Abstract
Background:
Emerging evidence has indicated that interleukin-8 (IL-8) gene-251A/T polymorphism may affect individual susceptibility to sepsis. However, the results of published studies are inconclusive. The aim of this meta-analysis was to elucidate the association between this polymorphism and the risk and mortality of sepsis.
Methods:
Relevant publications were searched from PubMed, EmBase, and Web of Science databases up to January 31, 2021, with studies only in English. The reference lists of the retrieved studies were investigated as well. Pooled odds ratio (OR) with 95% confidence interval (CI) was calculated to figure out the relationship between IL-8-251 A/T polymorphisms and the risk and mortality of sepsis. All of the data were analyzed with Stata 16.0.
Results:
The results of this meta-analysis will be submitted to a peer-reviewed journal for publication.
Conclusion:
This meta-analysis will summarize the relationship between IL-8-251 A/T polymorphism and the risk and mortality of sepsis.
Keywords: interleukin-8, meta-analysis, polymorphism, protocol, sepsis
1. Introduction
Sepsis is a life-threatening organ disorder in which the host fails to control severe infection.[1,2] In high-income countries, 28 million people die of septicemia each year.[3] The causes of sepsis include severe infections of lung, abdomen, blood, and urethra.[4–6] Among them, pulmonary infection accounts for about 64% of all cases of septicemia.[7] Multiple organ dysfunction syndrome is the most common and serious complication secondary to sepsis, and it is one of the main factors of sepsis death in the world.[8,9] The mortality rate of hospitalized patients with sepsis is 25% to 30%.[10] Early identification could improve the prognosis of sepsis.[11,12] Therefore, the treatment of patients with sepsis mainly depends on early identification and timely treatment.
The change of immune function is considered as a key factor in the pathogenesis of sepsis.[13] The host immune system generates a series of substances such as cytokines in response to infection or injury. Interleukin (IL)-8 is a pro-inflammatory cytokine that is involved in the inflammatory reaction at the early stage of sepsis. Inflammation is one of the most important clinical manifestations of sepsis.[14–16] During inflammation, mononuclear macrophages secrete IL-8 from the blood in tissues.[17] The upregulation of IL-8 in vitro indicates the deterioration of the disease and the higher tendency to death.[18,19] In addition, it has been reported that IL-8 is associated with the progression of sepsis.[20,21] IL-8 blocking therapy is beneficial to the prognosis of septicemia by blocking systemic inflammatory response.
As the most common genetic variation, single nucleotide polymorphism (SNP) has attracted more and more attentions in the research on sepsis. According to previous studies, it has been obvious that single nucleotide polymorphism can predict the risk and prognosis of sepsis. It was reported that a functional SNP, -251A/T, in the promoter region of IL-8 gene can influence the expression of IL-8. Several recent studies have been carried out to explore the correlation between the SNP of IL-8–251 A/T (rs4073) polymorphism and sepsis susceptibility.[22–27] However, the results were conflicting. Thus, this study was aimed to investigate the association between the IL-8-251 A/T polymorphism and the risk and mortality of sepsis by meta-analysis.
2. Methods
2.1. Study registration
The protocol of this review was registered in OSF (OSF registration number: DOI 10.17605/OSF.IO/EPR3Y), and followed the statement guidelines of preferred reporting items for systematic reviews and meta-analyses protocol[28] on the basis of reports.
2.2. Inclusion criteria
The publications fulfilling the following criteria were included: an original study evaluating the association between IL-8-251 A/T polymorphism and the risk and/or mortality of sepsis; objects in each study were from the same epoch; including a case group of sepsis; including a control group; including precise sample size of IL-8-251 A/T polymorphism of case and control groups that could be directly extracted or calculated based on the information available.
2.3. Exclusion criteria
The exclusion criteria are as follows: repetition of the published studies; a meta-analysis or a review; study with insufficient or incorrect data.
