SLC6A1 患者和组织视角:SLC6A1 连接的建立、研究和持续努力。

Therapeutic advances in rare disease Pub Date : 2024-09-28 eCollection Date: 2024-01-01 DOI:10.1177/26330040241283734
Jacob Tiller, Melissa B DeLeeuw, Jing-Qiong Kang, Amber Freed
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引用次数: 0

摘要

本文介绍了 "SLC6A1 连接"(SLC6A1 Connect)组织的成立过程,该组织为确诊患有 SLC6A1 的患者和家属提供资源,同时提供有关该疾病的最新科学概述。安布尔-弗里德(Amber Freed)在生下两对可爱的双胞胎后,注意到她的儿子麦克斯韦尔(Maxwell)错过了运动发育的里程碑,而且经常发呆。这些迹象最终导致了 SLC6A1 变异的诊断。SLC6A1 基因位于 3 号染色体的短臂上,该基因编码γ-氨基丁酸 (GABA) 转运体 1 (GAT-1) 蛋白。这种转运体负责抑制性神经递质 GABA 的再摄取。该转运体通常会将 GABA 从两个神经元之间的突触间隙中清除,从而限制大脑的过度兴奋,这可能会导致癫痫发作和运动障碍,安博尔在儿子麦克斯韦身上就发现了这一点。安布尔意识到,她儿子的病情几乎没有任何治疗方案,因此她开始与科学家和医生建立联系。最初,她飞去见史蒂文-格雷博士,并与他一起制定了治疗变异基因的基因替代疗法研究计划以及临床试验设计。不仅如此,他们还需要筹集四百万美元来资助这些努力。弗里德成立了 "SLC6A1 连接"(SLC6A1 Connect)组织,以筹集资金和提高认识,并组建了一个由热心研究人员和家庭组成的网络。从那时起,该组织已经筹集了 200 多万美元,并不断发展壮大,为患者家庭提供支持。该组织甚至每年都会与全球的家庭、科学家和生物技术或制药公司举办研讨会。此外,我们还详细介绍了该组织现在如何为家庭提供信息资源,帮助他们了解变异背后的科学原理以及帮助孩子的方法,如注册链接和基因检测选项。这些努力促使该组织与范德比尔特大学医学中心、UT 西南医学中心、克利夫兰诊所等机构的科学家以及许多工业制药合作伙伴开展合作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SLC6A1 patient & organization perspective: founding of SLC6A1 connect, research, and ongoing efforts.

This paper describes the founding of the SLC6A1 Connect organization, which offers resources to patients and families with SLC6A1 diagnoses while keeping current with a scientific overview of the disorder. Following the birth of her two lovely twins, Amber Freed noticed how her son, Maxwell, missed motor development milestones and would often stare. Eventually, these signs led to a diagnosis of an SLC6A1 variant. The SLC6A1 gene is located on the short arm of chromosome 3 and the gene encodes for the gamma-aminobutyric acid (GABA) transporter 1 (GAT-1) protein. This transporter is responsible for the reuptake of the inhibitory neurotransmitter, GABA. The transporter usually removes GABA from the synapse space between two neurons, limiting over-excitability in the brain, which can lead to seizures and motor deficits as Amber noticed in her son, Maxwell. Amber realized that there were nearly no treatment options for her son's condition so she began forming connections with scientists and doctors. Initially, she flew to see Dr. Steven Gray, with whom she developed a research plan for a gene replacement therapy to treat the variant along with a design for a clinical trial. Not only this but they needed to raise four million dollars to fund these endeavors. Freed founded the SLC6A1 Connect organization to raise money and awareness and put together a network of dedicated researchers and families. Since then, the organization has raised over two million dollars and grown to offer families a base of support. The organization even hosts a yearly symposium with families, scientists, and biotech or pharmaceutical companies worldwide. In addition, we detail how the organization now offers informational resources to families to help them understand the science behind the variant and ways to help their children such as registry links and genetic testing options. These endeavors have led the organization to collaborate with scientists based on institutions such as Vanderbilt University Medical Center, UT Southwestern Medical Center, the Cleveland Clinic, and many industrial pharmaceutical partners.

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