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. Author manuscript; available in PMC: 2017 Dec 1.
Published in final edited form as: Cerebellum. 2016 Dec;15(6):663–679. doi: 10.1007/s12311-015-0728-y

Table 1.

Current consensus criteria for the diagnosis of Multiple System Atrophy (MSA), according to Gilman et al. 2008.1

Definite MSA Autopsy-confirmed case with neuropathologic evidence of widespread and abundant CNS α-synuclein–positive glial cytoplasmic inclusions in association with striatonigral and/or olivopontocerebellar neurodegeneration
Probable MSA Sporadic, progressive, adult (>30 years) -onset disease characterized by
  • Autonomic failure involving

    • Urinary incontinence (with erectile dysfunction in males); OR

    • Orthostatic blood pressure drop of at least 30 points systolic or 15 points diastolic within 3 minutes after standing from a recumbent position

AND one of the following predominant motor features
  • Poorly levodopa-responsive parkinsonism (defined as bradykinesia with rigidity, tremor, or postural instability); OR

  • A cerebellar syndrome consisting of gait ataxia with cerebellar dysarthria, limb ataxia, or cerebellar oculomotor dysfunction

Possible MSA Sporadic, progressive, adult (>30 years) -onset disease characterized by
  • Parkinsonism (defined as bradykinesia with rigidity, tremor, or postural instability); OR

  • A cerebellar syndrome consisting of gait ataxia with cerebellar dysarthria, limb ataxia, or cerebellar oculomotor dysfunction

AND at least one of the following symptoms that suggest autonomic dysfunction including
  • Urinary urgency

  • Urinary frequency or incomplete bladder emptying

  • Erectile dysfunction in males

  • Significant orthostatic blood pressure drop not meeting the criterion for Probable MSA

AND at least one of the following additional features for MSA-P or MSA-C
  • MSA-P or MSA-C

    • Babinski sign with hyperreflexia

    • Stridor

  • MSA-P

    • Rapidly progressive parkinsonism

    • Poor response to levodopa

    • Postural instability within 3 years of motor onset

    • Gait ataxia, cerebellar dysarthria, limb ataxia, or cerebellar oculomotor dysfunction

    • Dysphagia within 5 years of motor onset

    • Atrophy on MRI of putamen, middle cerebellar pedunle, pons, or cerebellum

    • Hypometabolism on FDG-PET in putamen, brainstem, or cerebellum

  • MSA-C

    • Parkinsonism (bradykinesia and rigidity)

    • Atrophy on MRI of putamen, middle cerebellar peduncle, or pons

    • Hypometabolism on FDG-PET in putamen

    • Presynaptic nigrostriatal dopaminergic denervation on SPECT or PET