Published online before print August 3, 2006, doi: 10.1161/01.STR.0000236500.15976.f3
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(Stroke. 2006;37:2375.)
© 2006 American Heart Association, Inc.
Research Reports |
Thyroid Autoimmunity and Spontaneous Cervical Artery Dissection
From the Dipartimento di Scienze Mediche e Chirurgiche, Stroke Unit, Neurologia Vascolare (A.P.) and the Dipartimento di Radiologia, I Radiologia (F.F.), Spedali Civili di Brescia, Brescia, Italia; the Dipartimento di Scienze Mediche e Chirurgiche, Clinica Neurologica (E.D., A.G., A.P.) and the Dipartimento di Scienze Mediche e Chirurgiche, Medicina Interna (G.M., A.G.), Università degli Studi di Brescia, Brescia, Italia; and the Dipartimento di Medicina di Laboratorio (G.R.), III Laboratorio di Analisi Chimico-Cliniche, Spedali Civili di Brescia, Italia.
Correspondence to Alessandro Pezzini, MD, Stroke Unit, Neurologia Vascolare, Spedali Civili di Brescia, P.le Spedali Civili, 1, 25100 Brescia, Italia. E-mail ale_pezzini{at}hotmail.com
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Abstract |
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Background and Purpose— The possibility that a disorder of immunity might have a role in the mechanism of local inflammatory alterations leading to spontaneous cervical artery dissection (sCAD) has been recently advocated.
Methods— We explored this hypothesis in a case-control study, including patients with sCAD (n=29) and patients with non-CAD ischemic stroke (non-CAD; n=29). Serum levels of antithyroperoxidase, antithyroglobulin, and antithyroid-stimulating hormone receptor antibodies, antinuclear antibodies, antineutrophil cytoplasmic antibodies, antidouble-stranded deoxyribonucleic acid antibodies, antiextractable nuclear antigen antibodies, rheumatoid factor, C3 and C4 complement fraction, and cryoglobulins were measured in all subjects.
Results— Antithyroid autoimmunity was found in 31.0% (9 of 29) of patients with sCAD and 6.9% (2 of 29) of patients with non-CAD ischemic stroke (P=0.041).
Conclusions— Autoimmunity may be involved in the process of local inflammation related to sCAD occurrence. The hypothesis that the arterial disease might be one phenotypic expression of a generalized activation of immunity warrants further investigations.
Key Words: cerebral infarction • dissection • thyroiditis, autoimmune
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Introduction |
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Increasing evidence supports the assumption that a general susceptibility state may be involved in the pathogenesis of spontaneous cervical artery dissection (sCAD) and that inflammation might have a role in this process. The epidemiology of sCAD with seasonal peaks in autumn and spring, the clinical observation that acute infections may act as triggering factors, the finding of elevated levels of inflammatory markers in serum of patients with sCAD,1 and the pathologic evidence of inflammatory infiltrates in the wall of intracranial and coronary dissected arteries2,3 suggest that local inflammatory alterations might be a crucial step in the cascade of events leading to sCAD in predisposed individuals. Whether this implicates the activation of specific immune-mediated mechanisms is unknown at present. Recently, the hypothesis of an association between sCAD and thyroid disease has been suggested in sparse case reports4 prompting speculation on the pathogenic role of immunity in such a link. In fact, apart from the well-known association of thyroid dysfunction with vascular diseases, thyroid autoimmunity may lead to peripheral vascular damage independently on thyroid function. To explore the hypothesis of this relation, we search for thyroid autoimmunity, the most common of the autoimmune conditions, in a prospective case-control study, including patients with sCAD and patients with cerebral infarct of different pathogenesis (non-CAD).
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Subjects and Methods |
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Patients consecutively admitted to our department during a 24-month period were included. The diagnosis of CAD was confirmed by magnetic resonance imaging-magnetic resonance angiography or conventional angiography.5 Dissections occurring as an immediate consequence of a major trauma were labeled "traumatic" and excluded. Patients with non-CAD ischemic stroke, selected from those who experienced first-ever acute cerebral ischemia, after exclusion of the subgroup with CAD-related infarction, served as controls. Only subjects with computed tomography and/or magnetic resonance image-proven cerebral infarction, comparable to sCAD patients on sex and age (±5 years), were recruited.
In all subjects, serum levels of antithyroperoxidase and antithyroglobulin antibodies were measured by microparticle enzyme immunoassay (Abbott Diagnostics) and antithyroid-stimulating hormone receptor antibodies by radioreceptor assay (Brahms). Serum levels of free-thyroxin, free-triiodothyronine, and thyroid-stimulating hormone were measured by routine hospital assays. Antinuclear antibodies and the perinuclear and cytoplasmic patterns of antineutrophil cytoplasmic antibodies were assessed by indirect immunofluorescence (Bio-Rad); antidouble-stranded deoxyribonucleic acid antibodies by radio immunosorbent assay (IBL); antiextractable nuclear antigen antibodies by enzyme-linked immunosorbent assay (Innogenetics); rheumatoid factor and C3 to C4 complement fraction by nephelometry (Dade Behring); and cryoglobulins by standard procedure.
