Open Access

Personality traits in chronic daily headache patients with and without psychiatric comorbidity: an observational study in a tertiary care headache center

  • Marialuisa Rausa1,
  • Sabina Cevoli1,
  • Elisa Sancisi1,
  • Daniela Grimaldi1,
  • Gabriella Pollutri2,
  • Michela Casoria2,
  • Daniela Grieco2,
  • Alberto Bisi2,
  • Pietro Cortelli1,
  • Euro Pozzi2 and
  • Giulia Pierangeli1Email author
The Journal of Headache and Pain201314:22

DOI: 10.1186/1129-2377-14-22

Received: 1 December 2012

Accepted: 19 February 2013

Published: 4 March 2013

Abstract

Background

Previous studies suggest that patients with Chronic Daily Headache (CDH) have higher levels of anxiety and depressive disorders than patients with episodic migraine or tension-type headache. However, no study has considered the presence of psychiatric comorbidity in the analysis of personality traits. The aim of this study is to investigate the prevalence of psychiatric comorbidity and specific personality traits in CDH patients, exploring if specific personality traits are associated to headache itself or to the psychiatric comorbidity associated with headache.

Methods

An observational, cross-sectional study. Ninety-four CDH patients with and without medication overuse were included in the study and assessed by clinical psychiatric interview and Mini International Neuropsychiatric Interview (M.I.N.I.) as diagnostic tools. Minnesota Multiphasic Personality Inventory-2 (MMPI-2), Hamilton Depression Rating Scale (HAM-D) were afterwards administered. Patients with and without psychiatric comorbidity were compared. Further analyses were made by splitting the whole group according to the headache diagnosis and the presence or not of medication overuse.

Results

Psychiatric comorbidity was detected in 44 patients (46.8%) (group A) and was absent in the remaining 50 patients (53.2%) (group B). Mood and anxiety disorders were the most frequently diagnosed (43.6%).

In the overall group, mean scores of MMPI-2 showed a high level in the so-called neurotic triad; in particular the mean score in the Hypochondriasis subscale was in the pathologic area (73.55 ± 13.59), while Depression and Hysteria scores were moderate but not severe (62.53 and 61.61, respectively). In content scales, score in Health Concern was also high (66.73).

Group A presented higher scores compared to Group B in the following MMPI-2 subscales: Hypochondriasis (p = .036), Depression (p = .032), Hysteria (p < .0001), Hypomania (p = .030). Group B had a high score only in the Hypochondriasis subscale. No significant differences were found between chronic migraine (CM)-probable CM (pCM) plus probable medication overuse headache (pMOH) and chronic tension-type headache (CTTH)-probable CTTH (pCTTH) plus pMOH patients or between patients with and without drug overuse.

Conclusions

The so-called “Neurotic Profile” reached clinical level only in CDH patients with psychiatric comorbidity while a high concern about their general health status was a common feature in all CDH patients.

Keywords

Chronic daily headache Medication overuse headache Psychiatric comorbidity MMPI-2

Background

Chronic daily headache (CDH) is not a universally recognized diagnosis but an umbrella term for a group of headache disorders occurring at least 15 days per month [13]. Unfortunately the classification and definition of CDH are still plagued with difficulties [4]. The CDH population comprises individuals with chronic tension-type headache (CTTH) and chronic migraine (CM), both of which may be associated with medication overuse [57]. The majority of patients reporting CDH have a history of episodic headache, mainly migraine without aura (MWOA), evolving into a chronic form over the years [8]. CDH is a major clinical concern and a common health risk, with a prevalence of approximately 3% to 5% in the adult population worldwide [911]. Identifying risk factors for progression has emerged as a major public health priority. Psychiatric comorbidity has been one of the risk factors most widely investigated for headache chronification due the significant role it may play in this process [1216] and because it might be linked to medication overuse in migraineurs [17]. Many epidemiological and clinical studies have confirmed the elevated risk for mood and anxiety disorders in migraine and in CDH [1823]. In particular, patients with CDH showed higher levels of anxiety and depressive disorders than patients with episodic migraine [19]. Some studies [19, 24, 25] hypothesized that patients with medication overuse headache (MOH) may differ psychologically from other headache patients because of a dependence-related behavior, but this hypothesis was not confirmed by more recent findings [2628].

