Within the past two decades, seasonal affective disorder (SAD) has been increasingly diagnosed and treated. The concept of SAD, at least initially, was viewed by some with scepticism (Reference Eastwood and PeterEastwood & Peter, 1988), but it has steadily gained in credence and is included in DSM-IV (American Psychiatric Association, 1994) as major depressive episodes with seasonal pattern. Winter symptoms of lowered mood, increased lethargy, increased appetite and increased sleep length are very common away from the equator (Reference Kasper, Wehr and BartkoKasper et al, 1989), giving rise to debate about the point where a dividing line between ‘health’ and ‘illness’ might most appropriately be drawn on what appears to be a normally distributed continuum. Predictably, when SAD is defined more narrowly, estimates of community prevalence are lower but still significantly high at 1.4-3.5% (Reference Blazer, Kessler and SwartzBlazer et al, 1998; Reference Eagles, Wileman and CameronEagles et al, 1999). Given these levels of community prevalence, it seems almost certain that the majority of sufferers go undiagnosed and untreated. We hypothesised that sufferers of SAD would be consulting in primary care with increased frequency, that they would often present with physical manifestations of SAD and that they would generate increased numbers of prescriptions, tests/investigations and referrals for specialist care.
METHOD
The subjects in this study were identified first through the screening procedures described in previously published papers (Eagles et al, Reference Eagles, Naji and Gray1998, Reference Eagles, Wileman and Cameron1999; Reference Andrew, Wileman and HowieAndrew et al, 2001) and the service use data reported in the present paper derive from the aggregated sample from the two previous studies. Eleven large group practices based in and around Aberdeen participated, covering a total population of close to 120 000 people and employing about 60 general practitioners. Patients aged 16-64 years were approached while waiting to see their general practitioner during the month of January and were invited to complete the Seasonal Pattern Assessment Questionnaire (SPAQ; Reference Rosenthal, Genhart, Sack, Hudson and PopeRosenthal et al, 1987). Of 7927 people attending their general practitioner, 5249 (66.2%) adequately completed the SPAQ, and those who fulfilled the criteria for SAD on this instrument were invited for interview. Of 505 who were cases of SAD on the SPAQ, 274 (54.3%) attended for interview before the end of February. Of these, 127 (46.4%) also fulfilled DSM—IV criteria for recurrent major depressive disorder with seasonal pattern (American Psychiatric Association, 1994) and scored at least 15 on the Structured Interview Guide for the Hamilton Rating Scale for Depression—Seasonal Affective Disorder version (SIGH-SAD; Reference HamiltonHamilton, 1967; Reference Williams, Link and RosenthalWilliams et al, 1988; Reference Terman and WilliamsTerman & Williams, 1994), with a score of at least 6 on the atypical symptoms questions. These 127 patients, fulfilling all three sets of criteria for SAD were designated ‘interview-confirmed cases’. Of these 127 patients, 123 had primary care case records available and thus were included in the present study.
Each interview-confirmed case of SAD (none of whom had been diagnosed previously with SAD) was matched by gender and by age (to within 1 year) with two subjects who had attended the same general practice during January but who scored 6 or less on the global seasonality score of the SPAQ, this score indicating that they rated themselves as experiencing little or no significant seasonal fluctuation in their well-being. These 246 people were designated as ‘non-seasonal controls’. It is perhaps worth noting that although the control group rated themselves as being without meaningful seasonal fluctuation in well-being, no rating was made of their current mood and the control group was not intended to be one without possible depressive symptomatology of a non-seasonal nature.
