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Hypoalbuminemia linked to myocardial dysfunction in recent-onset nephrotic syndrome: a cross-sectional case control 3DSTE study



Although myocardial dysfunction in the context of longstanding steroid-resistant nephrotic syndrome (NS) has been the focus of many series, the detection of myocardial involvement in recent-onset NS has not taken sufficient attention. The primary outcome parameter of our study is the detection of myocardial dysfunction in the initial episode of NS (first 4 weeks after the onset), while the secondary outcome parameter is the determination of the best predictor of such dysfunction among systolic blood pressure, diastolic blood pressure, the duration of the initial episode of NS, and biochemical parameters such as serum albumin and cholesterol.


Forty NS patients during the initial episode of NS (first 4 weeks from the onset) were examined for anthropometric data as well as for serum albumin and cholesterol. Motion-mode echocardiography was used to determine Fractional shortening, while 3D echocardiography was applied to determine left ventricular (LV) ejection fraction (EF) and GLS (global longitudinal strain). Finally, we employed combined conventional and tissue doppler to determine LV E/e′ ratio (ratio of early transmitral inflow and average early diastolic basal septal and mitral annular velocities). Forty healthy, age- and sex-matched controls were enrolled to control advanced echocardiographic parameters.


LV GLS was markedly reduced in cases compared to controls, denoting subtle systolic dysfunction, while, LV E/e′ ratio was significantly higher in cases denoting diastolic dysfunction in early NS. Hypoalbuminemia was found to be the best predictor of both LV GLS and LV E/e′ ratio.


Myocardial dysfunction should be considered in any NS patient even in recent-onset NS, the severity of hypoalbuminemia seems to be the best determinant of this dysfunction either by increasing endothelial dysfunction or through triggering inflammation. Further studies are needed on the mechanism by which hypoalbuminemia induces myocardial dysfunction in NS patients


Nephrotic syndrome (NS) is a clinical condition characterized by massive proteinuria, hypoalbuminemia, hypercholesterolemia, and generalized edema. It is the most common renal disease of childhood with normal renal function [1].

Nephrotic syndrome (NS) is associated with increased cardiovascular morbidity and mortality, the appearance of which is related to excessive loss of albumin in urine, oxidative stress, or steroid therapy (leading to obesity, glucose utilization disorders, and increased arterial hypertension). Moreira-Rodrigues and colleagues describe the occurrence of impaired left ventricular function in the murine model of nephrotic syndrome [2]. The report links the occurrence of such dysfunction to the upregulation of cytokines and chronic inflammation. Furthermore, Hara et al. linked proteinuria to hyper-inflammation in the context of Hodgkin disease. Proteinuria may therefore be an important factor in the development of chronic inflammation in NS with subsequent myocardial involvement [3].

The shortest use of steroids can lead to myocardial complications as demonstrated by Shokr et al. who described a case of ST elevation myocardial infarction after a short course of dexamethasone. This may be explained by the role of steroids in impairing myocardial oxygen and glucose uptake. Moreover, their prolonged use can increase systemic blood pressure leading to pressure overload on the cardiomyocytes [4].

To our knowledge, there is no single report to date about myocardial involvement in cases with nephrotic syndrome and normal kidney functions. Most of the available data describe the occurrence of various forms of myocardial insult in the context of chronic nephrotic syndrome patients with elevated kidney functions.

Moreover, advanced echocardiographic techniques such as tissue Doppler imaging and speckle tracking echo echocardiography, offer a greater opportunity to assess the systolic and diastolic function of the LV. The assessment of segmental systolic function by STE leads to a better reflection of segmental contribution to the overall function, which makes it superior to the classic M-mode-derived EF.

The primary outcome parameter of this study is to confirm or rule out the presence of myocardial dysfunction in NS; while the secondary outcome parameter is to determine the best predictor of myocardial involvement in NS.


