Harvard Medical School, Boston, MA, USA.
Department of Neurology, BIDMC Comprehensive Headache Center, Beth Israel Deaconess Medical Center, Boston, MA, USA.
J Headache Pain. 2024 Jun 18;25(1):102. doi: 10.1186/s10194-024-01808-0.
Large conductance calcium-activated potassium (BK) channels have been implicated in the neurobiological underpinnings of migraine. Considering the clinical similarities between migraine and persistent post-traumatic headache (PPTH), we aimed to examine whether MaxiPost (a BK channel opener) could induce migraine-like headache in persons with PPTH.
This is a randomized double-blind, placebo-controlled, two-way crossover study from September 2023 to December 2023. Eligible participants were adults with PPTH after mild traumatic brain injury who reported having no personal history of migraine. The randomized participants received a single dose of either MaxiPost (0.05 mg/min) or placebo (isotonic saline) that was infused intravenously over 20 minutes. The two experiment sessions were scheduled at least one week apart to avoid potential carryover effects. The primary endpoint was the induction of migraine-like headache after MaxiPost as compared to placebo within 12 hours of drug administration. The secondary endpoint was the area under the curve (AUC) values for headache intensity scores between MaxiPost and placebo over the same 12-hour observation period.
Twenty-one adult participants (comprising 14 females and 7 males) with PPTH were enrolled and completed both experiment sessions. The proportion of participants who developed migraine-like headache was 11 (52%) of 21 participants after MaxiPost infusion, in contrast to four (19%) participants following placebo (P = .02). Furthermore, the median headache intensity scores, represented by AUC values, were higher following MaxiPost than after placebo (P < .001).
Our results indicate that BK channel opening can elicit migraine-like headache in persons with PPTH. Thus, pharmacologic blockade of BK channels might present a novel avenue for drug discovery. Additional investigations are nonetheless needed to confirm these insights and explore the therapeutic prospects of BK channel blockers in managing PPTH.
NCT05378074.
大电导钙激活钾(BK)通道与偏头痛的神经生物学基础有关。鉴于偏头痛和持续性创伤后头痛(PPTH)之间存在临床相似性,我们旨在研究 MaxiPost(一种 BK 通道开放剂)是否会在患有 PPTH 的人中引起偏头痛样头痛。
这是一项 2023 年 9 月至 2023 年 12 月进行的随机、双盲、安慰剂对照、双向交叉研究。合格的参与者是轻度创伤性脑损伤后患有 PPTH 的成年人,他们报告没有偏头痛的个人病史。随机参与者接受单剂量 MaxiPost(0.05mg/min)或安慰剂(等渗盐水)静脉输注 20 分钟。两个实验疗程至少间隔一周,以避免潜在的交叉效应。主要终点是在药物给药后 12 小时内与安慰剂相比,MaxiPost 诱导偏头痛样头痛。次要终点是在相同的 12 小时观察期内,MaxiPost 和安慰剂之间头痛强度评分的曲线下面积(AUC)值。
21 名患有 PPTH 的成年参与者(包括 14 名女性和 7 名男性)入组并完成了两个实验疗程。在 MaxiPost 输注后,21 名参与者中有 11 名(52%)出现偏头痛样头痛,而安慰剂组有 4 名(19%)参与者(P=0.02)。此外,MaxiPost 后头痛强度评分的中位数(表示为 AUC 值)高于安慰剂后(P<0.001)。
我们的结果表明,BK 通道开放可以在患有 PPTH 的人中引起偏头痛样头痛。因此,BK 通道的药理学阻断可能为药物发现提供新途径。然而,仍需要进一步的研究来证实这些发现,并探索 BK 通道阻滞剂在管理 PPTH 中的治疗前景。
NCT05378074。