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ISSN: 2161-0959
Journal of Nephrology & Therapeutics
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Low Dietary Intake of Vitamin D and Vitamin D Deficiency in Hemodialysis Patients

Maria Krassilnikova, Katya Ostrow, Amanda Bader, Peter Heeger and Anita Mehrotra*

Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, USA

*Corresponding Author:
Anita Mehrotra
Department of Medicine
Mount Sinai School of Medicine
One Gustave Levy Place
Box 1243, NY, 10029, USA
Tel: 212-241-5153
Fax: 212-987-0389
E-mail: [email protected]

Received Date: March 31, 2014; Accepted Date: May 09, 2014; Published Date: May 15, 2014

Citation: Krassilnikova M, Ostrow K, Bader A, Heeger P, Mehrotra A (2014) Low Dietary Intake of Vitamin D and Vitamin D Deficiency in Hemodialysis Patients. J Nephrol Ther 4:166. doi:10.4172/2161-0959.1000166

Copyright: © 2014 Krassilnikova M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Background: The purpose of this study was to test the hypothesis that decreased dietary intake of Vitamin D contributes to Vitamin D deficiency in end-stage renal disease (ESRD) patients on hemodialysis (HD).

Methods: We performed a cross-sectional study of 58 hemodialysis outpatients from two Mount Sinai Medical Center (MSMC)-affiliated outpatient HD units in New York City and 648 outpatients at MSMC with CKD stages I-IV. Serum 25(OH)D concentrations were measured from August 2010 to July of 2011 in recruited hemodialysis patients (n=58) and linked with results of dietary and lifestyle surveys. The Mount Sinai Data Warehouse (electronic medical record) was used to capture 25(OH) Vitamin D levels for outpatients with CKD stages I-IV who had Vitamin D testing during the same time period.

Results: The prevalence of Vitamin D insufficiency/deficiency in the HD cohort was 96.6%. Mean (SD) and median (IQR) 25(OH)D concentrations were 15.65 (6.82) and 13.55 (10.15) ng/mL, respectively. Dietary surveys showed a median weekly Vitamin D intake of 1044 IU (IQR=808, vs. a recommended weekly allowance of 4200 IU) and specific avoidance of foods containing both Vitamin D and phosphorus. In contrast, mean and median 25(OH)D concentrations in patients with CKD stages I-IV were 25.66 (13.44) and 23.60 (15.48) ng/mL (p<0.001 vs. HD patients).

Conclusions: Vitamin D deficiency is more prevalent in HD patients than in pre-dialysis patients with CKD and is associated with decreased dietary intake of Vitamin D. Dialysis restrictions imposed to reduce dietary phosphorus intake likely contributes to the development of hypovitaminosis D in ESRD patients.

Keywords

Hemodialysis diet; Phosphorus; Vitamin D deficiency

Introduction

Vitamin D deficiency (serum 25(OH)D levels <20 ng/mL), and insufficiency (serum 25(OH)D levels <30 ng/mL), [1] are common in patients with chronic kidney disease (CKD), [2] including patients with end-stage renal disease (ESRD) on maintenance hemodialysis (HD) despite treatment with 1,25(OH)2D (or its equivalent) to prevent/reverse osteopenia [3-5]. Vitamin D deficiency is associated with increased morbidity and decreased survival in patients with CKD and ESRD [3,6]. The etiologies of hypovitaminosis D in the ESRD population are not clear, but include limited sunlight exposure, reduced UVB-induced Vitamin D synthesis in the skin, and disturbed Vitamin D metabolism [2,7-9]. In the United States, a significant source of Vitamin D is the consumption of Vitamin D fortified foods, in particular dairy products [10]. Whether the physician/nutritionist imposed, phosphorus-restricted, “renal diet” impacts serum Vitamin D levels HD patients has not been studied.

To understand this issue, we undertook a cross-sectional study of HD patients at two outpatient dialysis units in New York City, examining Vitamin D status (serum 25(OH)D), sun exposure, and dietary Vitamin D intake using a dietary and lifestyle survey tool. We compared Vitamin D status to that of a cohort of pre-dialysis outpatients with CKD to address the impact of HD on Vitamin D levels.

