- Research article
- Open Access
The inclusion of N-terminal pro-brain natriuretic peptide in a sensitive screening strategy for systemic sclerosis-related pulmonary arterial hypertension: a cohort study
Arthritis Research & Therapyvolume 15, Article number: R193 (2013)
Pulmonary arterial hypertension (PAH) is a major cause of mortality in systemic sclerosis (SSc). Screening guidelines for PAH recommend multiple investigations, including annual echocardiography, which together have low specificity and may not be cost-effective. We sought to evaluate the predictive accuracy of serum N-terminal pro-brain natriuretic peptide (NT-proBNP) in combination with pulmonary function tests (PFT) (‘proposed’ algorithm) in a screening algorithm for SSc-PAH.
We evaluated our proposed algorithm (PFT with NT-proBNP) on 49 consecutive SSc patients with suspected pulmonary hypertension undergoing right heart catherisation (RHC). The predictive accuracy of the proposed algorithm was compared with existing screening recommendations, and is presented as sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV).
Overall, 27 patients were found to have pulmonary hypertension (PH) at RHC, while 22 had no PH. The sensitivity, specificity, PPV and NPV of the proposed algorithm for PAH was 94.1%, 54.5%, 61.5% and 92.3%, respectively; current European Society of Cardiology (ESC)/European Respiratory Society (ERS) guidelines achieved a sensitivity, specificity, PPV and NPV of 94.1%, 31.8%, 51.6% and 87.5%, respectively. In an alternate case scenario analysis, estimating a PAH prevalence of 10%, the proposed algorithm achieved a sensitivity, specificity, PPV and NPV for PAH of 94.1%, 54.5%, 18.7% and 98.8%, respectively.
The combination of NT-proBNP with PFT is a sensitive, yet simple and non-invasive, screening strategy for SSc-PAH. Patients with a positive screening result can be referred for echocardiography, and further confirmatory testing for PAH. In this way, it may be possible to shift the burden of routine screening away from echocardiography. The findings of this study should be confirmed in larger studies.
Systemic sclerosis (SSc) is a multisystem connective tissue disease resulting in a number of end-organ complications due to the pathogenic processes of vasculopathy, fibrosis and autoimmunity . Systemic sclerosis-related pulmonary arterial hypertension (SSc-PAH) is a particularly severe complication, affecting approximately 10% of SSc patients, and is one of the leading causes of mortality in these patients .
The early detection of SSc-PAH has emerged as an essential component of disease management. A number of studies have demonstrated the significantly better prognosis of patients presenting in lower World Health Organization functional classes (WHO-FC) (that is I and II), compared to patients presenting with more advanced functional impairment (WHO-FC III or IV) [3, 4]. Other studies have suggested that early commencement of therapy may delay the progression of SSc-PAH, and lead to improvements in functional class [5, 6]. Recently, the benefits of screening for SSc-PAH were observed in a study that showed a significantly higher three-, five- and eight-year survival rate in patients identified by a screening program compared with patients diagnosed during the course of routine clinical care, when symptoms and/or signs directed further investigation (81%, 73% and 64% vs. 31%, 25% and 17%, respectively) .
Right heart catherisation (RHC) is currently the only confirmatory test for PAH, but its invasive nature makes it unsuitable for screening. Instead, non-invasive screening strategies are used to risk-stratify patients for RHC. Current guidelines recommend transthoracic echocardiography (TTE), either with or without diffusing capacity for carbon monoxide (DLCO), as the strategy of choice; however, there are some important limitations with this approach [8–10]. While echocardiography and DLCO perform well when PAH is advanced, neither test has sufficiently high sensitivity for the detection of early disease, nor for the exclusion of PAH . Further, variations in echocardiography technique, the accuracy of measurements and interpretation of results poses challenges for the clinician, especially in community-based practice where the quality of echocardiography can be variable. In fact, the systolic pulmonary artery pressure at echocardiography (sPAPTTE) cannot be obtained in 20 to 39% of patients due to technical and patient-related factors such as obesity or concomitant interstitial lung disease (ILD) [12, 13]. Lastly, the cost-effectiveness of echocardiography-based screening remains to be evaluated, and it may be improved by rationalising the use of these screening tools.
We have previously proposed a ‘first-tier’ screening algorithm for SSc-PAH utilising serum N-terminal pro-brain natriuretic peptide (NT-proBNP) levels and pulmonary function tests (PFTs) . NT-proBNP is an easily measured biomarker released by cardiac myocytes in response to increased ventricular wall stress. A number of studies have reported the potential utility of NT-proBNP in SSc-PAH, including the study by Allanore et al. wherein a high NT-proBNP level (>97th percentile of normal) identified SSc patients who went on to develop pre-capillary pulmonary hypertension (pre-CPH) over a median follow-up period of 29 months [15–18]. We demonstrated that combining NT-proBNP and PFTs to select patients with positive screening results for referral for echocardiography had a high sensitivity and specificity for SSc-PAH confirmed by subsequent RHC. This approach has the potential to shift the burden of routine screening away from using echocardiography in every patient to limiting its use in a more targeted fashion to assist in the selection of patients for RHC.
For a screening algorithm for SSc-PAH to be validated, it should be compared with the diagnostic gold standard in an unselected group of SSc patients. In this case, RHC would be required in every patient but this could be difficult to do without selection bias as this test is not without risk. In the first instance, we set out to evaluate the predictive accuracy of the proposed screening algorithm in a group of patients at risk of SSc-PAH and to compare this with the screening guidelines recommended by the Australian Scleroderma Cohort Study (ASCS)  and European Society of Cardiology/European Respiratory Society (ESC/ERS) , both of which rely on annual echocardiography.
