| Elevated
Autoimmune Antibody Titers in Cervical Dystonia Versus Controls
D.D. Duane, M. Clark, L. Gottlob
Arizona
Dystonia Institute/Arizona State University
Scottsdale/Tempe,
Arizona
Objective: To
determine if elevated serologic titers of a variety of autoimmune
antibodies is more frequent in cervical dystonia patients as contrasted
with controls.
Background:
Although genetic mechanisms are conceded to predominate in the genesis
of focal, as well as in generalized dystonia, the specific etiology
and pathophysiology of focal dystonia remains unknown. Other neurologic
disorders with demonstrated autoimmune etiologic mechanisms were
initially suspected as autoimmune because (1) there was an increased
association with conditions characterized by disordered immune mechanisms
and/or (2) by the presence of either specific neurotoxic antibodies
or of other autoimmune antibodies. Prior reports have suggested
that there is an increased rate of autoimmune disorders in those
with focal dystonia. Whether there is an increased rate of autoimmune
antibodies in cervical dystonia is not clear as a prior report suggested
only a borderline significance (p = 0.1) rate of elevated autoimmune
antibody titers in women with cervical dystonia (CD) versus female
controls.
Design/Methods:
Retrospective analysis of 254 cervical dystonia patients (188 female,
mean age 55 years) serially evaluated between 01/88 and 07/94 by
a protocol which included serologic assay of antinuclear (ANA),
thyroid microsomal and thyroglobulin antibodies (Thyroid), rheumatoid
factor (RhF) and a miscellaneous group of three gastrointestinal
antibodies (Gut) and serum protein electrophoresis (SPEP). Results
were contrasted with 137 control (88 female, mean age 52 years)
evaluated during the same time frame with the same serologic assay
profile, suffering with subacute or chronic spine pain. Positive
titers were ANA > 1:80; thyroid microsomal > 1:400, thyroglobulin
> 42 ng/ml; RhF > 39 ng/mi; Gut-antiparietal antibody >
1:80, antismooth muscle > 1:80, antimitochondrial > 1:80 and
gamma globulin >1.7 gm/dl. Statistical analysis was by G test.
Results: Positive
ANA: CD -- 45 female (24%), 15 male (23%), Control -- 9 female (10%),
4 male (8%), p =.005. Positive thyroid antibodies: CD -- 20 female
(10.6%), 5 male (7.5%), Control -- 5 female (5.7%), 2 male (4%),
p =.1. Positive RhF: CD -- 11 female (5.9%), 2 male (3%), Control
-- 10 female (11.4%), 1 male (2%), p-NS. Gut: CD -- 7 female (3.7%),
3 male (4.5%), Control -- 1 female (1.1%), 2 male (4.1%), p = NS.
Conclusions:
CD patients do generate elevated levels of ANA and possibly thyroid
antibodies. Whether this observation represents a link to an autoimmune
etiology or an additional expression of the genetics of focal dystonia
requires further analysis.
Poster
presentation, American Academy of Neurology, Seattle, Washington.
May 11, 1995. Duane D, Clark M, Gottlob L: Elevated autoimmune antibody
titers in cervical dystonia versus controls. Neurology, 1995; (supplement
4):456.
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