Ream Margie A, Lam Wendy K K, Grosse Scott D, Ojodu Jelili, Jones Elizabeth, Prosser Lisa A, Rose Angela M, Marie Comeau Anne, Tanksley Susan, DiCostanzo Katie P, Kemper Alex R
Division of Child Neurology, Nationwide Children's Hospital, Columbus, Ohio.
Duke Clinical and Translational Science Institute, Duke University School of Medicine, Durham, North Carolina.
Pediatrics. 2025 Apr 1;155(4). doi: 10.1542/peds.2024-069152.
Krabbe disease (KD), which affects 0.3-2.6 per 100 000 live births, is an autosomal recessive lysosomal disorder caused by variants in the GALC gene that reduce galactosylceramidase (GALC) activity, leading to psychosine accumulation, cerebral white matter degeneration, and peripheral neuropathy. The most common form, infantile KD (IKD), has onset by 12 months with irritability, feeding difficulty, neurologic regression, and, when untreated, death in early childhood. Hematopoietic stem cell transplantation (HSCT) for IKD approximately 1 month after birth can improve long-term survival but has about a 10% risk of mortality within 100 days, and affected individuals can still have significant functional impairment. Newborn screening for KD is based on low GALC levels in dried-blood spots. Second-tier testing to assess whether an elevated psychosine concentration is present in the same dried-blood spot improves the specificity of screening for IKD. Without newborn screening, diagnosis of IKD is generally made after significant clinical symptoms develop, past when HSCT can be effective. The benefit of newborn detection of later-onset phenotypes of KD is uncertain. In 2024, the US Secretary of Health and Human Services added IKD to the Recommended Uniform Screening Panel after a recommendation by the Advisory Committee on Heritable Disorders in Newborns and Children. For IKD newborn screening to be as effective as possible, it is important to have systems in place to support families in making challenging decisions soon after diagnosis about whether to pursue HSCT and to ensure rapid access to HSCT if chosen.
克拉伯病(KD)的发病率为每10万例活产中有0.3 - 2.6例,是一种常染色体隐性溶酶体疾病,由GALC基因变异导致半乳糖神经酰胺酶(GALC)活性降低引起,进而导致精神鞘氨醇蓄积、脑白质变性和周围神经病变。最常见的形式是婴儿型KD(IKD),发病于12个月内,表现为易激惹、喂养困难、神经功能衰退,若不治疗,会在幼儿期死亡。出生后约1个月对IKD进行造血干细胞移植(HSCT)可提高长期生存率,但100天内有大约10%的死亡风险,且患者仍可能有明显的功能障碍。KD的新生儿筛查基于干血斑中GALC水平较低。通过二级检测评估同一干血斑中精神鞘氨醇浓度是否升高,可提高IKD筛查的特异性。若不进行新生儿筛查,IKD通常在出现明显临床症状后才得以诊断,此时已错过HSCT有效的时机。新生儿检测KD迟发型表型的益处尚不确定。2024年,在美国新生儿和儿童遗传性疾病咨询委员会的建议下,美国卫生与公众服务部部长将IKD纳入了推荐统一筛查项目。为使IKD新生儿筛查尽可能有效,建立相关系统以支持家庭在诊断后尽快做出关于是否进行HSCT的艰难决策,并确保若选择HSCT能快速获得治疗,这一点很重要。