Ugurlu Erhan, Kilic-Toprak Emine, Altinisik Goksel, Kilic-Erkek Ozgen, Cengiz Betul, Kucukatay Vural, Senol Hande, Akbudak Ismail Hakki, Ekbic Yusuf, Bor-Kucukatay Melek
Pamukkale University.
Sarcoidosis Vasc Diffuse Lung Dis. 2016 Dec 23;33(4):308-316.
Hemorheological properties are important determinants of tissue oxygenation. Although hemorheological alterations in various lung diseases have been well-defined, no information is available about the effects of idiopathic interstitial pneumonia (IIP) on hemorheological parameters.
The aim of this study was to investigate hemorheological parameters (erythrocyte deformability, aggregation, and plasma viscosity -PV) and associated oxidative stress indices in patients with IIP.
The study enrolled 31 patients (9 Idiopathic pulmonary fibrosis (IPF), 10 non-specific Interstitial Pneumonia (NSIP), 12 Cryptogenic Organising Pneumonia (COP) and 33 healthy controls. Erythrocyte deformability and aggregation were measured by an ektacytometer. PV was determined by a cone-plate rotational viscometer and oxidative stress via a commercial kit.
Erythrocyte aggregation, total oxidant status (TOS) and oxidative stress index (OSI) of IIP patients were higher than controls whereas erythrocyte deformability, PV and total antioxidant status (TAS) were unaltered.
Increment of oxidative stress in IIP seems to depend on enhancement of oxidants, rather than alteration of antioxidants. The issue that, elevated erythrocyte aggregation may further impair tissue oxygenation by disturbing microcirculation in IIP, may be considered in the follow up and development of new treatment protocols for this disease.
血液流变学特性是组织氧合的重要决定因素。尽管各种肺部疾病中的血液流变学改变已得到明确界定,但关于特发性间质性肺炎(IIP)对血液流变学参数的影响尚无相关信息。
本研究旨在调查IIP患者的血液流变学参数(红细胞变形性、聚集性和血浆粘度 - PV)以及相关的氧化应激指标。
该研究纳入了31例患者(9例特发性肺纤维化(IPF)、10例非特异性间质性肺炎(NSIP)、12例隐源性机化性肺炎(COP))和33名健康对照者。通过血细胞变形仪测量红细胞变形性和聚集性。通过锥板旋转粘度计测定PV,并通过商用试剂盒测定氧化应激。
IIP患者的红细胞聚集性、总氧化剂状态(TOS)和氧化应激指数(OSI)高于对照组,而红细胞变形性、PV和总抗氧化剂状态(TAS)未改变。
IIP中氧化应激的增加似乎取决于氧化剂的增强,而非抗氧化剂的改变。在该疾病的随访和新治疗方案的制定中,可能需要考虑红细胞聚集性升高可能通过扰乱IIP中的微循环进一步损害组织氧合这一问题。