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Speckle tracking derived reference values of myocardial deformation and impact of cardiovascular risk factors – Results from the population-based STAAB cohort study


Authors: Caroline Morbach aff001;  Bettina N. Walter aff001;  Margret Breunig aff001;  Dan Liu aff001;  Theresa Tiffe aff001;  Martin Wagner aff001;  Götz Gelbrich aff003;  Peter U. Heuschmann aff001;  Stefan Störk aff001
Authors place of work: Comprehensive Heart Failure Center, University and University Hospital Würzburg, Würzburg, Germany aff001;  Department of Medicine I, Cardiology, University Hospital Würzburg, Würzburg, Germany aff002;  Institute of Clinical Epidemiology and Biometry, University of Würzburg, Würzburg, Germany aff003;  Clinical Trial Center, University Hospital Würzburg, Würzburg, Germany aff004
Published in the journal: PLoS ONE 14(9)
Category: Research Article
doi: https://doi.org/10.1371/journal.pone.0221888

Summary

Aims

We aimed to provide reference values for speckle-tracking derived systolic and diastolic myocardial deformation markers, and to determine their relation with age, sex, and cardiovascular risk factors.

Methods and results

The Characteristics and Course of Heart Failure STAges A/B and Determinants of Progression (STAAB) cohort study recruited a representative sample of the population of Würzburg, Germany, aged 30–79 years. In a sample of 1818 participants (52% female, mean age 54±12 years) global longitudinal peak systolic strain (GL-PSS, n = 1218), systolic (GL-SSR, n = 1506), and early (GL-EDSR, n = 1506) and late diastolic strain rates (GL-LDSR, n = 1500) were derived from 2D speckle tracking analysis. From a subgroup of 323 individuals without any cardiovascular risk factor, sex- and age-specific reference values were computed. GL-PSS, GL-SSR, and GL-EDSR were associated with sex, GL-EDSR decreased and GL-LDSR increased with age. In the total sample, dyslipidemia was associated with altered GL-PSS, GL-SSR, and GL-EDSR in women but not in men, whereas obesity was associated with less favorable GL-PSS and GL-EDSR in either sex. Hypertension impacted more adversely on systolic and diastolic myocardial deformation in women compared to men (all p<0.01).

Conclusion

The female myocardium appeared more vulnerable to high blood pressure and dyslipidemia when compared to men, while obesity was associated with adverse myocardial deformation in either sex. The reference values for echocardiographic myocardial deformation provided for a non-diseased population and their here reported associations with cardiovascular risk factors will inform future observational and intervention studies regarding i) effect sizes and power calculation, ii) cross-study comparisons, and iii) categorization of myocardial deformation in specific patient groups.

Keywords:

Biology and life sciences – Physical sciences – Research and analysis methods – People and places – Population groupings – Medicine and health sciences – Physiology – Physiological parameters – Diagnostic medicine – Endocrinology – Endocrine disorders – metabolic disorders – Body weight – Physics – Age groups – Vascular medicine – Imaging techniques – Classical mechanics – obesity – Diagnostic radiology – Radiology and imaging – blood pressure – hypertension – Epidemiology – Medical risk factors – Ultrasound imaging – echocardiography – Deformation – Damage mechanics

Introduction

Echocardiography is the most frequently used method in the assessment of cardiac function. Conventional measurements like left ventricular (LV) ejection fraction are of limited utility to detect changes over time, hence, more sensitive methods are required. Strain as a measure of myocardial deformation carries incremental information on the change of the LV shape during the cardiac cycle [1]. Strain imaging may detect subtle alterations in cardiac function [2]. Two-dimensional speckle-tracking assesses myocardial motion by tracking speckles in the ultrasonic image. This method determines strain and strain rates avoiding Doppler-associated angulation errors and tethering artifacts with a good correlation to sonomicrometry and tagged magnetic resonance imaging (r = 0.87) [3]. Typically, the impairment in longitudinal deformation precedes deterioration of radial and/or circumferential deformation [4, 5].

The ability to quantify abnormal function relies on the definition of “normal”. Longitudinal systolic strain has consistently been reported more negative in women compared to men [613] indicating the necessity to apply sex-specific normal values. In contrast, the association of systolic strain patterns with age are contradictory [614], and knowledge on the association of diastolic myocardial deformation with age and sex is scarce. Importantly, there are no reference values available for speckle-tracking derived diastolic strain rates.

The adjustment of LV function to physiologic ageing is heavily influenced by the presence and individual expression of cardiovascular (CV) risk factors [15]. However, knowledge on their age-modifying effect on systolic and/or diastolic myocardial deformation is scarce. These small-scaled studies predominantly investigated selected age groups and isolated risk factors [5, 1628]

We therefore aimed a) to establish speckle tracking derived sex- and age-specific normal values for systolic and diastolic myocardial deformation from a carefully selected group of individuals in sinus rhythm free of CV risk factors, and b) to determine the impact of age, sex, and classical CV risk factors on myocardial deformation.

Methods

Study population and recruitment

This is a prospectively planned analysis of the Characteristics and Course of Heart Failure Stages A-B and Determinants of Progression (STAAB) Cohort Study, based on consecutive participants from the general population of Würzburg, Germany, enrolled up to December 31, 2015. The detailed study design and methodology has been published [29]. A brief description is given in the supporting information.

