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Association of antiphospholipid antibodies with active digital ulceration in systemic sclerosis
  1. Mickaël Martin1,
  2. Camille Martinez2,
  3. Laurent Arnaud3,
  4. Jean-Christophe Weber4,
  5. Vincent Poindron5,
  6. Gilles Blaison2,
  7. Pierre Kieffer6,
  8. Bernard Bonnotte7,
  9. Sabine Berthier7,
  10. Denis Wahl8,9,
  11. Francois Maurier10,
  12. Jean-Loup Pennaforte11,
  13. Philip Bielefeld7,
  14. Nadine Magy-Bertrand12,
  15. Hervé Devilliers7 and
  16. Thierry Martin5
  1. 1Internal Medicine, Poitiers University Hospital, Poitiers, France
  2. 2Internal Medicine, Colmar Civilian Hospitals, Colmar, France
  3. 3Rheumatology, National Reference Center for Rare Autoimmune Diseases (RESO), Strasbourg University Hospital, Strasbourg, France
  4. 4Internal Medicine, National Reference Center for Rare Autoimmune Diseases (RESO), Strasbourg University Hospital, Strasbourg, France
  5. 5Clinical Immunology, National Reference Center for Rare Autoimmune Diseases (RESO), Strasbourg University Hospital, Strasbourg, France
  6. 6Internal Medicine, Mulhouse Regional Hospital Center, Mulhouse, France
  7. 7Internal Medicine and Clinical Immunology, Dijon University Hospital, Dijon, France
  8. 8Vascular Medicine, Regional Center for Rare Vascular and Systemic Autoimmune Diseases, Nancy University Hospital, Vandoeuvre-Les-Nancy, France
  9. 9Medicine Faculty, University of Lorraine, Vandoeuvre-Les-Nancy, France
  10. 10Internal Medicine, Metz-Thionville Regional Hospital Center, Metz, France
  11. 11Rheumatology, Reims University Hospital, Reims, France
  12. 12Internal Medicine, Besancon University Hospital, Besançon, France
  1. Correspondence to Dr Mickaël Martin; mickael-martin{at}outlook.com

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Key messages

What is already known about this subject?

  • Antiphospholipid antibodies (aPL) prevalence seemed increased in patients with systemic sclerosis (SSc), but their clinical signification is unclear.

What does this study add?

  • Description of aPL positivity and antiphospholipid syndrome prevalence in a multicentre cross-sectional SSc cohort (confirmed and high aPL titre level).

  • Anti-beta-2 glycoprotein 1 (β2GP1) positivity is an independent factor associated with active digital ulceration.

How might this impact on clinical practice?

  • aPL and especially anti-β2GP1 should be screened in SSc to detect patients potentially at higher risk of developing digital ulcers.

Raynaud’s phenomenon (RP) in systemic sclerosis (SSc) can be severe with active digital ulceration (ADU) and gangrene. RP physiopathology includes early endothelial cell injury, vascular dysfunction and sometimes microvascular thrombosis.1 Antiphospholipid antibodies (aPL) activate endothelial cells and platelets by complexes of beta-2 glycoprotein 1 (β2GP1) and anti-β2GP12 and could therefore contribute to the initiation of and/or aggravate SSc-related RP. aPL prevalence seems increased in patients with SSc compared with controls,3 but aPL-associated clinical features are often contradictory. The aims of this study were to assess aPL and antiphospholipid syndrome (APS) prevalence in patients with SSc and their association with ADU.

Consecutive patients aged more than 18 years, fulfilling the American College of Rheumatology/EULAR classification criteria for SSc4 and followed in seven French expert centres for autoimmune diseases labelled by the French national network for autoimmune disease care, were enrolled prospectively during 8 months. Patients with other associated autoimmune disease were excluded. All patients provided written informed consent. SSc subtype was classified based on LeRoy and Medsger’s criteria,5 and skin involvement was assessed according to the modified Rodnan skin score (mRSS).6 Interstitial lung disease (ILD) was defined by subpleural ground-glass opacities and/or interstitial reticular pattern with or without fibrosis on high-resolution CT. Raynaud’s activity and the presence of digital ischaemia was determined using a previously published severity score: 0—no Raynaud’s; 1—Raynaud’s with/without vasodilator required; 2—Digital Pitting Scars; 3—Digital Tip Ulcerations and 4—Digital Gangrene.7 ADU was defined as a score ≥3.8 Pulmonary arterial hypertension (PAH) was defined by median pulmonary arterial pressure (mPAP) ≥25 mm Hg and pulmonary arterial wedge pressure ≤15 mm Hg, not related to lung diseases and/or chronic thromboembolism. Screening for lupus anticoagulant (LA), anticardiolipin (aCL) and anti-β2GP1 antibodies was systematically carried out in each centre and confirmed at least 12 weeks apart. Only persistent aPL were considered.9 LA was detected according to the international recommendations.10 Positivity for immunoglobulin (Ig)G/IgM aCL and anti-β2GP1 in immunosorbent assay was defined as ‘overall’ (titres more than 15–20 U/mL, according to each manufacturer’s guidelines) and ‘high’ (titres >40 U/mL9). APS was diagnosed according to international definition.9 Statistical analysis was performed using SAS V.9.4. Comparison for scaled variables were performed using Student’s t-test. Association between qualitative variables was determined with Pearson’s χ2 or Fisher’s exact tests. Factors independently associated with ADU were studied by logistic regression model. Dependent variables were selected using a manual backward procedure with p=0.05 as threshold for exit. The procedure initially included all factors associated with severe RP with a p-value below 0.1 in bivariate analysis. Subanalyses were performed considering only ‘high’ titres of aCL and/or anti-β2GP1.9 The alpha risk was set at 5% and statistical tests were performed bilaterally with p<0.05 considered as significant. Data are available upon request.

