- Research article
- Open Access
Relationship between hsTnI and coronary stenosis in asymptomatic women with rheumatoid arthritis
BMC Cardiovascular Disorders volume 16, Article number: 184 (2016)
Rheumatoid arthritis (RA) is a condition associated with accelerated progression of atherosclerosis in affected individuals. Myocardial assessment using exercise testing in such patients, however, is often difficult to perform. Our objective was to determine the factors associated with severe coronary stenosis using computed tomography (CT) angiography of the coronary arteries in asymptomatic patients with RA.
Forty-four women with RA were examined using CT angiography to detect atherosclerotic involvement and significant coronary stenosis (>50 %). CT findings were correlated with the cardiovascular risk score, and with classical and most recent parameters of atherosclerosis.
CT angiography of the coronary arteries revealed severe stenosis (>70 %) in 9 % of patients. High-sensitivity troponin I level was associated with severe coronary stenosis (odds ratio 6.37; 95 % confidence interval 1.53 − 26.48; P = 0.011). Adjustment for confounders did not alter this result (P = 0.039). In contrast, classical and modified Systemic Coronary Risk Evaluation scores had no value in predicting severe stenosis (P ≥ 0.49).
The present study showed the possible benefits of a coronary CT angiography in women with RA and asymptomatic ischemic coronary heart disease. Increased levels of high-sensitivity troponin I may be a potential indication for this type of examination. However, further studies are needed to confirm these results.
Rheumatoid arthritis (RA) is an inflammatory autoimmune disease associated with a higher prevalence of cardiovascular (CV) disease, both of which are linked to the presence of traditional risk factors for atherosclerosis as well as chronic inflammation. Accelerated atherosclerosis of the coronary and cerebrovascular arteries is the main cause of morbidity and mortality in RA . Patients with RA have a 45 % higher risk for all CV events than the general population, the risk for myocardial infarction is even higher (68 %) . In addition, 30-day mortality after the first acute coronary event is 80 % higher in patients with RA than in the general population . Early identification of high-risk patients and the initiation of preventive measures is, therefore, very important.
Classical CV Systematic Coronary Risk Evaluation (SCORE) may underestimate the actual risk in patients with RA, in whom inflammation plays a major role [4, 5]. Thus, the European League Against Rheumatism (EULAR) recommends multiplying the risk measured by SCORE by a factor of 1.5 in selected RA patients . This applies to patients meeting 2 or more of the following criteria: duration of disease >10 years; positivity for rheumatoid factor or anti-citrulline antibodies; and the presence of certain extra-articular symptoms .
Currently, several imaging methods for the detection of coronary atherosclerotic lesions are available. Non-contrast CT is frequently used for assessment of calcium burden using Agatston calcium score . Coronary CT angiography (cCTA) is, at present, used routinely in the diagnosis of coronary heart disease (CHD). This non-invasive method has high accuracy in detection of coronary stenosis and particularly predictive value in patients with negative findings [8–10].
The aim of the present study was to detect the following in asymptomatic patients with RA: the prevalence of significant coronary stenosis measured by cCTA; how coronary atherosclerosis diagnosed by CT examination correlates with classical or modified cardiovascular SCORE systems; and the predictive value of biomarkers in assessing the severity of coronary stenosis.
The prospectively designed single centre study included patients with RA who were at least 1 year on biological treatment observed in specialized outpatient clinic for rheumatological diseases during March and December 2013. Exclusion criteria were: 1) no other CV disease apart from arterial hypertension; 2) negative family medical history for diseases of the CV system; 3) current smoking; 4) symptoms suggesting the possibility of CHD; 5) contraindication to iodine contrast agent administration (allergy on iodine contrast agent and severe renal insufficiency). As RA is 3 times more frequent in women than in men, in those subjects eligible for this study, were only 2 men. To achieve higher homogeneity of our study we decide not to include them into present analysis. We further not included 1 patient because of allergy to iodine, 2 other women refused to participate.
All included patients were referred to cCTA and to take blood samples for laboratory assessment. Basic medical data, including co-morbidities, medications used, resting blood pressure, heart rate, height and weight were collected. Body mass index was calculated as body weight (kg)/height2 (m2). The stage of RA and the diagnosis of arterial hypertension, diabetes mellitus and dyslipidaemia were identified from medical documentation. The dose of corticosteroids used was recalculated as the equivalent dose of prednisone.
