Vitamin D Status in Patients With Severe Sepsis: A Randomized Clinical Trial

Sepsis is a clinical entity that complicates infections [1]. Without early recognition and timely management, it can rapidly progress to severe sepsis, septic shock, and culminate in multiple organ dysfunction syndrome. The incidence of severe sepsis is between 300 to 1000 cases per 100,000 persons [2] and is projected to increase annually due to an aging population, increasing burden of chronic disease, and greater use of invasive procedures, chemotherapy, and immunosuppressive agents [3]. Severe sepsis is the leading cause of mortality in critically ill patients, with healthcare costs exceeding $16 billion annually [4]. Despite evolving clinical guidelines for sepsis [5-7], and intense research, only a modest reduction in case fatality rates has been documented over the last two decades [8]. Aside from early administration of antibiotics, there is no effective stand-alone or adjuvant pharmacological intervention to improve survival in patients with severe sepsis.

The degree of immune dysfunction precipitated by an inciting infection is thought to correlate with the severity of sepsis. Recently, key cells of the immune system were shown to express the vitamin D receptor (VDR) [9]. Additionally, macrophages and neutrophils activated through VDR up-regulate expression of endogenous antimicrobial peptides (AMPs) that are active against a broad spectrum of infectious agents [10]. AMPs, influenced by vitamin D status, likely represent an important first-line of defense against microbial invasion. While circulating 25-hydroxyvitamin D (25OHD) is the most abundant vitamin D metabolite [11], under normal circumstances, 85-90% of 25OHD is tightly bound to vitamin D binding protein (DBP) and is unavailable to activate innate immune responses during acute stress [12]. The remaining 10-15% is more readily bioavailable (b25OHD), and is composed of the free and albumin-bound components of 25OHD. Fluid loading, albumin wasting, and increased DBP expression during critical illness may affect 25OHD homeostasis [13].

Low vitamin D status (25OHD <20ng/mL) is associated with increased mortality in critical illness [14]. Forty to 70% of septic patients have low vitamin D status [15-17], yet little is known about the impact of vitamin D3 (vitD3) supplementation in this patient population. As such, the investigators propose a randomized, double-blinded, placebo-controlled trial to test the hypothesis that early, rapid correction of low vitamin D status, as an adjunct to established treatment guidelines, will improve clinical outcomes and measurably alter immune profile in patients with severe sepsis. Patients will be assigned to a single dose of vitD3 (400,000 IU) or placebo (n=300/arm) within 24 hours of new-onset severe sepsis, followed by weekly doses of vitD3 (25,000 IU) or placebo, respectively, up to 90 days to assess clinical outcomes and key biomarkers.

AIM 1: To determine if early administration of vitD3 (vs placebo) improves clinical outcomes in patients with low vitamin D status and severe sepsis. Hypothesis 1a: Early vitD3 decreases 90-day mortality after onset of severe sepsis (Primary Outcome). Hypothesis 1b: Early vitD3 decreases sequential organ failure assessment scores in the first 5 days after onset of severe sepsis. Hypothesis 1c: Early vitD3 decreases non-home discharge rate in those who survive severe sepsis.

AIM 2: To determine if early administration of vitD3 (vs placebo) modulates b25OHD, AMPs, and key cytokines in patients with low vitamin D status and severe sepsis. Hypothesis 2a: Early vitD3 increases b25OHD in the first 5 days after the onset of severe sepsis. Hypothesis 2b: Early vitD3 increases expression of AMPs, cathelicidin (LL-37) and β-defensin (hBD-2). Hypothesis 2c: Early vitD3 decreases pro-inflammatory cytokine (IL-1β, IL-6) and increases anti-immunoparalytic cytokine (IL-10, IFN-γ) expression.