Size and burden of depressive disorders in Europe

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Abstract

We review epidemiological studies of depression in Europe. Community surveys are essential. Methodological differences in survey methods, instruments, nuances in language and translation limit comparability, but consistent findings are emerging. Western European countries show 1 year prevalence of major depression of around 5%, with two-fold variation, probably methodological, and higher prevalences in women, the middle-aged, less privileged groups, and those experiencing social adversity. There is high comorbidity with other psychiatric and physical disorders. Depression is a major cause of disability. Incidence has been less studied and lifetime incidence is not clear, with longitudinal studies required. There is pressing need for prevalence studies from Eastern Europe. The considerable differences in health care systems among European countries may impact on proportions of depressives receiving treatment and its adequacy, particularly in the key area of primary care, and require further study. There is a need for public health programmes aimed at improving treatment, reducing rates and consequences of depressive disorders.

Introduction

The term depression covers a spectrum, ranging from a normal mood of unhappiness to an abnormal, severe and incapacitating disorder. These phenomena appear to range along a continuum without clear cut points (Melzer et al., 2002). As depression becomes more severe it also becomes more pervasive, including additional symptoms. Modern definitions for disorder, as in ICD-10 Depressive Episode (World Health Organisation, 1992) and DSM-IV Major Depression (American Psychiatric Association, 1994), depend upon the presence of a specific number of symptoms to define a severity threshold, lasting at least 2 weeks, with distress or disability, and without the qualifying features of a number of other disorders. Dysthymia, a chronic or lifelong disorder, sets a milder severity threshold, but a minimum length of 2 years.

Statistics on treatment contacts miss the many cases not reaching health care, mandating community surveys. Within a continuum of severity, cut-off points, precise diagnostic definitions and instruments inevitably influence the results. Public health information on treatment needs should be based on thresholds for benefit in treatment trials but severity measures from these are rarely used in surveys. Below ICD-10/DSM IV depression thresholds are two phenomena which are more frequent: depressive symptoms, for which rates are very high (Boyd and Weissman, 1982), and so-called ‘common mental disorder’, mild mixed disorder usually including depressive and anxiety symptoms, but still with only a proportion fitting criteria for specific disorders.

This review primarily concerns defined disorder at ICD-10/DSM IV level, specifically depressive episode/major depression. Dysthymia adds a small amount to this, but most dysthymics ultimately develop depressive episodes (Keller, 1994). The main instruments in current use, the CIDI (Robins et al., 1988) and the SCAN (Wing et al., 1990) and their predecessors from the 1970s and 1980s, the DIS (Robins et al., 1981, Wittchen, 1994), and the PSE (Wing et al., 1978) use somewhat different case definitions and algorithms. Instruments employ either skilled clinician interviewers (SCAN), or fully structured interviews given by lay interviewers (CIDI). Direct comparisons consistently show that the two methods give different findings at symptom and case-diagnosis levels in general populations and also on co-morbidity (Brugha et al., 1999, Brugha et al., 2001), but better agreement for patients attending services. In primary care attenders, using lay interviewers against the psychiatrist administered SCAN, Jordanova et al. (2004) found the CIDI highly valid, and the CIS-R moderately valid.

In comparisons among European countries, with different languages and cultures, even with careful translation and testing, nuances still occur in language, and in readiness of response. There is little evidence available on the effects of this and its influence on rates reported from different European countries, which could be substantial. In order to compare regions or countries it is crucial that identical procedures and methods are used throughout. The most consistent rates found are for 12 months and 6 months.

Section snippets

Review of European prevalence studies

Table 1 presents findings from a review of selected European surveys, meeting rigorous specific comparability criteria. All were carried out on regional or national general population probability samples mostly including populations of at least one million people with at least 1000 completed interviews, and using interviews employing ICD-10 or DSM depression diagnoses. Ages were from 16 or 18 years upwards and there was no specialised selection criterion for a demographic subgroup. Published

Incidence and lifetime rates

In contrast to the large numbers of prevalence studies, studies of annual episode rates and first episode incidence are limited. They require two or more waves, the first to establish prevalent cases, the second new cases. The Dutch NEMESIS survey of population aged 18–64 found first incidence of major depression for males of 1.72 per 100 person-years and 3.90 for females (Bijl et al., 2002).