The CV SCORE (SCORE) and modified SCORE (mSCORE) were calculated in accordance with previously published recommendations [4, 6]. The CV SCORE takes into account patient’s sex, age, smoking status, systolic blood pressure and concentration of total cholesterol. Resulting number represents individual 10 year risk for fatal CV event. Modified SCORE multiplies the risk measured by SCORE by a factor of 1.5 in selected RA patients .
The Ethical Committee at the Faculty Hospital in Pilsen validated the study protocol, and all patients provided written informed consent. The study conformed to the provisions of the World Medical Association’s Declaration of Helsinki.
Standard biochemical parameters were assessed in the laboratory at the Faculty Hospital in Pilsen. The estimated glomerular filtration rate (eGFR) was calculated using the Modification of Diet in Renal Disease (MDRD) formula. Albuminuria is expressed as a urinary albumin-to-creatinine ratio (ACR). High-sensitivity cardiac troponin I (hsTnI) was measured using the Architect i2000 platform with STAT High Sensitive Troponin-I assay (Abbott Diagnostics, USA) (limit of quantification 4–10 ng/l, 10 % coefficient of variation 4.7 ng/l, 99th percentile 26.2 ng/l, percentage of measurable values in healthy population >80 %). Plasma levels of osteoprotegerin were measured using multiplex immunoanalyses based on xMAP® technology, commercially available kits MILLIPLEX MAP Human Bone Panel 1A magnetic (Merck-Millipore Corporation, USA) and the MAGPIX instrument (Luminex Corporation, USA). xMAP® technology and the MAGPIX system uses color-coded magnetic microspheres coated by antibodies to perform quantitative sandwich immunoanalysis of proteins in a variety of sample matrices.
CT examinations were performed using a second-generation dual-source CT device (SOMATOM Definition Flash, Siemens HealthCare, Forchheim, Germany). Initially, a non-contrast scan for calcium scoring quantification was performed. Cardiac CTA was monitored by retrospective electrocardiographic gating (128 × 0.6 mm; rotation 280 ms; adaptive pitch factor 0.2 − 0.4; optimized setting of tube voltage and tube current using CareDose and CarekV). Fifty millilitres of iodine contrast agent (400 mgI/l) was administered at a rate of 6 ml/s.
Assessment of the examinations was performed in consensus by 2 radiologists experienced in CT heart examination (20 and 10 years, respectively). Calcium score was calculated using a dedicated Syngo. CaScoring application (Siemens Healthcare, Forchheim, Germany). The total calcium score, without differentiation of individual coronary arteries, was used for the analysis.
Coronary arteries were assessed according to the degree of luminal stenosis (mild: 10 % − 40 %; moderate: 40 % − 70 % and severe: >70 %). The significance of the degree of stenosis was assessed for each patient, and the characteristics of plaques were assessed according to individual segments .
For statistical analysis, SAS software version 9.3 (SAS Institute Inc, USA) was used. The results are presented as arithmetic mean ± standard deviation, median with inter-quartile range (IQR) or as a proportion (percentage). For the purpose of statistical analysis, the subjects were divided into three groups according to maximal stenotic involvement of coronary arteries: without stenosis or mild stenosis according to cCTA (coronary stenosis <40 % [n = 28]); moderate stenosis (40 % − 70 % [n = 12]); and a group with severe stenosis (>70 % [n = 4]).
Differences among the groups were assessed using the paired Student’s t test, the Kruskal-Wallis test and the Fisher’s exact test. Correlations were expressed using the Spearman correlation coefficient. For the purposes of regression analysis, non-normally distributed variables were normalized using logarithmic transformation. Factors associated with a positive finding in CTAG were analysed using logistic regression. Significant attention was devoted to the selection of potential confounders. First, potentially significant covariables (age, arterial hypertension, dyslipidaemia, stage of RA, albuminuria, hs troponin I, dose of corticoids) were sought with a stepwise logistic regression analysis, which included only factors demonstrated to be significant in the univariate analysis. The final regression model included only parameters that remained in the models permanently.
