在军事飞行员中导航法布里病。

IF 0.9 4区 医学 Q4 BIOPHYSICS
Tanner Carlock, Eric Kincaid-Sharp, Christopher Orsello, Aven W Ford, Bashir B El-Khoury
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引用次数: 0

摘要

背景:法布里病(FD)是一种罕见的x连锁溶酶体贮积障碍,由α -半乳糖苷酶a (α -gala)活性不足引起,导致鞘糖脂积累,并导致广泛的全身性症状,包括神经、肾脏、心脑血管表现。虽然这种疾病的发病率约为十万分之一,但其发病率可能被低估了,而且以前没有记录在案的飞行员病例。病例报告:一名有FD家族史的30岁美国空军C-5飞行员在基因检测后被诊断为致病性半乳糖苷酶α基因变异。初步评估显示蛋白尿肾病和其他正常的神经系统检查提示早期FD,提示开始使用赖诺普利、氯吡格雷预防中风,以及美国食品和药物管理局新批准的伴侣治疗米加司他。患者对治疗的耐受性良好,对治疗有适当的反应,生化参数(α -半乳糖A活性和血浆globotriaosylsphingosine水平)的改善和临床稳定性证明了这一点。经过8个月的多学科监测和综合评估,他获得了有时间限制的航空医疗豁免,并成功重返飞行岗位。讨论:FD是一种罕见的进行性遗传病,由半乳糖苷酶α基因变异引起,导致α -半乳糖a缺乏和鞘糖脂积累,导致神经、肾脏、心脏和脑血管并发症。尽管有较高的航空医疗风险,特别是由于中风和脑血管问题,但FD患者可能有资格在密切监测和多学科护理下执行有限的飞行任务。持续评估新疗法和个性化航空医疗豁免可以在平衡安全和操作要求的同时支持患有FD的飞行员。卡洛克T,金凯德-夏普E, Orsello C,福特AW, El-Khoury BB。在一个军事飞行员身上导航法布里病。航空航天Med Hum Perform. 2025;96(6): 525 - 529。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating Fabry Disease in a Military Aviator.

Background: Fabry disease (FD) is a rare, X-linked lysosomal storage disorder caused by deficient alpha-galactosidase A (alpha-Gal A) activity, leading to the accumulation of glycosphingolipids and resulting in a wide spectrum of systemic symptoms, including neurological, renal, cardiovascular, and cerebrovascular manifestations. While the disease affects approximately 1 in 100,000 individuals, its incidence may be underreported, and no cases in aviators have previously been documented.

Case report: A 30-yr-old U.S. Air Force C-5 pilot with a family history of FD was diagnosed with a pathogenic galactosidase alpha gene variant after genetic testing. Initial evaluations revealed proteinuric kidney disease and an otherwise normal neurological workup indicating early FD, prompting initiation of lisinopril, clopidogrel for stroke prevention, and the newly Food and Drug Administration-approved chaperone therapy migalastat. The patient tolerated treatment well with appropriate response to therapy as demonstrated by improved biochemical parameters (alpha-Gal A activity and plasma globotriaosylsphingosine levels) and clinical stability. After 8 mo of multidisciplinary monitoring and comprehensive evaluation, he was granted a time-limited aeromedical waiver and successfully returned to flying duties.

Discussion: FD is a rare, progressive genetic disorder caused by galactosidase alpha gene variants, resulting in alpha-Gal A deficiency and glycosphingolipid accumulation, leading to neurological, renal, cardiac, and cerebrovascular complications. Despite higher aeromedical risks, especially due to stroke and cerebrovascular issues, FD patients may qualify for restricted flight duties under close monitoring and multidisciplinary care. Continued evaluation of novel therapies and individualized aeromedical waivers can support aviators with FD while balancing safety and operational requirements. Carlock T, Kincaid-Sharp E, Orsello C, Ford AW, El-Khoury BB. Navigating Fabry disease in a military aviator. Aerosp Med Hum Perform. 2025; 96(6):525-529.

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来源期刊
Aerospace medicine and human performance
Aerospace medicine and human performance PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH -MEDICINE, GENERAL & INTERNAL
CiteScore
1.10
自引率
22.20%
发文量
272
期刊介绍: The peer-reviewed monthly journal, Aerospace Medicine and Human Performance (AMHP), formerly Aviation, Space, and Environmental Medicine, provides contact with physicians, life scientists, bioengineers, and medical specialists working in both basic medical research and in its clinical applications. It is the most used and cited journal in its field. It is distributed to more than 80 nations.
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