For this study, we included consecutive SSc patients from the ASCS who were considered to be at high risk for PAH according to the ASCS screening guidelines and hence referred for RHC. We then evaluated the performance of the ‘proposed algorithm’ and ESC/ERS screening recommendations on this group of patients. The ASCS is a prospective, multi-centre study of risk and prognostic factors for cardiopulmonary outcomes in SSc. All patients fulfil either American College of Rheumatology (ACR) or Leroy and Medsger criteria for SSc [20, 21]. The ASCS has been approved by the human research ethics committees of the 13 participating Australian centres (St Vincent’s Hospital Melbourne, Royal Perth Hospital, Royal Adelaide Hospital, Queen Elizabeth Hospital, Sunshine Coast Rheumatology, Prince Charles Hospital, John Hunter Hospital, Royal Prince Alfred Hospital, Royal North Shore Hospital, St George Hospital, Canberra Rheumatology, Monash Medical Centre and The Menzies Research Institute Tasmania), and patients provide written informed consent at recruitment.
Patients involved in our previous derivation study were excluded . While there were no specific exclusion criteria for the patients in this study, patients screening positive to the ASCS undergo careful adjudication before progression to RHC where they have demonstrated previous evidence of clinically relevant left heart disease.
Current ASCS recommendations are that all patients undergo an annual clinical assessment, TTE and PFTs. Any patient identified as having possible PAH (sPAPTTE ≥40 mmHg, and/or DLCOcorr ≤50% predicted with forced vital capacity (FVC) >85%, and/or fall in DLCOcorr ≥20% on the previous year, or unexplained dyspnoea), especially in the presence of symptoms and without adequate explanation on high-resolution computed tomography (HRCT) lung and/or ventilation/perfusion (V/Q) scanning, undergoes RHC .
Current ESC/ERS guidelines are based on TTE, and recommend a lower-limit threshold value of a triscuspid regurgitant velocity (TRV) >2.8 m/s or sPAPTTE >36 mmHg for consideration of RHC .
Based on current guidelines, PH was defined as a mean pulmonary artery pressure (mPAP) ≥25 mmHg at RHC; therefore, no PH was defined as mPAP <25 mmHg . Pre-CPH was defined as mean pulmonary artery pressure (mPAP) >25 mmHg at rest and pulmonary capillary wedge pressure (PCWP) ≤15 mmHg. If the PCWP exceeded 15 mmHg, disease of the left side of the heart (LHD-PH), or post-capillary PH were diagnosed. PAH was defined as pre-capillary PH on RHC with no more than mild ILD on HRCT, and a FVC, (litres) >70% predicted. ILD-PH was defined as pre-CPH with moderate or severe changes of ILD on HRCT with FVC ≤70% predicted [12, 22].
Cardiac and pulmonary assessments
TTE, PFTs and NT-proBNP were all determined within one month of RHC. Left ventricular systolic and diastolic function and right ventricular systolic function were determined by two-dimensional TTE. sPAPTTE was estimated by Doppler echocardiography at rest, based on peak velocity of the tricuspid regurgitant jet and estimation of right atrial pressure of 5 to 10 mmHg based on the diameter and respiratory variation of the inferior vena cava. TTE was performed only at tertiary centres for SSc assessment. Pulmonary involvement was assessed by PFTs and/or HRCT. HRCTs were reported as no, mild, moderate or severe ILD by a radiologist based on total extent of lung disease. All DLCOcorr (ml/mmHg/min) values are reported as % of predicted values, corrected for haemoglobin .
Serum samples and NT-proBNP measurement
All patients had serum collected for NT-proBNP measurement at the time of TTE and PFTs, which were within one month of their RHC, and in cases of PAH, prior to the commencement of advanced pulmonary vasodilator therapy. Blood samples were collected at rest into tubes containing EDTA. Samples were centrifuged and stored at -80°C until used. NT-proBNP was measured using the Elecsys proBNP II sandwich immunoassay on the modular analytics E170 (Roche Diagnostics, Mannheim, Germany). The measurement range of this assay is between 5 pg/mL and 35000 pg/mL.
Proposed screening algorithm
As derived in our previous study, the proposed screening algorithm is comprised of two components: PFTs (component A) and NT-proBNP (component B) (Figure 1) . For ease of application, we have rounded the screening cut points of PFT and NT-proBNP to the nearest significant number. Therefore, component A is present if DLCOcorr <70% with an FVC/DLCOcorr ≥1.8, and component B is present if NT-proBNP ≥210 pg/ml. In this model, the screen is ‘positive’ if either component A, component B, or components A and B are present, and a screen is ‘negative’ if both component A and component B are absent. All patients with a positive screen move on to transthoracic echocardiography together with further tests such as lung HRCT, V/Q scanning and six-minute walk test (6MWT) as clinically indicated, while those who screen negative undergo repeat screening at regular intervals. The purpose of echocardiography and further tests is to evaluate contributing (for example, right and left ventricular systolic or diastolic dysfunction, interstitial lung disease and thromboembolic disease) and prognostic factors (right ventricular dysfunction and pericardial effusion) for pulmonary hypertension, on a case-by-case basis, that may have resulted in a positive screen. If no alternative explanation is found for a positive screen, patients should undergo confirmatory RHC testing, regardless of sPAPTTE at echocardiography.
