Department of Neurology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
J Neuromuscul Dis. 2023;10(4):555-566. doi: 10.3233/JND-230029.
GNE myopathy is an ultra-rare muscle disease characterized by a reduction in the synthesis of sialic acid derived from pathogenic variants in the GNE gene. No treatment has been established so far.
We evaluated the safety and efficacy of oral supplementation of aceneuramic acid in patients with GNE myopathy.
This multicenter, placebo-controlled, double-blind study comprised genetically confirmed GNE myopathy patients in Japan who were randomly assigned into treatment groups of sialic acid-extended release (SA-ER) tablets (6 g/day for 48 weeks) or placebo groups (4:1). The primary endpoint of effectiveness was set as the change in total upper limb muscle strength (upper extremity composite [UEC] score) from the start of administration to the final evaluation time point.
Among the 20 enrolled patients (SA-ER group, 16; placebo group, 4), 19 completed this 48-week study. The mean value of change in UEC score (95% confidence interval [CI]) at 48 weeks was -0.1 kg (-2.1 to 2.0) in the SA-ER group and -5.1 kg (-10.4 to 0.3) in the placebo group. The least squares mean difference (95% CI) between the groups in the covariance analysis was 4.8 kg (-0.3 to 9.9; P = 0.0635). The change in UEC score at 48 weeks was significantly higher in the SA-ER group compared with the placebo group (P = 0.0013) in the generalized estimating equation test repeated measurement analysis. In one patient in the SA-ER group, who was found to be pregnant 2 weeks after drug administration fetal death with tangled umbilical cord occurred at 13 weeks after the discontinuation of treatment. No other serious adverse effects were observed.
The present study indicates that oral administration of SA-ER tablets is effective and safe in patients with GNE myopathy in Japan.
GNE 肌病是一种极为罕见的肌肉疾病,其特征是由于 GNE 基因的致病性变异导致唾液酸的合成减少。到目前为止,还没有确立治疗方法。
我们评估了口服唾液酸延长释放(SA-ER)片剂在 GNE 肌病患者中的安全性和疗效。
这项多中心、安慰剂对照、双盲研究纳入了日本经基因确认的 GNE 肌病患者,他们被随机分为唾液酸延长释放片剂(6 g/天,持续 48 周)治疗组或安慰剂组(4:1)。有效性的主要终点设定为从开始给药到最终评估时间点的总上肢肌肉力量(上肢综合评分[UEC]评分)的变化。
在 20 名入组患者中(SA-ER 组 16 例,安慰剂组 4 例),有 19 名完成了这项 48 周的研究。SA-ER 组在 48 周时 UEC 评分的平均值(95%置信区间[CI])变化为-0.1 kg(-2.1 至 2.0),安慰剂组为-5.1 kg(-10.4 至 0.3)。协方差分析中两组间的最小二乘均值差(95%CI)为 4.8 kg(-0.3 至 9.9;P=0.0635)。在广义估计方程重复测量分析中,SA-ER 组在 48 周时的 UEC 评分变化明显高于安慰剂组(P=0.0013)。在 SA-ER 组的 1 名患者中,该患者在给药后 2 周发现怀孕,在治疗停止后 13 周发生脐带缠绕死胎。未观察到其他严重不良反应。
本研究表明,在日本的 GNE 肌病患者中,口服 SA-ER 片剂是有效且安全的。