The written and computerised primary care records of interview-confirmed SAD cases and non-seasonal controls were scrutinised. Use of health care services was recorded over a 5-year period, stretching back from May of the year in which they completed the screening procedures. The following data were recorded:
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(a) numbers of primary care consultations;
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(b) symptoms presented at each consultation, which were classified, where possible, by ‘bodily system’ (cardiovascular, gastrointestinal, etc.); specific note was made of symptoms that previously had been described as associated with SAD, namely pain, headache, infection, tiredness/lethary, weight gain/bingeing, sleep disturbance, depression, anxiety/panic, palpitations, alcohol misuse, diarrhoea/irritable bowel syndrome and premenstrual syndrome;
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(c) prescriptions issued, again classified by bodily system and sub-classified by the notations used in the British National Formulary (Joint Formulary Committee, 1999);
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(d) tests and investigations ordered;
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(e) specialist referrals;
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(f) hospital admissions.
After complete description of the study to the subjects, written informed consent was obtained.
Statistical analysis
Data within the above parameters of health care use were not normally distributed and therefore the Mann—Whitney test was used to compare median values between SAD cases and controls, while recognising that non-parametric statistics may be less sensitive to differences between groups. The χ2 test was used to compare the proportions of subjects in the two groups having symptoms, prescriptions and test/investigations, classified into either zero or at least unity on each parameter. This classification was used because the majority of subjects tended to have had none, one or two within each parameter, with only a few having a large number. Because as many as 20 comparisons between SAD cases and controls were sometimes made, P values of <0.025 were taken as a conservative indication of statistical significance.
RESULTS
Screened and interviewed subjects
Details of the screening and interviewing processes have been given elsewhere (Eagles et al, Reference Eagles, Naji and Gray1998, Reference Eagles, Wileman and Cameron1999). In brief, 34% of 7937 surgery attenders did not complete a SPAQ, and there are no data to estimate whether these non-responders would have differed in their likelihood of suffering seasonal morbidity. Of the 505 cases of SAD on the SPAQ, nearly half did not attend for interview before the end of February. People who were not interviewed were significantly younger than those who were (Reference Eagles, Wileman and CameronEagles et al, 1999), presumably reflecting willingness and/or availability to participate, but no other differences were detected.
Patients and controls
Among the interview-confirmed SAD patients, 21 (17%) were male and 102 (83%) were female, with double these numbers and the same percentages for controls. The mean age of patients was 39 years (s.d.=10.8) and was the same as that of controls (s.d.=11.0).
Main findings
Table 1 shows some of the main differences in use of health care services between patients with SAD and controls. Apart from hospital admissions (which were rare in both groups), there was excess use of services on all parameters by the patients with SAD.
Service use over a 5-year period by patients with seasonal affective disorder (SAD) and by non-seasonal controls
| Patients with SAD1(n=123) | Controls1(n=246) | 95% CI for differences between medians | Mann—Whitney Pvalues | |
|---|---|---|---|---|
| Primary care consultations | 34 (19-48) | 23 (14-38) | 4-12 | <0.001 |
| Prescriptions | 28 (15-48) | 18 (10-31) | 4-12 | <0.001 |
| Tests/investigations | 6 (3-12) | 4 (2-8) | 0-2 | 0.021 |
| Specialist referrals | 3 (1-4) | 1 (0-3) | 0-1 | <0.001 |
| Hospital admissions | 0 (0-0) | 0 (0-0) | 0-0 | 0.27 |
Symptoms presented
Tables 2 and 3 give details of the symptoms presented more often by sufferers of SAD at consultations over 5 years. Table 2 categorises symptoms by bodily system. Nearly 15% of all recorded symptoms could not be classified reliably, and these were grouped as miscellaneous/unclassifiable. This arose either because the presenting complaint was not sufficiently clearly recorded or, more usually, because the aetiology of the symptom (e.g. nausea, chest pain, fatigue) could not be assigned reliably to a particular bodily system. Patients with SAD presented with symptoms in a greater number of different bodily systems (median 4 (interquartile range=3-5) v. 3 (2-4) in controls; Mann—Whitney P<0.001); 59%, as against 30% of controls, presented with symptoms in four or more different systems. Table 3 relates to symptoms that have been linked previously to the presentation of SAD. Among these symptoms, it is reassuring that those of depression, tiredness/lethargy and weight gain/bingeing are more common because these would be regarded as central components of the disorder. Anxiety/panic also are more common, which presumably accounts for the excess of presentations with palpitations. The three types of symptoms that might generally be considered as less clearly linked to SAD but were significantly more common in patients with SAD were pain, infection and premenstrual syndrome.
