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Cardiac function assessed by myocardial deformation in adult polycystic kidney disease patients



Patients with autosomal dominant polycystic kidney disease (ADPKD) have an increased risk of cardiovascular morbidity and mortality. Impaired left ventricular (LV) global longitudinal strain (GLS) can be a sign of subclinical cardiac dysfunction even in patients with otherwise preserved ejection fraction (EF). Transmitral early filling velocity to early diastolic strain rate (E/SRe) is a novel measure of LV filling pressure, which is often affected early in cardiac disease.


A total of 110 ADPKD patients not on dialysis were included in this prospective study. All patients underwent an extensive echocardiographic examination including two-dimensional speckle tracking. GLS and strain rates were measured. The distribution of GLS and E/SRe was determined and patient characteristics were compared by median levels of GLS (− 17.8%) and E/SRe (91.4 cm). Twenty healthy participants were included as control group.


There was a significantly worse GLS in the ADPKD patients (mean: − 17.8 ± 2.5%) compared to the healthy controls (mean: − 21.9 ± 1.9%), p < 0.001. The same was true for E/SRe (mean: 10.0 ± 0.3 cm) compared to the control group (mean: 6.5 ± 0.3 cm), p < 0.001. In simple logistic regression, male gender (OR: 4.74 [2.10–10.71], p < 0.001), fasting glucose (odds ratio (OR) 1.05 [1.01–1.10], p = 0.024), htTKV (OR: 1.07 [1.01–1.13], p = 0.013), HDL cholesterol (OR: 0.97 [0.94, 0.996], p = 0.025), triglycerides (OR: 1.01 [1.00–1.02], p = 0.039), hemoglobin (OR: 1.50 [1.11–2.04], p = 0.009), and β-blocker use (OR: 1.07 [1.01, 1.13], p = 0.013) were all associated with higher GLS. After multivariate logistic regression with backward model selection, only male gender (OR: 5.78 [2.27–14.71], p < 0.001) and β-blocker use (OR: 14.00 [1.60, 122.51], p = 0.017) remained significant. In simple logistic regression models, BMI (OR: 1.11 [1.02–1.20], p = 0.015), systolic blood pressure (OR: 1.03 [1.00–1.06], p = 0.027) and β-blocker use (OR: 17.12 [2.15–136.20], p = 0.007) were associated with higher E/SRe - a novel measure of left ventricular filling pressure. After backward elimination, only β-blocker use (OR: 17.22 [2.16, 137.14], p = 0.007) remained significant.


Higher GLS and E/SRe are common in ADPKD patients, even in patients with preserved eGFR and normal left ventricular EF. GLS and E/SRe may aid in cardiovascular risk stratification in patients with ADPKD as they represent early markers of cardiac dysfunction.

Peer Review reports


Individuals with autosomal dominant polycystic kidney disease (ADPKD) have a high prevalence of cardiovascular (CV) disease associated with significant morbidity and mortality [1]. Death due to cardiovascular disease has been reported to be as high as 33% in ADPKD patients with end-stage renal disease, primarily due to ischemic heart disease and congestive heart failure [1].

Left ventricular hypertrophy is a strong independent risk factor for CV morbidity and mortality and is highly prevalent in ADPKD patients, even in the absence of hypertension [2, 3]. Although results from more recent studies suggest a lower occurrence of cardiac remodeling in ADPKD patients, possibly due to earlier antihypertensive treatment [4], structural and functional abnormalities remain common in these patients [5]. Furthermore, both hypertensive and normotensive ADPKD patients show significant diastolic dysfunction, suggesting cardiac pathology early in ADPKD [5]. Although these abnormalities become more severe at advanced stages of chronic kidney disease (CKD), they can be detected in individuals with preserved eGFR [6].

Previous understanding of CV risk in ADPKD has been achieved primarily through measurements of echocardiograms and cardiac magnetic resonance imaging [3, 4]. The recent results of the HALT-PKD study demonstrated that early treatment with angiotensin-converting enzyme inhibitors (ACEI) to a goal systolic blood pressure < 110 mmHg was associated with a greater decline in left ventricular mass index among individuals aged 15–49 with early-stage ADPKD compared to a standard blood pressure target [7]. These results may encourage earlier diagnosis and treatment of family members at risk for ADPKD. More sensitive echocardiographic techniques well-correlated to CV risk are needed in this younger asymptomatic group. Two-dimensional speckle-tracking is a technique that assesses regional deformation along infinitesimally small axes [8]. Global longitudinal strain (GLS), assessed by two-dimensional speckle tracking, has emerged as a new measure of left ventricular (LV) dysfunction [9]. GLS is a direct non-invasive quantitative measure of the myocardial contractility of the left ventricle. The lower (i.e. more negative) GLS is, the better contractility (Fig. 1). GLS can be altered despite preserved LV ejection fraction (LVEF) in various conditions predisposing to cardiovascular morbidity, including pre-diabetics with normal blood pressure [10], diabetes [11] and hypertension [12]. A peak GLS in the range of − 20% ± 2% can be expected in a healthy person [13].

