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Reduced left atrial contractile strain with speckle tracking analysis predicts abnormal plasma NTproBNP in an asymptomatic community population



The left atrium (LA) is closely related to left ventricular diastolic function. Two-dimensional speckle tracking strain and strain rate (SR) imaging has been applied in the study of LA function. We intended to explore the relationship between global LA deformation parameters and plasma NTproBNP levels in asymptomatic community residents with normal ejection fraction and normal LA volume.


A cross-sectional sample of Beijing residents underwent comprehensive Doppler echocardiography and medical record review in 2009. Global LA longitudinal strain and SR indexes were obtained in the apical four-chamber view. LA stiffness index (LASI) was calculated as the ratio of early diastolic velocity of transmitral flow/early diastolic mitral annular motion velocity (E/E') to LA reservoir strain.


A total of 620 individuals (mean age = 65.8 years, left ventricular ejection fraction = 70.8%, LA volume index = 17.9 ml/m2) were investigated in our study. 117 individuals had increased plasma NTproBNP (≥ 125 pg/ml). LA reservoir and contractile function by LA strain and SR indexes were significantly reduced in the abnormal NTproBNP group compared with the normal NTproBNP group. Multiple regression analysis indicated that LA contractile strain was a negative predictor of plasma NTproBNP in addition to indexed LA volume and E/E'. LASI was higher in the abnormal NTproBNP group and was significantly correlated with NTproBNP (r = 0.342, P < 0.001). The area under ROC analysis for LASI in predicting elevated plasma NTproBNP was 0.690, similar with LA contractile strain, E/E’ and LAVI. The cut-off value of LASI was 0.612.


LA reservoir and contractile functions demonstrated by LA strain and SR were significantly impaired in the community-based population with increased plasma NTproBNP levels. LA contractile strain adds incremental information in predicting abnormal NTproBNP levels. As a single index, LASI showed similar diagnostic value with LAVI and E/E’ in predicting abnormal NTproBNP.

Peer Review reports


Left atrial (LA) function is a useful barometer of LV diastolic function and vital for overall cardiac performance. LA mechanical function includes reservoir, conduit and pump function which contribute to left ventricular filling at different stages of the cardiac cycle [1]. Two-dimensional speckle tracking strain and strain rate(SR) imaging has been proposed as a new tool to evaluate LA function with considerable feasibility and reproducibility [2]. LA reservoir strain can predict elevated LV filling pressures [3, 4], classify left ventricular diastolic dysfunction [5, 6], discriminate heart failure with preserved ejection fraction (HFpEF) more accurately than conventional echocardiographic measures or the guidelines algorithm [7, 8], and is also associated with the prognosis in patients with HFpEF [9, 10].

N-terminal pro-brain natriuretic peptide (NTproBNP), secreted mainly by the ventricles in case of volume expansion and pressure overload, is a noninvasive marker of elevated LV filling pressure, and is regarded as an important diagnostic and prognostic tool in patients with heart failure [11]. The upper limit of normal plasma NT-proBNP is 125 pg/ml in the non-acute setting according to the 2016 ESC heart failure guideline [12]. Plasma NTproBNP was once regarded as a suboptimal screening test for preclinical ventricular dysfunction in community-based populations [13], but evidence from a meta-analysis of 40 prospective studies also supports the potential role of NTproBNP in the assessment of cardiovascular risk in general populations [14].

We investigated the relevance of LA deformation parameters assessed by two-dimensional speckle tracking imaging with plasma NTproBNP levels in a community-based population with normal left ventricular ejection fraction (LVEF) and normal LA volume. We speculate that LA function by LA strain and SR indexes in people with increased NTproBNP might be different from those with normal NTproBNP. We aim to determine the role of LA deformation parameters in predicting plasma NTproBNP levels, and to assess which of the indexes, separately or in combination, is a better correlate.



Our study enrolled the cohort in the community of the Capital Steel Corporation set up by Beijing Hypertension League Institute, including 1058 subjects, aged between 37–86 years old in 2005 [15]. Among them, 779 subjects took part in the follow-up in 2009. Clinical characteristics, echocardiographic examinations, and fasting samples were collected. The cross-sectional data of 734 subjects with full records were identified. Of these, 16 subjects were excluded for inadequate electrocardiograms or poor imaging quality. 19 subjects were excluded for history of atrial fibrillation or flutter. 26 subjects had reduced LVEF (< 50%) and 4 subjects with NYHA class III were excluded. 31 chronic kidney disease subjects with an estimated glomerular filtration rate (eGFR) < 60 ml/min.1.73m2 and 14 subjects with moderate or severe valvular diseases were excluded. Then, 4 subjects with enlarged LA (LA volume index > 34 ml/m2) were excluded to avoid enlarged LA as a confounding factor on LA phasic function. The final study consisted of 620 individuals (Fig. 1 flow chart). The study was in compliance with the Declaration of Helsinki and approved by the Ethics Committee of Peking University First Hospital. All subjects gave their written informed consent for participation.