The mean age of 44 women included in present study was 60.2 years (range 50 − 70 years). Twenty-two women (50.0 %) were treated for arterial hypertension, 3 (6.8 %) had diabetes mellitus and 19 (43.2 %) had dyslipidaemia, of whom 16 were taking a statin.
The basic characteristics of the patients according to severity of coronary stenosis are summarized in Table 1. Arterial hypertension and dyslipidaemia were more prevalent in women with positive findings in the coronary arteries than in those with negative findings.
The median calcium score for the entire group was 21.5 (IQR 0 – 65.0). In our study, 21 (47.7 %) women had calcium score of 0; 15 (34.1 %) women had values between 1 and 100; and 8 (18.2 %) women had calcium score over 100. In all women with calcium score 0 we did not detected any atherosclerotic plaque. In the same line, 3 of 4 women with severe stenosis had calcium score higher than 100. Altogether 103 coronary segments with an atherosclerotic involvement were detected in 22 patients. Severe (>70 %) stenosis was observed in 4 patients, moderate stenosis in 12 patients and mild stenosis in 6 patients. The median number of coronary stenosis in the entire group was 1 (IQR 0 – 3.5) and there were distributed as follows: right coronary artery - 42 (40.8 %) lesions; left anterior descending artery - 37 (35.9 %) lesions; left circumflex artery - 24 (23.3 %) lesions. We found no lesion in left main artery. Only in 2 (9.1 %) patients we detected >40 % stenosis in 2 branches, the others had single vessel affected. Table 2 summarizes the values of biochemical parameters, CV risk SCORE and parameters of coronary atherosclerosis. Women with severe coronary stenosis exhibited significantly more severe micro-albuminuria, and higher hsTn1 and osteoprotegerin levels. As expected, the severity of coronary stenosis correlated with the calcium score and the number of coronary lesions.
Figure 1 illustrates the hsTnl values, micro-albuminuria and calcium scores among the groups according to the severity of coronary stenosis.
Patients with severe coronary stenosis on cCTA were referred to coronary angiography. The findings were confirmatory to cCTA. On the basis of subsequent cardiologic examination, 2 patients were referred to coronary artery bypass surgery. Undergoing percutaneous coronary intervention was recommended to the remaining 2 patients to mitigate the risk of angina pectoris symptoms in the future.
Factors associated with severe coronary artery stenosis using logistic regression
The only parameter consistently associated with severe coronary stenosis was hsTnl (univariate analysis, odds ratio [OR] 6.37; 95 % confidence interval [CI] 1.53 – 26.48; P = 0.011). Albuminuria reached borderline statistical significance (OR 2.39; 95 % CI 0.99 – 5.75; P = 0.052). Plasma levels of osteoprotegerin were not associated with severe coronary stenosis (OR 3.6; 95 % CI 0.52 – 17.96; P = 0.22). After adjustment for albuminuria and osteoprotegerin level, the hsTnl value remained significantly associated with severe coronary stenosis assessed by cCTA (OR 5.39; 95 % CI 1.09 – 26.64; P = 0.039).
Table 3 shows the correlation coefficients between calculated cardiovascular risk, hsTnl, albuminuria and the calcium score, and the number of coronary lesions. It is evident that the classical SCORE and mSCORE for CV risk were less strongly correlated with the number of coronary lesions than hsTnl values. The presence of albuminuria was not correlated with the calcium score or the number of coronary lesions.
Figure 2 presents receiver-operator curves for classical SCORE and mSCORE, hsTnl and micro-albuminuria for the prediction of severe coronary stenosis. In this setting, SCORE (area under the curve [AUC] = 0.56) and mSCORE (AUC = 0.53) had no predictive value for severe stenosis. SCORE and mSCORE values in subjects with severe coronary stenosis fluctuated between 0 and 7. In contrast, hsTnl and albuminuria (ie, ACR) appeared to be biomarkers with very good sensitivity and specificity (AUC = 0.92 for both parameters).
In our study involving 44 women with rheumatoid arthritis without clinical symptoms of ischemic heart disease, we found that 9 % of them had severe coronary stenosis detected by coronary CT angiography. The classical cardiovascular risk SCORE or modified risk SCORE were not associated with coronary stenosis. On the other hand, high sensitivity Troponin I was correlated with the number and severity of coronary artery lesions.