Personality traits assessed by the Minnesota Multiphasic Personality Inventory-2 (MMPI-2) [29] disclosed that patients with CDH showed the so-called “neurotic MMPI-2 profile” characterized by high scores in the first three scales: Hs (Hypochondriasis), D (Depression), and Hy (Hysteria) [30, 31]. A recent study [27] comparing MMPI scores in MOH, episodic headache patients and healthy controls, showed that MOH and episodic headache patients displayed similar patterns, differentiating only in Hypochondriasis scale, and that there were no differences between the three groups in scales measuring dependence-related behavior. Another recent study [28] compared MOH sufferers and drug-addicted patients by means of MMPI-2 dependency scales showing that the two groups did not share personality characteristics linked to dependence. The authors argued that rather than a “true” addiction behavior, a different kind of “dependence” characterized headache patients related to the need to avoid pain. No study has hitherto explored if dependence behaviors in MOH patients are related to the psychiatric comorbidity often associated with CDH.

Aims of the present study were to: 1) investigate the prevalence of psychiatric comorbidity and specific personality traits in CDH patients, 2) investigate if specific personality traits characterize only patients with psychiatric comorbidity or were associated with the headache type.

Methods

One hundred and five consecutive adult patients referred to the Headache Centre of the Department of Neurological Sciences of the University of Bologna and satisfying inclusion criteria for CDH (≥15 days/months for at least 3 months) with or without medication overuse, were recruited by expert neurologists (S.C., E.S., G.P.). Headache and drug overuse were classified according to the original [5] and the revised International Classification of Headache Disorders-II (ICHD-II) criteria [6]. Exclusion criteria were: age <18, secondary CDH assessed by clinical examination, biochemical tests or neuroimaging studies.

The study protocol included a psychiatric evaluation by means of a clinical assessment set up by expert psychiatrists (M.C., D.G., A.B.) and of the Mini International Neuropsychiatric Interview (M.I.N.I.) [32] in order to identify subjects with psychiatric comorbidity. Moreover the Hamilton Depression Rating Scale (HAM-D) [33] and the Minnesota Multiphasic Personality Inventory-2 (MMPI-2) [29, 34] questionnaires were administered..

M.I.N.I. [32] is a short structured diagnostic interview for psychiatric disorders as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV) [35] and by the International Classification of Diseases, 10th edition (ICD-10) [36]. It generates a positive diagnosis for the main Axis I DSM-IV disorders: mood, anxiety, eating and substance-related disorders. It also explores psychotic symptoms to exclude probable lifetime or current psychotic disorders.

HAM-D [33] is a depression test measuring the severity of clinical depression symptoms. It is a 21-item multiple choice questionnaire assessing depression in four levels: score under 7: no depression, score from 8 to 17: mild depression, score from 18 to 24: moderate depression, score over 25: severe depression.

MMPI-2 [29, 34] is a 567 true-false item questionnaire composed of three validity and ten clinical scales. The questionnaire also includes content scales (clusters of items concerning the same psychological dimension and behavioral area) and supplementary scales which evaluate broad personality traits, generalized emotional distress and behavioral dyscontrol. For each scale, a T-score of 65 was considered as the level of clinical significance in the 95th percentile. MMPI-2 questionnaires were selected on the basis of the three validity scales.

M.I.N.I. and HAM-D were administered by a psychiatrist, while MMPI-2 was self-reported.

The institutional review board of the Department of Neurological Sciences of the University of Bologna approved the study protocol and all participants gave written informed consent. The study was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki.

Data analysis

Descriptive statistics (means ± SD) were conducted on the sample features. The sample was divided into two groups according to M.I.N.I. results: patients with and without psychiatric comorbidity (Group A and Group B, respectively). Analysis of skewedness and kurtosis showed that data had a normal distribution. Further analyses were made by splitting the whole group according to the presence or absence of medication overuse, and according to the headache diagnosis: CM or probable CM (pCM) plus probable MOH (pMOH) vs CTTH or probable CTTH (pCTTH) plus pMOH according to the ICDH-II and MOH, CM and CTTH according to the ICDH-II revised criteria. Moreover we consider which preventive therapy patients were assuming.

Chi-squared and Student’s T-test were performed to compare data between groups. Data were analyzed using the statistical software SPSS 19.0 (Statistical Package for Social Science). Significance level was set at p < .05.

Results

Descriptive analysis

Ninety-four out of 105 patients with CDH and consecutively referred to the Headache Center were recruited. Eleven refused to participate in the study, 94 accepted to partecipate and signed an informed consent. All partecipating patients received a psychiatric evaluation by means of a clinical assessment and of the M.I.N.I. [32]. Seven patients withdrew their consent. To the 87 patients left, the HAM-D [33] and the MMPI-2 [29, 34] questionnaires were administered.

