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Sex- and age- specific normal values of left ventricular functional and myocardial mass parameters using threshold-based trabeculae quantification

  • Zsófia Gregor,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Visualization, Writing – original draft

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Anna Réka Kiss,

    Roles Conceptualization, Data curation, Investigation, Methodology, Writing – original draft

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Liliána Erzsébet Szabó,

    Roles Data curation, Investigation, Methodology

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Attila Tóth,

    Roles Conceptualization, Investigation, Methodology, Software, Validation

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Kinga Grebur,

    Roles Data curation, Investigation, Methodology

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Márton Horváth,

    Roles Data curation, Investigation, Methodology

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Zsófia Dohy,

    Roles Data curation, Investigation, Methodology

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

  • Béla Merkely,

    Roles Conceptualization, Funding acquisition, Resources, Supervision

    Affiliations Heart and Vascular Center of Semmelweis University, Budapest, Hungary, Department of Sports Medicine, Semmelweis University, Budapest, Hungary

  • Hajnalka Vágó,

    Roles Conceptualization, Funding acquisition, Investigation, Resources, Supervision

    Affiliations Heart and Vascular Center of Semmelweis University, Budapest, Hungary, Department of Sports Medicine, Semmelweis University, Budapest, Hungary

  • Andrea Szűcs

    Roles Conceptualization, Investigation, Methodology, Supervision, Validation, Writing – review & editing

    szucsand@gmail.com

    Affiliation Heart and Vascular Center of Semmelweis University, Budapest, Hungary

Abstract

Background

The threshold-based (TB) trabeculated and papillary muscle mass (TPM) quantification method for cardiac MRI (CMR) calculates different values than conventional contouring techniques. We aimed to identify the sex- and age-related normal reference ranges for left ventricular (LV) myocardial mass values, volumetric and functional parameters and the correspondence of these parameters using the TB method.

Methods

Healthy European adults (n = 200, age: 39.4 ± 12 years, males: 100) were examined with CMR and evaluated with a TB postprocessing method. They were stratified by sex and age (Group A: 18–29, Group B: 30–39, Group C: 40–49, Group D: >50 years). The calculated parameters were indexed to body surface area (i).

Results

The normal reference ranges for the studied parameters were assessed in each age group. Significant biometric differences in LV parameters and mass-to-volume ratios were found between males and females, and the left ventricular compacted myocardial mass (LVCMi) and TPMi differences remained significant after stratification by age. Unlike other LV volumetric and functional parameters and mass-to-volume ratios, the TPMi, the LVCMi and the TPMi-to-LVCMi ratio did not differ among age groups in males or females. This finding was strengthened by the lack of correlation between TPMi and age.

Conclusions

Age- and sex-related normal reference ranges for LV volumetric and functional parameters and LVCMi and TPMi values were established using a TB postprocessing method. TPMi, LVCMi and their ratio did not change over time. The TPMi-to-LVCMi and the mass-to-volume ratios might have clinical utility in the differential diagnosis of conditions with LV hypertrabeculation.

Introduction

Several studies have been published about left ventricular (LV) functional parameters in both pathological and physiological conditions [13]. The border between normal and excessive LV trabeculation is undefined [2,4,5]; however, normal values of the trabecular mass might assist with the diagnosis of pathological conditions with hypertrabeculation, e.g., left ventricular noncompaction (LVNC), hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and congenital heart diseases.

A number of studies have already been performed in various populations using different methods and vendors since trabeculae quantification became available [68].

However, the established values of LV trabeculation are not comparable due to the use of different techniques, the lack of intervendor agreements, and the heterogeneous study populations.

The threshold-based (TB) trabeculated and papillary muscle (TPM) quantification method is based on the differing signal intensities of blood and myocardium and has been proven to be an excellent evaluation method with better interobserver agreement than conventional techniques [911]. The determined volumes are lower and the ejection fraction (EF) and myocardial mass values are higher when using this method than when using standard contouring techniques based on endocardial and epicardial contours [12]. Therefore, novel reference ranges are required.

