Anti-C1q antibodies antedate patent active glomerulonephritis in patients with systemic lupus erythematosus
© Meyer et al.; licensee BioMed Central Ltd. 2009
Received: 28 January 2009
Accepted: 10 June 2009
Published: 10 June 2009
Autoantibodies against C1q correlate with lupus nephritis. We compared titers of anti-C1q and anti-dsDNA in 70 systemic lupus erythematosus patients with (n = 15) or without (n = 55) subsequent biopsy-proven lupus nephritis.
The 15 patients with subsequent lupus nephritis had anti-C1q assays during clinical flares (mean Systemic Lupus Erythematosus Disease Activity Index (SLEDAI), 10.0 ± 4.7; range, 3 to 22) before the diagnosis of lupus nephritis (median, 24 months; range 3 to 192). Among the 55 others, 33 patients had active lupus (mean SLEDAI, 10.3 ± 6.2; range, 4 to 30) without renal disease during follow-up (median 13 years; range 2 to 17 years) and 22 had inactive lupus (mean SLEDAI, 0; range, 0 to 3).
Anti-C1q titers were elevated in 15/15 (100%) patients who subsequently developed nephritis (class IV, n = 14; class V, n = 1) and in 15/33 (45%) patients without renal disease (P < 0.001). The median anti-C1q titer differed significantly between the groups (P = 0.003). Anti-C1q titers were persistently positive at the time of glomerulonephritis diagnosis in 70% (7/10) of patients, with no difference in titers compared with pre-nephritis values (median, 147 U/ml; interquartile range (IQR), 69 to 213 versus 116 U/ml; 50 to 284, respectively). Titers decreased after 6 months' treatment with immunosuppressive drugs and corticosteroids (median, 76 U/ml; IQR, 33 to 106) but remained above normal in 6/8 (75%) patients. Anti-dsDNA antibodies were increased in 14/15 (93.3%) patients with subsequent nephritis and 24/33 (72.7%) patients without nephritis (P = ns). Anti-C1q did not correlate with anti-dsDNA or the SLEDAI in either group.
Anti-C1q elevation had 50% positive predictive value (15/30) and 100% (18/18) negative predictive value for subsequent class IV or V lupus nephritis.
Active proliferative glomerulonephritis is a serious manifestation of systemic lupus erythematosus (SLE) that may exist at disease onset or may develop later on during a flare. Clinical nephritis develops in about 50% of patients with SLE. Early diagnosis and rapid treatment of lupus nephritis are crucial to improving survival in SLE patients . The prognostic significance of lupus nephritis indicates a need for identifying early biomarkers that predict nephritis development [2–4].
A major pathogenic hypothesis is that SLE involves defective renal clearance of immune complexes. Among immunological parameters, consumption of the early components of the classical complement pathway, such as C1q and C4, is strongly associated with the development of active SLE . Low C1q levels, although occasionally caused by a rare genetic abnormality, are usually related to consumption by immune complexes such as dsDNA–anti-dsDNA or nucleosomes–antinucleosomes [6, 7]. Another cause of low C1q levels is the presence of anti-C1q antibodies with the formation of C1q/anti-C1q immune complexes . Anti-C1q antibodies have been described in patients with SLE [9–11] or other autoimmune diseases [12, 13]. Their correlations with hypocomplementemia and glomerulonephritis suggest that anti-C1q may play a pathogenic role [14, 15].
The aims of the present study were to determine the prevalence of anti-C1q antibodies in SLE patients with or without lupus nephritis after a long follow-up period and to test the predictive value of the anti-C1q assay for subsequent lupus nephritis. We also compared anti-C1q versus anti-dsDNA antibodies (another candidate for predicting lupus nephritis) regarding their ability to identify patients at high risk for lupus nephritis [2, 16–19].
Materials and methods
In this single-center retrospective study, 70 adults meeting at least four of the 11 American College of Rheumatology criteria for the classification of SLE  were recruited. These 70 patients were chosen among 115 SLE patients followed longitudinally by one of the authors (OCM). Patients were selected based on the availability of stored serum samples.
