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Could low grade bacterial infection contribute to low back pain? A systematic review

Abstract

Background

Recently, there has been both immense interest and controversy regarding a randomised, controlled trial which showed antibiotics to be effective in the treatment of chronic low back pain (disc herniation with Modic Type 1 change). While this research has the potential to result in a paradigm shift in the treatment of low back pain, several questions remain unanswered. This systematic review aims to address these questions by examining the role of bacteria in low back pain and the relationship between bacteria and Modic change.

Methods

We conducted electronic searches of MEDLINE and EMBASE and included studies that examined the relationship between bacteria and back pain or Modic change. Studies were rated based on their methodological quality, a best-evidence synthesis was used to summarise the results, and Bradford Hill’s criteria were used to assess the evidence for causation.

Results

Eleven studies were identified. The median (range) age and percentage of female participants was 44.7 (41–46.4) years and 41.5% (27–59%), respectively, and in 7 of the 11 studies participants were diagnosed with disc herniation. Nine studies examined the presence of bacteria in spinal disc material and all identified bacteria, with the pooled estimate of the proportion with positive samples being 34%. Propionibacterium acnes was the most prevalent bacteria, being present in 7 of the 9 studies, with median (minimum, maximum) 45.0% (0–86.0) of samples positive. The best evidence synthesis found moderate evidence for a relationship between the presence of bacteria and both low back pain with disc herniation and Modic Type 1 change with disc herniation. There was modest evidence for a cause-effect relationship.

Conclusions

We found that bacteria were common in the spinal disc material of people undergoing spinal surgery. There was moderate evidence for a relationship between the presence of bacteria and both low back pain with disc herniation and Modic Type 1 change associated with disc herniation and modest evidence for causation. However, further work is needed to determine whether these organisms are a result of contamination or represent low grade infection of the spine which contributes to chronic low back pain.

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Background

There has been both immense interest and controversy regarding a recent randomised, controlled trial (RCT) which showed antibiotic treatment to be effective in the treatment of chronic low back pain in individuals with herniated discs and associated Modic Type 1 changes (bone oedema) on magnetic resonance imaging (MRI) [1]. The RCT was based on the hypothesis that some individuals with a disc herniation develop chronic low back pain due to a secondary infection that occurs in the disc. While this research has the potential to result in a paradigm shift in the treatment of low back pain, it has not currently been translated into clinical practice. These findings have some similarities to the discovery of Helicobacter pylori and the shift it led to in the way peptic ulcers are treated. However, a greater understanding of the evidence underlying this RCT is required before a change in practice can be justified. Moreover, although the potential for good is high, the potential for harm in selecting for antimicrobial resistance with the prolonged use of broad spectrum antibiotics is also significant.

This recent RCT by Albert et al. [1] was based on the findings of their previous biopsy study which suggested that those who developed early Modic Type 1 changes were more likely to have infection with Propionibacterium acnes (P. acnes) [2]. However, there are several questions that remain unanswered; have other studies investigated the presence of bacteria in people with low back pain, and if so, what bacteria were identified, what were the associated participant and clinical characteristics, what evidence is there that bacteria are associated with low back pain, and are Modic changes markers for bacterial infection. This systematic review aims to address these questions by examining the evidence for the presence of bacteria in spinal structures of patients undergoing lumbar spine surgery and investigating the relationship between bacterial infection and Modic change. This work has the potential to provide a greater understanding of the evidence behind a potentially effective and safe treatment approach for individuals with chronic low back pain and disc herniation, thus significantly reducing the individual suffering and societal burden associated with this condition.

Methods

This systematic review was conducted according to the 2009 PRISMA statement [3,4].

Search strategy

A computerised search strategy was performed using MEDLINE and EMBASE from January 1946 until March 2014. We used the following MeSH headings and key words; ‘bacteria’, ‘infection’, ‘propionibacterium acnes’, ‘microbial’, ‘low back pain’, ‘Modic change’, and ‘lumbar surgery’. The search was limited to human studies of adults published in the English language. We also searched the reference lists of studies included in this review.

