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The Journal of Headache and Pain

Official Journal of the "European Headache Federation" and of "Lifting The Burden - The Global Campaign against Headache"

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Open Access

Comorbidity between headache and epilepsy in a pediatric headache center

  • Irene Toldo1Email author,
  • Egle Perissinotto2,
  • Francesca Menegazzo1,
  • Clementina Boniver1,
  • Stefano Sartori1,
  • Leonardo Salviati1,
  • Maurizio Clementi1,
  • Pasquale Montagna3 and
  • Pier Antonio Battistella1
The Journal of Headache and Pain201011:191

https://doi.org/10.1007/s10194-010-0191-6

Received: 16 October 2009

Accepted: 12 January 2010

Published: 29 January 2010

Abstract

The purpose of this study was to analyse the comorbidity between headache and epilepsy in a large series of children with headache (1,795). Fifty-six cases (3.1%) suffered from idiopathic headache and idiopathic or cryptogenic epilepsy or unprovoked seizures. There was a strong association between migraine and epilepsy: in migraineurs (46/56) the risk of epilepsy was 3.2 times higher when compared with tension-type headache, without significant difference between migraine with and without aura (P = 0.89); children with epilepsy had a 4.5-fold increased risk of developing migraine than tension-type headache. In cases with comorbidity, focal epilepsies prevailed (43/56, 76.8%). Migraineurs affected by focal epilepsies (36/56) had a three times higher risk of having a cryptogenic epilepsy (27/36, 75%) than an idiopathic epilepsy (9/36, 25%) (P = 0.003). In migraine with aura, epilepsy preceded migraine in 71% of cases. Photosensitivity (7/56, 12.5%) and positive family history for epilepsy (22/56, 39%) were frequent in cases with comorbidity.

Keywords

HeadacheMigraineEpilepsyComorbidityChildren

Introduction

Migraine and epilepsy are both common neurological disorders, although migraine is more frequent, and can occur as comorbid conditions [16]. An association between migraine and epilepsy has been demonstrated in several studies, mainly based on adults affected by epilepsy [1, 5, 6]. In children an association between migraine and some epilepsy syndromes has been reported, but data are conflicting and studies have been limited by the small numbers of patients and to the lack of clearly stated diagnostic criteria of childhood migraine [7].

The growing knowledge of the genetic bases of familial hemiplegic migraine (FHM) [8] and the findings of epileptic seizures occurring independent of the migraine attacks in FHM families [9] have stimulated the interest on the comorbidity between migraine and epilepsy.

The purpose of this study was to analyse the comorbidity between headache and epilepsy in a large series of children and to find out possible correlations among the type of headache, the type of epilepsy of probands and the family history for headache and epilepsy.

Methods

This is a retrospective case–control study of 1,795 patients under 18 years of age consecutively diagnosed as affected by headache at the pediatric Headache Center of the Department of Pediatrics of Padua Hospital between 1995 and 2008. We reviewed the medical records of all 1,795 patients, which contain pre-established questions concerning family and personal history of headache, and past medical history, which includes a section on seizures and epilepsy. From the total study population, we identified 56 patients with a diagnosis of idiopathic headache associated with idiopathic or cryptogenic epilepsy or unprovoked seizure. Patients with secondary headache or symptomatic epilepsy were excluded from the study. The study protocol and consent/assent forms were approved by our Institutional Review Board.

All 56 children included in the research and their parents were informed about the complete study protocol by letter and subsequently were contacted by telephone. They were asked to participate in a structured interview conducted in 2008 by a board certified child neurologist, regarding headache, epilepsy, and “periodic syndromes” in their child and other family members. Particular attention was devoted to the clinical features of headache and epilepsy. All 56 patients underwent brain neuroimaging (MRI or CT) and EEG with electrode placement according to the International 10–20 System. We reviewed all clinical, electrophysiological, and neuroimaging data. Forty-one patients were clinically reevaluated at a control visit in the second semester of 2008, while the other 15 patients participated only to the telephone clinical interview for follow-up.

