Insights into the Classification of Myasthenia Gravis

نویسندگان

  • Tetsuya Akaishi
  • Takuhiro Yamaguchi
  • Yasushi Suzuki
  • Yuriko Nagane
  • Shigeaki Suzuki
  • Hiroyuki Murai
  • Tomihiro Imai
  • Masakatsu Motomura
  • Kazuo Fujihara
  • Masashi Aoki
  • Kimiaki Utsugisawa
چکیده

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.

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عنوان ژورنال:

دوره 9  شماره 

صفحات  -

تاریخ انتشار 2014