Selective serotonin reuptake inhibitors (SSRIs), the most commonly prescribed antidepressant drugs, have a variable and incomplete efficacy. In order to better understand SSRI action, we explored the hypothesis that SSRIs do not affect mood per se but amplify the influence of the living conditions on mood. To this aim, we exploited the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) data set, selected a subpopulation of 591 patients with an overlapping clinical history and analyzed treatment outcome according to dosage −20 or 40 mg per day of citalopram. We found that sociodemographic characteristics affected treatment response in the same direction in the two dose groups, but these effects reached statistical significance only in the 40 mg per day dose group. In the latter, higher improvement rate was associated with having a working employment status (P=0.0219), longer education (P=0.0053), high income (P=0.01) or a private insurance (P=0.0031), and the higher remission rate was associated with having a working employment status (P=0.0326) or longer education (P=0.0484). Moreover, the magnitude of the effect of the sociodemographic characteristics on mood, measured as the percent of patients showing a positive outcome when exposed to favorable living conditions, was much greater—up to 37-fold—in the 40 compared to the 20 mg per day dose group. Overall, our results indicate that citalopram amplifies the influence of the living conditions on mood in a dose-dependent manner. These findings provide a potential explanation for the variable efficacy of SSRIs and might lead to the development of personalized strategies aimed at enhancing their efficacy.
Antidepressant drugs are the current standard treatment for major depressive disorder (MDD) and, among these, selective reuptake inhibitors (SSRIs) are the most commonly prescribed. However, their efficacy is variable and incomplete: 60–70% of depressed patients do not experience remission and 30–40% do not show a significant response.1 One of the main reasons for such incomplete efficacy is the poor comprehension of their mechanisms of action. A new hypothesis, the undirected susceptibility to change hypothesis, predicts that SSRI treatment does not drive changes in mood per se but, by increasing brain plasticity, creates a window of opportunity for a change in mood that is driven by the quality of the living conditions.2 In particular, the serotonin increase induced by SSRIs enhances brain plasticity and thus renders the individual more susceptible to the influence of the living conditions. The main consequence is the lack of a univocal outcome of SSRI administration: in a favorable environment treatment leads to a reduction of symptoms; by contrast, in a stressful environment it may lead to a worse prognosis. As a further consequence, SSRIs are expected to amplify the influence of living conditions on mood in a dose-dependent manner. Such hypothesis is supported by preclinical data3, 4, 5 showing that fluoxetine treatment leads to an improvement of the depression-like phenotype when administered in an enriched condition, while it leads to a worsening when administered in a stressful condition. In addition, SSRI treatment consequences on selected end points, such as vulnerability to obesity, have been shown to be dependent on the quality of the environment.6, 7 Finally, a number of clinical studies have shown that the environment moderates the effects of antidepressant treatment.1, 8, 9, 10, 11, 12, 13 However, the approaches used so far in these studies do not allow for assessing the effect of SSRIs on the susceptibility to the influence of the living conditions.
The main aim of the present study was to test whether SSRI treatment amplifies the influence of the living conditions on mood in a dose-dependent manner. We thus exploited the data collected in the framework of the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study. We considered a subpopulation of 591 patients having similar MDD severity and overlapping treatment history, and analyzed the efficacy of treatment between weeks 4 and 6 according to the dose received—either 20 or 40 mg per day of citalopram. Longer or different treatment periods or other patients’ groups could not be considered without losing data validity because of the limitations imposed by the STAR*D trial design. The socioeconomic characteristics included in the analysis are proxy of the quality of the patient's life environment and widely considered reliable indicators of socioeconomic status.14 Our prediction was that the 40 mg per day dose, compared to the 20 mg per day dose, would amplify the influence of sociodemographic characteristics on patients’ mood, since it should increase plasticity to a higher degree and thus lead to greater susceptibility to the environment. We therefore predicted citalopram to affect susceptibility to the living conditions in a dose-dependent manner. In addition, since we hypothesized that the environment drives the change in MDD induced by SSRIs, we predicted that patients living in conditions associated to a high quality of life should show a more effective response to treatment.