The diagnosis of headache was based on the International Classification of Headache Disorders (ICHD-II) criteria [10]. The diagnosis of epilepsy was based on clinical and EEG data and classified according to the International Classification of Epilepsy and Epilepsy Syndromes [11, 12]. Focal cryptogenic epilepsies were further classified on the basis of the origin of epileptogenic focus (frontal, temporal, parietal, or occipital lobe).

All the data were entered into a database and analyzed with SAS statistical package (9.2 version). Data were analyzed by a chi-square statistic technique and, in case of low sample, by the exact Fischer test. We calculated measures of association between variables expressed by the odds ratio (OR), for which the confidence interval (CI) to 95% was determined; for each test the level of significance was set at 0.05.

Results

Information concerning headache and seizures was collected from 1,795 headache patients under 18 years of age consecutively diagnosed at the Headache Center of the Department of Pediatrics of the University of Padua between 1995 and 2008 (Table 1). Fifty-six patients (N = 56/1,795, 3.1%) were identified as having comorbidity between primary headache and idiopathic or cryptogenic epilepsy or unprovoked seizures. There were 20 males (35.7%) and 36 females (64.3%) with a male-to-female ratio of 1:1.8. The average age at headache onset was 8.6 years (range 3–17 years, SD 4.3 years), while the average age at epilepsy onset was 7.8 years (range 1–24 years, SD 4.0 years). In 25 subjects (44%) epilepsy preceded headache, in 16 subjects (28.6%) headache started in the same year of epilepsy, and in 15 cases (27.4%) headache preceded epilepsy. In patients affected by migraine with aura (MA), epilepsy preceded migraine in 71% of the cases.
Table 1

Clinical characteristics of our population

 

N

%

Sex

 Male

835

46.5

 Female

960

 

Total

1,795

 

Migraine

957

53.3

 MO

836

 

 MA

121

 

Male to female ratio (M/F)

1/1.1

 

Tension type

686

38.2

 ETTH

621

 

 CTTH

65

 

Male to female ratio (M/F)

1/1.3

 

Other headache types

152

8.5

 Other primary headaches

132

 

 Headache attributed to psychiatric disorder

14

 

 Secondary headaches

6

0.3

Seizures

68

 

 Cases selecteda

56

3.1

aInclusion criteria: idiopathic or cryptogenic epilepsy or unprovoked seizures

MO migraine without aura, MA migraine with aura, ETTH episodic tension type headache, CTTH chronic tension type headache

Headache

A total of 46 out of 56 subjects (82.1%) had migraine, with a second level of diagnosis of migraine without aura (MO) in 69.6% (N = 39) and of MA in 12.5% (N = 7) of cases while 10 subjects (17.9%) had episodic tension type headache (ETTH); no other types of headache were reported.

Among the 1,795 patients, comparing the distribution of headache type in cases, respectively, with and without epilepsy, we found that the prevalence of migraine in cases with epilepsy (N = 46/56, 82.1%) was significantly higher compared to cases without epilepsy (N = 911/1739, 52%) (P = 0.0006). The risk of migraine in patients with epilepsy was on average 4.5 times higher compared to the risk of ETTH, without a significant difference between MO and MA (respectively, 4.6 and 5.0, P = 0.89). The ratio between MA and MO was 1:5.6 (N = 7/39).

Nineteen out of 56 cases (34%) had post-ictal headache, fulfilling the ICHD-II criteria (7.6.2) [10]. Many patients (N = 16/19, 84%) with post-ictal headache had migraine attacks independent of epileptic seizures; however, migraineurs did not have an increased risk of post-ictal headache compared to patients with ETTH (P = 0.58). Among the seven patients with MA, nobody experienced episodes of migralepsy.