Study subjects

This case-control cross-sectional observational study was conducted from December 2019 to July 2020. Forty patients (group 1) with fulfilling the clinical and laboratory criteria of nephrotic syndrome during the initial episode (first four weeks of the disease onset during initial steroid therapy) [5] were enrolled from the nephrology unit in our institution’s Children Hospital. The exclusion criteria were any preexisting arrhythmia, congenital or acquired heart disease, or any concurrent systemic disease (obesity, diabetes, and systemic lupus erythematosus) that might impair myocardial functions as well as any abnormal kidney functions. Forty age, sex, and body surface area matched controls (group 2) were included in the study to benchmark echocardiographic parameters.

Study methods

History taking and physical examination

Patients were subjected to a full clinical history including data from age and sex as well as the onset of nephrotic syndrome, duration, and response to steroid use. Physical examination by a nephrologist included a blood pressure (BP) assessment and anthropometric data were collected to include weight and height.

Biochemical assessment

Blood-EDTA were immediately centrifuged (20 min, 2500 rpm, 4 °C), and plasma was stored at − 80 °C until use. Serum albumin, cholesterol, creatinine, and urea were evaluated in the clinical pathology department of our institution’s Children Hospital.

Echocardiographic assessment

Transthoracic echocardiography was performed using a General Electric (Vivid-7/9, Horten, Norway) machine with 3- and 5-MHz transducers according to the age of the patient. It also has tissue velocity imaging capabilities.

  • Conventional echocardiography included motion-mode and Doppler echocardiographic parameters averaged over 3 cardiac cycles. All measurements were performed according to the guidelines for performance of echocardiogram by the American Society of Echocardiography [6]. Left ventricular fraction shortening and ejection fraction were calculated according to the Teichholz method [7].

  • Conventional and tissue doppler imaging (TDI) was utilized to assess LV diastolic function by calculating the LV E/e′ ratio: the ratio between the early transmitral filling (E) and average early diastolic mitral annular and basal septal velocities. For statistical purposes, an LV E/e′ ratio ≥ 9 was considered suggestive of diastolic dysfunction [8]

Three-dimensional echocardiography

Full-volume acquisition of the left ventricle was obtained by harmonic imaging from the apical approach. Six ECG-gated consecutive beats were acquired during end-expiratory breath-hold to left ventricular full volume. The software automatically identified the Left Ventricular cavity endocardial border. The operator performed all the necessary adjustments manually in order to correctly place the endocardial border. After the adjustments, the software provided the left ventricular volumes, ejection fraction, and three-dimensional-derived global longitudinal strain. For statistical purposes, an LV GLS ratio ≤ 15 was considered suggestive of systolic dysfunction [9].

Statistical analysis

Data were analyzed using IBM© (International Business Machines) SPSS© (The Statistical Package for the Social Sciences) Statistics version 23 (Armonk, New York, United States of America).

Normally distributed numerical variables were presented as mean and Standard Deviation and inter-group differences were compared using the unpaired t test.

Scatter plots were designed to express the relationship between serum albumin on one hand and LV GLS and LV E/e′ ratio on the other hand.

A P-value < 0.05 was considered statistically significant.


Table 1 shows the demographic criteria of cases and controls, cases were matched for age, sex, height, and weight compared to controls. The cases’ weight was non-significantly higher than that of controls, probably due to edema.

Table 1 Demographic criteria of cases and controls

Table 2 shows a comparison between basic and advanced echocardiographic parameters between the two study groups: speckle tracking echocardiography (STE) and tissue Doppler imaging (TDI). Diastolic dysfunction was observed in cases compared to controls as shown by a significantly higher LV E/e′ (NS: 10±3 vs. Controls: 5±1.9). LV GLS was reduced in cases compared to controls significant of LV systolic dysfunction (NS:17 ± 1 vs. controls: 23 ± 1). Conventional FS was not significantly different between cases and controls.

