Nutritional vitamin D supplementation and health-related outcomes in hemodialysis patients: a protocol for a systematic review and meta-analysis
© Mehrotra et al.; licensee BioMed Central. 2015
Received: 30 September 2014
Accepted: 19 January 2015
Published: 21 February 2015
The prevalence of vitamin D deficiency in hemodialysis patients is high. While most hemodialysis patients are treated with activated vitamin D (1,25[OH]2D) to prevent renal osteodystrophy, clinical practices of the screening and treatment of 25(OH)2D deficiency are highly variable. It is unclear if nutritional vitamin D supplementation with D2 or D3 provides an additional clinical benefit beyond that provided by activated vitamin D treatment in this population.
We will conduct a systematic review of nutritional vitamin D (D2/D3) supplementation and health-related outcomes in hemodialysis patients according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The primary objective is to assess the impact of nutritional vitamin D supplementation on clinical outcomes relevant in hemodialysis patients, such as mortality, cardiovascular events, infections, and fractures. Secondary outcomes will include anemia, hyperparathyroidism, medication use (erythrocyte-stimulating agents, activated vitamin D), and quality of life. We will search MEDLINE, Scopus, Web of Science, and ClinicalTrials.gov for randomized, controlled trials of nutritional vitamin D supplementation (ergocalciferol/D2 or cholecalciferol/D3) in chronic hemodialysis patients. The Cochrane Risk Assessment Tool will be used to assess the quality of eligible studies. We will perform meta-analyses using standard techniques for the outcomes listed above if pooling is deemed appropriate/sufficient. The results of this systematic review may highlight gaps in our knowledge of the relevance of nutritional vitamin D in end-stage renal disease, allowing for the informed design of clinical trials assessing the impact of nutritional vitamin D therapy in the hemodialysis population in the future.
Systematic review registration
KeywordsVitamin D 25(OH)D Ergocalciferol (D2) Cholecalciferol (D3) Hemodialysis Clinical trial Systematic review Protocol
Over 600,000 individuals live with end-stage renal disease (ESRD) in the United States . Among ESRD patients on hemodialysis (HD) as a renal replacement therapy, cardiovascular disease is the leading cause of death, and large cohort studies have shown that non-traditional cardiovascular risk factors, such as vitamin D deficiency, are associated with increased mortality in this population [2-8]. Whether or not this risk is mitigated by treatment of vitamin D deficiency is unknown.
Vitamin D is a steroid hormone, traditionally known for its role in the regulation of calcium, phosphorus, and bone metabolism. It can be derived from dietary sources (D2 and D3) and/or produced in the skin by exposure to UV light (D3). It is 25-hydroxylated in the liver and then undergoes 1-alpha-hydroxylation to its active form, 1,25-dihydroxyvitamin D [1,25(OH)2D], by 1-alpha-hydroxylase (CYP27B1) in the kidney (in the context of normal renal function) as well as in extra-renal sites. 1,25(OH)2D binds to the intracellular vitamin D receptor (VDR) to alter gene transcriptional profiles and mediate downstream effects .
Vitamin D deficiency is widespread among the general population  and is highly prevalent in patients with ESRD on hemodialysis. The concentration of 25(OH)D is the main clinical indicator of vitamin D status and is used to define vitamin D deficiency . According to the Institute of Medicine (IOM), there is an elevation in the risk of experiencing adverse health consequences of vitamin D deficiency at 25(OH)D concentrations <20 ng/mL . Multiple reports from various centers worldwide have documented that over 80% of HD patients have serum vitamin D levels within the insufficient/deficient range [13,14]. 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 [15-18]. Because renal CYPR27B1 is essentially absent in patients with ESRD, the levels of circulating 1,25(OH)2D are also commonly well below the normal range, contributing to secondary hyperparathyroidism and bone loss. While many of these ESRD patients are treated with 1,25(OH)2D (or its equivalent) during hemodialysis for the prevention of uremic bone disease, this alone may not fully satisfy the vitamin D requirement. Increasing experimental evidence indicates that many vitamin D target tissues, including intestinal and immune cells, express CYP27B1 and the VDR [19-21]. Recent data suggest that local production of 1,25(OH)2D is required to obtain maximal calcium absorption, expression of antimicrobial peptides, and anti-inflammatory effects [19-25]. Because 25(OH)D is the immediate precursor of 1,25(OH)2D, low serum 25(OH)D concentrations are thus hypothesized to prevent the production of 1,25(OH)2D in target tissues, potentially promoting inflammation and reducing other vitamin D effects.