Materials and methods
This paper is based on the STAR*D (ClinicalTrials.gov, number NCT00021528) study data. The design details of STAR*D are described accurately elsewhere.15 In brief, STAR*D was a multisite, prospective, randomized, multistep clinical trial conducted in the United States of America aimed to determine which of several treatments would be most effective for outpatients with nonpsychotic MDD.16 The study was conducted at 18 primary care and 23 psychiatric care centers and enrolled 4041 nonpsychotic MDD patients, aged 18–75, with a baseline score ⩾14, on the 17-item Hamilton Depression Rating Scale (HAM-D17).
MDD symptom severity in the STAR*D clinical trial was measured longitudinally using the 16-item Quick Inventory of Depressive Symptomatology (QIDS). The QIDS is a briefer version of the more commonly used 30-item Inventory of Depressive Symptomatology—IDS. The QIDS is available in the clinician and self-rated version and has been designed to assess the severity of depressive symptoms through the evaluation of all the criterion symptom domains designated by the American Psychiatry Association Diagnostic and Statistical Manual of Mental Disorders—4th edition (DSM-IV) to diagnose a major depressive episode. Each item was scored on a scale from 0 to 3 points: 0 indicating no problem and 3 indicating severe problem. Total score ranges from 0, that is, not depressed, to 27, that is, most depressed. For further details on the validity, reliability, generalizability, scoring and interpretation, see http://www.ids-qids.org/.
At Level 1, all participants were treated with citalopram, a SSRI, for a minimum of 8 weeks and were encouraged to complete 12 weeks to maximize benefit. All participants started treatment with a dose of 20 mg per day citalopram, with clinical visits at 2, 4, 6, 9 and 12 weeks. To ensure satisfactory dosing for an appropriate period of time, treatment was conducted using measurement-based care. This included flexible dosing recommendations based on symptom and side effect at each treatment visit.17 According to the Guidelines for discontinuing participants from the randomized treatment study, patient drop out could be due to a number of reasons including participant request and decision by clinicians to discontinue the study is in the best interest of the participant.
Dose adjustments were decided according to the QIDS-Clinician-rate (QIDS-C16) score: QIDS-C16⩽5, continue current dose; QIDS-C16=6–8, continue or increase current dose according to the clinician assessment; QIDS-C16⩾9, increase current dose. In addition, if the reduction in baseline symptom severity was found to be <20% at week 4, the initial dose (20 mg per day) was raised to 40 mg per day, assuming tolerable side effects. At week 4, participants with intolerable side effects could move to the next treatment level.17
In the present study, data from level 1 of STAR*D were considered. Only patients having similar MDD severity and overlapping treatment history were included in the analysis. In particular, we selected patients treated with a dose of 20 mg per day for the first 4 weeks following enrollment, showing a QIDS-SR16 score equal to 6–10 (mild depression) on week 4 and whose information concerning the QIDS score on week 6 was available (Supplementary Figure S1). Longer or different treatment periods or other patients’ groups could not be considered without losing data validity because of the limitations imposed by the STAR*D trial design. In particular, according to the recommendations of the clinical trial design, patients with high QIDS score that indicates moderate, severe and very severe depression are compulsorily assigned to a dose increase. Including patients with all QIDS scores in the analysis would lead to bring severe depressed and potentially non-responding patients in the high dose group, erroneously leading to the conclusion that the high dose is less effective. The subset of patients considered in the present study show no meaningful clinical difference in depressive symptomatology (measured as QIDS-SR16 score at enrollment, at week 4 and as difference between week 4 and enrollment) according to the dose assignment (see Results section and Table 1). We therefore analyzed treatment efficacy between weeks 4 and 6 according to the dose received, either 20 or 40 mg per day of citalopram.
