Incidence and health burden of 20 rare neurological diseases in South China from 2016 to 2022: a hospital-based observational study.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Jingjing Li, Shujin Tang, Jiaoxing Li, Xin Huang, Yu Liu, Jinsheng Zeng, Yuhua Fan
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引用次数: 0

Abstract

Background: Rare neurological diseases (RNDs) result in severe health burdens worldwide. Data from China are limited. We aimed to investigate the health burden of 20 RNDs in Guangdong Province (GD), which contains two-thirds of the population of South China.

Methods: The hospitalization data of 20 RNDs were described using hospital-based front sheet data from 3,037 hospitals of GD from 2016 to 2022. The 20 RNDs included amyotrophic lateral sclerosis (ALS), Charcot-Marie-Tooth Disease, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, congenital myotonia, congenital myasthenic syndrome, Dravet syndrome, Fabry disease, hereditary spastic paraplegia, Huntington disease, Leber hereditary optic neuropathy, mitochondrial encephalopathy (ME), multi-focal motor neuropathy, myotonic dystrophy, primary hereditary dystonia, progressive muscular dystrophy (PMD), spinal and bulbar muscular atrophy, spinal muscular atrophy (SMA), spinocerebellar ataxia, Wilson disease (WD) and X-linked adrenoleukodystrophy. Age were presented as mean and standard deviation while length of hospital stay as median and interquartile range (25th and 75th percentiles). The other variables were described as number and percentage. The data were analyzed by Joinpoint regression.

Results: There were 9,351 cases, including 330 ICU and 155 death cases. The average age was 33.7 ± 22.0 y, and 63.8% of patients were male. From 2016 to 2022, the number of RND (and juvenile RND) cases were 1034 (184), 1174 (293), 1443 (374), 1422 (320), 1331 (337), 1432 (409) to 1515 (515). ICU (and juvenile ICU) cases rose from 28 (3), 34 (6), 24 (4), 38 (11), 46 (13), 54 (24) to 106 (56). Joinpoint regression showed significant upward trend in percentages of juvenile and juvenile ICU cases (APC = 8.13, P< 0.05; APC = 28.42, P< 0.05). The fop five RNDs were WD, ASL, PMD, ME, and SMA, which accounted for 79.7% of all, 99.1% of ICU, and 94.8% of death cases.

Conclusions: We demonstrated that the increase in health burden of RNDs was mainly evident in juveniles in South China from 2016 to 2022. The top 5 RNDs accounted for majority of the critical patients.

2016 - 2022年华南地区20种罕见神经系统疾病发病率及健康负担的医院观察研究
背景:罕见神经系统疾病(RNDs)在世界范围内造成严重的健康负担。来自中国的数据有限。我们的目的是调查广东省20个农村地区(GD)的卫生负担,广东省人口占中国南方人口的三分之二。方法:采用2016 - 2022年广东省3037家医院住院病历资料,对20例rnd的住院情况进行描述。20例rnd包括肌萎缩性侧索硬化症(ALS)、腓骨肌萎缩性侧索硬化症、大脑常染色体显性动脉病变伴皮质下梗死和脑白质病、先天性肌强直、先天性肌无力综合征、Dravet综合征、Fabry病、遗传性痉挛性瘫痪、亨廷顿病、Leber遗传性视神经病变、线粒体脑病(ME)、多局点运动神经病、肌强直营养不良、原发性遗传性肌张力障碍、进行性肌营养不良(PMD)、脊髓和球性肌萎缩、脊髓性肌萎缩(SMA)、脊髓小脑性共济失调、威尔逊病(WD)和x连锁肾上腺脑白质营养不良。年龄表示为平均值和标准差,住院时间表示为中位数和四分位数范围(25和75百分位数)。其他变量描述为数量和百分比。采用Joinpoint回归对数据进行分析。结果:共9351例,其中重症监护330例,死亡155例。平均年龄33.7±22.0 y,男性占63.8%。2016 - 2022年,RND(及少年RND)病例数分别为1034例(184例)、1174例(293例)、1443例(374例)、1422例(320例)、1331例(337例)、1432例(409例)~ 1515例(515例)。ICU(及青少年ICU)病例由28例(3例)、34例(6例)、24例(4例)、38例(11例)、46例(13例)、54例(24例)增至106例(56例)。联合点回归显示,青少年和青少年ICU病例百分比有显著上升趋势(APC = 8.13, P< 0.05;Apc = 28.42, p < 0.05)。排名前5位的rnd分别是WD、ASL、PMD、ME和SMA,占全部病例的79.7%,占ICU的99.1%,占死亡病例的94.8%。结论:研究表明,2016年至2022年,中国南方地区RNDs健康负担的增加主要体现在青少年身上。rnd排名前5位的患者占危重患者的大多数。
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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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