To the best of our knowledge, no studies have been performed to determine the normal reference ranges for LV functional parameters and myocardial mass values using the TB method. In addition, there are no data about sex- and age-specific normal values of the LV trabecular mass.

We aimed to describe the normal reference ranges for LV functional parameters, compacted myocardial mass (LVCM), TPM and the correspondences of these parameters based on a healthy European population divided by sex and age using the TB method.

Materials and methods

Study population

Two hundred healthy adult European volunteers were enrolled in this single-center study (mean age: 39.4 ± 12 years, males: 100, mean EF: 68.7 ± 5.1%). Each participant completed a questionnaire about demographic characteristics, cardiovascular symptoms, medical history, medication and sport activity. The following exclusion criteria were applied: presence of any congenital cardiac abnormalities or acquired ischemic heart diseases, arrhythmias, valvular heart diseases, cardiomyopathies, other cardiac diseases or sudden cardiac death in the family history. Furthermore, participants with extracardiac disorders, including hypertension-related, pulmonary, nephrology, gastrointestinal, metabolic, autoimmune, hormonal, psychiatric, oncologic or neuromuscular diseases or other hereditary conditions, were excluded. None of the participants had received medical therapy. Athletes with competitive sport activity (>6 hours/week) were also ruled out [13].

In addition to cardiac MRI (CMR) examinations, blood pressure measurements and 12-lead resting electrocardiography were performed for each participant.

The study population was divided by age as follows: 20–29 years (Group A, n = 50), 30–39 years (Group B, n = 50), 40–49 years (Group C, n = 50) and ≥ 50 years (Group D, n = 50), and each subgroup contained an equal number of male and female participants. The baseline characteristics are seen in Table 1.

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Table 1. Baseline characteristics of the total population and the subgroups.

https://doi.org/10.1371/journal.pone.0258362.t001

All procedures performed in this study were in accordance with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Ethical approval was obtained from the Central Ethics Committee of Hungary, and all participants provided written informed consent.

Image acquisition and analysis

CMR examinations were performed on 1.5 T MRI scanners (Achieva, Philips Medical System and MAGNETOM Aera, Siemens Healthineers).

Retrospectively gated, balanced steady-state free precession (bSSFP) cine images were acquired in conventional two-chamber, three-chamber and four-chamber long-axis views. Breathhold short-axis cine images from base to apex were obtained. Contrast agent was not administered.

Medis Suite software was used for the postprocessing analysis (Medis Suite, version 3.2, Medis Medical Imaging Systems).

The LV parameters were calculated by a TB algorithm of the software (MassK module of the Medis Suite program). The method is based on the differential signal intensity of blood and myocardium. The program identifies each voxel within the epicardial contour as either blood or myocardium according to the chosen threshold, which was set to the default (50%). Endocardial contours include LV trabeculation and papillary muscle; therefore, the voxels detected as myocardium within the endocardial borders are identified as trabeculation (Fig 1). Unlike conventional postprocessing techniques based on manually contoured endocardial and epicardial borders [9], the TB semiautomatic quantification method is highly reproducible and is independent of the experience of the observer. The details of this technique and the above mentioned advantages were emphasized in several studies [911,14].

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Fig 1. The threshold-based (TB) method.

The program identifies each voxel within the left ventricular epicardial contour (green line) as either blood or myocardium according to the chosen threshold. Inside the endocardial contour (red line) the green area represents the trabeculated and papillary muscle mass (TPMi).

https://doi.org/10.1371/journal.pone.0258362.g001

The end-diastolic and end-systolic phases were identified, and semiautomatic tracing of the epicardial and endocardial contours was corrected manually in all slices from base to apex. The contours were made by two observers (ZG with 4 years of experience, and ARK with 5 years of experience) with excellent interobserver variability, and it was determined by the global intraclass correlation coefficient, which was 0.92 (interpreted as follows: 0.4–0.75 = fair to good, and greater than 0.75 = excellent).