The efficacy of the two dosing regimens was analyzed in relation to a number of sociodemographic characteristics considered as proxy of the socioeconomic status and the quality of the living environment of the patient:14 sex, race, marital status, employment status, insurance status, education, income, experience of traumatic events and drug abuse. In addition, we analyzed the following descriptors of the onset and progression of the psychopathology: age at onset of first major depressive episode (MDE), number of MDE, difference in QIDS-SR16 score between enrollment and week 4. Education was shown as years of schooling completed; we considered two levels of education:
MDD symptom severity was measured using the QIDS-SR16. Remission was defined as a QIDS-SR16 score ⩽5. In order to determine the effects of citalopram treatment, according to sociodemographic characteristics, we considered three variables: (i) percent of patients showing an improvement, measured as a reduction ⩾1 in QIDS-SR16 score between week 4 and 6; (ii) percent of patients achieving remission, measured as the attainment of a QIDS-SR16 score ⩽5 at week 6; and (iii) variation in the QIDS-SR16 score, measured between weeks 4 and 6.
Of the 4041 participants, a sample of 591 patients was identified according to the selection criteria (Supplementary Figure S1). Summary statistics are presented as percentages for discrete variables, and as means and s.d. for continuous variables. Logistic regression models were used to assess the association of all sociodemographic characteristics with QIDS-SR16 score improvement and remission rate, within each dose group, and to compute odds ratios. The Wald test was used to compute the overall significance of the categorical sociodemographic factors presenting more than two levels. The use of the odds ratios as a measure of risk is debatable and its approximation to the relative risk (RR) is acceptable only when the risk of the event (in the present study, the improvement or remission) in the control group (in the present study, the favorable sociodemographic condition) is very low, that is, under the so-called 'rare disease assumption'.18 For this reason, we additionally computed the percent of improvement or remission in the favorable (that is, associated to a high quality of life) and in the unfavorable (that is, associated to a low quality of life) sociodemographic condition, and the RR of unfavorable versus favorable condition, with the corresponding 95% confidence interval. Finally, the preventive fraction (1−RR) was computed to estimate the effect size and thus the magnitude of influence of the living conditions on the outcome. As in our study the outcome measured is a beneficial one, that is improvement or remission, values of 1−RR>0 indicate that the unfavorable condition decreases the probability of the beneficial outcome compared to the favorable condition, and vice versa. The variation in the QIDS-SR16 score between weeks 4 and 6 was analyzed with analyses of variance including sociodemographic characteristics as between-subject factors. Separate analyses of variance were performed for each sociodemographic characteristic within the two treatment doses. Post hoc comparisons were performed using the Tukey’s test. The variation in percent of improvement, stationary and worsening according to sociodemographic characteristics has been analyzed independently in the two dose groups with X2-test.
Of 591 patients who comprised the evaluable sample, 357 (60.4%) were treated with 20 mg of citalopram per day and 234 (39.6%) with 40 mg of citalopram per day between weeks 4 and 6. Females comprised two-thirds of the sample and minority representation was robust. The two dose groups did not show any meaningful clinical difference before receiving different citalopram doses (Supplementary Table S1). At enrollment, their QIDS-SR16 scores were almost overlapping (20 mg per day dose group: mean 14.14, s.d. 3.78; 40 mg per day dose group: mean 14.7, s.d. 3.79). The two groups did not differ also in QIDS-SR16 score at week 4 (20 mg per day dose group: mean 7.93, s.d. 1.39; 40 mg per day dose group: mean 8.16, s.d. 1.44). Finally, as shown in Table 1, no difference between the 20 and 40 mg per day dose groups was found in response to treatment as both showed an almost overlapping reduction of QIDS-SR score during the first 4 weeks of treatment, when all patients received the 20 mg per day dose. Table 1 summarizes further baseline characteristics of the two groups.