Symptoms presented (classified by bodily system) over a 5-year period more commonly by patients with seasonal affective disorder (SAD) than by non-seasonal controls
| Symptom type | Median number (interquartile range) of presentations | Per cent presenting at least once | ||
|---|---|---|---|---|
| Patients with SAD (n=123) | Controls (n=246) | Patients with SAD (n=123) | Controls (n=246) | |
| Gastrointestinal | 2 (0-5)* | 1 (0-3)* | 69.9 | 63.0 |
| Psychiatric/psychological | 4 (1-11)*** | 0 (0-2)*** | 79.7††† | 45.9††† |
| Urinary | 1 (0-3)*** | 0 (0-2)*** | 57.7†† | 41.1†† |
| Musculoskeletal | 4 (1-11)* | 3 (1-6)* | 85.4 | 77.2 |
| Miscellaneous/unclassifiable | 5 (2-9)*** | 4 (1-7)*** | 92.7 | 89.0 |
Specific symptoms presented over a 5-year period more often by patients with seasonal affective disorder (SAD) than by non-seasonal controls
| Symptom type | Median number (interquartile ranges) of presentations | Per cent presenting at least once | ||
|---|---|---|---|---|
| Patients with | Controls | Patients with | Controls | |
| SAD (n=123) | (n=246) | SAD (n=123) | (n=246) | |
| Pain | 6(2-3)** | 4(1-9)** | 91.1 | 85.8 |
| Infection | 9(4-15)** | 7(3-12)** | 96.7 | 94.3 |
| Tiredness/lethargy | 0(0-1)*** | 0(0-0)*** | 25.2††† | 11.1††† |
| Weight gain/bingeing | 0(0-0)** | 0(0-0)** | 8.1†† | 1.6†† |
| Depression | 1(0-4)*** | 0(0-0)*** | 55.3††† | 18.7††† |
| Anxiety/panic | 0(0-2)** | 0(0-1)** | 39.0 | 27.6 |
| Palpitations | 0(0-0)*** | 0(0-0)*** | 4.9†† | 0†† |
| Premenstrual syndrome | 0(0-0)*** | 0(0-0)*** | 17.1††† | 5.7††† |
Prescriptions issued
Table 4 presents the data on prescriptions issued more often to patients with SAD during the 5 years studied. To be most meaningful, some of these data are shown in prescriptions for a particular bodily system, whereas others are subdivided into more specific types of medication. When prescriptions were grouped by bodily system, patients with SAD received prescriptions covering more of the 12 bodily systems (median 6 (interquartile range=4-8) ν. 6 (4-7); Mann—Whitney P=0.006); among patients with SAD, 36% received prescriptions covering eight or more bodily systems, as compared with 20% of controls.
Prescriptions over a 5-year period issued more often to patients with seasonal affective disorder (SAD) than to non-seasonal controls
| Type of prescription | Median number (interquartile range) of prescriptions | Per cent receiving at least one prescription | ||
|---|---|---|---|---|
| Patients with | Controls | Patients with | Controls | |
| SAD (n=123) | (n=246) | SAD (n=123) | (n=246) | |
| Gastrointestinal | 1(0-3)* | 0(0-1.25)* | 52.0 | 42.7 |
| Cardiovascular | 0(0-1)* | 0(0-0)* | 32.5† | 20.3† |
| Respiratory | 0(0-2)* | 0(0-1)* | 48.8 | 41.9 |
| Hypnotic/anxiolytic | 0(0-1)*** | 0(0-0)*** | 30.9††† | 15.5††† |
| Antidepressant | 1(0-5)*** | 0(0-0)*** | 54.5††† | 20.3††† |
| Analgesic | 1(0-3)*** | 0(0-2)*** | 66.7††† | 47.6††† |
| Antibiotics | 6(2-12)*** | 4(2-9)*** | 91.9 | 89.0 |
| Sex hormones | 0(0-1)*** | 0(0-0)*** | 35.8††† | 19.9††† |
Tests and investigations
Three tests and investigations were carried out more frequently on patients with SAD. Median numbers of full blood counts (Mann—WhitneyP=0.01) and thyroid function tests and erythrocyte sedimentation rates (ESRs) (Mann—Whitney P=0.002 for both) were higher. During the 5 years, a greater proportion of patients with SAD had thyroid function tests (42% ν. 26%, χ2=7.92, 1 d.f.,P=0.005) and ESRs (33% ν. 18%, χ2=9.55, 1 d.f.,P=0.002).