Fig. 1

Example of GLS measurement. Abbreviations: GLS = global longitudinal strain

In a population of asymptomatic dialysis patients, two-dimensional speckle-tracking showed significantly higher (less negative) values of left ventricular peak longitudinal strain and early diastolic strain when compared to healthy individuals [14]. Speckle tracking echocardiography has been used to detect and evaluate myocardial ischemia, valvular heart disease, dyssynchrony, arrhythmias, cardiomyopathies and assessment of diastolic function [8]. Furthermore, speckle tracking has been demonstrated to detect myocardial fibrosis in more advanced stages of kidney disease [15], and is an important feature of uremic cardiomyopathy in these patients.

Two-dimensional speckle-tracking has not previously been used to assess cardiac function in individuals with ADPKD. The aim of our study was 1) to investigate the distribution of GLS as assessed by two-dimensional speckle-tracking in asymptomatic patients with ADPKD and 2) to identify clinical variables associated with higher (less negative) strain measurements in these patients.


Study population

We performed a cross-sectional study in the Baltimore PKD Center Core ADPKD cohort. Patients ≥18 years old with ADPKD as defined by the modified Pei-Ravine criteria [16] and with eGFR> 15 ml/min/1.73m2 were eligible to participate in a prospective observational cohort study at the Baltimore PKD Center at the University of Maryland School of Medicine. Patients with prior kidney transplant, pregnancy, uncontrolled diabetes (defined as a glycated hemoglobin > 7% or use of more than one anti-diabetic medication), current participation in an interventional pharmaceutical clinical trial, any systemic disease (e.g., lupus) likely to lead to kidney disease, or suspected kidney disease other than ADPKD were excluded. Participants were enrolled from 2013 through 2017. Family and personal medical history including absence of cardiac disease was obtained by nephrologist investigators through patient interview and review of medical records. Serum glucose, lipids and creatinine (using an IDMS-traceable assay) were measured after an overnight fast, and GFR was estimated using the creatinine-based CKD-Epi estimating equation [17]. Albuminuria was estimated as the ratio of urinary albumin to creatinine in a spot morning sample. Blood pressure was measured in the seated position and the average of 3 measures was calculated. Abdominal MRI was performed, and total kidney volume was calculated by a single radiologist blinded to the clinical characteristics and cardiac measurements of participants. TKV was indexed to height (htTKV, expressed in cc/meters). Echocardiograms were performed on all participants at baseline. Of the 126 patients enrolled in this cohort, N = 16 were excluded due to missing echocardiogram images or inadequate image quality for speckle tracking analysis, leaving 110 patients included in this study.

A control group consisting of 20 healthy age and gender matched controls were included as a comparison. All controls underwent an extensive echocardiographic examination and personal medical history was obtained. Healthy controls did not undergo abdominal MRI, therefore TKV could not be measured for the controls.


Experienced clinicians and sonographers performed all echocardiographic examinations under a standard echocardiography protocol using 2-dimensional-, spectral- and tissue Doppler. All images were acquired on Philips cardiology ultrasound systems (EPIC7, iE33), stored as DICOM images on the Synapse Cardiovascular platform (Fuji Medical, version 4.0.8 SR1) at the University of Maryland Medical Center, and analyzed offline at UCSF using vendor-independent post-processing software TomTec-Arena 2D-CPA by a trained investigator.

Conventional two-dimensional echocardiography: Left ventricle dimensions (interventricular septal thickness (IVSd), LV internal diameter (LVIDd) and LV posterior wall thickness (PWTd)) were measured on the parasternal long-axis projection. This was done in end-diastole at the tip of the mitral valve leaflets as per ASE guidelines [13]. LV mass was calculated using area length method using 2D and then divided by body surface area to get LV mass index (LVMI). LA diameter was measured in the parasternal long-axis view by using the leading edge to leading edge method. LV ejection fraction (LVEF) was measured using the modified Simpson’s biplane method in the apical 4- and 2-chamber projections.

Pulsed-wave (PW) Doppler imaging was used in the 4-chamber view to obtain peak early filling (E-wave), atrial filling (a-wave) and deceleration time (DT). PW tissue Doppler imaging was used to obtain early (e’) peak myocardial diastolic velocity at the lateral and septal mitral annular segments. The mean was calculated and used for determining E/e’.

