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AB0437 Predictivity of serum biomarkers for disease activity in a prospectively followed-up takayasu arteritis cohort: is serum amyloid a protein better than conventional acute phase markers?
  1. A. Omma1,
  2. B. Erer1,
  3. N. Alpay1,
  4. N. Gurel Polat2,
  5. A. Gul1,
  6. M. Inanc1,
  7. S. Kamali1
  1. 1Department Of Internal Medicine, Division Of Rheumatology
  2. 2Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey

Abstract

Background Takayasu arteritis (TA) is a chronic vasculitis with an indolent course. Reliable diagnostic and activity markers have not yet been demonstrated.

Objectives We aimed to evaluate the predictivity of conventional acute phase proteins (ESR, CRP) and other non-conventional inflammation and endothelial activity markers such as serum amilod A (SAA) protein, interleukin-6 (IL-6) and von Willebrand factor (vWF) in a TA cohort, prospectively followed-up.

Methods Fourty-eight TA patients diagnosed according to ACR 1990 criteria and followed-up ≥ 6 months, 37 patients with granulomatosis with poliangiitis (GPA) diagnosed according to ACR 1990 criteria and 28 healthy controls (HC) were included into the study. Demographic and clinical features of TA, GPA and HCs were recorded into a predefined protocol. ESR, CRP, SAA, IL-6 and vWF levels were analysed initially in all groups and at 3rd, 6th, 12th months visits in TA and GPA groups. Westergreen method for ESR, nephelometric assay for CRP, SAA and ELISA method for IL-6 and vWF were used. Disease activity was evaluated by Kerr criteria for TA and BVAS2003 for GPA. TA and GPA cohorts were stratified to the subgroups according to the activity. Comparisons were performed by Mann Whitney U test in subgroups. ROC curve analysis was used to identify the sensitivity and specificity of laboratory parameters for predicting activity.

Results Mean age and disease duration were found as 40±13 yrs, 121±115 mo for TA, 47±13 yrs, 65±42 mo for GPA and mean age was 38±9 for HCs. Females were significantly high in TA cohort (%) when compared to GPA (%) (p<0,001). The percentage of active disease was 40%, 31%, 35%, 29% for TA and 32%, 19%, 11%, 13% for GPA at initial 3rd, 6th and 12th months, respectively. ESR, CRP and SAA levels were significantly high in active TA at the initial, 3rd and 6th months visits (41±20 vs 21±12, p=<0.001 for ESR, 20±20 vs 6±10 p=<0.001 for CRP, 23±23 vs 12±29, p=0.001 for SAA at initial visit, 41±19 vs 24±17, p=0.002 for ESR, 26±28 vs 6±8, p= 0.004 for CRP, 38±59 vs 12±17, p=0.02 for SAA at the 3rd visit, 41±17 vs 24±12, p= <0.001 for ESR, 16±18 vs 4±5, p= 0.01 for CRP, 22±30 vs 10±16, p=0.002 for SAA at the 6th visit). SAA was the only marker that demonstrate the significance between subgroups at the 12th month (12±10 vs 8±11, p= 0.007). In active GPA subgroup, SAA and vWF at the 3rd visit and vWF at the 6th visit were found significantly high compared to inactive patients. Sensitivity and specificity were found as 88-70%, 79-84% for ESR levels of 35 mm/h, 83-65%, 86-84% for CRP levels of 5-8 mg/L 72-50%, 90-80% for SAA levels of 10-11 mg/L at the initial and 6th months visits in TA cohort. At the 12th month visit, SAA levels of 9 mg/L, was the only marker reaching the significant sensitivity (50%) and spesificity (83%) for predicting activity.

References In a well established and prospective cohort of TA, SAA has found to be a comparable sensitivity and specificity with ESR and CRP for predicting activity. It’s been observed that sensitivity of ESR, CRP had a trend towards to decrease in time which could be related to the decreasing activity during the follow-up. SAA was the only laboratory parameter which maintained its specificity in contrast to conventional biomarkers.

Disclosure of Interest None Declared

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