Based on published data demonstrating the prevalence of vitamin D deficiency in hemodialysis patients and the possible extra-skeletal benefits of nutritional vitamin D supplementation, it is imperative to establish recommendations to guide clinical practice and research in this arena. The purpose of the proposed systematic review is to provide the best available evidence on the treatment of vitamin D deficiency in the hemodialysis population and, if the evidence is inadequate, to highlight areas where further original research is required.
We will conduct a systematic review to determine the clinical impact of nutritional vitamin D supplementation on outcomes in hemodialysis patients (concurrently treated with 1,25[OH]2D). The pre-specified primary outcomes will be mortality, cardiovascular events, infections, and fractures. The secondary outcomes will include anemia, hyperparathyroidism, medication use (erythrocyte-stimulating agents, activated vitamin D), and quality of life. These pre-defined outcomes may be adjusted during the review, depending on the outcomes identified in eligible studies.
Types of studies
Only randomized, controlled trials (RCTs) of nutritional vitamin D (D2/ergocalciferol and/or D3/cholecalciferol) supplementation will be included in this systematic review. The choice to restrict the review to randomized controlled trials was made to eliminate the bias and confounding inherent in observational and uncontrolled studies of nutritional vitamin D repletion in this population. We may, however, find a paucity of eligible studies using this restriction strategy. If we are unable to find at least five eligible RCTs for the purposes of this systematic review, we will broaden our inclusion criteria (see below) to include non-randomized and/or uncontrolled interventional studies of nutritional vitamin D supplementation in HD patients using the Cochrane Effective Practice and Organization of Care (EPOC) approach to categorize the types of studies .
We will employ a broad electronic search strategy, using MEDLINE, Scopus, and Web of Science to identify published abstracts and manuscripts of randomized controlled trials of nutritional vitamin D supplementation in hemodialysis patients. To identify unpublished studies and assess publication bias, we will also search ClinicalTrials.gov for registered clinical trials of nutritional vitamin D supplementation in hemodialysis patients. With the goal of prioritizing sensitivity while remaining specific to clinical trials, the search strategy will include the relevant key terms: ‘cholecalciferol’ or ‘D3’ or ‘ergocalciferol’ or ‘D2’ and ‘hemodialysis’ and ‘trial’. We will also review the references of included manuscripts to potentially identify any missed trials. The corresponding authors of all identified eligible studies (published and unpublished) will be contacted to provide de-identified data for the purposes of meta-analysis.
Study screening and inclusion
All abstracts returned using the search strategy above will be screened by two independent investigators (WL and TJ) using the inclusion/exclusion criteria outlined below. In cases where an abstract is not available, the full text of the manuscript will be reviewed and evaluated instead. If the two independent investigators disagree on whether or not a particular study meets the inclusion criteria for the review, a third investigator (AM) will serve as a ‘tiebreaker’. The full text of all studies deemed eligible for inclusion will then be reviewed by all investigators for analysis.
We will include all randomized controlled trials of nutritional vitamin D (D2/ergocalciferol and/or D3/cholecalciferol) supplementation in adult and pediatric male and female chronic hemodialysis patients, regardless of outcome(s) measured. Only randomized, controlled interventional studies will be included. However, we will not restrict studies based on outcome(s) assessed, as we anticipate a limited number of true RCTs. We acknowledge that the type of nutritional supplementation (D2 vs D3), dose and preparation of supplement(s), and degree of vitamin D deficiency will vary among studies, but in order to maximize the total study population, we will not require any one particular supplement formulation/regimen or dosing schedule. Studies published in languages other than English will be translated and included if they otherwise meet all inclusion/exclusion criteria. As mentioned above, if we are unable to find at least five eligible RCTs for the purposes of this systematic review, we will broaden our inclusion criteria to include non-randomized and/or uncontrolled interventional studies of nutritional vitamin D supplementation in HD patients.