Sociodemographic characteristics and dosage associated with improvement
According to our hypothesis, the two citalopram dosages amplified the influence of sociodemographic characteristics on the percent of patients showing an improvement in a dose-dependent manner. In the 20 mg per day dose group, patients' response was not significantly affected by sociodemographic characteristics. By contrast, in the 40 mg per day dose group, sociodemographic characteristics were associated to significantly different outcomes. In the latter group, a higher rate of improvement was associated with having a working employment status, more than 16 years of education, high income and a private insurance (Table 2). In order to appreciate the influence of the environment in each dose group, its magnitude was measured as the preventive fraction (1−RR). The comparison of the preventive fraction, indicating the percent of patients showing a positive outcome when exposed to a favorable environment, between the two dose groups shows that the influence of sociodemographic characteristics on treatment outcome was overall markedly higher in the 40 mg per day dose group. In particular, the magnitude of the influence of the employment status (unemployed versus employed) and education (
Rate of remission
As for the rate of improvement, the two citalopram dosages produced a different amplification of the influence of the sociodemographic characteristics on the percent of patients achieving remission. In particular, in the 40 mg per day group, a significantly higher rate of remission was found to be associated with being employed and having longer education (Table 3). The magnitude of the influence of the employment status (unemployed versus employed) and education (
Variation in the QIDS-SR16 score
The variation in the QIDS-SR16 score produced results in line with the previous ones, as it significantly differed according to sociodemographic variables only in the 40 mg per day dose group. In particular, in this group, being of Caucasian ethnicity (F (1,232)=5.334, P=0.0218), having a private insurance (F (2,185)=4.427, P=0.0132), a high income (F (2,225)=3.629, P=0.0281) or more years of education (F (1,187)=11.344, P=0.0009) was associated with a significant larger reduction of QIDS-SR16 score (Figure 1). Post hoc analysis revealed a significant reduction of the QIDS-SR16 comparing high versus low income (P<0.05) and having a private versus a public insurance (P<0.05).
The results of the present study show that citalopram amplifies the influence of the living conditions on mood in a dose-dependent manner as sociodemographic characteristics modify treatment response in the same direction in the two dose groups, but in the 40 mg per day dose group the effect is much larger and reaches statistical significance. In addition, the magnitude of the influence of the living conditions on mood is much greater—up to 37-fold—in the 40 compared to the 20 mg per day dose group. These results support the undirected susceptibility to change hypothesis,2 which predicts that, as SSRI increases the susceptibility to the environment, treatment outcome is more profoundly affected by the quality of the living conditions in patients receiving high dosages of SSRIs.
The STAR*D clinical trial provides a unique opportunity to investigate the role of citalopram as amplifier of the influence of the living conditions on mood. It has allowed to consider a subpopulation of patients with similar MDD severity and overlapping treatment history in order to analyze the amplification of the influence of the sociodemographic features induced by different dosages of citalopram. Given the clear ethical limitations to perform a clinical trial aimed at directly measuring the effects of the SSRIs in amplifying the beneficial, but especially the detrimental effects of the environment in patients, the STAR*D data set is the best alternative to test the undirected susceptibility to change hypothesis. In addition, the STAR*D clinical trial is the largest ecologically valid 'real world' study of outpatients with nonpsychotic major depressive disorder to date.1, 19
Sociodemographic characteristics modified treatment outcome in the same direction in the two dose groups, but these changes did not reach statistical significance in the 20 mg per day dose group. By contrast, in the 40 mg per day dose group, each one of five sociodemographic characteristics—income, education, ethnicity, insurance and employment—significantly affected treatment outcome. In addition, the magnitude of the effect of the sociodemographic characteristics on mood, measured as the percent of patients showing a positive outcome when exposed to a favorable environment, was dose-dependent. In particular, the influence of the living conditions was much greater in the 40 than in the 20 mg per day dose group: improvement rate went from a minimum of fivefold for employment status to a maximum of 37-fold for education while remission rate went from twofold for education to eightfold for income.