Epilepsy

Epilepsy was significantly more frequent in migraineurs (N = 46/957, 4.8%) than in patients with ETTH (N = 10/686, 1.5%) (P = 0.0001). The risk of epilepsy (OR) in migraineurs was 3.2 times higher (CI of 95% = 1.7–6.2) compared to patients with ETTH and did not differ significantly between MO and MA cases. The most frequent type of epilepsy was focal epilepsy (N = 43/56, 76.8%) among which focal cryptogenic epilepsies prevailed (N = 32/56, 57.1%) (Table 2). The distribution of epilepsy type (focal idiopathic, focal cryptogenic, generalized, and isolated seizures) did not differ between migraine and ETTH (P = 0.77), neither between MO and MA (P = 0.9).
Table 2

Distribution of headache diagnosis on the basis of type of epilepsy

 

Total

N = 56 (%)

Migraine

N = 46 (%)

Episodic tension type headache

N = 10 (%)

Focal cryptogenic epilepsy

32 (57.1)

27/32 (84)

5/32 (16)

 Site determined

27

22/27

5/5

  Frontal

9

6/9

3/9

  Temporo-occipital

18

16/18

2/18

 Site not determined

5

5/27

0/5

Focal idiopathic epilepsy

11 (19.7)

9/11 (82)

2/11 (18)

 Rolandic

9

7/9

2/9

 Occipital

2

2/2

0/2

Idiopathic generalized epilepsy

10 (17.9)

8/10 (80)

2/10 (20)

Isolated unprovoked seizures

3 (5.3)

2/3 (67)

1/3 (33)

However, among migraineurs with focal epilepsy, the risk of having a cryptogenic epilepsy was about three times higher than an idiopathic epilepsy (P = 0.003). In the subjects affected by migraine and focal cryptogenic epilepsies (N = 27), those originating in temporal and occipital lobes (N = 16) prevailed on frontal epilepsies (N = 6) (P = 0.06).

On interictal EEG during intermittent photic stimulation (IPS), seven (N = 7/56, 12.5%) patients had a photoparoxysmal response (PPR), two of whom also had a photoconvulsive response. PPR was characterized by generalized discharges in most of the cases (N = 6/7, 85.7%), and only one patient had bilateral discharges on occipital regions during IPS.

An ictal EEG recording was performed in 14 (25%) patients, and half of them (7/14) had focal seizures recorded. In particular five cases presented focal seizures with parossistic activity on left temporal (1/5), left central (1/5) with also an electrical status epilepticus during slow sleep on EEG, frontal bilateral (1/5), right frontal (2/5) and two cases had a focal epileptic status (1 right temporo-occipital, 1 right fronto-temporal). In the remaining seven cases, two had palpebral myoclonia, four had absences (one of whom absence status), and one had subtle focal seizures during ictal EEG.

In other six cases a post-ictal EEG recording was obtained.

Family history of migraine and epilepsy in probands

A positive family history of headache and migraine was found respectively, in 73.2% (N = 41/56) and in 66% (N = 37/56) of our cases. In the latter, 81% (N = 30/37) had at least one-first-degree relative affected by migraine, mainly on maternal than on paternal lineage (respectively, N = 23/30, 77% vs. N = 8/30, 27%). All first-degree familial MA cases (N = 3/56) were exclusively of maternal origin. There was not any statistical significant correlation between the positive family history of migraine and the type of headache or epilepsy of the probands. A positive family history of non-symptomatic epilepsy was found in 39% (N = 22/56) of probands and 12.5% (N = 7/56) of probands had at least one-first-degree relative affected by epilepsy.

Discussion

In previous studies, the prevalence of migraine in epileptic populations was estimated to be 8–24% [1, 2, 5, 6] and the risk of migraine was 2.4 times higher among adults with epilepsy than in those without [1, 5, 6]. The prevalence of migraine in children with partial epilepsy was 21% in benign rolandic epilepsy and 17% in cryptogenic/symptomatic epilepsy [7].

In the last 20 years, few studies have been performed concerning the comorbidity between headache and epilepsy in children [3, 4, 7, 1317] and the majority of them are based on series of subjects affected by epilepsy [3, 4, 7, 13, 14, 16, 17]. Due to the different methodologies used they are quite difficult to compare. To our knowledge, this is the first study that evaluated the occurrence of epilepsy in a large series of children affected by headache, using the recent ICHD-II criteria [10] and with a longitudinal follow-up.