According to the original ICHD-II criteria [5], four subjects (4.2%) had a diagnosis of CM, 18 ( 19.1%) of CTTH, 43 (45.7%) had a diagnosis of pCM plus pMOH, and 29 (30.9%) of pCTTH plus pMOH. According to ICHD-II revised criteria [6], four subjects (4.2%) had a diagnosis of CM, 18 (19.2%) of CTTH, and 72 (76.6%) of MOH.

Table 1 shows patients’ demographic and headache features. Drug overuse was significantly higher in pCM + pMOH patients compared to pCTTH + pMOH patients (43 vs 29, χ2 = 11.631; p < .001).
Table 1

Patients’ demographic and headache characteristics

Gender

 

Male, n (%)

22 (23.4)

Female, n (%)

72 (76.6)

Age (yrs), mean ± sd (min-max)

48.51 ±14.31 (19-75)

Educational level

n (%)

Elementary/secondary school,

50 (53,2)

High or graduate school, n (%)

44 (44.7)

Types of headache at onset

n (%)

MWOA

78 (83.0)

MWOA + MWA

8 (8.5)

ETTH

5 (5.3)

CTTH

3 (3.2)

Age of chronification (yrs), mean ± sd

38.10 ±14.95

Duration of chronification (yrs), mean ± sd

10.21 ± 10.63

Type of CDH

n (%)

(Revised ICHD-II diagnosis)

MOH 72 (76.6)

CTTH 18 (19.2)

CM 4 (4.2)

Type of CDH

n (%)

(ICDH-II diagnosis)

CM 4 (4,2%)

pCM, pMOH 43 (45,7%)

CTTH 18 (19.2%)

pCTTH, pMOH 29 (30.8%)

CTTH = chronic tension-type headache; ETTH = episodic tension-type headache; MWA = migraine with aura; MWOA = migraine without aura; MOH = medication overuse headache, CM = chronic migraine, pCM = probable CM, pCTTH = probable CTTH, pMOH = probable MOH.

Psychiatric comorbidity

Descriptive analysis of M.I.N.I. showed that 44 patients (46.8%) presented psychiatric comorbidity (group A), whereas 50 patients (53.2%) did not present any psychiatric comorbidity (group B) (Table 2). In particular, within group A, 20 patients (21.2%) were classified as mood disorder sufferers, 16 patients (17%) had an anxiety disorder, six patients (6.4%) had anxiety and mood disorder and two patients (2.1%) had other psychiatric disorders (eating disorders).
Table 2

Psychiatric comorbidity

 

Group A

Group B

Total

Mood disorder

Anxiety disorder

Mood and anxiety disorder

Other psychological disorder

  

CM

1 (1.1%)

0 (0%)

0 (0%)

0 (0%)

3 (2.1%)

4 (4.2%)

pCM plus pMOH

8 (8.5%)

7 (7.4%)

2 (2.1%)

1 (1.1%)

25 (26.6%)

43 (45.7%)

CTTH

4 (4.2%)

1 (1.1%)

3 (3.1%)

0 (0%)

10 (10.6%)

18 (19.1%)

pCTTH plus pMOH

7 (7.4%)

8 (8.5%)

1 (1.1%)

1 (1.1%)

12 (12.8%)

29 (30.8%)

Total

20 (20.2%)

16 (17.0%)

6 (6.4%)

2 (2.1%)

50 (53.2%)

94 (100%)

CM = Chronic migraine, pCM = probable chronic migraine, pMOH = probable medication overuse headache, CTTH = chronic tension-type headache, pCTTH = probable chronic tension-type headache (according to the original ICHD-II criteria). Group A = patients with psychiatric comorbidity Group B = patients without psychiatric comorbidity.

No significant differences in psychiatric comorbidity frequency were found between CM or pCM plus pMOH and CTTH or pCTTH plus pMOH patients (p = .219), or between patients with and without drug overuse (p = .534). No significant differences were found in the percentage of Group A and Group B patients assuming antidepressant or mood stabilizer as preventive therapies (10/44 Group A and 16/50 Group B, χ2 = 0.596; p = .440).

MMPI-2

Among the 94 patients, only 87 correctly completed the questionnaire, and 4 questionnaires were excluded because they did not achieve validity’s level described in the MMPI-2 manual. Statistical analyses were made in the 10 clinical scales. In the overall group, mean scores of MMPI-2 showed a high level in the so-called neurotic triad. In particular the mean score in the Hypochondriasis subscale was in the pathologic area (73.55 ± 13.59), while Depression and Hysteria scores were moderate but not severe (62, 53 and 61.61, respectively). Secondary analyses were made on content and supplementary MMPI-2 scales. In content scales, score in Health Concern was also high (66.73).

