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Vitamin D Deficiency and Risk for Cardiovascular Disease

Suzanne Judd, MPH, PhD2 and Vin Tangpricha, MD, PhD1,3,4
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Abstract

Vitamin D is an important pro-hormone for optimal intestinal calcium absorption for mineralization of bone. Since the vitamin D receptor is present in multiple tissues, there has been interest in evaluating other potential functions of vitamin D, particularly in cardiovascular diseases. Cross-sectional studies have reported that vitamin D deficiency is associated with increased risk of cardiovascular disease, including hypertension, heart failure and ischemic heart disease. Initial prospective studies have also demonstrated that vitamin D deficiency increases the risk of developing incident hypertension or sudden cardiac death in individuals with pre-existing cardiovascular disease. Very few prospective clinical studies have been conducted to examine the effect of vitamin D supplementation on cardiovascular outcomes. The mechanism for how vitamin D may improve cardiovascular disease outcomes remains obscure; however, potential hypotheses include the down regulation of the renin-angiotensin-aldosterone system, direct effects on the heart and vasculature or improvement of glycemic control. This review will examine the epidemiologic and clinical evidence for vitamin D deficiency as a cardiovascular risk factor and to explore potential mechanisms for the cardio-protective effect of vitamin D.

Keywords: Vitamin D, cholecalciferol, ergocalciferol cardiovascular disease, hypertension

INTRODUCTION

The classic function of vitamin D is to increase the intestinal absorption of calcium for proper mineralization of bone1. The active form of vitamin D, 1,25-dihydroxyvitamin D (1,25(OH)2D), acts as a steroid hormone by binding to the vitamin D receptor (VDR) which is present in many cells throughout the body including cardiomyocytes2, vascular smooth muscle3 and endothelium4. Recent evidence has demonstrated that individuals deficient in vitamin D are more likely to have cardiovascular disease or are at risk of developing incident cardiovascular disease. The mechanism for how vitamin D may protect individuals from cardiovascular disease has not been fully elucidated. Several mechanisms have been proposed including negatively regulating renin to lower blood pressure, improving vascular compliance, decreasing parathyroid hormone levels and improving glycemic control. The purpose of this review is to summarize the epidemiologic and early pre-clinical and clinical evidence for a protective role for vitamin D in the cardiovascular system.

PHYSIOLOGY OF VITAMIN D

Vitamin D can be produced in the skin as vitamin D3 upon exposure to ultraviolet- B (UVB) from the sun or obtained from the diet as vitamin D2 or vitamin D3. After vitamin D enters the body, it circulates bound to vitamin D binding protein (DBP) and is rapidly converted to its major circulating form, 25-hydroxyvitamin D (25(OH)D) by the liver. Under the influence of parathyroid hormone (PTH), 25(OH)D is converted by the 1-alpha-hydroxylase (1α-OHase) in the kidney to form the hormonal form of vitamin D, 1,25-dihydroxyvitamin D (1,25(OH)2D). Other tissues in the body have the 1α-OHase and can convert 25(OH)D to 1,25(OH)2D5. However, only the renal 1α-OHase significantly contributes to circulating 1,25(OH)2D levels. It is speculated that the presence of the extra-renal 1α-OHases allow 25(OH)D to be converted to 1,25(OH)2D to work as a paracrine or autocrine hormone

Circulating 1,25(OH)2D enters the target cell, either in its free form or facilitated by megalin, and binds to the vitamin D receptor (VDR) in the cytoplasm which then translocates to the nucleus and heterodimerizes with the retinoic x receptor (RXR)6. The 1,25(OH)2D-VDR-RXR complex then binds to vitamin D response elements (VDRE) on DNA to increase transcription of vitamin D regulated genes. Classic functions regulated by vitamin D include genes important for mineralization of bone and calcium transport in the intestine7. Non-classic or novel functions of vitamin D under investigation include genes important for innate immunity, cancer proliferation, muscle (both skeletal and smooth) function and endothelial cell proliferation5.

Vitamin D status is best determined by a serum 25(OH)D as opposed to 1,25(OH)2D, for several reasons including 1) its long circulating half life (~3 weeks versus ~8 hours), 2) the concentration of 25(OH)D is 1000x higher in circulation compared to 1,25(OH)2D (ng/mL vs pg/mL) and 3) the production of 1,25(OH)2D is mainly under the influence of PTH which tightly regulates calcium levels. Thus, 1,25(OH)2D levels could be elevated in individuals with severe vitamin D deficiency in order to maintain normal serum calcium levels. As a mediator of cardiovascular disease, it is believed that 25(OH)D is the best biomarker to describe vitamin D status, although this has not been proven.

