- Research article
- Open Access
Associations of specific phobia and its subtypes with physical diseases: an adult community study
BMC Psychiatry volume 16, Article number: 155 (2016)
Specific phobia is the most prevalent anxiety disorder in the community and is associated with substantial impairment. Comorbidity with physical diseases is assumed and has important implications for etiology, treatment, or prevention of the comorbid conditions. However, due to methodological issues data are limited and subtypes of specific phobia have not been investigated yet. We examined the association of specific phobia and its subtypes with physical diseases in a representative community sample with physician-diagnosed physical diseases and diagnostic criteria of specific phobia.
Data of the German Mental Health Survey from 4181 subjects aged 18–65 years were used. Specific phobia was diagnosed using M-CIDI/DIA-X interview; physical diseases were assessed through a self-report questionnaire and a medical interview. Logistic regression analyses adjusted for sex were calculated.
Specific phobia was associated with cardiac diseases, gastrointestinal diseases, respiratory diseases, arthritic conditions, migraine, and thyroid diseases (odds ratios between 1.49 and 2.53). Among the subtypes, different patterns of associations with physical diseases were established. The findings were partially replicated in the Swiss PsyCoLaus Study.
Our analyses show that subjects with specific phobia have an increased probability for specific physical diseases. From these analyses etiological mechanisms of specific phobia and physical disease can be deduced. As subtypes differed in their patterns of associations with physical diseases, different etiological mechanisms may play a role. The findings are highly relevant for public health in terms of prevention and therapy of the comorbid conditions.
Specific phobia is the most prevalent anxiety disorder in the community [1, 2]. It is associated with significant impairment and distress  and with a loss of work days . Further, specific phobia is a predictor for increased suicidal tendency  and it is thought to be a risk factor for the later development of other mental disorders such as major depression [6, 7] or anxiety disorders . Additionally, specific phobia is highly comorbid with other mental disorders, especially with anxiety disorders and mood disorders [9, 10].
Research has suggested that besides being comorbid with other mental disorders, specific phobia may be highly comorbid with physical diseases, too. Having any anxiety disorder during the last year has been associated with neurological, vascular, respiratory, gastrointestinal, metabolic, bone, and infectious diseases [11–14]. Further, a longitudinal analysis showed that self-reported gastrointestinal disease predicted the onset of specific phobia in older adults during the next three years . Subjects with coronary heart disease reported elevated levels of phobic anxiety  and phobic anxiety is associated with cardiac mortality . Among men with high levels of phobic anxiety, an increased prevalence rate of Parkinson’s disease was found compared to men with low levels of phobic anxiety . Further, a review revealed that subjects with chronic obstructive pulmonary disease reported a prevalence of 10–17 % of specific phobia . Community studies in addition established an association between specific phobia and migraine , respiratory diseases , ulcer , vascular diseases  and heart diseases .
Most research has suggested a link between specific phobia and physical diseases. However, there are methodological issues that limit the generalizability of the findings. First, not all studies used Diagnostic and Statistical Manual of Mental Disorders (DSM)  or International Classification of Diseases (ICD)  diagnostic criteria of specific phobia. Second, the physical diseases were mainly assessed by self-report rather than diagnosed by a physician. Third, most studies focused on one specific physical disease and therefore provide limited information on the association with different physical diseases.
Knowledge of the comorbidity of specific phobia and physical diseases could influence research on the etiology of both physical diseases and specific phobia through the detection of possible etiological mechanisms. It is also highly relevant for public health because some studies have suggested that anxiety can complicate the treatment of chronic medical diseases and may therefore be associated with worse treatment outcomes [26, 27].
DSM-IV differentiates among five specific phobia subtypes (animal type, natural type, blood-injection-injury type, situational type and other type), which primarily differ with respect to content of subjective fear . Variation with respect to age of onset among the subtypes has also been observed . Further, some studies established differences among the comorbidity patterns with other mental disorders [28, 30, 31]: Youths with specific phobias of the natural type reported more depressive symptoms and showed higher prevalence rates of other anxiety disorders than youths with animal phobias ; situational phobia was associated with more panic attacks than other specific phobia subtypes ; and individuals with blood-injection phobia had a higher prevalence of marijuana abuse, depression, panic disorder, obsessive-compulsive disorder, or social phobia compared to individuals without blood-injection phobia [31, 33, 34]. Additionally, subjects with specific phobia of the natural type reported more somatic symptoms than subjects with animal phobia .
As for the different associations with mental disorders, subtypes of specific phobia may also show different comorbidity patterns with physical diseases. Psychobiological aspects might help to explain why these differences may be expected: There is evidence suggesting that different physiological processes in some biological systems may be involved in the different fear reaction of specific phobia subtypes . Subjects with animal phobia show triggered elevations in heart rate, blood pressure, norepinephrine, and epinephrine when they are exposed to the phobic stimulus. Subjects with blood-injection phobia on the other hand show an initial rise in heart rate and blood pressure followed by vasovagal fainting characterized by bradycardia and hypotension [31, 33]. Further, some evidence suggests partially distinct neurobiological substrates of blood-injection and animal phobia [35, 36]. A study investigating the neural response during the presentation of phobia-specific stimuli established that subjects with animal phobia showed activation in dorsal anterior cingulate and anterior insula, in comparison to subjects with Blood Injection Phobia showing activation in the thalamus and visual/attention areas .