Cardiovascular risk factors

Prevalence of diabetes mellitus, CV disease (previous myocardial infarction, coronary artery disease, stroke, peripheral artery disease), and current pharmacotherapy was assessed by physician-led face-to-face interview. Assessment of smoking status, height, weight, and blood pressure, and an oral glucose tolerance test were performed according to standard operating procedures by trained and certified personnel [29]. Fasting lipid profile and glycosylated hemoglobin (HbA1c) were measured at the central laboratory of the University Hospital Würzburg. CV risk factors were defined according to current recommendations as follows: hypertension = blood pressure ≥140/90 mmHg [30] or anti-hypertensive pharmacotherapy; dyslipidemia = low density lipoprotein ≥190 mg/dl [31] or lipid-lowering pharmacotherapy; obesity = body mass index >30 kg/m2 [32]; diabetes mellitus = HbA1c >6.5%, fasting plasma glucose >7.0 mmol/l or 2h-plasma glucose >11.1 mmol/l [33] or anti-diabetic medication; smoking = current or ex-smoker.

All individuals with valid assessment of myocardial deformation entered the analyses regarding the impact of CV risk factors on myocardial deformation. For determination of normal values, we defined a sub-sample of healthy individuals, i.e. subjects in sinus rhythm and free from CV risk factors or CV disease.

Echocardiography

The characteristics and effectiveness of performance measures of the echocardiographic quality assurance program established for the STAAB cohort study have been published [29, 34]. Image acquisition was performed by trained and certified sonographers on one echocardiography machine (Vivid S6®, M4S Sector Array Transducer operating at 1.5–4.3 MHz, GE Healthcare, Horten, Norway) with consistent system presets according to a pre-specified protocol [29, 34]. A minimum of three cardiac cycles was recorded. Standard LV apical views were acquired avoiding LV foreshortening with a frame rate of 50 to 80s-1, thus compatible with speckle tracking analysis. For tissue Doppler imaging (TDI) based reference assessments of myocardial deformation, additionally, small-angled images with high frame rates (80–100 s-1) were collected from the LV septal and lateral walls.

LV myocardial deformation was assessed offline using Q-Analysis (EchoPAC® PC Version 113, GE Healthcare, Buckinghamshire, Great Britain). Timing of aortic valve closure was determined using continuous-wave Doppler across the aortic valve. Systolic as well as early and late diastolic SR at the time of peak S, peak E and peak A, respectively, were measured in each apical view and averaged to generate global longitudinal systolic (GL-SSR) as well as early diastolic (GL-EDSR) and late diastolic SR (GL-LDSR). Global longitudinal peak systolic strain (GL-PSS) was automatically averaged from individually calculated segmental strain values. If more than two out of 18 LV segments were insufficiently tracked, the individual was excluded from GL-PSS analysis. Nevertheless, all LV segments that could be analyzed entered segment-specific analyses. For variability assessment and in accordance with standard operating procedures of the quality control program [29, 34], 10 recordings were interpreted by two observers and by one observer twice, 10–14 days apart, blinded to the previous results. For validation of speckle tracking versus TDI based strain imaging, TDI based GL-EDSR of the LV mid-septum and mid-lateral wall was determined in 25 random subjects (detailed description provided in supporting information).

Data analysis

Statistical analysis was performed using SPSS (Version 23, SPSS Inc., Chicago, USA). Descriptives of quantitative data are provided as mean and standard deviation. The relationship of global strain and SR with age and risk factors was examined by analysis of covariance. Main and interaction effects of CV risk factors on GL-PSS and SR were assessed using a general linear model. Age and sex were defined as main effects for analyses in the healthy sub-sample, and “no CV risk factor” plus individual CV risk factor for analyses in the total sample, respectively. P-values <0.05 were considered statistically significant. Observer variability was assessed using Bland-Altman 95% limits of agreement.

Results

In the frame of the first planned interim analysis, we analyzed 1818 STAAB participants (mean age 54±12 years, 51.5% women). Of those, 542 (30%) participants qualified for the sub-sample of healthy individuals (49±11 years, 58% women) and 1276 exhibited at least one CV risk factor (Table 1, Fig 1).

Fig. 1.

Number of individuals in each sub-sample in whom strain parameters could be derived.

<h2>Number of individuals in each sub-sample in whom strain parameters could be derived.</h2>

GL-PSS = global longitudinal peak systolic strain, GL-SSR = global longitudinal systolic strain rate, GL-EDSR = global longitudinal early diastolic strain rate, and GL-LDSR = global longitudinal late diastolic strain rate.

Tab. 1.

Clinical and echocardiographic characteristics of study participants, and subgroups without and with cardiovascular risk factors.

<h2>Clinical and echocardiographic characteristics of study participants, and subgroups without and with cardiovascular risk factors.</h2>

Owing to the preselection on risk, participants with CV risk factors featured numerous differences compared to the healthy group: they were older, had higher body mass index, blood pressure, cholesterol values, and also a higher HbA1c (Table 1). Accordingly, most echocardiographic markers matched with this adverse profile. Participants with CV risk factors had lower values for LVEF, GL-PSS, and all types of SR, but higher values for E/e´, LV end-diastolic diameter, septal and posterior wall thickness, and left atrial size. Of note, heart rate and frame rate of echocardiographic image acquisition were similar between groups (Table 1).

