University of Cincinnati College of Medicine.
Division of Human Genetics, Cincinnati Children's Hospital Medical Center.
Psychiatr Genet. 2024 Aug 1;34(4):86-90. doi: 10.1097/YPG.0000000000000372. Epub 2024 Jun 4.
X-linked creatine transporter deficiency is caused by hemizygous or heterozygous pathogenic variants in SLC6A8 that cause neuropsychiatric symptoms because of impaired uptake of creatine into tissues throughout the body. Small cohorts have suggested that supplementation of creatine, arginine, and glycine can stop disease progression in males, but only six cases of supplementation in females have been published. Here, we present a female with a de-novo pathogenic SLC6A8 variant who had ongoing weight loss, mild intellectual disability, and neuropsychiatric symptoms. Magnetic resonance spectroscopy of the brain showed reduced creatine on all acquired spectra. The patient was started on creatine-monohydrate, l -arginine, and l -glycine supplementation, and she had significant symptomatic improvement within the following 3 weeks. After 8 months of supplementation, magnetic resonance spectroscopy showed improved creatine concentrations with normalizing semiquantitative ratios with other brain metabolites. Current data supports clinicians trialing creatine, arginine, and glycine supplements for female patients with creatine transporter deficiency.
X 连锁肌氨酸转运蛋白缺乏症是由 SLC6A8 的杂合或纯合致病性变异引起的,由于全身组织对肌氨酸的摄取受损,会导致神经精神症状。小队列研究表明,肌氨酸、精氨酸和甘氨酸的补充可以阻止男性疾病的进展,但仅发表了 6 例女性补充的病例。在这里,我们介绍了一名女性患者,她携带新出现的致病性 SLC6A8 变异,持续体重减轻、轻度智力障碍和神经精神症状。脑磁共振波谱显示所有采集的图谱中肌酸减少。该患者开始使用肌酸一水合物、L-精氨酸和 L-甘氨酸补充剂,在接下来的 3 周内症状显著改善。补充 8 个月后,磁共振波谱显示肌酸浓度改善,与其他脑代谢物的半定量比值正常化。目前的数据支持临床医生为肌氨酸转运蛋白缺乏症的女性患者试用肌氨酸、精氨酸和甘氨酸补充剂。