Fig. 1
figure 1

Flow chart of the study population

Assessment of clinical parameters

Cardiovascular diseases and risk factors were confirmed based on a review of data collected from hospitalizations and outpatient records. Fasting blood samples were collected for analysis using standard techniques. eGFR was calculated using modified MDRD equations based on Chinese patients [16]. NTproBNP was tested by eletrochemiluminescence immunoassay (Elecsys, Roche Diagnostics, Germany). According to the 2016 ESC heart failure guideline, the upper limit of normal plasma NTproBNP in the non-acute setting is 125 pg/ml, which suggests that patients with normal NTproBNP concentrations are unlikely to have heart failure [12]. Tests of biochemical indexes were completed in the clinical laboratory of Peking University First Hospital, and a quality control standard (ISO 15189) was achieved.

Standard echocardiography

Echocardiographic examinations were performed using a Vivid 7 ultrasound system (GE Healthcare, Horten, Norway) equipped with a 2–4 MHz transducer with a frame rate of at least 50 frames per second according to the guidelines [17, 18]. Images in cineloop format from 3 consecutive beats were stored for a offline analysis. The maximal LA volume (LAV) was calculated using the biplane dimension-length formula: LAV (ml) = π/6 × (anteroposterior diameter) × (longitudinal diameter) × (transverse diameter) [18]. The LAV index (LAVI) was calculated as LAV/body surface area (BSA). Left ventricular mass (LVM) was calculated with the Devereux formula: LVM (g) = 0.8 × 1.04 × [(left ventricular end-diastolic internal diameter + intraventricular septal thickness + left ventricular posterior wall thickness)3- (left ventricular end-diastolic internal diameter)3] + 0.6 [18]. The LVM index (LVMI) was subsequently calculated as LVM/BSA. LVEF was assessed by modified biplane Simpson’s method. Transmitral flow velocities were obtained including peak velocities during early diastole (E) and late diastole (A). Values shown for peak early (E’) and late (A’) diastolic mitral annular velocities were averages of the values obtained at septal and lateral positions.

Measurements of LA strain and SR

Strain measures the myocardial deformation during a cardiac cycle, and strain rate (SR) measures the tissue velocity gradient within the myocardium. LA strain (ε) and SR were analysed by the 2D speckle tracking technique using EchoPAC software (Version 11.0, GE Healthcare) according to Sergio Mondillo’s method [19], by two experienced investigators who were blinded to clinical and other echocardiographic characteristics of the population. The grayscale 2D images acquired in the standard 4-chamber apical views were used. The software divided the LA wall into 6 segments, lateral and septal annular, lateral and septal mid-cavity and lateral and septal rear segments. LA global longitudinal strain and SR measurements were obtained as the average values (white dotted line as shown in Fig. 2).

Fig. 2
figure 2

Left atrial strain and strain rate measured by speckle tracking imaging on apical four-chamber views

The zero reference for LA strain is set at the onset of the P wave. The first peak negative strain (εCT) corresponds to the LA contractile function, and the following peak positive strain (εCD) corresponds to the LA conduit function. εR, as the sum of εCD and εCT, corresponds to LA reservoir function (Fig. 2). LASI is calculated as the ratio of E/Eʹ to LA reservoir strain [20].

The LA SR pattern is characterized by a positive wave occurring during ventricular systole and two negative waves during ventricular diastole. Peak positive global SR (SRs) reflects LA reservoir function, the first peak negative SR (SRe) reflects LA conduit function, and the second peak negative SR (SRa) reflects LA contractile function [21] (Fig. 2). For negative LA strain and SR variables, absolute values were used.

Intra-observer and inter-observer variability

Intra-observer and inter-observer variability of LA strain and SR indexes was assessed in 20 randomly selected subjects. To assess intra-observer variability, selected images were analyzed at a different time by the same observer. To assess inter-observer variability, selected images were analyzed by another observer blinded to the values.