Short-axis images were applied to calculate the following LV parameters using the TB method: end-diastolic volume (EDV), end-systolic volume (ESV), stroke volume (SV), cardiac output (CO), EF, end-diastolic total myocardial mass and end-diastolic TPM. In our study, LVCM was calculated as the difference between LV end-diastolic total muscle mass and TPM. In the following, we used only LVCM and TPM for the characterization of the myocardial mass.

All of the measured parameters were indexed to body surface area (i). The trabeculated and papillary muscle mass-to-myocardial mass (TPMi/LVCMi), the myocardial mass-to-end-diastolic volume (LVCMi/EDVi) and the trabeculated and papillary muscle mass-to-end-diastolic volume (TPMi/EDVi) ratios were created to assess the correspondence of the LV parameters.

Statistical analysis

The Kolmogorov-Smirnov test was used to assess data distribution. Continuous variables were reported either as the mean ± standard deviation (SD) or the median [interquartile range] as appropriate. The 95% confidence intervals (CIs) were calculated to assess the normal range for LV parameters. Independent-sample t-tests were applied to compare parameters that fit a normal distribution; otherwise, the Mann-Whitney test was used. The comparison of the functional parameters of the different age groups was performed with one-way analysis of variance (ANOVA) with the Tukey–Kramer post hoc test. Linear correlations were assessed using the Pearson correlation coefficient. A p value < 0.05 was considered statistically significant. The intraclass correlation coefficients (ICCs) were calculated to assess interobserver variability. The statistical analysis was performed using MedCalc Statistical Software version 17.9.5. (MedCalc Software).

Results

Sex- and age-specific normal values of LV parameters

The normal reference ranges of the LV functional parameters, the LVCM, the TPM and the derived parameters were assessed in the total study population and in each age group divided by sex (Table 2).

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Table 2. Reference ranges of age and sex related left ventricular parameters and changes with the age.

https://doi.org/10.1371/journal.pone.0258362.t002

Regarding the total population, the following functional parameters differed significantly between sexes: the EDVi, ESVi, LVCMi and TPMi were higher and the EF was lower in males than in females.

After dividing the participants by age and sex, unlike the functional parameters, the LVCMi and TPMi values differed significantly in all age groups; however, the difference in the TPMi/LVCMi ratio remained nonsignificant between sexes (Table 2). The LVCMi/EDVi and TPMi/EDVi ratios also showed significant differences between sexes in the age groups (Table 2).

Changes of the LV parameters with age

In the analysis of age-related changes in LV functional parameters, the EDVi, the ESVi, the SVi and the COi decreased with age: Group A had the highest and Group D had the lowest values in both sexes (Table 2). Although no significant differences were found between the groups, the EF showed a weak positive correlation with age (r = 0.14, p = 0.04).

Regarding the changes in myocardial masses, the TPMi, the LVCMi, and their ratios did not differ among age groups in males or females. However, due to the changes in volumetric parameters, LVCMi/EDVi and TPMi/EDVi were also altered among the age groups, showing an increase in both sexes (Table 2).

Correlations between TPM and phenotype characteristics

According to an analysis of the relationship between TPMi and the phenotypic characteristics of the total population, with the exception of age and COi, all of the observed parameters correlated with TPMi: the strongest relationship was with LVCMi, which was followed by BSA, ESVi and EDVi (Fig 2).

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Fig 2. Correlations with the TPMi in the total population.

EDVi: End-diastolic volume index, ESVi: End-systolic volume index, SVi: Stroke volume index, COi: Cardiac output index, EF: Ejection fraction, LVCMi: LV end-diastolic compacted myocardial mass index, TPMi: LV end-diastolic papillary and trabeculated muscle mass index, BMI: Body mass index, BSA: Body surface area. *p< 0.05.

https://doi.org/10.1371/journal.pone.0258362.g002

After dividing the population by sex and age, these significant differences mostly disappeared (Table 3).

