Objectives To assess the relationship between disease duration and the prevalence/distribution of nailfold videocapillaroscopy (NVC) patterns, named according to the current classification as 'early', 'active' and 'late', in a large cohort of systemic sclerosis (SSc) patients. Methods A cross-sectional analysis was conducted on 1689 patients undergoing standardized NVC. Clinical-serological data and treatments were collected. Statistical comparisons and multivariable logistic regression models were applied, including analyses based on disease duration. Results The prevalence of NVC patterns was as follows: 'early' 21.6%, 'active' 47.4%, 'late' 25.7% and normal/non-specific 5.3%. The distribution by disease duration showed that the three main patterns were always present. While the 'early' and 'active' progressively decreased (from 30.3% and 51.9% in patients with <= 5 yrs, to 14.6% and 43.5% in those >10 yrs, P < 0.01), the 'late' pattern increased from 13.2% (<= 5 yrs) to 36.0% (>10 yrs) (P < 0.001) and was associated with internal organ involvement, anti-topoisomerase antibodies and more therapies (P < 0.01). Conversely, the 'early' and 'active' patterns were associated with the limited-cutaneous subset (P < 0.01) and anti-centromere antibodies (P < 0.001). Multivariable analysis confirmed a strong association between the 'late' pattern and skin/peripheral vascular involvement. Notably, the presence of the 'late' pattern in patients with <= 2 yrs (10.9%) was significantly associated with scleroderma renal crisis (P = 0.012). Conclusion SSc-NVC patterns are not strictly time-dependent and can be observed at any stage of the disease, suggesting that microvascular damage progression is heterogeneous across different disease periods. Therefore, a revised classification of NVC changes considering both disease duration and NVC severity could improve its prognostic accuracy.
Prevalence, distribution and associations of the scleroderma capillaroscopic patterns: new insights from the Italian SPRING-SIR registry / De Angelis, R.; Ferri, C.; Cipolletta, E.; Riccieri, V.; Battista, M. D.; Bajocchi, G.; Bellando-Randone, S.; Bruni, C.; Orlandi, M.; Zanframundo, G.; Foti, R.; Cuomo, G.; Ariani, A.; Rosato, E.; Lepri, G.; Girelli, F.; Zanatta, E.; Bosello, S. L.; Cavazzana, I.; Ingegnoli, F.; De Santis, M.; Cacciapaglia, F.; Murdaca, G.; Abignano, G.; Pettiti, G.; Rossa, A. D.; Caminiti, M.; Iuliano, A. M.; Ciano, G.; Beretta, L.; Bagnato, G.; Lubrano, E.; De Andres, I.; Idolazzi, L.; Saracco, M.; Agnes, C.; Campochiaro, C.; Fornaro, M.; Lumetti, F.; Spinella, A.; Cocchiara, E.; De Luca, G.; Codullo, V.; Visalli, E.; Iandoli, C.; Gigante, A.; Pellegrino, G.; Pigatto, E.; Lazzaroni, M. G.; De Lorenzis, E.; Motta, F.; Tonutti, A.; Mennillo, G.; Pagano-Mariano, G.; Furini, F.; Vultaggio, L.; Parisi, S.; Peroni, C. L.; Bianchi, G.; Fusaro, E.; Sebastiani, G. D.; Govoni, M.; D'Angelo, S.; Cozzi, F.; Franceschini, F.; Guiducci, S.; Giuggioli, D.; Dagna, L.; Doria, A.; Salvarani, C.; Iannone, F.; Matucci-Cerinic, M.. - In: RHEUMATOLOGY. - ISSN 1462-0324. - 65:1(2026), pp. 1-13. [10.1093/rheumatology/keaf672]
Prevalence, distribution and associations of the scleroderma capillaroscopic patterns: new insights from the Italian SPRING-SIR registry
Ferri C.;Orlandi M.;Lumetti F.;Spinella A.;Giuggioli D.;Salvarani C.;
2026
Abstract
Objectives To assess the relationship between disease duration and the prevalence/distribution of nailfold videocapillaroscopy (NVC) patterns, named according to the current classification as 'early', 'active' and 'late', in a large cohort of systemic sclerosis (SSc) patients. Methods A cross-sectional analysis was conducted on 1689 patients undergoing standardized NVC. Clinical-serological data and treatments were collected. Statistical comparisons and multivariable logistic regression models were applied, including analyses based on disease duration. Results The prevalence of NVC patterns was as follows: 'early' 21.6%, 'active' 47.4%, 'late' 25.7% and normal/non-specific 5.3%. The distribution by disease duration showed that the three main patterns were always present. While the 'early' and 'active' progressively decreased (from 30.3% and 51.9% in patients with <= 5 yrs, to 14.6% and 43.5% in those >10 yrs, P < 0.01), the 'late' pattern increased from 13.2% (<= 5 yrs) to 36.0% (>10 yrs) (P < 0.001) and was associated with internal organ involvement, anti-topoisomerase antibodies and more therapies (P < 0.01). Conversely, the 'early' and 'active' patterns were associated with the limited-cutaneous subset (P < 0.01) and anti-centromere antibodies (P < 0.001). Multivariable analysis confirmed a strong association between the 'late' pattern and skin/peripheral vascular involvement. Notably, the presence of the 'late' pattern in patients with <= 2 yrs (10.9%) was significantly associated with scleroderma renal crisis (P = 0.012). Conclusion SSc-NVC patterns are not strictly time-dependent and can be observed at any stage of the disease, suggesting that microvascular damage progression is heterogeneous across different disease periods. Therefore, a revised classification of NVC changes considering both disease duration and NVC severity could improve its prognostic accuracy.| File | Dimensione | Formato | |
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