Statistical analysis

We analysed the differences between subjects with normal and increased plasma NTproBNP levels. Continuous variables with a normal distribution were expressed as the mean ± standard deviation (SD), and an independent t-test was used. Continuous variables with obvious skew distributions by Shapiro–Wilk analysis and histograms were expressed as medians and quartiles, and the Mann–Whitney U test was used. Categorical variables were compared using chi-square tests and Fisher’s exact tests as appropriate. Spearman correlation was used to analyse associations between echocardiographic parameters and NTproBNP. Forward conditional logistic regression was performed to explore the independent factors for the prediction of abnormal NTproBNP. Receiver operating characteristic (ROC) curves were used to determine the diagnostic performance of LA strain and SR indexes as well as other echocardiographic parameters to detect elevated NTproBNP. DeLong test was performed for comparison of ROC curves using MedCalc (Version 20.111, MedCalc Software Ltd, Ostend, Belgium). Comparisons of the intra-observer and inter-observer agreement of LA speckle-tracking parameters were assessed by Bland–Altman analysis using MedCalc (Version 20.111, MedCalc Software Ltd). Other data analysis was performed using SPSS 20.0 software (IBM-SPSS, Armonk, NY, USA). The results were considered statistically significant when the P value was < 0.05.


Clinical characteristics

Clinical characteristics and echocardiographic findings are shown in Table 1. Among all subjects (age = 65.8 ± 5.9), the plasma NTproBNP level was 62.5 (32.2–105.3) pg/ml. The average LVEF was 70.8 ± 9.4%, LVMI was 91.6 ± 22.5 g/m2, and LAVI was 17.9 ± 4.8 ml/m2.

Table 1 Clinical characteristics and echocardiographic parameters of the study subjects

The global LA εR, εCD and εCT were 21.61 ± 5.47%, 9.99 ± 4.41%, and 11.62 ± 3.70%, respectively. The global LA SRs, SRe and SRa were 1.09 ± 0.31 s−1, 0.91 ± 0.50 s−1, and 1.53 ± 0.53 s−1, respectively.

LA volume and deformation parameters in the abnormal NTproBNP group

Subjects were categorized into two groups by NTproBNP level: 503 subjects with NTproBNP < 125 pg/ml and 117 subjects with NTproBNP ≥ 125 pg/ml. Expected between-group differences were found in age, BMI, eGFR, the prevalence of coronary artery disease and heart failure history. Subjects with abnormal NTproBNP had higher LVMI and E/E’ ratios (P ≤ 0.01). No differences in LV diameters or LVEF were detected between the two groups.

Compared with the normal NTproBNP group, subjects with abnormal NTproBNP had significantly increased LAVI (20.1 ± 4.9 vs 17.4 ± 4.7 ml/m2, P ≤ 0.01), and decreased LA deformation indexes demonstrating impaired LA reservoir function (εR:19.93 ± 5.00% vs 22.00 ± 5.50%, SRs:0.97 ± 0.28/s vs 1.11 ± 0.31/s) and pump function (εCT: 10.30 ± 2.96% vs 11.93 ± 3.79%, SRa:1.32 ± 0.38/s vs 1.58 ± 0.54/s) (P ≤ 0.01), while LA conduit function by εCD and SRe remained similar. LASI was significantly higher in the abnormal NTproBNP group (0.68 ± 0.30 vs 0.51 ± 0.23, P ≤ 0.01) (Table 1).

Relationships between LA strain/SR indexes and NTproBNP

Spearman correlation analysis found that εR and εCT were only mildly negatively associated with plasma NTproBNP (r = -0.2 ~ -0.3, P < 0.001). LASI was significantly correlated with other echocardiographic parameters demonstrating raised left ventricular filling pressures (E', LAVI, TR velocity) and NTproBNP (Table 2). A scatter plot of LASI and NTproBNP (r = 0.342, P < 0.001) was shown in Fig. 3.

Table 2 Correlations between LA deformation parameters andNTproBNP &conventional echocardiographic measures, which demonstrate raised left ventricular filling pressures
Fig. 3
figure 3

Correlations between LASI and plasma NTproBNP levels in asymptomatic community population

After fully adjusting for confounding factors, multivariate logistic regression analysis demonstrated that εCT, LAVI, and E/E' > 14 were independent predictors of abnormal NTproBNP in addition to age, BMI and history of heart failure (Table 3). The odds ratio for εCT was below 1, suggesting negative impacts on plasma NTproBNP. LASI was not an independent influential factor of NTproBNP.

Table 3 Multivariate binary logistic regression analysis of clinical and echocardiographical variables to predict abnormal NTproBNP in the whole population

ROC analysis for abnormal NTproBNP

The diagnostic performance of LASI as a single index in predicting elevated NTproBNP (≥ 125 pg/ml) (AUC 0.690, cut-off value 0.612, specificity: 0.775, sensitivity:0.564), was similar with -εCT (AUC 0.650), LAVI (AUC 0.658) and E/E' (AUC 0.667), but better than -εR (AUC 0.608) by ROC analysis and DeLong test (Table 4, Fig. 4).