Notably, TPMi and EF had a negative correlation independent of sex in all age groups.

Discussion

In this study, we established age- and sex-related normal reference ranges for LV functional parameters and LVCMi and TPMi values using the TB method in a healthy European cohort. However, as trabeculated and papillary muscle mass is included in the endocardial contours but added to the myocardial mass instead of the volumetric values, the LV volumes and LV mass values differ significantly compared to those calculated with traditional techniques. Thus, novel normal ranges should be established, including reference ranges for LV trabeculation specific to both age and sex [9]. The accurate determination of the trabecular mass values is clinically relevant in conditions presenting with physiological and pathological LV hypertrabeculation [1517].

Sex- and age-specific normal values

Regarding the total population, the biometric differences between sexes were in accordance with previously published data, namely, males had significantly higher volumes and myocardial mass values and lower EF than females, regardless of the use of different postprocessing techniques [3,18,19]. After stratifying participants by age, the LVCMi and TPMi values differed significantly between sexes; however, some of the functional parameters did not show these significances because of the small numbers in the subgroups.

Previous studies described age-related changes in LV functional parameters, but we did not find information about sex-related differences based on age [1,2023].

For trabeculae quantification, Fernandez-Golfin and Bentatou described trabecular masses based on a conventional method in a diverse study population with healthy subjects, patients with valvular disorders and patients with cardiomyopathy and in a healthy population, but the groups were not divided by age [6,24]. Trabeculated myocardium volumes and percentiles have also been measured in a healthy population and in patients with hypertension, ischemic heart disease and different cardiomyopathies, but these studies did not stratify by age either [8,25]. Andre et al. and Cai et al. described the LV trabeculation of healthy subjects in different age groups but with differing techniques: the former group described the trabecular volume, while the latter group used fractal analysis [7,26].

To the best of our knowledge, there are no publications focusing on both age- and sex-related changes in LV trabecular mass; thus, we provide age- and sex-specific normal reference ranges for LV TPM.

Changes with increasing age

Analysis of the age-related changes in LV functional parameters in males and females revealed that all volumetric values decreased with age, and the difference between the youngest and oldest groups was significant. Our results are in line with other echocardiographic and CMR studies, namely, the volumetric parameters decreased in accordance with age [1,2729].

In our study, EF showed a weak positive correlation with age, which was strengthened by Fiechter et al. and Nikitin et al. [27,28], while other studies revealed that aging did not influence LV function [1,29,30].

Furthermore, we observed that the TPMi and LVCMi did not change in either males or females over time. We did not find information about age-dependent changes in the TPMi calculated with the TB method. Bentatou et al. were the only investigators who described that TPMi decreased with increasing age; however, the papillary muscles were included in the compact myocardial mass; this method differs from our technique, which considers papillary muscles in the trabeculated muscle mass [6].

Notably, depending on the analysis software, papillary muscle mass can be counted in either compact or trabeculated muscle mass, which might result in differences between investigators. However, Andre et al. described that this difference is not significant [24].

Opposing results regarding LVCMi have been reported: an echocardiographic study revealed an increase in LVCMi [31], while other studies conducted with CMR using conventional technique described a slight decrease with increasing age [27,32,33]. Moreover, in contrast to the above-mentioned results, the LVCMi did not change significantly with age in either males or females according to several CMR and echocardiographic investigations [1,21,34]. These results were confirmed with autopsy and are also in accordance with our findings [35]. The underlying pathophysiological mechanism could be the age-related loss of myocytes and compensatory reactive cellular hypertrophy, which maintains the total weight of the myocardium [36].

Normal values and changes in the ratios

The TPMi/LVCMi ratio was not significantly different between sexes, which might imply a sex-independent connection between trabecular mass and LV mass, and no changes were observed among the age groups.

