Hypovitaminosis D
Conditions
Keywords
cholecalciferol, vitamin D, sepsis, infection
Brief summary
Sepsis in a clinical entity that occurs in patients with serious infections. Though the severity of illness may vary, every year, approximately 1.6 million Americans are treated for sepsis. Even with timely interventions, anywhere from 16% to \>80% of patients with sepsis will not survive. Immune dysfunction is thought to play a critical role in the ability for infections to evolve into sepsis and to eventually lead to death. Recently, vitamin D has been identified as a key regulator of the immune system. While it remains unclear whether optimizing vitamin D status may improve outcomes in sepsis, little is known about the effects of vitamin D supplementation in patients with severe infections. As such, our goal is to study whether high doses of cholecalciferol (vitamin D3) can improve vitamin D status and boost certain aspects of the immune system in patients with sepsis.
Detailed description
Sepsis is a clinical syndrome that complicates severe infections. It is characterized by the cardinal signs of inflammation (e.g. vasodilation, leukocytosis, increased microvascular permeability) occurring in tissues that are remote from the site of an infection. Current theories about the onset and progression of the sepsis syndrome focus on dysregulation of inflammatory responses, including the possibility that a massive and uncontrolled release of pro-inflammatory mediators initiates a chain of events that lead to widespread tissue injury. The degree of immune dysfunction is thought to correlate with the severity of the sepsis syndrome. Sepsis syndrome can range from sepsis, to severe sepsis, septic shock, and multiple organ dysfunction syndrome (MODS). The mortality associated with each of these is estimated to be 16%, 20%, 46%, \>80%, respectively. The annual incidence of sepsis syndrome exceeds 1.6 million cases in the United States alone. Recently, cells of the innate and adaptive immune system have been shown to express the vitamin D receptor. Vitamin D appears to be necessary for interferon-γ dependent T cell responses to infection. In low vitamin D states, dysfunctional macrophage activity becomes evident. Vitamin D is also an important link between Toll Like Receptor (TLR) activation and antibacterial response. Human macrophages stimulated by TLR induce: 1) vitamin D receptor expression; 2) conversion of 25(OH)D to its most biologically active form of 1,25-dihydroxyvitamin D; and 3) production of cathelicidin (LL-37), an endogenous antimicrobial peptide with potent activity against bacteria, viruses, fungi, and mycobacteria. LL-37 is highly expressed in both the plasma and at natural barrier sites (e.g. skin, gut, lungs) and may represent an important first-line of defense for the innate immune system. In humans, cholecalciferol (vitamin D3) is either obtained through the diet or synthesized by skin upon exposure to ultraviolet B (UVB) radiation. Cholecalciferol is converted to 25(OH)D in the liver or by cells of the immune system. Serum 25(OH)D can be measured with relative ease and is the most abundant vitamin D metabolite. It is therefore, often used as a proxy for total body vitamin D status and 25(OH)D levels \<30 ng/mL characterize an insufficient state. A growing body of evidence suggests that a significant proportion (50-90%) of critically ill patients may have insufficient 25(OH)D levels during admission to the intensive care unit (ICU). 25(OH)D insufficiency, in turn, appears to be associated with a higher risk of mortality in critically ill patients. However, randomized, placebo-controlled trials (RCTs) aimed at studying the effect of vitamin D supplementation in critical illness are limited and have largely focused on superficial assessments of vitamin D status. While it is known that septic patients have nearly universally low 25(OH)D levels and that the vitamin D levels are inversely correlated with the severity of sepsis, little is known regarding the effects of vitamin supplementation in this patient cohort. Therefore, our goal is to determine whether vitamin D supplementation in patients highly suspected of sepsis syndrome may be effective in optimizing 25(OH)D levels and in improving host production of the antimicrobial polypeptide LL-37.
