and setting [x2(3)=8.3, p=0.040] ; there were no statistically signicant dierences according to gender [x2(3)=2.2, p=0.539]. The depressed groups were older [mean age of 43.9 (S.D.=10.5) years for the severe depression group and 44.9 (S.D.=11.1) years for the moderate depression group] than the control group [mean=40.1 (S.D.=12.6) years], with no dierences across levels of severity ; a higher proportion of individuals who were separated or divorced was related to higher levels of depression ; people with severe or moderate depression were more prevalent in the UK and Ireland and less prevalent in Spain ; and there were more people with severe or moderate depression living in an urban setting. There were statistically signicant

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Table 1. Comparison of SF-36 mean scores according to the severity of depressive symptoms Control Physical functioning Role limitations, physical Bodily pain General health perception Vitality/energy Social functioning Role limitations, emotional Mental health 92.0 (15.9) 89.4 (26.5) 83.2 (21.6) 82.4 (18.2) 72.2 (17.0) 94.9 (15.6) 92.0 (23.5) 82.8 (12.8) Mild 73.6 (25.2) 54.4 (40.7) 59.0 (27.9) 51.8 (23.6) 32.8 (16.9) 56.4 (27.0) 44.0 (39.2) 46.7 (15.0) Moderate 71.0 (27.7) 55.3 (43.8) 54.5 (31.3) 49.7 (24.1) 27.2 (18.5) 47.8 (29.3) 31.1 (36.4) 37.9 (17.8) Severe 67.4 (34.0) 51.4 (42.7) 52.0 (31.1) 47.6 (26.8) 19.4 (16.9) 38.9 (27.4) 15.4 (28.0) 31.8 (16.9) F 12.3 23.5 27.8 60.2 151.8 104.2 97.6 235.9 g2 0.066 0.119 0.141 0.257 0.465 0.376 0.358 0.576

Scores given as mean (standard deviation). All Fs had p<0.001.

dierences across the severity groups in the percentage of persons with long-term illness or disability [x2(3)=91.3, p<0.001], with higher percentages for the mild and moderate depression groups (30.2 % and 34.6 %, respectively) and lower percentages for the control (15.9 %) and severe depression (19.2 %) groups. There were also statistically signicant dierences across the severity groups in the number of days sick during the past 6 months [F(3, 288)=11.0, p<0.001]. According to the post-hoc analyses, the control group reported less days sick (mean=1.46, S.D.=0.84) than the depression groups, without dierences between the groups of people with depression. The one-way ANOVAs with depression severity as the independent variable and the eight subscales of the SF-36 as dependent variables resulted in signicant dierences (p<0.001) in all cases (see Table 1), with eect sizes (g2) ranging between 0.07 and 0.26 for the physical health variables and between 0.36 and 0.58 for the mental health variables. Post-hoc analyses (with p set to 0.00625 (0.05/8) controlling for type I errors associated with multiple comparisons) indicated that the control group had statistically signicantly higher scores (i.e. better QoL related to health status) on all of the eight subscales compared with the rest of the groups, with large eect sizes (e.g. ranging between 0.94 and 2.57 for the paired comparisons between controls and mild depression groups) (specic results for each paired comparison available on request from the corresponding author) ; with no dierences between the three levels of severity in people with depression, except for the subscale of mental health between mild and moderate depression, with a lower score for the moderate depression group [p<0.001, g=0.53, 95 % condence interval (CI) 0.60 1.26] and signicantly lower scores for the severe group compared with the mild group in emotional role limitations (p<0.001, g=0.79, 95 % CI 0.461.11), social functioning (p<0.001, g=0.64, 95 % CI 0.320.96),

