Key result
Patients with polycythemia vera had significantly higher mean arterial pressure (106.8 vs. 93.8 mmHg) and plasma cell-free hemoglobin (9.7 vs. 2.8 mg/dL) than healthy controls (p<=0.01).
Why the study?
Does isovolemic erythrocytapheresis reduce mean arterial pressure and cell-free hemoglobin in patients with polycythemia vera?
Observational (n=111)
Does isovolemic erythrocytapheresis reduce mean arterial pressure and cell-free hemoglobin in patients with polycythemia vera?
Absolute Event Rate: 106.8% vs 93.8%
p-value: p=<= 0.01
Accelerated scavenging of nitric oxide by cell-free hemoglobin, rather than high hematocrit, may be a primary driver of hypertension in patients with polycythemia vera, which can be reduced by erythrocytapheresis.
We tested the hypothesis that hypertension associated with polycythemia vera (PV) may be related to hemoglobin released from erythrocytes (cell-free hemoglobin, fHb). We assessed hematocrit, mean arterial pressure (MAP), blood viscosity, and the level of fHb and nitrite/nitrate (NOx) in the plasma of 73 PV patients and 38 healthy controls. The effect of isovolemic erythrocytapheresis (ECP) on the considered parameters was also studied. From the whole group of PV patients a subset of subjects with normal (normotensive patients, n = 16) and elevated MAP (hypertensive patients, n = 57) can be subtracted. It was found that in comparison with healthy controls, PV patients have significantly (p ≤ 0.01) elevated Hct (0.567 vs. 0.422), blood viscosity (5.45 vs. 3.56 cP), MAP (106.8 vs. 93.8 mmHg), plasma fHb (9.7 vs. 2.8 mg/dL), and NOx levels (34.1 vs. 27.5 μM). Compared with normotensive patients, hypertensive PV patients demonstrated a higher rise in fHb (10.2 vs. 8.0) and plasma NOx levels (35.8 vs. 31.0). In PV patients, fHb positively correlates with MAP (r = 0.489), NOx levels (r = 0.461), hematocrit (r = 0.428), and viscosity (r = 0.393). Blood viscosity positively correlated with hematocrit (r = 0.894), but not with other considered parameters. In PV patients MAP poorly correlated with hematocrit, whereas the correlation between MAP and NOx altered from - 0.325 (healthy control) to + 0.268 (PV patients). ECP procedure was associated with a significant (p < 0.01) reduction of hematocrit, fHb, blood viscosity, and MAP. In the normotensive subgroup of PV patients the ECP procedure did not affect MAP. It can be concluded that accelerated scavenging of nitric oxide by fHb rather than high Hct may be a key factor determining the development of hypertension in PV patients.
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Rusak et al. (2013) conducted an observational in Polycythemia vera (n=111). Polycythemia vera vs. Healthy controls was evaluated on Mean arterial pressure (MAP) (p=<= 0.01). Patients with polycythemia vera had significantly higher mean arterial pressure (106.8 vs. 93.8 mmHg) and plasma cell-free hemoglobin (9.7 vs. 2.8 mg/dL) than healthy controls (p<=0.01).
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