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. Author manuscript; available in PMC: 2010 Mar 12.
Published in final edited form as: Auton Neurosci. 2008 Oct 31;146(1-2):3–7. doi: 10.1016/j.autneu.2008.09.005

Table 1.

Ganglionic AChR antibody in patients with dysautonomia and other disorders*

Diagnostic Group % seropositive Antibody levels Reference
Autonomic disorders
Subacute AAG 40 – 50% 0.5 – 41.0 nM/L (Vernino et al., 2008; Vernino et al., 2000)
Chronic AAG 30 – 40%** 0.2 – 5.0 nmol/L (Klein et al., 2003)
Paraneoplastic AAG 10 – 20% 0.2 – 20.0 nmol/L (Vernino et al., 2000)
Postural tachycardia syndrome (POTS) 10 – 15% < 0.25 nmol/L (Thieben et al., 2007)
Idiopathic gastrointestinal dysmotility 5 – 10% < 0.4 nmol/L (Vernino et al., 2000)
Diabetic autonomic neuropathy < 10%
Multiple system atrophy (Shy-Drager) 0
Other disorders
Lambert-Eaton syndrome 5 – 10% 0.06 – 0.4 nmol/L (Vernino et al., 2000)
Myasthenia gravis without thymoma 3% < 0.25 nmol/L (Vernino et al., 2008)
Paraneoplastic disorders with thymoma 15 – 20% 0.06 – 2.0 nmol/L (Vernino et al., 2004b)
Paraneoplastic disorders with SCLC 3 – 5%
*

None of over 200 healthy control subjects were seropositive for ganglionic AChR antibodies.

**

The exact frequency is not known since antibody status may affect case definition