Subjects and Methods

Study design and data collection

The study was approved by the Institutional Review Board (IRB) of the Mount Sinai School of Medicine and in adherence with the Declaration of Helsinki. Patients from two outpatient hemodialysis units in New York City (Mount Sinai Medical Center and Terrence Cardinal Cooke) were recruited over the course of one year (from August 2010 to July of 2011) and enrolled into the study after providing written informed consent. Patients must have been receiving hemodialysis for at least two months prior to enrollment to be included in the study. Clinical and demographic characteristics of the patients (including self-reported race and ethnicity, past medical history, anthropometric parameters, medications, and clinically-indicated laboratory tests) were collected at the time of enrollment, and peripheral blood samples were obtained for 25(OH)D testing during the hemodialysis procedure. Serum 25(OH)D levels were determined commercially by the DiaSorin 25(OH)D competitive chemiluminescent immunoassay (CLIA) [11] in a CLIA-certified laboratory (Nationwide Laboratories, Ft. Lauderdale, FL, USA).

A dietary and lifestyle survey was performed in each study subject after enrollment describing sun exposure and dietary intake of Vitamin D-rich foods (attached as Supplemental Appendix A).

The Mount Sinai Data Warehouse was used to obtain de-identified Vitamin D data for a comparison group consisting of all outpatients with CKD stages I-IV (ICD-9 codes: 585.0, 585.1, 585.2, 585.3, 585.4). Patients with the above ICD-9 diagnoses and a 25(OH)D level measured between August 2010 and July 2011 were included in the query. For patients with multiple 25(OH)D levels during that time period, only the first level was included in the analysis. Any patients with a concomitant ICD-9 diagnosis of 585.5 and 585.6 were excluded to exclude any patients with ESRD on dialysis.

Statistical methods

Continuous data are reported as means (+/- SD) for normally distributed variables or medians (IQR) for non-normally distributed variables. Categorical data are reported as percentages of total. The Kolmogorov-Smirnov test was used to determine the distribution of continuous variables. Correlations between continuous variables (i.e. age and 25(OH)D level) were determined using a Spearman’s correlation coefficient. Comparison of continuous variables between groups was done using Mann-Whitney or Student’s t-test, as appropriate. Comparison of categorical variables was done using a Chi-square test or Fisher’s Exact test, as appropriate. Two-sided p<0.05 was considered to be statistically significant. All analyses were performed using SPSS version 19.0 (SPSS, Chicago, IL, USA).

Results

We performed serum 25(OH)D testing and dietary and lifestyle surveys in 58 patients with ESRD (Table 1). The majority of patients were male and of African ancestry, the average age of study participants was 59 years, the median time on dialysis was 4 years, and most patients developed ESRD as a result of diabetes and/or hypertension. Twenty-one (36.2%) patients reported taking a daily multivitamin and 41 (70.7%) patients reported taking phosphorus binders (calcium carbonate, calcium acetate, or sevelamer). Thirty-seven (63.8%) patients were receiving activated Vitamin D (1,25(OH)2D) in the form of intravenous doxercalciferol or paricalcitol during hemodialysis.

Age, years (mean +/- SD) 59 +/- 15
Gender: Male (%) 34 (58.6%)
Race: Black (%)
 White (%)
 Other (%)
39 (67.2%)
18 (31.0%)
1 (1.7%)
Ethnicity: Hispanic (%)
 Non-Hispanic (%)
19 (32.8%)
39 (67.2%)
Dialysis Vintage, years (median, IQR) 4 (6)
Smoking Status: Nonsmoker (%)
Current Smoker (%)
Former Smoker (%)
33 (56.9%)
7 (12.1%)
18 (31.0%)
Body Mass Index (BMI) (median, IQR) 26.95 (8.3)
Cause of ESRD: Hypertension (%)
Diabetes (%)
Glomerulonephritis (%)
Polycystic Kidney Disease (%)
Other (%)
16 (27.6%)
16 (27.6%)
5 (8.6%)
3 (5.2%)
18 (31.0%)
Comorbidities: Diabetes (%)
Peripheral vascular disease (%)
Coronary artery disease (%)
Hepatitis C (%)
Failed kidney transplant (%)
23 (39.7%)
13 (22.4%)
12 (20.7%)
10 (17.2%)
9 (15.5%)
Dialysis Access: Arteriovenous Fistula (%)
Arteriovenous Graft (%)
Tunneled Catheter (%)
37 (63.8%)
9 (15.5%)
12 (20.6%)

Table 1: Population Demographics (N=58)

The prevalence of Vitamin D insufficiency (25(OH)D<30ng/mL) was 96.6%. Over seventy percent (70.7%) of patients met criteria for Vitamin D deficiency (25(OH)D<20ng/mL), with 20.7% of patients severely deficient (25(OH)D<10ng/mL, Figure 1). Mean (SD) and median (IQR) 25(OH)D were 15.65 (6.82) and 13.55 (10.15) ng/mL, respectively. The distribution of 25(OH)D concentrations was similar regardless of the month of testing (Table S1), and patient characteristics did not vary between the deficient and insufficient/normal groups (Table 2).