Table 4 Receiver operating characteristic curve in predicting abnormal NTproBNP (NTproBNP ≥ 125 pg/ml) by MedCalc
Fig. 4
figure 4

Receiver operating characteristic curve in predicting abnormal NTproBNP levels

The ROC curve was further fitted through the predicted probability of the logistic regression model of increased NTproBNP listed in Table 3. The AUC for the regression model was 0.815 (Fig. 4), and the regresseion model was significantly better than other single echocardiographic indexes by DeLong test (P < 0.001), which showed that combining LA εCT and conventional echocardiographic measures (including LAVI and E/E') improved the diagnostic accuracy of abnormal BNP.

Reproducibility of LA speckle-tracking parameters

The inter-observer and intra-observer agreements of LA strain and strain rates were shown using mean difference bias and 2-SD limits of agreement (LOA) in Table 5.

Table 5 The intra-observer and inter-observer agreement analysis


In this study, we explored LA function by speckle tracking analysis in community people with normal LVEF, normal LA volume and no obvious heart failure symptoms. Impaired LA reservoir and pump function were found in subjects with abnormal NTproBNP. LA contractile strain was an independent factor of plasma NTproBNP and added incremental information in predicting abnormal NTproBNP levels to that provided by LA volume and E/E' assessment. LASI was correlated with plasma NTproBNP and showed similar diagnostic performance with conventional measures (including LA contractile strain, LAVI and E/E’) in predicting elevated NTproBNP.

Reduced LA function in community population

A meta-analysis revealed normal reference ranges for reservoir strain of 39% (95% CI, 38%-41%), for conduit strain of 23% (95% CI, 21%-25%), and for contractile strain of 17% (95% CI, 16%-19%) in healthy participants without cardiac risk factors [22]. In our study, the subjects had reduced LA strain (global LA εR 21.61 ± 5.47%, εCD 9.99 ± 4.41%, and εCT 11.62 ± 3.70%), probably due to heterogeneous characteristics and a high percentage of comorbid conditions such as hypertension (81.5%) and diabetes (28.4%). Hypertension and diabetes mellitus are both associated with morphologic and functional abnormalities of the LA. An earlier study has already shown that hypertension and diabetes are both associated with decreases in all LA strain and SR indexes [23].

Subjects in our study had a normal LA size and the average LAVI was 17.9 ± 4.8 ml/m2, while LA deformation mechanics were obviously impaired. It suggested that LA phasic function decreased prior to the onset of LA enlargement, which was in line with other studies involving hypertensive and diabetic patients [23,24,25]. LA dysfunction was associated with LA fibrosis [26], and LA strain may become a marker of LA fibrosis [27].

As acknowledged, there is a close interdependence between LV and LA function. With abnormal LV relaxation, LA conduit function decreases, while the relative contribution of LA reservoir and contractile function increases to maintain optimal LV end-diastolic volume, representing an important compensatory mechanism. However, with further progression of LV diastolic dysfunction and increased LA stiffness, the LA pump function decreases, and LA serves predominantly as a conduit [28, 29]. The progression of LA dysfunction is a key factor leading from left ventricular dysfunction to the development of heart failure [27]. In a study on women, LA reservoir and conduit function progressively decreased with increasing grades of left ventricular dysfunction (LVDD), whereas contractile function augmented in grade 1 LVDD before being reduced in patients with grade 2 LVDD [30]. Another study on hypertensive patients showed that LA reservoir and conduit function gradually decreased from enlarged LA to hypertrophic LV [24]. In our study, asymptomatic community subjects with abnormal NTproBNP had worsened LA reservoir and contractile function. These discrepancies could be due to distinct pathophysiological stages in patients with different diseases.

Relationship between LA strain and NTproBNP

Previous studies have demonstrated a significant negative correlation between LA reservoir strain and NTproBNP in patients with acute myocardial infarction [31, 32], suspected heart failure [33, 34] and end-stage renal disease on chronic hemodialysis [35] (r = -0.41 ~ -0.57). In Kurt's study, LA reservoir strain was more closely related to NTproBNP than LA contractile strain [36]. Unlike the aforementioned studies, LA reservoir and contractile strain were poorly correlated with NTproBNP in our community-based population (r = -0.2 ~ -0.3). However, LA contractile strain represented a distinct feature of predicting abnormal NTproBNP in the community population, independent of LAVI. As is known, LA enlargement was found to be an indicator for the severity and duration of increased LV filling pressure [37], and LAVI was positively correlated with plasma BNP levels [38]. Our results propose that LA function by strain might act as an early useful index in the community population before LA enlargement, and a combination of LA strain with LA size might provide more useful information. Future studies might provide new information on LA strain and the cardiovascular outcomes in community populations.

Role of LASI as a single index

LA stiffness index (LASI), as the ratio of E/e′ to LA reservoir strain, is a new derivative of the LA strain. The ratio of invasively measured PCWP and left atrial systolic strain is used to estimate LA stiffness, representing the change in pressure required to increase the volume of LA. Alternatively, the E/E' ratio is used instead of PCWP in conjunction with the LA strain as a noninvasive measure [20].