Group A showed significantly higher scores in the following MMPI-2 subscales when compared to Group B (Table 3): Hypochondriasis (p = .031), Depression (p = .008), Hysteria (p < .0001), Psychopatic Deviate (p = .025), Psychasthenia (p = .0,19), Schizophrenia p = .017), Hypomania (p = .025). Group B had a high score only in the Hypochondriasis subscale (70.38 ± 12.78).
Table 3

Mean and standard deviation ( Mean±sd) of MMPI-2 scores*

  

Total N = 74

Group A N = 39

Group B N = 35

P

MMPI

Hs (Hypochondriasis)

73.55 (13.60)

76.80 (13.79)

70.38 (12.78)

*0.03

Clinical Scales

D (Depression)

62.53 (12.61)

66.19 (12.49)

58,95 (11.81)

*0.00

 

Hy (Hysteria)

61.61 (13.36)

66.78 (12.93)

56.57 (11.87)

*0.00

 

Pd (Psychopathic Deviate)

53.85 (10.27)

56.39 (9,08)

51.38 (10.85)

*0.02

 

Mf (Masculinity-feminility)

46.99 (9.85)

47.76 (8.48)

46.23 (11.09)

*0.49

 

Pa (Paranoia)

55.49 (10.82)

56.63 (9.56)

54.38 (11.93)

*0.35

 

Pt (Psychasthenia)

57.47 (10.78)

60.27 (10.61)

56.74 (10.34)

*0.02

 

Sc (Schizophrenia)

55.75 (10.11)

58.41 (9.98)

53.14 (9.65)

*0.02

 

Ma (Hypomania)

46.62 (11.36)

49.44 (10.87)

43.88 (11.29)

*0.02

 

Si (Social introversion)

57.79 (10.94)

59.90 (10.56)

55.74 (11.03)

*0.08

*T-scores > 65 (considered to be the level of clinical significance) are in bold. Group A = patients with psychiatric comorbidity; Group B = patients without psychiatric comorbidity. Hyp + Dep + Hys = ”Neurotic profile”. * p < .05.

In the content scales, group A had high score in Health Concern (Group A = 69,24, Group B = 64,29; p > .05). The two groups did not show any high score in content scales, but differentiated in: Anxiety (Group A = 61,95, Group B = 57,40; p = .047), Depression (Group A = 60,76, Group B = 55,50; p = .025), Family Problems (Group A = 59,29, Group B = 54,40; p = .046); Work Interference (Group A = 58,56, Group B = 52,67; p = .021).

In the supplementary scales no high scores were found, but the two groups also differentiated in: Anxiety (Group A = 62,51, Group B = 56,60; p = .026) College Maladjustment (Group A = 64,95, Group B = 59,45; p = .026), Gender Feminine (Group A = 50,12, Group B = 44,57; p = .009), Post-Traumatic Stress disorder (Group A = 60,14, Group B = 54,88; p = .022); Addiction Potential Scale (Group A = 49.02, Group B = 43,38; p = .008).

No significant differences were found between CM or pCM plus pMOH and CTTH or pCTTH plus pMOH patients or between patients with and without drug overuse (Table 4).
Table 4

Mean and standard deviation ( Mean ± sd) of MMPI-2 scores in CM-pCM + pMOH versus CTTH-p CTTH + pMOH and MOH versus NO MOH

 

CM and pCM + pMOH

CTTH and pCTTH + pMOH

p

MOH

NO MOH

p

N = 42

N = 45

N = 66

N = 21

Hs (Hypochondriasis)

75.21 (11.66)

71.35 (14.82)

0.17

73.96 (13.07)

70.85 (14.64)

0.39

D (Depression)

63.90 (9.88)

60.37 (14.56)

0.18

63.57 (11.48)

57.38 (14.88)

0.09

Hy (Hysteria)

62.85 (10.28)

59.66 (15.39)

0.26

62.22 (12.97)

58.00 (13.70)

0.22

Pd (Psychopathic Deviate)

54.90 (9.82)

52.11 (9.82)

0.22

54.36 (9.82)

50.61 (12.26)

0.21

Mf (Masculinity-feminility)

47.90 (9.69)

47.04 (10.31)

0.69

47.68 (9.52)

46.76 (11.48)

0.74

Pa (Paranoia)

56.69 (9.93)

54.40 (12.12)

0.34

56.53 (10.35)

52.28 (12.97)

0.18

Pt (Psychasthenia)

58.02 (10.63)

56.13 (10.92)

0.42

57.04 (10.68)

57.04 (11.25)

0.99

Sc (Schizophrenia)

55.38 (10.05)

55.53 (10.36)

0.94

55.72 (10.15)

54.61 (10.35)

0.67

Ma (Hypomania)

47.92 (10.20)

45.60 (12.12)

0.33

46.75 (10.60)

46.61 (13.33)

0.96

Si (Social introversion)

57.76 (10.20)

57.51 (11.34)

0.91

58.22 (9.67)

55.76 (13.70)

0.45

T-scores > 65 (considered to be the level of clinical significance) are in bold. CM = Chronic migraine, pCM = probable chronic migraine, pMOH = probable medication overuse headache, CTTH = chronic tension-type headache, pCTTH = probable chronic tension-type headache (according to the original ICHD-II criteria).