We found a statistically significant association between migraine and epilepsy in our series. In fact the prevalence of migraine in cases with epilepsy (82.1%) was significantly higher than in those without epilepsy (52%) and children with epilepsy had a 4.5-fold increased risk of developing migraine than tension-type headache.

In a prospective study on 50 children with epilepsy, 46% had headache and 10 out of the 23 (43.5%) headache sufferers had migraine [13]. Most patients with headache were older than 10 years (54.5%) and had idiopathic epilepsy (65.2%) [13]. Different from this study, we found that the male-to-female ratio was significantly skewed in favor to females (P = 0.03), most patients with headache and epilepsy were younger than 10 years old (60%), and suffered from cryptogenic epilepsy (60%) (Table 3). Moreover, a positive family history for headache and migraine was found in many cases (respectively, 73.2%, P = 0.0005; 66%, P = 0.02) (Table 3). In the majority (95%) of the cases reported by Yamane et al. [13] the headache started in the same year as or after the diagnosis of epilepsy; this was also confirmed in our series.
Table 3

Comparison between our cases and other series reported in the literature [13]

Characteristics of patients

Present study

Yamane 2003

N = 56

χ2

N = 23

χ2

Gender

 Female

36

P = 0.03

13

P = 0.376

 Male

20

10

Age at headache onset

 <10 years

34

P = 0.13

5

P = 0.0001

 ≥10 years

22

18

Type of epilepsy

 Idiopathic

21

P = 0.13

15

P = 0.0003

 Cryptogenic

32

5

 Symptomatic

0

3

Seizure type

 Focal

43

P < 0.0001

14

P = 0.140

 Generalized

10

9

Family history of headache

 Positive

41

P = 0.0005

12

P = 0.546

 Negative

15

10

 n.a.

0

1

Family history of migraine

 Positive

37

P = 0.02

n.a.

n.a.

 Negative

19

  

Family history of epilepsy

 Positive

22

P = 0.11

n.a.

n.a.

 Negative

34

  

Type of headache

 Migraine

46

P < 0.0001

10

P = 0.132

 Tension type

10

4

 Not classified

0

9

Relationship between onset of headache and diagnosis of epilepsy

 Before epilepsy

15

P = 0.32

1

P = 0.001

 Same age

16

14

 After epilepsy

25

8

Temporal relationship between headache and epilepsy

 Yes

21

P = 0.06

9

P = 0.140

 No

35

14

Type of temporal relationship between headache and epilepsy

 Preictal

2

P = 0.0002

2

P = 0.157

 Postictal

19

19

n.a. not available

In the literature a strong association between MA and epilepsy has been suggested in both adults and children [14, 15, 18]. In adults, the MA prevalence was more elevated in cases with epilepsy (41%) compared to those without (25.8%) [18]. In a case–control study on children, the risk of unprovoked seizures was increased in MA (3.7-fold) but not in MO cases [14]. Differently, in our cases, MA did not increase the risk of epilepsy compared to MO and the prevalence of epilepsy was similar across the two groups of migraineurs (MO 5.4%, MA 5.8%). Moreover, in the majority of our cases (71%) epilepsy preceded MA and this finding is not consistent with a causative role for MA in epilepsy, as previously suggested [14]. It is more likely that MA and epilepsy share a common antecedent factor.

The prevalence of epilepsy in migraineurs varies from 1 to 17%, with a median of 5.9% [1, 2], substantially higher than the population prevalence of epilepsy which is 0.5–1% (http://www.who.int/topics/epilepsy). In a recent study on 134 children and adolescents with primary headache, the overall prevalence of epilepsy or unprovoked seizures was 4.4% [15]. Among the three cases affected by epilepsy, two had photosensitive epilepsy and one had temporal epilepsy and they all suffered from MA [15].

In our cases, the prevalence of idiopathic or cryptogenic epilepsy or unprovoked seizures was 3.1% in headache sufferers and 4.8% in migraineurs, similar to other reports [24, 15]. Moreover, in migraineurs, the risk of epilepsy was 3.2 times higher compared to subjects with ETTH, and the risk of epilepsy was not increased in MA compared to MO cases.