vitality/energy (p<0.001, g=0.79, 95 % CI 0.471.11) and mental health (p<0.001, g=0.95, 95 % CI 0.621.28). There were no statistically signicant dierences between the moderate and severe depression groups. Allowance for confounders in the ANOVAs led to qualitatively similar conclusions. When these analyses were carried out introducing all the confounders into the model, the main eect of severity remained signicant (p<0.001) for the eight SF-36 subscales, and the same pattern of specic dierences between groups in post-hoc comparisons was found. ANOVA comparing BDI scores between the groups of depression severity indicated a signicant eect [F(3, 546)=450.6, p<0.001]. Post-hoc analyses showed that the control group had a signicantly (p<0.001) lower score (BDI mean 3.62, S.D.=3.4) than the remaining groups ; the mild depression group (BDI mean=21.4, S.D.=7.7) had signicantly lower scores than the severe group (p<0.001) but without dierences compared with the moderate depression group (p=0.365, BDI mean=22.8, S.D.=7.3) ; and the severe group (BDI mean=29.3, S.D.=2.9) had signicantly higher scores than the rest of the groups (p<0.001). The MIMIC model including covariates presented a moderately adequate t to the data : CFI=0.925, GFI=0.992, TLI=0.887, x2/df=4.601, RMSEA=0.081. Given that the interest here was in analysing the effects of factors related to QoL, no further corrections were made on the model to improve the t. All regression weights were statistically signicant (p< 0.01), except for the direct path from depression status to one specic indicator of QoL. The model with the unstandardized weights and standard errors is depicted in Fig. 1 (specic results for each paired comparison available on request from the corresponding author). The direction of the weights indicates that depression status, being widowed, the presence of disability, being older, and being a woman are related to a decreased QoL.

Depression and quality of life


Table 2. Comparisons of SF-36 mean scores between depressed individuals with single or recurrent depression Single (n=227) 70.3 (28.8) 53.0 (43.0) 53.9 (29.8) 48.9 (24.5) 27.3 (17.7) 49.1 (28.2) 33.6 (38.7) 40.1 (17.7) Recurrent (n=76) 75.3 (24.3) 57.3 (40.4) 61.1 (29.3) 54.6 (24.3) 30.1 (19.4) 50.6 (30.1) 32.0 (34.2) 41.2 (18.2)

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SF-36 Physical functioning Role limitations, physical Bodily pain General health perception Vitality/energy Social functioning Role limitations, emotional Mental health

p 0.367 0.172 0.068 0.079 0.244 0.702 0.747 0.623

Hedges g (95 % CI) 0.18 (0.44 to x0.08) 0.10 (0.36 to x0.16) 0.24 (0.50 to x0.02) 0.23 (0.49 to x0.03) 0.15 (0.41 to x0.11) 0.05 (0.31 to x0.21) x0.04 (x0.22 to 0.30) 0.06 (0.32 to x0.20)

CI, Condence interval. Scores given as mean (standard deviation).

0.28 (2.45)

Depression
1 24.04 (2.23) 1.79 (0.16)

Functioning

Role

Physical Age
0.08 (0.03) 1

1.28 (0.11) 1.31 (0.12)

Pain

General health Disability


6.90 (1.43)

QoL
5.21 (1.02) 2.19 (0.20) 1 0.77 (0.03)

Mental role Social functioning Mental health

Widowed
1.68 (1.65)

Mental Gender
0.64 (0.02) 0.69 (0.02)

Energy
Fig. 1. The multiple-indicators multiple-causes (MIMIC) model. Depression and covariates eects on the quality of life (QoL) latent structural model : unstandardized weights. Standard errors are given in parentheses.

Finally, comparisons of means according to the type of depression (single depressive episode versus recurrent depression) indicated that there were no statistically signicant dierences between these two groups for any of the eight SF-36 subscale scores (see Table 2). The distribution of cases of mild, moderate or severe depression did not dier signicantly between the single- and recurrent-episode depression groups.

present results that depression has a negative eect, although this eect is not very marked. There were almost no dierences between each step from one to the next level of severity of depression. The main differences appeared in the step from normal mood state to depression. At this step QoL deteriorates, and from there generally remains, regardless of the level of severity according to the ICD-10 classication of depression or whether there is a single episode or recurrent depressive episodes. Depression and QoL In the sampled studied, the classication of depression into three levels of severity proposed by the ICD-10 is