Based on these empirical findings, we suggest that specific phobia subtypes are associated with different physical diseases that may be linked to distinct physiological processes. Analyses addressing similarities and differences among specific phobia subtypes are important to elucidate potential etiological pathways. However, to the best of our knowledge no study has evaluated the association between specific phobia subtypes and physical diseases in the community.
The aim of our study therefore was to analyze the association of DSM-IV specific phobia and its subtypes and a broad range of physical diseases in the German Health Interview and Examination Survey, Mental Health Supplement (GHS-MHS). We addressed the methodological limitations reported above by using a wide range of physician-diagnosed physical diseases and specific phobia assessed by a well-validated structured interview. Further, we aim to replicate the findings in a separate data set, the baseline investigation of the PsyCoLaus Study.
Based on the established associations between specific phobia and physical diseases in community samples as presented above, we specifically hypothesized for our community sample that
Having any specific phobia is associated with migraine
Having any specific phobia is associated with respiratory diseases
Having any specific phobia is associated with gastrointestinal diseases
Having any specific phobia is associated with cardiac diseases
Having any specific phobia is associated with vascular diseases
As there is not enough empirical knowledge to formulate specific hypotheses concerning the associations between subtypes of specific phobia and physical diseases, we further investigated these associations in an explorative manner.
Design and sample of the GHS-MHS
The GHS-MHS, conducted in 1997, was the first nationwide cross-sectional study for medical and social assessments in Germany. The GHS-MHS was commissioned by the German Ministry of Science, Research and Education and approved by the relevant institutional review board of the Robert Koch Institute (Berlin, Germany). The aim of the core study was the assessment of sociodemographic characteristics, physical diseases, impairments, and health-care utilization in a representative community sample of 7,124 subjects ages 18–79 years (overall response rate 61.5 %). The sample was stratified and randomized from 113 communities throughout Germany with 130 sampling units (step 1: selection of communities, step 2: selection of sampling units, step 3: selection of inhabitants) [2, 37]. The data were weighted and confidence intervals were calculated by the Huber–White sandwich method to account for the weighting scheme as well as the stratified sampling design .
Mental disorders were assessed in a two-stage design: The first stage entailed the administration of a 12-item screening questionnaire for mental disorders at the end of the medical examination of the core survey (the Composite International Diagnostic Screener) . The second stage involved the administration of a structured psychopathological interview, the Munich Composite International Diagnostic Interview (DIA-X/M-CIDI) to all core survey respondents who had been screened positive for a mental disorder and to a random sample of 50 % who screened negative . This subsample of the GHS is the sample of the Mental Health Supplement and included 4181 subjects aged 18–65 years. The M-CIDI interview was completed by 87.6 % of the subjects (conditional response rate). All subjects gave their written informed consent. Further descriptions of aims, design, and methods as well as sociodemographic characteristics of the whole GHS-MHS sample can be found elsewhere .
Specific phobia in the GHS-MHS
The fully structured DIA-X/M-CIDI interview was used for the diagnostic assessments in the GHS-MHS  covering both DSM-IV and ICD-10 criteria. Through the structured interview symptoms, syndromes, onset, duration and severity were assessed. Trained psychologists and physicians conducted the interview . The DIA-X/M-CIDI diagnostic algorithms were used to obtain the diagnostic findings reported in this paper . There was substantial test–retest reliability (kappa values between 0.56 and 0.81) ; the sensitivity of the DIA-X/M-CIDI diagnoses ranges from 87.5 % to 100 %, their specificity from 71.2 % to 100 % . The validity of the full diagnoses ranges from moderate to excellent when compared to diagnoses made by independent treating physicians in a sample of randomly chosen patients .
We used the 12-month DSM-IV diagnosis of specific phobia. Additionally, the 12-month diagnoses of the following subtypes of specific phobia were used: the animal subtype (referring to fear related to insects, snakes, birds, or other animals), the natural subtype (referring to fear related to height, storm, water), the blood-injection subtype (referring to fear related to seeing blood, injection, going to the dentist or hospital), the situational subtype (referring to flying in a plane, being in a small closed room, in a cellar, tunnel, or elevator), and the other subtype (referring to any other specific fear not matching any other subtype).
Physical diseases in the GHS-MHS
Physical diseases were assessed by a self-report questionnaire and a standardized computer-assisted medical interview by a general practice physician. Using the information on physical diseases in the self-report questionnaire, the physician collected data on age of onset, lifetime prevalence, 12-month prevalence, and point prevalence (4 weeks) of 44 physical diseases . Blood pressure and anthropometric measurements were conducted and blood and urine samples were collected. Diagnoses were then supplemented and revised based on these laboratory analyses . The present analyses are based on the physicians’ diagnoses during the medical interview.
Design and sample of the PsyCoLaus Study
As a replication study, we used the baseline investigation of the CoLaus/PsyCoLaus cohort study [43, 44]. CoLaus/PsyCoLaus conducted in Lausanne, Switzerland, was designed to study mental disorders and cardiovascular risk factors in the general population. The subjects aged 35–75 years were randomly selected through the population register of the city of Lausanne. All participants of the somatic investigation (CoLaus) aged between 35 and 66 years were asked to also undergo a comprehensive psychiatric evaluation (PsyCoLaus), resulting in a subsample of 3720 subjects (response rate: 67 %) . The psychiatric assessment took place between 2004 and 2008.
