Is late diagnosis of Duchenne muscular dystrophy still a reality?

被引:0
作者
Beckerq, Michele Michelin [1 ]
Gurgel-Giannetti, Juliana [2 ]
Araujo, Alexandra Prufer de Queiroz Campos [3 ]
Costa, Marcela Camara Machado [4 ]
Felix, Temis Maria [5 ]
Lorea, Claudia Fernandes [6 ]
Ortega, Adriana Banzzatto [7 ]
Zenyh, Michelle Silva [8 ]
Kowalskii, Thayne Woycinck [5 ]
Wincklerj, Pablo Brea [9 ]
Medeiros, Leonardo Simao [10 ]
Pinhati, Clara Catharino [11 ]
de Moura, Ana Carolina Monteiro Lessa [11 ]
Saute, Jonas Alex Morales [12 ,13 ,14 ]
Nardes, Flavia [15 ]
机构
[1] Hosp Clin Porto Alegre, Child Neurol Unit, Dept Pediat, Porto Alegre, RS, Brazil
[2] Univ Fed Minas Gerais UFMG, Fac Med UFMG, Dept Pediat, Belo Horizonte, Brazil
[3] Uiversidade Fed Rio de Janeiro UFRJ, Inst Puericnultura & Pediat MartagaGesteira, Dept Pediat IPPMG, Rio De Janeiro, Brazil
[4] Escola Bahiana Med & Saude Publ, Salvador, BA, Brazil
[5] Hosp Clin Porto Alegre, Med Genet Serv, Porto Alegre, RS, Brazil
[6] Univ Fed Rio Grande do Sul, Porto Alegre, Brazil
[7] Pequeno Principe Hosp, Dept Pediat Neurol, Curitiba, PR, Brazil
[8] Hosp Pequeno Principe, Curitiba, Brazil
[9] Hosp Clin Porto Alegre, Neuromuscular Dis Neurol Dept, Porto Alegre, Brazil
[10] Hosp Clin Porto Alegre, Nucl Med Serv, Depart000000ment Med Genet, Porto Alegre, Brazil
[11] Univ Fed Minas Gerais, Belo Horizonte, Brazil
[12] Univ Fed Rio Grande do Sul, Dept Internal Med, Neurol Div, Porto Alegre, Brazil
[13] Univ Fed Rio Grande Dul, Grad Program Med Med Sci, Porto Alegre, Brazil
[14] Hosp Clin Porto Alegre, Med Genet Div, Porto Alegre, Brazil
[15] Univ Fed Rio de Janeiro UFRJ, Dept Pediat IPPMG, Inst Puericultura & Pediat Gesteira, Rio De Janeiro, Brazil
关键词
Duchenne muscular dystrophy; Late diagnosis; Age of diagnosis; Delayed diagnosis; Time to diagnosis; BRAZILIAN CONSENSUS; GLUCOCORTICOIDS; REHABILITATION; MANAGEMENT; FAILURE; BOYS; LIFE;
D O I
10.1016/j.ejpn.2025.05.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Duchenne muscular dystrophy (DMD) is a progressive X-linked recessive neuromuscular disorder caused by pathogenic variants in the DMD gene manifesting in early childhood with progressive muscle weakness. First symptoms of muscle weakness usually appear around age of three, however, other signs of the disease like muscle hypertrophy, poor motor skills and social, language and motor delay can be detected earlier. Significant delays in the diagnostic process for DMD have been reported in many countries, with the diagnosis generally being made around five years. A collaborative historical cohort study was conducted to identify the age at diagnosis of DMD in five neuromuscular centers in Brazil, covering cases diagnosed between January 2019 and March 2024. In addition to data from the centers, data on age at diagnosis were obtained from The Brazilian National Network for Rare Diseases (RARAS). The final analytic cohort included 173 DMD individuals. The mean age at which patients were diagnosed with probable DMD based on clinical suspicion was 5.7 (+2.7) years, with diagnostic confirmation by genetic testing/muscle biopsy at 6.9 (+4.0) years, with medians of 6.0 and 6.8 years, respectively. The mean age at which parents noticed symptoms was 3.4 (+1.9) years with a median of 3.0 years. The most frequently observed initial symptoms by parents included frequent falls (35.5 %), gait abnormalities (31.4 %), difficulties in stair climbing (17.2 %), developmental delay (13.6 %), and difficulties in rising from the floor (8.9 %). The presence of co-occurring neurocognitive conditions was associated with a delay of 1.12 years (p symbolscript 0.008) in the median age at suspected diagnosis and 1.0 years in the median age at diagnosis confirmation (p symbolscript 0,022). These results suggest that while there have been improvements in the age of diagnosis of DMD in Brazil in recent decades, diagnosis still occurs later than ideal and then what has been achieved in high-income countries.
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页码:35 / 40
页数:6
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