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Residual symptoms and functioning in depression, does the type of residual symptom matter? A post-hoc analysis

BMC Psychiatry volume 13, Article number: 51 (2013) Cite this article

Abstract

Background

The degrees to which residual symptoms in major depressive disorder (MDD) adversely affect patient functioning is not known. This post-hoc analysis explored the association between different residual symptoms and patient functioning.

Methods

Patients with MDD who responded (≥50% on the 17-item Hamilton Rating Scale for Depression; HAMD-17) after 3 months of treatment (624/930) were included. Residual core mood-symptoms (HAMD-17 core symptom subscale ≥1), residual insomnia-symptoms (HAMD-17 sleep subscale ≥1), residual anxiety-symptoms (HAMD-17-anxiety subscale ≥1), residual somatic-symptoms (HAMD-17 Item 13 ≥1), pain (Visual Analogue Scale ≥30), and functioning were assessed after 3 months treatment. A stepwise logistic regression model with normal functioning (Social and Occupational Functioning Assessment Scale ≥80) as the dependent variable was used.

Results

After 3 months, 59.5% of patients (371/624) achieved normal functioning and 66.0% (412/624) were in remission. Residual symptom prevalence was: core mood symptoms 72%; insomnia 63%; anxiety 78%; and somatic symptoms 41%. Pain reported in 18%. Factors associated with normal functioning were absence of core mood symptoms (odds ratio [OR] 8.7; 95% confidence interval [CI], 4.6–16.7), absence of insomnia symptoms (OR 1.8; 95% CI, 1.2–2.7), episode length (4–24 weeks vs. ≥24 weeks [OR 2.0; 95% CI, 1.1–3.6]) and better baseline functioning (OR 1.0; 95% CI, 1.0–1.1). A significant interaction between residual anxiety symptoms and pain was found (p = 0.0080).

Conclusions

Different residual symptoms are associated to different degrees with patient functioning. To achieve normal functioning, specific residual symptoms domains might be targeted for treatment.

Background

Residual symptoms of depression cause significant functional impairment [1, 2]. This has been reported in patients who respond but are not remitters, partial remitters [1, 2], and even in remitters (typically defined as a score of ≤7 on the 17-item Hamilton Depression Rating scale [HAMD-17]) with residual symptoms [2]. Residual symptoms are also associated with persistent functional impairment [1]. However, little is known about the role of specific residual symptom domains, such as core symptoms, symptoms of anxiety, somatic symptoms, and non-painful symptoms.

Most research in patients with residual symptoms has focused on the relationship between residual symptoms and depressive relapse. Several studies have shown an increased risk of relapse [3, 4] and rapid relapse [5] in patients with residual symptoms after response without remission. A posthoc analysis from the Sequenced Treatment Alternatives to Relieve Depression [6] study showed that a greater number of residual symptom domains were associated with a higher probability of relapse in full symptomatic remitters. Although a few studies have evaluated the impact of residual symptoms on functional impairment [1, 2, 7, 8], to our knowledge, no published studies have examined the specific role of each residual symptom domain on functional impairment. This is definitely an area worthy of investigation, since the aim of treating depression is not only to achieve clinical remission, but also to return the patient to previous levels of functioning [9]. Knowledge of which residual symptom domains are associated with significant functional impairment and, to what degree would assist physicians in the implementation of specific strategies and treatments to increase the chances of achieving normal or previous levels of functioning.

The aim of this posthoc investigation was to assess the association of specific residual symptoms (core mood, insomnia, anxiety, somatic, and pain) with patient functioning in a large group of patients with an episode of major depressive disorder (MDD) who responded after 3 months of acute antidepressant treatment in routine clinical practice. Our hypothesis was that the strength of the association between residual symptoms and functioning would differ depending on the type of residual symptom.

Methods

This study is a post-hoc analysis done on a group of MDD patients who responded (improvement of ≥50% on the HAMD-17) after 3 months of acute treatment (n = 624). The analysis of the association between residual symptoms and functioning was done at three months of acute treatment. The source of data was based on a 1-year prospective observational study of a cohort of 930 outpatients with an index MDD episode [10]. As a non-interventional study, the patients were treated according to everyday clinical routine. The protocol was approved by the ethical review board of the Hospital Puerta de Hierro in Madrid, Spain, and all patients provided written informed consent before their inclusion in the study.