Table 2 Left ventricular echocardiographic parameters in cases vs. controls

In Table 3, cases were based on the presence or the absence of LV systolic dysfunction, into two groups (group 1A and group 1B). This is to compare the time of assessment from the onset of NS, and the duration of steroid therapy at the time of assessment as well as the baseline and follow-up serum cholesterol, serum albumin, and urine P/C ratio and the echocardiographic data. No significant difference was observed in the duration and dose of steroid therapy or in the duration of the illness at the time of assessment. The baseline serum albumin, cholesterol, and urine P/C ratio did not differ between the two study groups, whereas the serum albumin and urine P/C ratio as well as the weight difference (reflective of response to treatment and improvement of hypoalbuminemia) were significantly different between the two subgroups at the time of assessment with the serum albumin being lower and the urine P/C ratio higher in cases with systolic myocardial dysfunction at the time of assessment with lack of subsequent weight loss. This probably reflects a poorer response to steroid therapy with persistent hypoalbuminemia after two weeks of therapy.

Table 3 Duration of nephrotic syndrome, steroid therapy, laboratory, and echocardiographic data in cases with systolic dysfunction vs. cases without

Table 4 also divided the patients into two subgroups based on the presence or absence of LV diastolic dysfunction. Similar to Table 3, no significant difference was found in biochemical data and duration of steroid therapy between the two study groups except for the serum albumin and urine P/C ratio at the time of assessment and weight difference. The findings shown in Tables 3 and 4 suggest that there might be a close relationship between hypoalbuminemia and the occurrence of systo-diastolic myocardial dysfunction, while steroid therapy seems to be unchanged between cases with Systolic or Diastolic dysfunction and cases with preserved function.

Table 4 Duration of nephrotic syndrome, steroid therapy, laboratory, and echocardiographic data in cases with diastolic dysfunction dysfunction vs. cases without

Table 5 is a multivariate analysis of the best predictors of LV GLS and LV E/e′ ratio, serum albumin was the best predictor of both parameters, while duration and dose of steroid therapy did not achieve any statistical significance in predicting each of the systolic or diastolic dysfunction of the LV, which goes in agreement with the findings elicited in Tables 3 and 4.

Table 5 Multivariate analysis for the predictors of systolic and diastolic function of LV in nephrotic syndrome

Figures 1 and 2 are two scatter plots showing the relationship between serum albumin on one hand and both GLS and LV E/e′ ratio on the other hand. There was a significant positive correlation between GLS and serum albumin while a negative correlation was found between LV E/e′ ratio and serum albumin.

Fig. 1

Scatter plot showing relationship between LV GLS and serum albumin. Abbreviations: LV, left ventricular; GLS, global longitudinal strain

Fig. 2

Scatter plot showing the relationship between E/e′ ratio and serum albumin. Abbreviations: E/e′, ratio between early transmitral inflow velocity and average early diastolic mitral annular and basal septal velocities


It is widely recognized that NS is the commonest kidney disorder in the pediatric age group. It is characterized by massive proteinuria and dyslipidemia mainly involving hypercholesterolemia. Myocardial injury in new-onset NS is an understudied field. To our knowledge, the series studying the effect of NS on the cardiovascular system have mainly tackled myocardial injury in the context of chronic NS [2, 10]. Another recent point of focus has been the increased risk of coronary hypoperfusion in NS [11, 12].

Our report is by far the first to study the effect of new-onset NS on myocardial involvement. Our study subjects showed statistically significant systo-diastolic dysfunction compared to controls. Unlike the previously fixed belief that dyslipidemia, notably hypercholesterolemia associated with NS is the commonest predisposing factor for myocardial involvement, our multivariate analysis shows that serum cholesterol failed to be a statistically significant predictor of either systolic or diastolic dysfunction in NS [13].