HAM-D

We analyzed 87 valid questionnaires. The mean value of the total sample at Hamilton Depression Scale was 6.4 and it remained in the normative range indicative for absence of depression. Group A (n = 43) had a scale mean value indicative for the presence of mild depression (9.47 ± 4.26), significantly higher than group B (n = 42; 3.48 ± 3.24) (t = 7.37, p < .0001). No significant differences were found between CM or pCM plus pMOH and CTTH or pCTTH plus pMOH patients (p = .345) or between patients with and without drug overuse (p = .994).

Discussion

Our study evaluated the prevalence of psychiatric comorbidity and specific personality traits in CDH patients. Headache and drug overuse were classified using both the original [5] and the revised International Classification of Headache Disorders-II (ICHD-II) [6] criteria to clearly differentiate the type of prevalent headache (migraine vs tension-type headache) and the presence of drug overuse.

In our sample drug overuse is significantly increased in pCM + pMOH patients with respect to pCTTH + pMOH patients, probably due to the pain severity of their attacks.

Of the 94 subjects included in the sample, 46.8% showed psychiatric comorbidity. The disorders most frequently diagnosed were mood and anxiety disorders (43.6%). These data are in line with some previous literature [26, 3739], indicating that the most common psychiatric conditions related to migraine were depression, bipolar disorders, anxiety [19] and somatoform disorders. However, the relationship between CDH and psychiatric disorders is still matter of debate in the literature, this being also due to the different headache diagnostic criteria and the different methods adopted in most of the studies to assess psychiatric disorders [1216]. Verri and colleagues [21] found an association between CDH and at least one psychiatric disorder in 90% of their patients. Juang and colleagues [22] found that the frequency of any type of anxiety disorder was significantly higher in patients with CM than in those with CTTH. This was not confirmed in our sample in which no differences were found in psychiatric comorbidity between the migraine and the tension-type headache groups, and between patients with and without drug overuse. These findings are in agreement with the results obtained by Atasoy and colleagues [40] who analyzed psychiatric comorbidity in 89 MOH patients and did not find any difference in MOH patients with pre-existing episodic tension-type headache (ETTH) with respect to those with pre-existing MWOA.

Psychiatric comorbidity has often been clinically discussed rather than systematically studied. The use of M.I.N.I., a structured clinical psychiatric interview [41], helped us to establish a diagnosis on reliable and valid diagnostic criteria. Although M.I.N.I. is considered a somewhat overinclusive instrument in ‘making diagnosis’ [42], it indicated the presence of depression in our sample, while HAM-D results revealed that the mood disorder was milder than expected. Moreover, after clinical interviews, psychiatrists reported that psychiatric disorders in MOH appear in subthreshold forms rather than as full-blown disorders. Even if the percentage of patients assuming prophylactic therapies with antidepressant or mood stabilizer drugs was similar in both groups, with and without psychiatric comorbidity, we can not exclude a role of these drugs in the final results.

Previous MMPI-2 results stressed the presence of the “neurotic MMPI-2 profile” in headache patients, a profile characterized by a high level of depression, hypochondria and hysteria [27, 30, 31]. We found that in our sample, the neurotic triad was detected only in patients with psychiatric comorbidity, while patients without psychiatric comorbidity displayed a high score only in the Hypochondriasis subscale, indicating high concern for their health status. The presence of the “neurotic MMPI-2 profile” in chronic headache has already been the focus of previous studies [27, 28] arguing that these personality traits appeared to be a reaction to chronic pain rather than a specific feature of headache patients [43]. Our results suggest for the first time that the “neurotic MMPI-2 profile” was not associated to headache per se, but was a dominant feature in headache patients who showed comorbidity with psychiatric disorders. However the cross-sectional design of the study does not permit to reveal any casual relationship.