Speckle tracking was performed in the apical 4-, 2- and 3-chamber projections as recommended by current guidelines [13]. The tracing of the myocardial wall was done using a semiautomatic function. In cases of inaccurate tracing, the investigator would manually adjust the tracing. A total of 18 segments, 6 from each projection, were included. A total of 7 subjects had a maximum of 2 segments excluded in the cohort. All 3 apical projections were available for speckle tracking in all but 1 patient. GLS was calculated as the mean peak strain of the three apical projections. E/e’sr was calculated as E velocity (m/s) divided by the absolute value of global peak early diastolic strain rate (e’sr) averaged across 3 apical views. The investigator could exclude segments, if considered untraceable. Total study population was stratified according to the median GLS (− 17.8%) to identify clinical factors associated with higher (less negative) GLS. Our lab has previously reported good intra- and interobserver variability of both GLS and SRe with a small bias (GLS: mean difference ± 1.96 SDs was 0.1 ± 1.6% for the intraobserver analysis and − 0.8 ± 2.0% for the interobserver analysis) and (SRe: − 0.06 ± 0.25 for the intraobserver analysis and 0.06 ± 0.28 for the interobserver analysis) [18]. Diastolic function was assessed according to existing recommendations [19].

Statistical methods

We divided the cohort into groups with GLS above and below the median value (− 17.8%). Baseline demographic, clinical and echocardiographic data were compared between those with higher (below median) GLS and lower (above median) GLS. Kruskal-Wallis test was used for comparing non-Gaussian distributed continuous variables – estimated GFR, micro albumin/creatinine ratio, triglycerides, htTKV, left ventricle mass index, and E/e’ ratio. Student’s T-test was used for comparing continuous variables between groups, and Chi-squared test was used for comparing categorical variables. Student’s T-test was also used for comparing the control group to the ADPKD group. All covariates were tested for statistical differences between those with higher and lower GLS (stratified according to the population median of GLS (− 17.8%)) as has previously been done [20]. Correlations between eGFR and htTKV with GLS were defined using Pearson correlation coefficient. Covariates with a p-value < 0.15 in simple regression analyses were included in multiple linear regression with stepwise backward elimination. The threshold to remove was 0.05. Logistic regression was used to calculate odds ratios for the predictors of higher (worse) GLS and higher (worse) E/early diastolic strain rate, defined by ≤91.4 cm. Simple and multiple logistic regression models with backward elimination were built. Data analyses were performed using SAS 9.4 (SAS Institute, NC).


Baseline characteristics

Our cohort comprised 110 ADPKD patients (mean ± SD age 46.1 ± 13.3 years). Forty-eight (44%) were men and 92 (84%) were Caucasian. Clinical characteristics of the study population are displayed in Table 1. The mean ± SD of GLS was − 17.8 ± 2.5% (Fig. 2). GLS correlated weakly with eGFR (Pearson correlation coefficient = − 0.093) (Fig. 3a) and more strongly with htTKV (Pearson correlation coefficient = 0.144) (Fig. 3b). Patients with higher (worse) GLS were more likely to be male, have higher levels of fasting glucose and hemoglobin, be on ß-blockers and have lower levels of high-density lipoprotein despite no statistically significant differences in age, race, blood pressure and micro albumin/creatinine ratio (Table 1).

Table 1 Baseline characteristics
Fig. 2

Distribution of GLS in the study population. Abbreviations: GLS = global longitudinal strain

Fig. 3

a Scatterplot showing the correlation between eGFR and GLS. Abbreviations: GLS = global longitudinal strain, eGFR = estimated glomerular filtration rate. b Caption: Scatterplot showing correlation between htTKV values and GLS. Abbreviations: GLS = global longitudinal strain, htTKV = height-indexed total kidney volume

Comparison of control group to ADPKD group

There was a higher GLS in the ADPKD patients (mean: − 17.8 ± 2.5, 95%CI [− 18.3-(− 17.4)]) compared to the healthy controls (mean: − 22.0 ± 2.2, 95% CI [− 23.0-(− 21.0)]) (p < 0.001). E/SRe was increased (worse) in the ADPKD patients (mean: 100.3 ± 31.5 cm, 95% CI [94.4–100.6]) compared to the control group (mean: 65.2 ± 15.0 cm, 95% CI [58.2–72.3]) (p < 0.001). (Table 2).

