Almeida Vânia, Conceição Isabel, Fineza Isabel, Coelho Teresa, Silveira Fernando, Santos Manuela, Valverde Ana, Geraldo Argemiro, Maré Ricardo, Aguiar Teresa Carolina, Mendonça Carla, Martins João, Medeiros Luísa, Barroso Cândida, Vieira José Pedro, Moreno Teresa, Negrão Luis, Dias Margarida Silva, Lacerda Lúcia, Evangelista Teresinha
Serviço de Neurologia, Hospital de Santa Maria (Centro Hospitalar de Lisboa Norte, EPE), Av. Professor Egas Moniz, 1649-035 Lisboa, Portugal.
Serviço de Neurologia, Hospital de Santa Maria (Centro Hospitalar de Lisboa Norte, EPE), Av. Professor Egas Moniz, 1649-035 Lisboa, Portugal.
Neuromuscul Disord. 2017 Aug;27(8):777-781. doi: 10.1016/j.nmd.2017.03.010. Epub 2017 Mar 29.
Pompe disease is a rare metabolic disorder with available enzymatic replacement therapy. Contrasting with the classic infantile form, the others subtypes have a heterogeneous presentation that makes an early and accurate diagnosis difficult. We conducted a prospective, multicenter, observational study to identify undiagnosed patients. During a one-year period, patients followed in Portuguese neuromuscular outpatient clinics with proximal muscle weakness affecting upper and/or lower limbs, hyperCKemia in two or more determinations or hypotonia and hyperCKemia, were screened for acid α-glucosidase deficiency by dried blood spots. Lysosomal acid-alpha-1,4-glucosidase activity was determined by tandem mass spectrometry and positive results were confirmed by molecular study. From the 99 patients screened, Pompe disease was confirmed in 4, with age of onset ranging from 2.5 to 48 years, all with limb girdle muscle weakness, corresponding to a frequency of 4% in our cohort and 4.9% of limb girdle muscle weakness. Screening for Pompe disease in high risk populations, using dried blood spots, was already performed in some European populations. Apart from two negative Scandinavian studies, positive cases were confirmed in 2.8-7.9% of patients presenting with limb girdle muscle weakness and in 0-2.5% with isolated hyperCKemia.
庞贝病是一种罕见的代谢紊乱疾病,有可用的酶替代疗法。与经典的婴儿型不同,其他亚型表现各异,难以早期准确诊断。我们进行了一项前瞻性、多中心、观察性研究以识别未确诊患者。在一年时间里,对葡萄牙神经肌肉门诊中出现上肢和/或下肢近端肌无力、两次或更多次检测出现高肌酸激酶血症或肌张力减退和高肌酸激酶血症的患者,通过干血斑筛查酸性α-葡萄糖苷酶缺乏症。通过串联质谱法测定溶酶体酸性α-1,4-葡萄糖苷酶活性,阳性结果通过分子研究确认。在筛查的99例患者中,确诊4例庞贝病,发病年龄在2.5至48岁之间,均有肩胛带肌无力,在我们的队列中频率为4%,在肩胛带肌无力患者中占4.9%。一些欧洲人群已采用干血斑对高危人群进行庞贝病筛查。除了两项阴性的斯堪的纳维亚研究外,在表现为肩胛带肌无力的患者中,2.8%-7.9%确诊为阳性病例,在孤立性高肌酸激酶血症患者中,0%-2.5%确诊为阳性病例。