2.4. Publication search
Two investigators independently performed a systematically computerized search for English studies through PubMed, EmBase, and Web of Science databases up to January 31, 2021. The keywords for searching were the combination of “IL-8, interleukin-8, polymorphism, sepsis, septicemia, and septic shock.” Meanwhile, references of relevant literature reviews were screened to identify potentially relevant publications. The search strategy for PubMed is illustrated in Table 1, and the corresponding keywords would be used in other databases.
Table 1.
Search strategy in PubMed database.
| Number | Search terms |
| #1 | Sepsis[MeSH] |
| #2 | Pyaemia[Title/Abstract] |
| #3 | Pyemia[Title/Abstract] |
| #4 | Pyohemia[Title/Abstract] |
| #5 | Blood Poisoning[Title/Abstract] |
| #6 | Poisoning, Blood[Title/Abstract] |
| #7 | Septicemia[Title/Abstract] |
| #8 | Severe Sepsis[Title/Abstract] |
| #9 | Blood Poisonings[Title/Abstract] |
| #10 | Poisonings, Blood[Title/Abstract] |
| #11 | Pyaemias[Title/Abstract] |
| #12 | Pyemias[Title/Abstract] |
| #13 | Pyohemias[Title/Abstract] |
| #14 | Sepsis, Severe[Title/Abstract] |
| #15 | Septicemias[Title/Abstract] |
| #16 | or/1-15 |
| #17 | Interleukin-8[MeSH] |
| #18 | IL-8[Title/Abstract] |
| #19 | or/17-18 |
| #20 | polymorph∗[Title/Abstract] |
| #21 | susceptibility[Title/Abstract] |
| #22 | or/20-21 |
| #23 | #16 and #19 and #22 |
2.5. Data collection and analysis
2.5.1. Selection of studies
The 2 reviewers complete the screening process independently, and any differences are decided by a third reviewer. The screening process of the article includes reading the title, the abstract, and the full text, so as to determine whether it meets the inclusion criteria. The researchers record the reasons to exclude each study in light of the preferred reporting items for systematic reviews and meta-analysis guidelines and report the screening results. The flowchart is demonstrated in Figure 1.
Figure 1.
Flow diagram of study selection process.
2.5.2. Data extraction
All data were extracted by 2 independent investigators from included studies. Divergence was solved after discussion on every item. The following information was extracted from studies: first author, year of publication, country of the study and features of case and control groups such as ethnicity, age group, type of case and controls, genotype frequencies, genotyping method, and P value for Hardy–Weinberg equilibrium (HWE) of controls. In some studies, the risk and mortality of sepsis are discussed. In this case, the information was collected.
2.5.3. Methodology quality assessment
According to Newcastle-Ottawa Scale (NOS) by 2 researchers, the quality of included studies was evaluated.[29] Available data were extracted by 2 authors independently. Disagreements were dealt with by a third reviewer. The NOS values arrange from 0 to 9. Studies with the score of 6 are considered to be of high quality.[30]
2.5.4. Dealing with missing data
The reason for the loss of data in the period of data screening and extraction is identified here. We would attempt to contact the authors if the data of potential studies are insufficient, missing, or vague. These studies would be excluded only if the data are not available through the method described above.
2.5.5. Statistical analysis
The HWE for control subjects of each studies was evaluated by conducting a chi-square test, and P < .05 was seen as significant disequilibrium. Odds ratios (ORs) and the 95% confidence intervals (95% CIs) were calculated to evaluate the association between IL-8-251 A/T polymorphism and the risk or mortality of sepsis. The pooled ORs were executed for homozygote comparison, dominant and recessive models, allele comparison and heterozygote comparison. The heterogeneity was calculated by performing the χ2-based I2 test and the Q test. The fixed-effect model (the Mantel-Haenszel method) was chosen when the I2 value is <50%. Although the I2 is >50%, a random-effects model (DerSimonian and Laird method) was adopted. All of the statistical analyses were conducted by the STATA 16.0 (StataCorp, College Station, TX), and the P values were 2-sided. 2.5.6. Subgroup analysis
In the analysis on sepsis risk, subgroup analyses based on age group, ethnicity, restricted healthy controls were performed. Subgroup analysis on age and ethnicity in the mortality analysis was also made.
