1. Introduction
Venous thromboembolism (VTE) is a classical complication of chronic inflammatory diseases [
1], reported to be increased in many auto-immune and rheumatic diseases, including ANCA-associated vasculitis (AAV) [
2,
3,
4,
5,
6,
7,
8,
9]. The first studies specifically addressed in AAV were a case series of pediatric patients that developed deep vein thrombosis (DVT) shortly after disease diagnosis [
10] and a post-hoc analysis of the Wegener’s Granulomatosis Etanercept Trial (WGET) [
2,
11]. In this prospective trial, which was limited to patients with granulomatosis with polyangiitis (GPA), about 10% of patients developed VTE after a median time of 2.1 months from disease onset [
11]. The increased risk of VTE in AAV patients was confirmed in further retrospective studies [
4,
5]. Stassen et al. reported an incidence of 12% of VTE in a cohort of 193 patients with micropolyangitis (MPA) or GPA, followed for 6.1 years [
4]. A similar incidence was observed in a recent analysis performed in 417 patients that were included in randomized controlled trials conducted by the European Vasculitis Society [
5]. In this analysis, patients with severe renal disease had a higher rate of VTE. In the multivariate analysis, increased C-reactive protein level and increased creatinine cutaneous and gastrointestinal involvement at diagnosis were independently associated with VTE. However, the analysis of VTE risk factors was limited given the heterogeneity of patients pooled from four different studies, and by unavailability of detailed data at disease onset. Kronbichler et al. analyzed VTE frequency and risk factors in patients included in the RAVE study which aimed at evaluating rituximab as a remission induction regimen [
9,
12]. In these patients without severe kidney involvement, pulmonary hemorrhage, and positive PR3-ANCA, heart involvement and microscopic hematuria were found to be independently associated with VTE development. More recently, Isaacs et al. found PR3-ANCA, hypoalbuminemia, and BMI to be independent risk factors of VTE in a retrospective analysis in 162 AAV patients [
13].
Kidney involvement in AAV appears as a major prognostic factor [
14] and impaired kidney function has been reported as a risk factor of VTE [
5]. Finally, no study has specifically addressed VTE risk factors in ANCA-glomerulonephritis (ANCA-GN) patients and whether factors identified in past studies apply to ANCA-GN patients. Moreover, whether ANCA-GN patients experiencing VTE have a different prognosis remains to be studied.
The AAV Maine-Anjou registry includes all patients diagnosed with ANCA-GN from the Maine Anjou Region in France, encompassing one university and three regional hospitals [
15]. The registry gathers very detailed clinical and biological data of patients with ANCA-GN since 2000, as well as treatment management and outcomes.
Thus, in the present study, we used the AAV Maine-Anjou registry to study VTE episodes in patients with biopsy confirmed ANCA-GN. The primary objective was to analyze the incidence of VTE in ANCA-GN patients and the secondary objectives were to identify risk factors of VTE and to study the outcome of patients according to VTE occurrence.
4. Discussion
In the present study, we confirm a high incidence of VTE in ANCA-GN patients. Indeed, VTE occurred in 17.3% of patients at the end of follow-up, representing an estimated one-year incidence of 12.4%. While the univariate analysis identified age, low serum albumin at ANCA-GN onset, lack of statin therapy, and rituximab as significant risk factors of VTE; in the multivariate analysis, only statin therapy was significantly associated with a lower risk of VTE. To the best of our knowledge, this observation suggesting antithrombotic action of statins has not yet been reported in ANCA-GN patients and may open new therapeutic perspectives.
The antithrombotic action of statin therapy has been observed in human prospective randomized clinical trials [
20,
21]. A recent meta-analysis comprising more than three million participants from cohort studies and randomized control trials showed a significant risk reduction of DVT with a RR of 0.75 in patients on statin therapy as compared to patients on placebo [
22]. Interestingly, in this meta-analysis, a greater reduction risk of VTE was observed in the subgroup of patients with higher VTE risk (RR 0.46). Potential protective actions of statins may be explained by several ways. Indeed, several in vitro and in vivo animal and human studies have demonstrated an impact of statins on blood coagulation [
23,
24]. In addition to their anti-inflammatory action, statins have been shown to favor an anticoagulant state by reducing tissue factor expression, enhancing the protein C activity by increasing thrombomodulin expression on endothelial cells [
25], and by decreasing plasminogen activator inhibitor 1 and increasing tissue plasminogen activator [
26]. In the present study, lack of statin therapy conferred a 4.7-fold risk of developing VTE in our cohort. Thus, given that anti-thrombotic properties of statins may be stronger in patients at high VTE risk, we suggest that their anti-thrombotic action may be greatly enhanced in ANCA-GN patients, which could account for our results. Interestingly, patients under statin therapy at AAV diagnosis were more frequently under antiplatelet agents as compared to patients without statins. However, no difference was present as regards to hypertension or diabetes, nor to cholesterol concentration at ANCA-GN diagnosis between patients with and without statins. Moreover, the rate of statin therapy was not significantly different between centers suggesting the lack of a center effect.
