The incidence rate of pulmonary arterial hypertension and scleroderma renal crisis in systemic sclerosis patients with digital ulcers on endothelin antagonist receptors (ERAs) and phosphodiesterase-5 inhibitors (PDE5i)

Author:

Pestaña-Fernández Melani1ORCID,Rubio-Rivas Manuel1,Tolosa-Vilella Carles2,Guillén-Del-Castillo Alfredo3,Colunga-Argüelles Dolores4,Argibay Ana5,Marí-Alfonso Begoña2,Marín-Ballvé Adela6,Pla-Salas Xavier7,Chamorro Antonio-J8,Castro-Salomó Antoni9,Madroñero-Vuelta Ana Belén10,Sánchez-García María Esther11,Sáez-Comet Luis12,González-Echávarri Cristina13,Ortego-Centeno Norberto14,Vargas-Hitos José Antonio15,Todolí-Parra José Antonio16,Trapiella-Martínez Luis17,Lledó Gema María18,Freire Mayka19,Fonollosa-Pla Vicent3,Simeón-Aznar Carmen Pilar3,

Affiliation:

1. Unit of Autoimmune Diseases, Department of Internal Medicine, Hospital Universitario de Bellvitge-IDIBELL, L’Hospitalet de Llobregat, Barcelona, Spain

2. Department of Internal Medicine, Parc Taulí, Hospital Universitario, Sabadell, Barcelona, Spain

3. Unit of Autoimmune Diseases, Department of Internal Medicine, Hospital Universitario Vall d’Hebron, Barcelona, Spain

4. Department of Internal Medicine, Hospital Universitario Central de Asturias, Oviedo, Asturias, Spain

5. Unit of Systemic Autoimmune Diseases and Thrombosis, Department of Internal Medicine, Complejo Hospitalario Universitario de Vigo, Vigo, Pontevedra, Spain

6. Unit of Autoimmune Diseases, Department of Internal Medicine, Hospital Clínico Universitario Lozano Blesa, IIS Aragón, Zaragoza, Spain

7. Unit of Systemic Autoimmune Diseases, Department of Internal Medicine, Consorci Hospitalari de Vic, Vic, Barcelona, Spain

8. Department of Internal Medicine, Hospital Clínico Universitario de Salamanca, Universidad de Salamanca-IBSAL, Salamanca, Spain

9. Department of Internal Medicine. Hospital Universitario Sant Joan, Reus, Tarragona, Spain

10. Department of Internal Medicine, Hospital General San Jorge, Huesca, Spain

11. Department of Internal Medicine, Hospital Universitario Virgen de Valme, Sevilla, Spain

12. Department of Internal Medicine, Hospital Universitario Miguel Servet, Zaragoza, Spain

13. Autoimmune Diseases Research Unit, Department of Internal Medicine, Biocruces Bizkaia Health Research Institute, Hospital Universitario Cruces, University of the Basque Country, Barakaldo, Spain

14. Inst. Invest. Biosanitaria Ibs Granada, Department of Internal Medicine, Unit of Systemic Autoimmune Diseases, Department of Medicine, Facultad de Medicina, Hospital Universitario San Cecilio, Granada, Spain

15. Department of Internal Medicine, Hospital Universitario Virgen de las Nieves, Granada, Spain

16. Department of Internal Medicine, Hospital Universitario y Politécnico La Fe, Valencia, Spain

17. Unit of Systemic Autoimmune Diseases, Department of Internal Medicine, Hospital de Cabueñes, Gijón, Asturias, Spain

18. Department of Autoimmune Diseases, Hospital Clinic, Barcelona, Spain

19. Unit of Autoimmune Diseases, Department of Internal Medicine, Hospital Clínico Universitario de Santiago, Santiago de Compostela, A Coruña, Spain

Abstract

Abstract Introduction Endothelin antagonist receptors (ERAs) and phosphodiesterase-5 inhibitors (PDE5i) are beneficial in pulmonary arterial hypertension (PAH) and digital ulcers (DU) and prevent from DU recurrences. Our study aimed to determine the difference in the incidence rate of PAH and scleroderma renal crisis (SRC) in patients with SSc and DU (SSc-DU) under ERAs/PDE5i or without treatment. Methods We conducted a retrospective cohort study including SSc-DU patients from the Spanish Scleroderma Registry (RESCLE). The primary outcome was the incidence rate of PAH and SRC in patients under ERAs/PDE5i or not. Results Some 544 patients out of 1817 (29.9%) in the RESCLE database had DU, 221 (40.6%) under ERAs/PDE5i and 323 (59.4%) not. The incidence rate (95% CI) difference between patients under treatment or not under did not reach statistical significance in PAH [−0.1 (−4.8, 4.69), P = 0.988] or in SRC [0.7 (−2.2, 3.7), P = 0.620]. However, the time from the first DU to the diagnosis of SRC was delayed in treated patients [mean (s.d.) 7.6 (5.8) years vs 2.9  (5.3); P = 0.021]. The dcSSc subset was more prevalent in the treatment group (36 vs 26%; P = 0.018), along with anti-topoisomerase I antibodies (34 vs 18%; P < 0.001) and tendon friction rubs (12 vs 6%; P = 0.038), whereas the lcSSc subset was more prevalent in the no-treatment group (57 vs 66%; P = 0.031) along with ACA (37 vs 46%; P = 0.031). Conclusion There was no difference in the incidence rate of PAH and SRC between groups. However, treatment with ERAs and/or PDE5i appeared to delay the occurrence of SRC.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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