Specific phobia in the PsyCoLaus Study
The psychiatric evaluation in PsyCoLaus was based on the French version of the semi-structured Diagnostic Interview for Genetic Studies (DIGS; [45, 46]), which elicits DSM-IV axis I criteria and suicidal behavior and extensive information on the course and chronology of comorbid conditions. As the phobia section of the original DIGS interview was brief  it was replaced by the chapter from the semi-structured Schedule for Affective Disorders and Schizophrenia – Lifetime Version (SADS-LA) [47, 48]. The semi-structured interview revealed excellent inter-rater and fair to good test-retest reliability for major mood and psychotic disorders [49, 50]. Regarding anxiety disorders, applying the French translation of the SADS-LA, Leboyer et al.  found satisfactory test-retest reliability (mean interval 3.2 months) for panic disorder/agoraphobia (Yule’s Y = 0.43), Generalized Anxiety Disorder (GAD) (Yule’s Y = 0.61) and phobic disorders (Yule’s Y = 0.66). The Yule coefficient for the overall category of anxiety disorders was 0.49. Our own reliability study , based on a sample of 136 patients who also completed the combined DIGS – SADS-LA section for specific anxiety disorders, revealed perfect inter-rater agreement for all specific anxiety disorders except for agoraphobia (Yule’s Y = 0.96). The Yule’s Y coefficients for the 6-week test-retest reliability were 0.58 for panic disorder, 0.55 for agoraphobia, 0.44 for social phobia, 0.77 for specific phobia and 0.64 for OCD. Regarding GAD, no test-retest agreement was obtained.
During the interview, the subjects were asked if they had experienced symptoms of anxiety during certain situations related to the DSM-IV subtypes of specific phobia during their lifetime (e.g. “Did you feel anxious when you were flying in a plane?” or “Did you feel anxious when you were facing a certain animal?”). Subtypes were then derived from the information collected during the interview. For our analyses, the following subtypes were created based on DSM-IV criteria (comparable to those of the GHS-MHS): animal, natural, situational, blood-injection and the other subtype. As the ages of onset and offset of each disorder were assessed, 12 month prevalence of specific phobia and its subtypes could be established.
Physical diseases in the PsyCoLaus Study
Cardiovascular and metabolic diseases were assessed during the physical CoLaus evaluation through a medical interview, physical examinations and blood and urine tests. Moreover, in the medical part of the DIGS interview during the psychiatric evaluation information was collected on additional physical lifetime diseases. During this evaluation age at onset information for physical diseases were also collected.
For the present analyses, we used data from the CoLaus and PsyCoLaus Studies. Cardiac diseases and vascular diseases were diagnosed during the CoLaus Study by an adjudication committee according to the latest diagnostic criteria, and diagnoses of hypertension and diabetes were based on measurements of blood pressure and fasting glucose . For the other groups of diseases data stemmed from the medical part of the psychiatric interview. To enable comparison with the GHS-MHS, the same groups of physical diseases were built. However, in the groups of cardiac diseases, arthritic conditions and vascular diseases not all or different physical diseases were assessed among these groups in both studies (as indicated in Table 1).
Ethics, consent and permissions
All subjects of the GHS-MHS and the PsyCoLaus Study gave their written informed consent. The GHS-MHS was commissioned by the German Ministry of Science, Research and Education and approved by the relevant institutional review board of the Robert Koch Institute (Berlin, Germany). The Ethics Committee of the University of Lausanne approved both the physical (CoLaus) and psychiatric (PsyCoLaus Study) evaluation. All subjects gave their written informed consent .
Logistic regression analyses were used to evaluate the association of specific phobia and physical diseases in both the GHS-MHS and the PsyCoLaus Study (specific phobia as predictor, physical diseases as outcome). As specific phobia and physical diseases were both associated with sex, the associations between the two were controlled for sex. To further investigate the impact of sex on the results, we checked the interactions of sex and specific phobia on the association with physical diseases. Additionally, using the age of onset data available for both specific phobia and physical diseases, we evaluated the temporal order of onset of comorbid cases. We considered a p value <0.05 as statistically significant. The analyses in the GHS-MHS study were carried out using STATA 11.0 . The analyses in the PsyCoLaus Study were carried out using SPSS version 20 .
The 12-month prevalence of specific phobia and physical diseases in the GHS-MHS
In the GHS-MHS, the 12-month prevalence of specific phobia was 7.6 %, as shown in Table 1. The most prevalent subtype of specific phobia was the situational subtype (1.8 %), and the other subtype was the least prevalent (0.08 %). The most prevalent physical diseases were arthritic conditions with a 12-month prevalence of 25.9 %, followed by allergies (18.1 %). The least prevalent physical diseases were neurological diseases (0.5 %).
Association between specific phobia and physical diseases in the GHS-MHS (hypotheses 1–5)
As shown in Table 2, having any specific phobia was associated with cardiac diseases, gastrointestinal diseases, respiratory diseases, arthritic conditions, migraine, and thyroid diseases (odds ratios [ORs] ranging between 1.49, 95 % CI [1.15–1.92], for arthritic conditions and 2.53, CI [1.73–3.69], for gastrointestinal diseases). Additionally, having any specific phobia was associated with any physical disease (OR = 1.87, [1.30–2.68]). Therefore Hypotheses 1–4 could be confirmed, whereas Hypothesis 5 had to be rejected as no association between any specific phobia and vascular diseases could be proved.
Further, no significant interactions between sex and specific phobia on the association with physical diseases were established. Therefore associations do not differ among men and women.
Among subtypes, the situational subtype was associated with the most (4 of 10) physical diseases, whereas only one association was found between the natural subtype (migraine, OR = 2.40, 95 % CI [1.29–4.45]) and the blood-injection subtype (respiratory diseases, OR = 2.14, 95 % CI [1.05–4.36]) and physical diseases. Gastrointestinal diseases, respiratory diseases, migraine, and thyroid diseases were all associated with two subtypes.