Although the distribution of sex was balanced across the five age categories in the total sample (p = 0.41), subjects with CV risk factors were expectedly older than healthy subjects.

In a total of 1752 individuals with valid echocardiograms, feasibility was 70% for GL-PSS and 86% for strain rates, respectively. Age, body mass index, heart rate, and frame rate had no impact on feasibility to derive GL-PSS measurement, but individuals with valid GL-PSS were significantly more often male (624 men vs. 594 women, p = 0.01). The feasibility to derive any modality of SR was significantly associated with younger age, male sex, and lower body mass index (all p<0.05).

For GL-PSS, GL-SSR, GL-EDSR, and GL-LDSR, the 90th percentiles of the absolute difference of two interpretations were 0.8%, 0.05 s-1, 0.08 s-1, and 0.04 s-1 for repeated interpretation by the same observer, and 2.6%, 0.16 s-1, 0.01 s-1, and 0.03 s-1 for the interpretation by two observers, respectively. GL-EDSR derived by speckle tracking and TDI was 1.40±0.68 s-1 and 1.89±0.56 s-1, respectively; the correlation coefficient for both methods was r = 0.70 [95%CI 0.59–0.80] (Figure A in S1 File).

Normal values for myocardial deformation in individuals free from CV risk factors and CV disease

Systolic strain

GL-PSS values could be assessed in 323 healthy individuals and were normally distributed (Figure B in S1 File). In a linear model, there was a non-significant change of GL-PSS of -0.23% per age decade in men (p = 0.131) and of +0.29% per age decade in women (p = 0.054); however, the slopes for both sexes differed significantly (p = 0.015; Fig 2). Overall, regardless of age, GL-PSS was by 1.74% more negative in women compared to men (p<0.001). Sex-specific normal values per age decades are given in Tables 2 and 3.

Fig. 2.

Combined averaged a) global longitudinal peak systolic strain (GL-PSS, n = 323), b) systolic strain rate (GL-SSR, n = 410), c) early diastolic strain rate (GL-EDSR, n = 410), and d) late diastolic strain rate (GL-LDSR, n = 407) according to age and sex in individuals in sinus rhythm free from cardiovascular risk factors and cardiovascular disease (mean age 49±11 years, 55% females).

Tab. 2.

Speckle tracking derived markers of left ventricular myocardial deformation in male participants by age group.

<h2>Speckle tracking derived markers of left ventricular myocardial deformation in male participants by age group.</h2>
Tab. 3.

Speckle tracking derived markers of left ventricular myocardial deformation in female participants by age group.

<h2>Speckle tracking derived markers of left ventricular myocardial deformation in female participants by age group.</h2>

We provide sex-specific percentiles for GL-PSS (Figures C and D in S1 File) as well as age- and sex specific systolic strain values for each left ventricular segment (Tables A and B in S1 File). In women, basal septal, mid septal, basal inferior, as well as all anteroseptal segments showed a significantly less negative strain with increasing age, whereas in men systolic strain remained unchanged in all segments.

Strain rate

Sex-specific normal values per age decades are given in Tables 2 and 3. GL-SSR changed by -0.003 s-1 per age decade in men (p = 0.741), and +0.023 s-1 per decade in women (p = 0.007), with a significant difference between slopes (p = 0.032). Regardless of age, women had 0.072 s-1 more negative values compared to men (p<0.001; Fig 2).

GL-EDSR changed by -0.106 s-1 per age decade in men (p<0.001), and -0.175 s-1 per age decade in women (p<0.001), with a significant difference between slopes (p = 0.011). Regardless of age, women had 0.275/s-1 more positive values compared to men (p<0.001).

GL-LDSR changed by +0.074 s-1 per age decade in men (p<0.001), and +0.100 s-1 per age decade in women (p<0.001,) without a significant difference between slopes (p = 0.080). Regardless of age, women had 0.006 s-1 less positive values compared to men (p = 0.747).

Sex- and age-specific percentiles of GL-SSR, GL-EDSR, and GL-LDSR are detailed in Figures E-J in S1 File.

Impact of CV risk factors on myocardial deformation

1276 individuals exhibited at least one CV risk factor (56±12 years, 49% women). The number of individuals decreased with increasing number of prevalent CV risk factors and was evenly distributed over the decades (Figures K and L in S1 File).

In the total sample, GL-PSS was adversely affected by obesity in either sex (p<0.001), whereas an adverse effect of hypertension and dyslipidemia on GL-PSS was selectively observed in women (Table 4, Table C in S1 File). An adverse effect of dyslipidemia, hypertension, and obesity on GL-SSR was consistently observed in women only (Table 4, Table D in S1 File). GL-EDSR was negatively affected by hypertension and dyslipidemia, with a significantly more adverse effect in women, and by obesity in either sex (Table 4, Table E in S1 File). GL-LDSR was significantly increased in individuals with hypertension in either sex, with a significantly more adverse effect in women (Table 3, Table F in S1 File). Diabetes mellitus and smoking had no significant adverse effect on myocardial deformation (Tables C-F in S1 File)

Tab. 4.

Impact of cardiovascular risk factors on myocardial deformation in the total cohort and according to sex.

