Skull Base Research Center, The Five Senses Health Institute, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Department of Neurology, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Mov Disord Clin Pract. 2024 Jan;11(1):53-62. doi: 10.1002/mdc3.13933. Epub 2023 Dec 1.
Neurodegeneration with Brain Iron Accumulation (NBIA) disorder is a group of ultra-orphan hereditary diseases with very limited data on its course.
To estimate the probability of preserving ambulatory ability and survival in NBIA.
In this study, the electronic records of the demographic data and clinical assessments of NBIA patients from 2012 to 2023 were reviewed. The objectives of the study and factors impacting them were investigated by Kaplan-Meier and Cox regression methods.
One hundred and twenty-two genetically-confirmed NBIA patients consisting of nine subtypes were enrolled. Twenty-four and twenty-five cases were deceased and wheelchair-bound, with a mean disease duration of 11 ± 6.65 and 9.32 ± 5 years. The probability of preserving ambulation and survival was 42.9% in 9 years and 28.2% in 15 years for classical Pantothenate Kinase-Associated Neurodegeneration (PKAN, n = 18), 89.4% in 7 years and 84.7% in 9 years for atypical PKAN (n = 39), 23% in 18 years and 67.8% in 14 years for Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN, n = 23), 75% in 20 years and 36.5% in 33 years for Kufor Rakeb Syndrome (KRS, n = 17), respectively. The frequencies of rigidity, spasticity, and female gender were significantly higher in deceased cases compared to surviving patients. Spasticity was the only factor associated with death (P value = 0.03).
KRS had the best survival with the most extended ambulation period. The classical PKAN and MPAN cases had similar progression patterns to loss of ambulation ability, while MPAN patients had a slower progression to death. Spasticity was revealed to be the most determining factor for death.
神经铁沉积性神经变性(NBIA)障碍是一组超罕见遗传性疾病,其病程数据非常有限。
评估 NBIA 患者保持步行能力和存活的概率。
本研究回顾了 2012 年至 2023 年 NBIA 患者的电子病历和临床评估数据。通过 Kaplan-Meier 和 Cox 回归方法研究了研究目的和影响因素。
共纳入 122 例经基因证实的 NBIA 患者,包括 9 个亚型。24 例和 25 例患者死亡和坐轮椅,平均病程为 11±6.65 年和 9.32±5 年。经典泛酸激酶相关神经变性(PKAN,n=18)9 年内保持行走能力和生存的概率为 42.9%,15 年内为 28.2%;非典型 PKAN(n=39)7 年内为 89.4%,9 年内为 84.7%;线粒体膜蛋白相关神经变性(MPAN,n=23)18 年内为 23%,14 年内为 67.8%;Kufor Rakeb 综合征(KRS,n=17)20 年内为 75%,33 年内为 36.5%。与存活患者相比,死亡患者的僵硬、痉挛和女性频率明显更高。痉挛是与死亡相关的唯一因素(P 值=0.03)。
KRS 的生存率最高,步行能力维持时间最长。经典 PKAN 和 MPAN 病例的步行能力丧失进展模式相似,而 MPAN 患者的死亡进展较慢。痉挛被揭示为死亡的最决定性因素。