LASI [39, 40] or LA compliance (the reciprocal of LASI) [7] is useful in predicting elevated LV filling pressures and identifying patients with HFpEF. In our community-based population, LASI was also correlated with plasma NTproBNP and other echocardiographic parameters demonstrating raised left ventricular filling pressures (E', LAVI, TR velocity). In a study among systemic sclerosis patients, LASI was the best single index in predicting elevated NTproBNP compared with LAVI, LA strain and E/E' [41]. An increased LASI can be used as a marker of early target organ damage in hypertension in a recent paper [24]. In our asymptomatic community–based population, LASI failed to show superiority to conventional measures (LA contractile strain, E/E’ and LAVI) in predicting elevated NTproBNP. As a new index, LASI deserves more attention and further studies.

In our study, images were acquired on GE platform and LA strain indexes were analyzed using EchoPAC software (Version 11.0). Vendor differences are based primarily on strain algorithms. There are also some differences in the strain algorithm among different EchoPAC versions, according to the vendor. In a meta-analysis on speckle-tracking LA strain, the authors found no significant difference between EchoPAC and non-EchoPAC platforms, or difference between different iterations of EchoPAC software [22]. Therefore, we speculated the differences in LA strain indexes between our study and other studies were mainly caused by different pathophysiological states of patients. However, we should remain aware of the potential variations in techniques, and hopefully more comparable strain measurements from different software will be obtained in the future.

To our knowledge, this is one of the few studies to address the association between LA deformation parameters and plasma NTproBNP in asymptomatic communities.


The study was a cross-sectional study with a relatively small sample size and lacked clinical follow-up. There might be a selection bias in the collection of the cohort since limited subjects with LA enlargement were found in this population with a mean age of 66 years, and we excluded those subjects for further analysis. LV strain or SR indexes were not included in our analysis. LA strain and SR indexes were obtained in the apical four-chamber view, while the apical two-chamber view was not included. Several noncardiac presentations affect plasma NTproBNP values, such as ischemic stroke or chronic obstructive pulmonary disease, which might be confounding.


Our data suggested that LA reservoir and pump functions demonstrated by LA strain and SR were significantly impaired in the community-based population with abnormal plasma NTproBNP levels. LA reservoir strain adds incremental information in predicting abnormal NTproBNP levels to that provided by LA volume and E/E' assessment. LASI, as the ratio of E/e′ to LA reservoir strain, demonstrated similar diagnostic value with LAVI and E/E’ in the detection of abnormal NTproBNP.

Availability of data and materials

All available data can be obtained by contacting the corresponding author on reasonable request.



Left atrium (atrial)


Strain rate

εCD :

LA conduit strain, peak positive LA strain during early diastole of the left ventricle

εCT :

LA contractile strain, peak negative LA strain during late diastole of the left ventricle (atrial systole)

εR :

LA reservoir strain, the sum of εCD and εCT.


The first negative peak strain rate during early diastole of the left ventricle, corresponding to LA conduit function


The second negative peak strain rate during late diastole of the left ventricle (atrial systole), corresponding to LA pump function


Positive peak strain rate during systole of the left ventricle, corresponding to LA reservoir function


Peak velocity during late diastolic of mitral flow


Peak velocity during early diastolic of mitral flow


The average of septal and lateral mitral annular early diastolic peak velocity


The average of septal and lateral mitral annular late diastolic peak velocity


Peak velocity of tricuspid regurgitation


Left atrial stiffness index


Maximal left atrial volume index


Left ventricular diastolic diameter


Left ventricular mass index


Left ventricular ejection fraction


Heart failure with preserved ejection fraction


Coronary artery disease


Body mass index


Body surface area


Estimated glomerular filtration rate


Receiver operating characteristic


Limits of agreement


  1. Leung DY, Boyd A, Ng AA, Chi C, Thomas L. Echocardiographic evaluation of left atrial size and function: current understanding, pathophysiologic correlates, and prognostic implications. Am Heart J. 2008;156(6):1056–64.

    Article  PubMed  Google Scholar 

  2. Saraiva RM, Demirkol S, Buakhamsri A, Greenberg N, Popovic ZB, Thomas JD, Klein AL. Left atrial strain measured by two-dimensional speckle tracking represents a new tool to evaluate left atrial function. J Am Soc Echocardiogr. 2010;23(2):172–80.

    Article  PubMed  Google Scholar 

  3. Wakami K, Ohte N, Asada K, Fukuta H, Goto T, Mukai S, Narita H, Kimura G. Correlation between left ventricular end-diastolic pressure and peak left atrial wall strain during left ventricular systole. J Am Soc Echocardiogr. 2009;22(7):847–51.