Age of onset
As shown in Table 3, in the GHS-MHS across all physical diseases most comorbid cases had the onset of specific phobia before the onset of physical diseases.
In the CoLaus/PsyCoLaus Study, any specific phobia was associated with gastrointestinal, respiratory, arthritic conditions, allergic diseases and migraine (ORs ranging between 1.30, 95 % CI [1.04–1.63], for arthritic conditions and 1.68, 95 % CI [1.33–2.13], for migraine). Further, having any specific phobia was associated with having any physical disease (OR = 1.34, 95 % CI [1.07–1.68]). In this sample, Hypotheses 1–3 could be confirmed. As no associations between specific phobia and cardiac and vascular diseases could be established, Hypotheses 4 and 5 were rejected.
Among subtypes, the animal and natural subtype were associated with respiratory diseases (animal: OR = 1.62, 95 % CI [1.02–2.55]; natural: OR = 2.36, 95 % CI [1.16–4.82]) and migraine (animal: OR = 1.71, 95 % CI [1.09–2.69]; natural: OR = 2.38, 95 % CI [1.16–4.85]). Additionally, the natural subtype was associated with having any physical disease (OR = 3.03, 95 % CI [1.06–8.57]; No other associations were found between subtypes of specific phobia and physical diseases in the PsyCoLaus Study. Results of the PsyCoLaus data are available on request.
Further, similar to the GHS-MHS data across all physical diseases most comorbid cases had the onset of specific phobia before the onset of physical diseases (results available on request).
The aim of our study was to determine the association between specific phobia and its subtypes and physical diseases in a general population sample to extend information from earlier studies by using improved methods (physician-diagnosed physical diseases, standardized diagnostics of specific phobia, a wide range of physical diseases assessed within one sample). Our study suggests an association of specific phobia and several physical diseases in the community. In line with earlier studies, we found an association between specific phobia and respiratory diseases [11, 53], heart diseases [16, 17], vascular diseases  and cardiac diseases . An association with gastrointestinal diseases has also been found, but in comparison to our study the association did not remain significant after adjusting for sex . Additionally, we established an association between specific phobia and arthritic conditions, migraine, and thyroid diseases. We could replicate the associations between any specific phobia and gastrointestinal diseases, respiratory diseases, arthritic conditions and migraine in the PsyCoLaus Study. Associations with these physical diseases have already been documented within the GHS-MHS for the group of anxiety disorders . Further, our analyses did not provide evidence for associations between specific phobia and vascular diseases in both data sets. This is not in line with an earlier community based study that established associations between specific phobia and cardiovascular diseases . While we distinguished between cardiac and vascular diseases in two groups as shown in Table 1, the study by Goodwin et al. (2009) only used one group of cardiovascular diseases. Therefore it may be possible that the differences in the established associations may be due to methodological differences.
In addition, even though previous research showed that there are gender differences among specific phobia subtypes  and among certain physical diseases such as cardiac diseases , we did not establish differences in the associations between specific phobia subtypes and physical diseases among men and women.
Different models can be considered for the explanation of the comorbidity of specific phobia and physical diseases (specific phobia may be an antecedent or a consequent factor of a specific physical disease; there may be common biological or social factors that increase the risk of having both specific phobia and physical diseases; or a third variable may contribute to the comorbidity through an indirect mechanism). Our age at onset analyses show that in most cases specific phobia preceded the physical diseases. Therefore our data suggest that the most probable model at the moment is that a preceding specific phobia increases the risk of subsequent physical disease. Further it may be that a third variable contributes to the comorbidity through an indirect mechanism. The other sequence – a preceding physical disease and a subsequent specific phobia – is the least probable model based on our data. Such analyses can contribute to the deduction of possible etiological pathways of both specific phobia and physical diseases.
It has been suggested that certain pathophysiological mechanisms related to affective and anxiety disorders, such as sympathoadrenal hyperactivity, reduced heart-rate variability, heightened platelet activity, and endothelial dysfunction, may be of interest in the etiology of heart diseases, too . Additionally, ventricular arrhythmia and hyperventilation causing coronary spasm have been named as possible mechanisms by which phobic anxiety and therefore specific phobia cause coronary heart disease [16, 55].
As a plausible explanation for the comorbidity of gastrointestinal and anxiety disorders it has been suggested that anxiety could lead to an irritation of the gastrointestinal system, leading to a gastrointestinal disease . It has also been shown that the neurotransmitter serotonin, which is implicated in anxiety disorders in general and specifically in specific phobia , is also known to affect the gastrointestinal system .
It has been suggested that anxiety may lead to hyperventilation which is associated with asthma, too . Further, it has been discussed that shared etiological factors (either environmental or genetic) of some anxiety disorders and asthma may account for the comorbidity .
Arthritic conditions have mainly been associated with depression, but anxiety disorders seem to be rather common in subjects with arthritis, too . For the evaluation of possible shared etiological factors the following may be considered: certain cytokines and immunglobulins that seem to play a role in arthritic conditions may be associated with mental disorders, too .
Several studies have discussed the association of migraine and psychopathology [20, 63, 64]. Psychosocial factors related to stress and therefore specific phobia can act as a trigger for migraine . Additionally, a diminished serotonin level, which is also associated with anxiety disorders, has been detected in subjects with migraine . Further, psychosocial factors such as avoidance of certain situations during anxiety may trigger migraine .