Data are presented as means ± standard deviations (SD) for continuous variables, and numbers (percentages or proportions) for categorical variables, unless stated otherwise. Normally distributed variables were compared using the Student’s t test with unequal variances, whereas differences in frequency were determined using chi-square and Fisher’s exact tests. The Kruskall-Wallis and Mann-Whitney U test were used to compare the continuous variables among the smaller PH groups. The predictive accuracy of the proposed algorithm, which was also compared with the accuracy of the ERS/ESC algorithm in the same cohort, are presented as sensitivity, specificity, positive (PPV) and negative predictive value (NPV), with 95% confidence intervals (95% CIs). An ‘alternate case scenario’ analysis was also performed assuming a prevalence rate for PAH of 10%, lower than that seen in this study. Two-tailed P value ≤0.05 was considered statistically significant. All statistical analyses were performed using STATA 12.1 (Statacorp, College Station, TX, USA).
RHC was performed in 49 SSc patients as a result of their ASCS screening investigations (see Figure 2). Of these, 27 were found to have PH at RHC, while 22 had no PH. Of those with PH, the majority had PAH (n = 17), whilst the remainder had ILD-PH (n = 6) and LHD-PH (n = 4).
Table 1 outlines the results of the various ASCS screening investigations that led to RHC. Of the 27 patients with PH, 23 (85%) screened positive on echocardiography (sPAPTTE >40 mmHg), 11 (41%) screened positive on both echocardiography and PFT, and in only 2 patients was PFT the only positive test. In the PAH group, 16/17 patients screened positive on echocardiography, and 9/17 (53%) screened positive on both echocardiography and PFT. There was only one patient in the PAH group who had an unrecordable sPAPTTE; this patient had a DLCOcorr of 44% predicted, and was found to have early PAH (WHO FC II, mPAP of 26 mmHg at RHC).
Study demographics: PAH compared with no-PH
The patient demographics and characteristics of patients with PAH and no PH are compared in Tables 2 and 3; the features of the LHD-PH and ILD-PH are also shown. As can be seen, all the patients with PAH were female, with trends towards being older at the times of diagnosis of SSc and PAH. While a significantly greater proportion of the PAH group had anti-centromere antibodies (anti-cents), there were no significant differences in the frequency of Raynaud’s phenomenon (P = 0.178) and calcium channel blocker use (P = 0.128) between the groups. As expected, the PAH group had significantly higher sPAPTTE, and significantly lower DLCOcorr and 6MWD compared to the no PH group. Comparing the PAH and no PH groups, PAH was associated with a significantly higher mean ± SD NT-proBNP (1,074 ± 1,506 versus 303 ± 461, P = 0.008) and FVC/DLCOcorr ratio (2.1 ± 0.5 versus 1.45 ± 0.4, P = 0.0001). As NT-proBNP levels can be affected by older age, renal dysfunction, calcium channel blocker use, body mass index (BMI) and diabetes mellitus, we evaluated these relationships using simple linear regression. Here we found that that higher NT-proBNP levels were associated with older age (P <0.0001) and impaired renal function (P = 0.013), whilst lower NT-proBNP levels were associated with diabetes mellitus (P = 0.040). In this study, neither calcium channel blocker use (P = 0.862) nor BMI (P = 0.930) was associated with NT-proBNP levels.
Study demographics: comparing the types of PH
The PAH, LHD-PH and ILD-PH groups had a comparable age at SSc onset, age at the time of study, disease duration, disease subtype, antibody profile and 6MWD (all P >0.20). The groups also had a comparable mPAP (P = 0.527) and mean right atrial pressure (mRAP) (P = 0.562), but not pulmonary vascular resistance (PVR), with a significantly higher PVR seen in the PAH group compared with LHD-PH (P = 0.015). As expected, the group with ILD-PH had a significantly lower FVC (P = 0.0005) and DLCO (P = 0.031) than the PAH group.
While the highest absolute NT-proBNP levels were observed in ILD-PH (3,367 ± 3,337.0 pg/mL), there were no significant differences in NT-proBNP levels between the PH groups (P = 0.169). There was also no significant difference in the FVC/DLCOcorr ratio between the PH groups (P = 0.261).
Performance of the screening algorithm
The performance of the proposed NT-proBNP and PFT screening algorithm, as applied to this cohort, is presented in Table 4. The sensitivity, specificity, PPV and NPV for PAH were 94.1%, 54.5%, 61.5% and 92.3%, respectively. In comparison, the sensitivity, specificity, PPV and NPV of the ESC/ERS guidelines in this cohort, were 94.1%, 31.8%, 51.6% and 87.5%. Using the proposed algorithm, there was only one case of missed PAH. This patient had an mPAP of 48 mmHg at RHC; however, the patient was haemodynamically (mRAP 4.5 mmHg, cardiac output (CO) 8.2 L/min and PVR 4.5 Woods units) and functionally (WHO FC II, 6MWD 460 m) well preserved. Of the patients with PAH who were screen positive, 56% screened positive to NT-proBNP and PFTs, with 25% screening positive to NT-proBNP alone, and 19% with PFTs alone.
The performance of the proposed algorithm when compared with the ESC/ERS guidelines for pre-CPH and all patients with PH, is also presented in Table 4. As can be seen, the proposed algorithm was also effective at screening for pre-CPH and ‘all-cause’ PH; the sensitivity, specificity, PPV and NPV of the proposed algorithm for all-cause PH was 88.9%, 54.5%, 70.6% and 80.0%, respectively.