<h2>Impact of cardiovascular risk factors on myocardial deformation in the total cohort and according to sex.</h2>

Discussion

From a well-characterized, population-based cohort balanced for age and sex, we defined a sub-sample of healthy individuals (in sinus rhythm and free of CV risk factors and CV disease) and established reference values for global and segmental peak systolic strain and systolic SR of the LV. To the best of our knowledge, the current report is first to provide speckle-tracking derived reference values for early and late diastolic SR. Systolic and early, but not late, diastolic myocardial deformation showed a strong association with sex. Additionally, in contrast to systolic deformation parameters, diastolic SR markers were strongly affected by age: GL-EDSR decreased, while GL-LDSR increased with age.

In the total sample, CV risk factors differentially affected the various aspects of myocardial deformation. Further, sex-specific effects of CV risk factors on myocardial deformation were observed. This is compatible with the hypothesis that the myocardial sensitivity to individual risk factors is determined by sex.

Quality assurance

Assessment of acquisition variability and interpretation variability confirmed sound agreement between observers. Applying high quality standards to image and tracking quality, feasibility of GL-PSS in the total sample was 70%, which is comparable to other larger studies [11, 12]. Compared to TDI, speckle tracking derived GL-EDSR, which due to the highest velocity is most prone to undersampling by lower frame rates, indeed yielded a systematic deviation exhibiting slightly lower values (factor 0.7). Nevertheless, the good correlation between both methods and comparable standard deviation (1.40±0.68 s-1 versus 1.89±0.56 s-1) justify the clinical application of speckle tracking derived GL-EDSR. These findings emphasize the need for population-based normal values specifically derived from speckle tracking based strain imaging.

Systolic myocardial deformation in healthy individuals

In healthy individuals, GL-PSS and SR were found more negative in women compared to men [11], with disparate results regarding their association with age [11]. As age advances, the relationship of cardiac structure and function with age is confounded by the accumulation of traditional risk factors [15]. Most echocardiographic studies describing an association of GL-PSS with age did not systematically exclude individuals with CV risk factors or overt CV disease [11, 35, 36], which is the likely reason for these incongruent results.

We performed a detailed, physician-based assessment and thus established a well selected sub-sample of “truly healthy” individuals, i.e. in sinus rhythm and free from CV risk factors and CV disease. We here confirmed a more negative GL-PSS in women compared to men. Further, we found no significant change of systolic myocardial deformation with age in men, but significantly less positive GL-SSR with advancing age and a trend towards less negative GL-PSS accompanied by a significant impairment of segmental GL-PSS in septal and anteroseptal segments in women. This is in line with results from the EACVI NORRE study, where the pattern of worse systolic longitudinal LV function with advancing age in women was associated with more negative values of circumferential strain [37]. More detailed assessment of the underlying pathomechanisms including hormonal analyses and the evaluation of other than the conventional cardiovascular risk factors will be subjected to further research.

Diastolic myocardial deformation in healthy individuals

GL-EDSR is considered a comprehensive measure of early active LV relaxation. Importantly, diastolic SR yielded higher accuracy regarding the estimation of LV filling pressures compared to indices including the broadly used but angle dependent and mono-dimensional TDI measurement e´ [38, 39]. Further, GL-LDSR is considered a measure of late diastolic LV filling induced by active atrial contraction. Our analyses extend previous knowledge, as we found that GL-EDSR was significantly higher in women compared to men, whereas no sex-related difference was apparent regarding GL-LDSR. Further, GL-EDSR significantly decreased, whereas GL-LDSR significantly increased with age. This implies an increase of active atrial contribution to LV filling with advancing age, thus possibly compensating for the described decrease in active LV relaxation.

Impact of CV risk factors on systolic and diastolic myocardial deformation

A recent report from the MESA study employing cardiac magnet resonance tomography reported that CV risk status–besides sex and ethnicity–were major drivers of the progression of LV measures [15]. Using echocardiography, hypertensive heart disease with normal ejection fraction has been associated with reduced myocardial velocities and reduced regional function [40], and diabetes mellitus with worse LV remodeling and function [26, 28]. Results regarding the impact of obesity on myocardial function are inconsistent, reporting negative, positive or neutral associations of LV diastolic function patterns with the degree of obesity [5, 20, 22, 24, 25, 27, 41]. Two larger studies reported neutral findings [24, 25] and emphasized the importance of factors defining the metabolic syndrome rather than obesity itself. According to one report comparing 40 otherwise healthy smokers with age-matched controls, smoking intensity gradually impaired systolic and diastolic myocardial deformation patterns of both the left and the right ventricle [23]. Hence, evidence of the negative impact of CV risk factors on myocardial deformation is inconsistent, mainly due to heterogeneous study quality and relatively small samples looking at restricted age ranges and risk profiles.

To our knowledge, the current study is first to assess the individual impact of each of the established CV risk factors on systolic and diastolic myocardial deformation in a well-controlled representative cohort. Our results suggest a sex-specific sensitivity of the myocardium to individual CV risk factors. The vulnerability of the female myocardium to high blood pressure with subsequent alteration of the active early diastolic myocardial relaxation, for example, might be an explanation for the preponderance of females in HF with preserved ejection fraction. We did not observe any direct negative impact of smoking and diabetes mellitus on myocardial deformation at rest. These risk factors might act as dormant harmful factors affecting the vasculature, i.e. not affecting the myocardial function at rest until an ischemic damage has occurred. Further, all individuals with diabetes mellitus also exhibited at least one additional CV risk factor, which might have had a stronger impact on longitudinal LV function than diabetes mellitus.