2.5.6. Sensitivity analysis
The eligible study was sequentially removed to perform the sensitivity analysis.
2.5.7. Assessment of publication biases
Publication bias was assessed by Begg rank correlation and Egger linear regression. The publication bias was regarded as statistically significance when P < .05.[31,32]
2.5.8. Ethics and dissemination
The content of this article does not involve moral approval or ethical review and would be presented in print or at relevant conferences.
3. Discussion
IL-8 belongs to the COX2C subfamily of inflammatory mediators and participates in the regulation of inflammatory acute phase.[33] Studies have revealed that the promoter of IL-8 gene-251 A/T allele can upregulate the expression of IL-8 through transcriptional regulation.[34] Therefore, it plays an important role in the pathogenesis and progression of sepsis
The association between IL-8-251 A/T polymorphism and the risk or mortality of sepsis has been widely investigated.[22–27] Because of the controversial findings, a meta-analysis is necessary to bring some new insights into this topic. This study has the largest sample so far to address this issue.
This study has the following shortcomings. First, due to a change in the definition of sepsis, the selected study is unlikely to have the same definition, as our analysis includes studies over a longer period of time. Second, most of the subjects of the study are whites, and more researches are needed to further study other races. Sepsis is a complex disease, and its pathogenic factors include genetic and environmental factors. The results of this study did not adjust other confounding factors, so the interpretation of the results should be cautious. In spite of this, this study still ensures the truthfulness and reliability of the research results from the following points. On the one hand, this paper includes a large number of cases and controls from different studies, which significantly increases the testing efficiency of statistics. On the other hand, for the same population source or repeatedly published literature, only the larger or recent data results are included in the study to ensure that there is no obvious selection bias.
In summary, this meta-analysis will summarize the relationship between the IL-8-251 A/T polymorphism and the risk and mortality of sepsis. However, considering the limitations of this study, better design and larger sample size are needed to confirm this conclusion.
Author contributions
Data curation: Shiqiao Zhao and Junzuo Gong.
Formal analysis: Junzuo Gong.
Methodology: Junzuo Gong.
Project administration: Shu Luo.
Supervision: Songlin Yin.
Validation: Xiaofeng Li and Tianyi Mou.
Visualization and software: Shuangquan Zhao.
Writing – original draft: Shiqiao Zhao, Junzuo Gong and Shu Luo.
Writing – review & editing: Shiqiao Zhao, Junzuo Gong and Shu Luo.
Author contributions
Conceptualization: Shu Luo, Shiqiao Zhao.
Funding acquisition: Shu Luo.
Project administration: Shu Luo, Shiqiao Zhao.
Writing – original draft: Shu Luo, Shiqiao Zhao, Junzuo Gong.
Writing – review & editing: Shu Luo, Shiqiao Zhao, Junzuo Gong.
Data curation: Shiqiao Zhao.
Investigation: Junzuo Gong.
Resources: Songlin Yin.
Software: Songlin Yin.
Supervision: Songlin Yin.
Validation: Xiaofeng Li.
Visualization: Shuangquan Zhao, Tianyi Mou.
Footnotes
Abbreviations: CIs = confidence intervals, IL-8 = interleukin-8, NOS = Newcastle-Ottawa scale, OR = odds ratio, PRISMA-P = Preferred Reporting Items for Systematic Reviews and Meta-analysis Protocols, SNP = single-nucleotide polymorphism.
How to cite this article: Zhao S, Gong J, Yin S, Li X, Zhao S, Mou T, Luo S. The association between interleukin-8 gene-251 A/T polymorphism and sepsis: a protocol for systematic review and meta analysis. Medicine. 2021;100:15(e25483).
Ethics and dissemination: Ethical approval was not required for this study. The systematic review will be published in a peer-reviewed journal, presented at conferences, and shared on social media platforms.
