Vitamin D Deficiency and Replacement on Pulmonary and Endocrine Function in SCI

Overview

Studies have shown that individuals who have suffered a spinal cord injury are at an increased risk of Vitamin D deficiency compared to able-bodied individuals. It has recently been shown that Vitamin D deficiency is linked to a large number of diseases and conditions, including chronic lung disease, vascular problems, and insulin resistance. If this common nutritional deficiency is proven to be the cause of some of these diseases and conditions in persons with SCI, then it may easily be remedied with a cheap and effective therapeutic approach: vitamin D replacement therapy. Because of the high prevalence of vitamin D deficiency in persons with SCI, this therapy alone or in combination with other treatment options will be expected to significantly improve overall well being in the SCI population, decrease hospitalization rate, and the lower the financial burden of care.

Full Title of Study: “Effects of Vitamin D Deficiency and Its Replacement on Pulmonary and Endocrine Function in Persons With SCI”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Non-Randomized
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: December 2015

Detailed Description

Vitamin D deficiency is prevalent in individuals with Spinal Cord Injury (SCI). Recent studies have linked vitamin D with the prevention and/or treatment of a wide range of diseases, including chronic lung diseases. Patients with chronic lung diseases appear to be at increased risk for vitamin D deficiency for reasons that are not clear. Chronic lung diseases such as asthma and chronic obstructive lung disease (COPD) have been linked to vitamin D on a genetic basis. A recent observational study found a significant association between vitamin D deficiency and decreased pulmonary function in a large able-bodied population. The exact mechanisms involved have not been identified, but it has been postulated that vitamin D possesses a range of anti-inflammatory properties involving modulation of oxidative stress, or, possibly, protease/antiprotease balance and tissue damage/repair, mechanisms that have been shown to be important in the pathogenesis of chronic lung diseases. The relationship between vitamin D and the immune system is of utmost importance given that individuals with high cervical lesions express many obstructive aspects of pulmonary physiology commonly observed in individuals with asthma, in whom airway inflammation represents an underlying pathophysiological mechanism. In addition to a high prevalence of vitamin D deficiency, persons with SCI have a higher prevalence of insulin resistance (IR), impaired glucose tolerance (IGT) and diabetes mellitus (DM). In the general population, vitamin D deficiency has been shown to be associated with IR, IGT and DM. If treatment of vitamin D deficiency in persons with SCI is shown to be associated with improvement in insulin sensitivity and reductions in impaired glucose tolerance or DM, then progression to more severe carbohydrate disorders may be delayed or prevented.

Interventions

  • Drug: Vitamin D3
    • 4000 IU/day or 2000 IU/day for 12 weeks

Arms, Groups and Cohorts

  • No Intervention: Screening Study
    • To determine the prevalence and severity of vitamin D deficiency and glucose tolerance in persons with chronic SCI.
  • Experimental: Pulmonary Arm
    • Vitamin D3 Supplementation and Pulmonary Function: To determine the relationship between levels of vitamin D and overall pulmonary function, as measured by PFTs (spirometry and body plethysmography). To determine effects of vitamin D supplementations on overall pulmonary function and selected biomarkers of inflammation (FeNO, pH, 8- isoprostane levels).
  • Experimental: Endocrine Arm
    • Vitamin D3 Supplementation and Endocrine Function: To determine the effect of vitamin D replacement therapy on carbohydrate metabolism and insulin resistance in persons with vitamin D deficiency (<20ng/ml) and IGT, mild DM (e.g. fasting serum glucose <140 mg/dL) and/or IR.

Clinical Trial Outcome Measures

Primary Measures

  • Number of SCI participants with vitamin D deficiency
    • Time Frame: Screening study (1 visit, 2 hours)
    • Vitamin D levels will be obtained during screening.

Secondary Measures

  • Pulmonary function improvement as measured by PFTs in SCI with increased vitamin D levels
    • Time Frame: Change from baseline at 6 months
    • Pulmonary function change will be measured in vitamin D deficient SCI subjects by spirometry and body plethysmography at baseline, 3 months, and 6 months.

Participating in This Clinical Trial

Part 1: Screening for Vitamin D Deficiency Inclusion Criteria:

  • Between the ages of 18 and 75, – Chronic (>1 year) SCI; tetraplegia (C3-8), paraplegia, (T1-6) Exclusion Criteria:

  • Acute illness – Acute drug or alcohol use – Lack of mental capacity to give informed consent, – Pregnancy, – Currently receiving Vitamin D supplementation. Part 2A: Vitamin D and Pulmonary Function Inclusion Criteria:

  • Between the ages of 18 and 75, – Chronic SCI (>1 year, C3-T6) – Vitamin D deficiency as defined as a value <20 ng/ml. Exclusion Criteria:

  • Smoking, active or history of smoking during life time, – Any history of blast injuries to the chest, – Active respiratory disease, – Pregnancy, – Lack of mental capacity to give informed consent. – Recent (within 3 months) respiratory infection. – Receiving medications known to alter airway caliber. – Acute drug or alcohol use, – Currently receiving Vitamin D supplementation > 1000 units/day. Part 2B: Vitamin D, Carbohydrate Metabolism, and Insulin Resistance Inclusion Criteria:

  • Between the ages of 18 and 75, – Chronic SCI (>1 year, C3-T6) – Vitamin D deficiency as defined as a value <20 ng/ml, – Insulin Resistance (IR), Impaired glucose tolerance (IGT), and/or Diabetes Mellitus (DM). Exclusion Criteria:

  • Pregnancy, – Problems with the kidneys, – Lack of mental capacity to give informed consent, – Acute drug or alcohol use, – Currently receiving Vitamin D supplementation > 1000 units/day.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 75 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • James J. Peters Veterans Affairs Medical Center
  • Provider of Information About this Clinical Study
    • Principal Investigator: William A. Bauman, M.D., Research Center Director – James J. Peters Veterans Affairs Medical Center
  • Overall Official(s)
    • William Bauman, M.D., Principal Investigator, James J Peters VA Medical Center

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