Objectives: 1) To determine the degree and distribution and quantitate the
severity of autonomic impairment in painful neuropathy (PN). 2) To assess t
he role of autonomic testing in evaluating PN. Methods: The authors studied
92 patients with PN (60 women and 32 men, age 56.9 +/- 12.4 years) using:
1) autonomic reflex testing (ART), Quantitative Sudomotor Axon Reflex Test
(QSART), cardiac-vagal, head-up tilt, and surface skin temperature; 2) auto
nomic symptoms questionnaire; 3) nerve conduction (NCS) and laboratory stud
ies; 4) quantitative sensory testing; 5) skin biopsy; and 6) Composite Auto
nomic Symptoms Score (CASS) scale to grade ART results from 0 (normal) to 1
0 (autonomic failure). Results: Autonomic involvement in PN had characteris
tic features. Main symptoms were pain, secretory and skin vasomotor signs,
hypertension, and impotence. ART results were abnormal in 86 (93.5%) (CASS
< 4), QSART in 67 (72.8%), cardiac-vagal index in 58 (63%), skin temperatur
e in 51 (55.4%), orthostatic hypertension in 39 (42.3%), and family history
of PN in 26 (21%) of patients. Group 1 (abnormal NCS) (n = 45) had more se
vere ART and sensory abnormalities than the Group 2 (normal NCS) (n = 47):
1) CASS 2.0 <plus/minus> 0.96 vs 1.55 +/- 0.88 (p < 0.01), cardiac-vagal in
dex (p < 0.02), skin temperature (p < 0.02), hypertension (p < 0.03), cooli
ng (p < 0.002), and vibration (p < 0.0005) thresholds. Conclusions: Autonom
ic symptoms in painful neuropathy are predominantly cholinergic and form a
unique constellation of features that are distinct from other autonomic neu
ropathies.