Table 2 Control group and ADPKD group

Conventional and 2D speckle tracking results

Comparisons of echocardiographic parameters between those with higher and lower GLS are described in Table 3. On conventional echocardiogram, most measurements were not significantly different between groups of higher versus lower GLS. The difference in LVEF was statistically significant but was within the range of normal (60 versus 59%) for both groups. Similarly, although those with higher GLS had thicker interventricular septal diameter (IVSd) and thicker left ventricle posterior wall (PWTd) that reached statistical significance, the difference in these measures (0.04 cm, or 0.4 mm) was below the limit of detection by standard techniques (1 mm). On 2D speckle tracking, in the group with higher (less negative / worse) GLS, subjects had lower systolic and diastolic strain rates, increased E/SRe (a load-independent marker of LV filling pressure).

Table 3 Echocardiographic data

Covariate associations with GLS and E/SRe

In simple linear regression models, male gender, diastolic blood pressure, HDL, triglycerides, hemoglobin, β-blocker use were associated with higher GLS. After backwards elimination, age, male gender, triglycerides, diastolic blood pressure, eGFR and β-blocker use were independently associated with GLS (Table 4). In simple linear regression models, factors associated with greater E/SRe were systolic blood pressure, micro albumin/creatinine ratio, and β-blocker use. In the multiple model, systolic blood pressure and β-blocker use were associated with higher E/SRe (Table 5).

Table 4 Associations with GLS, Linear Regression
Table 5 Associations with E/SRe, Linear Regression

Logistic regression with GLS and E/diastolic strain rate

In simple logistic regression, male gender (OR: 4.74 [2.10, 10.71], p < 0.001), htTKV (OR: 1.07 [1.01–1.13], p = 0.013), fasting glucose (OR: 1.05 [1.01–1.10], p = 0.024), HDL (OR: 0.97 [0.94, 0.996], p = 0.025), hemoglobin (OR: 1.50 [1.11–2.04], p = 0.009), triglycerides (OR: 1.01 [1.00–1.02], p = 0.039), and β-blocker use (OR: 16.40 [2.06, 13.47], P = 0.008) were all associated with higher GLS (Table 6). htTKV was associated with GLS even after adjusting for eGFR (OR: 1.08 [1.02–1.15], p = 0.014). According to the results of multiple logistic regression with backward elimination, male gender (OR: 5.78 [2.27–14.71], p < 0.001) and β-blocker use (OR: 14 [1.60–122.51], p = 0.017) were found to be strongly associated with higher GLS.

Table 6 Associations with GLS: Logistic regression

The same method was used to investigate predictors of elevated filling pressure as assessed by E/SRe. Simple logistic regression showed that BMI (OR: 1.11 [1.02–1.20], p = 0.015), systolic blood pressure (OR: 1.03 [1.00–1.06], p = 0.027) and β-blocker use (OR: 17.12 [2.15–136.2], p = 0.007) were all independently associated with an increased E/SRe (> 91.4 cm). Based on the results of multiple variables logistic regression with stepwise backward elimination, only one variable remained significant: β-blocker use (OR: 17.22 [2.16–137.14], p = 0.007 (Table 7).

Table 7 Associations with E/SRe: Logistic regression

Sensitivity analysis

Because the number of individuals on beta blockers in this cohort was quite low, and because patients on beta blockers may represent a sub-group with more advanced cardiac dysfunction, we performed sensitivity analyses excluding individuals on beta blockers. In these analyses, the major findings in adjusted linear regression showed that age, gender, diastolic blood pressure, and estimated GFR were still significantly associated with higher GLS (Additional file 1 Table S1A), and systolic blood pressure and ACE inhibitor use remained significant predictors of E/SRe (Additional file 1 Table S1B). The major findings in logistic regression models with backward elimination showed that gender was significantly associated with higher GLS (Additional file 1 Table S2A), and BMI remained significantly associated with E/SRe (Additional file 1 Table S2B).


In this prospective cohort study of adult ADPKD patients with no history of cardiac disease, we described the distribution of GLS relative to established clinical predictors of disease severity in ADPKD. Given that GLS has been demonstrated as an early and sensitive predictor of cardiovascular morbidity and mortality in other patient populations [21,22,23], it is notable that the ADPKD patients in this study with otherwise normal conventional echocardiographic examinations displayed a relatively high GLS (mean: − 17.8% ± 2.5%) compared to the healthy age and gender matched control group (mean: − 21.9 ± 1.9%). The values found in our control group were similar to normative values in a large meta-analysis in healthy individuals (mean: − 19.7% +/− 0.4%) [24]. As both LVEF and GLS are measures of systolic function, this finding underscores the role of GLS as an early and sensitive marker of cardiac pathology. As patients may be encouraged to seek diagnosis earlier in light of recent findings of potential benefits of more aggressive blood pressure control as per HALT-PKD, GLS may represent a method by which to risk-stratify asymptomatic patients at risk for subclinical cardiovascular disease and adverse cardiovascular outcomes. Our findings of early subclinical dysfunction highlight the need to focus on early interventions to improve cardiovascular outcomes in ADPKD patients.

