Interruption of enzyme replacement therapy;
Clinical outcome;
Glycogen storage disease type 2;
Pompe disease;
CLINICAL-FEATURES;
CORONAVIRUS;
ADULTS;
ALPHA;
D O I:
10.1007/s00415-021-10475-z
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background Late-onset Pompe disease (LOPD) is a rare autosomal recessive disorder caused by mutations in the GAA gene, leading to progressive weakness of locomotor and respiratory muscles. Enzyme replacement therapy (ERT), administered every second week, has been proven to slow down disease progression and stabilize pulmonary function. Due to the COVID-19 pandemic in Germany, ERT was interrupted at our centre for 29 days. As reports on ERT discontinuation in LOPD are rare, our study aimed to analyse the impact of ERT interruption on the change in clinical outcome. Methods We performed a prospective cohort study in 12 LOPD patients. Clinical assessments were performed after ERT interruption and after the next three consecutive infusions. We assessed motor function by muscle strength testing, a 6-minute-walk-test, pulmonary function tests, and adverse events. For statistical analysis, an estimated baseline was calculated based on the individual yearly decline. Results The mean time of ERT interruption was 49.42 days (SD +/- 12.54). During ERT interruption, seven patients reported 14 adverse events and two of them were severe. Frequent symptoms were reduced muscle endurance/increased muscle fatigability and shortness of breath/worsening of breathing impairment. After ERT interruption, significant deterioration was found for MIP%pred (p = 0.026) and MRC%pred, as well as a trend to clinical deterioration in FVC%pred and the 6MWT(%pred). Conclusion Interruption of ERT was associated with a deterioration in the core clinical outcome measures. Therefore, an interruption of ERT should be kept as short as possible.
机构:
UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Hughes, D. S.
Norwood, F.
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Kings Coll Hosp London, Dept Neurol, London, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Norwood, F.
Sawicka, E.
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机构:
Princess Royal Univ Hosp, Dept Thorac Med, Kent, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Sawicka, E.
Milligan, A.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Milligan, A.
Pringle, S.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Pringle, S.
Bruce, R.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Bruce, R.
Goodwin, S.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Goodwin, S.
Jennings, A.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Jennings, A.
Richfield, L.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England
Richfield, L.
Mehta, A. B.
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UCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, EnglandUCL Royal Free & Univ Coll Med Sch, Lysosomal Storage Disorders Unit, London WC1E 6BT, England