Chuang et al. observed similar values for TPMi/LVCMi ratios measured with the conventional contouring technique, but they did not examine this relation in different age groups [8]. Fernandez described smaller ratios in a healthy subgroup with a lower number of patients using another method; however, this group was not divided by sex and age [24]. The normal values of TPMi/LVCMi ratio might have additive value in the diagnosis of different conditions with excessive LV trabeculation.

Regarding the mass/volume ratios, after dividing the total population by sex, the LVCMi/EDVi and TPMi/EDVi remained significantly different in most age groups, and this difference can be explained by the significantly different myocardial masses in males and females. Both the LVCMi/EDVi and TPMi/EDVi ratios increased with age due to the age-dependent decrease in volumetric parameters. These results are in accordance with those of other studies describing age-related changes in the LVCMi/EDVi ratio [1,31]. We found only one correspondence of age and trabeculation to EDV ratio; in contrast to our results, trabeculae were expressed as volumes, and the ratio had a weak negative correlation with age [8].

Czimbalmos et al. applied the LV mass-to-LV end-diastolic volume ratio to distinguish HCM from an athlete’s heart [16]. Thus, these myocardial mass-to-volume ratios could have possible clinical utility in enabling the differential diagnosis of pathological and physiological conditions associated with hypertrophy or hypertrabeculation.

Correlation with the TPMi

The lack of connection between TPMi and age in the total population corresponds to TPMi remaining unchanged over time after dividing the population by age; however, the underlying cause is still unknown based on other studies.

TPMi and LVCMi showed a strong positive correlation in the total population. Chuang et al. also described the trabeculation and LV mass correlation, although the amount of trabeculation was expressed as volumes [8]. Janik et al. described that papillary and trabecular masses correlate with ventricular mass; however, they observed a diverse population of patients with concentric or eccentric hypertrophy and normal controls, and the participants were not divided by sex or age [15].

In our study, there was a positive correlation between TPMi and BSA in the total population, but no data were found in the literature about this correspondence.

Similar to our study, in Chuang et al., Andre et al. and Bentatou et al.’s studies, LV trabeculae showed a strong relationship with EDV and ESV, measured either by volume or by myocardial mass [6,8,24].

In concordance with our results, the lack of connection between TrMi and BMI was also described previously [33].

After stratifying our total population by age, there was no correlation between TPMi and the other observed parameters, which can be explained by the small number of subgroups.

Interestingly, there was an inverse correlation between TPMi and EF, as in Bentatou’s research [6]. The inverse relationship between TPMi and EF might be explained by the association between lower EF and higher myocardial mass (e.g., in males), and LVCMi correlated with TPMi in our study.

Conclusions

We defined age- and sex-related normal values for LV functional parameters and myocardial and trabecular mass using a TB trabeculated and papillary muscle mass quantification method in a healthy European cohort. The TPMi, LVCMi and TPMi/LVCMi ratio were independent of sex and age, and this result is strengthened by the correlation between them.

Increasing the number of the subgroups would provide even more accurate results. Overall, normal values would be helpful for the determination of trabecular mass and myocardial mass/volume ratios, which might have clinical utility in the differential diagnosis of physiological and pathological conditions with LV hypertrabeculation.

Limitations

In the TB method, the papillary muscles are added to the trabeculated myocardial mass because of the nature of this technique. Although this study was performed on a large cohort, after dividing by sex and age, the number of subgroups decreased, which may have affected the statistical findings.

Different vendors and third party software companies may have differences in how they specifically implement the algorithm separating the trabecules and papillary muscles from the blood pool and the myocardium. A simple algorithm will not fit every scanner, and some fine-tuning is necessary for different MR vendors. So the different trabecular measuring techniques are not comparable because their intervendor agreements are not established yet.