The two groups also differentiated for scores in Addiction Potential Scale: patients with psychiatric comorbidity had higher scores than patients without, even if the scores fell in the normal range. Furthermore, the presence of medication overuse was not a discriminating factor. These data support Galli et al.’s [28] hypothesis that medication overuse in CDH patients might not be related to dependence, but rather might be a consequence of chronic pain. From this perspective, medication overuse could be seen as the only way patients know to cope with their pain and maintain a normal lifestyle. However, this hypothesis conflicts with other studies on dependence in patients with MOH [25]. Specific instruments are needed to assess dependence behavior in MOH patients as it seems to have different theoretical constructs from classic dependence behavior [27].

A high score in MMPI-2 Health Concern subscale was found in all CDH patients suggesting concern for their general health condition, and not only for their headache. This result is concordant with the elevated score also found in the Hypochondria clinical scale.

We acknowledge the limitations of the present study, the principal one being that it was performed in a tertiary care headache clinic so that the investigated sample may not represent the whole spectrum of CDH patients in the general population. Another limitation was that MMPI-2 was properly completed only by 83 of the 94 subjects included. Another major problem was the diagnostic distinction of CDH and drug overuse that remains controversial and could introduce a selection bias. We tried however to overcome this limitation, which is intrinsic to all studies investigating headache chronification, by applying the IHS revised criteria for headache diagnosis.

Conclusion

Our study showed that the so-called Neurotic Profile (high level of hypochondria, depression and hysteria) reached a clinical level only in patients with psychiatric comorbidity and that all CDH patients, independently from psychiatric comorbidity, had a high score in hypochondria evaluation suggesting a high concern for their general health status. Large population-based studies are needed to confirm this original finding and future prospective studies might also evaluate how hypocondria is a risk factor for transformation from episodic to chronic headache and if it is possible to modify this aspect by applying cognitive behavioral interventions.

Abbreviations

CDH: 

Chronic daily headache

CTTH: 

Chronic tension-type headache

pCTTH: 

Probable chronic tension-type headache

CM: 

Chronic migraine

pCM: 

Probable chronic migraine

MWOA: 

Migraine without aura

MWA: 

Migraine with aura

ETTH: 

Episodic tension-type headache

MOH: 

Medication overuse headache

pMOH: 

Probable medication overuse headache

MMPI-2: 

Minnesota Multiphasic Personality Inventory

ICHD-II: 

International classification of headache disorders-II

M.I.N.I: 

International neuropsychiatric interview

HAM-D: 

Hamilton depression rating scale

Declarations

Acknowledgment

With profound sadness we thank Prof. Pasquale Montagna, our peerless mentor, great friend, outstanding scientist, physician and man.

This work was partially supported by a research grant from the Isabella Seragnoli Foundation awarded to Marialuisa Rausa.

Authors’ Affiliations

(1)
Department of Biomedical and Neuromotor Sciences-DIBINEM, University of Bologna – IRCCS Istituto delle Scienze Neurologiche di Bologna
(2)
Department of Psychiatry, Bologna Local health Trust

