Literature DB >> 21297151

Unexplained iron deficiency in idiopathic and heritable pulmonary arterial hypertension.

Elaine Soon1, Carmen M Treacy, Mark R Toshner, Robert MacKenzie-Ross, Vijay Manglam, Mark Busbridge, Mark Sinclair-McGarvie, Jayantha Arnold, Karen K Sheares, Nicholas W Morrell, Joanna Pepke-Zaba.   

Abstract

BACKGROUND: Anaemia is common in left heart failure and is associated with a poorer outcome. Many patients with pulmonary arterial hypertension (PAH) are anaemic or iron-deficient. This study was performed to investigate the prevalence of iron deficiency in PAH and to identify possible causes.
METHODS: All patients with idiopathic or heritable PAH diagnosed in 1995-2008 were identified. Controls were selected from patients with chronic thromboembolic pulmonary hypertension (CTEPH). Full blood counts were examined and any abnormality was investigated. Patients were excluded if they had a cause for iron deficiency. The prevalence study was based on 85 patients with idiopathic PAH and 120 with CTEPH. A separate group of 20 patients with idiopathic PAH and 24 with CTEPH with matching haemodynamics were prospectively investigated for serum factors affecting iron metabolism.
RESULTS: The prevalence study identified a point prevalence of unexplained iron deficiency of 50% in premenopausal women with idiopathic PAH compared with 8% in premenopausal women with CTEPH (p=0.002); 14% in postmenopausal women with idiopathic PAH compared with 6% in postmenopausal women with CTEPH (p=0.16); 28% in men with idiopathic PAH men compared with 2% in men with CTEPH (p=0.002); and 60% in patients with heritable PAH. The serum study showed that patients with idiopathic PAH had lower serum iron and transferrin saturations than those with CTEPH. Interleukin-6 levels correlated with iron levels (r=-0.6, p=0.006) and transferrin saturations (r=-0.68, p=0.001) in idiopathic PAH but not in CTEPH.
CONCLUSIONS: The prevalence of unexplained iron deficiency is significantly higher in idiopathic PAH than in CTEPH. This may be linked to interleukin-6.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21297151     DOI: 10.1136/thx.2010.147272

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  41 in total

1.  High levels of zinc-protoporphyrin identify iron metabolic abnormalities in pulmonary arterial hypertension.

Authors:  Ilka Decker; Sudakshina Ghosh; Suzy A Comhair; Samar Farha; Wai Hong Wilson Tang; Margaret Park; Sihe Wang; Alan E Lichtin; Serpil C Erzurum
Journal:  Clin Transl Sci       Date:  2011-08       Impact factor: 4.689

Review 2.  The crossroads of iron with hypoxia and cellular metabolism. Implications in the pathobiology of pulmonary hypertension.

Authors:  Jeffrey C Robinson; Brian B Graham; Tracey C Rouault; Rubin M Tuder
Journal:  Am J Respir Cell Mol Biol       Date:  2014-12       Impact factor: 6.914

3.  Ironing out pulmonary arterial hypertension.

Authors:  Jodie L Babitt
Journal:  Proc Natl Acad Sci U S A       Date:  2019-06-06       Impact factor: 11.205

Review 4.  Sex, Gender, and Sex Hormones in Pulmonary Hypertension and Right Ventricular Failure.

Authors:  James Hester; Corey Ventetuolo; Tim Lahm
Journal:  Compr Physiol       Date:  2019-12-18       Impact factor: 9.090

5.  Iron chelation inhibits the development of pulmonary vascular remodeling.

Authors:  Chi-Ming Wong; Ioana R Preston; Nicholas S Hill; Yuichiro J Suzuki
Journal:  Free Radic Biol Med       Date:  2012-08-25       Impact factor: 7.376

6.  Hemodynamic response to treatment of iron deficiency anemia in pulmonary arterial hypertension: longitudinal insights from an implantable hemodynamic monitor.

Authors:  Muddassir Mehmood; Richa Agarwal; Amresh Raina; Priscilla Correa-Jaque; Raymond L Benza
Journal:  Pulm Circ       Date:  2016-12       Impact factor: 3.017

Review 7.  The Search for Disease-Modifying Therapies in Pulmonary Hypertension.

Authors:  Chen-Shan Chen Woodcock; Stephen Y Chan
Journal:  J Cardiovasc Pharmacol Ther       Date:  2019-02-17       Impact factor: 2.457

8.  Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia).

Authors:  Craig A Sable; Zakari Y Aliyu; Niti Dham; Mehdi Nouraie; Vandana Sachdev; Stanislav Sidenko; Galina Y Miasnikova; Lydia A Polyakova; Adelina I Sergueeva; Daniel J Okhotin; Vladimir Bushuev; Alan T Remaley; Xiaomei Niu; Oswaldo L Castro; Mark T Gladwin; Gregory J Kato; Josef T Prchal; Victor R Gordeuk
Journal:  Haematologica       Date:  2011-10-11       Impact factor: 9.941

9.  Elevation of plasma cell-free hemoglobin in pulmonary arterial hypertension.

Authors:  Evan L Brittain; David R Janz; Eric D Austin; Julie A Bastarache; Lisa A Wheeler; Lorraine B Ware; Anna R Hemnes
Journal:  Chest       Date:  2014-12       Impact factor: 9.410

10.  BMP type II receptors have redundant roles in the regulation of hepatic hepcidin gene expression and iron metabolism.

Authors:  Claire Mayeur; Patricio A Leyton; Starsha A Kolodziej; Binglan Yu; Kenneth D Bloch
Journal:  Blood       Date:  2014-07-29       Impact factor: 22.113

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.