Current EF and volume quantification uses a stack of thick short-axis slices, and 8–10 mm is usual for Z-direction spatial resolution. Moreover, trabecules and papillary muscles will not cross the slice in an exactly perpendicular fashion, which creates partial volume effects. Depending on the actual path of the trabecules, this will influence the threshold-based quantification. With the advent of advanced isotropic 4D cine techniques, this drawback will be less important in the future.

Acknowledgments

We thank the technicians who helped performing the cardiac magnetic resonance imaging examinations.

References

  1. 1. Petersen SE, Aung N, Sanghvi MM, Zemrak F, Fung K, Paiva JM, et al. Reference ranges for cardiac structure and function using cardiovascular magnetic resonance (CMR) in Caucasians from the UK Biobank population cohort. J Cardiovasc Magn Reson. 2017;19(1):18. pmid:28178995
  2. 2. Kawel N, Nacif M, Arai AE, Gomes AS, Hundley WG, Johnson WC, et al. Trabeculated (noncompacted) and compact myocardium in adults: the multi-ethnic study of atherosclerosis. Circ Cardiovasc Imaging. 2012;5(3):357–66. pmid:22499849
  3. 3. Kawel-Boehm N, Maceira A, Valsangiacomo-Buechel ER, Vogel-Claussen J, Turkbey EB, Williams R, et al. Normal values for cardiovascular magnetic resonance in adults and children. J Cardiovasc Magn Reson. 2015;17:29. pmid:25928314
  4. 4. Captur G, Syrris P, Obianyo C, Limongelli G, Moon JC. Formation and Malformation of Cardiac Trabeculae: Biological Basis, Clinical Significance, and Special Yield of Magnetic Resonance Imaging in Assessment. Can J Cardiol. 2015;31(11):1325–37. pmid:26440509
  5. 5. Paun B, Bijnens B, Butakoff C. Relationship between the left ventricular size and the amount of trabeculations. Int J Numer Method Biomed Eng. 2018;34(3). pmid:29124903
  6. 6. Bentatou Z, Finas M, Habert P, Kober F, Guye M, Bricq S, et al. Distribution of left ventricular trabeculation across age and gender in 140 healthy Caucasian subjects on MR imaging. Diagn Interv Imaging. 2018;99(11):689–98. pmid:30262171
  7. 7. Cai J, Bryant JA, Le TT, Su B, de Marvao A, O’Regan DP, et al. Fractal analysis of left ventricular trabeculations is associated with impaired myocardial deformation in healthy Chinese. J Cardiovasc Magn Reson. 2017;19(1):102. pmid:29241460
  8. 8. Chuang ML, Gona P, Hautvast GL, Salton CJ, Blease SJ, Yeon SB, et al. Correlation of trabeculae and papillary muscles with clinical and cardiac characteristics and impact on CMR measures of LV anatomy and function. JACC Cardiovasc Imaging. 2012;5(11):1115–23. pmid:23153911
  9. 9. Csecs I, Czimbalmos C, Suhai FI, Mikle R, Mirzahosseini A, Dohy Z, et al. Left and right ventricular parameters corrected with threshold-based quantification method in a normal cohort analyzed by three independent observers with various training-degree. Int J Cardiovasc Imaging. 2018;34(7):1127–33. pmid:29492774
  10. 10. Varga-Szemes A, Muscogiuri G, Schoepf UJ, Wichmann JL, Suranyi P, De Cecco CN, et al. Clinical feasibility of a myocardial signal intensity threshold-based semi-automated cardiac magnetic resonance segmentation method. Eur Radiol. 2016;26(5):1503–11. pmid:26267520
  11. 11. Freling HG, van Wijk K, Jaspers K, Pieper PG, Vermeulen KM, van Swieten JM, et al. Impact of right ventricular endocardial trabeculae on volumes and function assessed by CMR in patients with tetralogy of Fallot. Int J Cardiovasc Imaging. 2013;29(3):625–31. pmid:22945368
