Clinical course of neurogenic bladder dysfunction in human T-cell leukemia virus type-1-associated myelopathy/tropical spastic paraparesis: a nationwide registry study in Japan

被引:3
作者
Iijima, Naoki [1 ]
Yamauchi, Junji [1 ,2 ]
Yagishita, Naoko [2 ]
Araya, Natsumi [2 ]
Aratani, Satoko [2 ,3 ]
Tanabe, Kenichiro [2 ]
Sato, Tomoo [1 ,2 ]
Takata, Ayako [4 ]
Yamano, Yoshihisa [1 ,2 ]
机构
[1] St Marianna Univ, Div Neurol, Dept Internal Med, Sch Med, Kawasaki, Kanagawa, Japan
[2] St Marianna Univ, Div Neurol, Dept Rare Dis Res, Inst Med Sci,Sch Med, Kawasaki, Kanagawa 2168511, Japan
[3] LSI Medience Co, Tokyo, Japan
[4] St Marianna Univ, Dept Prevent Med, Sch Med, Kawasaki, Kanagawa, Japan
关键词
Human T-cell leukemia virus type 1; Human T-cell leukemia virus type 1-associated myelopathy; tropical spastic paraparesis; Neurogenic bladder; Urinary symptom score; Mirabegron; VOIDING DYSFUNCTION; SYMPTOMS;
D O I
10.1186/s13023-021-01990-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Most patients with human T-cell leukemia virus type 1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) develop neurogenic bladder dysfunction. However, longitudinal changes and treatment effects remain poorly understood. This study aimed to characterize the clinical course of urinary dysfunction in this population. Methods This prospective observational study included 547 patients enrolled in HAM-net, a nationwide registry for HAM/TSP in Japan. Urinary dysfunction severity was evaluated using the HAM/TSP-bladder dysfunction symptom score (HAM-BDSS) and the HAM/TSP-bladder dysfunction severity grade (HAM-BDSG). These specific measures were recently developed for assessing urinary dysfunction in HAM/TSP. We analyzed longitudinal changes over a 6-year follow-up period, associations between urinary and gait dysfunction, and treatment efficacy of urinary catheterization and mirabegron (a beta 3-adrenergic agonist for overactive bladder symptoms). Results The mean (standard deviation [SD]) age and disease duration at enrollment were 61.9 (10.7) years and 16.6 (11.6) years, respectively, and 74.6% of patients were women. Only 8.0% were free from urinary symptoms (HAM-BDSG 0), 65.4% had urinary symptoms or were on medication (HAM-BDSG I), and 23.2% and 3.3% used intermittent and indwelling catheters (HAM-BDSG II and III), respectively. HAM-BDSG and BDSS were worse in patients with greater gait dysfunction (p < 0.001 for both). During the 6-year follow-up, 66.7% of patients with HAM-BDSG 0 developed new urinary symptoms. Of those with HAM-BDSG I at enrollment, 10.8% started using urinary catheters. Importantly, HAM-BDSS significantly improved after initiating catheterization (mean [SD] change, - 8.93 [10.78], p < 0.001). The number of patients receiving mirabegron increased in the fourth year. Multivariable linear regression analysis significantly associated mirabegron with improvement in HAM-BDSS (- 5.82, 95% confidence interval - 9.13 to - 2.51, p = 0.001). Conclusions Urinary dysfunction affected 92% of patients and progressed over the 6-year follow-up. Urinary symptoms were more severe in patients with poorer gait function. Urinary catheterization and mirabegron were effective in relieving symptoms. Effective utilization of real-world data is key to establishing evidence for rare diseases, such as HAM/TSP.
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页数:10
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