OSF REGISTRATION NUMBER: DOI 10.17605/OSF.IO/EPR3Y.
SZ and JG contributed equally to this work.
Funding: This work is supported by the Sichuan Provincial Commission of Health and Family Planning (17PJ142).
The authors report no conflicts of interest.
Patient consent: Not required.
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
References
- [1].Singer M, Deutschman CS, Seymour CW, et al. The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA 2016;315:775–87. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [2].Donnelly JP, Safford MM, Shapiro NI, et al. Application of the Third International Consensus Definitions for Sepsis (Sepsis-3) Classification: a retrospective population-based cohort study. Lancet Infect DisV 17 2017;661–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [3].Adhikari NK, Fowler RA, Bhagwanjee S, et al. Critical care and the global burden of critical illness in adults. Lancet 2010;376:1339–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [4].Vincent JL, Rello J, Marshall J, et al. International study of the prevalence and outcomes of infection in intensive care units. JAMA 2009;302:2323–9. [DOI] [PubMed] [Google Scholar]
- [5].Vincent JL, Sakr Y, Sprung CL, et al. Sepsis in European intensive care units: results of the SOAP study. Crit Care Med 2006;34:344–53. [DOI] [PubMed] [Google Scholar]
- [6].Karlsson S, Varpula M, Ruokonen E, et al. Incidence, treatment, and outcome of severe sepsis in ICU-treated adults in Finland: the Finnsepsis study. Intensive Care Med 2007;33:435–43. [DOI] [PubMed] [Google Scholar]
- [7].Fleischmann C, Scherag A, Adhikari NK, et al. Assessment of global incidence and mortality of hospital-treated sepsis. Current estimates and limitations. Am J Respir Crit Care Med 2016;193:259–72. [DOI] [PubMed] [Google Scholar]
- [8].Bosurgi R. Sepsis: a need for new solutions. Lancet Infect Dis 2015;15:498–9. [DOI] [PubMed] [Google Scholar]
- [9].Bermejo-Martin JF, Andaluz-Ojeda D, Almansa R, et al. Preventing sepsis. Lancet Infect Dis 2015;15:1259–60. [DOI] [PubMed] [Google Scholar]
- [10].Cohen J, Vincent JL, Adhikari NK, et al. Sepsis: a roadmap for future research. Lancet Infect Dis 2015;15:581–614. [DOI] [PubMed] [Google Scholar]
- [11].Peake SL, Delaney A, Bailey M, et al. Goal-directed resuscitation for patients with early septic shock. N Engl J Med 2014;371:1496–506. [DOI] [PubMed] [Google Scholar]
- [12].Yealy DM, Kellum JA, Huang DT, et al. A randomized trial of protocol-based care for early septic shock. N Engl J Med 2014;370:1683–93. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [13].Monneret G, Venet F. Sepsis-induced immune alterations monitoring by flow cytometry as a promising tool for individualized therapy. Cytometry B Clin Cytom 2016;90:376–86. [DOI] [PubMed] [Google Scholar]
- [14].Vavrova L, Rychlikova J, Mrackova M, et al. Increased inflammatory markers with altered antioxidant status persist after clinical recovery from severe sepsis: a correlation with low HDL cholesterol and albumin. Clin Exp Med 2016;16:557–69. [DOI] [PubMed] [Google Scholar]
- [15].Alharbi A, Thompson JP, Brindle NP, et al. Ex vivo modelling of the formation of inflammatory platelet-leucocyte aggregates and their adhesion on endothelial cells, an early event in sepsis. Clin Exp Med 2019;19:321–37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [16].Brodská H, Malíčková K, Adámková V, et al. Significantly higher procalcitonin levels could differentiate Gram-negative sepsis from Gram-positive and fungal sepsis. Clin ExpMed 2013;13:165–70. [DOI] [PubMed] [Google Scholar]