In the 15 patients with lupus nephritis, we had stored (-20°C) serum samples obtained at least 3 months before the onset of clinical manifestations of nephritis, at a time when the disease was active (Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) ≥ 4). Clinical nephritis was suspected if urinalysis showed proteinuria >0.5 g/dl on a 24-hour urine collection and/or hematuria or cellular casts with or without increased serum creatinine. Renal biopsies were performed for all 15 patients with clinical nephritis. The findings were classified according to the World Health Organization and International Society of Nephrology/Renal Pathology Society . The renal disease was class IV in 14 patients and class V in one patient.
Characteristics of patients with systemic lupus erythematosus
Active lupus with nephritis (n = 15)
Active lupus without nephritis (n = 33)
Inactive lupus without nephritis (n = 22)
Age at serum sampling (years)
19 to 58
17 to 48
20 to 76
Duration of SLE (years) at serum sampling
0.25 to 36
0.1 to 14.1
1.1 to 49
Duration of follow-up (years) (from SLE diagnosis to last visit)
5.9 to 23
2 to 17
4 to 52
SLEDAI at first serum sampling (points)
0 to 3
Patients with class IV or class III glomerulonephritis were treated with either intermittent intravenous cyclophosphamide infusions (0.6 g/m2/infusion) (13 patients) or oral mycophenolate mofetil (two patients) and with high-dose prednisolone (1 mg/kg/day) with or without initial intravenous methylprednisolone pulses (1 g). The single patient with class V glomerulonephritis also had central nervous system involvement, and was given intermittent intravenous cyclophosphamide infusions (12 infusions in all) after an incomplete response to azathioprine and high-dose oral corticosteroids.
In 11 of the 15 patients with nephritis, we obtained the anti-C1q and anti-dsDNA titers at the time of renal biopsy (n = 10) and/or after 6 months' immunosuppressive treatment (and: n = 7/ or: n = 1). Of the eight patients whose anti-C1q status was determined after immunosuppressive treatment, three patients were in complete remission and five patients were in partial remission of the nephritis. Partial remission was defined as any of the following: decrease in urinary protein excretion by >50% and to <3 g/day with a serum albumin level of ≥ 30 g/l, and either stable renal function or a serum creatinine decrease to <130 μmol/l for patients whose baseline serum creatinine was 130 to 260 μmol/l. (None of the patients had a baseline creatinine level >260 μmol/l.)
The hospital ethics committee approved the present study and all participants gave their written informed consent. The study was conducted in accordance with the recommendations of the Helsinki declaration and all investigations were those routinely required to evaluate the patients, each of whom gave informed consent to all procedures.
All autoantibody assays were performed on the stored serum samples during the same run, by technicians who were blinded to the patient groups.
IgG anti-C1q antibodies were determined using an ELISA with purified human C1q (Bühlmann Laboratories, Schönenbuch, Switzerland), according to the manufacturer's recommendations. Briefly, undigested purified human C1q served as the antigen, and sera were diluted and incubated in high-salt buffer (1 M NaCl). Optical densities were measured at 450 nm and converted into units (U/ml) by plotting against the autoantibody titer of the standards given by the manufacturer. The cutoff value for defining a positive test was determined by the manufacturer as 20 U/ml. With this cutoff value, 20% of 40 blood donors tested in our laboratory had positive tests. We calculated an optimized cutoff value at the 98th percentile (that is, 32 U/ml), which decreased the proportion of normal blood donors with positive tests to 6%, as reported in the literature .
IgG anti-dsDNA antibodies were determined using an ELISA with enzyme-linked immunoassay technology (PHADIA GmBH, Freiburg, Germany), according to the manufacturer's instructions. The cutoff value for a positive test result (15 U/ml), as determined by the manufacturer by testing samples from 400 healthy blood donors, corresponds to the 98th percentile. The fluorescent signal was converted to international units (IU/ml) by plotting the value against the autoantibody titer of World Health Organization standardized calibrators (Wo80) supplied by the manufacturer.
Demographic, clinical, and histological characteristics are reported as the mean (standard deviation) or n (%), as appropriate. Results of the ELISAs are given as the median (interquartile range (IQR)). Nonparametric tests (Mann-Whitney U test, and Spearman's rank correlation test) and Fisher's exact test were used to compare the groups with and without lupus nephritis. Sigma Stat software, version 3.5 (Systat Software Inc., Chicago, IL, USA) was used for statistical analyses. P < 0.05 was considered significant.