Alternate case scenario analysis
Due to the higher than expected prevalence of PAH in this study (as patients had already screened positive to the ASCS algorithm in order to undergo RHC), we performed an alternate case scenario analysis with a PAH prevalence of 10%, as commonly reported in the literature (see Additional file 1) . Here we find that the adjusted sensitivity, specificity, PPV and NPV of the proposed algorithm for PAH was 94.1%, 54.5%, 18.7% and 98.8%, respectively. For comparison, the adjusted sensitivity, specificity, PPV and NPV of the ESC/ERS algorithm was 94.1%, 31.8%, 13.3% and 98.1%, respectively. Therefore, our proposed screening model captures almost all patients with PAH, and would have reduced the number of patients referred for echocardiography and potentially RHC by 50%.
Application of the proposed screening algorithm to ‘no PH’ group
In total, 22 patients were found to have ‘no PH’ at the time of RHC, despite screening positive on conventional screening. In contrast, the proposed screening algorithm of NT-proBNP with PFTs would have led to only 10 of these 22 patients being considered for RHC, thereby reducing the number of false positive screens and unnecessary RHCs. Application of the ESC/ERS algorithm to this cohort would have led to 15 of 21 being considered for RHC, with a further patient having an incomplete screen due to unrecordable TRV.
Next, we considered the clinical features of the no PH group according to the proposed algorithm. We found that those who screened positive but had no PH were significantly older (67.5 ± 11.7 versus 51.5 ± 9.5, P = 0.002) and had a higher mPAP at RHC (20.4 ± 3.6 mmHg versus 17.3 ± 3.0, P = 0.041), compared with those who screened negative. No other important differences were noted in clinical and laboratory characteristics (including disease duration, disease subtype, auto-antibodies (ANAs) renal function, calcium channel blocker use, BMI, presence of significant ILD, 6MWD, DLCO or sPAPTTE; data not shown). Six of the ten patients screening positively using the proposed algorithm had an mPAP 21 to 24 mmHg consistent with the potentially significant entity, borderline pulmonary hypertension.
In this study, we have confirmed that a screening algorithm comprised of NT-proBNP and PFT is a sensitive, non-invasive tool for SSc-PAH screening when applied in patients selected by the more intensive screening algorithm used in the ASCS. We were also able to show that compared with the ASCS and the ESC/ERS algorithms, this proposed algorithm could lead to fewer RHCs being performed, even in those patients with estimated sPAP >40 mmHg on echocardiogram. These results suggest that rather than referring all patients for echocardiography ± DLCO, which is the current practice according to major screening guidelines, only patients who are ‘positive’ in this ‘first-tier’ screen could be referred for echocardiography (+/-HRCT, 6WMD and V/Q if abnormal), and then definitive RHC if PH is still suspected. This requires further validation in a larger group of SSc patients who have been referred for RHC irrespective of their apparent risk of having PH. However, the ethical implications of subjecting low-risk patients to RHC would limit the feasibility of such a study. Nonetheless, it may be possible to better utilise echocardiography and rationalise the use of limited resources.
The success of any given screening tool for SSc-PAH depends on achieving high sensitivity and NPV, ensuring that there are very few or no missed PAH cases, especially because of the potentially serious morbidity and mortality of this complication. At the same time, it is important to limit the number of false positive screens to an acceptable level because diagnostic RHC is invasive. The combination of NT-proBNP and PFT achieved a high sensitivity and NPV of 94.1% and 92.3%, respectively, which was at least comparable to the current ESC/ERS screening guidelines in this cohort, and broadly comparable to the recently presented DETECT study in which patients selected for risk of PAH based on DLCO <60% all had RHC . In fact, the specificity and PPV achieved with the proposed algorithm was better than that seen with application of the ERS/ESC guidelines, with 20% fewer patients without PH being referred for RHC. The decision to perform RHC in this study was based on screening positive to the ASCS screening algorithm (detailed in Methods), and the prevalence of PAH in the highly selected participants in this study was higher than the usually accepted prevalence of 10%. To account for this, we performed an ‘alternate case scenario’ analysis, which confirmed the utility of the screening tool, which continued to outperform the ERS/ESC model, and would have led to a reduction in numbers of patients referred for echocardiography and further tests.
One patient with PAH was not identified using the proposed screening algorithm. Although this patient was shown to have an mPAP of 48 mmHg at RHC, haemodynamics and functional status were well preserved and not typical of moderate PAH (see Results section). However, this missed PAH case highlights the ongoing need for having a high level of suspicion in PAH screening. Indeed, the PFT component of the proposed algorithm in this patient showed a low and unexplained DLCOcorr (53% predicted), which in the presence of symptoms, would almost certainly have triggered further diagnostic evaluation.
The combination of NT-proBNP with PFTs helps overcome the limitations of either test performed in isolation. Similar to other studies, we have shown that PAH cannot be excluded by normal NT-proBNP values and that NT-proBNP lacks sufficient sensitivity as a stand-alone test for SSc-PAH [15–17, 24]. In addition, whilst a linear decline in DLCO for over 10 years has been demonstrated in patients, prior to diagnosis of PAH, often resulting in a high FVC/DLCO ratio, neither DLCO or FVC/DLCO demonstrates sufficient sensitivity and NPV to be relied upon for the exclusion of PAH [25, 26]. In this study, we have demonstrated the complementary roles of NT-proBNP with PFTs, since the absence of either component led to a missed PAH diagnosis in 23 to 29%. Thus, NT-proBNP and PFT combine to provide an efficient and practical ‘first-tier’ screening tool in identifying the SSc patient who should be considered for further cardiopulmonary assessment.
