Hypovitaminosis D correction and high-sensitivity C-reactive protein levels in hypertensive adults

Nathan Carlson1, Robert Mah2, Maria Aburto3

  • 1Family Physician and Faculty of the Family Medicine Residency Program at the Fontana Medical Center in CA. nathan.d.carlson@kp.org Biostatistician in Research and Evaluation for the Southern California Permanente Medical Group in Pasadena, CA. lie.h.chen@kp.org.

The Permanente Journal
|December 24, 2013
PubMed

Insights

Correcting vitamin D deficiency in adults with hypertension did not significantly lower high-sensitivity C-reactive protein (hs-CRP) levels, a marker of cardiovascular inflammation. Most participants achieved normal vitamin D levels after treatment.

Area of Science:

  • Cardiology
  • Endocrinology
  • Nutritional Science

Background:

  • Hypovitaminosis D is a potential risk factor for cardiovascular disease.
  • High-sensitivity C-reactive protein (hs-CRP) is a key biomarker for cardiovascular inflammation and risk.
  • The effect of vitamin D repletion on hs-CRP in humans remains unclear.

Purpose of the Study:

  • To evaluate the laboratory accuracy of 25-hydroxyvitamin D (25-OH-vitamin D) and hs-CRP assays.
  • To determine if hs-CRP levels decrease after correcting hypovitaminosis D in hypertensive adults.

Main Methods:

  • Prospective, unblinded study design.
  • 108 adults with hypertension and low vitamin D levels were treated.
  • Ergocalciferol (50,000 IU weekly for 12 weeks) was administered.

Main Results:

  • Mean 25-OH-vitamin D increased from 20.07 ng/mL to 43.92 ng/mL.
  • 91% of subjects achieved normal vitamin D levels (>30 ng/mL).
  • No statistically significant change in hs-CRP levels was observed post-treatment.

Conclusions:

  • Correction of hypovitaminosis D did not lead to a significant reduction in hs-CRP levels.
  • Weekly ergocalciferol effectively corrected vitamin D deficiency in most participants.
  • Further research may be needed to explore the relationship between vitamin D and cardiovascular inflammation markers.
Abstract

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