- [17].Hoffmann E, Dittrich-Breiholz O, Holtmann H, et al. Multiple control of interleukin-8 gene expression. J Leukoc Biol 2002;72:847–55. [PubMed] [Google Scholar]
- [18].Mera S, Tatulescu D, Cismaru C, et al. Multiplex cytokine profiling in patients with sepsis. APMIS 2011;119:155–63. [DOI] [PubMed] [Google Scholar]
- [19].Wacharasint P, Nakada TA, Boyd JH, et al. AA genotype of IL-8 -251A/T is associated with low PaO(2)/FiO(2) in critically ill patients and with increased IL-8 expression. Respirology (Carlton, Vic) 2012;17:1253–60. [DOI] [PubMed] [Google Scholar]
- [20].Macdonald SP, Stone SF, Neil CL, et al. Sustained elevation of resistin, NGAL and IL-8 are associated with severe sepsis/septic shock in the emergency department. PLoS One 2014;9:e110678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [21].Miyoshi T, Yamashita K, Arai T, et al. The role of endothelial interleukin-8/NADPH oxidase 1 axis in sepsis. Immunology 2010;131:331–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [22].Georgitsi MD, Vitoros V, Panou C, et al. Individualized significance of the -251 A/T single nucleotide polymorphism of interleukin-8 in severe infections. Eur J Clin Microbiol Infect Dis 2016;35:563–70. [DOI] [PubMed] [Google Scholar]
- [23].Hu D, Wang H, Huang X, et al. Investigation of association between IL-8 serum levels and IL8 polymorphisms in Chinese patients with sepsis. Gene 2016;594:165–70. [DOI] [PubMed] [Google Scholar]
- [24].Zhao XF, Zhu SY, Hu H, et al. [Association between interleukin-8 rs4073 polymorphisms and susceptibility to neonatal sepsis]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2020;22:323–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [25].Fu P, Xie S, Zhang X. IL-8 gene locus is associated with risk, severity and 28-day mortality of sepsis in a Chinese population. Clin Exp Med 2019;19:571–6. [DOI] [PubMed] [Google Scholar]
- [26].Baghel K, Srivastava RN, Chandra A, et al. TNF-(, IL-6, and IL-8 cytokines and their association with TNF-(-308 G/A polymorphism and postoperative sepsis. J Gastrointest Surg 2014;18:1486–94. [DOI] [PubMed] [Google Scholar]
- [27].Yousef AA, Suliman GA, Mabrouk MM. The value of admission serum IL-8 monitoring and the correlation with IL-8 (-251A/T) polymorphism in critically ill patients. ISRN Inflamm 2014;2014:494985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [28].Shamseer L, Moher D, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ (Clinical research ed) 2015;350:g7647. [DOI] [PubMed] [Google Scholar]
- [29].Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol 2010;25:603–5. [DOI] [PubMed] [Google Scholar]
- [30].Zhang Q, Jin Y, Li X, et al. Plasminogen activator inhibitor-1 (PAI-1) 4G/5G promoter polymorphisms and risk of venous thromboembolism—a meta-analysis and systematic review. VASA Zeitschrift fur Gefasskrankheiten 2020;49:141–6. [DOI] [PubMed] [Google Scholar]
- [31].Lewis SJ, Zammit S, Gunnell D, et al. Bias in meta-analysis detected by a simple, graphical test. BMJ Clin Res 1997;315:629–34. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [32].Duval S, Tweedie R. Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis. Biometrics 2000;56:455–63. [DOI] [PubMed] [Google Scholar]
- [33].Raychaudhuri SP, Jiang WY, Farber EM, et al. Upregulation of RANTES in psoriatic keratinocytes: a possible pathogenic mechanism for psoriasis. Acta Dermatovenereol 1999;79:09–11. [DOI] [PubMed] [Google Scholar]
- [34].Hull J, Ackerman H, Isles K, et al. Unusual haplotypic structure of IL8, a susceptibility locus for a common respiratory virus. Am J Hum Genet 2001;69:413–9. [DOI] [PMC free article] [PubMed] [Google Scholar]