Importantly, the proposed screening model shifts the burden of routine screening away from echocardiography, and instead reserves echocardiography for high-risk, screen ‘positive’ patients where a detailed assessment (including an assessment of direct and indirect signs of PH, tricuspid annular plane systolic excursion (TAPSE), right and left ventricular systolic and diastolic function, valvular heart disease and pericardial effusion) is important. In this way, it may be possible to better rationalise the use of a limited resource like echocardiography. This strategy may also prove more cost-effective and convenient. In Australia, the cost of NT-proBNP combined with PFT is $A197, which is significantly less than the cost of echocardiography combined with PFT at $A367. Furthermore, the proposed algorithm would have resulted in 50% fewer false positive screens in this cohort with a resultant reduction in the number of RHCs, further reducing costs and any morbidity associated with this invasive procedure. NT-proBNP assays have also become much more widely available owing to the usefulness of NT-proBNP in the diagnosis, prognosis and risk stratification of patients with congestive cardiac failure [27–29]. These factors together suggest that NT-proBNP together with PFT might be a practical and efficient ‘first-tier’ screen that better utilises existing resources. A formal cost-effectiveness analysis is the next step in confirming these findings.
The usefulness of the proposed algorithm is not limited to screening for PAH. Multiple causes of pulmonary hypertension can contribute to dyspnoea in an individual SSc patient, including ILD-PH and LHD-PH. In addition to a high sensitivity and NPV, we have shown that the PPV for all causes of PH is 70.6% using the proposed algorithm, enabling the clinician to direct further investigation of these patients where appropriate. Further, the established value of NT-proBNP in identifying cardiac dysfunction, coupled with the utility of PFTs in the assessment of ILD, makes this algorithm a useful tool for dyspnoea evaluation in SSc patients.
So far we have considered all patients screening positive to the proposed algorithm but with no PH at RHC, as false positives. However, the false positive patients identified using the proposed algorithm had a significantly higher mPAP at RHC than those identified with the existing algorithm, and six of ten patients considered false positives had borderline PH with an mPAP of 21 to 24 mmHg. While further follow-up is required to determine the prognosis of this group, the ability to identify a subset of patients widely considered to have abnormal pulmonary artery pressures remains a desirable feature of our proposed screening algorithm .
While this study provides important observations, there are some limitations that must be acknowledged. First, the study participants were an enriched population selected for RHC on the basis of screening positive to the ASCS algorithm. To account for this selection bias, we compared the performance of the ‘proposed’ algorithm with the ESC/ERS guidelines on the same cohort; we also evaluated the performance of the proposed algorithm using an alternate case scenario analysis estimating the prevalence of PAH at 10% . Therefore, it remains for the performance of the proposed algorithm to be evaluated and applied as a first-line screening strategy for SSc-PAH, in a larger study population. Second, the reported NPV refers only to the high-risk population selected for RHC. While this is an inherent limitation of our study design, ethical considerations make it difficult to perform RHC on patients who have apparently ‘normal’ non-invasive risk assessment for SSc-PAH. As a result, RHC is generally reserved for evaluation of patients at high risk for PAH. This has been typical for most studies that have applied a predefined screening algorithm for PAH to an unselected population of SSc patients [15, 31–37]. Even in the recently published DETECT study, the largest SSc cohort to undergo RHC, patients were selected for RHC on the basis of an uncorrected DLCO (% predicted) of less than 60 . The third limitation is that the overall study population is small, and the findings need to be confirmed in a larger population of SSc patients. There was also only a small number of patients with significant LV dysfunction across the groups, potentially limiting the generalisability of the findings to this group. However, significant LV dysfunction would be expected to raise NT-proBNP levels, triggering referral of these patients for echocardiography. Similarly, there were no patients in the study with an estimated glomerular filtration rate (eGFR) <30 ml/min, a factor known to raise NT-proBNP levels. This severity of chronic kidney disease is not typical for the general SSc patient undergoing screening; however, it may be more prudent to retain echocardiography as first-line screening for this group, particularly given the increased risk of atherosclerotic cardiovascular disease in this group. Last, the study does not address the question of the timing and frequency of repeat screening. In keeping with current international recommendations and emerging evidence, we would recommend at least annual screening, from the time of SSc diagnosis . Furthermore, while the study performed well in this cohort of patients with ‘early’ PAH, the utility of the proposed algorithm for early PAH remains to be established by using the proposed algorithm as a first-line screening tool.
We have confirmed that the combination of NT-proBNP and PFT is a sensitive, yet simple and non-invasive, screening strategy for SSc-PAH. Patients screening positive can be referred for echocardiography, and further confirmatory testing for PAH. In this way, it would appear possible to rationalise the use of existing resources.
Six-minute walk distance
Anti- topoisomerase-1 antibody
Australian Scleroderma Cohort Study
Body mass index
Diffusion capacity of lung for carbon monoxide, corrected for haemoglobin
Estimated glomerular filtration rate
European Society of Cardiology/European Respiratory Society
Forced expiratory volume in one second
Forced vital capacity
Forced vital capacity/diffusion capacity of lung for carbon monoxide, corrected for haemoglobin
High-resolution computed tomography
Interstitial lung disease
Left heart disease
Mean pulmonary artery pressure
Mean right atrial pressure
Negative predictive value
N-terminal pro-brain natriuretic peptide
Pulmonary arterial hypertension
Pulmonary capillary wedge pressure
Pulmonary function test
Positive predictive value
Pre-capillary pulmonary hypertension
Pulmonary vascular resistance
Right heart catherisation
Systolic pulmonary artery pressure
Systemic sclerosis-related pulmonary arterial hypertension
Tricuspid regurgitant velocity
World Health Organization functional class.
