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Vitamin D has shown to play an important role in those with multiple sclerosis, chronic obstructive pulmonary disease (COPD), and even depression; now it looks like the same can be said about those with stage 3 or 4 chronic kidney disease (CKD).
Vitamin D has shown to play an important role in those with multiple sclerosis, chronic obstructive pulmonary disease (COPD), and even depression; now it looks like the same can be said about those with stage 3 or 4 chronic kidney disease (CKD).
In a poster session at the Endocrine Society’s annual meeting (ENDO 2016) in Boston, Massachusetts, researchers assessed disease activity associated with vitamin D levels.
“Vitamin D insufficiency (VDI) is defined as serum total 25-hydroxyvitamin D (25D) below 30 ng/mL in clinical practice guidelines applicable to secondary hyperparathyroidism (SHPT) in CKD,” wrote Stuart M Sprague, DO, from Northshore University Health System-University of Chicago, and colleagues.
Although current methods to raise VDI above 30 ng/mL have been sufficient, they do not control SHPT — which previous research has said is essential in order to maximally lower elevated intact parathyroid hormone (iPTH) in patients with CKD.
The team conducted two identical trials to evaluate the impact of modified-release calcifediol (MRC) on elevated plasma iPTH. A total of 429 patients (average age around 65) with low serum 25D levels (10 to 30 ng/mL) and stage 3 or 4 CKD were included in the studies. The average serum 25D ranged from 16.5 to 21.5 ng/mL and mean plasma iPTH was 134.8 to 156.5 pg/mL. In addition, the averge eGFR was 30.1 to 32.3 mL/min.1.73m².
Two-thirds of the participants received oral MRC for 26 weeks while the remaining one-third unknowingly took a placebo. Those who took MRC started by taking 30 µg/d at night and if plasma iPTH remained above 70 pg/mL after 12 weeks, the dose increased to 60 µg/d. A total of 356 of the 429 patients (83%) completed the study where the researchers then recorded their 25D levels.
“More than 95% of subjects treated with MRC achieved serum 25D levels of greater than 30 ng/mL at end of treatment,” the authors confirmed. No matter if the patient had stage 3 or 4 CKD, their mean 25D levels rose with MRC. Also, average plasma iPTH serum collagen type 1 C-telopeptide and serum procollagen type 1 N-terminal propeptide decreased with more 25D.
However, the vitamin D treatment did not affect serum calcium (Ca) or phosphorus (P), or urine Ca or P.
“These findings indicate that serum 25D levels recommended for non-CKD patients are insufficient to control SHPT in stage 3 or 4 CKD and that higher, more effective levels (>60 ng/mL) can be safely achieved with daily MRC,” the team concluded.
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