It is worth noting that, in line with our hypothesis and with previous studies showing that a favorable and supportive environment increases antidepressant efficacy,1, 10, 11, 13, 20 the present results indicate not only that citalopram amplifies the influence of the living conditions on mood, but also that the quality of the living environment drives the change in mood. In particular, in the 40 mg per day dose group, where this change reaches statistical significance, improvement and remission were shown at significantly higher rates by patients living in conditions associated with a high quality of life, such as having a working employment status, more than 16 years of education and a high income. The exception concerns insurance where those individuals having public insurance showed the worse outcome, even compared to those having no insurance.21 This is concordant with previous studies reporting, for instance, that having public insurance predicts the highest attrition.17 In addition, higher rates of improvement and remission were associated with being of Caucasian ethnicity. The sociodemographic characteristics here found to affect treatment outcome have been previously shown to both determine rates of major depression morbidity and mortality22 and affect SSRI outcome.1 According to our hypothesis,2 even a worsening of symptomatology could be predicted when citalopram treatment is administered in an adverse environment. However, only a very limited worsening of the QIDS-SR score was expected in patients receiving the treatment while living in an unfavorable condition (Figure 1) because of the implementation of the STAR*D guidelines for discontinuing participants, which recommend that patients drop out of the study when clinicians consider that discontinuation is in the best interest of the participant. Nevertheless, an effect of treatment, both for better and for worse,23 can be appreciated when considering the percent of patients showing improvement or worsening according to the quality of the living conditions in the two dose groups (Supplementary Figure S2). Indeed, the 40, compared to 20 mg per day dose, leads to an increase not only of the percent of improvements in patients living in a favorable environment, but also of the percent of worsening in patients living in an unfavorable environment. For instance, in the 20 mg per day dose group, patients with a college degree showing an improvement were 62% and patients with a high school degree showing a worsening were 21%. In the 40 mg per day group, these percent rise up, respectively, to 71% and 35%. As further example, in the 20 mg per day dose group, patients with a high income showing an improvement were 58% and patients with a low income showing a worsening were 35% while, in the 40 mg per day group, these are, respectively, 68% and 40% (Supplementary Figure S2).
Taking into account the role of SSRIs as amplifier of the influence of living conditions on mood—and, consequently, the quality of the environment as a moderator of SSRI treatment outcome24—may explain the inconsistency of the findings in the literature about SSRI efficacy. Indeed, overlooking the environment as the key stratifying factor in treatment response might have led to the reported contradictory results in antidepressant outcome. The conceptual shift in considering the action of SSRIs from being the causative factor for recovering from major depression to acting as a permissive factor for the influence of the living conditions on the psychopathology allows to reconcile experimental and clinical data that apparently do not fit together.2 For instance, the theoretical framework currently available in the literature leads to the paradox that the same molecular mechanism of action has two opposite outcomes: high extracellular serotonin levels are beneficial when induced by SSRI administration, but confer a high risk to develop psychopathology when associated to the s variant of the serotonin-transporter-linked polymorphic region (5-HTTLPR). This discordant picture can be coherently interpreted in light of our results and the undirected susceptibility to change hypothesis, positing that high serotonin levels lead to increased plasticity and thus to high susceptibility to change, which may promote either an improvement or a worsening, according to the quality of the environment.2 It is worth noting that the effects of citalopram described in the present paper may represent only part of the action of SSRIs on mood as the main target of these drugs, that is, the serotoninergic system, has a high molecular complexity and is involved in a wide range of physiological functions.
