Progression of nailfold capillaroscopic patterns and correlation with organ involvement in systemic sclerosis: a 12 year study

被引:33
|
作者
Sulli, A. [1 ,2 ]
Paolino, S. [1 ,2 ]
Pizzorni, C. [1 ,2 ]
Ferrari, G. [1 ,2 ]
Pacini, G. [1 ,2 ]
Pesce, G. [3 ]
Carmisciano, L. [4 ]
Smith, V. [5 ]
Cutolo, M. [1 ,2 ]
机构
[1] Univ Genoa, IRCCS Osped Policlin San Martino, Dept Internal Med, Res Lab, Viale Benedetto XV 6, I-16132 Genoa, Italy
[2] Univ Genoa, IRCCS Osped Policlin San Martino, Dept Internal Med, Acad Div Clin Rheumatol, Viale Benedetto XV 6, I-16132 Genoa, Italy
[3] Univ Genoa, IRCCS Osped Policlin San Martino, Dept Internal Med, Lab Autoimmun, Genoa, Italy
[4] Univ Genoa, Biostat Sect, Dept Hlth Sci, Genoa, Italy
[5] VIB Ghent Univ, Inflammat Res Ctr, Dept Internal Med, Dept Rheumatol,Ghent Univ Hosp, Ghent, Belgium
基金
比利时弗兰德研究基金会;
关键词
systemic sclerosis; nailfold videocapillaroscopy; patterns; microangiopathy; Raynaud's phenomenon; autoantibodies; connective tissue diseases; PERIPHERAL-BLOOD PERFUSION; RAYNAUDS-PHENOMENON; VIDEOCAPILLAROSCOPY ASSESSMENT; MICROVASCULAR DAMAGE; DIGITAL ULCERS; AUTOANTIBODIES; RELIABILITY; BOSENTAN; ILOPROST; CLASSIFICATION;
D O I
10.1093/rheumatology/kez374
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The aim of this observational study was to investigate the evolution of scleroderma microangiopathy throughout different nailfold videocapillaroscopy (NVC) patterns ('early', 'active', 'late') as well as the prevalence of organ involvement in SSc patients during a 12-year follow-up. Methods: Thirty-four SSc patients showing at baseline (first capillaroscopic analysis) the 'early' NVC pattern of microangiopathy were enrolled and followed for 12 years (s.d. 2). Complete NVC analysis and clinical and serological findings were collected. Patients were in a standard therapeutic care setting. Statistical analysis was carried out by non-parametric tests. Results: After a 12-year follow-up, the 'early' NVC pattern changed from baseline in 76% of the patients. The NVC pattern was found to be 'active' in 9 patients (26%), 'late' in 13 (38%) and characterized by non-specific capillary abnormalities in 4 (12%). In the subgroup whose microangiopathy progressed from the 'early' to the 'late' NVC pattern, the median time of progression from the 'early' to the 'active' pattern was significantly shorter (11 months) when compared with patients who progressed from the 'early' to the 'active' NVC pattern (55 months) (P = 0.002). The median time of progression between NVC patterns was significantly shorter in SSc patients showing either a nucleolar ANA pattern or Scl70 autoantibodies (P = 0.048). Organ involvement was progressively greater in SSc patients with 'early', 'active' and 'late' NVC patterns, respectively. Conclusions: This longitudinal study confirms over a 12-year follow-up the evolution of specific NVC patterns associated with the progressive severity of organ involvement in SSc patients in a standard clinical care setting.
引用
收藏
页码:1051 / 1058
页数:8
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