Strengths and limitations

Strain imaging depends on optimal image quality. Hence, feasibility is lower compared to routine echocardiography. Nevertheless, applying high quality standards, we achieved a feasibility comparable to other large cohort studies [11, 36]. The current analysis omitted radial and circumferential deformation as we focused on longitudinal myocardial deformation, which is affected first along the pathophysiological cascade [4]. CV risk factors were assessed very carefully. Nevertheless, more detailed analyses including pharmacotherapy and quality of cardiovascular risk factor control were not performed due to the sample size.

Clinical impact and conclusion

Healthy aging seems to be associated with a selective decrease in systolic function in women. By contrast, active LV relaxation decreases with advancing age in either sex, necessitating the left atrium to contribute increasingly more to left ventricular filling. Further, the female myocardium appears more vulnerable to high blood pressure and dyslipidemia when compared to men, while obesity might reduce myocardial deformation to a similar extent in either sex.

The here presented sex- and age-specific speckle-tracking derived reference values for systolic and, importantly, also for diastolic myocardial deformation, will help to classify myocardial deformation in patients more reliably. Reference values of strain and strain rates and their here reported association with CV risk factors will inform future observational and intervention studies regarding i) effect sizes and power calculation, ii) cross-study comparisons, and iii) categorization of myocardial deformation in specific patient groups.

Supporting information

S1 File [docx]
Supplementary methods: Study population and recruitment, myocardial deformation imaging–detailed, Tissue-Doppler derived strain rate imaging, and data analysis.


Zdroje

1. Pedrizzetti G, Mangual J and Tonti G. On the geometrical relationship between global longitudinal strain and ejection fraction in the evaluation of cardiac contraction. J Biomech. 2014;47:746–9. doi: 10.1016/j.jbiomech.2013.12.016 24411099

2. Stampehl MR, Mann DL, Nguyen JS, Cota F, Colmenares C and Dokainish H. Speckle strain echocardiography predicts outcome in patients with heart failure with both depressed and preserved left ventricular ejection fraction. Echocardiography. 2015;32:71–8. doi: 10.1111/echo.12613 24816065

3. Perk G, Tunick PA and Kronzon I. Non-Doppler two-dimensional strain imaging by echocardiography—from technical considerations to clinical applications. J Am Soc Echocardiogr. 2007;20:234–43. 17336748

4. Mizuguchi Y, Oishi Y, Miyoshi H, Iuchi A, Nagase N and Oki T. The functional role of longitudinal, circumferential, and radial myocardial deformation for regulating the early impairment of left ventricular contraction and relaxation in patients with cardiovascular risk factors: a study with two-dimensional strain imaging. J Am Soc Echocardiogr. 2008;21:1138–44. doi: 10.1016/j.echo.2008.07.016 18926389

5. Share BL, La Gerche A, Naughton GA, Obert P and Kemp JG. Young Women With Abdominal Obesity Have Subclinical Myocardial Dysfunction. Can J Cardiol. 2015;31:1195–201. doi: 10.1016/j.cjca.2015.02.004 26002065

6. Yingchoncharoen T, Agarwal S, Popovic ZB and Marwick TH. Normal ranges of left ventricular strain: a meta-analysis. J Am Soc Echocardiogr. 2013;26:185–91. doi: 10.1016/j.echo.2012.10.008 23218891

7. Kleijn SA, Pandian NG, Thomas JD, Perez de Isla L, Kamp O, Zuber M, Nihoyannopoulos P, Forster T, Nesser HJ, Geibel A, Gorissen W and Zamorano JL. Normal reference values of left ventricular strain using three-dimensional speckle tracking echocardiography: results from a multicentre study. Eur Heart J Cardiovasc Imaging. 2015;16:410–6. doi: 10.1093/ehjci/jeu213 25345661

8. Bernard A, Addetia K, Dulgheru R, Caballero L, Sugimoto T, Akhaladze N, Athanassopoulos GD, Barone D, Baroni M, Cardim N, Hagendorff A, Hristova K, Ilardi F, Lopez T, de la Morena G, Popescu BA, Penicka M, Ozyigit T, David Rodrigo Carbonero J, van de Veire N, Stephan Von Bardeleben R, Vinereanu D, Luis Zamorano J, Martinez C, Magne J, Cosyns B, Donal E, Habib G, Badano LP, Lang RM and Lancellotti P. 3D echocardiographic reference ranges for normal left ventricular volumes and strain: results from the EACVI NORRE study. Eur Heart J Cardiovasc Imaging. 2017;18:475–483. doi: 10.1093/ehjci/jew284 28329230

9. Cheng S, Larson MG, McCabe EL, Osypiuk E, Lehman BT, Stanchev P, Aragam J, Benjamin EJ, Solomon SD and Vasan RS. Age- and sex-based reference limits and clinical correlates of myocardial strain and synchrony: the Framingham Heart Study. Circ Cardiovasc Imaging. 2013;6:692–9. doi: 10.1161/CIRCIMAGING.112.000627 23917618