CROSS-SECTIONAL AND EPIDEMIOLOGIC EVIDENCE EVALUATING VITAMIN D STATUS AND CARDIOVASCULAR DISEASE RISK

Several observations in the early 1980s and 1990s suggested that an environmental factor such as vitamin D could explain differences in mortality from ischemic heart disease (IHD). Fleck recognized higher mortality rates with increased distance from the equator8. Grimes et al also recognized that mortality from IHD was inversely proportional to the amount of hours of sunlight in the United Kingdom 9. He proposed vitamin D as a protective factor by regulating serum cholesterol levels or by inhibiting Chlamydia pneumoniae, once thought to be a cause of coronary heart disease. Douglas et al recognized that incidence and mortality rates from coronary heart disease demonstrated a strong seasonal pattern with higher rates in the winter, when vitamin D levels are lowest 10. Rostand reported that blood pressure increased with increasing distance from the equator and suggested that cutaneously synthesized vitamin D could be playing a role in the regulation of blood pressure11.

The National Health and Nutritional Examination Surveys (NHANES) (1988-1994, 2000-2004) conducted in the United States have provided a means to explore cross-sectional associations between vitamin D status and cardiovascular disease (CVD). Kendrick et al reported that individuals surveyed in NHANES 1988-1994 with vitamin D deficiency (25(OH)D <20 ng/mL) had higher prevalence of self reported angina, myocardial infarction and heart failure compared to individuals with higher levels of vitamin D, (OR (95% CI) 1.20 (1.01, 1.36))12. In the most recent NHANES 2000-2004 survey, vitamin D deficiency (25(OH)D <20 ng/mL) was associated with increased prevalence of self reported coronary heart disease, heart failure and peripheral vascular disease13. Several cardiovascular risk factors have been associated with lower vitamin D status including hypertension, diabetes, elevated body mass index (>30), elevated triglyceride level and microalbuminuria in NHANES 1988-199414,15. Prevalence of peripheral arterial disease is also increased comparing lowest quartile of 25(OH)D to highest quartile of 25(OH)D16. Judd et al determined in non-hypertensive individuals from NHANES 1988-1994, optimal vitamin D status (>32 ng/mL) provided a 20% reduction in the rate of blood pressure rise with age17. In contrast, smaller cross-sectional studies from Germany18 and the Netherlands19 have not been able to confirm an association between vitamin D status and blood pressure in older adults.

Melamed et al examined all cause mortality by quartile of 25(OH)D and found that the lowest quartile of 25(OH)D had significantly increased adjusted mortality rate ratios (MRR (95% CI) 1.28 (1.11-1.48) compared to individuals with the highest quartile of 25(OH)D20. There was a trend towards increased mortality rate in the lowest quartile of 25(OH)D due to cardiovascular mortality; however, this did not reach statistical significance (MRR (95% CI) 1.22 (0.90 - 1.65)). Thus, several epidemiologic findings seem to suggest that poor vitamin D status is associated with poor cardiovascular outcomes.

COHORT AND CASE-CONTROL STUDIES EVALUATING VITAMIN D STATUS AND CARDIOVASCULAR DISEASE RISK

Several studies have evaluated a baseline measurement of vitamin D status and prospectively evaluated long-term cardiovascular outcomes in subjects with no previous history of CVD. During a 10 year follow-up period, men in the Health Professionals Follow-up Study (HPFS) without previous CVD and vitamin D deficiency (25(OH)D < 15 ng/mL) exhibited a 2-fold increased rate of myocardial infarction.21. In the Framingham Offspring Study, subjects with no previous history of CVD and severe vitamin D deficiency (25(OH)D <10 ng/mL) experienced a hazard ratio of 1.80 (95% CI, 1.05 - 3.08) for developing a first cardiovascular event after 5 years of follow-up compared to subjects with higher levels of 25(OH)D (>15 ng/mL)22.

