Cargando…

Insights into the Classification of Myasthenia Gravis

BACKGROUND AND PURPOSE: Myasthenia gravis (MG) is often categorized into thymoma-associated MG, early-onset MG with onset age <50 years, and late-onset MG with onset age ≥50 years. However, the boundary age of 50 years old between early- and late-onset MG remains controversial, and each category...

Descripción completa

Detalles Bibliográficos
Autores principales: Akaishi, Tetsuya, Yamaguchi, Takuhiro, Suzuki, Yasushi, Nagane, Yuriko, Suzuki, Shigeaki, Murai, Hiroyuki, Imai, Tomihiro, Motomura, Masakatsu, Fujihara, Kazuo, Aoki, Masashi, Utsugisawa, Kimiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156422/
https://www.ncbi.nlm.nih.gov/pubmed/25192469
http://dx.doi.org/10.1371/journal.pone.0106757
Descripción
Sumario:BACKGROUND AND PURPOSE: Myasthenia gravis (MG) is often categorized into thymoma-associated MG, early-onset MG with onset age <50 years, and late-onset MG with onset age ≥50 years. However, the boundary age of 50 years old between early- and late-onset MG remains controversial, and each category contains further subtypes. We attempted to classify MG from a statistical perspective. METHODS: We analyzed 640 consecutive MG patients using two-step cluster analysis with clinical variables and discrimination analysis, using onset age as a variable. RESULTS: Two-step cluster analyses categorized MG patients into the following five subtypes: ocular MG; MG with thymic hyperplasia (THMG); generalized anti-acetylcholine receptor antibody (AChR-Ab)-negative MG; thymoma-associated MG; and generalized AChR-Ab-positive (SP) MG without thymic abnormalities. Among these 5 subtypes, THMG showed a distribution of onset age skewed toward a younger age (p<0.01), whereas ocular MG and SPMG without thymic abnormalities showed onset age skewed toward an older age (p<0.001 and p<0.0001, respectively). The other 2 subtypes showed normal distributions. THMG appeared as the main component of early-onset MG, and ocular MG and SPMG without thymic abnormalities as the main components of late-onset MG. Discrimination analyses between THMG and ocular MG and/or SPMG without thymic abnormalities demonstrated a boundary age of 45 years old. CONCLUSIONS: From a statistical perspective, the boundary age between early- and late-onset MG is about 45 years old.