10. Menting ME, McGhie JS, Koopman LP, Vletter WB, Helbing WA, van den Bosch AE and Roos-Hesselink JW. Normal myocardial strain values using 2D speckle tracking echocardiography in healthy adults aged 20 to 72 years. Echocardiography. 2016;33:1665–1675. doi: 10.1111/echo.13323 27550630

11. Dalen H, Thorstensen A, Aase SA, Ingul CB, Torp H, Vatten LJ and Stoylen A. Segmental and global longitudinal strain and strain rate based on echocardiography of 1266 healthy individuals: the HUNT study in Norway. Eur J Echocardiogr. 2010;11:176–83. doi: 10.1093/ejechocard/jep194 19946115

12. Moreira HT, Nwabuo CC, Armstrong AC, Kishi S, Gjesdal O, Reis JP, Schreiner PJ, Liu K, Lewis CE, Sidney S, Gidding SS, Lima JAC and Ambale-Venkatesh B. Reference Ranges and Regional Patterns of Left Ventricular Strain and Strain Rate Using Two-Dimensional Speckle-Tracking Echocardiography in a Healthy Middle-Aged Black and White Population: The CARDIA Study. J Am Soc Echocardiogr. 2017;30:647–658 e2. doi: 10.1016/j.echo.2017.03.010 28511859

13. Park JH, Lee JH, Lee SY, Choi JO, Shin MS, Kim MJ, Jung HO, Park JR, Sohn IS, Kim H, Park SM, Yoo NJ, Choi JH, Kim HK, Cho GY, Lee MR, Park JS, Shim CY, Kim DH, Shin DH, Shin GJ, Shin SH, Kim KH, Kim WS and Park SW. Normal 2-Dimensional Strain Values of the Left Ventricle: A Substudy of the Normal Echocardiographic Measurements in Korean Population Study. J Cardiovasc Ultrasound. 2016;24:285–293. doi: 10.4250/jcu.2016.24.4.285 28090256

14. Kaku K, Takeuchi M, Tsang W, Takigiku K, Yasukochi S, Patel AR, Mor-Avi V, Lang RM and Otsuji Y. Age-related normal range of left ventricular strain and torsion using three-dimensional speckle-tracking echocardiography. J Am Soc Echocardiogr. 2014;27:55–64. doi: 10.1016/j.echo.2013.10.002 24238753

15. Liu CY, Lai S, Kawel-Boehm N, Chahal H, Ambale-Venkatesh B, Lima JAC and Bluemke DA. Healthy aging of the left ventricle in relationship to cardiovascular risk factors: The Multi-Ethnic Study of Atherosclerosis (MESA). PLoS One. 2017;12:e0179947. doi: 10.1371/journal.pone.0179947 28640873

16. Bjornstad P, Truong U, Pyle L, Dorosz JL, Cree-Green M, Baumgartner A, Coe G, Regensteiner JG, Reusch JE and Nadeau KJ. Youth with type 1 diabetes have worse strain and less pronounced sex differences in early echocardiographic markers of diabetic cardiomyopathy compared to their normoglycemic peers: A RESistance to InSulin in Type 1 ANd Type 2 diabetes (RESISTANT) Study. J Diabetes Complications. 2016;30:1103–10. doi: 10.1016/j.jdiacomp.2016.04.008 27133451

17. Szelenyi Z, Fazakas A, Szenasi G, Tegze N, Fekete B, Molvarec A, Hadusfalvy-Sudar S, Janosi O, Kiss M, Karadi I and Vereckei A. The mechanism of reduced longitudinal left ventricular systolic function in hypertensive patients with normal ejection fraction. J Hypertens. 2015;33:1962–9; discussion 1969. doi: 10.1097/HJH.0000000000000624 26154942

18. Huang J, Yan ZN, Rui YF, Fan L, Shen D and Chen DL. Left Ventricular Systolic Function Changes in Primary Hypertension Patients Detected by the Strain of Different Myocardium Layers. Medicine (Baltimore). 2016;95:e2440. doi: 10.1097/MD.0000000000002440 26765428

19. Almeida AL, Teixido-Tura G, Choi EY, Opdahl A, Fernandes VR, Wu CO, Bluemke DA and Lima JA. Metabolic syndrome, strain, and reduced myocardial function: multi-ethnic study of atherosclerosis. Arq Bras Cardiol. 2014;102:327–35. doi: 10.5935/abc.20140040 24844874

20. Pascual M, Pascual DA, Soria F, Vicente T, Hernandez AM, Tebar FJ and Valdes M. Effects of isolated obesity on systolic and diastolic left ventricular function. Heart. 2003;89:1152–6. doi: 10.1136/heart.89.10.1152 12975404

21. Wong CY, O'Moore-Sullivan T, Leano R, Byrne N, Beller E and Marwick TH. Alterations of left ventricular myocardial characteristics associated with obesity. Circulation. 2004;110:3081–7. 15520317

22. Wierzbowska-Drabik K, Chrzanowski L, Kapusta A, Uznanska-Loch B, Plonska E, Krzeminska-Pakula M, Kurpesa M, Rechcinski T, Trzos E and Kasprzak JD. Severe obesity impairs systolic and diastolic heart function—the significance of pulsed tissue Doppler, strain, and strain rate parameters. Echocardiography. 2013;30:904–11. doi: 10.1111/echo.12164 23496241

23. Eroglu E, Aydin S, Yalniz F, Kalkan AK, Bayrak F and Degertekin M. Chronic cigarette smoking affects left and right ventricular long-axis function in healthy young subjects: a Doppler myocardial imaging study. Echocardiography. 2009;26:1019–25. doi: 10.1111/j.1540-8175.2009.00924.x 19558517

24. Dobson R, Burgess MI, Sprung VS, Irwin A, Hamer M, Jones J, Daousi C, Adams V, Kemp GJ, Shojaee-Moradie F, Umpleby M and Cuthbertson DJ. Metabolically healthy and unhealthy obesity: differential effects on myocardial function according to metabolic syndrome, rather than obesity. Int J Obes (Lond). 2016;40:153–61.

