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Clinical Studies |
Centro per lo Studio, Prevenzione, Diagnosi e Cura delle Tireopatie, Istituto di Oftalmologia (E.S., F.N., C.M.) and Radiologia (F.F.), Università di Parma, Parma, Italy; and Thyroid-Eye Research Program, Allegheny-Singer Research Institute (J.R.W.), Pittsburgh, Pennsylvania 15212-4772
Address all correspondence and requests for reprints to: Dr. Mario Salvi, Cattedra di Endocrinologia, Università di Parma, via Gramsci 14, 43100 Parma, Italy.
In the present study we have recorded visual evoked cortical potentials
(VECP) in 88 patients affected by autoimmune thyroid disease and
thyroid-associated ophthalmopathy (TAO) without clinical signs of optic
neuropathy. At the time of ophthalmological examination, 37 of these
patients were hyperthyroid, 41 were euthyroid, and 8 were hypothyroid;
2 were not assessed. Twenty-nine normal subjects served as controls. We
performed pattern reversal visual stimulation and recorded the
amplitude and latency of the cortical electric response at 100 ms (P100
wave). There were no differences in the mean P100 amplitude of TAO
patients and normal subjects. The mean P100 latency in patients was
105.6 ± 0.5 ms, significantly higher than that in normal subjects
(102.0 ± 0.5 ms; P < 0.00003). Latency in
euthyroid patients did not differ from that in either hypo- or
hyperthyroid patients. The VECP test was positive (latency,
110.0 ms)
in 21 (23.8%) TAO patients. In patients with proptosis greater than 21
mm, latency was 106.7 ± 0.7 ms, significantly higher than that in
patients with normal Hertel measurements (104.3 ± 0.6 ms;
P < 0.01). Latency was not increased in patients
with acute inflammatory signs compared to those with inactive eye
disease and in patients with altered extrinsic motility. In patients
with an abnormal visual field study, the mean latency was 110.3 ±
1.5 ms, significantly higher than that in patients with a normal visual
field (104.7 ± 0.4; by t test,
P < 0.000003). In conclusion, we observed a
prolongation of the latency of the evoked cortical response in patients
with TAO without subjective visual complaints and without optic nerve
compression. We believe that the study of VECP in TAO is complementary
to the study of the visual field in identifying early optic nerve
dysfunction in the absence of decreased visual acuity.
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