Headache in idiopathic/genetic epilepsy: Cluster analysis in a large cohort
Author
DERİCİOĞLU, NEŞE
BAKLAN, BARIŞ
GENÇ, BÜLENT OĞUZ
Atalar, Arife Cimen
TÜRK, BENGİ GÜL
Ekizoglu, Esme
Gok, Duygu Kurt
BAYKAL, Betül
ÖZGE, AYNUR
Ayta, Semih
Altindag, Ebru Aykutlu
Karahan, Gokcen
Koc, Guray
Misirli, Handan
ÖZTURA, İBRAHİM
ASLAN KARA, KEZBAN
ÇAKAR, MERVE MELODİ
Turkmen, Nur
BULUT, ONUR
Karadas, Omer
Sahin, Ozlem Kesim
FERİK, SEVGİ
Pekoz, Mehmet Taylan
Topaloglu, Pinar
Ozek, Sibel Ustun
Duzgun, Ulkuhan
Yayla, Vildan
Gomceli, Yasemin
Acar, Zeynep Unlusoy
ERDOĞAN, FÜSUN FERDA
YENİ, SEHER NAZ
Tasdelen, Bahar
VELİOĞLU, SİBEL
Yapici, Zuhal
MİDİ, İPEK
SAYGI, SERAP
Celebi, Ulufer
Darol, Elif Sarica
AĞAN YILDIRIM, KADRİYE
Ayca, Senem
GAZİOĞLU, SİBEL
Okudan, Zeynep Vildan
Sirin, Nermin Gorkem
Bebek, Nerses
Altun, Ilknur Guclu
Yalcin, Ayse Destina
Surmeli, Reyhan
ERDİNÇ, OĞUZ OSMAN
Erdal, Abidin
İLHAN ALGIN, DEMET
KUTLU, GÜLNİHAL
Bek, Semai
Erdal, Yuksel
Ozon, Akcay Ovunc
Reyhani, Aylin
Guldiken, Baburhan
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Objective The link between headache and epilepsy is more prominent in patients with idiopathic/genetic epilepsy (I/GE). We aimed to investigate the prevalence of headache and to cluster patients with regard to their headache and epilepsy features. Methods Patients aged 6-40 years, with a definite diagnosis of I/GE, were consecutively enrolled. The patients were interviewed using standardized epilepsy and headache questionnaires, and their headache characteristics were investigated by experts in headache. Demographic and clinical variables were analyzed, and patients were clustered according to their epilepsy and headache characteristics using an unsupervised K-means algorithm. Results Among 809 patients, 508 (62.8%) reported having any type of headache; 87.4% had interictal headache, and 41.2% had migraine. Cluster analysis revealed two distinct groups for both adults and children/adolescents. In adults, subjects having a family history of headache, >= 5 headache attacks, duration of headache >= 24 months, headaches lasting >= 1 h, and visual analog scale scores > 5 were grouped in one cluster, and subjects with juvenile myoclonic epilepsy (JME), myoclonic seizures, and generalized tonic-clonic seizures (GTCS) were clustered in this group (Cluster 1). Self-limited epilepsy with centrotemporal spikes and epilepsy with GTCS alone were clustered in Cluster 2 with the opposite characteristics. For children/adolescents, the same features as in adult Cluster 1 were clustered in a separate group, except for the presence of JME syndrome and GTCS alone as a seizure type. Focal seizures were clustered in another group with the opposite characteristics. In the entire group, the model revealed an additional cluster, including patients with the syndrome of GTCS alone (50.51%), with >= 5 attacks, headache lasting >4 h, and throbbing headache; 65.66% of patients had a family history of headache in this third cluster (n = 99). Significance Patients with I/GE can be clustered into distinct groups according to headache features along with seizures. Our findings may help in management and planning for future studies.
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