Serum HMGB1 in febrile seizures

被引:1
|
作者
Hautala, Maria K. [1 ,2 ]
Mikkonen, Kirsi H. [1 ,2 ,3 ,4 ,5 ]
Pokka, Tytti M. L. [6 ,7 ]
Rannikko, Sirpa K. [8 ]
Koskela, Ulla V. [1 ,2 ]
Rantala, Heikki M. J. [1 ,2 ]
Uhari, Matti K. [1 ,2 ]
Glumoff, Virpi [8 ]
Helander, Heli M. [1 ,2 ]
机构
[1] Univ Oulu, Med Res Ctr Oulu MRC Oulu, Res Unit Clin Med, POB 23, Oulu 90029, Finland
[2] Oulu Univ Hosp, Dept Pediat & Adolescent Med, POB 23, Oulu 90029, Finland
[3] Univ Helsinki, Childrens Hosp, Div Child Neurol, Epileps Helsinki, POB 347, Helsinki 00029, Finland
[4] Helsinki Univ Hosp, Pediat Res Ctr, POB 347, Helsinki 00029, Finland
[5] Univ Helsinki, POB 347, Helsinki 00029, Finland
[6] Oulu Univ Hosp, Res Serv Unit, POB 10, Oulu 90029, Finland
[7] Univ Oulu, Res Unit Clin Med, POB 8000, Oulu 90014, Finland
[8] Univ Oulu, Med Res Lab Unit, POB 8000, Oulu 90014, Finland
关键词
Febrile seizure; Pathogenesis; Cytokine; HMGB1; MOBILITY GROUP BOX-1; TOLL-LIKE RECEPTOR; CHILDREN; ASSOCIATION; EPILEPSY;
D O I
10.1016/j.eplepsyres.2024.107381
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The role of high-mobility group box 1 (HMGB1) in the pathogenesis of febrile seizures (FSs) is unclear. In our controlled follow-up study, we compared serum levels of HMGB1 (s-HMGB1) in the same individuals after the first FS, during febrile episodes without a FS, after recurrent FS, during healthy periods after FS, and between patients and controls. In all, 122 patients with FSs were included in the final analysis, including 18 with recurrent FSs with a complete follow-up protocol. We recruited 30 febrile children and 18 matched febrile children without seizures as controls. S-HMGB1 was lower in patients with recurrent FSs after the first FS than that in matched febrile control children (median 1.12 mu g/L (0.14-2.95) vs 1.79 mu g/L (0.33-47.90), P<0.04). We did not find any other differences in s-HMGB1 between the groups. S-HMGB1 did not differ in different types of FSs. We updated a meta-analysis of s-HMGB1 in patients with FSs and found that the differences were significant only in the studies conducted in East Asian populations. We conclude that S-HMGB1 does not seem to be a key factor in the pathogenesis of FSs but differences in HMGB1 concentrations could explain some of the ethnicity related susceptibility to FSs.
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页数:8
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