Arginine, glycine, and creatine supplementation improves symptoms in a female with creatine transporter deficiency.

IF 1.5 4区 医学 Q4 GENETICS & HEREDITY
Psychiatric Genetics Pub Date : 2024-08-01 Epub Date: 2024-06-04 DOI:10.1097/YPG.0000000000000372
Kara Tauer, Caroline Theile, Joshua W Owens, Kim M Cecil, Amelle Shillington
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引用次数: 0

Abstract

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.

补充精氨酸、甘氨酸和肌酸可改善肌酸转运体缺乏症女性患者的症状。
X 连锁肌酸转运体缺乏症是由 SLC6A8 的半杂合子或杂合子致病变体引起的,由于全身组织对肌酸的摄取能力受损,因此会导致神经精神症状。小规模队列研究表明,补充肌酸、精氨酸和甘氨酸可阻止男性患者的疾病进展,但目前仅发表了六例女性患者补充肌酸的病例。在此,我们介绍了一名患有去原位致病性 SLC6A8 变异的女性患者,她的体重持续下降,并伴有轻度智力障碍和神经精神症状。脑部磁共振波谱检查显示,所有获得的波谱中肌酸含量都有所降低。患者开始补充一水肌酸、L-精氨酸和 L-甘氨酸,并在随后的 3 周内症状得到明显改善。补充肌酸 8 个月后,磁共振波谱显示肌酸浓度有所提高,与其他脑代谢物的半定量比率趋于正常。目前的数据支持临床医生为肌酸转运体缺乏症女性患者试用肌酸、精氨酸和甘氨酸补充剂。
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来源期刊
Psychiatric Genetics
Psychiatric Genetics 医学-神经科学
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
3 months
期刊介绍: ​​​​​​The journal aims to publish papers which bring together clinical observations, psychological and behavioural abnormalities and genetic data. All papers are fully refereed. Psychiatric Genetics is also a forum for reporting new approaches to genetic research in psychiatry and neurology utilizing novel techniques or methodologies. Psychiatric Genetics publishes original Research Reports dealing with inherited factors involved in psychiatric and neurological disorders. This encompasses gene localization and chromosome markers, changes in neuronal gene expression related to psychiatric disease, linkage genetics analyses, family, twin and adoption studies, and genetically based animal models of neuropsychiatric disease. The journal covers areas such as molecular neurobiology and molecular genetics relevant to mental illness. Reviews of the literature and Commentaries in areas of current interest will be considered for publication. Reviews and Commentaries in areas outside psychiatric genetics, but of interest and importance to Psychiatric Genetics, will also be considered. Psychiatric Genetics also publishes Book Reviews, Brief Reports and Conference Reports.
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