  12. 12. Riffel JH, Schmucker K, Andre F, Ochs M, Hirschberg K, Schaub E, et al. Cardiovascular magnetic resonance of cardiac morphology and function: impact of different strategies of contour drawing and indexing. Clin Res Cardiol. 2019;108(4):411–29. pmid:30203190
  13. 13. Pelliccia A, Caselli S, Sharma S, Basso C, Bax JJ, Corrado D, et al. European Association of Preventive Cardiology (EAPC) and European Association of Cardiovascular Imaging (EACVI) joint position statement: recommendations for the indication and interpretation of cardiovascular imaging in the evaluation of the athlete’s heart. Eur Heart J. 2018;39(21):1949–69. pmid:29029207
  14. 14. Jaspers K, Freling HG, van Wijk K, Romijn EI, Greuter MJ, Willems TP. Improving the reproducibility of MR-derived left ventricular volume and function measurements with a semi-automatic threshold-based segmentation algorithm. Int J Cardiovasc Imaging. 2013;29(3):617–23. pmid:23053857
  15. 15. Janik M, Cham MD, Ross MI, Wang Y, Codella N, Min JK, et al. Effects of papillary muscles and trabeculae on left ventricular quantification: increased impact of methodological variability in patients with left ventricular hypertrophy. J Hypertens. 2008;26(8):1677–85. pmid:18622248
  16. 16. Czimbalmos C, Csecs I, Toth A, Kiss O, Suhai FI, Sydo N, et al. The demanding grey zone: Sport indices by cardiac magnetic resonance imaging differentiate hypertrophic cardiomyopathy from athlete’s heart. PLoS One. 2019;14(2):e0211624. pmid:30763323
  17. 17. Szucs A, Kiss AR, Gregor Z, Horvath M, Toth A, Dohy Z, et al. Changes in strain parameters at different deterioration levels of left ventricular function: A cardiac magnetic resonance feature-tracking study of patients with left ventricular noncompaction. Int J Cardiol. 2021. pmid:33577906
  18. 18. Chung AK, Das SR, Leonard D, Peshock RM, Kazi F, Abdullah SM, et al. Women have higher left ventricular ejection fractions than men independent of differences in left ventricular volume: the Dallas Heart Study. Circulation. 2006;113(12):1597–604. pmid:16567580
  19. 19. Natori S, Lai S, Finn JP, Gomes AS, Hundley WG, Jerosch-Herold M, et al. Cardiovascular function in multi-ethnic study of atherosclerosis: normal values by age, sex, and ethnicity. AJR Am J Roentgenol. 2006;186(6 Suppl 2):S357–65.
  20. 20. Le Ven F, Bibeau K, De Larochelliere E, Tizon-Marcos H, Deneault-Bissonnette S, Pibarot P, et al. Cardiac morphology and function reference values derived from a large subset of healthy young Caucasian adults by magnetic resonance imaging. Eur Heart J Cardiovasc Imaging. 2016;17(9):981–90. pmid:26354980
  21. 21. Le TT, Tan RS, De Deyn M, Goh EP, Han Y, Leong BR, et al. Cardiovascular magnetic resonance reference ranges for the heart and aorta in Chinese at 3T. J Cardiovasc Magn Reson. 2016;18:21. pmid:27071974
  22. 22. Alfakih K, Plein S, Thiele H, Jones T, Ridgway JP, Sivananthan MU. Normal human left and right ventricular dimensions for MRI as assessed by turbo gradient echo and steady-state free precession imaging sequences. J Magn Reson Imaging. 2003;17(3):323–9. pmid:12594722
  23. 23. Faganello G, Collia D, Furlotti S, Pagura L, Zaccari M, Pedrizzetti G, et al. A new integrated approach to cardiac mechanics: reference values for normal left ventricle. Int J Cardiovasc Imaging. 2020;36(11):2173–85. pmid:32671607