Lifetime rates are problematic. Most estimates have used the CIDI, or the DIS, which enquire

Associated factors

Although study differences limit comparisons of rates, a systematic review of approximately 200 European epidemiological studies (Fryers et al., 2004), found that associations with risk factors within studies were generally consistent.

Impairment and disability

Major depression is disabling and this has been shown in many studies. For instance, in the ESMeD study mood disorders and anxiety disorders ranked more highly than a number of common physical disorders for work days lost (ESEMeD/MHEDEA 2000 Investigators, 2004b). In a German primary care study depressed patients had 11 times as many days with total impairment as non-depressed patients (Wittchen and Pittrow, 2002). In the UK Whitehall studies, psychiatric disorder, largely neurosis, was the

Economic burden

Depression produces substantial economic costs, both through costs of health and social care, and from other costs such as work days lost. A recent review deals with European studies (Lothgren, 2004). Six studies, four from the UK and one each from Sweden and Spain, were examined in detail. Cost estimates varied widely, with total costs per patient year at 2003 prices in three studies varying from 1171 to 16581, mainly from direct medical costs (446–15822). More data are required before useful

Interventions

The extremely large treatment efficacy literature gives no evidence that basic efficacy differs among European countries.

Antidepressant medications produce around 30% more subjects showing good improvement than does placebo. The older anti-depressants have low costs. Favoured individual drugs vary by country, reflecting local preferences and marketing. Most antidepressant trials have used secondary care psychiatric samples but there is evidence of benefit in milder general practice major

Course and outcome

Depression is often a recurrent disorder (Paykel, 2001). Acute short term outcome is fairly good, with most patients showing some improvement, a small proportion remaining chronic and unremitted, but around 20–30% showing partial remission with residual symptoms. However around 30% of subjects relapse in the first year and in the long term 70–80% have at least one further episode.

The many European studies permit only partial review. A recent British 10 year follow-up found recurrence in 67% and

Health care and primary care

A pathway with many determinants leads from the community to various levels of health care, including primary care, specialist outpatient and inpatient care. European countries differ quite widely in health care systems, mode of funding (state, insurance, private), extent to which health care is primary care or specialist based. The impact of these differences on proportions of people treated in various settings has not been sufficiently studied.

Available studies have often used different ways

Possible breakthroughs

Major advances are likely in the next 20 years in knowledge of aetiology of depression, but it will be some time before these impact on rates. For social factors, use of longitudinal cohort studies is proving a most valuable tool to study early factors which are not reliably reported in retrospective studies. Biologically we have entered an era of rapid molecular genetic advance. Establishment of specific genes in affective disorder has been slow, probably because there are many genes of small

Established findings and gaps

This section summarises what is known and the research gaps which remain.

Considerable progress has been made in epidemiological methods in the last 30 years. Further research needs to be undertaken regarding effects of language and culture and effects of these on the rates reported from different European countries. Other major advances in reducing survey error do not appear near and it is more practical to accept current methods, standardised carefully. Equivalent survey procedures need to be

Recommendations

  • 1.

    The prevalence of depression has been studied extensively in Western Europe. There are variations in prevalence among studies, but these do not appear greater than can be explained by inevitable methodological factors. Social and demographic risk factors are well established and consistent. Further prevalence studies are not a high priority in these settings. However, in the new EU entrants, less well studied and with more adverse economic and social conditions, prevalence studies are needed,

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    This paper was prepared in the framework of the European College of Neuropharmacology (ECNP) Task Force project on “Size and Burden of Mental Disorders in Europe” (PI: Hans-Ulrich Wittchen). The paper also serves as input for the European Brain Council (EBC; www.ebc-eurobrain.net) Initiative “Cost of Disorders of the Brain” (Steering committee: Jes Olesen, Bengt Jönsson, Hans-Ulrich Wittchen).

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