Urine and Plasma Complement Ba Levels During Disease Flares in Patients With Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis

被引:3
作者
Almaani, Salem [1 ,14 ]
Song, Huijuan [1 ]
Suthanthira, Meshora [1 ]
Toy, Christopher [2 ]
Fussner, Lynn A. [1 ]
Meara, Alexa [1 ]
Nagaraja, Haikady [1 ]
Cuthbertson, David [3 ]
Khalidi, Nader A. [4 ]
Koening, Curry L. [5 ]
Langford, Carol A. [6 ]
Mcalear, Carol A. [7 ]
Moreland, Larry W. [8 ]
Pagnoux, Christian [9 ,10 ]
Seo, Philip [11 ]
Specks, Ulrich [12 ]
Sreih, Antoine G. [7 ]
Warrington, Kenneth J. [12 ]
Monach, Paul A. [13 ]
Merkel, Peter A. [7 ]
Rovin, Brad [1 ]
Birmingham, Daniel [1 ]
机构
[1] Ohio State Univ, Wexner Med Ctr, Dept Med, Columbus, OH USA
[2] Colorado State Univ, Dept Soil & Crop Sci, Ft Collins, CO USA
[3] Univ S Florida, Hlth Informat Inst, Tampa, FL USA
[4] McMaster Univ, St Josephs Healthcare Hamilton, Hamilton, ON, Canada
[5] UT Hlth Austin, Div Rheumatol, Austin, TX USA
[6] Cleveland Clin, Div Rheumatol, Cleveland, OH USA
[7] Univ Penn, Div Rheumatol, Philadelphia, PA USA
[8] Univ Colorado, Div Rheumatol & Clin Immunol, Denver, CO USA
[9] Univ Toronto, Mt Sinai Hosp, Div Rheumatol, Toronto, ON, Canada
[10] Univ Hlth Network, Univ Toronto, Toronto, ON, Canada
[11] Johns Hopkins Med, Div Rheumatol, Baltimore, MD USA
[12] Mayo Clin, Mayo Clin Coll Med, Dept Med, Rochester, MN USA
[13] Vet Affairs Boston Healthcare Syst, Boston, MA USA
[14] Ohio State Univ, Div Nephrol, Wexner Med Ctr, Suite 4100,1664 Neil Ave, Columbus, OH 43201 USA
来源
KIDNEY INTERNATIONAL REPORTS | 2023年 / 8卷 / 11期
关键词
ANCA-associated vasculitis; biomarker; complement; ACTIVATION; PATHWAY;
D O I
10.1016/j.ekir.2023.08.017
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Although the alternative complement pathway has been implicated in the pathogenesis of antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV), the specific nature of its involvement is unclear. This study measured levels of urine and plasma complement fragment Ba at multiple time points in a group of patients with AAV.Methods: The complement fragment Ba was measured by enzyme-linked immunosorbent assay in serial urine and plasma samples from 21 patients with AAV who developed a renal flare, 19 who developed a nonrenal flare, and 20 in long-term remission. Urine Ba levels were corrected for urine creatinine con-centration. Changes in Ba levels were modeled using mixed linear-effect models. A logistic regression model was fit to predict a renal flare using Ba levels at the time of flare versus the nonrenal flare and long-term remission groups.Results: Data from 60 patients with AAV were used for this analysis; 53% were male, 93% were White, and 74% had antiproteinase3-ANCA. Urine Ba levels increased at renal flare (P < 0.001) but remained stable during a nonrenal flare or long-term remission. Plasma Ba levels were stable over time in all groups. Urine Ba levels predicted a renal flare with an area under the curve of 0.76 (P < 0.001), with a cutoff of 12.53 ng/ mg urine creatinine yielding a sensitivity of 76.2% and a specificity of 68.4%.Conclusion: Urine Ba levels, but not plasma Ba levels, are increased at the time of a renal flare in AAV, suggesting intrarenal complement activation and highlighting the potential use of this biomarker for surveillance of active renal vasculitis.
引用
收藏
页码:2421 / 2427
页数:7
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