Updated birth prevalence and relative frequency of mucopolysaccharidoses across Brazilian regions

• Autor(a) principal: Josahkian,Juliana Alves
• Data de Publicação: 2021
• Outros Autores: Trapp,Franciele Barbosa, Burin,Maira Graeff, Michelin-Tirelli,Kristiane, Magalhães,Ana Paula Pereira Scholz de, Sebastião,Fernanda Medeiros, Bender,Fernanda, Mari,Jurema Fátima De, Brusius-Facchin,Ana Carolina, Leistner-Segal,Sandra, Málaga,Diana Rojas, Giugliani,Roberto
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Genetics and Molecular Biology
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000100103
• topic: Lysosomal storage diseases; metabolic diseases; mucopolysaccharidoses; epidemiology; Brazil

Abstract The mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by 11 enzyme deficiencies, classified into seven types. Data on the birth prevalence of each MPS type are available for only a few countries, and the totality of cases may be underestimated. To determine the epidemiological profile of MPS in each Brazilian region, we analyzed data collected between 1982 and 2019 by a national reference laboratory and identified 1,652 patients. Using data between 1994 and 2018, the birth prevalence (by 100,000 live births) for MPS was 1.57. MPS II was the most common type of MPS in Brazil, and its birth prevalence was 0.48 (0.94 considering only male births). Regarding the number of cases per region, MPS II was the most frequent in the North and Center-West (followed by MPS VI), and also in the Southeast (followed by MPS I); MPS I and MPS II were the most common types in the South; and MPS VI was the most common in the Northeast (followed by MPS II). The differences observed in the relative frequencies of MPS types across Brazilian regions are likely linked to founder effect, endogamy, and consanguinity, but other factors may be present and need further investigation.