Discussion The main aim of the present study was to analyse the relationship between level of depression severity and QoL related to health status. It seems clear from the

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R. Nuevo et al. in-patients in Denmark discharged between 1994 and 1999 with a diagnosis of a single depressive episode, testing its power to predict risk of relapse and suicide, with the result that patients with increasing levels of severity were signicantly associated with a higher risk. Hamalainen et al. (2004), in a population study in Finland, showed that more severe depressive episodes are associated with a predictably larger use of health services. The current classication has been questioned by some researchers (Parker and Manicavasagar, 2005 a, b ; Parker, 2006), who argue that the ICD-10 describes depressive disorder as a single condition varying by severity, and that this model has not generated any replicable biological changes or correlates at a satisfactory level, and has not been informative in identifying treatment-specic eects. In our study, the subjects with mild depressive episodes presented a signicant dierence in QoL compared with subjects without depression. This difference is greater than that seen between the dierent severity groups. Moreover, in follow-up studies, it has been reported that mild depressive patients are ve times more likely to have depressive disorder after 1 year (Kessing, 2004 ; Lyness et al. 2006). Mild depression may occur independently of a lifetime history of depressive disorder (Rapaport et al. 2002). Our ndings support the necessity of having specic treatment guidelines for mild depressive episodes. The only guidelines that make specic recommendations for mild depressive episodes are the National Institute for Health and Clinical Excellence (NICE) Guidelines (NCCMH, 2004) for treatment of depression in primary and secondary care settings, which are an example of a union of categorical and dimensional approaches. They use a stepped care approach that recognizes the dierent treatment requirements for dierent levels of severity of depression as dened in the ICD-10. Our ndings show that, in terms of QoL, the ICD-10 classication of depressive episodes into three levels (mild, moderate and severe) is only validated for the two extremes. We found signicant dierences between controls and mild depression, scant dierences between mild and severe, and almost no dierence between mild and moderate and between moderate and severe episodes of depression. The classication system used to diagnose depressive disorders is very important for determining the epidemiology of the disorders and planning treatment management strategies in health resourcing ; and if the classication does not have a proper validation, it is doomed to failure. Current ICD-10 classication of depression severity has only been validated in clinical samples, including in-patients (Kessing, 2004).

not valid in terms of its impact on QoL. The current system for distinguishing between mild, moderate and severe depression is categorical, involving a simple addition of symptoms, with no consideration of the weight according to its importance or intensity. It could be that dierent symptoms have dierent weight in the impact on QoL of depressive subjects, and the inclusion of additional symptoms to those with the highest weights is not indicating an increase in severity of depression. Recurrent depression was not found to be associated with worse QoL compared with a single episode of depression. This lack of dierence in degree of QoL between recurrent and single episodes could be explained, hypothetically, by the fact that individuals with recurrent depression adapt to their situation, and therefore they give more positive answers to the SF-36 than subjects in their rst episode. Another hypothesis could be that individuals with recurrent depression know their disorder and seek treatment earlier (Merikangas et al. 1994 ; Kruijshaar et al. 2003 ; Paykel, 2003), or that their health-care professionals know their disorder better and therefore treat them earlier and more successfully, so their depressive episodes are shorter, which could increase their QoL, diminishing dierences with single depression. The present sample is from a community setting, and could present dierences with a clinical setting, where the observation that recurrent depression is more disabling than a single depressive episode was originally made (OLeary et al. 2000). The comparisons between the categories of depressive episode and severity in the BDI scores also indicated that the threshold between mild and moderate depression could be arbitrary ; the control group had lower scores than the rest of groups, severe group had higher scores but there were no dierences between mild and moderate. Validation of the current classications of depressive episodes The current model for classication of mood disorders takes the depressive episode as a categorical entity ; the model is unitary, with disorders dierentiated largely on the basis of severity (Kessing, 2007). The way ICD-10 handles severity has been praised, and recommended for preservation in future editions (Paykel, 2002). There have been very few studies that validate this classication of severity levels of depressive episodes with other clinical correlates, such as biological markers, prognosis, outcomes and treatment responses. This classication has only been validated by Kessing (2004), in a sample comprising all psychiatric