An increased rate of subjects with specific phobia has been documented in thyroid disease compared to subjects in the general population [65, 66]. Common neurochemical abnormalities have been identified as a possible link between anxiety and thyroid disease .
Beside the association between specific phobia and physical diseases, different patterns of associations between the subtypes of specific phobia and physical diseases have been detected. Most associations were found between the situational subtype and physical diseases. This is in line with a finding from an earlier study that situational phobia has higher rates of comorbid psychopathology than animal and natural phobias . Another study found more somatic symptoms in subjects with natural phobia compared to subjects with animal phobia , which might suggest a somatic vulnerability of the natural subtype. In our study, however, the natural subtype was only associated with one physical disease.
The different patterns of associations between the subtypes and physical diseases may point toward different etiological mechanisms that need to be addressed in future studies. As blood-injection phobia is—alone of the subtypes—associated with vasovagal fainting , it could be, for instance, that people with this phobia profit from their rather low blood pressure, leading to a reduction of their risk for certain physical ailments, such as cardiovascular diseases or hypertension. Unfortunately, power issues precluded evaluating the impact of blood pressure on the association of specific phobia and cardiovascular diseases. This should therefore be evaluated in future studies.
The current study has a number of limitations. First, the subjects assessed were between 18 and 65 years of age. Therefore the results cannot be generalized to younger or older subjects. Second, some diagnoses may rely more on self-report data (e.g. arthritis) than other (e.g. diabetes) . This could lead to over-reporting of certain symptoms in subjects with specific phobia. Third, no conclusions concerning the causal nature of the associations between specific phobia and physical diseases can be drawn. Longitudinal evaluation of the associations found is needed. Fourth, although the sample size is 4181 subjects, the combination of physical diseases and specific phobia led to relatively small cell sizes, especially in the subtype analyses in the GHS-MHS. Fifth, the comparability of the GHS-MHS and PsyCoLaus study was limited with respect to methodology used and data collected, as different timeframes (12 months vs. lifetime diagnosis of physical diseases) and different age ranges of subjects (18–65 vs. 35–66 years) were used. Further, not all physical diseases were assessed in both studies. Accordingly, it was not surprising that the results from the GHS-MHS study could be partially replicated. Several associations were only observed in the GHS-MHS study, which could be attributable to the younger age of the sample. Indeed, in the older CoLaus/PsyCoLaus sample the prevalence of almost all physical diseases was considerably higher than in the GHS-MHS study and it is therefore possible that an increased number of age related factors predisposing to these diseases could have blurred their association with specific phobia in CoLaus/PsyCoLaus.
Despite these limitations, our study shows that specific phobia is highly comorbid with different physical diseases. Moreover, the different subtypes show different patterns of comorbidity with physical diseases in a community sample.
The comorbidity of specific phobia and physical diseases has been rarely evaluated until now. However, the findings in our community sample support the importance of further research within this field, as the comorbidity may influence the burden of subjects affected [13, 14]. Additionally, this knowledge may be highly relevant for health care policy as studies showed that anxiety disorders may be associated with noncompliance  or worse treatment outcome of the physical disease . This means that therapy of anxiety symptoms may not only lead to a reduction of anxiety but also to a better therapy outcome of the physical disease.
Last but not least given that our cross-sectional associations are proved in a longitudinal model and we presume a causal relationship between specific phobia and the different physical diseases this may also have important implications for prevention. Therapy of specific phobia may then reduce the probability of specific physical diseases.
Our community study shows that specific phobia is associated with an increased probability of specific physical diseases and that the subtypes may differ in their comorbidity patterns with physical diseases. These findings are highly relevant for etiological considerations and crucial for public health aspects, such as treatment, and prevention of the comorbid conditions.
Availability of data and materials
As the data of the GHS-MHS were obtained from a third party, namely the Robert Koch Institute, we cannot make the data available. However, data from the GHS-MHS are available as a Public Use File from Dr. Frank Jacobi, Institute of Clinical Psychology and Psychotherapy, Chemnitzer Str. 46, 01187 Dresden, Germany; e-mail: firstname.lastname@example.org. For further information about the GHS Core Survey and its Public Use File, contact Dr. Heribert Stolzenberg, Robert Koch Institute, Nordufer 20, 13353 Berlin, Germany; e-mail: email@example.com. Due to legal reasons it is not possible to make the data of the PsyCoLaus Study available.
Diagnostic Interview for Genetic Studies
Diagnostic and Statistical Manual of Mental Disorders
Generalized Anxiety Disorder
German Health Interview and Examination Survey, Mental Health Supplement
International Classification of Diseases
Munich Composite International Diagnostic Interview
Schedule for Affective Disorders and Schizophrenia – Lifetime Version
Alonso J, Angermeyer MC, Bernert S, Bruffaerts R, Brugha T, Bryson H, et al. Prevalence of mental disorders in Europe: results from the European Study of the Epidemiology of Mental Disorders (ESEMeD) project. Acta Psychiatr Scand. 2004;109(s420):21–7.
Jacobi F, Wittchen H-U, Holting C, Hoefler M, Pfister H, Muller N, et al. Prevalence, co-morbidity and correlates of mental disorders in the general population: Results from the German Health Interview and Examination Survey (GHS). Psychol Med. 2004;34:597–611. doi:10.1017/S0033291703001399.
Wittchen H, Jacobi F, Rehm J, Gustavsson A, Svensson M, Svensson B, et al. The size and burden of mental disorders and other disorders of the brain in Europe 2010. Eur Neuropsychopharmacol. 2011;21(9):655–79.
