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Arthritis Res Ther. 2012; 14(3): R143.
Published online 2012 June 12. doi:  10.1186/ar3876
PMCID: PMC3446526
N-terminal pro-brain natriuretic peptide in a novel screening algorithm for pulmonary arterial hypertension in systemic sclerosis: a case-control study
Vivek Thakkar,1 Wendy M Stevens,1 David Prior,2 Owen A Moore,1 Jillian Byron,1 Danny Liew,3 Karen Patterson,4 Pravin Hissaria,4,5 Janet Roddy,6 Jane Zochling,7 Joanne Sahhar,8 Peter Nash,9 Kathleen Tymms,10 David Celermajer,11 Eli Gabbay,12 Peter Youssef,13 Susanna M Proudman,14 and Mandana Nikpourcorresponding author1,15
1Department of Rheumatology, St Vincent's Hospital Melbourne, 41 Victoria Parade, Fitzroy, Victoria 3065, Australia
2Department of Cardiology, St Vincent's Hospital Melbourne, 41 Victoria Parade, Fitzroy, Victoria 3065, Australia
3Department of Epidemiology, Biostatistics and Health Research, Royal Melbourne Hospital, Grattan Street, Parkville, Victoria 3050
4Institute of Medical and Veterinary Science/SA Pathology, 72 King William Road, North Adelaide, South Australia 5000, Australia
5Departments of Clinical Immunology and Immunopathology, Royal Adelaide Hospital, North Terrace, South Australia 5000, Australia
6Department of Rheumatology, Royal Perth Hospital, Wellington Street (GPO Box X2213), Perth, Western Australia 6001, Australia
7Department of Rheumatology, The Menzies Institute, Private Bag 23, Hobart, Tasmania 7001, Australia
8Department of Rheumatology, Monash Medical Centre, 246 Clayton Road, Clayton, Melbourne, Victoria 3168, Australia
9Sunshine Coast Rheumatology, PO Box 368, Maroochydore, Sunshine Coast, Queensland 4558, Australia
10Canberra Rheumatology, 40 Markus Clarke Street, Canberra, Australian Capital Territory 2601, Australia
11Department of Cardiology, Royal Prince Alfred Hospital, Missendon Road, Camperdown, New South Wales 2050, Australia
12Advanced Lung Disease Unit and Pulmonary Hypertension Service, Royal Perth Hospital, GPO Box X2213, Perth, WA 6001, Australia
13Institute of Rheumatology and Orthopaedics, Royal Prince Alfred Hospital, Queen Elizabeth II Building, Missendon Road, Camperdown, New South Wales 2050, Australia
14Department of Rheumatology, Royal Adelaide Hospital, North Terrace, Adelaide, South Australia 5000
15The University of Melbourne Department of Medicine, St Vincent's Hospital Melbourne, 41 Victoria Parade, Fitzroy, Victoria 3065, Australia
corresponding authorCorresponding author.
Vivek Thakkar: Vivek.Thakkar/at/svhm.org.au; Wendy M Stevens: Wendy.Stevens/at/svhm.org.au; David Prior: David.Prior/at/svhm.org.au; Owen A Moore: droamoore/at/gmail.com; Jillian Byron: Jill.Byron/at/svhm.org.au; Danny Liew: Danny.Liew/at/mh.org.au; Karen Patterson: Karen.Patterson/at/health.sa.gov.au; Pravin Hissaria: Pravin.Hissaria/at/health.sa.gov.au; Janet Roddy: Janet.Roddy/at/health.wa.gov.au; Jane Zochling: jane.zochling/at/utas.edu.au; Joanne Sahhar: jsdixon/at/bigpond.com; Peter Nash: pnash/at/tpg.com.au; Kathleen Tymms: Canberra_rheumatology/at/bigpond.com; David Celermajer: david.celermajer/at/email.cs.nsw.gov.au; Eli Gabbay: EGabbay/at/respiratorywest.com.au; Peter Youssef: pyoussef/at/med.usyd.edu.au; Susanna M Proudman: sproudman/at/internode.on.net; Mandana Nikpour: mnikpour/at/medstv.unimelb.edu.au
Received March 23, 2012; Accepted June 12, 2012.
Abstract
Introduction
Pulmonary arterial hypertension is a major cause of mortality in systemic sclerosis. N-terminal pro-brain natriuretic peptide (NT-proBNP) has emerged as a candidate biomarker that may enable the early detection of systemic sclerosis-related pulmonary arterial hypertension (SSc-PAH). The objective of our study was to incorporate NT-proBNP into a screening algorithm for SSc-PAH that could potentially replace transthoracic echocardiography (TTE) as a more convenient and less costly "first tier" test.
Methods
NT-proBNP levels were measured in patients from four clinical groups: a group with right heart catheter (RHC)-diagnosed SSc-PAH before commencement of therapy for PAH; a group at high risk of SSc-PAH based on TTE; a group with interstitial lung disease; and systemic sclerosis (SSc) controls with no cardiopulmonary complications. NT-proBNP levels were compared by using ANOVA and correlated with other clinical variables by using simple and multiple linear regression. ROC curve analyses were performed to determine the optimal cut point for NT-proBNP and other clinical variables in prediction of PAH.
Results
NT-proBNP was highest in the PAH group compared with other groups (P < 0.0001), and higher in the risk group compared with controls (P < 0.0001). NT-proBNP was positively correlated with systolic pulmonary artery pressure (PAP) on TTE (P < 0.0001), and mean PAP (P = 0.013), pulmonary vascular resistance (P = 0.005), and mean right atrial pressure (P = 0.006) on RHC. A composite model wherein patients screened positive if NT-proBNP was ≥ 209.8 pg/ml, and/or DLCOcorr was < 70.3% with FVC/DLCOcorr ≥ 1.82, had a sensitivity of 100% and specificity of 77.8% for SSc-PAH.
Conclusion
We have proposed a screening algorithm for SSc-PAH, incorporating NT-proBNP level and PFTs. This model has high sensitivity and specificity for SSc-PAH and, if positive, should lead to TTE and confirmatory testing for PAH. This screening algorithm must be validated prospectively.
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