Depression and quality of life In the context of the current revision of classication systems such as DSM-IV and ICD-10, the issues around a dimensional versus a categorical approach towards aective disorders are being increasingly addressed (Judd & Akiskal, 2000 ; Andrews et al. 2007 ; Kessing, 2007). The results of the present work suggest that if a dimension could be assumed to be within the group of depressive disorders (although with a not very steep slope), then there is a point of rarity from no depression to the less severe forms of depression. The discontinuity in QoL between mild depression and not having depression, and then the continuity across severity of depression, indicates that the minimum presentations of depression should be included in diagnostic systems and should merit attention from the health services. Nevertheless, it is not clear whether the threshold established by current systems is capturing the exact point of the discontinuity of impact. Given the potential clinical relevance of identifying persons at risk of depression, research should try to sharpen the distinction between relevant and notrelevant depressive symptoms. Factors aecting QoL The data from the MIMIC model also suggest that other factors are related to QoL when they are added to the presence of depression in the model. Specically, apart from the eect of depression, being widowed, the presence of disability, being older, and being a woman are related to a decreased QoL. Therefore, those characteristics could have a relevant impact on the QoL of the patient, they could be mediating or moderating the eect of depressive symptoms on QoL and would have an impact on patient care. Thus, these results and the adequate t of the model highlight the idea that depression (versus not depression) is relevant to QoL even when relevant covariates are taken into account, and that a relevant change on impact occurs from normality to depression. Limitations Our sample comes from a multi-centre study across ve countries, so some results might have been explained by country dierences rather than by severity or type of depression ; for this reason we controlled by country on all the analyses, together with potential eects on demographic characteristics across samples. The number of subjects with severe depression with psychotic features (n=6) was so small that we were unable to analyse them as a dierent group and test the hypothesis that the presence of psychotic symptoms could add an aggravating factor to the

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depressive episode. This is the only weighted symptom in the current ICD classication, and when present the level of depression is automatically severe. Conclusions The results of this study support the relationship between level of depression and QoL, but provide indirect evidence against the three thresholds suggested by the ICD-10 for dierentiating among dierent levels of depression. Only the threshold between normal and depression is clearly established, and among levels of depression, only the extreme poles were clearly distinguished in terms of QoL. We consider that in the re-emergence of this nosology, an expert consensus is an important element for establishing diagnostic guidelines. However, the guidelines need to be empirically validated before introducing major changes in the current classication system. Acknowledgements This study was partially supported by the Instituto n Biome dica de Salud Carlos III, Centro de Investigacio en Red de Salud Mental, CIBERSAM, Spain. Declaration of Interest None. References
Andrews G, Brugha T, Thase ME, Duy FF, Rucci P, Slade T (2007). Dimensionality and the category of major depressive episode. International Journal of Methods in Psychiatric Research 16 (Suppl. 1), S41S51. Arbuckle JL (2006). Amos (Version 7.0). [Computer program]. SPSS : Chicago. Ayuso-Mateos JL, Lasa L, Vazquez-Barquero JL, Oviedo A, Diez-Manrique JF (1999). Measuring health status in psychiatric community surveys : internal and external validity of the Spanish version of the SF-36. Acta Psychiatrica Scandinavica 99, 2632. Ayuso-Mateos JL, Vazquez-Barquero JL, Dowrick C, Lehtinen V, Dalgard OS, Casey P, Wilkinson C, Lasa L, Page H, Dunn G, Wilkinson G (2001). Depressive disorders in Europe : prevalence gures from the ODIN study. British Journal of Psychiatry 179, 308316. Beck AT, Ward CH, Mendelson M, Mock J, Erbaugh J (1961). An inventory for measuring depression. Archives of General Psychiatry 4, 561571. Bentler PM (1990). Comparative t indexes in structural models. Psychological Bulletin 107, 238246. Bijl RV, Ravelli A (2000). Current and residual functional disability associated with psychopathology : ndings from The Netherlands Mental Health Survey and Incidence Study (NEMESIS). Psychological Medicine 30, 657668.

