This study aimed to detect by nailfold videocapillaroscopy (NVC) the presence of age-related capillary morphological patterns in a large cohort of subjects affected by primary Raynaud's phenomenon (PRP). NVC was performed in 877 patients affected by PRP, divided into three age groups: < 35, 35-55 and > 55 years. The following qualitative parameters were assessed and compared in the three groups of patients: apical dilations, irregular (non-homogeneous) dilations, venous branch dilations, microhaemorrhages, tortuosities and subpapillary venous plexus visibility. Patients with either irregular dilations or venous branch dilations were found significantly younger than those without (p < 0.0001). The presence of either irregular or venous branch dilations seems to exclude the presence of apical dilations. Patients with microhaemorrhages were found significantly younger than those without (p = 0.05), and 81 % of patients without microhaemorrhages did not show irregular and venous branch dilations. The subpapillary venous plexus seems more visible in subjects with age < 35, as well as in those with age > 55 years (p < 0.0001). A statistically significant negative correlation was found between presence of apical and irregular dilations (p < 0.0001), apical dilations and venous branch dilations (p = 0.02), apical dilations and tortuosities (p = 0.0005), microhaemorrhages and tortuosities (p < 0.0001) and venous branch dilations and tortuosities (p = 0.02). Finally, a statistically significant positive correlation was found between irregular and venous branch dilations (p < 0.0001), irregular dilations and microhaemorrhages (p < 0.0001) and venous branch dilations and microhaemorrhages (p < 0.0001). In conclusion, our study detected different age-related morphological capillary changes mainly in younger patients with PRP, as well as statistically significant correlations between the presence of different capillary variables.
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Fernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, PortugalFernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
Caetano, Joana
Coimbra, Matilde
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Fernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, PortugalFernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
Coimbra, Matilde
Lopes, Monica
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Fernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, PortugalFernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
Lopes, Monica
Amaral, Marta
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Fernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
NOVA Med Res, Lisbon, PortugalFernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
Amaral, Marta
Oliveira, Susana
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Fernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, PortugalFernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
Oliveira, Susana
Alves, Jose Delgado
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Fernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal
NOVA Med Res, Lisbon, PortugalFernando Fonseca Hosp, Dept Med 4, Syst Autoimmune Dis Unit, Amadora, Portugal