Alonso J, Angermeyer M, Bernert S, Bruffaerts R, Brugha T, Bryson H, et al. Disability and quality of life impact of mental disorders in Europe: results from the European Study of the Epidemiology of Mental Disorders (ESEMeD) project. Acta Psychiatr Scand. 2004;109(s420):38–46.
Nock MK, Hwang I, Sampson NA, Kessler RC. Mental disorders, comorbidity and suicidal behavior: results from the National Comorbidity Survey Replication. Mol Psychiatry. 2009;15(8):868–76.
Goodwin RD. Anxiety disorders and the onset of depression among adults in the community. Psychol Med. 2002;32:1121–4.
Bittner A, Goodwin RD, Wittchen H-U, Beesdo K, Hoefler M, Lieb R. What characteristics of primary anxiety disorders predict subsequent major depressive disorder? J Clin Psychiatry. 2004;65(5):618–26.
Trumpf J, Margraf J, Vriends N, Meyer AH, Becker ES. Specific phobia predicts psychopathology in young women. Soc Psychiatry Psychiatr Epidemiol. 2010;45(12):1161–6.
Stinson FS, Dawson DA, Chou SP, Smith S, Goldstein RB, Ruan WJ, et al. The epidemiology of DSM-IV specific phobia in the USA: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Psychol Med. 2007;37(07):1047–59.
Kessler RC, Chiu WT, Demler O, Walters EE. Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry. 2005;62:617–27. doi:10.1001/archpsyc.62.6.617.
Sareen J, Jacobi F, Cox BJ, Belik SL, Clara I, Stein MB. Disability and poor quality of life associated with comorbid anxiety disorders and physical conditions. Arch Intern Med. 2006;166(19):2109–16. doi:10.1001/archinte.166.19.2109.
Harter MC, Conway KP, Merikangas KR. Associations between anxiety disorders and physical illness. Eur Arch Psychiatry Clin Neurosci. 2003;253(6):313–20. doi:10.1007/s00406-003-0449-y.
Witthauer C, Gloster AT, Meyer AH, Goodwin RD, Lieb R. Comorbidity of infectious diseases and anxiety disorders in adults and its association with quality of life: a community study. Frontiers Public Health. 2014;2:80.
Witthauer C, Gloster AT, Meyer AH, Lieb R. Physical diseases among persons with obsessive compulsive symptoms and disorder: a general population study. Soc Psychiatry Psychiatr Epidemiol. 2014;1–10.
El-Gabalawy R, Mackenzie CS, Pietrzak RH, Sareen J. A longitudinal examination of anxiety disorders and physical health conditions in a nationally representative sample of US older adults. Exp Gerontol. 2014
Kawachi I, Colditz GA, Ascherio A, Rimm EB, Giovannucci E, Stampfer MJ, et al. Prospective study of phobic anxiety and risk of coronary heart disease in men. Circulation. 1994;89:1992–7. doi:10.1161/01.CIR.89.5.1992.
Watkins LL, Blumenthal JA, Davidson JR, Babyak MA, McCants CB, Sketch MH. Phobic anxiety, depression, and risk of ventricular arrhythmias in patients with coronary heart disease. Psychosom Med. 2006;68(5):651–6.
Weisskopf MG, Chen H, Schwarzschild MA, Kawachi I, Ascherio A. Prospective study of phobic anxiety and risk of Parkinson’s disease. Mov Disord. 2003;18:646–51. doi:10.1002/mds.10425.
Willgoss TG, Yohannes AM. Anxiety disorders in patients with COPD: A systematic review. Respir Care. 2013;58:858–66. doi:10.4187/respcare.01862.
Merikangas KR, Angst J, Isler H. Migraine and psychopathology: Results of the Zurich cohort study of young adults. Arch Gen Psychiatry. 1990;47:849–53. doi:10.1001/archpsyc.1990.01810210057008.
Kessler RC, Ormel J, Demler O, Stang PE. Comorbid mental disorders account for the role impairment of commonly occurring chronic physical disorders: Results from the National Comorbidity Survey. J Occup Environ Med. 2003;45:1257. doi:10.1097/01.jom.0000100000.70011.bb.
Goodwin RD, Davidson KW, Keyes K. Mental disorders and cardiovascular disease among adults in the United States. J Psychiatr Res. 2009;43:239–46. doi:10.1016/j.jpsychires.2008.05.006.
Scott KM, de Jonge P, Alonso J, Viana MC, Liu Z, O‘Neill S, et al. Associations between DSM-IV mental disorders and subsequent heart disease onset: Beyond depression. Int J Cardiol. 2013;168:5293–9. doi:10.1016/j.ijcard.2013.08.012.
American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 4th edition. Washington, DC: American Psychiatric Association; 1994.
World Health Organization. Tenth revision of the international classification of diseases. Geneva, Switzerland: World Health Organization; 1993.
Dahlen I, Janson C. Anxiety and depression are related to the outcome of emergency treatment in patients with obstructive pulmonary disease. CHEST J. 2002;122:1633–7. doi:10.1378/chest.122.5.1633.
DiMatteo MR, Lepper HS, Croghan TW. Depression is a risk factor for noncompliance with medical treatment: Meta-analysis of the effects of anxiety and depression on patient adherence. Arch Intern Med. 2000;160:2101–7. doi:10.1001/archinte.160.14.2101.