Likewise, steroid use was thought to be an important inducer of myocardial dysfunction, specifically proved in animal models and in humans as well. Bauer and associates succeeded in demonstrating that steroid intake for 8 weeks at a dose of 5mg/kg/day induces deterioration of myocardial dysfunction in mouse models. Bispo and colleagues also demonstrated myocardial insult in a case report of a patient receiving anabolic steroids for 10 weeks. Our study, however, failed to show any relationship between steroid use and the observed myocardial dysfunction. This might be due to the lower dose of steroids compared to the mentioned series (2mg/kg/day). Another factor that might be implicated in the absence of the steroid effect is the relatively short period of steroid use compared to the Bauer and Bispo series. The average duration of steroid use was 4 weeks, while the duration of steroid use needed to induce myocardial dysfunction seems to be close to 8–10 weeks [14, 15].

The only significant predictor of myocardial injury in NS was serum albumin. Serum albumin was found to be negatively correlated with LV E/e′ ratio and positively correlated with LV GLS. The contribution of serum albumin to myocardial dysfunction during the initial episode of NS seems to be a virgin piece of land.

Several possible explanations can be offered to justify the role of decreased albumin in inducing myocardial dysfunction in the context of NS. The first of which is the major role of albumin in scavenging free oxygen radicals and decreasing inflammation. Furthermore, Hara et al. [3] correlated the levels of proteinuria with inflammatory markers in patients with Lymphoma and concluded that higher proteinuria is associated with higher levels of acute-phase reactants in non-Hodgkin lymphoma. On top of that, Dirajlal-Fargo and colleagues reported that decreased albumin can be an important pathogenic factor in the inflammatory process leading to the development of carotid atherosclerosis [16]. The persistent hypoalbuminemia in cases showing myocardial dysfunction was coupled with persistent albuminuria and failure of significant weight loss suggesting early evidence of failure of response to steroids.

Finally, yet importantly, hypoalbuminemia has been implicated in the induction of endothelial dysfunction. Yu et al. [13] underlined the role of albumin leak in the development of microvascular injury in peritoneal dialysis patients. Nevertheless, Caraba and colleagues proved that there is a state of endothelial dysfunction in NS patients. Such endothelial dysfunction might impair coronary perfusion leading to subsequent ventricular dysfunction [17].


This paper points at early myocardial injury in cases with NS. Hypoalbuminemia seems to play a central role in the induction of such dysfunction. Despite the known role of steroid use in triggering such dysfunction, the relatively short duration and a low dose of steroid use in our study subjects wasn’t enough to justify this role. Furthermore, Hypoalbuminemia might be operating either through triggering myocardial inflammation or through impairing myocardial perfusion via endothelial dysfunction. Further studies are needed to unleash the mechanisms by which hypoalbuminemia operate to induce myocardial dysfunction.

Availability of data and materials

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



Blood Pressure




Global longitudinal strain


Left ventricle

LV E/e′:

The ratio between the early transmitral filling (E) and average early diastolic mitral annular and basal septal velocities


Nephrotic syndrome


Speckle tracking echocardiography


Tissue Doppler imaging


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To our families who are bearing the weight of our sacrifice of time to our patients. If our families were not understanding to the depth of our struggle, we would have never been able to keep the same level of dedication to our patients. To our students that we involve in each step of our researches to make them flourish in this field and take the lead the soonest the possible.

Author information




M.H conceived the idea, A.S revised the patients’ selection, S.Y and M.T participated in data collection, A.A and M.S performed and interpreted Echocardiography. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Antoine AbdelMassih.

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The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant Egyptian guidelines on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008, and has been approved by the institutional committee of the Faculty of Medicine, Cairo University. Ethical committee approval number is: I-231546. A written consent was fulfilled by each of the study participants.

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The authors declare that they have no competing interests.

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AbdelMassih, A., Haroun, M., Samir, M. et al. Hypoalbuminemia linked to myocardial dysfunction in recent-onset nephrotic syndrome: a cross-sectional case control 3DSTE study. Egypt Pediatric Association Gaz 69, 24 (2021).

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  • Recent-onset nephrotic syndrome
  • Myocardial dysfunction
  • Hypoalbuminemia