Bearden David, Steenhoff Andrew P, Dlugos Dennis J, Kolson Dennis, Mehta Parth, Kessler Sudha, Lowenthal Elizabeth, Monokwane Baphaleng, Anabwani Gabriel, Bisson Gregory P
*Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, PA; †Botswana-UPenn Partnership, Philadelphia, PA; ‡Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; §Division of Infectious Disease, Children's Hospital of Philadelphia, Philadelphia, PA; ‖Division of Neurology, Hospital of the University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA; ¶Texas Children's Cancer and Hematology Centers, Baylor College of Medicine, Houston, TX; #Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA; **Department of Pediatrics, University of Botswana, Gaborone, Botswana; ††Botswana-Baylor Children's Clinical Centre of Excellence, Gaborone, Botswana; and ‡‡Division of Infectious Disease, Hospital of the University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA.
J Acquir Immune Defic Syndr. 2015 Jun 1;69(2):193-9. doi: 10.1097/QAI.0000000000000563.
Seizures are common among patients with HIV/AIDS in the developing world and are associated with significant morbidity and mortality. Early treatment with combination antiretroviral therapy (cART) may reduce this risk by decreasing rates of central nervous system infections and HIV encephalopathy.
A case-control study of new-onset epilepsy among children aged 0-18 years with perinatally acquired HIV/AIDS followed in Gaborone, Botswana, during the period 2003-2009 was conducted. Children with epilepsy were identified and compared with age- and sex-matched controls without epilepsy with respect to timing of cART initiation. Early treatment was defined as treatment with cART before the age of 12 months, at a CD4% of greater than 25 in children aged 1-5 years, or at an absolute CD4 count of >350 cell per cubic millimeter in children aged 5 years and older.
We identified 29 cases of new-onset epilepsy and 58 age- and sex-matched controls. The most common identified etiologies for epilepsy were central nervous system infections and direct HIV neurotoxicity. Only 8 (28%) of the children who developed epilepsy received early treatment compared with 31 (53%) controls (odds ratio: 0.36, 95% confidence interval: 0.14 to 0.92, P = 0.03). This effect was primarily driven by differences in rates of epilepsy among children who initiated treatment with cART between the ages of 1 and 5 years (11% vs. 53%, odds ratio: 0.11, 95% confidence interval: 0.01 to 1.1, P = 0.06).
Earlier initiation of cART may be protective against epilepsy in children with HIV.
在发展中国家,癫痫在艾滋病毒/艾滋病患者中很常见,且与高发病率和死亡率相关。早期联合抗逆转录病毒疗法(cART)治疗可能通过降低中枢神经系统感染率和艾滋病毒脑病发生率来降低这种风险。
对2003年至2009年期间在博茨瓦纳哈博罗内随访的0至18岁围产期感染艾滋病毒/艾滋病儿童中新发癫痫进行了一项病例对照研究。确定癫痫患儿,并就开始cART治疗的时间与年龄和性别匹配的无癫痫对照进行比较。早期治疗定义为12个月龄前接受cART治疗、1至5岁儿童CD4%大于25时接受治疗或5岁及以上儿童绝对CD4计数>350个细胞/立方毫米时接受治疗。
我们确定了29例新发癫痫病例和58例年龄和性别匹配的对照。确定的癫痫最常见病因是中枢神经系统感染和直接艾滋病毒神经毒性。发生癫痫的儿童中只有8例(28%)接受了早期治疗,而对照中有31例(53%)(优势比:0.36,95%置信区间:0.14至0.92,P = 0.03)。这种效应主要是由1至5岁开始接受cART治疗的儿童中癫痫发生率的差异驱动的(11%对53%,优势比:0.11,95%置信区间:0.01至1.1,P = 0.06)。
更早开始cART治疗可能对艾滋病毒感染儿童的癫痫有预防作用。