The clinical characteristics of the study patients are presented in Table 1. No significant differences were found between the groups for the sex ratio, ethnicity, median age at serum sampling, median follow-up duration from SLE diagnosis to the last visit, or median SLEDAI at serum sampling in the two groups with active SLE. The only significant difference between the groups was a longer median duration of SLE in the nephritis group (6 years; range, 0.25 to 36 years) compared with the group without nephritis (2.1 years; range, 0.1 to 14.1 years) (P < 0.003). The median time from serum sampling to the diagnosis of lupus nephritis (15 patients) was 1.2 years (range, 0.3 to 16 years). The time from serum sampling to lupus nephritis was <12 months in 5 patients and ≥ 12 months in 10 patients (1 to 2 years in four patients, 2 to 5 years in five patients, and 16 years in one patient). Lupus treatment at the time of serum sampling in the 15 patients with subsequent nephritis involved low-dose prednisolone (<0.5 mg/kg/day) and hydroxychloroquine in eight patients, high-dose prednisolone (≥ 0.5 mg/kg/day) and intermittent intravenous cyclophosphamide in two patients, low-dose prednisolone and oral azathioprine (2 mg/kg/day) or methotrexate (0.4 mg/kg/week) in two patients each, and hydroxychloroquine with no corticosteroid in one patient.
The time between serum sampling and subsequent clinical lupus nephritis varied widely, from 3 months to 16 years. We therefore divided the nephritis patients into two subgroups, one with sampling-to-nephritis times <12 months (n = 5) and the other with longer times (n = 10). Anti-C1q antibody titers were not significantly different between these two groups (median, 82 U/ml vs. 117 U/ml).
Anti-dsDNA antibodies were detected in 14 (93.3%) of 15 patients with subsequent lupus nephritis, compared with 24 (72.7%) of 33 patients with active SLE and no nephritis (P = ns) and nine (73%) patients with inactive SLE and no nephritis (P = ns). The median plasma anti-dsDNA titer in the 15 patients with nephritis was 115 IU/ml (IQR, 74 to 296 IU/ml), compared with 24 IU/ml (IQR, 10 to 70 IU/ml) in the 33 patients with active SLE and no nephritis (P = 0.01) and 13 IU/ml (IQR, 5 to 23 IU/ml) in the 22 patients with inactive SLE (P = 0.008) (Figure 1b). The NPV of anti-dsDNA antibodies for subsequent lupus nephritis was 9/10 (90%). The only patient who subsequently developed nephritis but had negative anti-dsDNA antibodies (2 IU/ml) had class V membranous glomerulonephritis 31 months after serum sampling.
At renal biopsy, the anti-dsDNA antibody test was positive (30 IU/ml). The sensitivity of anti-dsDNA for subsequent active proliferative lupus nephritis was 14/14 (100%), the PPV was 14/38 (37%), and the NPV was 9/10 (90%). Combining anti-C1q and anti-dsDNA led only to a slight improvement in the PPV (58.3% instead of 50%); both antibodies were positive in 10 out of 33 (30.3%) patients with active nonrenal lupus and in four out of 22 (18.2%) patients with inactive lupus. The NPV decreased to 95.8% when both antibodies were used in combination.
At the time of renal biopsy, nine out of 10 patients were positive for anti-dsDNA antibodies; the remaining patient, who previously had a weakly positive titer (19 IU/ml), had a negative titer at the time of biopsy (14 IU/ml) (Figure 2b). Finally, six out of eight patients had persistently low anti-dsDNA titers after 6 months of high-dose immunosuppressive drugs.
The aim of the present study was to determine whether anti-C1q antibodies predicted the subsequent development of lupus nephritis. Among previous studies, all but one  involved testing for anti-C1q at the time of the renal biopsy showing active proliferative or nonproliferative lupus nephritis [9, 23–29]. In this setting, anti-dsDNA and other immunological parameters such as low complement hemolytic 50, C3, and C4 or the presence of antinucleosome showed moderate sensitivity and a moderate NPV for lupus nephritis [10, 19, 30–32]. We looked at anti-C1q titers at a time when the patients had no evidence of nephritis. Patients in whom nephritis developed subsequently were more likely to have anti-C1q antibodies (100%) than the other patients (45%), although the SLEDAI (excluding renal parameters) at the time of sampling was similar in the two groups before the first renal manifestation. The median anti-C1q titer was higher in the group with subsequent nephritis.