Interventions
DIETARY_SUPPLEMENTCholecalciferol
7ml syringe of cholecalciferol suspension given through nasogastric (NG) or orogastric (OG) tube
DIETARY_SUPPLEMENTPlacebo
7ml syringe of placebo cholecalciferol suspension given through nasogastric (NG) or orogastric (OG) tube
Sponsors
Massachusetts General Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* English or Spanish speaking * Within 24 hours of a suspected diagnosis of sepsis * Meeting criteria for sepsis (defined as suspected or confirmed infection AND at least one diagnostic criteria in each of the following groupings): 1. Vital signs: 1. Temperature: \>38.3 Celsius (C) or \<36 Celsius (C) 2. Heart rat e: \>90/min, or \>2 standard deviation above normal 3. Tachypnea (\>20 breaths per minute) 4. Altered mental status 5. Positive fluid balance (\>20 mL/Kg over 24 hrs) 6. Glucose \>140 mg/dL in the absence of diabetes mellitus 2. Inflammatory markers: 1. white blood cell (WBC): \>12,000 or \<4,000 2. Normal WBC count with \>10% immature forms 3. c-reactive protein (CRP) \>2 standard deviation above normal value 4. Pro- calcitonin \>2 standard deviation above normal value 3. Hemodynamic 1. Systolic blood pressure (SBP) \<90 millimeters mercury (mmHg), Mean Arterial Pressure (MAP) \<70mmHg or SBP decrease \>40mmHg 2. Vasopressor therapy to maintain MAP \>65mmHg 4. Organ dysfunction 1. Arterial hypoxemia arterial oxygen partial pressure/fractional inspired oxygen (PaO2/FiO2) \<300 2. Acute Oliguria (UoP \<0.5 mL/Kg/hr for at least 2 hours) 3. Cr increase \>0.5 mg/dL 4. Coagulopathy: internationals normalized ratio (INR) \>1.5 or a-partial prothrombin time (aPTT) \>60 sec 5. Thrombocytopenia: Platelet (PLT) \<100 thousand (K) 6. Hyperbilirubinemia: Total Bilirubin (Tbili) \>4 mg/dL 5. Tissue perfusion 1. Lactate \>2 mmol/L 2. Decrease cap refill or mottling
Exclusion criteria
* Pregnant females or immediate post-partum status * Comfort measures only status * Inability to provide informed consent or have a surrogate consent * History of renal stones within the past year * History of hypercalcemia within the past year * Baseline serum total calcium \>10 mg/dL * Established diagnosis associated with increased risk of hypercalcemia (e.g. metastatic cancer, sarcoidosis, multiple myeloma, primary hyperparathyroidism) * History of severe anemia (Hematocrit \<25%) * Medications that affect vitamin D metabolism (e.g. antiepileptics, tuberculosis medication * Already enrolled or planning to enroll in a research study that would conflict with full participation in the current study or confound the observation or interpretation of the study findings
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Patients will be followed between the onset of suspected sepsis and for an average duration of 7 days | Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. Vitamin D status at the onset of a suspected case of sepsis will be compared to vitamin D status between 5-9 days after supplementation with cholecalciferol or placebo. To assess vitamin D status, we will measure serum and urine: 1) 25-hydroxyvitamin D; 2) 1,25-dihydroxyvitamin D; 3) 24,25-dihydroxyvitamin D; 4) Fibroblast growth factor 23; 5) Vitamin D binding protein; 6) LL-37; 7) Parathyroid hormone; 8) Albumin; 9) Calcium; and 10) Phosphorus levels. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Patients will be followed between the onset of suspected sepsis and for an average duration of 7 days | Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. Immunological profile at the onset of a suspected case of sepsis will be compared to the immunological profile between 5-9 days after supplementation with cholecalciferol or placebo. To assess the immunological profile, we will measure serum LL-37. |
| Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | Patients will be followed between the onset of suspected sepsis and for an average duration of 90 days | Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. The incidence of infection-related complications will be assessed between the onset of suspected sepsis and 80-100 days after supplementation with cholecalciferol or placebo. To assess the incidence of infection-related complications, we will measure rates of: 1) ICU length of stay; and 2) hospital length of stay |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Cholecalciferol Dose II Oral suspension cholecalciferol 400,000 IU
Cholecalciferol: 7ml syringe of cholecalciferol suspension given through NG or OG tube | 10 |