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R. Nuevo et al.
Kruijshaar ME, Hoeymans N, Bijl RV, Spijker J, Essink-Bot ML (2003). Levels of disability in major depression : ndings from the Netherlands Mental Health Survey and Incidence Study (NEMESIS). Journal of Aective Disorders 77, 5364. Lasa L, Ayuso-Mateos JL, Vazquez-Barquero JL, Diez-Manrique FJ, Dowrick CF (2000). The use of the Beck Depression Inventory to screen for depression in the general population : a preliminary analysis. Journal of Aective Disorders 57, 261265. Lyness JM, Heo M, Datto CJ, Ten Have TR, Katz IR, Drayer R, Reynolds III CF, Alexopoulos GS, Bruce ML (2006). Outcomes of minor and subsyndromal depression among elderly patients in primary care settings. Annals of Internal Medicine 144, 496504. Merikangas KR, Wicki W, Angst J (1994). Heterogeneity of depression. Classication of depressive subtypes by longitudinal course. British Journal of Psychiatry 164, 342348. NCCMH (2007). Depression (Amended) : Management of Depression in Primary and Secondary Care. Developed by the National Collaborating Centre for Mental Health (NCCMH) for the National Institute for Health and Clinical Excellence (NICE). Clinical Guidelines CG23. NICE : London. Oord DR, Boyle MH, Campbell D, Goering P, Lin E, Wong M, Racine YA (1996). One-year prevalence of psychiatric disorders in Ontarians 1564 years of age. Canadian Journal of Psychiatry 41, 559563. OLeary D, Costello F, Gormley N, Webb M (2000). Remission onset and relapse in depression. An 18-month prospective study of course for 100 rst admission patients. Journal of Aective Disorders 57, 159171. Parker G, Manicavasagar V (2005 a). Depression sub-typing : independence and interdependence. In Modelling and Managing the Depressive Disorders (ed. G. Parker and V. Manicavasagar), pp. 2128. Cambridge University Press : Cambridge. Parker G, Manicavasagar V (2005 b). A declaration of independence. In Modelling and Managing the Depressive Disorders (ed. G. Parker and V. Manicavasagar), pp. 313. Cambridge University Press : Cambridge. Parker G (2006). Through a glass darkly : the disutility of the DSM nosology of depressive disorders. Canadian Journal of Psychiatry 51, 879886. Paykel ES (2002). Mood disorders : review of current diagnostic systems. Psychopathology 35, 9499. Paykel ES (2003). Life events and aective disorders. Acta Psychiatrica Scandinavica 108 (Suppl. 418), 6166. Rapaport MH, Judd LL, Schettler PJ, Yonkers KA, Thase ME, Kupfer DJ, Frank E, Plewes JM, Tollefson GD, Rush AJ (2002). A descriptive analysis of minor depression. American Journal of Psychiatry 159, 637643. Ravindran AV, Matheson K, Griths J, Merali Z, Anisman H (2002). Stress, coping, uplifts, and quality of life in subtypes of depression : a conceptual frame and emerging data. Journal of Aective Disorders 71, 121130. Reise SP, Widaman KF, Pugh RH (1993). Conrmatory factor analysis and item response theory : two approaches