Vitamin D status and risk of CVD has also been evaluated in subjects with established cardiovascular disease or end stage kidney disease (ESRD). In over 3000 subjects undergoing coronary angiography, severe vitamin D deficiency (25(OH)D <10 ng/mL) had 3 - 5 times risk of dying from sudden cardiac death or heart failure over a 7 year follow-up period compared to optimal levels of vitamin D (25(OH)D >30 ng/mL)23. Further, in these same subjects, vitamin D deficiency imparted a 50% increase in fatal stroke24. Subjects in the lowest quartile for 25(OH)D had increased hazard ratios for all cause and cardiovascular mortality compared to subjects in the highest quartile for 25(OH)D25. Similar findings have been reported in incident hemodialysis patients26. An earlier and smaller study from India did not establish any benefit from having optimal levels of 25(OH)D in subjects with established CVD27. In contrast, they reported that very high levels of 25(OH)D (>89 ng/mL) were associated increased risk of ischemic heart disease.

Several studies have examined the relationship between vitamin D status and incident hypertension. Men and Women participating in the HPFS and the Nurses' Health Study with vitamin D deficiency (< 15 ng/mL) had 3 - 6 fold increased risk of developing incident hypertension over a 4 year follow-up period compared to subjects with optimal vitamin D status28. Similar protection with having optimal vitamin D status and the development of incident hypertension was seen in the Nurses Health Study II, a group of younger female subjects29. A large cohort study from the United Kingdom also reported that vitamin D status was inversely related to the development of components of the metabolic syndrome including hypertension30.

RANDOMIZED CONTROLLED TRIALS OF VITAMIN D SUPPLMENTATION AND RISK OF CARDIOVASCULAR DISEASE

Given the early epidemiologic associations between vitamin D and hypertension, early studies of vitamin D supplementation have focused on vitamin D as a potential anti-hypertensive agent. A randomized controlled trial conducted in elderly German women demonstrated that modest amounts of vitamin D (400IU) plus calcium given over 8 week period significantly reduced systolic blood pressure by 9%31. Krause et al randomized 18 subjects with stage I hypertension to UVA exposure to skin (which does not produce vitamin D) and to UVB exposure to skin (which produces vitamin D3) and demonstrated that systolic and diastolic blood pressure significantly decreased after 6 weeks of therapy in those subjects receiving UVB therapy, suggesting that cutaneously produced vitamin D resulted in lowered blood pressure32. In contrast, several smaller studies conducted primarily in elderly subjects have demonstrated no effect of vitamin D supplementation on blood pressure in Denmark33, in Taiwan34, and in the UK35. The Women's Health Initiative Study (WHI) conducted in the U.S. demonstrated no significant difference in systolic or diastolic blood pressure in women randomized to calcium and vitamin D (400 IU) at the end of 7 years of follow-up. Therefore, studies on vitamin D supplementation have not consistently demonstrated a positive effect on regulating blood pressure. However, several caveats should be noted including relatively low doses of vitamin D used as the intervention (typically ~400 IU), most studies did not demonstrate adequate improvement of 25(OH)D to optimal levels (>30 ng/mL), and adherence was low particular in the WHI study.

Very few studies have been conducted to evaluate vitamin D supplementation on risk of cardiovascular mortality. Two studies prospectively examined vitamin D supplementation on cardiovascular mortality. In the WHI, women randomized to vitamin D 400 IU daily and 1000 mg of calcium had no difference in all cause or cardiovascular mortality36. In a European study by Trivedi et al, elderly individuals receiving a daily equivalent dose of 800 IU of vitamin D did not have improved cardiovascular survival compared to controls37. A recent meta-analysis examined 9 randomized controlled trials and found a 8% reduction in all cause mortality with supplementation of very modest amounts of vitamin D (~500 IU). In this meta-analysis, cardiovascular mortality was reported only by two studies as discussed above36,37. The Institutes of Medicine currently recommend a daily intake of 400 - 600 IU of vitamin D for adults. Several experts believe this intake level is inadequate for adults to maintain a optimal vitamin D status and a daily intake of close to 1000 IU of vitamin D is required to maintain health38.

PROPOSED PROTECTIVE MECHANISMS FOR VITAMIN D IN CARDIOVASCULAR DISEASE

The mechanism for how vitamin D may protect against cardiovascular disease has not been fully elucidated. Proposed mechanisms include effects on the renin-angiotensin system, on glycemic control, inflammatory cytokines, direct effects on the vasculature and regulation of parathyroid hormone levels and calcium deposition in vascular smooth muscle22,39,40. Studies to examine these mechanisms have been conducted mainly in pre-clinical studies with very little information available from clinical trials.

