The prevalence of myasthenia gravis (MG) among middle-aged and older patien
ts has increased. Patients with early-onset MG live longer than before, but
there is also an increase in late-onset MG (onset of the disease after the
age of 50 years in patients with no clinical or paraclinical evidence of a
thymoma). Epidemiological data support using the age of 50 years to separa
te early- and late-onset MG. The main immunological difference between earl
y- and late-onset MG is the presence of antibodies to muscle titin, which a
re detected in approximately 50% of patients with late-onset MG. Treatment
of late-onset MG has to be tailored both to the age of the patient and to t
he immunological findings of that particular form of MG.