RETRACTED ARTICLE: Evaluation of the Relationship Between Serum Vitamin D Level and Severity of Sepsis

AUTHORS

Koorosh Ahmadi 1 , Morteza Talebi Doluee 2 , Seyyed Mohsen Pouryaghobi 3 , Fermoozan Nikpasand 4 , Morteza Hariri 5 , Elham Pishbin ORCID 2 , *

1 Department of Emergency Medicine, Alborz University of Medical Sciences, Karaj, IR Iran

2 Department of Emergency Medicine , Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad , IR Iran

3 Department of Anesthesiology, Alborz University of Medical Sciences, Karaj, IR Iran

4 Faculty of Medicine, Islamic Azad University, Tehran, IR Iran

5 Emergency Medicine Resident, School of Medicine, Mashhad University of Medical Sciences, Mashhad, IR Iran

How to Cite: Ahmadi K, Talebi Doluee M, Pouryaghobi S M, Nikpasand F, Hariri M, et al. RETRACTED ARTICLE: Evaluation of the Relationship Between Serum Vitamin D Level and Severity of Sepsis, Iran Red Crescent Med J. 2016 ; 18(2):e12257. doi: 10.5812/ircmj.12257.

ARTICLE INFORMATION

Iranian Red Crescent Medical Journal: 18 (2); e12257
Published Online: February 20, 2016
Article Type: Research Article
Received: May 19, 2013
Revised: August 17, 2013
Accepted: December 28, 2015
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Abstract

Background: On the basis of the literature, vitamin D is known as an important medium in bodily immune function, and it therefore may play a role in the pathogenesis of sepsis.

Objectives: In this study, we aimed to evaluate the relationship between vitamin D serum levels and sepsis severity.

Patients and Methods: This study was a case-control study that evaluated adult patients admitted to the emergency department of Imam Reza hospital with suspected sepsis. These patients were enrolled in the study as the case group. In addition, healthy individuals without the sepsis diagnostic criteria were included in the control group. For all of the study participants, vitamin D levels were evaluated. The acute physiology age chronic health evaluation (APACHE) was used to evaluate disease severity in the case group. A difference of P < 0.05 was regarded as statistically significant.

Results: A total of 112 patients were assessed: 56 in the control group and 56 in the case group. In the case group, 18 patients had sepsis, 25 patients had severe sepsis, and 13 patients were in septic shock. The mean ages of the patients in the case and control groups were 57.7 ± 15.15 and 58.6 ± 15.05 years, respectively (P = 0.741). Vitamin D levels in the case group were lower than in the control group (16.3 ± 10.7 versus 27.9 ± 11.46 ng/mL), and the difference between the groups was significant (P < 0.001). Mean vitamin D levels in the severe sepsis and septic shock groups were lower than in the sepsis group, and the mean level in the septic shock group was lower than in the severe sepsis group (P = 0.001). In the case group, there was a significant reverse correlation between APACHE II criteria and vitamin D levels (P < 0.001, r = -0.586).

Conclusions: The results of this study indicated that patients with sepsis had lower serum vitamin D levels than healthy controls. Also, patients with more severe disease had lower serum vitamin D levels, but to evaluate causation and determine whether vitamin D supplementation could be effective in reducing the risk or severity of sepsis, randomized controlled trials should be conducted.

Keywords

Vitamin D Sepsis Septic Shock APACHE II Criteria

Copyright © 2016, Iranian Red Crescent Medical Journal. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

1. Background

Vitamin D has been best described and investigated for its role in bone and calcium-phosphate homeostasis. After researchers found that vitamin D receptors and 25-hydroxyvitamin D-1α-hydroxylase (1α-OHase) are distributed throughout bodily tissues, not only in the skeleton, assessing the relationship between this vitamin and several diseases became an attractive field of research. Scientists have also demonstrated that the vitamin D response element exists in more than 900 genes (1).

Current knowledge about the other important roles of this vitamin in other body systems and mechanisms is poor, but several studies have shown that vitamin D has an influence on several chronic diseases, such as diabetes, cardiovascular disease, lung disease, autoimmune disorders, and common cancers (2-6).

Recent studies and clinical trials provide evidence that vitamin D affects the innate and adaptive immune system activity, including activation and differentiation of dendritic cells, macrophages, and B and T lymphocytes (7).

The prevalence rates in an Iranian population of mild, moderate, and severe vitamin D deficiency were 14.2%, 57.6%, and 9.5%, respectively (8). Chapuy et al. reported similar results of a high prevalence of vitamin D insufficiency in normal adults (9).

Recently, researchers have found an association between low levels of serum 25 (OH) D and increased risk of infection (10). The severity of an infection is negatively correlated to serum vitamin D concentrations. These findings proposed another important role for this vitamin in the progression of sepsis pathogenesis (11-13). The incident of influenza A infections were also reduced with vitamin D supplementation in a clinical trial (14).

