Burden of illness and mortality in men with Adrenomyeloneuropathy: a retrospective cohort study.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-07-17 DOI:10.1186/s13023-024-03276-w
Joshua L Bonkowsky, Bridget Healey, Naomi C Sacks, Ronaé McLin, Philip L Cyr, Eileen K Sawyer, Christopher D Stephen, Florian Eichler
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Abstract

Background: Adrenomyeloneuropathy (AMN) is a neurodegenerative disease phenotype of X-linked adrenoleukodystrophy (ALD), resulting in progressive myeloneuropathy causing spastic paraparesis, sensory ataxia, and bowel/bladder symptoms. We conducted a retrospective cohort study using two large administrative databases to characterize mortality and the burden of illness in adult men with AMN in the US.

Results: Healthcare resource use was assessed using a national commercial insurance claims database (2006-2021). Males with AMN ages 18-64 years and no evidence of cerebral ALD or other peroxisomal disorders were included and 1:4 matched on demographic characteristics to individuals without AMN. All study participants were followed for as long as observable. Patients with AMN were also identified in the Medicare Limited Dataset (2017-2022); mortality and age at death were compared with all Medicare enrollees. We identified 303 commercially insured men with AMN. Compared with non-AMN, individuals with AMN had significantly more inpatient hospital admissions (0.44 vs. 0.04 admissions/patient/year), outpatient clinic (8.88 vs. 4.1 visits/patient/year), outpatient hospital (5.33 vs. 0.99 visits/patient/year), and home healthcare visits (4.66 vs. 0.2 visits/patient/year), durable medical equipment claims (0.7 vs. 0.1 claims/patient/year), and prescription medication fills (18.1 vs. 5.4 fills/patient/year) (all p < 0.001). Average length-of-stay per hospitalization was also longer in AMN (8.88 vs. 4.3 days; p < 0.001). Rates of comorbidities were significantly more common in AMN compared to controls, including peripheral vascular disease (4.6% vs. 0.99%), chronic pulmonary disease (6.3% vs. 2.6%), and liver disease (5.6% vs. 0.88%), all p < 0.001. Among individuals age < 65 with Medicare disability coverage, mortality rates were 5.3x higher for adult AMN males (39.3% vs. 7.4%) and the age at death significantly younger (47.0 ± 11.3 vs. 56.5 ± 7.8 years), both p < 0.001. Among Medicare beneficiaries ages ≥ 65 mortality rates were 2.2x higher for men with AMN vs. those without AMN (48.6% vs. 22.4%), p < 0.001.

Conclusion: AMN imposes a substantial and underrecognized health burden on men, with higher healthcare utilization, greater medical comorbidity, higher mortality rates, and younger age at death.

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肾上腺肌萎缩性神经病男性患者的疾病负担和死亡率:一项回顾性队列研究。
背景:肾上腺肌髓神经病(AMN)是X连锁肾上腺白质营养不良症(ALD)的一种神经退行性疾病表型,会导致进行性肌髓神经病,引起痉挛性瘫痪、感觉共济失调和肠/膀胱症状。我们利用两个大型行政数据库开展了一项回顾性队列研究,以了解美国成年男性 AMN 患者的死亡率和疾病负担:我们使用全国商业保险理赔数据库(2006-2021 年)对医疗资源使用情况进行了评估。研究对象包括年龄在 18-64 岁之间、无脑 ALD 或其他过氧化物酶体疾病证据的 AMN 男性患者,他们与无 AMN 患者的人口统计学特征比例为 1:4。对所有研究参与者进行了长期跟踪观察。在医疗保险有限数据集(2017-2022 年)中也发现了 AMN 患者;死亡率和死亡年龄与所有医疗保险参保者进行了比较。我们发现了 303 名患有 AMN 的商业保险男性患者。与非 AMN 患者相比,AMN 患者的住院次数(0.44 次/患者/年 vs. 0.04 次/患者/年)、门诊次数(8.88 次/患者/年 vs. 4.1 次/患者/年)、门诊医院次数(5.33 次/患者/年 vs. 0.99 人次/患者/年)、家庭保健就诊(4.66 人次/患者/年 vs. 0.2 人次/患者/年)、耐用医疗设备索赔(0.7 vs. 0.1 索赔/患者/年)和处方药配药(18.1 vs. 5.4 配药/患者/年)(均为 p 结论:AMN 对患者造成了巨大且过低的医疗费用:急性髓系白血病给男性带来了巨大的健康负担,但这一负担并未得到充分认识,因为他们需要更多的医疗保健服务、更高的医疗并发症、更高的死亡率以及更年轻的死亡年龄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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