25. Russo C, Sera F, Jin Z, Palmieri V, Homma S, Rundek T, Elkind MS, Sacco RL and Di Tullio MR. Abdominal adiposity, general obesity, and subclinical systolic dysfunction in the elderly: A population-based cohort study. Eur J Heart Fail. 2016;18:537–44. doi: 10.1002/ejhf.521 27109744

26. Kishi S, Gidding SS, Reis JP, Colangelo LA, Venkatesh BA, Armstrong AC, Isogawa A, Lewis CE, Wu C, Jacobs DR, Jr., Liu K and Lima JA. Association of Insulin Resistance and Glycemic Metabolic Abnormalities With LV Structure and Function in Middle Age: The CARDIA Study. JACC Cardiovasc Imaging. 2017;10:105–114. doi: 10.1016/j.jcmg.2016.02.033 27544896

27. Zarich SW, Kowalchuk GJ, McGuire MP, Benotti PN, Mascioli EA and Nesto RW. Left ventricular filling abnormalities in asymptomatic morbid obesity. Am J Cardiol. 1991;68:377–81. 1858679

28. Jensen MT, Sogaard P, Andersen HU, Bech J, Fritz Hansen T, Biering-Sorensen T, Jorgensen PG, Galatius S, Madsen JK, Rossing P and Jensen JS. Global longitudinal strain is not impaired in type 1 diabetes patients without albuminuria: the Thousand & 1 study. JACC Cardiovasc Imaging. 2015;8:400–10. doi: 10.1016/j.jcmg.2014.12.020 25746329

29. Wagner M, Tiffe T, Morbach C, Gelbrich G, Stork S, Heuschmann PU and Consortium S. Characteristics and Course of Heart Failure Stages A-B and Determinants of Progression—design and rationale of the STAAB cohort study. Eur J Prev Cardiol. 2017;24:468–479. doi: 10.1177/2047487316680693 27879413

30. Mancia G, Fagard R, Narkiewicz K, Redon J, Zanchetti A, Bohm M, Christiaens T, Cifkova R, De Backer G, Dominiczak A, Galderisi M, Grobbee DE, Jaarsma T, Kirchhof P, Kjeldsen SE, Laurent S, Manolis AJ, Nilsson PM, Ruilope LM, Schmieder RE, Sirnes PA, Sleight P, Viigimaa M, Waeber B, Zannad F, Redon J, Dominiczak A, Narkiewicz K, Nilsson PM, Burnier M, Viigimaa M, Ambrosioni E, Caufield M, Coca A, Olsen MH, Schmieder RE, Tsioufis C, van de Borne P, Zamorano JL, Achenbach S, Baumgartner H, Bax JJ, Bueno H, Dean V, Deaton C, Erol C, Fagard R, Ferrari R, Hasdai D, Hoes AW, Kirchhof P, Knuuti J, Kolh P, Lancellotti P, Linhart A, Nihoyannopoulos P, Piepoli MF, Ponikowski P, Sirnes PA, Tamargo JL, Tendera M, Torbicki A, Wijns W, Windecker S, Clement DL, Coca A, Gillebert TC, Tendera M, Rosei EA, Ambrosioni E, Anker SD, Bauersachs J, Hitij JB, Caulfield M, De Buyzere M, De Geest S, Derumeaux GA, Erdine S, Farsang C, Funck-Brentano C, Gerc V, Germano G, Gielen S, Haller H, Hoes AW, Jordan J, Kahan T, Komajda M, Lovic D, Mahrholdt H, Olsen MH, Ostergren J, Parati G, Perk J, Polonia J, Popescu BA, Reiner Z, Ryden L, Sirenko Y, Stanton A, Struijker-Boudier H, Tsioufis C, van de Borne P, Vlachopoulos C, Volpe M and Wood DA. 2013 ESH/ESC guidelines for the management of arterial hypertension: the Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). Eur Heart J. 2013;34:2159–219. doi: 10.1093/eurheartj/eht151 23771844

31. European Association for Cardiovascular P, Rehabilitation, Reiner Z, Catapano AL, De Backer G, Graham I, Taskinen MR, Wiklund O, Agewall S, Alegria E, Chapman MJ, Durrington P, Erdine S, Halcox J, Hobbs R, Kjekshus J, Filardi PP, Riccardi G, Storey RF, Wood D, Guidelines ESCCfP and Committees. ESC/EAS Guidelines for the management of dyslipidaemias: the Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). Eur Heart J. 2011;32:1769–818. doi: 10.1093/eurheartj/ehr158 21712404