Specialist referrals
Three types of specialist referrals were more common among patients with SAD. Reassuringly, psychiatry/psychology referrals were more common for patients with SAD, of whom 27.6% were referred as against 8.1% (Mann—Whitney P<0.001) of controls. The two other specialities that had significantly increased numbers of referrals were physiotherapy (Mann—Whitney P=0.005) and gynaecology (Mann—Whitney P=0.016). Referrals in general were higher among patients with SAD (see Table 1), with 52% (as against 28% of controls) having three or more specialist referrals during the 5-year period.
DISCUSSION
Summary of findings
We found that patients with SAD, when compared with two age-matched and gender-matched controls, were much heavier users of health care services; they saw their general practitioners more frequently, they received more prescriptions, they had more tests and investigations and they were referred to more secondary care specialists. Not only were patients with SAD high consumers of health care, but they presented with a greater diversity of different symptoms. Presentations with depression, anxiety, weight gain and lethargy were predictable, but it is more noteworthy that patients with SAD also presented more often with pain, infection and premenstrual syndrome and with symptoms in the urinary, musculoskeletal and gastrointestinal systems. The prescriptions they received reflected not only high rates of presentation but a more diverse variety of presenting symptoms than controls. The higher number of tests ordered no doubt reflects diagnostic uncertainties, whereas full blood counts and thyroid function tests are likely to represent appropriate investigation of low mood and/or tiredness and lethargy. Not only psychiatrists and psychologists, but also physiotherapists and gynaecologists, saw more patients with SAD than they saw controls.
These findings are novel and have significance with regard to the diagnosis, aetiology, comorbidity and management of SAD. These issues are potentially wide-ranging and the discussion below will attempt to provide a summary rather than do full justice to all of them.
Analogies with service use in non-seasonal depression
In contrast with SAD, there is a considerable literature on the presentation, the identification, the treatment and the service use of patients with other types of depression in primary care settings. Because these findings constitute comparative data that may be of relevance to our own study, a very brief précis of some relevant points will follow.
Patients with depression present commonly in primary care but their depression often goes undetected (Reference Paykel and PriestPaykel & Priest, 1992). Depression frequently is associated with somatic symptoms, especially in primary care settings (Reference Paykel and PriestPaykel & Priest, 1992; Reference Brody, Thompson and LarsonBrody et al, 1995), and not only do somatic presentations render detection of depression less likely (Reference Brody, Thompson and LarsonBrody et al, 1995) but patients with depression who somatise are often particularly frequent consulters in primary care (Reference Portegijs, van der Horst and ProotPortegijs et al, 1996). Depressed patients are generally high consumers of health care services. They are high users of primary care services, they receive more tests and investigations, they have more out-patient visits and they are more often admitted to general hospitals (Reference Simon, Von Korff and BarlowSimonet al, 1995; Reference Rost, Zhang and FortneyRostet al, 1998). It is striking, however, that within this high demand for health care only a very small proportion of the expense relates to the treatment of the depressive disorder itself (Reference Rost, Zhang and FortneyRost et al, 1998).