Becker ES, Rinck M, Tuerke V, Kause P, Goodwin R, Neumer S, et al. Epidemiology of specific phobia subtypes: Findings from the Dresden Mental Health Study. Eur Psychiatry. 2007;22(2):69–74. doi:10.1016/j.eurpsy.2006.09.006.
Fyer AJ. Current approaches to etiology and pathophysiology of specific phobia. Biol Psychiatry. 1998;44(12):1295–304.
Park S, Cho MJ, Chang SM, Jeon HJ, Cho S-J, Kim B-S, et al. Prevalence, correlates, and comorbidities of adult ADHD symptoms in Korea: Results of the Korean epidemiologic catchment area study. Psychiatry Res. 2011;186:378–83. doi:10.1016/j.psychres.2010.07.047.
LeBeau RT, Glenn D, Liao B, Wittchen H-U, Beesdo-Baum K, Ollendick T, et al. Specific phobia: A review of DSM-IV specific phobia and preliminary recommendations for DSM-V. Depress Anxiety. 2010;27:148–67. doi:10.1002/da.20655.
Ollendick TH, Raishevich N, Davis TE, Sirbu C, Oest L-G. Specific phobia in youth: Phenomenology and psychological characteristics. Behav Ther. 2010;41:133–41. doi:10.1016/j.beth.2009.02.002.
Bienvenu OJ, Eaton WW. The epidemiology of blood-injection-injury phobia. Psychol Med. 1998;28(5):1129–36.
Kim S-J, Kim B-N, Cho S-C, Kim J-W, Shin M-S, Yoo H-J, et al. The prevalence of specific phobia and associated co-morbid features in children and adolescents. J Anxiety Disord. 2010;24(6):629–34.
Caseras X, Giampietro V, Lamas A, Brammer M, Vilarroya O, Carmona S, et al. The functional neuroanatomy of blood-injection-injury phobia: a comparison with spider phobics and healthy controls. Psychol Med. 2010;40(1):125.
Lueken U, Kruschwitz JD, Muehlhan M, Siegert J, Hoyer J, Wittchen H-U. How specific is specific phobia? Different neural response patterns in two subtypes of specific phobia. Neuroimage. 2011;56(1):363–72.
Jacobi F, Wittchen HU, Holting C, Sommer S, Lieb R, Hofler M, et al. Estimating the prevalence of mental and somatic disorders in the community: aims and methods of the German National Health Interview and Examination Survey. Int J Methods Psychiatr Res. 2002;11(1):1–18.
Wittchen H, Hoefler M, Gander F, Pfister H, Storz S, Uestun B, et al. Screening for mental disorders: performance of the Composite International Diagnostic Screener (CIDI-S). Int J Methods Psychiatr Res. 1999;8:59–70.
Wittchen H, Pfister H. DIA-X-Interviews: Manual für das Screening-Verfahren und Interview; Interviewheft Längsschnittuntersuchung (DIA-X-Lifetime); Ergänzungsheft (DIA-X-Lifetime): Interviewheft Querschnittsuntersuchung (DIA-X-12 Monate); Ergänzungsheft (DIA-X-12 Monate); PC-Programm zur Durchführung des Interviews (Längs- und Querschnittuntersuchung); Auswertungsprogramm. Frankfurt: Swets & Zetilinger; 1997
Pfister H, Wittchen HU. M-CIDI Computerprogramm. Munich: Max Planck Institut für Psychiatrie, Klinisches Institut; 1995.
Wittchen HU, Lachner G, Wunderlich U, Pfister H. Test-retest reliability of the computerized DSM-IV version of the Munich-Composite International Diagnostic Interview (M-CIDI). Soc Psychiatry Psychiatr Epidemiol. 1998;33(11):568–78.
Reed V, Gander F, Pfister H, Steiger A, Sonntag H, Trenkwalder C, et al. To what degree does the composite international diagnostic interview (CIDI) correctly identify DSM-IV disorders? Testing validity issues in a clinical sample. Int J Methods Psychiatr Res. 1998;7:142–55.
Firmann M, Mayor V, Vidal PM, Bochud M, Pecoud A, Hayoz D, et al. The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome. BMC Cardiovasc Disord. 2008;8(1):6.
Preisig M, Waeber G, Vollenweider P, Bovet P, Rothen S, Vandeleur C, et al. The PsyCoLaus study: methodology and characteristics of the sample of a population-based survey on psychiatric disorders and their association with genetic and cardiovascular risk factors. BMC Psychiatry. 2009;9(1):9.
Nurnberger JI, Blehar MC, Kaufmann CA, York-Cooler C, Simpson SG, Harkavy-Friedman J, et al. Diagnostic Interview for Genetic Studies: rationale, unique features, and training. Arch Gen Psychiatry. 1994;51(11):849–59.
Leboyer M, Barbe B, Gorwood P, Teherani M, Allilaire JF, Preisig M, et al. Diagnostic interview for genetic studies (DIGS): inter-rater and test-retest reliability of the French version. Eur Arch Psychiatry Clin Neurosci. 1999;249:174–9.
Endicott J, Spitzer RL. A diagnostic interview: the schedule for affective disorders and schizophrenia. Arch Gen Psychiatry. 1978;35(7):837–44.
Mannuzza S, Fyer AJ, Klein DF, Endicott J. Schedule for Affective Disorders and Schizophrenia Lifetime Version modified for the study of anxiety disorders (SADS-LA): rationale and conceptual development. J Psychiatr Res. 1986;20(4):317–25.
Preisig M, Fenton BT, Matthey M-L, Berney A. Ferrero Fo. Diagnostic interview for genetic studies (DIGS): inter-rater and test-retest reliability of the French version. Eur Arch Psychiatry Clin Neurosci. 1999;249(4):174–9.