References

  1. Halker RB, Hastriter EV, Dodick DW: Chronic daily headache: an evidence-based and systematic approach to a challenging problem. Neurology 2011,76(2):S37–43.PubMedView Article
  2. Scher AI, Stewart WF, Liberman J, Lipton RB: Prevalence of frequent headache in a population sample. Headache 1998, 38: 497–506. 10.1046/j.1526-4610.1998.3807497.xPubMedView Article
  3. Castillo J, Munoz J, Guitera V, Pascual J: Kaplan Award 1998. Epidemiology of chronic daily headache in the general population. Headache 1999, 39: 190–196. 10.1046/j.1526-4610.1999.3903190.xPubMedView Article
  4. Manzoni GC, Bonavita V, Bussone G, Cortelli P, Narbone MC, Cevoli S, D’Amico D, De Simone R, Torelli P: Chronic migraine classification: current knowledge and future perspectives. J Headache Pain 2011, 12: 585–592. 10.1007/s10194-011-0393-6PubMed CentralPubMedView Article
  5. Headache Classification Committee of the International Headache Society: The International Classification of Headache Disorders, 2nd edition. Cephalalgia 2004,24(Suppl 1):9–160.
  6. Olesen J, Bousser M-G, Diener H-C: Headache Classification Committee. New appendix criteria open for a broader concept of chronic migraine. Cephalalgia 2006, 26: 742–746.PubMedView Article
  7. Sancisi E, Cevoli S, Pierangeli G: Application of ICHD-II and revised diagnostic criteria to patients with chronic daily headache. Neurol Sci 2007, 28: 2–8. 10.1007/s10072-007-0741-0PubMedView Article
  8. Mathew NT, Stubits E, Nigam MR: Transformation of episodic migraine into daily headache: Analysis of factors. Headache 1982, 22: 66–68. 10.1111/j.1526-4610.1982.hed2202066.xPubMedView Article
  9. Colas R, Munoz P, Temprano R, Gomez SW, Pascual J: Chronic daily headache with drug analgesic overuse. Epidemiology and impact on quality of life. Neurology 2004, 62: 1338–1342. 10.1212/01.WNL.0000120545.45443.93PubMedView Article
  10. Diener HC, Limmroth V: Medication-overuse headache: A worldwide problem. Lancet Neurol 2004, 3: 475–483. 10.1016/S1474-4422(04)00824-5PubMedView Article
  11. Jonsson P, Hedenrud T, Linde M: Epidemiology of medication overuse headache in the general Swedish population. Cephalalgia 2011, 31: 1015–22. 10.1177/0333102411410082PubMedView Article
  12. Guidetti V, Galli F, Fabrizi P: Headache and psychiatric comorbidity: Clinical aspects and outcome in an 8-year follow-up study. Cephalalgia 1998, 18: 455–462. 10.1046/j.1468-2982.1998.1807455.xPubMedView Article
  13. Pompili M, Serafini G, Di Cosimo D, Dominici G, Innamorati M, Lester D, Forte A, Girardi N, De Filippis S, Tatarelli R, Martelletti P: Psychiatric comorbidity and suicide risk in patients with chronic migraine. Neuropsychiatr Dis Treat 2010, 6: 81–91.PubMed CentralPubMedView Article
  14. Buse DC, Silberstein SD, Manack AN, Papapetropoulos S, Lipton RB: Psychiatric comorbidities of episodic and chronic migraine. J Neurol 2012.
  15. Heckman BD, Merrill JC, Anderson T: Race, psychiatric comorbidity, and headache characteristics in patients in headache subspecialty treatment clinics. Ethn Health 2012.
  16. Serafini G, Pompili M, Innamorati M, Negro A, Fiorillo M, Lamis DA, Erbuto D, Marsibilio F, Romano A, Amore M, D’Alonzo L, Bozzao A, Girardi P, Martelletti P: White matter hyperintensities and self-reported depression in a sample of patients with chronic headache. J Headache Pain 2012, 13: 661–667. 10.1007/s10194-012-0493-yPubMed CentralPubMedView Article
  17. Radat F, Sakh D, Lutz G, El Amrani M, Ferreri M, Bousser MG: Psychiatric comorbidity is related to headache induced by chronic substance use in migraineurs. Headache 1999, 39: 477–480. 10.1046/j.1526-4610.1999.3907477.xPubMedView Article
  18. Radat F, Swendsen J: Psychiatric comorbidity in migraine: a review. Cephalalgia 2005, 25: 165–178. 10.1111/j.1468-2982.2004.00839.xPubMedView Article
  19. Radat F, Creac’h C, Swendsen JD: Psychiatric comorbidity in the evolution from migraine to medication overuse headache. Cephalalgia 2005, 25: 519–522. 10.1111/j.1468-2982.2005.00910.xPubMedView Article
  20. Baskin SM, Lipchik GL, Smitherman TA: Mood and anxiety disorders in chronic headache. Headache 2006,46(suppl 3):S76-S87.PubMedView Article
  21. Verri AP, Proietti Cecchini A, Galli C, Granella F, Mandrini G, Nappi G: Psychiatric comorbidity in chronic daily headache. Cephalalgia 1998,18(suppl 21):45–49.PubMed
  22. Juang K-D, Wang S-J, Fuh J-L, Lu S-R, Su T-P: Comorbidity of depressive and anxiety disorders in chronic daily headache and its subtypes. Headache 2000, 40: 818–823. 10.1046/j.1526-4610.2000.00148.xPubMedView Article