We included studies which examined i) the role of bacteria in low back pain and ii) the relationship between the presence of bacteria and Modic changes. Studies where participants had low back pain secondary to a previous bacterial exposure or current systemic infection were excluded.

Information was extracted and tabulated on the characteristics of the identified studies and their cohorts, the prevalence and type of bacteria identified, the methods used for bacterial identification and to minimize contamination, the results of studies examining the relationship between bacteria and Modic change, and evidence for a causal relationship.

Methodological quality

To assess the methodological quality of the included studies, two reviewers (DU and SMH) independently scored them using the adapted scoring system of Lievense et al. [5,6] (Table 1). Each of the items was scored as positive (1), negative (0), or unclear (?), with a maximum possible score of 100%. Where the reviewers disagreed and could not achieve consensus, a third reviewer (FC) gave a final judgement. High quality was defined as achieving a score above the mean of all quality scores.

Table 1 Criteria used to assess the methodological quality of selected cohort and cross-sectional studies (Lievense et al. [5,6])

As the criteria specific to the methodological assessment of RCTs is not included in the study by Lievense et al. [5,6], the PEDro scale [7] was used. The PEDro scale rates 11 aspects of the methodological quality of RCTs as being absent or present (Table 2). The total score ranges from 0 to 10, as the first item (eligibility criteria) is not included in the scoring. Studies that obtain a score of less than 6 points are considered to be of low quality, while those with a score of greater than 6 points are of high quality.

Table 2 The PEDro Scale [7] – criteria used to assess the methodological quality of selected randomised control trials

Best evidence synthesis

A best evidence synthesis was used to summarise the data (Table 3). It was not possible to perform a meta-analysis due to the heterogeneity between the studies. The studies were ranked according to their design, with cohort studies considered to be a higher level of evidence than case control and cross-sectional studies. The level of evidence of studies was determined in conjunction with the quality score calculated for each study.

Table 3 Criteria list for determining the level of evidence for best evidence synthesis, adapted from Lievense et al. [6,7]

Bradford Hill’s criteria for causation

We used Bradford Hill’s criteria to examine the evidence for causation [8]. These criteria, along with a description of each, are included in Table 4. The Bradford Hill’s criteria are commonly used to determine whether there is adequate evidence of a causal relationship between an incidence and a consequence.

Table 4 Evidence for a causal relationship between low virulent bacteria and low back pain according to Bradford Hill’s criteria

Results

Eleven studies were included in this systematic review (Figure 1; Table 5). Of these, one was a RCT, one had a cross-sectional and a longitudinal component, and nine were cross-sectional. Ten studies examined the presence of bacteria in people undergoing spinal surgery (Table 6) and four studies investigated the relationship between the presence of bacteria and Modic changes (Table 7).

Figure 1
figure 1

PRISMA flow diagram showing the flow of information through the different phases of the systematic review.

Table 5 Characteristics of the 11 identified studies
Table 6 Methods used for bacteria identification and to minimize contamination and prevalence, and type of bacteria identified
Table 7 Studies examining the relationship between the presence of low virulent bacteria and modic changes

What were the characteristics of people with low back pain that have bacterial infection?

Table 5 presents the characteristics of the study cohorts in the 11 identified studies. The average number of participants in the 11 studies was 74, with samples ranging from 10 to 207. The median (minimum, maximum) age and percentage of female patients was 44.7 (41, 46.4) years and 41.5% (27, 59), respectively. In five of the 11 studies, the participants were diagnosed with disc herniation alone [2,9-13], with the remaining six studies recruiting participants with discogenic radiculitis [14,15], radiculopathy and disc herniation [14,16,17], disc degeneration [10], disc herniation and Modic changes [1], and Modic changes only [15].