These data are consistent with the results of anti-C1q assays using a similar method in serum samples taken at the time of renal biopsy in 38 patients with proliferative (n = 26) or class V (n = 2) lupus nephritis . Anti-C1q was found in 97% of patients with active proliferative nephritis, compared with 35% of lupus patients with inactive nephritis and 25% of lupus patients without nephritis . Similar data were reported by Horak and colleagues in a series of 33 patients  and by Fang and colleagues in a series of 150 patients , all with lupus nephritis.
Our data indicate that the PPV of anti-C1q is only fair, as nearly one-half of the patients who still had no evidence of nephritis at follow-up completion had positive tests for anti-C1q, sometimes with very high titers. The mean follow-up was 11.3 years (median, 13 years) in this group, and we cannot rule out that nephritis will develop later on in some of the patients, particularly as the lower end of the follow-up range was only 2 years (three patients, including one patient with a very high anti-C1q titer).
With the caveat that we studied only a small number of patients, and that we studied only a single time measurement for a predictive value calculation of subsequent nephritis, the high NPV of anti-C1q is of interest. A high NPV is extremely helpful for identifying patients at low risk. All 14 patients with a subsequent diagnosis of class IV proliferative glomerulonephritis tested positive for anti-C1q at least 3 months before, and sometimes as long as 16 years before, the first clinical manifestation of renal disease. Anti-C1q antibody data at the time of renal biopsy showed good concordance with data obtained before the clinical manifestations of glomerulonephritis in seven out of 10 patients. One patient with an anti-C1q titer slightly above the cutoff value was diagnosed with class V glomerulonephritis 31 months later and had a high anti-C1q titer at the time of the renal biopsy. Another patient, whose anti-C1q titer was slightly above the cutoff value, was diagnosed 13 months later with class IV glomerulonephritis and had a negative anti-C1q test but was already treated with high-dose cyclophosphamide for extra-renal SLE manifestations.
The anti-C1q test may remain positive, however, even after 6 months of immunosuppressive therapy (five out of eight (62%) nephritis patients in our series, 30% in the study by Moroni and colleagues , and 47% in the study by Fang and colleagues ). In our study, this finding may be related to the fact that five out of eight patients achieved only partial responses. Other possibilities include inadequacy of the upper limit of normal determined in our laboratory in normal control individuals. We chose the 98th percentile as the upper limit of the normal, in keeping with many earlier studies. The high NPV of anti-C1q in our study is consistent with previous reports of anti-C1q values at the time of full-blown lupus nephritis [10, 23, 27–29, 32–36] or before the diagnosis of lupus nephritis . Moroni and colleagues reported a prospective 6-year study in 228 patients with lupus nephritis . Among flares of proliferative lupus nephritis, 20% occurred at a time when anti-C1q titers were below the cutoff value, and 30% of patients were in remission of their nephritis at a time when anti-C1q titers were elevated. The best model for predicting renal flares was a combination of anti-C1q with C3 and C4 .
Anti-C1q titers did not correlate with the SLEDAI in patients with subsequent lupus nephritis. These antibodies should not be taken as a general marker of disease activity, in contrast to anti-dsDNA antibodies . Our finding is in contrast with a recent report by Fang and colleagues that anti-C1q titers correlated well with the SLEDAI in 150 patients with renal SLE . This discrepancy may be ascribable to differences in the patient populations and anti-C1q assays. In the study by Fang and colleagues, the IgG subclass distribution of anti-C1q antibodies suggested that IgG2 anti-C1q might be pathogenic and that IgG3 anti-C1q might be the most specific biomarker for monitoring disease activity (among patients in remission, 100% became negative for IgG3 anti-C1q compared with 53% negative for IgG2 anti-C1q).
Our data suggest that anti-C1q may be a good serological marker for the subsequent development of active proliferative glomerulonephritis in patients with SLE. Patients without anti-C1q are at very low risk for severe proliferative glomerulonephritis (100% NPV in our study). Patients with anti-C1q antibodies have an approximately 50% risk for lupus nephritis within the next decade, and therefore require close renal monitoring.
enzyme-linked immunosorbent assay
negative predictive value
positive predictive value
systemic lupus erythematosus
Systemic Lupus Erythematosus Disease Activity Index.
The present study was supported by grants from the Association pour la Recherche et le Développement de l'Immuno-Rhumatologie.
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