  24. 24. Fernandez-Golfin C, Pachon M, Corros C, Bustos A, Cabeza B, Ferreiros J, et al. Left ventricular trabeculae: quantification in different cardiac diseases and impact on left ventricular morphological and functional parameters assessed with cardiac magnetic resonance. J Cardiovasc Med (Hagerstown). 2009;10(11):827–33. pmid:19543106
  25. 25. Choi Y, Kim SM, Lee SC, Chang SA, Jang SY, Choe YH. Quantification of left ventricular trabeculae using cardiovascular magnetic resonance for the diagnosis of left ventricular non-compaction: evaluation of trabecular volume and refined semi-quantitative criteria. J Cardiovasc Magn Reson. 2016;18(1):24. pmid:27142637
  26. 26. Andre F, Burger A, Lossnitzer D, Buss SJ, Abdel-Aty H, Gianntisis E, et al. Reference values for left and right ventricular trabeculation and non-compacted myocardium. Int J Cardiol. 2015;185:240–7. pmid:25804350
  27. 27. Fiechter M, Fuchs TA, Gebhard C, Stehli J, Klaeser B, Stahli BE, et al. Age-related normal structural and functional ventricular values in cardiac function assessed by magnetic resonance. BMC Med Imaging. 2013;13:6. pmid:23391039
  28. 28. Nikitin NP, Loh PH, de Silva R, Witte KK, Lukaschuk EI, Parker A, et al. Left ventricular morphology, global and longitudinal function in normal older individuals: a cardiac magnetic resonance study. Int J Cardiol. 2006;108(1):76–83. pmid:16516701
  29. 29. Kaku K, Takeuchi M, Otani K, Sugeng L, Nakai H, Haruki N, et al. Age- and gender-dependency of left ventricular geometry assessed with real-time three-dimensional transthoracic echocardiography. J Am Soc Echocardiogr. 2011;24(5):541–7. pmid:21345649
  30. 30. Ruan Q, Nagueh SF. Effect of age on left ventricular systolic function in humans: a study of systolic isovolumic acceleration rate. Exp Physiol. 2005;90(4):527–34. pmid:15769881
  31. 31. Shub C, Klein AL, Zachariah PK, Bailey KR, Tajik AJ. Determination of left ventricular mass by echocardiography in a normal population: effect of age and sex in addition to body size. Mayo Clin Proc. 1994;69(3):205–11. pmid:8133657
  32. 32. Yeon SB, Salton CJ, Gona P, Chuang ML, Blease SJ, Han Y, et al. Impact of age, sex, and indexation method on MR left ventricular reference values in the Framingham Heart Study offspring cohort. J Magn Reson Imaging. 2015;41(4):1038–45. pmid:24817313
  33. 33. Cheng S, Fernandes VR, Bluemke DA, McClelland RL, Kronmal RA, Lima JA. Age-related left ventricular remodeling and associated risk for cardiovascular outcomes: the Multi-Ethnic Study of Atherosclerosis. Circ Cardiovasc Imaging. 2009;2(3):191–8. pmid:19808592
  34. 34. Dannenberg AL, Levy D, Garrison RJ. Impact of age on echocardiographic left ventricular mass in a healthy population (the Framingham Study). Am J Cardiol. 1989;64(16):1066–8. pmid:2530879
  35. 35. Kitzman DW, Scholz DG, Hagen PT, Ilstrup DM, Edwards WD. Age-related changes in normal human hearts during the first 10 decades of life. Part II (Maturity): A quantitative anatomic study of 765 specimens from subjects 20 to 99 years old. Mayo Clin Proc. 1988;63(2):137–46. pmid:3276974
  36. 36. Olivetti G, Giordano G, Corradi D, Melissari M, Lagrasta C, Gambert SR, et al. Gender differences and aging: effects on the human heart. J Am Coll Cardiol. 1995;26(4):1068–79. pmid:7560601