RA is a disease associated with accelerated atherosclerosis and higher mortality after myocardial infarction in affected individuals [2, 3]. Early detection of significant CHD, thus, plays an important role in patient prognosis. Coronary CT angiography is non-invasive and safe method with possibility of excellent depiction of coronary plaques and stenosis assessment [12, 13].
High sensitivity cardiac troponins have demonstrated utility in estimating prognosis in general population and in patients with coronary heart disease, even in the range far below the 99th percentile (recommended cut-off value for diagnosis of acute myocardial infarction). deFillipi et al.  found a HR of 2.91 for cardiovascular mortality in older adults without known heart failure (>65 years; hsTnT > 12.94 ng/l vs < 3 ng/l). Omland et al.  (PEACE study) showed a HR 2.39 for cardiovascular mortality in stable CHD patients (hsTnT > 9.6 ng/l in men and > 7.4 ng/l in women) and Kavsak et al.  observed a HR 2.2 for cardiovascular mortality in stable patients at risk for CHD or chronic heart failure (hsTnI > 10 ng/l). Accordingly, hs troponins may be useful for risk stratification in patients with RA. In our study, hsTnl level had a high negative predictive value (18 of 21 patients without any coronary lesions had hsTnI < 3 ng/l).
Bradham et al. demonstrated that patients with RA had 49 % higher hsTnl levels than healthy individuals . In the same study, the hsTnl value correlated with the calcium score in univariate analysis; however, after adjustment for age, race, sex and Framingham risk score, this association was no longer statistically significant. Our data suggest that female RA patients with the highest concentrations of hsTnI tend to have severe coronary stenosis (adjusted OR 5.39).
Of note, 99th percentile derived from our population of RA women without any signs of acute myocardial ischemia was 25.7 ng/l, whereas 99th percentile of the reference female population was 15 ng/l . This fact should be probably considered in diagnostics of acute coronary syndromes in RA patients.
Moreover, we highlighted a potentially interesting connection between albuminuria and severe coronary stenosis. Albuminuria is a condition for which testing is readily available. Moreover, the presence of albuminuria increases CV risk by a factor of 2 − 4 . Sihvonen et al. demonstrated that in patients with RA, the presence of albuminuria (in the range of 20–200 μg/min) increases the risk of mortality by 180 % compared with patients without simultaneously increased ACR . In our study, albuminuria was correlated (borderline significance) with the severity of coronary stenosis, but not with the calcium score or the number of coronary lesions.
Other studies have demonstrated a connection between inflammatory markers and CV risk [1, 20, 21]. In our groups, however, we did not find any difference, either in erythrocyte sedimentation rate or C-reactive protein levels between women with positive and negative findings on cCTA.
Surprisingly, in our study classical or mSCORE systems did not correlate with the severity of coronary stenosis [4, 6]. On the other hand, calcium score enables to diagnose the severity of calcification in the coronary arteries. Increased calcium scores were detected in patients with RA  and were correlated with the occurrence of CV complications . In our cohort, the calcium score was a very good predictor of severe coronary stenosis (AUC = 0.94). Moreover, it was significantly correlated (r = 0.96) with the total number of coronary lesions. Given its ready availability and its non-invasive character, cCTA is a suitable method for the detection of coronary atherosclerosis. A negative finding has a particularly strong predictive value with regard to stenotic lesions . Coronary CTA is comparable with invasive angiography in its precision for assessing the degree of possible coronary arterial stenosis. However, its limitation lies mainly in its low specificity, which may overestimate stenosis, particularly in cases involving sclerotic plaque . However, high sensitivity of cCTA is more important factor in our study and a negative cCTA finding has a strong predictive value with regard to stenotic lesions .
The present study had several limitations. First, it investigated a relatively small group of women with RA; our results, thus, cannot be generalized to include men or women without RA. However, our patients were comprehensively examined using a CT method that achieves excellent results in diagnosing CHD . Second, the present study was cross-sectional in design; therefore, we have no long-term follow-up information regarding patient outcomes, although individuals with severe coronary stenosis have been shown to have a higher risk for major adverse cardiac events . Third, the low prevalence of severe coronary stenosis in our group may lead to a skewed interpretation of the results, although we used several different statistical methods to analyse our data with confirmatory results. Four, we did not perform any stress test to assess functional severity of stenosis detected on cCTA. Moreover, we performed an invasive coronary angiography only in patients with finding of severe stenosis (<70 %). However, all patients were completely asymptomatic and we focused on non-invasive examination with minimized radiation and overall burden.