Longitudinal strain is known to be influenced by several clinical factors such as diabetes [11], obesity [25] and hypertension [12] and generally declines in cardiac pathologic states before there is a noticeable reduction in LVEF. This may be due to the superior sensitivity of the strain technique when compared to conventional echocardiographic measures. Although LVEF and GLS are physiologically related, as they are both measures of systolic function, they reflect different aspects of the myocardial deformation thus explaining the weak correlation observed in this study. LVEF measures a change in volume and predominantly quantifies radial contraction, whereas GLS represents contraction of the longitudinal myocardial fibers. Sub-endocardial longitudinal fibers are sensitive to ischemia, and both fibrosis and lipid deposition have been shown to affect GLS [26, 27]. In mouse models of PKD, strain imaging has also demonstrated myocardial dysfunction, which is rescued by suppression of galectin-3, a protein regulator of fibrosis that may aggravate the cystic phenotype of autosomal recessive PKD [28].

As more cysts develop, the renin-angiotensin-aldosterone system (RAAS) is activated leading to high blood pressure very early in the pathogenesis [29]. Therefore, greater RAAS activation may explain the association of greater htTKV with lower GLS independent of blood pressure effects. A significant association was also seen between blood pressure and GLS. This association may be due to the fact that longitudinal strain is affected by hypertrophic LV remodeling and afterload conditions. This is especially true in patients suffering from ADPKD as these individuals are more prone to undergo hypertrophic LV remodeling due to uremic cardiomyopathy, early-onset hypertension, and hyperinsulinemia [3, 30, 15]. GLS may thus be able to detect even subtle increases in afterload in these otherwise asymptomatic individuals. However, as kidney disease in general affects cardiac function, it is difficult to conclude whether specific ADPKD-pathogenic mechanisms are responsible for the findings or whether kidney dysfunction alone was the cause. The association between htTKV and lower GLS independent of eGFR could indicate that ADPKD-specific mechanisms play a role, but it is likely a combination of both factors. The fact that hemoglobin was higher in the group with higher GLS could be due to the increased EPO concentration sometimes observed in more advanced stages of ADPKD leading to a higher level of hemoglobin [31, 32]. However this is mostly speculative and future studies are needed to elucidate how EPO concentrations and hemoglobin levels in ADPKD patients affects echocardiographic parameters.

Diastolic dysfunction assessed according to current recommendations [19] was present in only a small minority of participants. This was interesting, as elevated LV filling pressure assessed by E/SRe was found to be quite high in our population. This was especially true in the group with worse GLS (> − 17.8%), where the mean of E/SRe (111.29 ± 36.57) were similar to the ranges of this measure reported in studies of STEMI patients [33], heart failure patients [34] and even higher than in atrial fibrillation patients [35]. This has been suggested as a more sensitive non-invasive measure of LV filling pressure. In our population of ADPKD patients, a significant number appear to have elevated LV filling pressures when assessed by E/SRe, despite having relatively normal blood pressure, LVMI and preserved ejection fraction. We found BMI, systolic blood pressure and β-blocker use to be independent predictors of increased E/SRe. That BMI and systolic blood pressure were associated with elevated filling pressure may be due to the adverse effect on LV relaxation which co-morbid conditions such as hypertension and metabolic syndrome can have [26, 36]. The fact that β-blocker use was an independent predictor of both E/SRe and GLS is possibly due to reverse causality in which the group of patients using β-blockers may have more severe hypertension and/or more pronounced impaired cardiac function than the larger group of patients not using β-blockers.

We also found that more men had higher GLS than women. This is consistent with reports that CV disease in men with ADPKD is more severe [3] and it is well known that women have higher LVEF and lower GLS than men [21]. The lack of an association between albuminuria and GLS was surprising, and may represent a low prevalence of albuminuria in our cohort.

Our study had some limitations. This was a single-center study. Participants had relatively preserved renal function, and the majority were Caucasian. Although none of these patients had diabetes requiring insulin, we do not have data on measures of insulin sensitivity. Furthermore, we did not have information regarding treatment with erythropoietin stimulating agents (ESA). Nevertheless, this is the first study to our knowledge to apply speckle echo images in adults with ADPKD. Although speckle echo represents a novel technology not generally available in general clinical practice, strain measurements can be applied to standard echo images, making this approach potentially easier and more cost effective for clinical risk stratification than cardiac MRI [4]. Finally, although we adjusted for eGFR, we cannot account for residual confounding including by kidney dysfunction independent of ADPKD.