The major limitation of the present study is the short time frame (2-week period) over which data of the STAR*D clinical trial have been extracted. This period had to be chosen because it is the only one allowing to consider patients with overlapping clinical history. Longer or different treatment periods or other patient groups would have not allowed to keep data validity. By contrast, the fact that coherent significant results have been found in such a short time frame suggests that the described phenomenon is robust. Further limitations include open treatment design, the use of a single antidepressant agent (citalopram) and the lack of placebo control. Although data analyses did not include correction for multiple comparisons, the overall consistence of the results support their reliability. It is worth noting that depression treatment disparities experienced by different ethnicities may result from stigma, clinician failure to engage with the patient, poor patient activation, treatment adherence and other factors, including biological differences.25
In conclusion, acknowledging the role of SSRIs as amplifier of the influence of the living conditions on mood represents a critical step in developing a personalized medicine approach aimed at better matching patients with treatment and avoiding potential harmful consequences. The control of the patients' living environment could be achieved by training patients to cope with harsh conditions, for instance, through cognitive behavioral therapy,26 or taking them in charge through appropriate specialized services, as it is unlikely that people can rapidly and effectively change their living milieu. The cost of this approach is limited as no new psychoactive molecules need to be developed, while the benefits for the patients could be substantial. Finally, the undirected susceptibility to change hypothesis may contribute building a new theoretical framework capable to integrate the 'chemical imbalance theory' with other hypotheses acknowledging the importance of social–psychological factors in MDD, as both approaches are needed to explain the mechanisms underlying the recovery from the disease.
Trivedi MH, Rush AJ, Wisniewski SR, Nierenberg AA, Warden D, Ritz L et al. Evaluation of outcomes with citalopram for depression using measurement-based care in STAR*D: implications for clinical practice. Am J Psychiatry 2006; 163: 28–40.
Branchi I . The double edged sword of neural plasticity: increasing serotonin levels leads to both greater vulnerability to depression and improved capacity to recover. Psychoneuroendocrinology 2011; 36: 339–351.
Branchi I, Santarelli S, Capoccia S, Poggini S, D'Andrea I, Cirulli F et al. Antidepressant treatment outcome depends on the quality of the living environment: a pre-clinical investigation in mice. PLoS ONE 2013; 8: e62226.
Alboni S, Poggini S, Garofalo S, Milior G, El Hajj H, Lecours C et al. Fluoxetine treatment affects the inflammatory response and microglial function according to the quality of the living environment. Brain Behav Immun 2016; 58: 261–271.
Alboni S, van Dijk RM, Poggini S, Milior G, Perrotta M, Drenth T et al. Fluoxetine effects on molecular, cellular and behavioral endophenotypes of depression are driven by the living environment. Mol Psychiatry 2015; e-pub ahead of print 15 September 2015. doi:10.1038/mp.2015.142.
Bornstein SR, Schuppenies A, Wong ML, Licinio J . Approaching the shared biology of obesity and depression: the stress axis as the locus of gene-environment interactions. Mol Psychiatry 2006; 11: 892–902.
Mastronardi C, Paz-Filho GJ, Valdez E, Maestre-Mesa J, Licinio J, Wong ML . Long-term body weight outcomes of antidepressant-environment interactions. Mol Psychiatry 2011; 16: 265–272.
Downing RW, Rickels K . Predictors of response to amitriptyline and placebo in three outpatient treatment settings. J Nervous Ment Dis 1973; 156: 109–129.
Keitner GI, Ryan CE, Miller IW, Norman WH . Recovery and major depression: factors associated with twelve-month outcome. Am J Psychiatry 1992; 149: 93–99.
Perlis RH, Alpert J, Nierenberg AA, Mischoulon D, Yeung A, Rosenbaum JF et al. Clinical and sociodemographic predictors of response to augmentation, or dose increase among depressed outpatients resistant to fluoxetine 20 mg per day. Acta Psychiatr Scand 2003; 108: 432–438.
Rickels K, Jenkins BW, Zamostien B, Raab E, Kanther M . Pharmacotherapy in neurotic depression. Differential population responses. J Nervous Ment Dis 1967; 145: 475–485.
Ronalds C, Creed F, Stone K, Webb S, Tomenson B . Outcome of anxiety and depressive disorders in primary care. Br J Psychiatry 1997; 171: 427–433.