All case reports/series, review articles, observational studies, and non-randomized or uncontrolled interventional studies will be excluded. All animal studies will be excluded. We are also excluding studies of peritoneal dialysis (PD) and kidney transplant patients as these ESRD populations do not typically receive intravenous 1,25(OH)2D therapy, an important potential confounder.
Data extraction will be performed in a standardized fashion for all trials included in the final review using a pre-formatted database. All extracted data will be verified by a second investigator to ensure accuracy and completeness. Study investigator information, study sites/locations, sample size, inclusion/exclusion criteria, type and dose of nutritional vitamin D supplements, follow-up time, and patient characteristics (age, gender, race, dialysis vintage, comorbidities, dialysis access, medications) will be collected as variables for analysis. Baseline and follow-up 25(OH)D concentrations will also be collected, regardless of time of testing. All outcome variables will also be collected, regardless of number of studies with that outcome assessed.
The internal validity of all eligible randomized controlled trials will be evaluated using the Cochrane Risk Assessment Tool. The tool evaluates studies based on seven criteria: 1) randomization generation, 2) allocation concealment, 3) blinding of outcome assessors, 4) blinding patients/study personnel, 5) incomplete outcome data (that is, lost to follow-up), 6) selective outcome reporting, and 7) other risks of bias. Other features to be incorporated in the quality assessment include sample size and statistical analysis (was it appropriate?). In the event that we include non-randomized and/or uncontrolled interventional studies of nutritional vitamin D supplementation in HD patients (see ‘Types of studies’ above), we will use the Cochrane Effective Practice and Organization of Care Group Draft Risk of Bias Tool to assess quality and risk of bias .
We will develop a Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) diagram based on the search strategy and eligibility assessment to show the flow of included and excluded studies . We will describe all included studies in detail in the Results section of the manuscript. Study name/identification, patient population, and detailed design will be discussed, with a comparison of outcomes assessed by the various studies. The descriptive statistics from each trial will also be included and described in as much detail as is available from the parent trial(s).
We will pool treatment effect estimates where possible using standard statistical techniques and RevMan software. However, if combining data across studies is not feasible due to excessive heterogeneity of outcomes, we will use descriptive methods to present the results of all eligible studies. We did not specify the duration of therapy in our inclusion criteria in an effort to avoid being too restrictive, but we will attempt to account for differences in treatment duration during the data analysis. We will group both studies of ergocalciferol (D2) and cholecalciferol (D3) together initially, and we will then perform a subsequent sensitivity analysis for each treatment separately, as the bioavailability of these two agents may differ . Depending on the heterogeneity of dosing schedules, we may also perform separate analyses for differing dosing regimens. Finally, as follow-up time may vary from trial to trial, we will include time as a covariate in our final data analysis.
The National Kidney Foundation (NKF) Kidney Disease Outcomes Quality Initiative (KDOQI) guidelines do not address the treatment of vitamin D deficiency in hemodialysis patients beyond a recommendation for treatment with activated vitamin D during hemodialysis for the prevention of renal osteodystrophy . Perhaps this is due to a perception that treatment with activated vitamin D, or 1,25(OH)2D, bypasses any need for its precursor, 25(OH)D. However, emerging evidence indicates that vitamin D may play a role in human health that goes beyond bone and mineral metabolism . As such, determining the optimal strategy for screening and repletion of vitamin D deficiency in the ESRD population is of vital importance and is the purpose of the proposed systematic review.
We foresee several potential limitations with this systematic review: heterogeneity of clinical outcomes, substandard quality of existing studies, and a scarcity of randomized controlled trials, which are the focus of this project. Therefore, we anticipate that we may have to broaden our inclusion criteria to include non-randomized/uncontrolled interventional trials, particularly if we find fewer than five eligible RCTs for this review. We acknowledge that defining inclusion ‘sufficiency’ as five or more studies is somewhat arbitrary. However, we wanted to establish a priori a point at which we will consider changing our inclusion strategy to maximize the utility of performing a systematic review on this topic. We also anticipate that we may not be able to combine eligible studies for a meta-analysis, but we will nonetheless present our findings using descriptive methods, if necessary. This study protocol has been designed prior to any knowledge of the study data or outcomes from existing published (and non-published) literature. Hence, we are limited in our capacity to predict the results. Our hope is that the dissemination of this protocol will allow us to obtain feedback and constructive criticism of the methods of our study before it is conducted.