Higher (worse) GLS and elevated LV filling pressure assessed by E/SRe are common in patients suffering from autosomal dominant polycystic kidney disease, even those with preserved eGFR and LVEF. These measures may represent early markers of cardiac dysfunction that may be used for cardiovascular risk stratification in autosomal dominant polycystic kidney disease. Use of sensitive measurements from speckle echo may be of benefit in elucidating mechanisms of early cardiovascular disease onset in early stage ADPKD.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.



Autosomal dominant polycystic kidney disease


Body mass index


Chronic kidney disease




Ratio of transmitral early filling velocity to early diastolic strain rate


Estimated glomerular filtration rate


Global longitudinal strain


High density lipoprotein


Height indexed total kidney volume


Interventricular septal thickness


Left ventricular ejection fraction


Left ventricular internal diameter


Left ventricular mass index


Left ventricular posterior wall


  1. 1.

    Perrone RD, Ruthazer R, Terrin NC. Survival after end-stage renal disease in autosomal dominant polycystic kidney disease: contribution of extrarenal complications to mortality. Am J Kidney Dis Off J Natl Kidney Found. 2001;38(4):777–84.

    CAS  Article  Google Scholar 

  2. 2.

    Koren MJ, Devereux RB, Casale PN, Savage DD, Laragh JH. Relation of left ventricular mass and geometry to morbidity and mortality in uncomplicated essential hypertension. Ann Intern Med. 1991;114(5):345–52.

    CAS  Article  Google Scholar 

  3. 3.

    Chapman AB, Johnson AM, Rainguet S, Hossack K, Gabow P, Schrier RW. Left ventricular hypertrophy in autosomal dominant polycystic kidney disease. J Am Soc Nephrol JASN. 1997;8(8):1292–7.

    CAS  PubMed  Google Scholar 

  4. 4.

    Perrone RD, Abebe KZ, Schrier RW, Chapman AB, Torres VE, Bost J, et al. Cardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol CJASN. 2011;6(10):2508–15.

    Article  Google Scholar 

  5. 5.

    Oflaz H, Alisir S, Buyukaydin B, Kocaman O, Turgut F, Namli S, et al. Biventricular diastolic dysfunction in patients with autosomal-dominant polycystic kidney disease. Kidney Int. 2005;68(5):2244–9.

    Article  Google Scholar 

  6. 6.

    Ecder T, Schrier RW. Cardiovascular abnormalities in autosomal-dominant polycystic kidney disease. Nat Rev Nephrol. 2009;5(4):221–8.

    CAS  Article  Google Scholar 

  7. 7.

    Schrier RW, Abebe KZ, Perrone RD, Torres VE, Braun WE, Steinman TI, et al. Blood pressure in early autosomal dominant polycystic kidney disease. N Engl J Med. 2014;371(24):2255–66.

    Article  Google Scholar 

  8. 8.

    Gorcsan J, Tanaka H. Echocardiographic assessment of myocardial strain. J Am Coll Cardiol. 2011;58(14):1401–13.

    Article  Google Scholar 

  9. 9.

    Biering-Sørensen T, Solomon SD. Assessing contractile function when ejection fraction is Normal: a case for Strain imaging. Circ Cardiovasc Imaging. 2015;8(11):e004181.

    Article  Google Scholar 

  10. 10.

    Kowsari A-A, Hosseinsabet A. Evaluation of the right ventricular function in prediabetes: a 2-D speckle tracking echocardiographic study. Ultrasound Med Biol. 2016;42(6):1321–9.

    Article  Google Scholar 

  11. 11.

    Jensen MT, Sogaard P, Andersen HU, Bech J, Fritz Hansen T, Biering-Sørensen T, et al. Global longitudinal strain is not impaired in type 1 diabetes patients without albuminuria: the thousand & 1 study. JACC Cardiovasc Imaging. 2015;8(4):400–10.

    Article  Google Scholar 

  12. 12.

    Narayanan A, Aurigemma GP, Chinali M, Hill JC, Meyer TE, Tighe DA. Cardiac mechanics in mild hypertensive heart disease: a speckle-strain imaging study. Circ Cardiovasc Imaging. 2009;2(5):382–90.

    Article  Google Scholar 

  13. 13.

    Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr Off Publ Am Soc Echocardiogr. 2015;28(1):1–39.e14.

    Article  Google Scholar 

  14. 14.