Our study suggests the potential benefits of a coronary CT angiography in asymptomatic RA patients. In our hands, the hsTnl level was the best parameter for predicting of severe coronary stenosis assessed by CTAG. Classical or modified cardiovascular risk SCOREs were not effective in assessing the severity stenosis. However, further studies with larger patient cohorts and also correlation with clinical outcomes are needed before recommendation for measuring hsTnl levels in all patients with RA can be made.
Area under curve
Coronary CT angiography
Coronary heart disease
Computed tomography angiography
Estimated glomerular filtration rate
European league against rheumatism
High-sensitivity cardiac troponin I
Modification of diet in renal disease
Modified systematic coronary risk evaluation
Systematic coronary risk evaluation
Maradit-Kremers H, Nicola PJ, Crowson CS, Ballman KV, Gabriel SE. Cardiovascular death in rheumatoid arthritis: a population-based study. Arthritis Rheum. 2005;52:722–32.
Avina-Zubieta JA, Thomas J, Sadatsafavi M, Lehman AJ, Lacaille D. Risk of incident cardiovascular events in patients with rheumatoid arthritis: a meta-analysis of observational studies. Ann Rheum Dis. 2012;71:1524–9.
Van Doornum S, Brand C, King B, Sundararajan V. Increased case fatality rates following a first acute cardiovascular event in patients with rheumatoid arthritis. Arthritis Rheum. 2006;54:2061–8.
Perk J, De BG, Gohlke H, Graham I, Reiner Z, Verschuren M, et al. European Guidelines on cardiovascular disease prevention in clinical practice (version 2012). The Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts). Eur Heart J. 2012;33:1635–701.
Gómez-Vaquero C, Corrales A, Zacarias A, Rueda-Gotor J, Blanco R, Gonzalez-Juanatey C, et al. SCORE and REGICOR function charts underestimate the cardiovascular risk in Spanish patients with rheumatoid arthritis. Arthritis Res Ther. 2013;15:R91.
Peters MJ, Symmons DP, McCarey D, Dijkmans BA, Nicola P, Kvien TK, et al. EULAR evidence-based recommendations for cardiovascular risk management in patients with rheumatoid arthritis and other forms of inflammatory arthritis. Ann Rheum Dis. 2010;69:325–31.
Agatston AS, Janowitz WR, Hildner FJ, Zusmer NR, Viamonte Jr M, Detrano R. Quantification of coronary artery calcium using ultrafast computed tomography. J Am Coll Cardiol. 1990;15:827–32.
Scheffel H, Stolzmann P, Alkadhi H, Azemaj N, Plass A, Baumueller S, et al. Low-dose CT and cardiac MR for the diagnosis of coronary artery disease: accuracy of single and combined approaches. Int J Cardiovasc Imaging. 2010;26:579–90.
Sun Z, Aziz YF, Ng KH. Coronary CT angiography: how should physicians use it wisely and when do physicians request it appropriately? Eur J Radiol. 2012;81(4):e684–7.
Meinel FG, Bayer RR, Zwerner PL, De Cecco CN, Schoepf UJ, Bamberg F. Coronary computed tomographic angiography in clinical practice: state of the art. Radiol Clin North Am. 2015;53:287–96.
Wang S, Yiu KH, Mok MY, Ooi GC, Khong PL, Mak KF, et al. Prevalence and extent of calcification over aorta, coronary and carotid arteries in patients with rheumatoid arthritis. J Intern Med. 2009;266:445–52.
Saremi F, Achenbach S. Coronary plaque characterization using CT. AJR Am J Roentgenol. 2015;204:W249–60.
Eckert J, Schmidt M, Magedanz A, Voigtlander T, Schmermund A. Coronary CT angiography in managing atherosclerosis. Int J Mol Sci. 2015;16:3740–56.
deFilippi CR, de Lemos JA, Christenson RH, Gottdiener JS, Kop WJ, Zhan M, et al. Association of serial measures of cardiac troponin T using a sensitive assay with incident heart failure and cardiovascular mortality in older adults. JAMA. 2010;304:2494–502.