nephrology-therapeutics-serum-cohort

Figure 1: Serum 25(OH)D (ng/mL) of the HD cohort (n=58)

  Deficient (n=41) Non-Deficient (n=17) P-value
Age, years (mean +/- SD) 60 +/- 16 58 +/- 13 0.731
Gender: Male (%) 25 (61.0%) 9 (52.9%) 0.572
Race:
Black (%)
White (%)
Other (%)

30 (73.2%)
10 (24.4%)
1 (2.4%)

9 (52.9%)
8 (47.1%)
0 (0.0%)
0.208
Dialysis Vintage, years (median, IQR) 4 +/- 6 3.5 +/- 6 0.644
Body Mass Index (BMI) (median, IQR) 27.8 (6.4) 26.7 (12.5) 0.718

Table 2: Patient Characteristics of Deficient (25(OH)D<20ng/mL) versus Non-deficient Study Subjects

We found no statistically significant associations between 25(OH)D concentration and age, gender, race, ethnicity, dialysis vintage, smoking status, or body mass index (BMI). There were also no significant associations between 25(OH)D and other laboratory parameters of mineral metabolism, nutrition, and inflammation, including serum calcium, phosphorus, intact parathyroid hormone (PTH), albumin, and ferritin (Table 3).

  Value Spearman’s correlation coefficient (rho) P-value
Calcium, mg/dL, median (IQR) 9,2 (1.0) -0.242 0.067
Phosphorus, mg/dL, mean +/- SD 5.8 +/- 1.4 -0.018 0.895
Intact Parathyroid Hormone, pg/mL, median (IQR) 373 (413) -0.047 0.725
Albumin, g/dL, median (IQR) 3.9 (0.4) -0.095 0.479
Ferritin, ng/mL, median (IQR) 454 (321) -0.080 0.551

Table 3: Laboratory Markers of Mineral Metabolism, Nutrition, and Inflammation and Correlation with serum 25(OH)D

Lifestyle surveys revealed that in the summer, patients spent a median number of 7 days/week outside for more than 15 minutes; in the winter, they spent a median number of 3 days/week outside for more than 15 minutes. Thirteen (22.4%) patients reported regular sunscreen use.

Dietary surveys showed a median weekly vitamin D intake of 1044 IU (IQR=808), well below the Institute of Medicine’s (IOM) recommended dietary allowance (RDA) of Vitamin D of 600 IU/day, or 4200 IU/week [12]. The median number of servings/week of specific Vitamin D-rich foods consumed is given in Table 4. The avoidance of dairy products (milk, yogurt, and cheese) was as per the dialysis unit dietician recommendations, as these foods are also high in phosphorus.

Item Vit D (IU) per serving Amount per serving Median number servings/week (IQR) Total vit D/week (IU)
Fish 100-654 3oz 2(2) 200-1308
Milk 100 8oz 0.5 (2) 50
Yogurt 80 6oz 0 (0.75) 0
Cheese 6-12 1oz 6 (5) 36-72
Cereal 40 1cup 2 (4) 80
Eggs 20-25 1egg 5 (5) 100-125
        Total 520-1689 IU/week

Table 4: Median Intake of Vitamin D Rich Foods

The high prevalence of Vitamin D deficiency in HD patients and low intake of Vitamin D containing foods (which are also high in phosphates) suggested the possibility that initiating HD results in lower serum Vitamin D, in part because of imposed dietary restrictions to limit phosphate intake. In an effort to address this possibility, we compared serum 25(OH)D concentrations in the HD cohort with those of a cohort of 648 outpatients followed over the same time period at Mount Sinai Medical Center carrying diagnoses of chronic kidney disease stages (CKD) I-IV. This analysis revealed mean (SD) and median (IQR) 25(OH)D concentrations of 25.66 (13.44) and 23.60 (15.48) ng/mL, respectively in the CKD cohort, significantly higher than the serum concentrations in the HD patients (Figure 2 and 3, p<0.001).

nephrology-therapeutics-serum-cohort

Figure 2: Serum 25(OH)D (ng/mL) of the CKD cohort (n=648)

nephrology-therapeutics-serum-cohort

Figure 3: Serum 25(OH)D (ng/mL) of the CKD cohort (n=648) vs HD cohort (n=58)* *p < 0.001