    Kramann R, Erpenbeck J, Schneider RK, Röhl AB, Hein M, Brandenburg VM, et al. Speckle tracking echocardiography detects uremic cardiomyopathy early and predicts cardiovascular mortality in ESRD. J Am Soc Nephrol JASN. 2014;25(10):2351–65.

    CAS  Article  Google Scholar 

  15. 15.

    Saito M, Okayama H, Yoshii T, Higashi H, Morioka H, Hiasa G, et al. Clinical significance of global two-dimensional strain as a surrogate parameter of myocardial fibrosis and cardiac events in patients with hypertrophic cardiomyopathy. Eur Heart J Cardiovasc Imaging. 2012;13(7):617–23.

    Article  Google Scholar 

  16. 16.

    Pei Y, Obaji J, Dupuis A, Paterson AD, Magistroni R, Dicks E, et al. Unified criteria for ultrasonographic diagnosis of ADPKD. J Am Soc Nephrol JASN. 2009;20(1):205–12.

    CAS  Article  Google Scholar 

  17. 17.

    Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF, Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150(9):604–12.

    Article  Google Scholar 

  18. 18.

    Biering-Sørensen T, Hoffmann S, Mogelvang R, Zeeberg Iversen A, Galatius S, Fritz-Hansen T, et al. Myocardial strain analysis by 2-dimensional speckle tracking echocardiography improves diagnostics of coronary artery stenosis in stable angina pectoris. Circ Cardiovasc Imaging. 2014;7(1):58–65.

    Article  Google Scholar 

  19. 19.

    Nagueh SF, Smiseth OA, Appleton CP, Byrd BF, Dokainish H, Edvardsen T, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. Eur Heart J Cardiovasc Imaging. 2016;17(12):1321–60.

    Article  Google Scholar 

  20. 20.

    Lassen MCH, Biering-Sørensen SR, Olsen FJ, Skaarup KG, Tolstrup K, Qasim AN, et al. Ratio of transmitral early filling velocity to early diastolic strain rate predicts long-term risk of cardiovascular morbidity and mortality in the general population. Circ Cardiovasc Imaging. 2017(3).

  21. 21.

    Biering-Sørensen T, Biering-Sørensen SR, Olsen FJ, Sengeløv M, Jørgensen PG, Mogelvang R, et al. Global longitudinal Strain by echocardiography predicts long-term risk of cardiovascular morbidity and mortality in a low-risk general population: the Copenhagen City heart study. Eur Heart J. 2019;40(6):518-25.

    Article  Google Scholar 

  22. 22.

    Nasir K, Rosen BD, Kramer HJ, Edvardsen T, Bluemke DA, Liu K, et al. Regional left ventricular function in individuals with mild to moderate renal insufficiency: the multi-ethnic study of atherosclerosis. Am Heart J. 2007;153(4):545–51.

    Article  Google Scholar 

  23. 23.

    Russo C, Jin Z, Elkind MSV, Rundek T, Homma S, Sacco RL, et al. Prevalence and prognostic value of subclinical left ventricular systolic dysfunction by global longitudinal strain in a community-based cohort. Eur J Heart Fail. 2014;16(12):1301–9.

    Article  Google Scholar 

  24. 24.

    Yingchoncharoen T, Agarwal S, Popović ZB, Marwick TH. Normal ranges of left ventricular strain: a meta-analysis. J Am Soc Echocardiogr Off Publ Am Soc Echocardiogr. 2013;26(2):185–91.

    Article  Google Scholar 

  25. 25.

    Wong CY, O’Moore-Sullivan T, Leano R, Byrne N, Beller E, Marwick TH. Alterations of left ventricular myocardial characteristics associated with obesity. Circulation. 2004;110(19):3081–7.

    Article  Google Scholar 

  26. 26.

    Ng ACT, Delgado V, Bertini M, van der Meer RW, Rijzewijk LJ, Hooi Ewe S, et al. Myocardial steatosis and biventricular strain and strain rate imaging in patients with type 2 diabetes mellitus. Circulation. 2010;122(24):2538–44.

    Article  Google Scholar 

  27. 27.

    Kosmala W, Przewlocka-Kosmala M, Szczepanik-Osadnik H, Mysiak A, O’Moore-Sullivan T, Marwick TH. A randomized study of the beneficial effects of aldosterone antagonism on LV function, structure, and fibrosis markers in metabolic syndrome. JACC Cardiovasc Imaging. 2011;4(12):1239–49.

    Article  Google Scholar 

  28. 28.