Katsumoto TR, Whitfield ML, Connolly MK: The pathogenesis of systemic sclerosis. Annu Rev Pathol. 2011, 6: 509-537. 10.1146/annurev-pathol-011110-130312.
Steen VD, Medsger TA: Changes in causes of death in systemic sclerosis, 1972-2002. Ann Rheum Dis. 2007, 66: 940-944. 10.1136/ard.2006.066068.
Condliffe R, Kiely DG, Peacock AJ, Corris PA, Gibbs JSR, Vrapi F, Das C, Elliot CA, Johnson M, DeSoyza J, Torpy C, Goldsmith K, Hodgkins D, Hughes RJ, Pepke-Zaba J, Coghlan JG: Connective tissue disease-associated pulmonary arterial hypertension in the modern treatment era. Am J Respir Crit Care Med. 2009, 179: 151-157. 10.1164/rccm.200806-953OC.
Launay D, Sitbon O, Le Pavec J, Savale L, Tcherakian C, Yaici A, Achouh L, Parent F, Jais X, Simonneau G, Humbert M: Long-term outcome of systemic sclerosis-associated pulmonary arterial hypertension treated with bosentan as first-line monotherapy followed or not by the addition of prostanoids or sildenafil. Rheumatology. 2009, 49: 490-500.
Galiè N, Rubin LJ, Hoeper MM, Jansa P, Al-Hiti H, Meyer GMB, Chiossi E, Kusic-Pajic A, Simonneau G: Treatment of patients with mildly symptomatic pulmonary arterial hypertension with bosentan (EARLY study): a double-blind, randomised controlled trial. Lancet. 2008, 371: 2093-2100. 10.1016/S0140-6736(08)60919-8.
Rubin L, Pulido T, Channick R, Delcroix M, Galie N, Ghofrani A, Jansa P, Le Brun FO, Mehta S, Mittelholzer C, Perchenet L, Sastry BKS, Sitbon O, Souza R, Torbicki A, Simonneau G: Effect of Macitentan on morbidity and mortality in pulmonary arterial hypertension (PAH): results from the SERAPHIN Trial. Chest. 2012, 142: 1026A-10.1378/chest.1456207.
Humbert M, Yaici A, de Groote P, Montani D, Sitbon O, Launay D, Gressin V, Guillevin L, Clerson P, Simonneau G, Hachulla E: Screening for pulmonary arterial hypertension in patients with systemic sclerosis: clinical characteristics at diagnosis and long-term survival. Arthritis Rheum. 2011, 63: 3522-3530. 10.1002/art.30541.
Galie N, Hoeper MM, Humbert M, Torbicki A, Vachiery JL, Barbera JA, Beghetti M, Corris P, Gaine S, Gibbs JS, Gomez-Sanchez MA, Jondeau G, Klepetko W, Opitz C, Peacock A, Rubin L, Zellweger M, Simonneau G: Guidelines for the diagnosis and treatment of pulmonary hypertension: the task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT). Eur Heart J. 2009, 30: 2493-2537.
McLaughlin VV, Archer SL, Badesch DB, Barst RJ, Farber HW, Lindner JR, Mathier MA, McGoon MD, Park MH, Rosenson RS, Rubin LJ, Tapson VF, Varga J: ACCF/AHA 2009 expert consensus document on pulmonary hypertension. J Am Coll Cardiol. 2009, 53: 1573-1619. 10.1016/j.jacc.2009.01.004.
National Pulmonary Hypertension Centres of the UK: Consensus statement on the management of pulmonary hypertension in clinical practice in the UK and Ireland. Heart. 2008, 94: i1-i41.
Mukerjee D, St George D, Knight C, Davar J, Wells AU, Du Bois RM, Black CM, Coghlan JG: Echocardiography and pulmonary function as screening tests for pulmonary arterial hypertension in systemic sclerosis. Rheumatology (Oxford). 2004, 43: 461-466. 10.1093/rheumatology/keh067.
Kowal-Bielecka O, Avouac J, Pittrow D, Huscher D, Behrens F, Denton CP, Foeldvari I, Humbert M, Matucci-Cerinic M, Nash P, Opitz CF, Rubin LJ, Seibold JR, Strand V, Furst DE, Distler O: Echocardiography as an outcome measure in scleroderma-related pulmonary arterial hypertension: a systematic literature analysis by the EPOSS group. J Rheumatol. 2009, 37: 105-115.
Mathai SC, Sibley CT, Forfia PR, Mudd JO, Fisher MR, Tedford RJ, Lechtzin N, Boyce D, Hummers LK, Housten T, Zaiman AL, Girgis RE, Hassoun PM: Tricuspid annular plane systolic excursion is a robust outcome measure in systemic sclerosis-associated pulmonary arterial hypertension. J Rheumatol. 2011, 38: 2410-2418. 10.3899/jrheum.110512.
Thakkar V, Stevens WM, Prior D, Moore OA, Byron J, Liew D, Patterson K, Hissaria P, Roddy J, Zochling J, Sahhar J, Nash P, Tymms K, Celermajer D, Gabbay E, Youssef P, Proudman SM, Nikpour M: N-terminal pro-brain natriuretic peptide in a novel screening algorithm for pulmonary arterial hypertension in systemic sclerosis: a case-control study. Arthritis Res Ther. 2012, 14: R143-10.1186/ar3876.