Discussion

Our results extend previously published studies indicating a high prevalence of Vitamin D deficiency/insufficiency among HD outpatients by providing new insight into the etiology of this observation [3-5]. While others have suggested that patient race, time of year of testing (due to limited sunlight exposure), and rates of sunscreen use can impact serum Vitamin D levels [13], our data indicate that these factors are largely inconsequential in our patient population, as all HD patients appeared to be at risk. In contrast, as we found a) avoidance of phosphate rich, Vitamin D containing foods by the HD patients and b) that patients with CKD (not on dialysis) have higher serum 25(OH)D concentrations than HD patients, our data suggest that dialysis-imposed dietary restrictions contribute to the hypovitaminosis D. Since many patients struggle to adhere to phosphate binder regimens, they are often counseled against dairy product consumption by their nephrologists and renal dieticians. Nutritional guidelines for dialysis patients are consistent with this conclusion as they recommend limited intake of Vitamin D-containing dairy products [14]. Serial measurements of Vitamin D levels in prospectively followed cohorts of CKD patients as they initiate dialysis are needed to formally prove this hypothesis.

We acknowledge that other factors may influence Vitamin D status in HD patients, including physiological effects of progression of renal disease that impair Vitamin D metabolism (i.e. elevated fibroblast growth factor-23 levels) [15], and limited ultraviolet-B (UVB) exposure. The majority of patients surveyed in our study had enough sun exposure (at least during the summer) to achieve maximal cutaneous Vitamin D synthesis [16]. 22.4% of patients in our study reported regular sunscreen use. Sunscreen, when used appropriately, reduces the capacity of the skin to produce vitamin D3 by 95% [17]. Regardless, physiological or environmental circumstances that hinder the production of D3 in the skin are generally compensated for by increased dietary intake of vitamin D [18], which did not occur in our cohort. HD patients in our study consumed well below the Institute of Medicine’s (IOM) recommended dietary allowance (RDA) of Vitamin D of 600 IU/day, or 4200 IU/week [12], and essentially none were being treated with Vitamin D supplements. It is also possible that oral Vitamin D supplementation, which can be administered to CKD patients, was discontinued as the patients initiated dialysis, contributing to lower serum Vitamin D levels over time, although this is purely speculative.

Despite the high prevalence of 25(OH)D deficiency among dialysis patients, screening for Vitamin D deficiency is not standard of care in many dialysis units. Perhaps this is due to a perception that treatment with activated Vitamin D(1,25(OH)2D) bypasses any need for its precursor (25(OH)D). Most chronic hemodialysis patients are treated for secondary hyperparathyroidism with intravenous activated Vitamin D or its analogs (i.e. doxercalciferol or paricalcitol), as renal 1-alpha hydroxylase is decreased or absent in these patients, and intact parathyroid hormone levels are used to guide therapy. The impact of 25(OH)D deficiency and its treatment on secondary hyperparathyroidism and renal bone disease in dialysis patients is not known, and no guidelines for therapy in this population exist.

Vitamin D (25(OH)D) has many biological effects beyond those affecting bone metabolism, including potent immunomodulatory and anti-inflammatory effects [19,20]. Up to two-thirds of dialysis patients are characterized by a malnutrition-inflammation syndrome [21], and many display disturbances in both innate and adaptive immunity [22-32]. This raises the intriguing hypothesis that Vitamin D deficiency could contribute to the inflammation and immune abnormalities found in this patient population, making it imperative that we understand the etiology of this problem and pursue solutions. Larger prospective studies of cohorts of patients with CKD progressing to ESRD are necessary to achieve this goal, as our study is limited by its single-center nature, small sample size, and reliance on patient recall for dietary history.

In conclusion, our data build upon previous work by providing evidence that the high prevalence (>90%) of Vitamin D deficiency and insufficiency among hemodialysis outpatients accompanies decreased consumption of Vitamin D-rich foods, a phenomenon which may be inadvertently caused by dialysis-imposed dietary restrictions. As evidence suggests that Vitamin D deficiency has negative health consequences and that oral Vitamin D repletion can be administered safely to dialysis patients, [20,33,34] our findings support the need for controlled studies to address the impact of Vitamin D repletion (via supplements and/or dietary modifications) on dialysis patient health.

Support and Conflict of Interest Statement

This study was funded by grants from the National Kidney Foundation (to PSH) and American Heart Association (to AM) as well as grant UL1TR000067 from the National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH). The authors have no other relevant conflicts of interests.

Acknowledgements

We would like to thank the physicians, staff, and patients at the Mount Sinai Medical Center and Terrence Cardinal Cooke dialysis units for their participation. This study was funded by grants from the National Kidney Foundation (to PSH) and American Heart Association (to AM) as well as grant UL1TR000067 from the National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH).

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