Participants

As described in detail elsewhere [10], adult outpatients with nonpsychotic MDD, single or recurrent episode, according to DSM-IV-TR® [11] were included. Patients had a baseline total score of ≥15 on the HAMD-17) [12] and at least a moderate (≥4) baseline score on the Clinical Global Impression-Severity (CGI-S) scale [13]. Patients suffering from Axis I main psychiatric disorder, dementia, Alzheimer’s disease, organic brain syndrome, or cognitive impairment were excluded from the study.

Patients from this study who responded (improvement of ≥50% on the HAMD-17) after 3 months of acute antidepressant treatment were included in the present analysis.

Measures and definitions

The HAMD-17 was used to assess the severity of depression and its improvement. Remission was defined as a HAMD-17 score of ≤7 and a response as an improvement of 50% or more from the baseline score. Functioning was measured using the Social and Occupational Functioning Assessment Scale (SOFAS) [14], a 100-point single-item scale used to indicate the individual’s level of social and occupational functioning across a continuum ranging from a state of optimum functioning to a state of important functional impairment. It measures only the level of social and occupational functioning without taking symptoms into account. Thus, a value of 1 represents the hypothetically most impaired individual and 100 the hypothetically healthiest individual. It is completed by a clinician using information from any clinical source. The two highest ranges on the SOFAS, 81–90 and 91–100, describe individuals who not only are without significant psychopathology, but who also exhibit many traits often considered to be components of positive mental health. A SOFAS score ≥80 was used to define normal levels of functioning [15]. The baseline and 3-month follow-up visits were included in this analysis.

Based on Dombrovski [16], we defined the presence of residual core mood symptoms as a score of 1 or more on the HAMD-17 core symptom subscale (depressed mood [Item 1], guilt [Item 2], suicide [Item 3], and anergia/anhedonia [Item 7]). The presence of residual insomnia symptoms was defined as a score of 1 or more on the HAMD-17 sleep subscale insomnia items (early [Item 4], middle [Item 5], and late [Item 6]). The presence of residual anxiety symptoms was defined as a score of 1 or more on the HAMD-17 anxiety subscale (agitation [Item 9], psychic anxiety [Item 10], somatic anxiety [Item 11], and hypochondriasis [Item 15]), and of residual somatic symptoms as a score of 1 or more for item 13 of the HAMD-17.

The Visual Analog Scale (VAS) for Pain was used to assess pain [17], defining the presence of pain as a VAS-overall pain ≥30 mm, which includes patients with at least moderate pain, and had been previously used for the identification of clinically significant pain [18]. The visual analog scale for pain is an instrument widely used in research studies to measure the level of pain. Its simplicity, reliability, and validity, make the VAS the optimal tool for describing pain [19, 20]. Pain was measured by the VAS- overall pain, where the patient scores on a 100 point scale the level of overall pain in the last week.

Analysis

Demographic and clinical data at baseline were described by means of percentages (qualitative variables) or mean ± standard deviation (quantitative variables).

A stepwise logistic regression model was developed to evaluate the association between the residual symptom domains and patient functioning, with a normal level of functioning after 3 months of antidepressant treatment (SOFAS total score ≥80) as the dependent variable, and the following factors as the independent variables in the initial model: Age as a continuous variable, gender, marital status, working status, education status, baseline functioning (SOFAS score), baseline depression severity (HAMD-17), presence of previous episodes of depression, medical co-morbidities, length of current episode, residual symptoms at 3 months (core mood symptoms, insomnia symptoms, anxiety symptoms, somatic symptoms), and pain at 3 months. All the independent variables were included in a full model and then removed stepwise by backward selection (threshold for the p-value = 0.05). Interactions between variables were tested at 3 months (likelihood ratio). Only patients with complete information on the variables previously described were included in the model (n = 600). The reduced model was reported in terms of odds ratios (OR) and their 95% confidence intervals (CI); the fit of the final model was assessed using the Hosmer-Lemeshow goodness-of-fit test [21].

Receiver operating characteristics curves were plotted to determine and compare the sensitivity and specificity of the residual symptom domains and of the pain, as indicators of normal levels of functioning according to the SOFAS (SOFAS score ≥80) after 3 months of treatment. Areas under the curve (AUC) using the trapezoidal rule and their associated asymptotic 95% CIs were calculated. The AUC varies from 0.5 (no apparent accuracy) to 1.0 (perfect accuracy). SAS 9.2 for Windows (SAS Institute Inc., USA) was used for the statistical analysis.

Results

Patient disposition, demographics, and clinical characteristics

Of the evaluable sample (N = 930), 624 patients responded to antidepressant treatment and were therefore included in the present analysis. Table 1 shows the socio-demographic and clinical characteristics of the study sample of responders.

