TY - JOUR
T1 - Red cell distribution width and platelet count as biomarkers of pulmonary arterial hypertension in patients with connective tissue disorders
AU - Bellan, Mattia
AU - Giubertoni, Ailia
AU - Piccinino, Cristina
AU - Dimagli, Arnaldo
AU - Grimoldi, Federico
AU - Sguazzotti, Maurizio
AU - Burlone, Michela Emma
AU - Smirne, Carlo
AU - Sola, Daniele
AU - Marino, Paolo
AU - Pirisi, Mario
AU - Sainaghi, Pier Paolo
N1 - Publisher Copyright:
© 2019 Mattia Bellan et al.
PY - 2019
Y1 - 2019
N2 - Introduction/Objective. In the present paper, we aimed to test the value of the red cell distribution width (RDW) coefficient of variation as a candidate biomarker for pulmonary arterial hypertension (PAH) in patients with connective tissue disorders (CTD), correlating it with the degree of cardiopulmonary impairment in these patients. Methods. The study population included N = 141 patients with CTD and N = 59 patients affected by pulmonary hypertension of other etiologies, all referred to the Pulmonary Hypertension Clinic of the Cardiology Division of an Academic Hospital in Northern Italy for evaluation (including right catheterization). Clinical, instrumental, and laboratory data were collected and related to RDW and other full blood count indexes. Results. Twenty out of 141 CTD patients (14%) received a diagnosis of PAH. In comparison to those without PAH, CTD patients with PAH displayed a larger RDW (14.9% (13.5-17.2) vs. 13.8% (13.1-15.0); p = 0 02) and a lower platelet count (205 (177-240) × 109/l vs. 244 197 5-304 2 × 109/l; p = 0 005). Moreover, with respect to CTD patients without PAH, RDW was significantly larger also in PH of other etiologies. In contrast, the platelet count was significantly lower only in CTD-related PAH, with a value > 276 × 109/l being 100% sensitive in ruling out PAH. Finally, RDW, but not the platelet count, was related directly to systolic pulmonary arterial pressure (r = 0 381; p = 0 0008) and right ventricle diameter (r = 0 283; p = 0 015) and inversely to diffusing capacity of the lung for carbon monoxide (r = -0 325; p = 0 014). Conclusion. RDW is a promising candidate biomarker for the screening and the prognostic stratification of PAH in CTD patients.
AB - Introduction/Objective. In the present paper, we aimed to test the value of the red cell distribution width (RDW) coefficient of variation as a candidate biomarker for pulmonary arterial hypertension (PAH) in patients with connective tissue disorders (CTD), correlating it with the degree of cardiopulmonary impairment in these patients. Methods. The study population included N = 141 patients with CTD and N = 59 patients affected by pulmonary hypertension of other etiologies, all referred to the Pulmonary Hypertension Clinic of the Cardiology Division of an Academic Hospital in Northern Italy for evaluation (including right catheterization). Clinical, instrumental, and laboratory data were collected and related to RDW and other full blood count indexes. Results. Twenty out of 141 CTD patients (14%) received a diagnosis of PAH. In comparison to those without PAH, CTD patients with PAH displayed a larger RDW (14.9% (13.5-17.2) vs. 13.8% (13.1-15.0); p = 0 02) and a lower platelet count (205 (177-240) × 109/l vs. 244 197 5-304 2 × 109/l; p = 0 005). Moreover, with respect to CTD patients without PAH, RDW was significantly larger also in PH of other etiologies. In contrast, the platelet count was significantly lower only in CTD-related PAH, with a value > 276 × 109/l being 100% sensitive in ruling out PAH. Finally, RDW, but not the platelet count, was related directly to systolic pulmonary arterial pressure (r = 0 381; p = 0 0008) and right ventricle diameter (r = 0 283; p = 0 015) and inversely to diffusing capacity of the lung for carbon monoxide (r = -0 325; p = 0 014). Conclusion. RDW is a promising candidate biomarker for the screening and the prognostic stratification of PAH in CTD patients.
UR - http://www.scopus.com/inward/record.url?scp=85069269902&partnerID=8YFLogxK
U2 - 10.1155/2019/4981982
DO - 10.1155/2019/4981982
M3 - Article
SN - 0278-0240
VL - 2019
JO - Disease Markers
JF - Disease Markers
M1 - 4981982
ER -