One hundred and sixty-eight patients were included. Their characteristics are summarised in table 1. LA was detected in 17 (10%) patients. Overall, aCL and/or anti-β2GP1 were present in 14 (8%) and 14 (8%) patients, respectively. Positivity for ≥1 aPL was found in 31 (18%) patients and triple positivity in three (2%). Seven (4%) patients had definite APS, without obstetric APS. Anti-Scl70 positivity was more frequent in the APS group (71% vs 34%, p=0.046). No association was observed between APS and other SSc-related manifestations, including PAH (online supplementary table 1). Among the 31 aPL-positive patients, 12 had ADU among whom all received calcium channel inhibitors, seven had bosentan, nine had low-dose aspirin while three received vitamin K antagonists or unfractioned heparin for APS (online supplementary table 2). Forty-eight patients (28.6%) had ADU (table 2). In univariate analysis, factors associated with ADU were positivity for anti-β2GP1 IgG (p<0.001), anti-Scl70 (p=0.006) and higher mean mRSS (6.0 vs 14.0, p<0.001). Anti-β2GP1 positivity and mRSS remained significant in multivariate analysis (OR 8.71, 95% CI 1.31 to 55.43; p=0.02 and OR 1.06, 95% CI 1.02 to 1.11; p=0.007, respectively). When considering only ‘high’ aPL titres, anti-β2GP1 and anti-β2GP1 IgG remained significant (p=0.003 both) in univariate analysis, and anti-β2GP1 IgM was also associated with ADU(p=0.04). In multivariate analysis, only mRSS remained significantly associated with ADU (OR 1.07, 95% CI 1.02 to 1.11; p=0.005) with a trend towards anti-β2GP1 positivity (OR 5.27, 95% CI 0.97 to 28.62; p=0.054) (online supplementary table 3)(online supplementary table 3). aPL, APS and past thrombotic event prevalences according to the different RP subsets are depicted in online supplementary table 4.

Table 1

Patient characteristics

Table 2

Factors associated with ADU

Overall, aPL prevalence in our population (18%) is consistent with those recently reported in worldwide (14%) and European (15%) SSc populations,11 despite pronounced heterogeneity between studies in terms of aPL definition and technical methodology. We report an estimated APS prevalence in SSc of 4%. Notwithstanding its rare occurrence, the association between APS and anti-Scl70 merits further evaluation.

Overall, anti-β2GP1 positivity was independently associated with ADU. A recent metanalysis did not find any association between overall aPL, LA, aCL or anti-β2GP1 positivity and digital ulcers.11 Only three studies have specifically evaluated IgG and/or IgM aCL prevalence in patients with SSc with or without digital ulcer, and no difference was observed.3 Only one study has shown an independent association between active digital ischaemia and IgM anti-β2GP1 positivity, using the same definition of ADU as us.8 On the other hand, another study reported an association between aCL positivity and elevated von Willebrand antigen factor.12 Taken together, these results suggest possible associations between aPL positivity and endothelial injury in SSc, and this relationship deserves further evaluation.

The main strength of our study was to only consider confirmed aPL and subanalyses with high titres of aPL, thereby avoiding potential bias of transient and non-clinically relevant aPL. Moreover, distinction of each aPL type and isotype was made for assessment of potential associations with ADU. Lastly, our results reflect a real-life prevalence study of aPL in SSc with aPL assays having been performed in each centre.

Our study has several limitations. First, the lack of power precluded multivariate analysis for aCL and anti-β2GP1 isotypes and probably explains the loss of significance for the association between ‘high’ anti-β2GP1 positivity and ADU. Moreover, the low number of patients with APS calls for cautious interpretation of the data. Second, thrombosis history was collected retrospectively, leading to potential memorisation and selection bias.

In conclusion, this study found an aPL prevalence in SSc of 18%. Anti-β2GP1 positivity is an independent factor associated with ADU and might be preferentially related to positivity of antiB2GP1 IgG isotype. These data provide additional insights into the role of aPL in SSc vasculopathy.

References

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Footnotes

  • Contributors All authors approved the entirety of the submitted material and contributed actively to the study and all of them meet the journal’s criteria for authorship.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval The study was approved by local ethics committee.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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