Vitamin D as a negative regulator of renin

Pioneering work by Yan Chun Li at the University of Chicago has re-invigorated interest in vitamin D as an anti-hypertensive agent. His group clearly established that vitamin D receptor (VDR) knock-out mice have elevated blood pressure, cardiac hypertrophy and elevated activation of the renin-angiotensin-aldosterone system (RAAS) which can be reversed with an angiotensin converting enzyme inhibitor41. Furthermore, wild type mice given injections of 1,25(OH)2D3 demonstrated suppression of renin mRNA expression41. Several novel vitamin D analogues have also been demonstrated to inhibit renin expression in vitro, possibly leading to the development of specific cardio-selective vitamin D compounds for the treatment of hypertension without calcemic effects42. In a follow-up study, Li and colleagues demonstrated that 1,25(OH)2D inhibits renin gene expression by sequestering cAMP response element binding (CREB ), a necessary factor for the transcription of renin mRNA43. These very intriguing observations have yet to be translated in rigorous randomized controlled trials of vitamin D or its analogues on hypertension and signaling of the RAAS.

Vitamin D as a factor in improving insulin sensitivity

The pancreas possesses the vitamin D receptor (VDR) and the 1-alpha-hydroxylase and thus has the vitamin D machinery for circulating 25(OH)D to be converted to 1,25(OH)2D to work as a paracrine or autocrine hormone Early studies have suggested that vitamin D deficient rodents are not able to adequately secrete insulin compared to vitamin D sufficient controls44. Several small observational and case-control studies have been published to suggest that vitamin D deficiency is associated with insulin resistance or impaired insulin secretion45,46. Several studies including one published by Scragg et al demonstrated that lower vitamin D status was associated with increased risk of diabetes and better insulin sensitivity 47,48. In a longitudinal study of Finnish men and women, a 40% reduction in risk of developing Type II diabetes was observed after 17 years of follow-up in those with 25(OH)D levels > 28 ng/mL at baseline49. One prospective study evaluated the effect of vitamin D supplementation (400 IU daily) on fasting glucose and found that subjects with impaired fasting glucose at baseline had less of a rise in fasting glucose concentrations over a 3 year period compared to subjects randomized to placebo50. Taken together, this early evidence suggests that vitamin D may have an important role in regulating glycemic control which may also contribute to a benefical effect on cardiovascular outcomes.

Vitamin D as a direct factor on cardiac tissues and the vasculature

A few in vitro and in vivo studies have evaluated the role of vitamin D acting directly on cardiac tissue, especially in response to injury. Rahman et al demonstrated that matrix metalloproteinases (MMP), proteins that contribute to aberrant cardiomyocyte remodeling in response to injury and atherosclerosis, were up-regulated in vitamin D receptor knockout mice51. Vitamin D receptor knock-out mice have impaired cardiac relaxation and contractility52 and develop left ventricular hypertrophy41,53.

Clinical studies have evaluated the role of vitamin D directly on the vasculature. A cross-sectional study of 52 subjects with ESRD demonstrated a significant positive correlation between vitamin D status and arterial compliance measured by brachial artery flow mediated dilation and a negative correlation between aortic pulse wave velocity, both findings indicating decreased vascular compliance54. Vitamin D (1,25-hydroxyvitamin D) inhibited pro-fibrotic markers in vitro using mesenchymal multipotent cells, suggesting that vitamin D may also have a direct effect on the vasculature in response to injury55. Diabetic patients who ingested a single large dose of vitamin D (100,000 IU) had significant improvement in endothelial function measured by flow mediated dilation and decrease in blood pressure56. Finally, a recent randomized controlled trial of vitamin D supplementation in subjects with heart failure demonstrated significant reductions in inflammatory cytokines involved in the pathophysiology of heart failure57.

CONCLUSION

Vitamin D insufficiency is very common in the United States and world-wide. Several recent epidemiologic studies have demonstrated a strong association between vitamin D insufficiency and risk of cardiovascular disease, risk of diabetes and metabolic syndrome. Several prospective studies have suggested that vitamin D deficiency predisposes individuals to increased risk of incident hypertension, ischemic heart disease, sudden cardiac death or heart failure. Initial randomized clinical trials of vitamin D in the treatment of hypertension have yielded mixed results; however, the study design of these trials limits definitive conclusions. No large randomized clinical trial using vitamin D or its analogues on cardiovascular endpoints have been published to date.