Allanore Y, Borderie D, Avouac J, Zerkak D, Meune C, Hachulla E, Mouthon L, Guillevin L, Meyer O, Ekindjian OG, Weber S, Kahan A: High N-terminal pro–brain natriuretic peptide levels and low diffusing capacity for carbon monoxide as independent predictors of the occurrence of precapillary pulmonary arterial hypertension in patients with systemic sclerosis. Arthritis Rheum. 2008, 58: 284-291. 10.1002/art.23187.
Mukerjee D, Yap LB, Holmes AM, Nair D, Ayrton P, Black CM, Coghlan JG: Significance of plasma N-terminal pro-brain natriuretic peptide in patients with systemic sclerosis-related pulmonary arterial hypertension. Respir Med. 2003, 97: 1230-1236. 10.1016/S0954-6111(03)00254-3.
Williams MH, Handler CE, Akram R, Smith CJ, Das C, Smee J, Nair D, Denton CP, Black CM, Coghlan JG: Role of N-terminal brain natriuretic peptide (N-TproBNP) in scleroderma-associated pulmonary arterial hypertension. Eur Heart J. 2006, 27: 1485-1494.
Coghlan JG, Denton CP, Grunig E, Bonderman D, Distler O, Khanna D, Muller-Ladner U, Pope JE, Vonk MC, Doelberg M, Chadha-Boreham H, Heinzl H, Rosenberg DM, McLaughlin VV, Seibold JR: Evidence-based detection of pulmonary arterial hypertension in systemic sclerosis: the DETECT study. Ann Rheum Dis. , : -in press
Proudman S, Byron J, Zochling J, Youssef P, Nash P, Tymms K, Chan M, Sturgess A, Schreiber L, Hill C, Celermajer D, Sahhar J, Stevens W: An on-line screening tool for cardiopulmonary complications of scleroderma-the Australian Scleroderma Screening Program. Arthritis Rheum. 2009, 60: S641-10.1002/art.24350.
Masi AT, The Subcommittee for Scleroderma Criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee: Preliminary criteria for the classification of systemic sclerosis (scleroderma). Arthritis Rheum. 1980, 23: 581-10.1002/art.1780230510.
LeRoy EC, Medsger TA: Criteria for the classification of early systemic sclerosis. J Rheumatol. 2001, 28: 1573-1576.
Avouac J, Airo P, Meune C, Beretta L, Dieude P, Caramaschi P, Tiev K, Cappelli S, Diot E, Vacca A, Cracowski JL, Sibilia J, Kahan A, Matucci-Cerinic M, Allanore Y: Prevalence of pulmonary hypertension in systemic sclerosis in European Caucasians and metaanalysis of 5 studies. J Rheumatol. 2010, 37: 2290-2298. 10.3899/jrheum.100245.
Macintyre N, Crapo RO, Viegi G, Johnson DC, van der Grinten CP, Brusasco V, Burgos F, Casaburi R, Coates A, Enright P, Gustafsson P, Hankinson J, Jensen R, McKay R, Miller MR, Navajas D, Pedersen OF, Pellegrino R, Wanger J: Standardisation of the single-breath determination of carbon monoxide uptake in the lung. Eur Respir J. 2005, 26: 720-735. 10.1183/09031936.05.00034905.
Allanore Y, Borderie D, Meune C, Cabanes L, Weber S, Ekindjian OG, Kahan A: N-terminal pro-brain natriuretic peptide as a diagnostic marker of early pulmonary artery hypertension in patients with systemic sclerosis and effects of calcium-channel blockers. Arthritis Rheum. 2003, 48: 3503-3508. 10.1002/art.11345.
Steen V, Medsger TA: Predictors of isolated pulmonary hypertension in patients with systemic sclerosis and limited cutaneous involvement. Arthritis Rheum. 2003, 48: 516-522. 10.1002/art.10775.
Hsu VM, Moreyra AE, Wilson AC, Shinnar M, Shindler DM, Wilson JE, Desai A, Seibold JR: Assessment of pulmonary arterial hypertension in patients with systemic sclerosis: comparison of noninvasive tests with results of right-heart catheterization. J Rheumatol. 2008, 35: 458-465.
Moe GW, Howlett J, Januzzi JL, Zowall H: N-terminal pro-B-type natriuretic peptide testing improves the management of patients with suspected acute heart failure: primary results of the Canadian prospective randomized multicenter IMPROVE-CHF study. Circulation. 2007, 115: 3103-3110. 10.1161/CIRCULATIONAHA.106.666255.
Chen AA, Wood MJ, Krauser DG, Baggish AL, Tung R, Anwaruddin S, Picard MH, Januzzi JL: NT-proBNP levels, echocardiographic findings, and outcomes in breathless patients: results from the ProBNP Investigation of Dyspnoea in the Emergency Department (PRIDE) echocardiographic substudy. Eur Heart J. 2006, 27: 839-845. 10.1093/eurheartj/ehi811.
Hartmann F, Packer M, Coats AJ, Fowler MB, Krum H, Mohacsi P, Rouleau JL, Tendera M, Castaigne A, Anker SD, Amann-Zalan I, Hoersch S, Katus HA: Prognostic impact of plasma N-terminal pro-brain natriuretic peptide in severe chronic congestive heart failure: a substudy of the Carvedilol Prospective Randomized Cumulative Survival (COPERNICUS) trial. Circulation. 2004, 110: 1780-1786. 10.1161/01.CIR.0000143059.68996.A7.
