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Review
. 2012 Jan;21(1):72-9.
doi: 10.1097/MNH.0b013e32834de4ee.

Vitamin D: roles in renal and cardiovascular protection

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Review

Vitamin D: roles in renal and cardiovascular protection

Yan C Li. Curr Opin Nephrol Hypertens. 2012 Jan.

Abstract

Purpose of review: Great progress has been made in recent years in understanding the expanding roles of the vitamin D endocrine system beyond calcemic regulation, including pathophysiological actions in the kidney and the cardiovascular system. The purpose of this review is to update the recent advance regarding the effects of vitamin D and its analogs on the renal and cardiovascular system.

Recent findings: Vitamin D deficiency is not only widely associated with chronic kidney disease and cardiovascular disease in humans, but may also accelerate the disease progression. Dysregulation of vitamin D metabolism caused by renal insufficiency contributes to the low vitamin D status. Preclinical and clinical studies have demonstrated impressive therapeutic outcome with low-calcemic vitamin D analogs in renal and cardiovascular disease. The mechanism underlying the renal and cardiovascular protection involves regulation of multiple signaling pathways by vitamin D including nuclear factor κB, Wnt/β-catenin and the renin-angiotensin system.

Summary: The renal and cardiovascular protective activity of vitamin D revealed in recent studies has profound clinical implications. Nutritional correction of vitamin D deficiency and treatment with vitamin D analogs could be therapeutic options for renal and cardiovascular problems. New vitamin D analogs with better renal and cardiovascular therapeutic efficacy are highly desired. More randomized trials are needed to address these issues.

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Figures

Figure 1
Figure 1
Although 1,25 (OH) D3 has the greatest affinity for the vitamin D receptor, because of their similar chemical structures and much higher levels, ergocalcifetol is also a physiologically important agonist.

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References

    1. Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357:266–281. - PubMed
    1. Levin A, Bakris GL, Molitch M, et al. Prevalence of abnormal serum vitamin D, PTH, calcium, and phosphorus in patients with chronic kidney disease: results of the study to evaluate early kidney disease. Kidney Int. 2007;71:31–38. - PubMed
    1. Levin A, Le Barbier M, Er L, et al. Incident isolated 1,25(OH)2D3 deficiency is more common than 25(OH)D deficiency in CKD. J Nephrol. 2011 - PubMed
    1. Urena-Torres P, Metzger M, Haymann JP, et al. Association of Kidney Function, Vitamin D Deficiency, and Circulating Markers of Mineral and Bone Disorders in CKD. Am J Kidney Dis. 2011 - PubMed
    1. Patel NM, Gutierrez OM, Andress DL, et al. Vitamin D deficiency and anemia in early chronic kidney disease. Kidney Int. 2010;77:715–720. - PubMed

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