Spillmann M, Borus JS, Davidson KG, Worthington JJ 3rd, Tedlow JR, Fava M . Sociodemographic predictors of response to antidepressant treatment. Int J Psychiatr Med 1997; 27: 129–136.
Adler NE, Ostrove JM . Socioeconomic status and health: what we know and what we don't. Ann N Y Acad Sci 1999; 896: 3–15.
Fava M, Rush AJ, Trivedi MH, Nierenberg AA, Thase ME, Sackeim HA et al. Background and rationale for the sequenced treatment alternatives to relieve depression (STAR*D) study. Psychiatr Clin N Am 2003; 26: 457–494, x.
Rush AJ, Fava M, Wisniewski SR, Lavori PW, Trivedi MH, Sackeim HA et al. Sequenced treatment alternatives to relieve depression (STAR*D): rationale and design. Controlled Clin Trials 2004; 25: 119–142.
Warden D, Rush AJ, Wisniewski SR, Lesser IM, Thase ME, Balasubramani GK et al. Income and attrition in the treatment of depression: a STAR*D report. Depress Anxiety 2009; 26: 622–633.
Schmidt CO, Kohlmann T . When to use the odds ratio or the relative risk? Int J Public Health 2008; 53: 165–167.
Warden D, Rush AJ, Trivedi MH, Fava M, Wisniewski SR . The STAR*D Project results: a comprehensive review of findings. Curr Psychiatr Rep 2007; 9: 449–459.
Jain FA, Hunter AM, Brooks JO 3rd, Leuchter AF . Predictive socioeconomic and clinical profiles of antidepressant response and remission. Depress Anxiety 2013; 30: 624–630.
Hahn B, Flood AB . No insurance, public insurance, and private insurance: do these options contribute to differences in general health? J Health Care Poor Underserved 1995; 6: 41–59.
Lorant V, Croux C, Weich S, Deliege D, Mackenbach J, Ansseau M . Depression and socio-economic risk factors: 7-year longitudinal population study. Br J Psychiatry 2007; 190: 293–298.
Belsky J . The differential susceptibility hypothesis: sensitivity to the environment for better and for worse. JAMA Pediatr 2016; 170: 321–322.
Kraemer HC, Frank E, Kupfer DJ . Moderators of treatment outcomes: clinical, research, and policy importance. JAMA 2006; 296: 1286–1289.
Schraufnagel TJ, Wagner AW, Miranda J, Roy-Byrne PP . Treating minority patients with depression and anxiety: what does the evidence tell us? Gen Hosp Psychiatry 2006; 28: 27–36.
Wiles N, Thomas L, Abel A, Ridgway N, Turner N, Campbell J et al. Cognitive behavioural therapy as an adjunct to pharmacotherapy for primary care based patients with treatment resistant depression: results of the CoBalT randomised controlled trial. Lancet 2013; 381: 375–384.
This study was funded by the Italian Ministry of Health, Ricerca Finalizzata RF-2011-02349921 to IB and Olga Mayenfisch foundation to Irmgard Amrein. IB was partially supported by EU, Marie Curie IEF fellowship for Experienced Researcher n: 302881—Acronym: MODELMOOD. We warmly thank Professor Carmine Pariante (King's College London, UK) and Dr Francesca Cirulli (Istituto Superiore di Sanità, Rome, Italy) for critical reading and Dr Irmgard Amrein (Institute of Anatomy, University of Zurich, Zurich, Switzerland), Prof David Wolfer (Institute of Anatomy, University of Zurich, Zurich, Switzerland) and Silvia Poggini (Istituto Superiore di Sanità, Rome, Italy) for help and support.
The funders of the study had no role in the study design or conduct, data collection, data management, data analysis, data interpretation or writing of the report.
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on the Translational Psychiatry website
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Chiarotti, F., Viglione, A., Giuliani, A. et al. Citalopram amplifies the influence of living conditions on mood in depressed patients enrolled in the STAR*D study. Transl Psychiatry 7, e1066 (2017). https://doi.org/10.1038/tp.2017.35
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