There are clear similarities between our study's findings and those for non-seasonal depression. Our own study design did not permit comparison of subjects with SAD against subjects with non-seasonal depression, because our initial selection through screening was based on seasonality of symptoms and not on depression, but such a comparison would be potentially edifying.
Other studies of SAD in primary care
Our own group previously has reported increased rates of consultation in a smaller comparison of 33 patients each against one control (Reference Eagles, Naji and GrayEagles et al, 1998), and only when a larger sample was compared with two controls per case could a small autumn and winter excess of consultations be demonstrated among patients with SAD (Reference Andrew, Wileman and HowieAndrew et al, 2001). The most striking finding was of an increased rate of consultation by patients with SAD across the months of the years studied.
Only one other study has looked directly at SAD among patients consulting in primary care. Schlager et al (Reference Schlager, Froom and Jaffe1995) screened a ‘convenience sample’ of 303 patients attending a family medicine ambulatory centre in New York state during January and February and found that between 8.9% and 9.6% (the figure depending upon how the SPAQ was interpreted) satisfied the criteria for SAD. Schlager et al (Reference Schlager, Froom and Jaffe1995) did not attempt to quantify service use but noted that over half of the patients with SAD reported seasonal pain variation.
Other studies have used less direct methods. Blacker et al (Reference Blacker, Thomas and Thompson1997) found a peak of primary care presentations with major depression in the winter months, although this did not reach statistical significance, and they suspected that any winter excess in depression might be linked to higher rates of infectious illness. Other studies have found peaks of depressive presentations and antidepressant prescribing in winter (Reference Williams and DunnWilliams & Dunn, 1981; Reference Skegg, Skegg and McDonaldSkegg et al, 1986), although such peaks may occur also during the summer months (Reference Skegg, Skegg and McDonaldSkegg et al, 1986). Thus, hitherto there has been little direct evidence about the presentation of SAD, or the burden for care it imposed, in primary care settings.
Comorbidity of SAD
Anxiety was reported by 72% of the first series of patients with SAD described by Rosenthal et al (Reference Rosenthal, Sack and Gillin1984) and may be regarded more as a central component of the disorder than as a comorbid phenomenon. Panic disorder previously has been associated with winter depression (Reference Halle and DilsaverHalle & Dilsaver, 1993) and the fact that there were nine presentations with palpitations among our patients with SAD and none among our controls may further testify to this link.
Premenstrual depression also was reported commonly among Rosenthal et al's (Reference Rosenthal, Sack and Gillin1984) original series, and the relationship between SAD and premenstrual syndrome since has been established further (Reference Maskall, Lam and MisriMaskall et al, 1994). Our patients with SAD presented more commonly than controls with premenstrual problems and were more likely to receive prescriptions for sex hormones. The comorbidity of premenstrual syndrome and SAD may be important to note because seasonal premenstrual syndrome can respond to light therapy (Reference Maskall, Lam and MisriMaskall et al, 1994).
There is good evidence of a link between winter depression and disordered eating, certainly among identified clinical samples (e.g. Reference Blouin, Blouin and AubinBlouin et al, 1992). Again, the importance of this association may relate to the response of seasonal bulimia to light therapy (Reference Lam, Goldner and SolyomLamet al, 1994). In our study, although patients with SAD presented with weight gain or binge eating more often than controls did, such presentations were relatively uncommon.
Seasonal pain was reported in Schlager et al's (Reference Schlager, Froom and Jaffe1995) primary care sample of SAD sufferers and has been described also in about 50% of a clinical sample of patients with SAD (Reference Dilsaver, Del Medico and QamarDilsaver et al, 1993). Our findings of increased presentations with pain and increased analgesic prescriptions among patients with SAD are in accord with those studies. The relationship between pain and depressed mood, however, may not be a seasonal phenomenon (Reference Von KnorringVon Knorring, 1975).