In 2011, Ginde et al. conducted a study to assess the severity of infection in patients with serum 25 (OH) D levels of < 75 nmol/L, and found that patients with a basic 25 (OH) D level of < 75 nmol/L, compared to those with >75 nmol/L, were more likely to develop severe sepsis (P = 0.006) and to have a sepsis-related organ failure assessment (SOFA) score of ≥ 2 (P = 0.049) and an Acute Physiology Age Chronic Health Evaluation (APACHE II) score of ≥ 25 (P = 0.06) (15).

There is evidence of the significant relationship of vitamin D serum levels and the risk of infection and its consequences; however, some studies had different results and did not reach the significance level (16-19). Due to this controversy, there should be more studies to investigate this relationship, given the importance of its application in critically ill patients at risk for infection or sepsis.

2. Objectives

The aim of this study was to provide additional evidence about serum vitamin D levels and their correlation with the severity of sepsis in patients referred to the emergency department.

3. Patients and Methods

3.1. Study Design

This was a case-control study. All patients over 18 years of age who were referred to the emergency department of Imam-Reza hospital, and hospitalized due to possible sepsis, were assessed for enrollment in the study as the case group (n = 56). We divided these 56 patients into three subgroups: sepsis, severe sepsis, and septic shock. Patients that met two or more criteria for systemic inflammatory response syndrome, and who were diagnosed with sepsis due to an infectious cause, were designated as the first subgroup. Sepsis patients were assigned to the second subgroup (severe sepsis) if there were one or more signs of organ dysfunction or hypo perfusion, such as metabolic acidosis, acutely altered mental status, oliguria, or acute respiratory distress syndrome. Patients with severe sepsis that did not respond to fluid resuscitation were considered to have septic shock and were placed in the third subgroup. Patients who did not sign the consent form, or who refused to continue in the study, were excluded. For each patient in the case group, we enrolled a healthy, age- and sex-matched individual without any of the diagnostic sepsis criteria, to form the control group.

3.2. Investigated Variables

We measured APACHE II scores, which are approved for determining the severity of infection or disease, and the serum vitamin D levels for each patient. Before any treatments, 5 ml of blood was drawn from each patient, then centrifuged (4,000 RPM for 5 minutes) to separate blood cells from serum. The serum samples were then stored at -80°C until analysis. The samples were sent to the central laboratory of Imam-Reza hospital for serum vitamin D assays. Vitamin D was determined with the chemiluminescence immunoassay (CLIA) technique using LIAISON® 25 OH Vitamin D Total assay (DiaSorin) kits on the LIAISON analyzer. Other demographic variables, such as age and sex, were collected by a questionnaire.

3.3. Ethical Issues

The study was conducted in accordance with the principles of the 1996 declaration of Helsinki and good clinical practice standards, under the supervision of the Mashhad University of Medical Sciences ethics committee. All patients signed informed consent.

3.4. Statistical Analysis

To compare quantitative variables between the two groups, if the data were normally distributed, an independent-samples t-test was used. To compare quantitative variables between more than two groups, one-way ANOVA was used to analyze the data. If the data were not normally distributed, equivalent non-parametric tests were used. All data were analyzed with SPSS 16.0 statistical software (SPSS Inc., Champaign, IL, USA).

We used the Pearson chi-squared test to analyze qualitative variables, and if the data were not eligible for the test, other appropriate tests were used, such as Fisher’s exact or the likelihood ratio. To assess correlations between quantitative data, the Pearson correlation test was used. In all cases, a significance level of P < 0.05 was set.

4. Results

A total of 112 eligible individuals were enrolled in this study, with 56 patients in the case group and 56 subjects in the control group. The case group included 18 patients with sepsis, 25 with severe sepsis, and 13 with septic shock. The demographic and baseline characteristics of the two groups are shown in Table 1.

Table 1. Characteristics of the Subjects in the Case and Control Groups (N = 56)a
VariableCase GroupControl GroupP Value
Age, yb57.7 ± 15.1558.6 ± 15.050.741
Gender, %0.571
Male48.253.6
Female51.846.4
Temperature (rectal)b38.37 ± 0.898--
Mean arterial pressureb80.6 ± 16.49--
AaDO2 or PaO2b75.1 ± 12.56--
Heart rate, median [IQR]109 (104 - 111)--
Respiratory rate, median [IQR]29 (26 - 39)--
Hematocritb33.2 ± 5.82--
Sodium (serum)b135.2 ± 11.07--
Potassium (serum)b4.11 ± 1.26--
White blood cell countb15320 ± 5388--
Glasgow Coma Scale, median (IQR)12 (11 - 15)--
Ph (arterial)b7.33 ± 0.11--
Serum vitamin D levels, ng/mLb16.31 ± 10.7027.91 ± 11.46< 0.001
Serum vitamin D levels, No. (%)0.002
Deficiency48 (85.7)33 (58.9)-
Normal8 (14.3)23 (41.1)-

a< 30 ng/mL was considered vitamin D deficiency; ≥ 30 ng/mL was considered normal.

bValues are expressed as mean ± SD.