Three studies reported the use of a control group; Albert’s RCT included an intervention group receiving antibiotic treatment and a placebo group [1], Stirling et al. [17] recruited patients with trauma, tumours, or scoliosis for their controls, and, similarly, Coscia et al. [11] included patients with trauma or neuromuscular deformity. Four of the 11 studies specified the inclusion and exclusion criteria they used [2,10,16]; with previous use of antibiotics [2,10], allergy to antibiotics [1], and previous surgery [10,16] reported to be exclusions. None of the studies specified osteomyelitis or discitis as exclusion criteria.

What was the prevalence and type of bacteria identified in studies examining participants undergoing spinal surgery?

Table 6 presents the prevalence and type of bacteria identified in 10 studies examining participants undergoing spinal surgery. Nine studies investigated the presence of bacteria in spinal disc material, with one study examining the vertebral body with Modic Type 1 change. Of the nine studies that examined disc material, the median (minimum, maximum) percentage of culture positive samples was found to be 22.0% (6.7, 53.3). The data are presented as a forest plot (Figure 2) with the pooled estimate of the proportion with positive cultures being 34%. Eight of these nine studies identified more than one bacteria, with the study by Ben-Galim et al. [10] only reporting the presence of coagulase-negative staphylococci. While a variety of bacteria were identified, P. acnes was the most prevalent, being present in seven of the nine studies and the most common bacteria in six of the nine studies. A median (minimum, maximum) of 45% (0, 86.0) of samples were positive for P. acnes, followed by coagulase-negative staphylococci, which was present in 14% (0, 100) of cases. The study by Wedderkopp et al. [15], which investigated the presence of bacteria in the vertebral body, reported 8.3% of cultures to be positive, with staphylococcus epidermis and coagulase-negative staphylococci each being present in 50% of cultures.

Figure 2
figure 2

Forest plot showing the proportion of positive cultures in the nine studies examining the presence of bacteria in disc material in patients undergoing spinal surgery.

There were a variety of methods used to identify bacteria and minimize contamination. Nine of the 10 studies used an open procedure to obtain biopsies, with one study by Wedderkopp et al. [15] using a closed, needle approach. Six studies used cultures to identify bacteria [9-11,13,15,16], two studies used culture and serology [14,17], and the remaining two used PCR with [2] or without culture [12]. Studies obtained between one and five specimens for assessment. The duration of culturing varied considerably between the studies, ranging from 5 to 7 days [4,10,14,15,17] to 2 to 3 weeks [11,12,16,18]. Moreover, only three of the 10 studies performed genetic analysis to determine the species of P. acnes identified [4,14,15]. With respect to minimizing contamination, five of the studies simply stated that aseptic or sterile techniques were used [10,11,13,15,17], while the others reported a wide variety of techniques including flaming scalpels [2], using bipolar diathermy [12], and collecting specimens in sterile cups and syringes [9,16].

Are Modic changes markers of bacterial infection in low back pain?

Only four of the 11 studies we identified examined Modic changes. The RCT by Albert et al. [1] examined differences in Modic Type 1 changes after antibiotic treatment and found a reduction in their volume in the treatment group compared to the placebo group (P = 0.05). In Albert et al.’s biopsy study [2], low virulent bacteria were identified in participants who did and did not develop new Modic Type 1 changes, and conversely, those that had no bacteria present also developed Modic Type 1 changes. However, overall, a significant association between anaerobic bacteria and Modic Type 1 change was reported (5.60; 95% CI, 1.51–21.95; P = 0.004). The study by Arndt et al. [9] reported no significant association between the presence of bacteria and Modic Type 1 and 2 changes on MRI, and Wedderkopp et al. [15] reported that there was no evidence of bacteria in vertebrae with Modic Type 1 changes.

What did the best evidence synthesis show with regards to the role of bacteria in low back pain and the relationship between bacteria and Modic changes?