In conclusion, the proposed systematic review will provide insight into the clinical impact of nutritional vitamin D repletion in hemodialysis patients concurrently receiving treatment with activated vitamin D. The results have the potential to inform national and international guidelines on the care and management of vitamin D deficiency in this population. The review will also help to highlight areas requiring further research on this topic.
end-stage renal disease
Institute of Medicine
Kidney Disease Outcomes Quality Initiative
National Kidney Foundation
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
randomized controlled trial
vitamin D receptor
AM is supported by UL1TR000067 from the National Center for Advancing Translational Sciences.
- Collins AJ, Foley RN, Herzog C, Chavers B, Gilbertson D, Herzog C, et al. US Renal Data System 2012 Annual Data Report. Am J Kidney Dis. 2013;61:A7. e1-476.View ArticlePubMedGoogle Scholar
- Brookhart MA, Schneeweiss S, Avorn J, Bradbury BD, Liu J, Winkelmayer WC. Comparative mortality risk of anemia management practices in incident hemodialysis patients. JAMA. 2010;303:857–64.View ArticlePubMedGoogle Scholar
- Wolf M, Shah A, Gutierrez O, Ankers E, Monroy M, Tamez H, et al. Vitamin D levels and early mortality among incident hemodialysis patients. Kidney Int. 2007;72:1004–13.View ArticlePubMedGoogle Scholar
- Servilla KS, Singh AK, Hunt WC, Harford AM, Miskulin D, Meyer KB, et al. Anemia management and association of race with mortality and hospitalization in a large not-for-profit dialysis organization. Am J Kidney Dis. 2009;54:498–510.View ArticlePubMedGoogle Scholar
- Foley RN, Parfrey PS, Harnett JD, Kent GM, Murray DC, Barre PE. The impact of anemia on cardiomyopathy, morbidity, and and mortality in end-stage renal disease. Am J Kidney Dis. 1996;28:53–61.View ArticlePubMedGoogle Scholar
- Ofsthun N, Labrecque J, Lacson E, Keen M, Lazarus JM. The effects of higher hemoglobin levels on mortality and hospitalization in hemodialysis patients. Kidney Int. 2003;63:1908–14.View ArticlePubMedGoogle Scholar
- Gracia-Iguacel C, Gallar P, Qureshi AR, Ortega O, Mon C, Ortiz M, et al. Vitamin D deficiency in dialysis patients: effect of dialysis modality and implications on outcome. J Ren Nutr. 2010;20:359–67.View ArticlePubMedGoogle Scholar
- Pecovnik-Balon B, Jakopin E, Bevc S, Knehtl M, Gorenjak M. Vitamin D as a novel nontraditional risk factor for mortality in hemodialysis patients. Ther Apher Dial. 2009;13:268–72.View ArticlePubMedGoogle Scholar
- Bikle D. Nonclassic actions of vitamin D. J Clin Endocrinol Metab. 2009;94:26–34.View ArticlePubMedGoogle Scholar
- Looker AC, Johnson CL, Lacher DA, Pfeiffer CM, Schleicher RL, Sempos CT. Vitamin D status: United States, 2001–2006. NCHS Data Brief. 2011;59:1–8.PubMedGoogle Scholar
- Holick MF. Vitamin D, deficiency. N Engl J Med. 2007;357:266–81.View ArticlePubMedGoogle Scholar
- Pramyothin P, Holick MF. Vitamin D supplementation: guidelines and evidence for subclinical deficiency. Curr Opin Gastroenterol. 2012;28:139–50.View ArticlePubMedGoogle Scholar
- Jean G, Terrat JC, Vanel T, Hurot JM, Lorriaux C, Mayor B, et al. Daily oral 25-hydroxycholecalciferol supplementation for vitamin D deficiency in haemodialysis patients: effects on mineral metabolism and bone markers. Nephrol Dial Transplant. 2008;23:3670–6.View ArticlePubMedGoogle Scholar
