Table 2.

SSc-PAH diagnosed according to right heart catheterization criteria – longitudinal studies.

Capillaroscopic Ch aracteristicsSignificant AssociationNon-significant AssociationConclusion
Quantitative
  DensityCapillary loss at inclusionN/ASSc-PAH (HR 3.92, 95% CI 0.8 8–17.36, p = 0.074)31Progressive capillary loss was unequivocally associated with incident SSc-PAH in 2 longitudinal studies
Progressive capillary lossSSc-PAH (p = 0.04; HR 18.53, 95% CI 1.28–78.33, p = 0.033)30,31N/A
  DimensionPresence of giant capillaries at inclusionN/ASSc-PAH (HR 0.68, 95% CI 0.28–2.09, p = 0.638)31No association
Progression of giant capillariesN/ASSc-PAH (HR 0.31, 95% CI 0.15–1.07, p = 0.062)31
  MorphologyAbnormal morphology at inclusionSSc-PAH (HR 11.12, 95% CI 1.19–103.79, p = 0.036)31N/AAbnormal morphology at inclusion was more commonly associated with incident SSc-PAH in 1 longitudinal study
Progression of abnormal morpholo gySSc-PAH, p = 0.0430SSc-PAH (HR 1.14, 95% CI 0.22–5.86, p = 0.872)31
  HemorrhagesPresence of hemorrhages at inclusionN/ASSc-PAH (HR 0.98, 95% CI 0.42–2.30, p = 0.969)31No association
Progression of hemorrhagesN/ASSc-PAH (HR 0.44, 95% CI 0.05–3.55, p = 0.443)31
Semiquantitative
  NVC scoreN/AN/ANot investigated
  Avascular area gradeN/AN/ANot investigated
Qualitative
  Progression to a severe NVC pattern (active/late vs normal/early)SSc-PAH (p = 0.05/p = 0.01; HR 5.12, 95% CI 1.23–21.27)30,31N/AProgression to a severe NVC pattern (active/late) was unequivocally associated with incident SSc-PAH in 2 longitudinal studies
  • SSc-PAH: systemic sclerosis–related pulmonary arterial hypertension; NVC: nailfold videocapillaroscopy; N/A: not applicable.