Omland T, de Lemos JA, Sabatine MS, Christophi CA, Rice MM, Jablonski KA, et al. A sensitive cardiac troponin T assay in stable coronary artery disease. N Engl J Med. 2009;361:2538–47.
Kavsak PA, Xu L, Yusuf S, McQueen MJ. High-sensitivity cardiac troponin I measurement for risk stratification in a stable high-risk population. Clin Chem. 2011;57:1146–53.
Bradham WS, Bian A, Oeser A, Gebretsadik T, Shintani A, Solus J, et al. High-sensitivity cardiac troponin-I is elevated in patients with rheumatoid arthritis, independent of cardiovascular risk factors and inflammation. PLoS ONE. 2012;7:e38930.
Apple FS, Ler R, Murakami MM. Determination of 19 cardiac troponin I and T assay 99th percentile values from a common presumably healthy population. Clin Chem. 2012;58:1574–81.
Sihvonen S, Korpela M, Mustonen J, Laippala P, Pasternack A. Renal disease as a predictor of increased mortality among patients with rheumatoid arthritis. Nephron Clin Pract. 2004;96:c107–14.
Gonzalez-Gay MA, Gonzalez-Juanatey C, Lopez-Diaz MJ, Pineiro A, Garcia-Porrua C, Miranda-Filloy JA, et al. HLA-DRB1 and persistent chronic inflammation contribute to cardiovascular events and cardiovascular mortality in patients with rheumatoid arthritis. Arthritis Rheum. 2007;57:125–32.
Goodson NJ, Symmons DP, Scott DG, Bunn D, Lunt M, Silman AJ. Baseline levels of C-reactive protein and prediction of death from cardiovascular disease in patients with inflammatory polyarthritis: a ten-year followup study of a primary care-based inception cohort. Arthritis Rheum. 2005;52:2293–9.
Yiu KH, Mok MY, Wang S, Ooi GC, Khong PL, Lau CS, et al. Prognostic role of coronary calcification in patients with rheumatoid arthritis and systemic lupus erythematosus. Clin Exp Rheumatol. 2012;30:345–50.
Kim SM, Choi JH, Chang SA, Choe YH. Additional value of adenosine-stress dynamic CT myocardial perfusion imaging in the reclassification of severity of coronary artery stenosis at coronary CT angiography. Clin Radiol. 2013;68:e659–68.
Zeb I, Abbas N, Nasir K, Budoff MJ. Coronary computed tomography as a cost-effective test strategy for coronary artery disease assessment - a systematic review. Atherosclerosis. 2014;234:426–35.
Bettencourt N, Chiribiri A, Schuster A, Ferreira N, Sampaio F, Pires-Morais G, et al. Direct comparison of cardiac magnetic resonance and multidetector computed tomography stress-rest perfusion imaging for detection of coronary artery disease. J Am Coll Cardiol. 2013;61:1099–107.
Nakazato R, Arsanjani R, Achenbach S, Gransar H, Cheng VY, Dunning A, et al. Age-related risk of major adverse cardiac event risk and coronary artery disease extent and severity by coronary CT angiography: results from 15 187 patients from the International Multisite CONFIRM Study. Eur Heart J Cardiovasc Imaging. 2014;15:586–94.
This research was supported by MH–DRO (Faculty Hospital in Pilsen – FNPI, 00669806) and by the Charles University Research Fund (project number P36).
MH coordinated the study, contributed for data collection and for the paper draft. JB contributed for the study design and performed CT examination. JS performed statistical analysis and guided draft of the paper. DS contributed for data collection and participated in study design. DR contributed for data collection and performed biochemical analysis. JŠ contributed to the study design and for data collection. RR guided for study design and contributed to draft the paper. All authors read and approved the final manuscript.
The authors declare that they have no competing interest.
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Hromádka, M., Seidlerová, J., Baxa, J. et al. Relationship between hsTnI and coronary stenosis in asymptomatic women with rheumatoid arthritis. BMC Cardiovasc Disord 16, 184 (2016). https://doi.org/10.1186/s12872-016-0359-3
- Calcium score
- Coronary heart disease
- Coronary CT angiography
- High-sensitivity troponin
- Rheumatoid arthritis