In subjects with raised levels of antithyroid antibodies, impaired thyroid function, or both, thyroid echotomography was performed to determine thyroid morphology using equipment with a 12-MHz linear-array transducer. The diagnosis of autoimmune thyroiditis (AT) was based on positive serum titers of antithyroperoxidase, antithyroperoxidase and antithyroglobulin, or both, and/or on the echographic pattern of the thyroid gland on ultrasound of diffuse or irregular hypoechogenicity.6 Graves disease was diagnosed on the basis of serum positivity for antithyroid-stimulating hormone receptor antibodies with clinical or subclinical hyperthyroidism accompanied by high I131 thyroid uptake.
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Results |
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The study group was composed of 29 patients with sCAD (male/female, 15/14; median age, 44 years; range, 21 to 64 years) and 29 patients with non-CAD (male/female, 15/14; median age, 45 years; range, 26 to 64 years). Large-vessel or small-vessel atherosclerosis was the presumed cause of infarct in seven non-CAD cases (24.1%), cardiac/transcardiac embolism in 12 cases (41.4%), and other etiologies in the remaining 10 cases (34.5%). Increased levels of thyroid autoantibodies were found in 9 (31.0%) patients with sCAD. Biochemical and ultrasonographic findings were consistent with AT in 7 of these 9 patients. Five were euthyroid with normal circulating thyroid hormone levels, whereas 1 was classified as having a subclinical hypothyroidism and underwent thyroxin therapy. In 1 patient (no. 2), the diagnosis of AT had been made 13 years before sCAD occurrence, and he was being treated with hormone replacement therapy (100 µg thyroxine daily) because of overt hypothyroidism. The remaining 2 patients had a 6-year and 1-year history, respectively, of treatment for Graves disease. Of these 9 subjects, 6 were also antinuclear antibodies-positive (4 with a "speckled" pattern), 1 had antibodies to antidouble-stranded deoxyribonucleic acid, and 1 was positive for perinuclear antineutrophil cytoplasmic antibodies. In 1 patient (no. 7), the diagnosis of Pemphigus vulgaris had been made 3 years before the vascular event (Table).
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Only 2 (6.9%) subjects with non-CAD ischemic stroke had positive antithyroid antibodies titers (P=0.041). AT was the presumed diagnosis in these cases (not shown).
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Discussion |
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Thyroid autoimmunity is the paradigm for autoimmune diseases. In the present study, we observed a higher prevalence of thyroid autoimmunity in the group of patients with sCAD than in the group of patients with non-CAD ischemic stroke, and than that observed in the general population, in which it occurs in a percentage of 10% to 12%. Although the study design does not allow elucidation of the mechanism whereby thyroid autoimmunity is associated with sCAD, our findings suggest the hypothesis of a specific pathogenic relation of these 2 entities. One possible interpretation for such a link is that immunologic mechanisms may contribute to the chronic vascular damage underlying arterial dissection. From this point of view, autoimmunity should be considered a biologic determinant of sCAD. Actually, although AT is traditionally labeled as an "organ-specific" autoimmune disease, a systemic immune dysregulation has been suggested based on the demonstration of activated phenotypes in the peripheral blood of patients with this disease.7 Therefore, sCAD might be one phenotypic expression of a generalized activation of immunity. According to this view, it might be that antithyroid antibodies do not directly contribute to the pathogenic process, but only serve as indicators of autoimmunity. Alternatively, crossreactivity between thyroid gland and vascular tissues might be operant.
Although a direct relation between AT and sCAD seems the most likely mechanism, the alternative hypothesis of a reverse causation cannot be excluded a priori. In this regard, the activation of the immune process should be interpreted as the consequence of a primary disorder of the arterial wall.
Apart from the exact mechanism, a number of indirect evidence provides arguments to support our hypothesis of a link between sCAD and autoimmunity. First, inflammatory infiltrates have been described in a substantial percentage of spontaneous coronary dissections3 at times in combination with cystic medial necrosis. Whether the inflammatory reaction is the cause or the consequence of the dissecting process is difficult to determine from histopathologic changes alone. However, the absence of such infiltrates in cases of iatrogenic-traumatic dissections, the reported association with immune disorders, also including AT,8 and the rapid disappearance of these arterial abnormalities after immunosuppressive treatment in some cases9 support the concept of a direct relation between autoimmunity and dissection. Second, autoimmunity has been proposed as a pathogenic mechanism of some disease entities such as segmental arterial mediolysis, related to sCAD occurrence.4,10 In line with this hypothesis is the observation that proinflammatory cytokines such as tumor necrosis factor-
and interleukin-1ß, which can be activated by immune mechanisms, may induce the proteolytic process and contribute to the degradation of the extracellular matrix proteins, a crucial process in the pathogenesis of sCAD.11 Finally, the hypothesis that genetically determined susceptibility to inflammatory stimuli might predispose to sCAD has been recently advocated.12,13
In conclusion, our results provide arguments to the hypothesis that the activation of an immune-mediated process may be involved in the pathogenesis of sCAD probably by determining an underlying susceptibility state to disease occurrence and justify further investigations to clarify the nature of these mechanisms.
Received May 19, 2006; accepted June 9, 2006.
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References |
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