ABSTRACT Background: The headaches are a heterogeneous clinical manifestations characterized not only by pain but also by a severe multifactorial disabilities, often associated with other comorbidities that severely affects the patient’s quality of life. And ‘it is known for some time the risk of cerebrovascular disease in migraine patients. Numerous studies showed the association between the enzyme MTHFR mutations , the T allele and genotype TTand migraine, particularly migraine with aura. Aim of the study: On the basis of theliterature data we propose to evaluate the prevalence of the MTHFR mutation in the population of patients admitted to a headache center of the childhood. Materials and methods: Weexamined 226 children, aged 5-17 years,admitted to “Headache Center” of Children Neuropsychiatry of Hospital San Salvatore L’Aquila, from 2013 to the year 2015. The diagnosis of headache are made according toICHD III criteria. The identifi cation of the MTHFR C677T polymorphism of the enzyme was carried out by the Real-time PCR qualitative. The statistical analysis by SAS System. Results: Diagnosis of migraine without aura in 96 patients, migraine with aura in 39, in 18 chronic migraine, Frequent episodic tension-type headache in 40, chronic tension type headache in 20 and in 13 other headaches. 61 patients are without mutation, 85 with heterozygous mutation, and 28 homozygous. Therefore, the mutation is present in 147 patients with a percentage of 65%. The heterozygous mutation is present in 50.56% of females and 47.06% males; the homozygous in 10.19% and 12.94% in females than males. In migraineurs the mutation is present in 66.67% compared with patients with tension-type headache (33.33%), homozygous is the 70.37% versus 29.63% (p <0.001). Homocysteine levels are elevated only nell’8.69% of mutated patients, of which 5/12 patients have a mutation in homozygosity. Conclusions: We confi rme the statistical association between MTHFR mutationboth in the heterozygous and homozygous forms and migraines.The migraines with aura, unlike the literature, does not seem to have a important role. Also the homocysteine not seems statistically affect the trends of the forms of headaches examined.

The Methylenetetrahydrofolate Reductase and Polymorphism C677T in the Children with Headache

TOZZI, Elisabetta
;
PICCOROSSI, ALESSANDRA;GAMMELLA, CRISTINA;Verrotti, Alberto;SECHI, ENZO
2017-01-01

Abstract

ABSTRACT Background: The headaches are a heterogeneous clinical manifestations characterized not only by pain but also by a severe multifactorial disabilities, often associated with other comorbidities that severely affects the patient’s quality of life. And ‘it is known for some time the risk of cerebrovascular disease in migraine patients. Numerous studies showed the association between the enzyme MTHFR mutations , the T allele and genotype TTand migraine, particularly migraine with aura. Aim of the study: On the basis of theliterature data we propose to evaluate the prevalence of the MTHFR mutation in the population of patients admitted to a headache center of the childhood. Materials and methods: Weexamined 226 children, aged 5-17 years,admitted to “Headache Center” of Children Neuropsychiatry of Hospital San Salvatore L’Aquila, from 2013 to the year 2015. The diagnosis of headache are made according toICHD III criteria. The identifi cation of the MTHFR C677T polymorphism of the enzyme was carried out by the Real-time PCR qualitative. The statistical analysis by SAS System. Results: Diagnosis of migraine without aura in 96 patients, migraine with aura in 39, in 18 chronic migraine, Frequent episodic tension-type headache in 40, chronic tension type headache in 20 and in 13 other headaches. 61 patients are without mutation, 85 with heterozygous mutation, and 28 homozygous. Therefore, the mutation is present in 147 patients with a percentage of 65%. The heterozygous mutation is present in 50.56% of females and 47.06% males; the homozygous in 10.19% and 12.94% in females than males. In migraineurs the mutation is present in 66.67% compared with patients with tension-type headache (33.33%), homozygous is the 70.37% versus 29.63% (p <0.001). Homocysteine levels are elevated only nell’8.69% of mutated patients, of which 5/12 patients have a mutation in homozygosity. Conclusions: We confi rme the statistical association between MTHFR mutationboth in the heterozygous and homozygous forms and migraines.The migraines with aura, unlike the literature, does not seem to have a important role. Also the homocysteine not seems statistically affect the trends of the forms of headaches examined.
File in questo prodotto:
File Dimensione Formato  
IJND-ID15 (1).pdf

accesso aperto

Tipologia: Documento in Versione Editoriale
Licenza: Dominio pubblico
Dimensione 229.69 kB
Formato Adobe PDF
229.69 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/116971
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact