Decreased Serum 25-hydroxyvitamin D Level Causes Interventricular Septal Hypertrophy in Patients on Peritoneal Dialysis: Cardiovascular Aspects of Endogenous Vitamin D Deficiency

Esen, Bennur; Sahin, Irfan; Atay, Ahmet Engin; Saglam Gokmen, Emel; Harmankaya Kaptanogullari, Ozlem; Yılmaz, Mürvet; Kucuk, Suat Hayri; Kahvecioglu, Serdar; Seyahi, Nurhan

doi:https://doi.org/10.1155/2016/2464953

International Journal of Nephrology

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Research Article | Open Access

Volume 2016 | Article ID 2464953 | https://doi.org/10.1155/2016/2464953

Decreased Serum 25-hydroxyvitamin D Level Causes Interventricular Septal Hypertrophy in Patients on Peritoneal Dialysis: Cardiovascular Aspects of Endogenous Vitamin D Deficiency

Bennur Esen,¹Irfan Sahin,²Ahmet Engin Atay,³Emel Saglam Gokmen,³Ozlem Harmankaya Kaptanogullari,⁴Mürvet Yılmaz,⁴Suat Hayri Kucuk,⁵Serdar Kahvecioglu,⁶and Nurhan Seyahi⁷

Academic Editor: Alessandro Amore

Received11 Jul 2016

Accepted01 Nov 2016

Published27 Nov 2016

Abstract

Introduction. In the present study, we aimed to analyze the relation of vitamin D with echocardiographic indexes in patients with end stage renal disease (ESRD) receiving renal replacement therapy (RRT). Methods. A total of 98 patients, 64 patients on hemodialysis (HD) (29F/35M, mean age 56.75 ± 18.63 years) and 34 age matched patients on peritoneal dialysis (PD) (21F/13M, mean age 58.11 ± 10.63 years), with similar duration of ESRD and RRT were enrolled into this cross-sectional study. Echocardiographic examination was performed after dialysis session at normovolemic status. Fasting blood samples were obtained before dialysis session. Results. Patients on PD and female patients in both groups had significantly lower level of 25-OH-D3 level when compared to patients on HD or male patients (p: 0.0001 and p: 0.0001). When all participants were considered, there was no significant association between 25-OH-D3 and echocardiographic parameters; however, in patients on PD, a significant negative correlation was determined between 25-OH-D3 and diastolic blood pressure, interventricular septal hypertrophy (ISH), and left ventricular mass index (LVMI) (r: −0.424, p: 0.012; r: −0.508, p: 0.004; r: 0.489, p: 0.04, resp.). Conclusion. Low serum 25-hydroxyvitamin D levels is associated with ISH and LVMI in PD patients.

1. Introduction

Besides its action on bone-mineral metabolism, vitamin D has numerous physiologic effects including cell growth and differentiation of immune system [1]. Also vitamin D deficiency (VDD) has a well-known association with endothelial dysfunction [2]. In vitro studies indicated a favourable antiproliferative effect of vitamin D replacement on relaxation of cardiomyocytes and diastolic functions of heart [3, 4].

Cardiovascular disorders (CVD) account most common cause of mortality in ESRD. On the other hand, chronic kidney disease (CKD) is associated with accelerated development of CVD [5]. Patients with CKD tend to have accelerated atherosclerosis, valvular calcification, asymmetric septal hypertrophy, and arrhythmias when compared to general population. Innovations in renal replacement procedures prolong survival in ESRD patients and consequent increase in CVD risk [6].

Vitamin D receptors have been identified in several extrarenal organ systems including cardiac myocytes and endothelial cells [7]. In animal studies, researchers have demonstrated an association between VDD and increased contractility and deteriorated systolic functions, both leading to myocardial hypertrophy [8]. Mose et al. showed that active vitamin D therapy for 6 months improved end-diastolic volume of left ventricule [9]. Similarly, active vitamin D and vitamin D receptor activators (paricalcitol) are related to decreased mortality and better cardiovascular risk profile. Low serum vitamin D level cause hypocalcemia and secondary hyperparathyroidism that are related to coronary artery calcification, cardiac failure, and mortality [8].

There is a strict relationship between VDD and CVD-related mortality; however exact mechanism is not clearly understood. We aimed to examine the effect of 25-OH-D3 on echocardiographic indices and cardiac functions in ESRD patients receiving RRT.

2. Material-Method

A cross-sectional study on 98 ESRD patients receiving RRT was conducted between January 2015 and March 2015 in Bagcilar Education and Research Hospital. Patients were divided into 2 subgroups: 64 patients on hemodialysis (HD) and 34 age matched patients on peritoneal dialysis (PD) with similar duration of ESRD and RRT. Ethics committee of Bagcilar Education and Research Hospital approved the study. Written informed consent was obtained from all participants.

Entire patients in each group were under dietary restrictions that is recommended by K/DOQI for patients on dialysis therapy [10]. Patients on PD and HD were regularly followed up in Dialysis Center and Nephrology outpatient service of Bagcilar Education and Research Hospital. Serum potassium, sodium, calcium, and hemogram analysis were performed by monthly intervals, and parathormon level was analyzed by 3-month intervals. Patients were informed about the results and, consequently, recommendations were updated by special dietitian. Also their first-degree relatives (parents, husbands, wives, or children) were integrated to follow-up procedure to augment patient’s continuity and accommodation. Similarly, patients in both groups were advised with exposure to sunlight not less than 1 hour/day. The study was performed between January and March 2015 in Istanbul to eliminate variations of seasonal exposure to sunlight. All the patients have the same ethnic background and were residents of the same region in European side of Istanbul city. All the patients survived during the study period

Exclusion criteria were anemia, obesity, acute inflammatory or infectious disease, malignancy, immobility, ongoing treatment with immunosuppressive agents, severe hypertension, hypohyperparathyroidism, pregnancy, left ventricular ejection fraction (LVEF) <50%, moderate-to-severe valvular disease, or age younger than 18 years. Data regarding demographic features and physical examination were recorded.

Blood samples were collected after 8-hour fasting period. Serum levels of calcium (Ca), phosphorus (P), albumin, alkalen phosphatase (ALP), and low density lipoprotein (LDL) were analyzed by photometric method in Siemens Advia 1800 device. Electrochemiluminescence immunoassay (ECLIA) method was used to analyze serum levels of parathormon (PTH) and 25-hydroxyvitamin D3. Vitamin D deficiencies were classified as severe, <5 ng/mL; moderate, 5–15 ng/mL; and mild, 15–29 ng/mL [11]. Vitamin D replacement was instituted on the basis of achieving a PTH level of <300 IU/L as recommended by K/DOQI [10]. The use of vitamin D replacement was recorded for each patient.

Echocardiographic examination was performed after dialysis session at normovolemic status. Normovolemia or dry weight was defined as postdialysis weight where the patient shows no sign of pulmonary or peripheral edema and do not have hypotension [12]. Fasting blood samples were obtained before dialysis session. All cases were examined by iE33 Echocardiography system to detect left ventricular end-diastolic dimension (LVEDD), left atrial diameter (LAD), left ventricular posterior wall thickness in diastole (LVPWT), interventricular septum thickness in diastole (IVST), and left ventricular ejection fraction (LVEF). Left ventricular mass was calculated according to the American Society of Echocardiography formula. Body mass index (BMI) was calculated by dividing weight into the square of height, body surface area (BSA) was calculated as ([height (cm) × weight (kg)]/3600)^1/2, and LV mass index was calculated by dividing LV mass into the BSA. Left ventricular hypertrophy was defined as LV mass index >115 g/m² (for men) and >95 g/m² (for women) [13]. The use of angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARB) was recorded for each patient.

2.1. Statistical Analysis

SPSS 22.0 (SPSS, Chicago, Illinois, USA) package programme was used for statistical analysis. Parametric variables were compared with independent t-test, ordinal data were compared with Mann–Whitney U test, and nonparametric variables were compared with chi-square test. Quantitative parameters were compared with Kruskal Wallis test. Spearman’s rho correlation test was used to evaluate the relation of parametric variables. A value <0.05 was considered significant.

3. Results

Group 1 consists of 64 patients on HD with a mean age of years and mean RRT duration of months. In group 2, there were 34 patients on PD with a mean age of years and mean RRT duration of months. The mean age and RRT duration of both groups were similar. Creatinine levels were similar in both groups. In most of the patients, daily urine output was below 200 mL/day; therefore renal clearance was negligible.

Serum levels of Ca, P, PTH, and alkalen phosphatase (ALP) were similar between patients on HD and PD. Lipid profile including LDL-c, HDL-c, and triglyceride level were similar between patients on HD and PD. Serum 25-OH-D3 level of patients on PD ( ng/mL) was significantly lower than patients on HD ( ng/mL) (p: 0.0001). Women in both groups had low 25-OH-D3 level when compared to male participants (p: 0.0001). Table 1 shows the biochemical and demographic data of both groups.

Two patients in PD group and 3 patients in HD group were receiving statin therapy. The mean ± SD systolic blood pressure of patients on HD and PD was mmHg and mmHg, respectively. The mean ± SD diastolic blood pressure of patients on HD and PD was mmHg and mmHg, respectively. Both mean systolic and diastolic pressure of patients on HD and PD were statistically similar. The ratio of antihypertensive drug use in PD and HD group was similar. Frequency of ACE-inhibitor or ARB use was 8.2% and 6.9% for HD and PD patients respectively. Also vitamin D was administered according to parathormon level of patients as recommended by K/DOQI clinical practice guidelines for bone metabolism and disease in CKD. Frequency of active vitamin D use was 91.8% and 93.1% for HD and PD patients, respectively.

Echocardiographic parameters were similar in HD and PD group (Table 2). When all patients were considered, correlation analysis indicated a significant association between 25-OHD3 and age (r: −0.226, p: 0.028). However, there was no significant association between 25-OHD3 and echocardiographic parameters.

In HD group, there was no significant association between 25-OH-D3 and echocardiographic parameters (Table 3). In PD group, a significant inverse correlation was determined between 25-OH-D3 and diastolic blood pressure, aortic velocity (Aovel), pulmonary velocity (Pvel), aortic regurgitation (AR), interventricular septal hypertrophy (IVSH), and left ventricular mass index (r: −0.424, p: 0.012; r: −0.433, p: 0.024; r: −0.498, p: 0.006; r: −0.430, p: 0.022; r: −0.508, p: 0.004; r: 0.489, p: 0.04; resp.) (Table 4).

4. Discussion

Our study indicates that female participants and patients on PD have lower 25-OH-D3 level. Additionally, PD patients but not HD patients with low 25-OH-D3 level have structural cardiovascular changes which may be related to high diastolic blood pressure, ISH, and LVMI.

CVD-related mortality risk of patients with CKD varies between 40% and 50% [14]. Low serum 25-OH-D3 levels are frequently seen in CKD patients. In a study by Taskapan et al., mild, moderate, and severe VDD was observed in 43,9%, 48,4%, and 4,4%, respectively, similar to our study [15]. A growing body of evidence indicates the relation of VDD with morbidity and mortality in patients with CKD. Ravani et al. showed that 25-OH-D3 independently and more accurately predicts progression of CKD and mortality in 168 patients with stages 2–5 CKD when compared to 1,25-OH-D3 [16]. Wang and Wells demonstrated a high CV event risk in a study on 230 PD patients with low serum 25-OH-D3 level [17]. Pekkanen et al. determined a relation between decreased LVEF and low serum 25-OH-D3 level [18].

Drechsler et al. showed a 3 times increased sudden cardiac death among patients with severe VDD (<25 nmol/L) when compared to patients with adequate vitamin D status (>75 nmol/L) [19]. In “Framingham Offspring Study,” patients with low serum 25-OH-D3 and without a history of CVD have high mortality rates [20]. All cause and CV related mortality rates were significantly higher in patients with low 25-OH-D level than normal 25-OH-D in patients that underwent coronary angiography and were followed up for 7.7 years [21].

Vitamin D metabolites have renoprotective effect by antiproteinuric, anti-inflammatory, and immunomodulatory properties and by suppression of renin-angiotensin-aldosterone system (RAAS) [22]. Low serum 25-OH-D level activates (RAAS) and increases fibroblast growth factor which are associated with progression of renal injury [23, 24]. Decreased serum 25-hydroxyvitamin D level leads to IVSH which is a significant predictor of cardiovascular morbidity in ESRD in pediatric population [25]. Additionally, low serum 25-OH-D3 have been related to increased inflammatory state which is involved in atherosclerosis and CVD [26, 27].

Hypertension, DM, dyslipidemia, age, volume-nutritional status, and dialysis adequacy are well-known CVD risk factors that are frequently seen in CKD patients [27]. All these factors are correlated with echocardiographic indexes including left ventricular diastolic diameter (LVdD), LVED, and ejection fraction (EF) [27]. Because calcium-phosphorus equilibrium as well as fluid and glycemic control has significant impact on cardiac myocytes (trophic effect of PTH on cardiac myocytes), echocardiographic examinations were performed after dialysis session at normovolemic status. In the Framingham Offspring Study, individuals with low 25-OH-D3 level had a hazard ratio of 1.62 for CVD risk [27]. Because fluid control is better in HD patients, PD patients have increased CVD and mortality risk [28].

Although it is out of our study object, vitamin D replacement has favourable impact on cardiac functions and diastolic dysfunction and is associated with regression of myocardial hypertrophy [29–31]. However authors of two large scaled human studies (PRIMO and OPERA trials) and an experimental animal study failed to demonstrate a beneficial effect of vitamin D therapy on structural and functional changes in myocardium [32–34]. It would be reasonable to state that maintaining an accurate vitamin D level has vital importance in ESRD because excessive vitamin D replacement may cause hypercalcemia and hyperphosphatemia where high CaxP level is also related to calciphylaxis and vascular or valvular calcification.

Low sample size and single point measurement of variables were two major limitations of the study. A large number of dialysis patients that have exclusion criteria mentioned in the material-method section were excluded. Additionally patients with low dialysis adequacy were also excluded to eliminate the effect of hypervolemia and electrolyte imbalance on echocardiographic indices. Cross-sectional design of the study was another major limitation that should be confirmed by RCTs. To the best of our knowledge, this was the first report that indicates the association of low endogenous vitamin D status with diastolic dysfunction and ventricular hypertrophy in PD patients. In contrast to majority of previous studies, our study participants were similar in terms of CVD risk factors including blood pressure, dyslipidemia, serum glucose, age, obesity, uric acid level, and dialysis adequacy that provided us with elimination of effect of these factors on echocardiographic indices. Possible explanation of correlation between vitamin D and echocardiographic indices in PD is that fluid control and volume status were better in HD patients that have significant impact on both cardiovascular health and echocardiographic indices. Also intravenous or oral administration of vitamin D may affect serum level and echocardiographic indices. Owing to the fact that CKD patients on RRT have predisposition to CVD, 25-OH-D3 may become a candidate marker to predict future CV events. Regular follow-up of serum 25-OH-D3 may provide complementary data on cardiovascular health status of dialysis patients. Large scaled studies would clarify the exact role of vitamin D on cardiovascular morbidity and mortality in CKD patients.

Competing Interests

The authors declare that there is no conflict interests.

References

S. Chen, G. P. Sims, X. X. Chen, Y. Y. Gu, S. Chen, and P. E. Lipsky, “Modulatory effects of 1,25-dihydroxyvitamin D₃ on human B cell differentiation,” The Journal of Immunology, vol. 179, no. 3, pp. 1634–1647, 2007.
View at: Publisher Site | Google Scholar
K. A. Nibbelink, D. X. Tishkoff, S. D. Hershey, A. Rahman, and R. U. Simpson, “1,25(OH)₂-vitamin D3 actions on cell proliferation, size, gene expression, and receptor localization, in the HL-1 cardiac myocyte,” Journal of Steroid Biochemistry and Molecular Biology, vol. 103, no. 3-5, pp. 533–537, 2007.
View at: Publisher Site | Google Scholar
T. D. O'Connell, J. E. Berry, A. K. Jarvis, M. J. Somerman, and R. U. Simpson, “1,25-Dihydroxyvitamin D3 regulation of cardiac myocyte proliferation and hypertrophy,” American Journal of Physiology—Heart and Circulatory Physiology, vol. 272, no. 4, pp. H1751–H1758, 1997.
View at: Google Scholar
J. J. Green, D. A. Robinson, G. E. Wilson, R. U. Simpson, and M. V. Westfall, “Calcitriol modulation of cardiac contractile performance via protein kinase C,” Journal of Molecular and Cellular Cardiology, vol. 41, no. 2, pp. 350–359, 2006.
View at: Publisher Site | Google Scholar
A. S. Go, G. M. Chertow, D. Fan, C. E. McCulloch, and C.-Y. Hsu, “Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization,” The New England Journal of Medicine, vol. 351, no. 13, pp. 1296–1370, 2004.
View at: Publisher Site | Google Scholar
T.-H. Kuo, D.-C. Yang, W.-H. Lin et al., “Compliance index, a marker of peripheral arterial stiffness, may predict renal function decline in patients with chronic kidney disease,” International Journal of Medical Sciences, vol. 12, no. 7, pp. 530–537, 2015.
View at: Publisher Site | Google Scholar
H. F. Deluca and M. T. Cantorna, “Vitamin D: its role and uses in immunology,” FASEB Journal, vol. 15, no. 14, pp. 2579–2585, 2001.
View at: Publisher Site | Google Scholar
S. Pilz, A. Tomaschitz, C. Drechsler, and R. A. de Boer, “Vitamin D deficiency and heart disease,” Kidney International Supplements, vol. 1, no. 4, pp. 111–115, 2011.
View at: Publisher Site | Google Scholar
F. H. Mose, H. Vase, T. Larsen et al., “Cardiovascular effects of cholecalciferol treatment in dialysis patients—a randomized controlled trial,” BMC Nephrology, vol. 15, article 50, 2014.
View at: Publisher Site | Google Scholar
“K/DOQI clinical practice guidelines for bone metabolism and disease in chronic kidney disease,” American Journal of Kidney Diseases, vol. 42, pp. S1–S201, 2003.
View at: Google Scholar
G. A. Block and F. K. Port, “Re-evaluation of risks associated with hyperphosphatemia and hyperparathyroidism in dialysis patients: recommendations for a change in management,” American Journal of Kidney Diseases, vol. 35, no. 6, pp. 1226–1237, 2000.
View at: Publisher Site | Google Scholar
J. K. Leypold and A. K. Cheung, “Evaluating volume status in hemodialysis patients,” Advances in Renal Replacement Therapy, vol. 5, pp. 64–74, 1998.
View at: Google Scholar
R. M. Lang, M. Bierig, R. B. Devereux et al., “Recommendations for chamber quantification: a report from the American Society of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology,” Journal of the American Society of Echocardiography, vol. 18, no. 12, pp. 1440–1463, 2005.
View at: Publisher Site | Google Scholar
“Causes of death,” American Journal of Kidney Diseases, vol. 34, no. 2, supplement 1, pp. S87–S94, 1999.
View at: Publisher Site | Google Scholar
H. Taskapan, I. Sahin, P. Tam, and T. Sikaneta, “Vitamin D and kidney,” International Journal of Endocrinology, vol. 2013, Article ID 164103, 2 pages, 2013.
View at: Publisher Site | Google Scholar
P. Ravani, F. Malberti, G. Tripepi et al., “Vitamin D levels and patient outcome in chronic kidney disease,” Kidney International, vol. 75, no. 1, pp. 88–95, 2009.
View at: Publisher Site | Google Scholar
T. J. Wang and Q. S. Wells, “Vitamin D deficiency and heart failure risk. Not so black and white?” JACC: Heart Failure, vol. 3, no. 5, pp. 357–359, 2015.
View at: Publisher Site | Google Scholar
M. P. Pekkanen, O. Ukkola, P. Hedberg et al., “Serum 25-hydroxyvitamin D is associated with major cardiovascular risk factors and cardiac structure and function in patients with coronary artery disease,” Nutrition, Metabolism and Cardiovascular Diseases, vol. 25, no. 5, pp. 471–478, 2015.
View at: Publisher Site | Google Scholar
C. Drechsler, M. Verduijn, S. Pilz et al., “Vitamin D status and clinical outcomes in incident dialysis patients: results from the NECOSAD study,” Nephrology Dialysis Transplantation, vol. 26, no. 3, pp. 1024–1032, 2011.
View at: Publisher Site | Google Scholar
V. Xanthakis, D. M. Enserro, J. M. Murabito et al., “Ideal cardiovascular health: associations with biomarkers and subclinical disease and impact on incidence of cardiovascular disease in the Framingham Offspring Study,” Circulation, vol. 130, no. 19, pp. 1676–1683, 2014.
View at: Publisher Site | Google Scholar
G. N. Thomas, B. Ó. Hartaigh, J. A. Bosch et al., “Vitamin D levels predict all-cause and cardiovascular disease mortality in subjects with the metabolic syndrome: the Ludwigshafen risk and cardiovascular health (LURIC) study,” Diabetes Care, vol. 35, no. 5, pp. 1158–1164, 2012.
View at: Publisher Site | Google Scholar
D. Santoro, D. Caccamo, S. Lucisano et al., “Interplay of vitamin D, erythropoiesis, and the renin-angiotensin system,” BioMed Research International, vol. 2015, Article ID 145828, 11 pages, 2015.
View at: Publisher Site | Google Scholar
K. Yokoyama, A. Nakashima, M. Urashima et al., “Interactions between serum vitamin D levels and vitamin D receptor gene foki polymorphisms for renal function in patients with type 2 diabetes,” PLoS ONE, vol. 7, no. 12, article e51171, 2012.
View at: Publisher Site | Google Scholar
K. Khademvatani, M. H. Seyyed-Mohammadzad, M. Akbari, Y. Rezaei, R. Eskandari, and A. Rostamzadeh, “The relationship between vitamin D status and idiopathic lower-extremity deep vein thrombosis,” International Journal of General Medicine, vol. 7, pp. 303–309, 2014.
View at: Publisher Site | Google Scholar
S. Uysal, A. G. Kalayci, and K. Baysal, “Cardiac functions in children with vitamin D deficiency rickets,” Pediatric Cardiology, vol. 20, no. 4, pp. 283–286, 1999.
View at: Publisher Site | Google Scholar
J. Donate-Correa, V. Domínguez-Pimentel, M. L. Méndez-Pérez et al., “Selective vitamin D receptor activation as anti-inflammatory target in chronic kidney disease,” Mediators of Inflammation, vol. 2014, Article ID 670475, 6 pages, 2014.
View at: Publisher Site | Google Scholar
B. Esen, A. E. Atay, I. Sahin et al., “The relation of serum 25-hydroxy vitamin D3 with inflammation and indirect markers of thrombotic activity in patients with end stage renal disease,” Journal of Clinical and Experimental Nephrology, vol. 1, pp. 1–6, 2016.
View at: Google Scholar
S. Lai, A. Molfino, G. E. Russo et al., “Cardiac, inflammatory and metabolic parameters: hemodialysis versus peritoneal dialysis,” Cardiorenal Medicine, vol. 5, no. 1, pp. 20–30, 2015.
View at: Publisher Site | Google Scholar
A. N. Kiani, H. Fang, L. S. Magder, and M. Petri, “Vitamin D deficiency does not predict progression of coronary artery calcium, carotid intima-media thickness or high-sensitivity C-reactive protein in systemic lupus erythematosus,” Rheumatology, vol. 52, no. 11, pp. 2071–2076, 2013.
View at: Publisher Site | Google Scholar
S. Lemmilä, H. Saha, V. Virtanen, I. Ala-Houhala, and A. Pasternack, “Effect of intravenous calcitriol on cardiac systolic and diastolic function in patients on hemodialysis,” American Journal of Nephrology, vol. 18, no. 5, pp. 404–410, 1998.
View at: Publisher Site | Google Scholar
N. P. Singh, V. Sahni, D. Garg, and M. Nair, “Effect of pharmacological suppression of secondary hyperparathyroidism on cardiovascular hemodynamics in predialysis CKD patients: a preliminary observation,” Hemodialysis International, vol. 11, no. 4, pp. 417–423, 2007.
View at: Publisher Site | Google Scholar
C. W. Park, Y. S. Oh, Y. S. Shin et al., “Intravenous calcitriol regresses myocardial hypertrophy in hemodialysis patients with secondary hyperparathyroidism,” American Journal of Kidney Diseases, vol. 33, no. 1, pp. 73–81, 1999.
View at: Publisher Site | Google Scholar
R. Thadhani, E. Appelbaum, Y. Pritchett et al., “Vitamin D therapy and cardiac structure and function in patients with chronic kidney disease: the PRIMO randomized controlled trial,” The Journal of the American Medical Association, vol. 307, no. 7, pp. 674–684, 2012.
View at: Publisher Site | Google Scholar
A. Y.-M. Wang, F. Fang, J. Chan et al., “Effect of paricalcitol on left ventricular mass and function in CKD-the OPERA trial,” Journal of the American Society of Nephrology, vol. 25, no. 1, pp. 175–186, 2014.
View at: Publisher Site | Google Scholar

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Copyright © 2016 Bennur Esen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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