Anticardiolipin, glutamic acid decarboxylase, and antinuclear antibodies in epileptic patients

被引:16
作者
Verrotti, A
Greco, R
Altobelli, E
Latini, G
Morgese, G
Chiarelli, F
机构
[1] Univ G dAnnunzio, Dept Pediat, Osped Policlin, I-66013 Chieti, Italy
[2] Univ G dAnnunzio, Dept Med, Sect Pediat, I-66013 Chieti, Italy
[3] Univ Aquila, Dept Epidemiol, I-67100 Laquila, Italy
[4] Natl Res Council Italy, Div Pediat, Perrino Hosp, Azienda Osped Di Summa,Clin Physiol Inst,IFC CNR, Lecce, Italy
[5] Univ Siena, Dept Pediat, I-53100 Siena, Italy
关键词
anticardiolipin antibodies; glutamic acid decarboxylase antibodies antinuclear antibodies; epilepsy; SYSTEMIC-LUPUS-ERYTHEMATOSUS; ANTIPHOSPHOLIPID ANTIBODIES; PARTIAL SEIZURES; AUTOANTIBODIES; ASSOCIATION; DISEASE; PREVALENCE;
D O I
10.1007/s102380300013
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To explore the hypothesis that raised anticardiolipin antibodies, glutamic acid decarboxylase, and antinuclear antibodies may be associated with epilepsy and/or pharmacoresistance, we studied titers in 74 epileptic patients and 50 controls. Epileptic patients were divided into two groups according to their response to anticonvulsant therapy. Group I included 52 children (30 females and 22 males with a mean age+/-SD of 7.0+/-2.4 years) suffering from different types of epilepsy who were treated with various anticonvulsants. Group 11 included 22 children (10 females and 12 males with a mean age of 6.2+/-3.6 years) suffering from therapy resistant epilepsy. We found that the prevalence of anticardiolipin antibodies was significantly higher in epileptic patients than in controls, while there was no significant difference between patients who were seizure free and those with uncontrolled epilepsy. No significant difference was found in glutamic acid decarboxylase antibodies between epileptic children and controls, and between patients who were seizure free and those with uncontrolled epilepsy. A significant difference in the incidence of antinuclear antibodies was found between epileptic children and controls, while no difference was found between well-controlled and drug-resistant epilepsy. In conclusion, the prevalence of anticardiolipin and antinuclear antibodies was higher in patients with epilepsy than in controls. There was no significant difference in serum glutamic acid decarboxylase antibodies between epileptic children and controls, and between patients who were seizure free and those with uncontrolled epilepsy.
引用
收藏
页码:32 / 36
页数:5
相关论文
共 37 条
[1]   IMMUNOLOGICAL ASPECTS OF EPILEPSY [J].
AARLI, JA .
BRAIN & DEVELOPMENT, 1993, 15 (01) :41-50
[2]   Partial seizures associated with antiphospholipid antibodies in childhood [J].
Angelini, L ;
Granata, T ;
Zibordi, F ;
Binelli, S ;
Zorzi, G ;
Besana, C .
NEUROPEDIATRICS, 1998, 29 (05) :249-253
[3]   PROPOSAL FOR REVISED CLASSIFICATION OF EPILEPSIES AND EPILEPTIC SYNDROMES [J].
不详 .
EPILEPSIA, 1989, 30 (04) :389-399
[4]   CEREBROVASCULAR-DISEASE AND ANTIPHOSPHOLIPID ANTIBODIES IN SYSTEMIC LUPUS-ERYTHEMATOSUS, LUPUS-LIKE DISEASE, AND THE PRIMARY ANTIPHOSPHOLIPID SYNDROME [J].
ASHERSON, RA ;
KHAMASHTA, MA ;
GIL, A ;
VAZQUEZ, JJ ;
CHAN, O ;
BAGULEY, E ;
HUGHES, GRV .
AMERICAN JOURNAL OF MEDICINE, 1989, 86 (04) :391-399
[5]  
ASHERSON RA, 1993, ANN MED INTERNE, V144, P367
[6]   THE ANTIPHOSPHOLIPID-THROMBOSIS SYNDROMES - FACT, FICTION, CONFUSION, AND CONTROVERSY [J].
BICK, RL .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1993, 100 (05) :477-480
[7]   The binding of some human antiendothelial cell antibodies induces endothelial cell apoptosis [J].
Bordron, A ;
Dueymes, M ;
Levy, Y ;
Jamin, C ;
Leroy, JP ;
Piette, JC ;
Shoenfeld, Y ;
Youinou, PY .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (10) :2029-2035
[8]  
BOUMA PAD, 1992, CLIN NEUROL NEUROSUR, V94, pS54
[9]   NEUROLOGICAL DISEASE ASSOCIATED WITH ANTICARDIOLIPIN ANTIBODIES IN PATIENTS WITHOUT SYSTEMIC LUPUS-ERYTHEMATOSUS - CLINICAL AND IMMUNOLOGICAL FEATURES [J].
CHANCELLOR, AM ;
CULL, RE ;
KILPATRICK, DC ;
WARLOW, CP .
JOURNAL OF NEUROLOGY, 1991, 238 (07) :401-407
[10]   Antiphospholipid antibodies permeabilize and depolarize brain synaptoneurosomes [J].
Chapman, J ;
Cohen-Armon, M ;
Shoenfeld, Y ;
Korczyn, AD .
LUPUS, 1999, 8 (02) :127-133