Papassotiriou I, Kanavakis E, Stamoulakatou A, Kattamis C
Hematology Laboratory, Aghia Sophia Children's Hospital, Athens, Greece.
Pediatr Hematol Oncol. 1997 Jul-Aug;14(4):323-34. doi: 10.3109/08880019709041592.
To evaluate the degree of tissue hypoxia in patients with hemoglobinopathy H disease, whole blood oxygen affinity was estimated and analyzed in 33 patients. Twenty patients with iron deficiency anemia, matched for degree of anemia, served as controls. The results were as follows: Whole blood oxygen equilibrium curves of patients with HbH disease are biphasic because of a combination of the rectangular hyperbolic curve of HbH and the normal sigmoid curve of HbA and are shifted toward the left (P50 3.66 +/- 0.33 kPa). Patients with iron deficiency anemia have right-shifted oxygen equilibrium curves (P50 4.02 +/- 0.13 kPa) compared with normal. Oxygen release to the tissues in HbH disease is decreased (1.4 +/- 0.3 mmol/L) as compared with iron-deficient patients (1.6 +/- 0.2 mmol/L) with a similar degree of anemia. Red cell indices vary between the two groups. In patients with HbH disease the mean corpuscular hemoglobin concentration was 268 +/- 17 g/L as compared with 294 +/- 18 g/L in iron deficiency anemia. These findings indicate that whole blood oxygen affinity is a reliable index of tissue oxygenation in patients with hemoglobinopathy H.
为评估血红蛋白病H病患者的组织缺氧程度,对33例患者的全血氧亲和力进行了估算和分析。选取20例贫血程度与之匹配的缺铁性贫血患者作为对照。结果如下:由于HbH的矩形双曲线和HbA的正常S形曲线共同作用,HbH病患者的全血氧平衡曲线呈双相,且向左移位(P50为3.66±0.33kPa)。与正常情况相比,缺铁性贫血患者的氧平衡曲线右移(P50为4.02±0.13kPa)。与贫血程度相似的缺铁性贫血患者(1.6±0.2mmol/L)相比,HbH病患者向组织释放的氧量减少(1.4±0.3mmol/L)。两组之间的红细胞指数有所不同。HbH病患者的平均红细胞血红蛋白浓度为268±17g/L,而缺铁性贫血患者为294±18g/L。这些发现表明,全血氧亲和力是血红蛋白病H患者组织氧合的可靠指标。