Kovacs G, Berghold A, Scheidl S, Olschewski H: Pulmonary arterial pressure during rest and exercise in healthy subjects: a systematic review. Eur Respir J. 2009, 34: 888-894. 10.1183/09031936.00145608.
Cavagna L, Caporali R, Klersy C, Ghio S, Albertini R, Scelsi L, Moratti R, Bonino C, Montecucco C: Comparison of brain natriuretic peptide (BNP) and NT-proBNP in screening for pulmonary arterial hypertension in patients with systemic sclerosis. J Rheumatol. 2010, 37: 2064-2070. 10.3899/jrheum.090997.
Ciurzynski M, Bienias P, Irzyk K, Rymarczyk Z, Kostrubiec M, Szewczyk A, Glinska-Wielochowska M, Zylkowska J, Kurzyna M, Pruszczyk P: Usefulness of echocardiography in the identification of an excessive increase in pulmonary arterial pressure in patients with systemic sclerosis. Kardiol Pol. 2011, 69: 9-15.
Frea S, Capriolo M, Marra WG, Cannillo M, Fusaro E, Libertucci D, Morello M, Gaita F: Echo Doppler predictors of pulmonary artery hypertension in patients with systemic sclerosis. Echocardiogr. 2011, 28: 860-869. 10.1111/j.1540-8175.2011.01467.x.
Hachulla E, Gressin V, Guillevin L, Carpentier P, Diot E, Sibilia J, Kahan A, Cabane J, Francès C, Launay D, Mouthon L, Allanore Y, Tiev KP, Clerson P, de Groote P, Humbert M: Early detection of pulmonary arterial hypertension in systemic sclerosis: A French nationwide prospective multicenter study. Arthritis Rheum. 2005, 52: 3792-3800. 10.1002/art.21433.
Hachulla E, de Groote P, Gressin V, Sibilia J, Diot E, Carpentier P, Mouthon L, Hatron P-Y, Jego P, Allanore Y, Tiev KP, Agard C, Cosnes A, Cirstea D, Constans J, Farge D, Viallard JF, Harle JR, Patat F, Imbert B, Kahan A, Cabane J, Clerson P, Guillevin L, Humbert M: The three-year incidence of pulmonary arterial hypertension associated with systemic sclerosis in a multicenter nationwide longitudinal study in France. Arthritis Rheum. 2009, 60: 1831-1839. 10.1002/art.24525.
Jansa P, Becvar R, Ambroz D, Palecek T, Tomcik M, Skacelova S, Aschermann M, Linhart A: Pulmonary arterial hypertension associated with systemic sclerosis in the Czech Republic. Clin Rheumatol. 2011, 31: 557-561.
Mukerjee D, St George D, Coleiro B, Knight C, Denton CP, Davar J, Black CM, Coghlan JG: Prevalence and outcome in systemic sclerosis associated pulmonary arterial hypertension: application of a registry approach. Ann Rheum Dis. 2003, 62: 1088-1093. 10.1136/ard.62.11.1088.
Hachulla E, Launay D, Mouthon L, Sitbon O, Berezne A, Guillevin L, Hatron PY, Simonneau G, Clerson P, Humbert M: Is pulmonary arterial hypertension really a late complication of systemic sclerosis?. Chest. 2009, 136: 1211-1219. 10.1378/chest.08-3042.
We wish to thank the following people for assistance with sample preparation and data collection: Edmund Lau, Tamera Corte, Alison Batty, Kerry Cooper, Kathleen Elford, Dot Fowler, Barbara Gemmell, Trish Lewis, Helen Marsden, Leah McWilliams and Bev Wilson. We wish to thanks the patients who participated in this study and St Vincent’s Hospital Melbourne IT department for their expert advice and continued support of the Australian Scleroderma Cohort Study and Database. Dr Thakkar was funded by a National Health and Medical Research Council of Australia Scholarship (APP 1038612) and The Australian Scleroderma Interest Group Clinical Research Fellowship. Dr Nikpour holds a David Bickart Clinician Research Fellowship from the University of Melbourne Faculty of Medicine, Dentistry and Health Sciences. Other sources of funding include Scleroderma Australia, Arthritis Australia, St Vincent’s Research Endowment Foundation, Pfizer (including a Pfizer CardioVascular Lipid research grant), Actelion Australia, Bayer, CSL Biotherapies and GlaxoSmithKline Australia.
The authors declare that they have no competing interests.
VT contributed to the study design, collection and analysis of data, interpretation of results, and preparation of the manuscript. WS contributed to the study design, collection of data, interpretation of results, and preparation of the manuscript. DP contributed to the interpretation of results and preparation of the manuscript. PY contributed to the interpretation of results and preparation of the manuscript. DL contributed to the interpretation of results and preparation of manuscript. EG contributed to the interpretation of results and preparation of the manuscript. JR contributed to the collection of data and preparation of the manuscript. JW contributed to the collection of data and preparation of the manuscript. JZ contributed to the collection of data and preparation of the manuscript. JS contributed to the collection of data and preparation of the manuscript. PN contributed to the interpretation of results and preparation of the manuscript. SL contributed to the collection of data and preparation of the manuscript. MR contributed to the collection of data and preparation of the manuscript. SP contributed to the study design, collection of data, interpretation of results, and preparation of the manuscript. MN contributed to the study design, collection and analysis of data, interpretation of results, and preparation of the manuscript. All authors have read and approved the final version of the paper.