Bijl RV, Ravelli A, van Zessen G (1998). Prevalence of psychiatric disorder in the general population : results of The Netherlands Mental Health Survey and Incidence Study (NEMESIS). Social Psychiatry and Psychiatric Epidemiology 33, 587595. Bonicatto SC, Dew MA, Zaratiegui R, Lorenzo L, Pecina P (2001). Adult outpatients with depression : worse quality of life than in other chronic medical diseases in Argentina. Social Science and Medicine 52, 911919. Browne MW (1984). Asymptotically distribution-free methods for the analysis of covariance structures. British Journal of Mathematical and Statistical Psychology 37, 6283. Buist-Bouwman MA, Ormel J, de Graaf R, Vollebergh WA (2004). Functioning after a major depressive episode : complete or incomplete recovery ? Journal of Aective Disorders 82, 363371. da Silva Lima AF, de Almeida Fleck MP (2007). Subsyndromal depression : an impact on quality of life ? Journal of Aective Disorders 100, 163169. Dowrick C, Casey P, Dalgard O, Hosman C, Lehtinen V, Vazquez-Barquero JL, Wilkinson G (1998). Outcomes of Depression International Network (ODIN). Background, methods and eld trials. ODIN Group. British Journal of Psychiatry 172, 359363. Dunn G, Pickles A, Tansella M, Vazquez-Barquero JL (1999). Two-phase epidemiological surveys in psychiatric research. British Journal of Psychiatry 174, 95100. Goldberg DP, Gater R, Sartorius N, Ustun TB, Piccinelli M, Gureje O, Rutter C (1997). The validity of two versions of the GHQ in the WHO study of mental illness in general health care. Psychological Medicine 27, 191197. Hamalainen J, Isometsa E, Laukkala T, Kaprio J, Poikolainen K, Heikkinen M, Lindeman S, Aro H (2004). Use of health services for major depressive episode in Finland. Journal of Aective Disorders 79, 105112. Jorngarden A, Wettergen L, von Essen L (2006). Measuring health-related quality of life in adolescents and young adults : Swedish normative data for the SF-36 and the HADS, and the inuence of age, gender, and method of administration. Health and Quality of Life Outcomes 4, 91. Judd LL, Akiskal HS (2000). Delineating the longitudinal structure of depressive illness : beyond clinical subtypes and duration thresholds. Pharmacopsychiatry 33, 37. Keller MB, Klein DN, Hirschfeld RM, Kocsis JH, McCullough JP, Miller I, First MB, Holzer III CP, Keitner GI, Marin DB (1995). Results of the DSM-IV mood disorders eld trial. American Journal of Psychiatry 152, 843849. Kessing LV (2004). Severity of depressive episodes according to ICD-10 : prediction of risk of relapse and suicide. British Journal of Psychiatry 184, 153156. Kessing LV (2007). Epidemiology of subtypes of depression. Acta Psychiatrica Scandinavica 115 (Suppl. 433), 8589. Kessler RC, McGonagle KA, Zhao S, Nelson CB, Hughes M, Eshleman S, Wittchen HU, Kendler KS (1994). Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey. Archives of General Psychiatry 51, 819.

Depression and quality of life


for exploring measurement invariance. Psychological Bulletin 114, 552566. Sprangers MA, de Regt EB, Andries F, van Agt HM, Bijl RV, de Boer JB, Foets M, Hoeymans N, Jacobs AE, Kempen GI, Miedema HS, Tijhuis MA, de Haes HC (2000). Which chronic conditions are associated with better or poorer quality of life ? Journal of Clinical Epidemiology 53, 895907. Stewart AL, Hays RD, Ware Jr. JE (1988). The MOS short-form general health survey. Reliability and validity in a patient population. Medical Care 26, 724735. Vilagut G, Ferrer M, Rajmil L, Rebollo P, Permanyer-Miralda G, Quintana JM, Santed R, Valderas JM, Ribera A, Domingo-Salvany A, Alonso J (2005). The Spanish version of the Short Form 36 Health

2077

Survey : a decade of experience and new developments [in Spanish]. Gaceta Sanitaria 19, 135150. Wells KB, Sherbourne CD (1999). Functioning and utility for current health of patients with depression or chronic medical conditions in managed, primary care practices. Archives of General Psychiatry 56, 897904. WHO (1992). The ICD-10 Classication of Mental and Behavioural Disorders : Clinical Descriptions and Diagnostic Guidelines. World Health Organization : Geneva. WHO (1994). Schedules for Clinical Assessment in Neuropsychiatry : Version 2.0. World Health Organization : Geneva. WHO (2001). World Health Report 2001. Mental Health : New Understanding, New Hope. World Health Organization : Geneva.

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