Table 1 Baseline demographic and clinical characteristics
Full size table

Residual symptom prevalence

After 3 months of acute antidepressant treatment, the most frequent residual symptom was anxiety in 78.2% of patients (95% CI, 74.8–81.4), followed by core mood symptoms in 72.1% (95% CI, 68.4–75.6), residual insomnia in 63.0% (95% CI, 59.1–66.8) and somatic symptoms in 41.3% (95% CI, 37.4–45.3). Pain was reported in 18.4% (95% CI, 15.5–21.7) of patients (Figure 1A). The severity of the residual symptoms and pain was mild (Table 2).

Figure 1
figure 1

A Prevalence of residual symptoms domains and pain. All patients, N = 624. B Prevalence of residual symptoms domains and pain, based on remission (HAMD-17 ≤7) N = 412, or non-remission (HAMD-17 >7) N = 212.

Full size image
Table 2 Residual symptoms, pain and HAMD-17 mean scores after 3 months of acute treatment, N = 624
Full size table

After 3 months treatment, 66.0% (412/624) of the patients were in remission (HAMD-17 ≤7). Figure 1B shows the prevalence of residual symptoms by remission status at 3 months. About 90% of remitters (88.3%; 95% CI, 84.8–91.3) had residual symptoms from at least one of the domains studied.

Residual symptoms and patient functioning

More than half of the patients (59.4%, 371/624) had a normal level of functioning. Factors associated with normal functioning were absence of core mood symptoms (OR 8.7; 95% CI, 4.6–16.7), absence of insomnia symptoms (OR 1.8; 95% CI, 1.2–2.7), shorter episode length (4–24 weeks vs. ≥24 weeks [OR 2.0; 95% CI, 1.1–3.6]) and better baseline functioning (OR 1.0; 95% CI, 1.0–1.1). A significant interaction was found between residual anxiety symptoms and pain (p = 0.0080). The absence of pain increased the chance of normal functioning in either the absence (OR 21.7; 95% CI, 3.5–132.5) or presence of residual anxiety (OR 1.7; 95% CI, 1.0–2.8). However, the absence of residual anxiety was found to increase the chance of normal functioning only if pain was not present (OR 5.2; 95% CI, 2.4.–11.3) (Table 3). Demographic variables, physical co-morbidities, baseline depression severity, previous depression episodes and residual somatic symptoms were not significantly related to functioning (Table 3).

Table 3 Association between residual symptoms domains, pain and functioning
Full size table

The AUC for the residual core mood symptoms was 0.84 (95% CI, 0.80–0.87). Lower AUCs were found for the other residual symptom domains and pain: anxiety 0.75 (95% CI, 0.71–0.78); pain 0.73 (95% CI, 0.69–0.77); insomnia 0.65 (95% CI, 0.60–0.69); and residual somatic symptoms 0.62 (95% CI, 0.58–0.66).

Discussion

This study evaluated the relationship between patient functioning and specific residual symptom domains (core mood, insomnia, anxiety, somatic symptoms) and pain symptoms in a large group of patients with MDD who responded after receiving acute treatment. Anxiety was the most prevalent residual symptom, followed by core mood symptoms. The strength of the association between the residual symptom domains studied and patient functioning differed depending on the type of symptoms. A more marked association was found for residual core mood symptoms. Residual insomnia was less strongly related to patient functioning, and residual somatic symptoms were not associated.

To our knowledge, this is the first study to investigate the role of specific residual symptoms on patient functioning in MDD. Most publications about residual symptoms in MDD focus on their description and on their relationship to relapse and recurrence of depression [6, 22–27]. More recent publications have evaluated their relationship to time to remission [6, 28]. Few studies have specifically investigated the relationship between residual symptoms and functional impairment, but instead have focused on the overall impact of these symptoms on functioning without a separate analysis of the type of residual symptom [1, 8, 29].

As reported previously, residual symptoms are very common after acute treatment, even in remitters [6, 22, 23]. In the present investigation, we found that almost 90% of remitters had at least one residual symptom domain of mild intensity. This is similar to figures reported by Nierenberg et al. [6] and Ioveno et al. [22]. Similar to other studies, the most common residual symptom domain in our patients was anxiety [6, 26]. Other studies have reported residual insomnia [23] and sleep disturbances [6, 22] to be the most common residual symptoms domains. These differences may be due to the use of different scales and definitions. Development of a consensus on the definition and measurement of residual symptoms would be desirable to enable results between studies to be compared, thus improving understanding.