In children, the association between migraine and some epilepsy syndromes, such as childhood epilepsy with occipital paroxysms and benign childhood epilepsy with centrotemporal spikes reported by some authors [2, 17, 1921], was not confirmed by subsequent studies [3, 22]. It has been recently reported that partial epilepsies (benign rolandic and focal cryptogenic/symptomatic epilepsy), regardless of etiology, are associated with higher rates of migraine in children [7].

Among our patients with comorbidity, focal epilepsies prevailed (76.8%), and in migraineurs the risk of having a focal cryptogenic epilepsy was threefold higher than idiopathic epilepsy.

A PPR was found in 12.5% of our cases with comorbidity, which is more elevated than the occurrence in healthy individuals aged 6–18 (1.4%), in patients with epilepsy (5%) and in children with idiopathic headaches (mean 8%; 8.9% in MO, 7.8% in MA, 6.7% in TTH) [15, 2326].

A positive family history of headache and migraine was found, respectively, in 73.2% and 66% of our cases. While we found no significant correlation between the positive family history of migraine and the type of headache or of epilepsy of the probands, a positive family history for epilepsy was present in 39% of our cases with comorbidity and it was more elevated compared to other series (9.5%) [15].

In the past years, three alternative models have been proposed to explain the comorbidity between migraine and epilepsy: (a) a simple unidirectional causal explanation; (b) shared environmental risk factors; or (c) shared genetic risk factors [6]. Similar to previous studies [16, 2729], our results are consistent with rejecting these three possibilities because epilepsy preceded migraine in the majority of our cases, and we did not find any statistical significant correlation between the positive family history of migraine and the type of headache or epilepsy of the probands.

Two rare conditions in which there is a complete overlapping between headache and epilepsy and raise problems of differential diagnosis are migralepsy and ictal headache [3033]. In both cases, EEG recording during the headache attacks is essential for diagnosis. Migralepsy (1.5.5 ICHD-II) is a particular condition wherein a seizure occurs during or within 1 h after a migraine aura, and it can mime occipital lobe seizures, which might be underrecognized without EEG recording [30]. Rarely, headache (not only migraine) might represent the sole ictal epileptic manifestation, and the new term “ictal epileptic headache” was proposed to be included in both classifications [3133]. In our series nobody experienced episodes of migralepsy or ictal epileptic headache.

At present many authors believe that an increased brain excitability might increase the risk of both migraine and epilepsy and could explain the comorbidity [18, 28, 34, 35]. There is considerable interest in the possibility that genetic polymorphisms in ion channels or in genes encoding other molecules involved in the generation and the maintenance of membrane contribute to epilepsy and migraine susceptibility [35].

In conclusion, comorbidity between headache and epilepsy is common in children and adolescents. Our results confirm a strong association between migraine and epilepsy, without significant difference between MO and MA. Migraine is associated with higher rates of focal epilepsies, in particular cryptogenic epilepsies. Recurrent attacks of migraine do not seem to cause epilepsy, since in the majority of our cases, and mainly in MA, epilepsy preceded migraine. In cases with comorbidity, migraineurs do not have a major risk of post-ictal headache compared to tension-type headache sufferers. Photosensitivity on EEG and positive family history for epilepsy are frequent in children with comorbidity between headache and epilepsy.

The analysis of the clinical relationship between headache (especially migraine) and epilepsy could contribute to understanding the pathogenetic mechanisms of these two conditions, mainly when they are comorbid. Further studies, based on the present diagnostic criteria of both disorders [1012], are needed.

Declarations

Conflict of interest

None.

Authors’ Affiliations

(1)
Department of Pediatrics, University of Padova, Padua, Italy
(2)
Department of Preventive Medicine and Public Health, University of Padova, Padua, Italy
(3)
Department of Neurological Sciences, University of Bologna, Bologna, Italy

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© Springer-Verlag 2010

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