Montesano Elizabeth, Garcia Maria E, Lyon Shannon, Worhach Jennifer, Wang Grace, Zhang Bo, August Joshua, Maski Kiran
Department of Neurology, Boston Children's Hospital, Boston, Massachusetts.
School of Medicine, Ponce Health Science University, Ponce, Puerto Rico.
J Clin Sleep Med. 2025 Jun 1;21(6):1081-1091. doi: 10.5664/jcsm.11628.
Most children/adolescents with narcolepsy type 1 (NT1) are treated with stimulants or modafinil, yet the cardiovascular effects of these medications have not been investigated in this population. We compared vital signs in youth with NT1 before and after exposure to stimulants/modafinil to test the hypotheses that these medications increase rates of elevated blood pressure (BP) and hypertension and that body mass index influences these outcomes.
In this retrospective study, we collected electronic medical data including vital signs and polysomnography/Multiple Sleep Latency Test results from 39 youth with NT1 aged 7-18 at 3 points over a 20-month period: baseline (drug-naïve/weaned), after initiating treatment, and after treatment optimization. We performed stepwise regression to determine predictors of baseline elevated BP/hypertension. We used McNemar's test and generalized estimating equations to assess the effects of stimulant/modafinil exposure on vital signs.
The prevalence of elevated BP/hypertension at baseline was 51% in our cohort and increased 21% from baseline to the final visit ( = .03). Systolic BP increased significantly with stimulant/modafinil exposure ( < .05), while diastolic BP and heart rate showed nonsignificant increases. Body mass index was associated with increased systolic BP and heart rate across the 3 time points but not at baseline.
Youth with NT1 are at risk for elevated BP/hypertension, particularly after stimulant/modafinil treatment. We recommend revising clinical guidelines to address this risk and advocate for controlled studies to better understand the cardiovascular risks and implications of these treatments in pediatric NT1.
Montesano E, Garcia ME, Lyon S, et al. Rising pressure to understand the risks of hypertension in children with narcolepsy type 1. . 2025;21(6):1081-1091.
大多数1型发作性睡病(NT1)儿童/青少年使用兴奋剂或莫达非尼进行治疗,然而这些药物对该人群的心血管影响尚未得到研究。我们比较了NT1青少年在使用兴奋剂/莫达非尼前后的生命体征,以检验以下假设:这些药物会增加血压升高(BP)和高血压的发生率,且体重指数会影响这些结果。
在这项回顾性研究中,我们收集了39名7 - 18岁NT1青少年在20个月内3个时间点的电子医疗数据,包括生命体征以及多导睡眠图/多次睡眠潜伏期测试结果:基线期(未使用药物/停药)、开始治疗后以及治疗优化后。我们进行逐步回归以确定基线血压升高/高血压的预测因素。我们使用McNemar检验和广义估计方程来评估兴奋剂/莫达非尼暴露对生命体征的影响。
在我们的队列中,基线时血压升高/高血压的患病率为51%,从基线到最后一次就诊增加了21%(P = .03)。随着兴奋剂/莫达非尼暴露,收缩压显著升高(P < .05),而舒张压和心率虽有升高但无统计学意义。在3个时间点上,体重指数与收缩压和心率升高相关,但在基线时不相关。
NT1青少年有血压升高/高血压的风险,尤其是在使用兴奋剂/莫达非尼治疗后。我们建议修订临床指南以应对这一风险,并倡导进行对照研究,以更好地了解这些治疗对儿童NT1的心血管风险及影响。
Montesano E, Garcia ME, Lyon S, et al. Rising pressure to understand the risks of hypertension in children with narcolepsy type 1.. 2025;21(6):1081 - 1091.