- Sawinski D, Uribarri J, Peace D, Yao T, Wauhop P, Trzcinka P, et al. 25-OH-vitamin D deficiency and cellular alloimmunity as measured by panel of reactive T cell testing in dialysis patients. Am J Transplant. 2010;10:2287–95.View ArticlePubMedPubMed CentralGoogle Scholar
- Mehrotra R, Kermah D, Budoff M, Salusky IB, Mao SS, Gao YL, et al. Hypovitaminosis D in chronic kidney disease. Clin J Am Soc Nephrol. 2008;3:1144–51.View ArticlePubMedPubMed CentralGoogle Scholar
- Doorenbos CR, van den Born J, Navis G, de Borst MH. Possible renoprotection by vitamin D in chronic renal disease: beyond mineral metabolism. Nat Rev Nephrol. 2009;5:691–700.View ArticlePubMedGoogle Scholar
- Jacob AI, Sallman A, Santiz Z, Hollis BW. Defective photoproduction of cholecalciferol in normal and uremic humans. J Nutr. 1984;114:1313–9.PubMedGoogle Scholar
- Helvig CF, Cuerrier D, Hosfield CM, Ireland B, Kharebov AZ, Kim JW, et al. Dysregulation of renal vitamin D metabolism in the uremic rat. Kidney Int. 2010;78:463–72.View ArticlePubMedGoogle Scholar
- Lemire JM, Adams JS, Kermani-Arab V, Bakke AC, Sakai R, Jordan SC. 1,25-Dihydroxyvitamin D3 suppresses human T helper/inducer lymphocyte activity in vitro. J Immunol. 1985;134:3032–5.PubMedGoogle Scholar
- Manolagas SC, Provvedini DM, Tsoukas CD. Interactions of 1,25-dihydroxyvitamin D3 and the immune system. Mol Cell Endocrinol. 1985;43:113–22.View ArticlePubMedGoogle Scholar
- Piemonti L, Monti P, Sironi M, Fraticelli P, Leone BE, Dal Cin E, et al. Vitamin D3 affects differentiation, maturation, and function of human monocyte-derived dendritic cells. J Immunol. 2000;164:4443–51.View ArticlePubMedGoogle Scholar
- Chen S, Sims GP, Chen XX, Gu YY, Lipsky PE. Modulatory effects of 1,25-dihydroxyvitamin D3 on human B cell differentiation. J Immunol. 2007;179:1634–47.View ArticlePubMedGoogle Scholar
- Griffin MD, Kumar R. Effects of 1alpha,25(OH)2D3 and its analogs on dendritic cell function. J Cell Biochem. 2003;88:323–6.View ArticlePubMedGoogle Scholar
- Provvedini DM, Tsoukas CD, Deftos LJ, Manolagas SC. 1,25-dihydroxyvitamin D3 receptors in human leukocytes. Science. 1983;221:1181–3.View ArticlePubMedGoogle Scholar
- Provvedini DM, Tsoukas CD, Deftos LJ, Manolagas SC. 1 alpha,25-Dihydroxyvitamin D3-binding macromolecules in human B lymphocytes: effects on immunoglobulin production. J Immunol. 1986;136:2734–40.PubMedGoogle Scholar
- Effective Practice and Organisation of Care (EPOC), EPOC Resources for review authors. Oslo: Norwegian Knowledge Centre for the Health Services. http://epocoslo.cochrane.org/epoc-specific-resources-review-authors. Accessed 14 Jan 2015.
- Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151:264–9. W264.View ArticlePubMedGoogle Scholar
- Lehmann U, Hirche F, Stangl GI, Hinz K, Westphal S, Dierkes J. Bioavailability of vitamin D(2) and D(3) in healthy volunteers, a randomized placebo-controlled trial. J Clin Endocrinol Metab. 2013;98:4339–45.View ArticlePubMedGoogle Scholar
- Kramer H, Berns JS, Choi MJ, Martin K, Rocco MV. 25-Hydroxyvitamin D testing and supplementation in CKD: an NKF-KDOQI controversies report. Am J Kidney Dis. 2014;64:499–509.View ArticlePubMedGoogle Scholar
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