The mean ages of the case and control groups were not significantly different (P = 0.741). Also, in the case group, the mean age of patients with septic shock was greater than in the other two groups, but the difference was not significant (P = 0.131). Males accounted for 48.2% and 53.6% of the patients in the case and control groups, respectively. No significant difference in sex distribution was observed between the case and control groups (P = 0.571) or among the case subgroups (P = 0.240) (Table 1).

The number of patients with underlying disease in the septic shock group was higher than in the other two groups. This number was greater in patients with severe sepsis compared to patients with sepsis. Statistical comparisons showed a significant difference between these groups (P = 0.024) (Table 2).

Table 2. Variables for the Case-Group Patientsa,b
VariableSepsis (n = 18)Severe Sepsis (n = 25)Septic Shock (n = 13)P Value
Age, y55.2 ± 12.6955.6 ± 17.3265.1 ± 12.100.131
Gender0.240
Male11 (61.1)9 (36)7 (53.8)
Female7 (38.9)16 (64)6 (46.2)
Chronic health problem0.024
Yes27.811 (44)10 (76.9)
No72.214 (56)3 (23.1)
Serum vitamin D levels, ng/mL23.6 ± 11.3113.5 ± 9.1611.5 ± 7.360.001, P1 = 0.003, P2 = 0.003, P3 = 0.809
Serum vitamin D levels0.144
Deficiency 13 (72.2)23 (92)12 (92.3)
Normal5 (27.8)2 (8)1 (7.7)
APACHE II, median (IQR)10 (8 - 12.25)28 (25 - 32)32 (28 - 35.5)< 0.001, P1 < 0.001, P2 < 0.001, P3 = 0.029

aValues are expressed as No. (%) unless otherwise indicated as mean ± SD.

bBelow 30 ng/mL was considered vitamin D deficiency and 30 ng/mL or higher was considered normal. Post hoc analysis was done with the Tukey test. P1 = sepsis vs. severe sepsis, P2 = sepsis vs. septic shock, P3 = severe sepsis vs. septic shock.

Serum vitamin D levels in the control group were higher than in the case group (P < 0.001). Patients with sepsis had higher levels of vitamin D compared with the other two groups. Similarly, the patients with severe sepsis had higher levels of vitamin D compared to the patients suffering from septic shock (P = 0.001) (Figure 1, Table 2).

Serum Vitamin D levels in the Control Group and the Case Subgroups
Figure 1. Serum Vitamin D levels in the Control Group and the Case Subgroups

Vitamin D deficiency was considered to be present when serum levels were < 30 ng/mL. The number of patients in the case group who were deficient for vitamin D was higher than in the control group (P = 0.002). However, no significant differences were observed between the case subgroups (P = 0.144).

APACHE II score comparisons between the case subgroups showed a significant difference (P < 0.001), with a higher score in the septic shock patients compared to the two other subgroups. In patients with severe sepsis, APACHE II scores were greater than in the sepsis group (Table 2).

There was a significant negative correlation (correlation coefficient = -0.586) between vitamin D levels and APACHE II scores (As seen in Table 3, the APACHE II classification (≥ 25 or < 25) and vitamin D levels were measured in all patients (n = 56), and the u-djusted odds ratio was calculated.(Figure 2) (OR = 5.47).

Scatter-Dot Diagram of Serum Vitamin D Levels and APACHE II Scores
Figure 2. Scatter-Dot Diagram of Serum Vitamin D Levels and APACHE II Scores
Table 3. Cross-Tabulated Serum Vitamin D Levels and APACHE II Scores (N = 56)a
APACHE IIVitamin D
DeficientNormal
≥ 25312
< 25176

aOdds ratio (CI95%): 5.47(0.99 - 30.13).

There was a negative correlation between serum vitamin D levels and age. The qualitative analysis also showed that vitamin D deficiency in patients aged 65 years or older was greater than in patients younger than 65. Serum vitamin D levels were higher in men than in women (P < 0.001).

5. Discussion

We conducted a case-control study to evaluate the relationship between serum vitamin D and sepsis severity. The results showed that serum levels of vitamin D in patients with sepsis compared with the control group of healthy individuals were significantly lower. Also, serum vitamin D levels were lower in patients with severe sepsis or septic shock. On the other hand, by considering 30 ng/mL of vitamin D as the lowest normal concentration, we demonstrated that the percentage of patients deficient for vitamin D was significantly higher in the case group than in the control group, but no significant difference was observed between the three case subgroups. The difference in these findings (vitamin D levels in the form of qualitative or quantitative variables) can be justified by the fact that using quantitative data is more accurate in a statistical analysis and leads to more precise results.