| Placebo Oral suspension of placebo cholecalciferol
Placebo: 7ml syringe of placebo cholecalciferol suspension given through NG or OG tube | 10 |
| Cholecalciferol Dose I Oral suspension cholecalciferol 200,000 IU
Cholecalciferol: 7ml syringe of cholecalciferol suspension given through NG or OG tube | 10 |
| Total | 30 |
Baseline characteristics
| Characteristic | Cholecalciferol Dose II | Total | Cholecalciferol Dose I | Placebo |
|---|---|---|---|---|
| 30 day mortality alive | 8 participants | 22 participants | 7 participants | 7 participants |
| 30 day mortality dead | 2 participants | 8 participants | 3 participants | 3 participants |
| 30 day readmission No | 10 participants | 28 participants | 10 participants | 8 participants |
| 30 day readmission Yes | 0 participants | 2 participants | 0 participants | 2 participants |
| Acute Physiology and Chronic Health Evaluation II (APACHE II) score | 23 scores on a scale | 22 scores on a scale | 21 scores on a scale | 22 scores on a scale |
| Age, Continuous | 62 years | 64 years | 64 years | 65 years |
| Body mass index | 30 kg/m^2 | 28 kg/m^2 | 28 kg/m^2 | 28 kg/m^2 |
| Day 1 data: 25 hydroxyvitaminD(25OHD),bioavailable 25 hydroxyvitamin D(B25OHD), cathelicidin (LL-37) Day 1 25OHD (ng/mL) | 17 ng/mL | 17 ng/mL | 15 ng/mL | 19 ng/mL |
| Day 1 data: 25 hydroxyvitaminD(25OHD),bioavailable 25 hydroxyvitamin D(B25OHD), cathelicidin (LL-37) Day 1 B25OHD (ng/mL) | 2.5 ng/mL | 1.9 ng/mL | 1.9 ng/mL | 1.4 ng/mL |
| Day 1 data: 25 hydroxyvitaminD(25OHD),bioavailable 25 hydroxyvitamin D(B25OHD), cathelicidin (LL-37) Day 1 LL-37 (ng/mL) | 51 ng/mL | 52 ng/mL | 52 ng/mL | 53 ng/mL |
| Day 1 data: high-sensitivity c-reactive protein (hs-CRP) | 119 mg/L | 119 mg/L | 208 mg/L | 106 mg/L |
| Day 1: total body fluid balance (TBB) | 1,518 mL | 1,592 mL | 1,730 mL | 1592 mL |
| Intensive Care Unit (ICU) type medical | 5 participants | 16 participants | 5 participants | 6 participants |
| Intensive Care Unit (ICU) type surgical | 5 participants | 14 participants | 5 participants | 4 participants |
| Positive culture Blood stream | 70 percentage | 190 percentage | 60 percentage | 60 percentage |
| Positive culture Pulmonary | 40 percentage | 130 percentage | 50 percentage | 40 percentage |
| Positive culture Urinary | 10 percentage | 30 percentage | 10 percentage | 10 percentage |
| Region of Enrollment United States | 10 participants | 30 participants | 10 participants | 10 participants |
| Sex: Female, Male Female | 4 Participants | 12 Participants | 4 Participants | 4 Participants |
| Sex: Female, Male Male | 6 Participants | 18 Participants | 6 Participants | 6 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — |
| other Total, other adverse events | 0 / 10 | 0 / 10 | 0 / 10 |
| serious Total, serious adverse events | 0 / 10 | 0 / 10 | 0 / 10 |
Outcome results
Primary
Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol
Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. Vitamin D status at the onset of a suspected case of sepsis will be compared to vitamin D status between 5-9 days after supplementation with cholecalciferol or placebo. To assess vitamin D status, we will measure serum and urine: 1) 25-hydroxyvitamin D; 2) 1,25-dihydroxyvitamin D; 3) 24,25-dihydroxyvitamin D; 4) Fibroblast growth factor 23; 5) Vitamin D binding protein; 6) LL-37; 7) Parathyroid hormone; 8) Albumin; 9) Calcium; and 10) Phosphorus levels.
Time frame: Patients will be followed between the onset of suspected sepsis and for an average duration of 7 days
| Arm | Measure | Group | Value (MEDIAN) |
|---|---|---|---|
| Placebo | Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Day 1 | 19 ng/mL |
| Placebo | Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Day 5 | 19 ng/mL |
| Cholecalciferol Dose I | Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Day 1 | 15 ng/mL |
| Cholecalciferol Dose I | Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Day 5 | 22 ng/mL |
| Cholecalciferol Dose II | Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Day 1 | 17 ng/mL |
| Cholecalciferol Dose II | Change in Vitamin D Status 5 Days Following Supplementation With Cholecalciferol | Day 5 | 29 ng/mL |
Secondary
Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol
Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. Immunological profile at the onset of a suspected case of sepsis will be compared to the immunological profile between 5-9 days after supplementation with cholecalciferol or placebo. To assess the immunological profile, we will measure serum LL-37.
