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Anti-C1q antibodies in systemic lupus erythematosus
- Orbai, A-M;
- Truedsson, L;
- Sturfelt, G;
- Nived, O;
- Fang, H;
- Alarcón, GS;
- Gordon, C;
- Merrill, Jt;
- Fortin, PR;
- Bruce, IN;
- Isenberg, DA;
- Wallace, DJ;
- Ramsey-Goldman, R;
- Bae, S-C;
- Hanly, JG;
- Sanchez-Guerrero, J;
- Clarke, AE;
- Aranow, CB;
- Manzi, S;
- Urowitz, MB;
- Gladman, DD;
- Kalunian, KC;
- Costner, MI;
- Werth, VP;
- Zoma, A;
- Bernatsky, S;
- Ruiz-Irastorza, G;
- Khamashta, MA;
- Jacobsen, S;
- Buyon, JP;
- Maddison, P;
- Dooley, MA;
- Van Vollenhoven, RF;
- Ginzler, E;
- Stoll, T;
- Peschken, C;
- Jorizzo, JL;
- Callen, JP;
- Lim, SS;
- Fessler, BJ;
- Inanc, M;
- Kamen, DL;
- Rahman, A;
- Steinsson, K;
- Franks, AG;
- Sigler, L;
- Hameed, S;
- Pham, N;
- Brey, R;
- Weisman, MH;
- McGwin, G;
- Magder, LS;
- Petri, M
Published Web Location
https://doi.org/10.1177/0961203314547791Abstract
OBJECTIVE: Anti-C1q has been associated with systemic lupus erythematosus (SLE) and lupus nephritis in previous studies. We studied anti-C1q specificity for SLE (vs rheumatic disease controls) and the association with SLE manifestations in an international multicenter study. METHODS: Information and blood samples were obtained in a cross-sectional study from patients with SLE (n = 308) and other rheumatologic diseases (n = 389) from 25 clinical sites (84% female, 68% Caucasian, 17% African descent, 8% Asian, 7% other). IgG anti-C1q against the collagen-like region was measured by ELISA. RESULTS: Prevalence of anti-C1q was 28% (86/308) in patients with SLE and 13% (49/389) in controls (OR = 2.7, 95% CI: 1.8-4, p < 0.001). Anti-C1q was associated with proteinuria (OR = 3.0, 95% CI: 1.7-5.1, p < 0.001), red cell casts (OR = 2.6, 95% CI: 1.2-5.4, p = 0.015), anti-dsDNA (OR = 3.4, 95% CI: 1.9-6.1, p < 0.001) and anti-Smith (OR = 2.8, 95% CI: 1.5-5.0, p = 0.01). Anti-C1q was independently associated with renal involvement after adjustment for demographics, ANA, anti-dsDNA and low complement (OR = 2.3, 95% CI: 1.3-4.2, p < 0.01). Simultaneously positive anti-C1q, anti-dsDNA and low complement was strongly associated with renal involvement (OR = 14.9, 95% CI: 5.8-38.4, p < 0.01). CONCLUSIONS: Anti-C1q was more common in patients with SLE and those of Asian race/ethnicity. We confirmed a significant association of anti-C1q with renal involvement, independent of demographics and other serologies. Anti-C1q in combination with anti-dsDNA and low complement was the strongest serological association with renal involvement. These data support the usefulness of anti-C1q in SLE, especially in lupus nephritis.
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