    Article  PubMed  Google Scholar 

  4. Cameli M, Sparla S, Losito M, Righini FM, Menci D, Lisi M, D’Ascenzi F, Focardi M, Favilli R, Pierli C, et al. Correlation of Left Atrial Strain and Doppler Measurements with Invasive Measurement of Left Ventricular End-Diastolic Pressure in Patients Stratified for Different Values of Ejection Fraction. Echocardiography. 2016;33(3):398–405.

  5. Singh A, Addetia K, Maffessanti F, Mor-Avi V, Lang RM. LA Strain for Categorization of LV Diastolic Dysfunction. JACC Cardiovasc Imaging. 2017;10(7):735–43.

    Article  PubMed  Google Scholar 

  6. Morris DA, Belyavskiy E, Aravind-Kumar R, Kropf M, Frydas A, Braunauer K, Marquez E, Krisper M, Lindhorst R, Osmanoglou E, et al. Potential Usefulness and Clinical Relevance of Adding Left Atrial Strain to Left Atrial Volume Index in the Detection of Left Ventricular Diastolic Dysfunction. JACC Cardiovasc Imaging. 2018;11(10):1405–15.

    Article  PubMed  Google Scholar 

  7. Reddy YNV, Obokata M, Egbe A, Yang JH, Pislaru S, Lin G, Carter R, Borlaug BA. Left atrial strain and compliance in the diagnostic evaluation of heart failure with preserved ejection fraction. Eur J Heart Fail. 2019;21(7):891–900.

    Article  PubMed  Google Scholar 

  8. Singh A, Medvedofsky D, Mediratta A, Balaney B, Kruse E, Ciszek B, Shah AP, Blair JE, Maffessanti F, Addetia K, et al. Peak left atrial strain as a single measure for the non-invasive assessment of left ventricular filling pressures. Int J Cardiovasc Imaging. 2019;35(1):23–32.

    Article  PubMed  Google Scholar 

  9. Freed BH, Daruwalla V, Cheng JY, Aguilar FG, Beussink L, Choi A, Klein DA, Dixon D, Baldridge A, Rasmussen-Torvik LJ, et al. Prognostic Utility and Clinical Significance of Cardiac Mechanics in Heart Failure With Preserved Ejection Fraction: Importance of Left Atrial Strain. Circ Cardiovasc Imaging. 2016;9(3):e003754.

  10. Santos AB, Roca GQ, Claggett B, Sweitzer NK, Shah SJ, Anand IS, Fang JC, Zile MR, Pitt B, Solomon SD, et al. Prognostic Relevance of Left Atrial Dysfunction in Heart Failure With Preserved Ejection Fraction. Circ Heart Fail. 2016;9(4): e002763.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Chow SL, Maisel AS, Anand I, Bozkurt B, de Boer RA, Felker GM, Fonarow GC, Greenberg B, Januzzi JL Jr, Kiernan MS, et al. Role of Biomarkers for the Prevention, Assessment, and Management of Heart Failure: A Scientific Statement From the American Heart Association. Circulation. 2017;135(22):e1054–91.

    Article  PubMed  Google Scholar 

  12. Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JGF, Coats AJS, Falk V, Gonzalez-Juanatey JR, Harjola VP, Jankowska EA, et al. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur Heart J. 2016;37(27):2129–200.

    Article  PubMed  Google Scholar 

  13. Redfield MM, Rodeheffer RJ, Jacobsen SJ, Mahoney DW, Bailey KR, Burnett JC Jr. Plasma brain natriuretic peptide to detect preclinical ventricular systolic or diastolic dysfunction: a community-based study. Circulation. 2004;109(25):3176–81.

    Article  PubMed  Google Scholar 

  14. Natriuretic Peptides Studies Collaboration, Willeit P, Kaptoge S, Welsh P, Butterworth AS, Chowdhury R, Spackman SA, Pennells L, Gao P, Burgess S, et al. Natriuretic peptides and integrated risk assessment for cardiovascular disease: an individual-participant-data meta-analysis. Lancet Diabetes Endocrinol. 2016;4(10):840–9.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Liu L, Zhao F, Yang Y, Qi LT, Zhang BW, Chen F, Ciren D, Zheng B, Wang SY, Huo Y, et al. The clinical significance of carotid intima-media thickness in cardiovascular diseases: a survey in Beijing. J Hum Hypertens. 2008;22(4):259–65.

    Article  PubMed  Google Scholar 

  16. Ma YC, Zuo L, Chen JH, Luo Q, Yu XQ, Li Y, Xu JS, Huang SM, Wang LN, Huang W, et al. Modified glomerular filtration rate estimating equation for Chinese patients with chronic kidney disease. J Am Soc Nephrol. 2006;17(10):2937–44.