Time frame: Patients will be followed between the onset of suspected sepsis and for an average duration of 7 days
| Arm | Measure | Group | Value (MEDIAN) |
|---|---|---|---|
| Placebo | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 1 LL-37 (ng/mL) | 53 ng/mL |
| Placebo | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 5 LL 37 (ng/mL) | 50 ng/mL |
| Cholecalciferol Dose I | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 1 LL-37 (ng/mL) | 52 ng/mL |
| Cholecalciferol Dose I | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 5 LL 37 (ng/mL) | 54 ng/mL |
| Cholecalciferol Dose II | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 1 LL-37 (ng/mL) | 51 ng/mL |
| Cholecalciferol Dose II | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 5 LL 37 (ng/mL) | 67 ng/mL |
Secondary
Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol
Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. Immunological profile at the onset of a suspected case of sepsis will be compared to the immunological profile between 5-9 days after supplementation with cholecalciferol or placebo. To assess the immunological profile, we will measure serum hsCRP.
Time frame: Patients will be followed between the onset of suspected sepsis and for an average duration of 90 days
| Arm | Measure | Group | Value (MEDIAN) |
|---|---|---|---|
| Placebo | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 1 hsCRP (mg/L) | 106 mg/L |
| Placebo | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | D 5 hsCRP (mg/L) | 53 mg/L |
| Cholecalciferol Dose I | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 1 hsCRP (mg/L) | 208 mg/L |
| Cholecalciferol Dose I | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | D 5 hsCRP (mg/L) | 98 mg/L |
| Cholecalciferol Dose II | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | Day 1 hsCRP (mg/L) | 119 mg/L |
| Cholecalciferol Dose II | Change in Immunological Profile 5 Days Following Supplementation With Cholecalciferol | D 5 hsCRP (mg/L) | 31 mg/L |
Secondary
Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis
Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. The incidence of infection-related complications will be assessed between the onset of suspected sepsis and 80-100 days after supplementation with cholecalciferol or placebo. To assess the incidence of infection-related complications, we will measure rates of: 1) ICU length of stay; and 2) hospital length of stay
Time frame: Patients will be followed between the onset of suspected sepsis and for an average duration of 90 days
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| Placebo | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | ICU length of stay | 12 days |
| Placebo | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | Hospital length of stay | 21 days |
| Cholecalciferol Dose I | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | ICU length of stay | 4 days |
| Cholecalciferol Dose I | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | Hospital length of stay | 13 days |
| Cholecalciferol Dose II | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | ICU length of stay | 3 days |
| Cholecalciferol Dose II | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | Hospital length of stay | 14 days |
Secondary
Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis
Subjects will receive 200,000 IU or 400,000 IU cholecalciferol suspension (vs. placebo) within 24 hours from the onset of a suspected case of sepsis during their hospitalization. The incidence of infection-related complications will be assessed between the onset of suspected sepsis and 80-100 days after supplementation with cholecalciferol or placebo. To assess the incidence of infection-related complications, we will measure rates of: 1\) 30 day hospital readmission; and 2) 30 day mortality.
Time frame: Patients will be followed between the onset of suspected sepsis and for an average duration of 90 days
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Placebo | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day readmission: no | 8 participants |
| Placebo | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day readmission: yes | 2 participants |
| Placebo | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day mortality: dead | 3 participants |
| Placebo | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day mortality:alive | 7 participants |
| Cholecalciferol Dose I | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day mortality:alive | 7 participants |
| Cholecalciferol Dose I | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day readmission: no | 10 participants |
| Cholecalciferol Dose I | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day mortality: dead | 3 participants |
| Cholecalciferol Dose I | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day readmission: yes | 0 participants |
| Cholecalciferol Dose II | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day mortality:alive | 8 participants |
| Cholecalciferol Dose II | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day readmission: yes | 0 participants |
| Cholecalciferol Dose II | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day mortality: dead | 2 participants |
| Cholecalciferol Dose II | Incidence of Infection-related Complications Within 90 Days From the Onset of a Suspected Case of Sepsis | 30 day readmission: no | 10 participants |