32. Fruhbeck G, Toplak H, Woodward E, Yumuk V, Maislos M, Oppert JM and Executive Committee of the European Association for the Study of O. Obesity: the gateway to ill health—an EASO position statement on a rising public health, clinical and scientific challenge in Europe. Obes Facts. 2013;6:117–20. doi: 10.1159/000350627 23548858

33. Authors/Task Force M, Ryden L, Grant PJ, Anker SD, Berne C, Cosentino F, Danchin N, Deaton C, Escaned J, Hammes HP, Huikuri H, Marre M, Marx N, Mellbin L, Ostergren J, Patrono C, Seferovic P, Uva MS, Taskinen MR, Tendera M, Tuomilehto J, Valensi P, Zamorano JL, Guidelines ESCCfP, Zamorano JL, Achenbach S, Baumgartner H, Bax JJ, Bueno H, Dean V, Deaton C, Erol C, Fagard R, Ferrari R, Hasdai D, Hoes AW, Kirchhof P, Knuuti J, Kolh P, Lancellotti P, Linhart A, Nihoyannopoulos P, Piepoli MF, Ponikowski P, Sirnes PA, Tamargo JL, Tendera M, Torbicki A, Wijns W, Windecker S, Document R, De Backer G, Sirnes PA, Ezquerra EA, Avogaro A, Badimon L, Baranova E, Baumgartner H, Betteridge J, Ceriello A, Fagard R, Funck-Brentano C, Gulba DC, Hasdai D, Hoes AW, Kjekshus JK, Knuuti J, Kolh P, Lev E, Mueller C, Neyses L, Nilsson PM, Perk J, Ponikowski P, Reiner Z, Sattar N, Schachinger V, Scheen A, Schirmer H, Stromberg A, Sudzhaeva S, Tamargo JL, Viigimaa M, Vlachopoulos C and Xuereb RG. ESC Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD: the Task Force on diabetes, pre-diabetes, and cardiovascular diseases of the European Society of Cardiology (ESC) and developed in collaboration with the European Association for the Study of Diabetes (EASD). Eur Heart J. 2013;34:3035–87. doi: 10.1093/eurheartj/eht108 23996285

34. Morbach C, Gelbrich G, Breunig M, Tiffe T, Wagner M, Heuschmann PU and Stork S. Impact of acquisition and interpretation on total inter-observer variability in echocardiography: results from the quality assurance program of the STAAB cohort study. Int J Cardiovasc Imaging. 2018.

35. Kuznetsova T, Herbots L, Richart T, D'Hooge J, Thijs L, Fagard RH, Herregods MC and Staessen JA. Left ventricular strain and strain rate in a general population. Eur Heart J. 2008;29:2014–23. doi: 10.1093/eurheartj/ehn280 18583396

36. Hung CL, Goncalves A, Shah AM, Cheng S, Kitzman D and Solomon SD. Age- and Sex-Related Influences on Left Ventricular Mechanics in Elderly Individuals Free of Prevalent Heart Failure: The ARIC Study (Atherosclerosis Risk in Communities). Circ Cardiovasc Imaging. 2017;10.

37. Sugimoto T, Dulgheru R, Bernard A, Ilardi F, Contu L, Addetia K, Caballero L, Akhaladze N, Athanassopoulos GD, Barone D, Baroni M, Cardim N, Hagendorff A, Hristova K, Lopez T, de la Morena G, Popescu BA, Moonen M, Penicka M, Ozyigit T, Rodrigo Carbonero JD, van de Veire N, von Bardeleben RS, Vinereanu D, Zamorano JL, Go YY, Rosca M, Calin A, Magne J, Cosyns B, Marchetta S, Donal E, Habib G, Galderisi M, Badano LP, Lang RM and Lancellotti P. Echocardiographic reference ranges for normal left ventricular 2D strain: results from the EACVI NORRE study. Eur Heart J Cardiovasc Imaging. 2017;18:833–840. doi: 10.1093/ehjci/jex140 28637227

38. Dokainish H, Sengupta R, Pillai M, Bobek J and Lakkis N. Usefulness of new diastolic strain and strain rate indexes for the estimation of left ventricular filling pressure. Am J Cardiol. 2008;101:1504–9. doi: 10.1016/j.amjcard.2008.01.037 18471466

39. Ersboll M, Andersen MJ, Valeur N, Mogensen UM, Fakhri Y, Thune JJ, Moller JE, Hassager C, Sogaard P and Kober L. Early diastolic strain rate in relation to systolic and diastolic function and prognosis in acute myocardial infarction: a two-dimensional speckle-tracking study. Eur Heart J. 2014;35:648–56. doi: 10.1093/eurheartj/eht179 23713080

40. Narayanan A, Aurigemma GP, Chinali M, Hill JC, Meyer TE and Tighe DA. Cardiac mechanics in mild hypertensive heart disease: a speckle-strain imaging study. Circ Cardiovasc Imaging. 2009;2:382–90. doi: 10.1161/CIRCIMAGING.108.811620 19808626

41. Peterson LR, Waggoner AD, Schechtman KB, Meyer T, Gropler RJ, Barzilai B and Davila-Roman VG. Alterations in left ventricular structure and function in young healthy obese women: assessment by echocardiography and tissue Doppler imaging. J Am Coll Cardiol. 2004;43:1399–404. 15093874


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