The potential for vitamin D to have a role in the prevention and/or treatment of cardiovascular disease has some biologic plausibility. Several studies have demonstrated that vitamin D receptor knockout mice have increased surrogate markers of cardiovascular disease including hypertension, left ventricular hypertrophy and increased proteinuria. One of the leading hypotheses for the protective effects of vitamin D is its negative regulation on the renin-angiotensin-aldosterone system. Other mechanisms may also include effects on cardiac remodeling, the vasculature, inflammatory markers and glycemic control.

The results of future trials should provide guidance on how to manage vitamin D status in clinical practice. There are currently no universal guidelines for the screening and treatment of vitamin D insufficiency. Furthermore, the adequate intake levels established by the Institutes of Medicine have been recognized to be inadequate and are currently in revision. In the meantime, it may be prudent to screen individuals who are at highest risk for vitamin D insufficiency (institutionalized elderly, osteoporotic individuals, chronically ill patients, African-American patients, especially those with cardiovascular disease58) and treat with vitamin D to a 25(OH)D level of 30 ng/mL. The current evidence does not strongly support screening for vitamin D deficiency in all patients with established CVD or who are at risk for CVD. For the general population, increasing vitamin D status with a daily supplement containing at least 1000 IU of may be sufficient, especially in areas with increased latitude from the equator or during the winter months.

Acknowledgments

The manuscript was supported in part by NIH K23 AR054334 (VT)

