Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Mol Genet Metab. 2023 Mar;138(3):107525. doi: 10.1016/j.ymgme.2023.107525. Epub 2023 Jan 25.
Glycogen storage disease type IV (GSD IV) is an ultra-rare autosomal recessive disorder caused by pathogenic variants in GBE1 which results in reduced or deficient glycogen branching enzyme activity. Consequently, glycogen synthesis is impaired and leads to accumulation of poorly branched glycogen known as polyglucosan. GSD IV is characterized by a remarkable degree of phenotypic heterogeneity with presentations in utero, during infancy, early childhood, adolescence, or middle to late adulthood. The clinical continuum encompasses hepatic, cardiac, muscular, and neurologic manifestations that range in severity. The adult-onset form of GSD IV, referred to as adult polyglucosan body disease (APBD), is a neurodegenerative disease characterized by neurogenic bladder, spastic paraparesis, and peripheral neuropathy. There are currently no consensus guidelines for the diagnosis and management of these patients, resulting in high rates of misdiagnosis, delayed diagnosis, and lack of standardized clinical care. To address this, a group of experts from the United States developed a set of recommendations for the diagnosis and management of all clinical phenotypes of GSD IV, including APBD, to support clinicians and caregivers who provide long-term care for individuals with GSD IV. The educational resource includes practical steps to confirm a GSD IV diagnosis and best practices for medical management, including (a) imaging of the liver, heart, skeletal muscle, brain, and spine, (b) functional and neuromusculoskeletal assessments, (c) laboratory investigations, (d) liver and heart transplantation, and (e) long-term follow-up care. Remaining knowledge gaps are detailed to emphasize areas for improvement and future research.
糖原贮积病 IV 型(GSD IV)是一种极为罕见的常染色体隐性遗传病,由 GBE1 中的致病性变异引起,导致糖原分支酶活性降低或缺乏。因此,糖原合成受损,导致积累不良分支的糖原,即多葡聚糖。GSD IV 的表型异质性程度显著,表现为宫内、婴儿期、幼儿期、青春期或中年至晚年。临床连续体包括肝脏、心脏、肌肉和神经系统表现,严重程度不一。GSD IV 的成人发病形式,称为成人多葡聚糖体病(APBD),是一种神经退行性疾病,其特征是神经性膀胱、痉挛性截瘫和周围神经病。目前,对于这些患者的诊断和管理尚无共识指南,导致误诊率、延迟诊断率和缺乏标准化临床护理的情况较高。为了解决这个问题,一组来自美国的专家制定了一套针对所有 GSD IV 临床表型(包括 APBD)的诊断和管理建议,以支持为 GSD IV 患者提供长期护理的临床医生和护理人员。该教育资源包括确认 GSD IV 诊断的实用步骤和医疗管理的最佳实践,包括(a)肝脏、心脏、骨骼肌、大脑和脊柱的影像学检查,(b)功能和神经肌肉骨骼评估,(c)实验室检查,(d)肝和心脏移植,以及(e)长期随访护理。详细说明了剩余的知识空白,以强调改进和未来研究的领域。