Patients in our study presented more often than controls did with infections and received more prescriptions for antibiotics, and people with SAD can report that they are especially prone to winter infections. Our findings could be seen as related to ‘help-seeking behaviour’ or may represent a comorbid biological phenomenon. Immune function certainty fluctuates seasonally (Reference Maes, Stevens and ScharpeMaes et al, 1994) and reduced winter immune function may be mediated through light deprivation via vitamin D (Reference Rosen, Livingston and RosenthalRosen et al, 1991); sufferers from winter depression have been shown to receive reduced daylight exposure during winter (Reference Espiritu, Kripke and Ancoli-IsraelEspiritu et al, 1994).
Other possible reasons for high service use
Patients with SAD might become high service users because of the SAD itself or because of associated comorbid conditions, but their service use patterns may have other explanations. One prosaic possibility is that depressive symptoms give rise to frequent primary care contact, which facilitates recognition, investigation and treatment of unrelated conditions that otherwise would have remained undiagnosed (Reference Simon, Von Korff and BarlowSimon et al, 1995). Depression also may lead to an amplification of symptoms and thus to a greater propensity to seek, and to expect, medical assistance (Reference BarskyBarsky, 1992). Our own study design was such that, in order to become a confirmed case of SAD, patients had to attend an additional interview and it is possible that this served to select people with SAD who were more focused upon their own health.
Other possible explanations have been explored in a previous paper (Reference Eagles, Naji and GrayEagles et al, 1998). Hotopf (Reference Hotopf1994) has suggested that SAD may constitute one component of ‘environmental hypersensitivity’, a condition characterised by multiple physical symptoms and somatisation and in which media-popularised ‘diseases of fashion’ can be adopted readily by the patient. Our method of patient identification — they did not self-diagnose and we actively screened and recruited them — perhaps makes this view less plausible. It may be that personality factors are of importance. Sufferers of SAD may be more neurotic, with a tendency to adopt an external locus of control (Reference Murray, Hay and ArmstrongMurray et al, 1995), and these factors may give rise to an amplification of dysphoria and an increased likelihood of seeking medical advice.
Service implications
Patients with SAD are consulting frequently in primary care and are high users of health care services but, perhaps partly because of the variety of symptoms with which they present, their SAD goes undiagnosed and untreated; none of the patients in our study had a diagnosis of SAD and in only a very few (from what was recorded in their case records) had the possibility ever been considered. Light therapy has been found to be beneficial for sufferers of SAD and to have few adverse effects (e.g. Reference Eastman, Young and FoggEastman et al, 1998). However, study participants often have comprised self-diagnosed volunteers referred on to specialist centres and this efficacy may not equate to that among patients in primary care. Our own group's trial (Reference Wileman, Eagles and AndrewsWileman et al, 2001) did not demonstrate superiority of bright white light over dim red light in patients with SAD identified in primary care, some of the subjects being those included in the present study. Therefore, before primary care professionals embark on any attempt at ‘assertive identification’ of patients with SAD, it would be important to have evidence that treatment does indeed lower morbidity among such patients and perhaps, therefore, results in reduced use of health services.
Clinical Implications and Limitations
CLINICAL IMPLICATIONS
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• Patients with seasonal affective disorder (SAD) make heavy demands on a range of health care services.
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• Sufferers of SAD present with a wide variety of physical complaints.
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• Generally SAD is not diagnosed, probably contributing to high numbers of tests and prescriptions.
LIMITATIONS
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• Patients with SAD were compared only with non-seasonal controls and not with patients suffering from non-seasonal depression.
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• Although relatively strict diagnostic criteria for SAD were deployed, it was not possible to validate the diagnosis externally.
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• It is not known whether identification and treatment of patients in primary care with SAD influence morbidity or service use.
Acknowledgements
We are grateful to all general practitioners and practice managers who helped to organise the screening and interviewing of their patients. Drs Mysore Dharmendra and Douglas Gray conducted patient interviews. The secretarial work was done by Lana Hadden.
eLetters
No eLetters have been published for this article.