Footnotes

The authors have no conflicts of interest to disclosure

REFERENCES

1. Khazai N, Judd SE, Tangpricha V. Calcium and vitamin D: skeletal and extraskeletal health. Curr Rheumatol Rep. 2008 Apr;10(2):110–7. [PMC free article] [PubMed]
2. Nibbelink KA, Tishkoff DX, Hershey SD, Rahman A, Simpson RU. 1,25(OH)2-vitamin D3 actions on cell proliferation, size, gene expression, and receptor localization, in the HL-1 cardiac myocyte. J Steroid Biochem Mol Biol. 2007 Mar;103(35):533–7. [PMC free article] [PubMed]
3. Wu-Wong JR, Nakane M, Ma J, Ruan X, Kroeger PE. Effects of Vitamin D analogs on gene expression profiling in human coronary artery smooth muscle cells. Atherosclerosis. 2006 May;186(1):20–8. [PubMed]
4. Merke J, Milde P, Lewicka S, Hügel U, Klaus G, Mangelsdorf DJ, Haussler MR, Rauterberg EW, Ritz E. Identification and regulation of 1,25-dihydroxyvitamin D3 receptor activity and biosynthesis of 1,25-dihydroxyvitamin D3. Studies in cultured bovine aortic endothelial cells and human dermal capillaries. J Clin Invest. 1989 Jun;83(6):1903–15. [PMC free article] [PubMed]
5. Holick MF. Vitamin D deficiency. N Engl J Med. 2007 Jul 19;357(3):266–81. [PubMed]
6. Rowling MJ, Kemmis CM, Taffany DA, Welsh J. Megalin-mediated endocytosis of vitamin D binding protein correlates with 25-hydroxycholecalciferol actions in human mammary cells. J Nutr. 2006 Nov;136(11):2754–9. [PMC free article] [PubMed]
7. Pike JW, Zella LA, Meyer MB, Fretz JA, Kim S. Molecular actions of 1,25-dihydroxyvitamin D3 on genes involved in calcium homeostasis. J Bone Miner Res. 2007 Dec;22(Suppl 2):V16–9. [PubMed]
8. Fleck A. Latitude and ischaemic heart disease. Lancet. 1989 Mar 18;1(8638):613. [PubMed]
9. Grimes DS, Hindle E, Dyer T. Sunlight, cholesterol and coronary heart disease. QJM. 1996 Aug;89(8):579–89. [PubMed]
10. Douglas AS, Dunnigan MG, Allan TM, Rawles JM. Seasonal variation in coronary heart disease in Scotland. J Epidemiol Community Health. 1995 Dec;49(6):575–82. Click here to read J Epidemiol Community Health. 1995 Dec;49(6):575-82. [PMC free article] [PubMed]
11. Rostand SG. Ultraviolet light may contribute to geographic and racial blood pressure differences. Hypertension. 1997 Aug;30(2 Pt 1):150–6. [PubMed]
12. Kendrick J, Targher G, Smits G, Chonchol M. 25-Hydroxyvitamin D deficiency is independently associated with cardiovascular disease in the Third National Health and Nutrition Examination Survey. Atherosclerosis. 2008 Nov 11; Epub ahead of print. [PubMed]
13. Kim DH, Sabour S, Sagar UN, Adams S, Whellan DJ. Prevalence of hypovitaminosis D in cardiovascular diseases (from the National Health and Nutrition Examination Survey 2001 to 2004) Am J Cardiol. 2008 Dec 1;102(11):1540–4. [PubMed]
14. Martins D, Wolf M, Pan D, Zadshir A, Tareen N, Thadhani R, Felsenfeld A, Levine B, Mehrotra R, Norris K. Prevalence of cardiovascular risk factors and the serum levels of 25-hydroxyvitamin D in the United States: data from the Third National Health and Nutrition Examination Survey. Arch Intern Med. 2007 Jun 11;167(11):1159–65. [PubMed]
15. Scragg R, Sowers M, Bell C. Serum 25-hydroxyvitamin D, ethnicity, and blood pressure in the Third National Health and Nutrition Examination Survey. Am J Hypertens. 2007 Jul;20(7):713–9. [PubMed]
16. Melamed ML, Muntner P, Michos ED, Uribarri J, Weber C, Sharma J, Raggi P. Serum 25-hydroxyvitamin D levels and the prevalence of peripheral arterial disease: results from NHANES 2001 to 2004. Arterioscler Thromb Vasc Biol. 2008 Jun;28(6):1179–85. [PMC free article] [PubMed]
17. Judd SE, Nanes MS, Ziegler TR, Wilson PW, Tangpricha V. Optimal vitamin D status attenuates the age-associated increase in systolic blood pressure in white Americans: results from the third National Health and Nutrition Examination Survey. Am J Clin Nutr. 2008 Jan;87(1):136–41. [PubMed]
18. Hintzpeter B, Mensink GB, Thierfelder W, Müller MJ, Scheidt-Nave C. Vitamin D status and health correlates among German adults. Eur J Clin Nutr. 2008 Sep;62(9):1079–89. [PubMed]
19. Snijder MB, Lips P, Seidell JC, Visser M, Deeg DJ, Dekker JM, van Dam RM. Vitamin D status and parathyroid hormone levels in relation to blood pressure: a population-based study in older men and women. J Intern Med. 2007 Jun;261(6):558–65. [PubMed]
