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激光辅助光学旋转细胞分析仪(LoRRca MaxSis)在红细胞膜疾病、酶缺陷及先天性红细胞生成异常性贫血诊断中的应用:一项对202例患者的单中心研究

Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.

作者信息

Zaninoni Anna, Fermo Elisa, Vercellati Cristina, Consonni Dario, Marcello Anna P, Zanella Alberto, Cortelezzi Agostino, Barcellini Wilma, Bianchi Paola

机构信息

UOC Oncoematologia, UOS Fisiopatologia delle Anemie, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

UO Epidemiologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

出版信息

Front Physiol. 2018 Apr 27;9:451. doi: 10.3389/fphys.2018.00451. eCollection 2018.

Abstract

Chronic hemolytic anemias are a group of heterogeneous diseases mainly due to abnormalities of red cell (RBC) membrane and metabolism. The more common RBC membrane disorders, classified on the basis of blood smear morphology, are hereditary spherocytosis (HS), elliptocytosis, and hereditary stomatocytoses (HSt). Among RBC enzymopathies, the most frequent is pyruvate kinase (PK) deficiency, followed by glucose-6-phosphate isomerase, pyrimidine 5' nucleotidase P5'N, and other rare enzymes defects. Because of the rarity and heterogeneity of these diseases, diagnosis may be often challenging despite the availability of a variety of laboratory tests. The ektacytometer laser-assisted optical rotational cell analyser (LoRRca MaxSis), able to assess the RBC deformability in osmotic gradient conditions (Osmoscan analysis), is a useful diagnostic tool for RBC membrane disorders and in particular for the identification of hereditary stomatocytosis. Few data are so far available in other hemolytic anemias. We evaluated the diagnostic power of LoRRca MaxSis in a large series of 140 patients affected by RBC membrane disorders, 37 by enzymopathies, and 16 by congenital diserythropoietic anemia type II. Moreover, nine patients with paroxysmal nocturnal hemoglobinuria (PNH) were also investigated. All the hereditary spherocytoses, regardless the biochemical defect, showed altered Osmoscan curves, with a decreased Elongation Index (EI) max and right shifted Omin; hereditary elliptocytosis (HE) displayed a trapezoidal curve and decreased EImax. Dehydrated hereditary stomatocytosis (DHSt) caused by mutations was characterized by left-shifted curve, whereas mutations were associated with a normal curve. Congenital diserythropoietic anemia type II and RBC enzymopathies had Osmoscan curve within the normal range except for glucosephosphate isomerase (GPI) deficient cases who displayed an enlarged curve associated with significantly increased Ohyper, offering a new diagnostic tool for this rare enzyme defect. The Osmoscan analysis performed by LoRRca MaxSis represents a useful and feasible first step screening test for specialized centers involved in the diagnosis of hemolytic anemias. However, the results should be interpreted by caution because different factors (i.e., splenectomy or coexistent diseases) may interfere with the analysis; additional tests or molecular investigations are therefore needed to confirm the diagnosis.

摘要

慢性溶血性贫血是一组异质性疾病,主要由于红细胞(RBC)膜和代谢异常所致。根据血涂片形态分类,较常见的红细胞膜疾病有遗传性球形红细胞增多症(HS)、椭圆形红细胞增多症和遗传性口形红细胞增多症(HSt)。在红细胞酶病中,最常见的是丙酮酸激酶(PK)缺乏症,其次是葡萄糖-6-磷酸异构酶、嘧啶5'核苷酸酶P5'N以及其他罕见的酶缺陷。由于这些疾病的罕见性和异质性,尽管有多种实验室检查可用,但诊断往往具有挑战性。激光辅助光学旋转细胞分析仪(LoRRca MaxSis)能够在渗透梯度条件下评估红细胞变形性(渗透扫描分析),是诊断红细胞膜疾病尤其是遗传性口形红细胞增多症的有用工具。目前在其他溶血性贫血方面的数据较少。我们评估了LoRRca MaxSis在140例红细胞膜疾病患者、37例酶病患者和16例II型先天性红细胞生成异常性贫血患者中的诊断效能。此外,还对9例阵发性夜间血红蛋白尿(PNH)患者进行了研究。所有遗传性球形红细胞增多症患者,无论生化缺陷如何,均显示渗透扫描曲线改变,最大伸长指数(EI)max降低且Omin右移;遗传性椭圆形红细胞增多症(HE)表现为梯形曲线且EImax降低。由突变引起的脱水遗传性口形红细胞增多症(DHSt)的特征是曲线左移,而突变则与正常曲线相关。II型先天性红细胞生成异常性贫血和红细胞酶病的渗透扫描曲线在正常范围内,但葡萄糖磷酸异构酶(GPI)缺乏症患者的曲线增大,Ohyper显著增加,为这种罕见的酶缺陷提供了一种新的诊断工具。LoRRca MaxSis进行的渗透扫描分析是参与溶血性贫血诊断的专业中心有用且可行的初步筛查试验。然而,结果应谨慎解释,因为不同因素(如脾切除术或并存疾病)可能干扰分析;因此需要额外的检查或分子研究来确诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4d/5934481/3e89ae0e5992/fphys-09-00451-g0001.jpg

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