Interestingly, we found the strongest association between patient functioning and residual core mood symptoms, and we also found a significant interaction with pain and anxiety. The absence of pain increased the chances of normal functioning, regardless of the presence of residual anxiety. However, the absence of residual anxiety increased the chances of normal functioning only if pain was not present. Of note, we found residual insomnia significantly less strongly related to patient functioning than residual core mood symptoms. In addition, no association was found for residual somatic symptoms. It is remarkable that baseline depression severity and previous depression episodes were not significantly related to functional impairment. This further supports the previous finding that residual symptoms are more important than previous episodes of depression in the prognosis of the patient [5].

The different degree of association of each residual symptom with patient functioning might have prognostic implications and requires further investigation. In line with this, several recent studies tried to identify which specific residual symptoms are predictive of relapse or recurrence [16, 26, 30, 31]. Residual anxiety symptoms were found to be predictive of relapse [26, 30, 31]. The picture for residual insomnia was less clear, with both positive [16, 30] and negative associations reported [6]. Although preliminary, these findings suggest that some residual symptoms present a greater risk for relapse than others.

This study has the following limitations: The primary study from which our data were drawn was not designed to assess residual symptoms, and our results are based on a post-hoc analysis. Our analysis has inherent limitations of post-hoc analysis; measures were those used in the source study. Antidepressant history, before baseline, was not collected, therefore percentage of naïve patients and already treated patients are unknown. This analysis has included a selected population of patients with MDD; patients who had a response to acute antidepressant treatment. This may limit the generalizability of the results to other types of patients not included in this analysis. Our research focused on selected residual symptoms domains and did not include domains such as fatigue or other symptoms not included in the HAMD-17. We also cannot rule out the possibility that a small proportion of the symptoms reported might have been treatment-emergent and not residual.

Conclusions

In summary, our results contribute to a better understanding of the role of specific residual symptoms domains on functional impairment in depression. We found that different residual symptoms have different degrees of association with patient functioning. This indicates that specific residual symptoms domains may be targets for intervention if normal functioning is the treatment objective.

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Acknowledgements

We thank Alistair Reeves for editing assistance, Ígor Martín from Chiltern International Inc. for his support with the statistical analysis, Irene Fregenal from Lilly Spain, Irene Fregenal from Lilly Spain for editing support, the principal investigators, and the patients for their voluntary participation. This study was funded by Eli Lilly and Company.

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Authors and Affiliations

  1. Department of Clinical Research Lilly, S.A. Avenida de la Industria 30, 28108, Alcobendas, Spain

    Irene Romera, Antonio Ciudad, Pepa Polavieja & Inmaculada Gilaberte

  2. Autonomous University of Barcelona, Barcelona, Spain

    Irene Romera

  3. Department of Psychiatry, Hospital Santa Creu i Sant Pau, Autonomous University of Barcelona / CIBERSAM, Barcelona, Spain

    Víctor Pérez

  4. Department of Psychiatry, Hospital Puerta de Hierro, Madrid, Spain

    Luis Caballero

  5. Department of Psychiatry, Joan March Hospital, Rediapp, Palma de Mallorca, Spain

    Miguel Roca

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  1. Irene Romera
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Correspondence to Irene Romera.

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Competing interests

Dr. Irene Romera, Dr. Antonio Ciudad, Pepa Polavieja and Dr. Inmaculada Gilaberte are employees of Eli Lilly. Dr. Irene Romera is also an affiliate with the Universidad Autónoma de Barcelona, Departamento de Psiquiatría. Dr. Victor Perez has received grant support from Eli Lilly, Lundbeck, Boehringer, Pfizer, Astra Zeneca, and GSK; has received honoraria from Servier, Eli Lilly, BMS-Otsuka, GSK, Astra Zeneca, and Boehringer; has served as a consultant for and/or on advisory boards for Eli Lilly, BMS, and AstraZeneca. Dr. Luis Caballero has served on advisory boards for Eli Lilly. Dr. Miguel Roca has received grant support from Almirall, Lundbeck and Janssen and served on advisory boards for Eli Lilly and Wyeth.

Authors’ contributions

IR, PP and IG, have been involved in the analysis. All authors have been involved in the interpretation of the data, decision to submit the manuscript for publication and have read and approved the final manuscript. IR has been involved in writing the manuscript.

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Romera, I., Pérez, V., Ciudad, A. et al. Residual symptoms and functioning in depression, does the type of residual symptom matter? A post-hoc analysis. BMC Psychiatry 13, 51 (2013). https://doi.org/10.1186/1471-244X-13-51

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