20. Melamed ML, Michos ED, Post W, Astor B. 25-hydroxyvitamin D levels and the risk of mortality in the general population. Arch Intern Med. 2008 Aug 11;168(15):1629–37. [PMC free article] [PubMed]
21. Giovannucci E, Liu Y, Hollis BW, Rimm EB. 25-hydroxyvitamin D and risk of myocardial infarction in men: a prospective study. Arch Intern Med. 2008 Jun 9;168(11):1174–80. [PMC free article] [PubMed]
22. Wang TJ, Pencina MJ, Booth SL, Jacques PF, Ingelsson E, Lanier K, Benjamin EJ, D'Agostino RB, Wolf M, Vasan RS. Vitamin D deficiency and risk of cardiovascular disease. Circulation. 2008 Jan 29;117(4):503–11. [PMC free article] [PubMed]
23. Pilz S, März W, Wellnitz B, Seelhorst U, Fahrleitner-Pammer A, Dimai HP, Boehm BO, Dobnig H. Association of vitamin D deficiency with heart failure and sudden cardiac death in a large cross-sectional study of patients referred for coronary angiography. J Clin Endocrinol Metab. 2008 Oct;93(10):3927–35. [PubMed]
24. Pilz S, Dobnig H, Fischer JE, Boehm BO, März W. Low vitamin D levels predict stroke in patients referred to coronary angiography. Stroke. 2008;39:2611–2613. [PubMed]
25. Dobnig H, Pilz S, Scharnagl H, Renner W, Seelhorst U, Wellnitz B, Kinkeldei J, Boehm BO, Weihrauch G, Maerz W. Independent association of low serum 25-hydroxyvitamin d and 1,25-dihydroxyvitamin d levels with all-cause and cardiovascular mortality. Arch Intern Med. 2008 Jun 23;168(12):1340–9. [PubMed]
26. Wolf M, Shah A, Gutierrez O, Ankers E, Monroy M, Tamez H, Steele D, Chang Y, Camargo CA, Jr, Tonelli M, Thadhani R. Vitamin D levels and early mortality among incident hemodialysis patients. Kidney Int. 2007 Oct;72(8):1004–13. [PubMed]
27. Rajasree S, Rajpal K, Kartha CC, Sarma PS, Kutty VR, Iyer CS, Girija G. Serum 25-hydroxyvitamin D3 levels are elevated in South Indian patients with ischemic heart disease. Eur J Epidemiol. 2001;17(6):567–71. [PubMed]
28. Forman JP, Giovannucci E, Holmes MD, Bischoff-Ferrari HA, Tworoger SS, Willett WC, Curhan GC. Plasma 25-hydroxyvitamin D levels and risk of incident hypertension. Hypertension. 2007 May;49(5):1063–9. [PubMed]
29. Forman JP, Curhan GC, Taylor EN. Plasma 25-hydroxyvitamin D levels and risk of incident hypertension among young women. Hypertension. 2008 Nov;52(5):828–32. [PMC free article] [PubMed]
30. Hyppönen E, Boucher BJ, Berry DJ, Power C. 25-hydroxyvitamin D, IGF-1, and metabolic syndrome at 45 years of age: a cross-sectional study in the 1958 British Birth Cohort. Diabetes. 2008 Feb;57(2):298–305. [PubMed]
31. Pfeifer M, Begerow B, Minne HW, Nachtigall D, Hansen C. Effects of a short-term vitamin D(3) and calcium supplementation on blood pressure and parathyroid hormone levels in elderly women. J Clin Endocrinol Metab. 2001 Apr;86(4):1633–7. [PubMed]
32. Krause R, Bühring M, Hopfenmüller W, Holick MF, Sharma AM. Ultraviolet B and blood pressure. Lancet. 1998 Aug 29;352(9129):709–10. [PubMed]
33. Myrup B, Jensen GF, McNair P. Cardiovascular risk factors during estrogennorethindrone and cholecalciferol treatment. Arch Intern Med. 1992 Nov;152(11):2265–8. [PubMed]
34. Pan WH, Wang CY, Li LA, Kao LS, Yeh SH. No significant effect of calcium and vitamin D supplementation on blood pressure and calcium metabolism in elderly Chinese. Chin J Physiol. 1993;36(2):85–94. [PubMed]
35. Scragg R, Khaw KT, Murphy S. Effect of winter oral vitamin D3 supplementation on cardiovascular risk factors in elderly adults. Eur J Clin Nutr. 1995 Sep;49(9):640–6. [PubMed]
36. Lacroix AZ, Kotchen J, Anderson G, Brzyski R, Cauley JA, Cummings SR, Gass M, Johnson KC, Ko M, Larson J, Manson JE, Stefanick ML, Wactawski-Wende J. Calcium Plus Vitamin D Supplementation and Mortality in Postmenopausal Women: The Women's Health Initiative Calcium-Vitamin D Randomized Controlled Trial. J Gerontol A Biol Sci Med Sci. 2009 Feb 16; Epub ahead of print. [PMC free article] [PubMed]
37. Trivedi DP, Doll R, Khaw KT. Effect of four monthly oral vitamin D3 (cholecalciferol) supplementation on fractures and mortality in men and women living in the community: randomised double blind controlled trial. BMJ. 2003 Mar 1;326(7387):469. [PMC free article] [PubMed]
38. Vieth R, Bischoff-Ferrari H, Boucher BJ, Dawson-Hughes B, Garland CF, Heaney RP, Holick MF, Hollis BW, Lamberg-Allardt C, McGrath JJ, Norman AW, Scragg R, Whiting SJ, Willett WC, Zittermann A. The urgent need to recommend an intake of vitamin D that is effective. Am J Clin Nutr. 2007 Mar;85(3):649–50. [PubMed]