Also, using a cut-off point of 30 ng/mL as the lowest normal concentration for vitamin D was based on previous studies, and may not be the lowest amount of vitamin D necessary for optimal immune system function.

We also investigated the relationship between vitamin D levels and APACHE II scores, and found that a there is a significant inverse correlation between these two variables. In patients with more severe sepsis (higher APACHE II scores), we saw lower serum vitamin D levels.

Jeng et al.’s study found that critically ill patients hospitalized in the ICU (with or without sepsis) had significantly lower levels of 25 (OH) D plasma concentrations compared to healthy individuals, and that plasma concentrations of proteins that bind to vitamin D were significantly lower in severely ill patients with sepsis than in severely ill patients without sepsis (13).

Chinese researchers conducted a study to assess the association between vitamin D levels and risk of infection, disease severity, and mortality rates. Su et al. enrolled 50 healthy individuals, 51 patients with sepsis in the ICU, and 105 patients with sepsis in the ICU in this study. In general, ICU patients had lower vitamin D levels (P < 0.01), but no significant difference was observed between those with sepsis and those without it. A weak negative relationship was observed between APACHE II scores, the simplified acute physiology score (SAPS) II, SOFA scores, and vitamin D concentrations. Also, 25 (OH) D levels were not significantly different with regard to the 28-day (P = 0.776) and 90-day (P = 0.389) survival rates. However, APACHE II and SAPS II scores were identified as risk factors for mortality due to sepsis (16).

All of these findings are consistent with our study results. Higgins et al. assessed the prevalence and severity of vitamin D deficiency in ICU patients, and the deficiency’s relationship to disease morbidity and mortality. Out of 196 ICU patients, 26% were vitamin D deficient (< 30 nmol/L) and 56% had insufficient levels (30 - 60 nmol/L). In addition, 25 (OH) D levels decreased in all patients after admission to the ICU, and were significantly lower 10 days later (P < 0.001). 25 (OH) D status had no association with any cause of death after 28 days. However, higher levels of 25 (OH) D were associated with early discharge from the ICU. Also, patients with 25 (OH) D deficiency showed no significant differences with patients who had adequate levels with regard to acquiring infections (P = 0.11) (20).

Many studies have shown that a lack of vitamin D is common in patients admitted to the ICU (21-24). Several additio-l studies have shown that the prevalence of vitamin D deficiency is high in patients admitted to the hospital (25-27).

Ginde et al. investigated the hypothesis that in patients with suspected infection and a serum 25 (OH) D level of < 75 nmol/L, a more severe infection might be present. Eighty-one patients with a median age of 62 years were included in the study and scored with APACHE II and SOFA. The results of that study suggested that patients with a basic 25 (OH) D level of < 75 nmol/L, compared to patients with > 75 nmol/L, were more likely to develop severe sepsis (69% vs. 29%; P = 0.006), and more likely to have a SOFA score of ≥ 2 (44% vs. 18%; P = 0.049) and an APACHE II score of ≥ 25 (19% vs. 0%; P = 0.06). In addition, after 24 hours, those patients with 25 (OH) D levels of < 75 nmol/L were more likely to experience failure of two or more organs (50% vs. 18%; P = 0.02). All four of the study’s patients who died during hospitalization had 25 (OH) D levels of < 75 nmol/L (15). That study showed the most similarity to the design of our study, as 75 nmol/L (approximately 30 ng/mL) of serum vitamin D was considered the lowest normal concentration. Also, the mean age of the patients was similar and the results were consistent with those of the present study.

The results of the present study indicated that patients with sepsis had lower serum vitamin D levels compared with healthy individuals, and that patients with more severe sepsis had even lower levels. Based on our findings and those of other similar studies, a high percentage of patients are vitamin D deficient. For further research in this field, we suggest randomized clinical trials with administration of vitamin D supplementation in patients diagnosed with sepsis, in order to investigate vitamin D’s therapeutic effects on disease progression and survival rates. The use of such supplementation, especially in high-risk patients such as the elderly, may reduce the risk of infection and mortality associated with sepsis.

One the limitations of the present study was the small number of cases in each of the case subgroups after they were divided according to sepsis, severe sepsis, or septic shock. Because of the limited number of patients in each subgroup, we were not able to perform multivariable a-lyses. There may be confounding factors, such as medical co-morbidities, drug history, season, and obesity. A larger sample size is necessary to assess the effects of these factors.

Footnotes

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