    Balbo BE, Amaral AG, Fonseca JM, de Castro I, Salemi VM, Souza LE, et al. Cardiac dysfunction in Pkd1-deficient mice with phenotype rescue by galectin-3 knockout. Kidney Int. 2016;90(3):580–97.

    CAS  Article  Google Scholar 

  29. 29.

    Fick GM, Duley IT, Johnson AM, Strain JD, Manco-Johnson ML, Gabow PA. The spectrum of autosomal dominant polycystic kidney disease in children. J Am Soc Nephrol JASN. 1994;4(9):1654–60.

    CAS  PubMed  Google Scholar 

  30. 30.

    Lumiaho A, Pihlajamäki J, Hartikainen J, Ikäheimo R, Miettinen R, Niemitukia L, et al. Insulin resistance is related to left ventricular hypertrophy in patients with polycystic kidney disease type 1. Am J Kidney Dis Off J Natl Kidney Found. 2003;41(6):1219–24.

    CAS  Article  Google Scholar 

  31. 31.

    Abbott KC, Agodoa LY. Polycystic kidney disease in patients on the renal transplant waiting list: trends in hematocrit and survival. BMC Nephrol. 2002;3:7.

  32. 32.

    Chandra M, Miller ME, Garcia JF, Mossey RT, McVicar M. Serum immunoreactive erythropoietin levels in patients with polycystic kidney disease as compared with other hemodialysis patients. Nephron. 1985;39(1):26–9.

    CAS  Article  Google Scholar 

  33. 33.

    Ersbøll M, Andersen MJ, Valeur N, Mogensen UM, Fakhri Y, Fahkri Y, et al. 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(10):648–56.

    Article  Google Scholar 

  34. 34.

    Kimura K, Takenaka K, Ebihara A, Okano T, Uno K, Fukuda N, et al. Speckle tracking global strain rate E/E’ predicts LV filling pressure more accurately than traditional tissue Doppler E/E’. Echocardiogr Mt Kisco N. 2012;29(4):404–10.

    Article  Google Scholar 

  35. 35.

    Hsu P-C, Lee W-H, Chu C-Y, Lee C-S, Yen H-W, Su H-M, et al. The ratio of early mitral inflow velocity to global diastolic strain rate as a useful predictor of cardiac outcomes in patients with atrial fibrillation. J Am Soc Echocardiogr Off Publ Am Soc Echocardiogr. 2014;27(7):717–25.

    Article  Google Scholar 

  36. 36.

    Høfsten DE, Løgstrup BB, Møller JE, Pellikka PA, Egstrup K. Abnormal glucose metabolism in acute myocardial infarction influence on left ventricular function and prognosis. JACC Cardiovasc Imaging. 2009;2(5):592–9.

    Article  Google Scholar 

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This work was supported by a grant from the Lundbeck Foundation to UCSF to fund Lundbeck Foundation Clinical Research Fellowship for Mats Højbjerg Lassen. Furthermore, Mats Højbjerg Lassen received a research grant from Gentofte & Herlev Hospital. The sponsors had no role in the study design, data collection, data analysis, data interpretation, or writing of the article. The Baltimore PKD Center and Drs. Seliger and Watnick are supported by a grant from the NIDDKP30 DK090868. MP is supported by NIH/NIDDKK23 DK099238 and a Doris Duke Charitable Foundation Clinical Scientist Development Award.

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Study design and interpretation of results: MHL, AQ, TBS, MP, acquisition of data and setting up the study: TW, SLS, JLTR, YL, SNH, MP, key inputs to manuscript preparation: HC, MAS, DN. All authors have read and approve of the final version of this manuscript.

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Correspondence to Mats C. H. Lassen.

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This study was approved by the regional institutional review board (University of California, San Francisco Institutional Review Board) and all participants gave written informed consent. Our database and clinical specimen protocols are approved by our IRB (# 14–15601, 13–11609).

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The authors declare that they have no competing interests.

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Additional file 1:

Table S1A. Associations with GLS, Linear Regression (those who were on Beta blocker were excluded from analysis). Table S1B. Associations with E/SRe, Linear Regression (those who were on Beta blocker were excluded from analysis). Table S2A. Associations with GLS: Logistic regression (those who were on Beta blocker were excluded from analysis). Table S2B. Associations with E/SRe: Logistic regression (those who were on Beta blocker were excluded from analysis). (DOCX 18 kb)

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Lassen, M.C.H., Qasim, A.N., Biering-Sørensen, T. et al. Cardiac function assessed by myocardial deformation in adult polycystic kidney disease patients. BMC Nephrol 20, 324 (2019).

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  • Autosomal dominant polycystic kidney disease
  • Two-dimensional speckle tracking echocardiography
  • Global longitudinal Strain