39. Zittermann A, Schleithoff SS, Koerfer R. Vitamin D and vascular calcification. Curr Opin Lipidol. 2007 Feb;18(1):41–6. [PubMed]
40. Fitzpatrick LA, Bilezikian JP, Silverberg SJ. Parathyroid hormone and the cardiovascular system. Curr Osteoporos Rep. 2008 Jun;6(2):77–83. [PubMed]
41. Li YC, Kong J, Wei M, Chen ZF, Liu SQ, Cao LP. 1,25-Dihydroxyvitamin D(3) is a negative endocrine regulator of the renin-angiotensin system. J Clin Invest. 2002 Jul;110(2):229–38. [PMC free article] [PubMed]
42. Qiao G, Kong J, Uskokovic M, Li YC. Analogs of 1alpha,25-dihydroxyvitamin D(3) as novel inhibitors of renin biosynthesis. J Steroid Biochem Mol Biol. 2005 Jun;96(1):59–66. [PubMed]
43. Yuan W, Pan W, Kong J, Zheng W, Szeto FL, Wong KE, Cohen R, Klopot A, Zhang Z, Li YC. 1,25-dihydroxyvitamin D3 suppresses renin gene transcription by blocking the activity of the cyclic AMP response element in the renin gene promoter. J Biol Chem. 2007 Oct 12;282(41):29821–30. [PubMed]
44. Norman AW, Frankel JB, Heldt AM, Grodsky GM. Vitamin D deficiency inhibits pancreatic secretion of insulin. Science. 1980 Aug 15;209(4458):823–5. [PubMed]
45. Mathieu C, Gysemans C, Giulietti A, Bouillon R. Vitamin D and diabetes. Diabetologia. 2005 Jul;48(7):1247–57. [PubMed]
46. Liu E, Meigs JB, Pittas AG, McKeown NM, Economos CD, Booth SL, Jacques PF. Plasma 25-hydroxyvitamin d is associated with markers of the insulin resistant phenotype in nondiabetic adults. J Nutr. 2009 Feb;139(2):329–34. [PMC free article] [PubMed]
47. Scragg R, Sowers M, Bell C. Serum 25-hydroxyvitamin D, diabetes, and ethnicity in the Third National Health and Nutrition Examination Survey. Diabetes Care. 2004 Dec;27(12):2813–8. [PubMed]
48. Chonchol M, Scragg R. 25-Hydroxyvitamin D, insulin resistance, and kidney function in the Third National Health and Nutrition Examination Survey. Kidney Int. 2007 Jan;71(2):134–9. [PubMed]
49. Mattila C, Knekt P, Männistö S, Rissanen H, Laaksonen MA, Montonen J, Reunanen A. Serum 25-hydroxyvitamin D concentration and subsequent risk of type 2 diabetes. Diabetes Care. 2007 Oct;30(10):2569–70. [PubMed]
50. Pittas AG, Harris SS, Stark PC, Dawson-Hughes B. The effects of calcium and vitamin D supplementation on blood glucose and markers of inflammation in nondiabetic adults. Diabetes Care. 2007 Apr;30(4):980–6. [PubMed]
51. Rahman A, Hershey S, Ahmed S, Nibbelink K, Simpson RU. Heart extracellular matrix gene expression profile in the vitamin D receptor knockout mice. J Steroid Biochem Mol Biol. 2007 Mar;103(35):416–9. [PubMed]
52. Tishkoff DX, Nibbelink KA, Holmberg KH, Dandu L, Simpson RU. Functional vitamin D receptor (VDR) in the t-tubules of cardiac myocytes: VDR knockout cardiomyocyte contractility. Endocrinology. 2008 Feb;149(2):558–64. [PMC free article] [PubMed]
53. Simpson RU, Hershey SH, Nibbelink KA. Characterization of heart size and blood pressure in the vitamin D receptor knockout mouse. J Steroid Biochem Mol Biol. 2007 Mar;103(35):521–4. [PMC free article] [PubMed]
54. London GM, Guérin AP, Verbeke FH, Pannier B, Boutouyrie P, Marchais SJ, Mëtivier F. Mineral metabolism and arterial functions in end-stage renal disease: potential role of 25-hydroxyvitamin D deficiency. J Am Soc Nephrol. 2007 Feb;18(2):613–20. [PubMed]
55. Artaza JN, Norris KC. Vitamin D reduces the expression of collagen and key profibrotic factors by inducing an antifibrotic phenotype in mesenchymal multipotent cells. J Endocrinol. 2009 Feb;200(2):207–21. [PMC free article] [PubMed]
56. Sugden JA, Davies JI, Witham MD, Morris AD, Struthers AD. Vitamin D improves endothelial function in patients with Type 2 diabetes mellitus and low vitamin D levels. Diabet Med. 2008 Mar;25(3):320–5. [PubMed]
57. Schleithoff SS, Zittermann A, Tenderich G, Berthold HK, Stehle P, Koerfer R. Vitamin D supplementation improves cytokine profiles in patients with congestive heart failure: a double-blind, randomized, placebo-controlled trial. Am J Clin Nutr. 2006 Apr;83(4):754–9. [PubMed]
58. Alsafwah S, Laguardia SP, Nelson MD, Battin DL, Newman KP, Carbone LD, Weber KT. Hypovitaminosis D in African Americans residing in Memphis, Tennessee with and without heart failure. Am J Med Sci. 2008 Apr;335(4):292–7. [PubMed]
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