Literature DB >> 22244549

Raised erythrocyte creatine in patients with pulmonary arterial hypertension--evidence for subclinical hemolysis.

Benjamin D Fox1, Toshika Okumiya, Liat Attas-Fox, Michael Kassirer, Yael Raviv, Mordechai R Kramer.   

Abstract

BACKGROUND: Pulmonary arterial hypertension (PAH) has been associated with hemolytic conditions such as sickle cell disease but the possible role of hemolysis in the pathogenesis or pathophysiology of other forms of PAH has not been studied. Erythrocyte lifespan is the gold-standard test of hemolysis and may be measured by assaying erythrocyte creatine (EC) levels. EC decreases as the erythrocyte ages, so patients with hemolysis have high EC levels.
METHODS: We measured EC and other parameters of hemolysis in patients with idiopathic and connective tissue associated PAH and normal controls.
RESULTS: In patients with PAH (n = 40), EC levels were higher than in controls n = 30 (patients EC 1.72 mcmol/g HgB 95%CI[1.51, 1.96], controls EC 1.05 mcmol/g HgB [0.93, 1.19], p < 0.0001). High levels of EC correlated with worse 6 min walk (r = -0.42, p < 0.0001) and worse functional class (p = 0.002). Other indirect indices of hemolysis (total lactate dehydrogenase, red cell distribution width) were also increased in patients with PAH relative to controls.
CONCLUSIONS: There is evidence of subclinical hemolysis in patients with PAH, and higher levels of hemolysis are associated with poorer exercise capacity. Copyright Â
© 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22244549     DOI: 10.1016/j.rmed.2011.12.005

Source DB:  PubMed          Journal:  Respir Med        ISSN: 0954-6111            Impact factor:   3.415


  4 in total

1.  Shortened mean erythrocyte age in female patients with type 2 diabetes mellitus.

Authors:  Masafumi Koga; Shinya Inada; Hiroko Ijima; Hideaki Jinnouchi; Yasuhiro Ono; Tsuyoshi Iwasaka; Toshika Okumiya
Journal:  J Clin Lab Anal       Date:  2018-10-18       Impact factor: 2.352

2.  The Hepcidin/Ferroportin axis modulates proliferation of pulmonary artery smooth muscle cells.

Authors:  Latha Ramakrishnan; Sofia L Pedersen; Quezia K Toe; Laura E West; Sharon Mumby; Helen Casbolt; Theo Issitt; Benjamin Garfield; Allan Lawrie; S John Wort; Gregory J Quinlan
Journal:  Sci Rep       Date:  2018-08-28       Impact factor: 4.379

3.  The clinical characteristics and long-term prognosis of pulmonary arterial hypertension associated with hereditary hemorrhagic telangiectasia.

Authors:  Wen Li; Chang-Ming Xiong; Qing Gu; Xiao-Tong Wang; Xiao-Ling Cheng; Li Huang; Tao Yang; Qin Luo; Zhi-Hui Zhao; Xin-Hai Ni; Zhi-Hong Liu; Jian-Guo He
Journal:  Pulm Circ       Date:  2018-02-26       Impact factor: 3.017

Review 4.  Pulmonary Arterial Hypertension: Iron Matters.

Authors:  Latha Ramakrishnan; Sofia L Pedersen; Quezia K Toe; Gregory J Quinlan; Stephen J Wort
Journal:  Front Physiol       Date:  2018-05-31       Impact factor: 4.566

  4 in total

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