Role of inflammatory markers in Takayasu arteritis disease monitoring

Document Type

Article

Abstract

BACKGROUND: Takayasu arteritis (TA) is an idiopathic large-vessel vasculitis that can result in significant morbidity and mortality secondary to progressive stenosis and occlusion. Monitoring disease progression is crucial to preventing relapse, but is often complicated by the lack of clinical symptoms in the setting of active disease. Although acute phase reactants such as ESR and CRP are generally used as an indicator of inflammation and disease activity, mounting evidence suggests that these markers cannot reliably distinguish active from inactive TA. CASE PRESENTATION: We report a 24-year-old Hispanic female with a 5-year history of TA who presented with stroke-like symptoms and evidence of left MCA occlusion on imaging, despite a history of decreasing inflammatory markers. CTA revealed complete occlusion of the left common carotid artery, left subclavian, and left MCA from their origins. It also revealed a striking compensatory circulation supplying the left anterior circulation as well as the left subclavian as a response to progressive stenosis. CONCLUSION: Monitoring ESR and CRP levels alone may not be a reliable method to evaluate disease progression in patients with TA, and should be taken in context with both patient's clinical picture and the imaging. We recommend that serial imaging be performed regularly in the setting of active disease to monitor progression and allow for immediate therapy in response to evidence of disease advancement, with a relaxation of the imaging interval once the disease is presumed inactive.

Medical Subject Headings

Biomarkers (blood); Blood Sedimentation; C-Reactive Protein (analysis); Carotid Stenosis (etiology, therapy); Collateral Circulation (physiology); Female; Humans; Inflammation Mediators (blood); Ischemia (etiology); Monitoring, Physiologic; Stroke (etiology); Takayasu Arteritis (diagnosis, physiopathology); Young Adult

Publication Date

3-28-2014

Publication Title

BMC neurology

E-ISSN

1471-2377

Volume

14

First Page

62

PubMed ID

24678735

Digital Object Identifier (DOI)

10.1186/1471-2377-14-62

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