Metabolic and genetic risk factors for migraine in children

被引:49
作者
Bottini, F
Celle, ME
Calevo, MG [1 ]
Amato, S
Minniti, G
Montaldi, L
Di Pasquale, D
Cerone, R
Veneselli, E
Molinari, AC
机构
[1] Giannina Gaslini Childrens Hosp, Serv Epidemiol & Biostat, Sci Directorate, Genoa, Italy
[2] Giannina Gaslini Childrens Hosp, Dept Paediat Haematol & Oncol, Thrombosis & Haemostasis Unit, Genoa, Italy
[3] Univ Genoa, Dept Paediat 1, Lab Standardizat Verificat Screening Metab & Endo, Genoa, Italy
[4] Univ Genoa, Dept Child Neuropsychiat, Genoa, Italy
关键词
childhood; folate metabolism; migraine; prothrombotic conditions; risk factors;
D O I
10.1111/j.1468-2982.2006.01107.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Migraine can induce ischaemic stroke, and is considered an independent risk factor for stroke in the young. To date, the nature of the link between migraine and stroke is essentially unknown. Forty-five children were studied. Homocysteine levels (fasting and post methionine load), vitamin B12 and plasma folate levels, factor V Leiden, factor II G20210A, methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C mutations were examined. Compared with controls, patients with migraine had higher levels of post-methionine load homocysteine values (19.5 +/- 4.9 vs. 16.9 +/- 1.9; P = 0.025) and significantly lower folate levels (5.8 +/- 2.6 vs. 7.5 +/- 2.1; P = 0.002). We found a trend toward an increased risk of migraine in subjects carrying a homozygous mutant genotype for MTHFR C677T and MTHFR A1298C polymorphisms. Genetic prothrombotic conditions do not seem to be related to migraine in the young, whereas the biochemical differences between migrainous patients and controls are an appealing topic for further investigation.
引用
收藏
页码:731 / 737
页数:7
相关论文
共 34 条
[1]  
Bassi B, 2003, J HEADACHE PAIN, V4, P138, DOI DOI 10.1007/S10194-003-0048-3
[2]  
CANO A, 2000, MIGRAINE AURA MIGRAI, P617
[3]   Migraine and prothrombotic genetic risk factors [J].
Corral, J ;
Iniesta, JA ;
Gonzalez-Conejero, R ;
Lozano, ML ;
Rivera, J ;
Vicente, V .
CEPHALALGIA, 1998, 18 (05) :257-260
[4]   Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population [J].
De Marco, P ;
Calevo, MG ;
Moroni, A ;
Arata, L ;
Merello, E ;
Finnell, RH ;
Zhu, HP ;
Andreussi, L ;
Cama, A ;
Capra, V .
JOURNAL OF HUMAN GENETICS, 2002, 47 (06) :319-324
[5]  
DE SV, 1998, BLOOD, V91, P3562
[6]   Ischemic stroke and migraine in childhood: Coincidence or causal relation? [J].
Ebinger, F ;
Boor, R ;
Gawehn, J ;
Reitter, B .
JOURNAL OF CHILD NEUROLOGY, 1999, 14 (07) :451-455
[7]  
Etminan M, 2005, BRIT MED J, V330, P345
[8]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[9]   APPLICABILITY OF THE 1988 IHS CRITERIA TO HEADACHE PATIENTS UNDER THE AGE OF 18 YEARS ATTENDING 21 ITALIAN HEADACHE CLINICS [J].
GALLAI, V ;
SARCHIELLI, P ;
CARBONI, F ;
BENEDETTI, P ;
MASTROPAOLO, C ;
PUCA, F .
HEADACHE, 1995, 35 (03) :146-153
[10]   INCIDENCE OF ACTIVATED PROTEIN-C RESISTANCE CAUSED BY THE ARG-506 GLN MUTATION IN FACTOR-V IN 113 UNRELATED SYMPTOMATIC PROTEIN C-DEFICIENT PATIENTS [J].
GANDRILLE, S ;
GREENGARD, JS ;
ALHENCGELAS, M ;
JUHANVAGUE, I ;
ABGRALL, JF ;
JUDE, B ;
GRIFFIN, JH ;
AIACH, M .
BLOOD, 1995, 86 (01) :219-224