    Article  PubMed  Google Scholar 

  17. Quinones MA, Otto CM, Stoddard M, Waggoner A, Zoghbi WA. Recommendations for quantification of Doppler echocardiography: a report from the Doppler Quantification Task Force of the Nomenclature and Standards Committee of the American Society of Echocardiography. J Am Soc Echocardiogr. 2002;15(2):167–84.

    Article  PubMed  Google Scholar 

  18. Lang RM, Bierig M, Devereux RB, Flachskampf FA, Foster E, Pellikka PA, Picard MH, Roman MJ, Seward J, Shanewise JS, et al. Recommendations for chamber quantification: a report from the American Society of Echocardiography’s Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology. J Am Soc Echocardiogr. 2005;18(12):1440–63.

  19. Mondillo S, Galderisi M, Mele D, Cameli M, Lomoriello VS, Zaca V, Ballo P, D’Andrea A, Muraru D, Losi M, et al. Speckle-tracking echocardiography: a new technique for assessing myocardial function. J Ultrasound Med. 2011;30(1):71–83.

  20. Cameli M, Mandoli GE, Loiacono F, Dini FL, Henein M, Mondillo S. Left atrial strain: a new parameter for assessment of left ventricular filling pressure. Heart Fail Rev. 2016;21(1):65–76.

    Article  PubMed  Google Scholar 

  21. To AC, Flamm SD, Marwick TH, Klein AL. Clinical utility of multimodality LA imaging: assessment of size, function, and structure. JACC Cardiovasc Imaging. 2011;4(7):788–98.

    Article  PubMed  Google Scholar 

  22. Pathan F, D’Elia N, Nolan MT, Marwick TH, Negishi K. Normal Ranges of Left Atrial Strain by Speckle-Tracking Echocardiography: A Systematic Review and Meta-Analysis. J Am Soc Echocardiogr. 2017;30(1):59–70-e58.

  23. Mondillo S, Cameli M, Caputo ML, Lisi M, Palmerini E, Padeletti M, Ballo P. Early detection of left atrial strain abnormalities by speckle-tracking in hypertensive and diabetic patients with normal left atrial size. J Am Soc Echocardiogr. 2011;24(8):898–908.

    Article  PubMed  Google Scholar 

  24. Zhao Y, Sun Q, Han J, Lu Y, Zhang Y, Song W, Cheng Y, Cong T, Liu Y, Jiang Y. Left atrial stiffness index as a marker of early target organ damage in hypertension. Hypertens Res. 2021;44(3):299–309.

    Article  PubMed  Google Scholar 

  25. Muranaka A, Yuda S, Tsuchihashi K, Hashimoto A, Nakata T, Miura T, Tsuzuki M, Wakabayashi C, Watanabe N, Shimamoto K. Quantitative assessment of left ventricular and left atrial functions by strain rate imaging in diabetic patients with and without hypertension. Echocardiography. 2009;26(3):262–71.

    Article  PubMed  Google Scholar 

  26. Kuppahally SS, Akoum N, Burgon NS, Badger TJ, Kholmovski EG, Vijayakumar S, Rao SN, Blauer J, Fish EN, Dibella EV, et al. Left atrial strain and strain rate in patients with paroxysmal and persistent atrial fibrillation: relationship to left atrial structural remodeling detected by delayed-enhancement MRI. Circ Cardiovasc Imaging. 2010;3(3):231–9.

    Article  PubMed  Google Scholar 

  27. Thomas L, Marwick TH, Popescu BA, Donal E, Badano LP. Left Atrial Structure and Function, and Left Ventricular Diastolic Dysfunction: JACC State-of-the-Art Review. J Am Coll Cardiol. 2019;73(15):1961–77.

    Article  PubMed  Google Scholar 

  28. Prioli A, Marino P, Lanzoni L, Zardini P. Increasing degrees of left ventricular filling impairment modulate left atrial function in humans. Am J Cardiol. 1998;82(6):756–61.

    Article  PubMed  Google Scholar 

  29. Dernellis JM, Stefanadis CI, Zacharoulis AA, Toutouzas PK. Left atrial mechanical adaptation to long-standing hemodynamic loads based on pressure-volume relations. Am J Cardiol. 1998;81(9):1138–43.

    Article  PubMed  Google Scholar 

  30. Brecht A, Oertelt-Prigione S, Seeland U, Rucke M, Hattasch R, Wagelohner T, Regitz-Zagrosek V, Baumann G, Knebel F, Stangl V. Left Atrial Function in Preclinical Diastolic Dysfunction: Two-Dimensional Speckle-Tracking Echocardiography-Derived Results from the BEFRI Trial. J Am Soc Echocardiogr. 2016;29(8):750–8.