  23. Pompili M, Di Cosimo D, Innamorati M, Lester D, Tatarelli R, Martelletti P: Psychiatric comorbidity in patients with chronic daily headache and migraine: a selective overview including personality traits and suicide risk. J Headache Pain 2009,10(4):283–90. 10.1007/s10194-009-0134-2PubMed CentralPubMedView Article
  24. Saper JR, Hamel RL, Lake AE 3rd: Medication overuse headache (MOH) is a biobehavioural disorder. Cephalalgia 2005, 25: 545–546. 10.1111/j.1468-2982.2005.00879.xPubMedView Article
  25. Fuh JL, Wang SJ, Lu SR, Juang KD: Does medication overuse headache represent a behavior of dependence? Pain 2005, 119: 49–55. 10.1016/j.pain.2005.09.034PubMedView Article
  26. Antonaci F, Nappi G, Galli F, Manzoni GC, Calabresi P, Costa A: Migraine and psychiatric comorbidity: a review of clinical findings. J Headache Pain 2011,12(2):115–25. 10.1007/s10194-010-0282-4PubMed CentralPubMedView Article
  27. Sances G, Galli F, Anastasi S, Ghiotto N, De Giorgio G, Guidetti V, Firenze C, Pazzi S, Quartesan R, Gallucci M, Nappi G: Medication-overuse headache and personality: a controlled study by means of the MMPI-2. Headache 2010,50(2):198–209. 10.1111/j.1526-4610.2009.01593.xPubMedView Article
  28. Galli F, Pozzi G, Frustaci A, Allena M, Anastasi S, Chirumbolo A, Ghiotto N, Guidetti V, Matarrese A, Nappi G, Pazzi S, Quartesan R, Sances G, Tassorelli C: Differences in the personalty profile of medication overuse headache sufferers and drug addict patients: a comparative study using MMPI-2. Headache 2011,51(8):1212–1227. 10.1111/j.1526-4610.2011.01978.xPubMedView Article
  29. Butcher JN, Dahlstrom WG, Graham JR, Tellegen A, Kaemmer B: The Minnesota Multiphasic Personality Inventory-2 (MMPI-2): Manual for administration and scoring. Minneapolis, MN: University of Minnesota Press; 1989.
  30. Bigal ME, Sheftell FD, Rapaport AM, Tepper SJ, Weeks R, Baskin SM: MMPI personality profiles in patients with primary chronic headache: A case-control study. Neurol Sci 2003,24(3):103–10. 10.1007/s10072-003-0094-2PubMedView Article
  31. Mongini F, Defilippi N, Negro C: Chronic daily headache. A clinical and psychological profile before and after the treatment. Headache 1997, 37: 83–87. 10.1046/j.1526-4610.1997.3702083.xPubMedView Article
  32. Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, Hergueta T, Baker R, Dunbar GC: The Mini.-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry 1998,59(20):22–33.PubMed
  33. Hamilton M: A rating scale for depression. Journal of Neurolog Neurosurg Psychiatry 1960, 23: 56–62. 10.1136/jnnp.23.1.56View Article
  34. Pancheri P, Sirigatti S: MMPI-2 (Adattamento Italiano). Firenze: Organizzazioni Speciali; 1995.
  35. American Psychiatric Association: Diagnostic and statistical manual of mental disorders. 4th edition. DC: Washington; 2000.
  36. World Health Organization: International statistical classification of disease and related health problems, Tenth Revision (ICD-10). Geneva: World Health Organization; 1992.
  37. Fasmer OB, Oedegaard KJ: Clinical characteristics of patients with major affective disorders and comorbid migraine. World J Biol Psychiatry 2011, 2: 149–155.View Article
  38. Kalayadjian A, Merikangas K: Physical and mental comorbidity of headache in a nationally representative sample of US adults. Psychosom Med 2008, 70: 773–780. 10.1097/PSY.0b013e31817f9e80View Article
  39. Beghi E, Bussone G, D’Amico D, Cortelli P, Cevoli S, Manzoni GC, Torelli P, Tonini MC, Allais G, De Simone R, D’Onofrio F, Genco S, Moschiano F, Beghi M, Salvi S: Headache, anxiety and depressive disorder: the HADAS study. J Headache Pain 2010, 11: 141–150. 10.1007/s10194-010-0187-2PubMed CentralPubMedView Article
  40. Atasoy HT, Atasoy N, Unal AE, Emre U, Sumer M: Psychiatric comorbidity in medication overuse headache patients with pre-existing headache type of episodic tension-type headache. Eur J Pain 2005,9(3):285–91. 10.1016/j.ejpain.2004.07.006PubMedView Article
  41. Lake AE 3rd, Rains JC, Penzien DB, Lipchik GL: Headache and psychiatric comorbidity: historical context, clinical implications, and research relevance. Headache 2005,45(5):493–506. 10.1111/j.1526-4610.2005.05101.xPubMedView Article
  42. Sheehan DV, Lecrubier Y, Sheehan KH, Janavs J, Weiller E, Keskiner A, Schinka J, Knapp E, Sheehan MF, Dunbar GC: The validity of the Mini International Neuropsychiatric Interview (MINI) according to the SCID-P and its reliability. Eur Psychiatry 1997,12(5):232–241. 10.1016/S0924-9338(97)83297-XView Article
  43. Mongini F, Ibertis F, Barbalonga E, Raviola F: MMPI-2 profiles in chronic daily headache and their relationship to anxiety levels and accompanying symptoms. Headache 2000, 40: 466–472. 10.1046/j.1526-4610.2000.00070.xPubMedView Article

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