In the two major previous studies that analyzed VTE in AAV patients, the incidence of VTE was 9.8% and 12%, thus lower than the incidence observed in the present study [
2,
4]. In the study from Kronbichler et al., there was a trend towards a higher incidence of VTE in the MEPEX trial that included patients with severe renal disease [
5], which is in accordance with the higher incidence of VTE in our study. The differences in VTE incidences may also be explained by heterogeneity in disease presentation, severity, and stages of disease (flare versus remission) of patients included in past studies [
2,
4].
We observed that most VTE occurred soon after AAV diagnosis when patients had active vasculitis. The median delay to VTE was about 3 months after ANCA-GN diagnosis, which corresponds to the remission-induction therapeutic phase. Given that no systematic VTE screening was performed in our study, it is probable that the true delay between AAV diagnosis and VTE occurrence may be shorter. Thus, most VTE occurred in a period when several risk factors of VTE are present, such as hospitalization, immobilization related to disease severity, and the need for central venous access for hemodialysis or plasmapheresis.
We were not able to study the role for endogenous hypercoagulable factors in our study. Only one third of patients were screened for APL and/or LA, not allowing to investigate relationship with VTE. We observed a low prevalence of APL and lupus anticoagulant in screened patients.
Interestingly, we observed that patients that experienced VTE within the first 3 months following AAV diagnosis developed more frequently ESRD. The kidney involvement of these patients as assessed by kidney biopsy was not significantly different as compared to other patients. We also did not observe any significant difference in treatment regimens that could explain this observation. Unfortunately, the low number of patients with this condition does not allow us to analyze causative factors extensively.
Interestingly, serum albumin appeared as a potential risk factor for VTE in ANCA-GN patients in our study. Indeed, we observed an association between serum albumin at baseline with an HR of 2.42 for each 10 g/L albumin decrease in the univariate analysis. The relationship between hypoalbuminemia and VTE is well documented in patients with nephrotic syndrome, where hypoalbuminemia is mainly the consequence high albuminuria [
27,
28], and has also been evidenced as an independent risk factor of VTE in a recent study conducted in AAV patients with and without renal involvement [
13]. In our study, proteinuria was not different between patients with and without VTE, suggesting that mechanisms other than proteinuria may be involved to explain more profound hypoalbuminemia in VTE patients. Finally, serum albumin was no longer associated with VTE in the multivariate analysis, maybe because our study was underpowered. Further studies should focus on this aspect to better understand the factor favoring venous thrombosis in ANCA-GN patients.
In contrast to previous studies [
5], we did not observe any association between VTE and AAV organ involvement, C-reactive protein level or BVAS at presentation. This may be explained by our design that only included patients with ANCA-GN with finally poor representation of patients with other organ involvement. The lack of association with inflammation may also be related to the fact that patients of our study had high disease activity at presentation mainly driven by their renal involvement (median BVAS 17.2), limiting any comparison between patients with severe and milder disease activity. In a recent post-hoc analysis of the RAVE trial [
12], Kronbichler et al. showed that heart involvement, pulmonary hemorrhage, PR3-ANCA, and microscopic hematuria were independently associated with VTE development. However, it is important to underline that patients with serum creatinine above 354 µmol/L were excluded from RAVE study [
12] and that kidney involvement of RAVE study patients was mild with a mean eGFR above 50 at baseline as compared to 20 mL/min/1.73 m
2 in our study. Finally, we were not able to identify “classical” risk factors found in previous studies, but found association with novel factors not yet or poorly reported. This may be related to the fact that patients in our cohort had a very detailed phenotype allowing us to analyze a large number of potential risk factors. Another explanation may be that that classical risk factors of VTE could be overcome in the context of ANCA-GN.
Our study has several limitations starting with its observational design. We did not perform systematic radiological screening of DVT, thus some VTE may have been missed. Moreover, we did not perform systematic screening of blood clotting and of APL antibodies and the use of thromboprophylaxis at ANCA-GN diagnosis was not collected. However, despite these limitations, this study is the first to analyze specifically the incidence and risk factors of VTE in a well characterized population of patients with ANCA-GN.
In conclusion, in line with previous studies, we show a high incidence of VTE in ANCA-GN patients, predominantly within the first months following ANCA-GN diagnosis. The present study identifies statin therapy as an independent risk factors of VTE in ANCA-GN patients, thus suggesting a protective role of statins and opening interesting research and therapeutic perspectives. Furthermore, these results give some suggestions for future research that should focus on the effect of albumin levels on VTE risk and on the impact of experiencing VTE on renal outcome. Thus, these results may help identifying ANCA-GN patients with higher VTE risk and defining specific preventive strategies.