Clinical Subgroups in Bilateral Meniere Disease

• Tipo: Artigo em Revista Científica Internacional
• Data: 2016

Autores

Frejo, L (Autor) Outra; Soto Varela, A (Autor) Outra; Santos Perez, S (Autor) Outra; Aran, I (Autor) Outra; Batuecas Caletrio, A (Autor) Outra; Perez Guillen, V (Autor) Outra; Perez Garrigues, H (Autor) Outra; Fraile, J (Autor) Outra; Martin Sanz, E (Autor) Outra; Tapia, MC (Autor) Outra; Trinidad, G (Autor) Outra; Garcia Arumi, AM (Autor) Outra; Gonzalez Aguado, R (Autor) Outra; Espinosa Sanchez, JM (Autor) Outra; Marques, P (Autor) FMUP; Perez, P (Autor) Outra; Benitez, J (Autor) Outra; Lopez Escamez, JA (Autor) Outra

Revista

Título: Frontiers in Neurology

Vol. 7

ISSN: 1664-2295

Editora: Frontiers Media

Indexação

ISI Web of Knowledge - 79 Citações

Scopus - 94 Citações

Outras Informações

ID Authenticus: P-00M-55J

DOI: 10.3389/fneur.2016.00182

Abstract (EN): Meniere disease (MD) is a heterogeneous clinical condition characterized by sensorineural hearing loss, episodic vestibular symptoms, and tinnitus associated with several comorbidities, such as migraine or autoimmune disorders (AD). The frequency of bilateral involvement may range from 5 to 50%, and it depends on the duration of the disease. We have performed a two-step cluster analysis in 398 patients with bilateral MD (BMD) to identify the best predictors to define clinical subgroups with a potential different etiology to improve the phenotyping of BMD and to develop new treatments. We have defined five clinical variants in BMD. Group 1 is the most frequently found, includes 46% of patients, and is defined by metachronic hearing loss without migraine and without AD. Group 2 is found in 17% of patients, and it is defined by synchronic hearing loss without migraine or AD. Group 3, with 13% of patients, is characterized by familial MD, while group 4, that includes 12% of patients, is associated by the presence of migraine in all cases. Group 5 is found in 11% of patients and is defined by AD. This approach can be helpful in selecting patients for genetic and clinical research. However, further studies will be required to improve the phenotyping in these clinical variants for a better understanding of the diverse etiological factors contributing to BMD.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 10