Natural history of respiratory muscle strength in spinal muscular atrophy: a prospective national cohort study

被引:15
|
作者
Veldhoen, Esther S. [1 ]
Wijngaarde, Camiel A. [2 ]
Hulzebos, Erik H. J. [3 ]
Wosten-van Asperen, Roelie M. [1 ]
Wadman, Renske, I [2 ]
van Eijk, Ruben P. A. [2 ,4 ]
Asselman, Fay Lynn [2 ]
Stam, Marloes [2 ]
Otto, Louise A. M. [2 ]
Cuppen, Inge [2 ]
Scheijmans, Feline E., V [2 ]
Verweij-van den Oudenrijn, Laura P. [1 ]
Bartels, Bart [3 ]
Gaytant, Michael A. [5 ]
van der Ent, Cornelis K. [6 ]
van der Pol, W. Ludo [2 ]
机构
[1] Univ Utrecht, Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Pediat Intens Care, POB 85090, NL-3508 AB Utrecht, Netherlands
[2] Univ Utrecht, Univ Med Ctr Utrecht, UMC Utrecht Brain Ctr, Dept Neurol, Utrecht, Netherlands
[3] Univ Utrecht, Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Child Dev & Exercise Ctr, Utrecht, Netherlands
[4] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Biostat & Res Support, Utrecht, Netherlands
[5] Univ Utrecht, Univ Med Ctr Utrecht, Ctr Home Mech Ventilat, Dept Pulmonol, Utrecht, Netherlands
[6] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Pediat Pulmonol, ERN LUNG, Utrecht, Netherlands
关键词
Neuromuscular; Spinal muscular atrophy; Respiratory muscle strength; Lung function; Natural history; NASAL INSPIRATORY PRESSURE; REFERENCE VALUES; SHAM CONTROL; CHILDREN; NUSINERSEN; MANAGEMENT; DIAGNOSIS; PULMONARY; ADULTS; TOOL;
D O I
10.1186/s13023-022-02227-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Respiratory complications are the most important cause of morbidity and mortality in spinal muscular atrophy (SMA). Respiratory muscle weakness results in impaired cough, recurrent respiratory tract infections and eventually can cause respiratory failure. We assessed longitudinal patterns of respiratory muscle strength in a national cohort of treatment-naive children and adults with SMA, hypothesizing a continued decline throughout life. Methods We measured maximal expiratory and inspiratory pressure (PEmax and PImax), Sniff Nasal inspiratory pressure (SNIP), peak expiratory flow (PEF), and peak cough flow (PCF) in treatment-naive patients with SMA. We used mixed-models to analyze natural history patterns. Results We included 2172 measurements of respiratory muscle function from 80 treatment-naive patients with SMA types 1c-3b. All outcomes were lower in the more severe phenotypes. Significant differences in PEF were present between SMA types from early ages onwards. PEF decline was linear (1-2%/year). PEF reached values below 80% during early childhood in types 1c-2, and during adolescence in type 3a. PEmax and PImax were severely lowered in most patients throughout life, with PEmax values abnormally low (i.e. < 80 cmH(2)O) in virtually all patients. The PEmax/PImax ratio was < 1 throughout life in all SMA types, indicating that expiratory muscles were most affected. All but SMA type 3b patients had a lowered PCF. Patients with types 2b and 3a had PCF levels between 160 and 270 L/min, those with type 2a around 160 L/min and patients with type 1c well below 160 L/min. Finally, SNIP was low in nearly all patients, most pronounced in more severely affected patients. Conclusions There are clear differences in respiratory muscle strength and its progressive decline between SMA types. We observed lower outcomes in more severe SMA types. Particularly PEF may be a suitable outcome measure for the follow-up of respiratory strength in patients with SMA. PEF declines in a rather linear pattern in all SMA types, with clear differences at baseline. These natural history data may serve as a reference for longer-term treatment efficacy assessments.
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页数:11
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