    Article  PubMed  Google Scholar 

  31. Dogan C, Ozdemir N, Hatipoglu S, Bakal RB, Omaygenc MO, Dindar B, Candan O, Emiroglu MY, Kaymaz C. Relation of left atrial peak systolic strain with left ventricular diastolic dysfunction and brain natriuretic peptide level in patients presenting with ST-elevation myocardial infarction. Cardiovasc Ultrasound. 2013;11:24.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Degirmenci H, Bakirci EM, Demirtas L, Duman H, Hamur H, Ceyhun G, Topal E. Relationship of left atrial global peak systolic strain with left ventricular diastolic dysfunction and brain natriuretic peptide level in patients presenting with non-ST elevation myocardial infarction. Med Sci Monit. 2014;20:2013–9.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Aung SM, Guler A, Guler Y, Huraibat A, Karabay CY, Akdemir I. Left atrial strain in heart failure with preserved ejection fraction. Herz. 2017;42(2):194–9.

    Article  PubMed  Google Scholar 

  34. Al Saikhan L, Hughes AD, Chung WS, Alsharqi M, Nihoyannopoulos P. Left atrial function in heart failure with mid-range ejection fraction differs from that of heart failure with preserved ejection fraction: a 2D speckle-tracking echocardiographic study. Eur Heart J Cardiovasc Imaging. 2019;20(3):279–90.

    Article  PubMed  Google Scholar 

  35. Abid L, Charfeddine S, Kammoun S. Relationship of left atrial global peak systolic strain with left ventricular diastolic dysfunction and brain natriuretic peptide level in end-stage renal disease patients with preserved left ventricular ejection fraction. J Echocardiogr. 2016;14(2):71–8.

    Article  PubMed  Google Scholar 

  36. Kurt M, Tanboga IH, Aksakal E, Kaya A, Isik T, Ekinci M, Bilen E. Relation of left ventricular end-diastolic pressure and N-terminal pro-brain natriuretic peptide level with left atrial deformation parameters. Eur Heart J Cardiovasc Imaging. 2012;13(6):524–30.

    Article  PubMed  Google Scholar 

  37. Abhayaratna WP, Seward JB, Appleton CP, Douglas PS, Oh JK, Tajik AJ, Tsang TS. Left atrial size: physiologic determinants and clinical applications. J Am Coll Cardiol. 2006;47(12):2357–63.

    Article  PubMed  Google Scholar 

  38. Kim H, Jun DW, Cho YK, Nam CW, Han SW, Hur SH, Kim YN, Kim KB. The correlation of left atrial volume index to the level of N-terminal pro-BNP in heart failure with a preserved ejection fraction. Echocardiography. 2008;25(9):961–7.

    Article  PubMed  Google Scholar 

  39. Kurt M, Wang J, Torre-Amione G, Nagueh SF. Left atrial function in diastolic heart failure. Circ Cardiovasc Imaging. 2009;2(1):10–5.

    Article  PubMed  Google Scholar 

  40. Lin J, Ma H, Gao L, Wang Y, Wang J, Zhu Z, Pang K, Wang H, Wu W. Left atrial reservoir strain combined with E/E’ as a better single measure to predict elevated LV filling pressures in patients with coronary artery disease. Cardiovasc Ultrasound. 2020;18(1):11.

  41. Porpaczy A, Nogradi A, Vertes V, Tokes-Fuzesi M, Czirjak L, Komocsi A, Faludi R. Left atrial stiffness is superior to volume and strain parameters in predicting elevated NT-proBNP levels in systemic sclerosis patients. Int J Cardiovasc Imaging. 2019;35(10):1795–802.

    Article  PubMed  PubMed Central  Google Scholar 

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The study was completed with the support of Ms. Shuyu Wang (Beijing Hypertension League Institute), Dr. Guobin Xu and Dr. Xuejing Wang (Department of Laboratory Medicine, Peking University First Hospital).


The study was supported by a grant from National Key Technology R&D Program (2006BAI01A02).

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Authors and Affiliations



Liu L, Zhang BW and Huo Y discussed and constituted the study design; Yang Y, Qi LT, Meng L and Ma W performed the echocardiographic examinations and collected the patient data. Liu L, Yang Y and Wang S analysed images. Liu L carried out statistical analysis and drafted the manuscript. All authors read, revised, and approved the manuscript.

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Correspondence to Baowei Zhang.

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The study protocol conforms to the ethical guidelines of the Declaration of Helsinki and was approved by the ethics committee of Peking University First Hospital. Informed consent was obtained from each participant.

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The authors declare no competing interests.

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Liu, L., Zhang, B., Yang, Y. et al. Reduced left atrial contractile strain with speckle tracking analysis predicts abnormal plasma NTproBNP in an asymptomatic community population. Cardiovasc Ultrasound 20, 27 (2022).

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