Rougemont-Buecking A, Rothen S, Jeanpretre N, Lustenberger Y, Vandeleur CL, Ferrero F, et al. Inter-informant agreement on diagnoses and prevalence estimates of anxiety disorders: direct interview versus family history method. Psychiatry Res. 2008;157(1):211–23.
StataCorp. Stata statistical software: release 11. In: StataCorp, editor. College Station, TX: StataCorp; 2009.
IBMCorp. IBM SPSS Statistics for Windows, Version 20.0: Released 2011. In: IBMCorp, editor. Armonk, NY: IBMCorp; 2011
Goodwin RD, Olfson M, Shea S, Lantigua RA, Carrasquilo O, Gameroff MJ, et al. Asthma and mental disorders in primary care. Gen Hosp Psychiatry. 2003;25:479–83. doi:10.1016/S0163-8343(03)00071-9.
Moller-Leimkuhler A. Gender differences in cardiovascular disease and comorbid depression. Dialogues Clin Neurosci. 2007;9(1):71.
Haines A, Imeson J, Meade T. Phobic anxiety and ischaemic heart disease. British Med J (Clinical research ed). 1987;295(6593):297.
Goodwin RD, Cowles RA, Galea S, Jacobi F. Gastritis and mental disorders. J Psychiatr Res. 2013;47:128–32.
Zohar J, Westenberg HGM. Anxiety disorders: a review of tricyclic antidepressants and selective serotonin reuptake inhibitors. Acta Psychiatr Scand. 2000;101:39–49. doi:10.1111/j.1600-0447.2000.tb10947.
Sikander A, Rana SV, Prasad KK. Role of serotonin in gastrointestinal motility and irritable bowel syndrome. Clin Chim Acta. 2009;403(1):47–55.
Roy-Byrne PP, Davidson KW, Kessler RC, Asmundson GJ, Goodwin RD, Kubzansky L, et al. Anxiety disorders and comorbid medical illness. Gen Hosp Psychiatry. 2008;30:208–25. doi:10.1016/j.genhosppsych.2007.12.006.
Goodwin RD, Fergusson DM, Horwood L. Asthma and depressive and anxiety disorders among young persons in the community. Psychol Med. 2004;34:1465–74. doi:10.1017/S0033291704002739.
El-Miedany YM, Rasheed AHE. Is anxiety a more common disorder than depression in rheumatoid arthritis? Joint Bone Spine. 2002;69:300–6. doi:10.1016/S1297-319X(02)00368-8.
Isik A, Koca SS, Ozturk A, Mermi O. Anxiety and depression in patients with rheumatoid arthritis. Clin Rheumatol. 2007;26:872–8. doi:10.1007/s10067-006-0407-y.
Smitherman TA, Penzien DB, Maizels M. Anxiety disorders and migraine intractability and progression. Curr Pain Headache Rep. 2008;12:224–9.
Gonda X, Rihmer Z, Juhasz G, Zsombok T, Bagdy G. High anxiety and migraine are associated with the s allele of the 5HTTLPR gene polymorphism. Psychiatry Res. 2007;149(1):261–6.
Placidi G, Boldrini M, Patronelli A, Fiore E, Chiovato L, Perugi G, et al. Prevalence of psychiatric disorders in thyroid diseased patients. Neuropsychobiology. 1998;38(4):222–5.
Lindemann CG, Zitrin CM, Klein DF. Thyroid dysfunction in phobic patients. Psychosomatics. 1984;25:603–6. doi:10.1016/S0033-3182(84)72995-1.
Depla MF, Margreet L, van Balkom AJ, de Graaf R. Specific fears and phobias in the general population: results from the Netherlands Mental Health Survey and Incidence Study (NEMESIS). Soc Psychiatry Psychiatr Epidemiol. 2008;43(3):200–8.
We thank the Robert Koch Institute for kindly providing the data of the GHS-MHS necessary for our analyses.
The German Health Survey (GHS) was supported by grant 01EH970/8 (German Federal Ministry of Research, Education and Science; BMBF). The reported data on mental disorders were assessed in the Mental Health Supplement of the GHS, conducted at the Max Planck Institute of Psychiatry, Munich, Germany. The principal investigator was Dr. Hans-Ulrich Wittchen. Reported somatic health status variables come from the GHS Core Survey, conducted at the Robert Koch Institute, Berlin, Germany. Principal investigators of the GHS-Core Survey were Dr. Bärbel-Maria Kurth and Dr. Wolfgang Thefeld.
The CoLaus and PsyCoLaus Study was supported by research grants from GlaxoSmithKline, the Faculty of Biology and Medicine of Lausanne, and the Swiss National Science Foundation (grants 3200B0-105993, 3200B0-118308, 33CSCO-122661, 33CS30-139468, and 33CS30-148401).
On behalf of all authors, the corresponding author states that there are no competing interests.
CW RL AHM VAG MP GW PV conceived and designed the study. CW RL AHM VAG MP GW PV performed the study. CW and AHM analyzed the data. CW RL VAG MP GW PV wrote the manuscript. CW RL AHM VAG MP GW PV critically revised the manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
Witthauer, C., Ajdacic-Gross, V., Meyer, A.H. et al. Associations of specific phobia and its subtypes with physical diseases: an adult community study. BMC Psychiatry 16, 155 (2016). https://doi.org/10.1186/s12888-016-0863-0
- Specific phobia
- Physical diseases
- Representative survey