Eleven studies examined the role of bacteria in low back pain (Table 5). This included one RCT and 10 cross-sectional studies. The mean methodological quality score of the 10 cross-sectional studies was 70%, with scores ranging from 56% to 78%. Four of the 10 observational studies were considered to be of high quality (according to the Lievense criteria), as they were given a quality score above the mean [2,11,14,16]. The RCT by Albert et al. [1] was also considered high quality as it scored greater than six on the PEDro scale. Overall, the best evidence synthesis indicated moderate evidence for a role of bacteria in low back pain with disc herniation.

Four studies examined the relationship between the presence of bacteria and Modic changes (Table 7). This included one RCT, one cohort study, and two cross-sectional studies. The RCT and cohort study were of high quality and the cross-sectional studies were of low quality. Overall, the best-evidence synthesis indicated moderate evidence for a relationship between the presence of bacteria and Modic Type 1 changes with disc herniation.

What evidence is there for causation according to Bradford Hill’s criteria?

Table 4 presents Bradford Hill’s criteria, an explanation of each criterion, and evidence for a causal relationship between low virulent bacteria and chronic back pain in relation to each criterion. While there was evidence for causation with respect to five of Bradford Hill’s criteria (plausibility, strength of the association, specificity, reversibility, and coherence), there was no or limited evidence for the remaining four criteria (temporal relationship, consistency, dose–response relationship, and analogy). Overall, this approach suggests that there is modest evidence for a cause-effect relationship, with a major criteria (reversibility) being present between low virulent bacteria and chronic low back pain. However, further work is needed to clarify the role of bacterial infection in the development of low back pain with disc herniation.

Discussion

This review identified 11 studies which examined the role of bacteria in individuals with low back pain. Ten studies reported the presence of bacteria in people undergoing spinal surgery, with P. acnes being the most commonly identified. Participants with bacterial infection were aged in their 40’s, were of both genders, and were most commonly diagnosed with lumbar disc herniation. The best evidence syntheses showed moderate evidence for low virulent bacteria having a role in low back pain with disc herniation and moderate evidence for a relationship between bacterial infection and Modic Type 1 change with disc herniation. There was also modest evidence for a causal relationship between the presence of bacteria and low back pain with disc herniation according to the Bradford Hill criteria.

All nine studies which examined the spinal disc material of individuals undergoing spinal surgery, found bacteria to be present in the disc, with pooled estimate of the proportion of positive cultures found to be 34%. P. acnes was the most common bacterium identified, being reported in seven of the nine studies, with a median (range) of 45.0% (0–86.0) of positive cultures. In contrast, the study by Wedderkopp et al. [15], which examined the presence of bacteria in the lumbar vertebrae, did not identify P. acnes in Modic Type 1 changes. While P. acnes is part of the normal human microbiota and has even been shown to stimulate protective responses against various cancers, there is growing evidence to suggest that it can have a pathological role in the human body, including being a cause of infections in injured structures and indwelling medical devices [18]. It is believed that the predominance of P. acnes, which is an anaerobic bacterium, may reflect the unusual environment in the disc where the lack of vascularity results in a very low oxygen tension and a low pH which provides ideal conditions for low virulent anaerobic bacteria to grow.

While each of the 10 studies identified bacteria in excised spinal tissue, there were inconsistencies between studies with respect to the prevalence of positive cultures and the types of bacteria identified. These inconsistencies may have been due to differences in study methodology, including the use of varying methods and time frames for detecting bacteria (cultures, PCR, and serology), culturing the biopsy material, and administering the antibiotic treatment. For instance, the two studies by Fritzell et al. [12] and Ben-Galim et al. [10], which did not report the presence of the P. acnes, used stringent methodology, including PCR to detect bacterial DNA and stringent aseptic biopsy methods, respectively, as well as longer time periods to culture the biopsies. Moreover, only six of the 10 studies reported on the administration of antibiotics, with three studies providing the dose before spinal tissue was excised [9,10,16] and three studies after tissue was removed [2,12,15].

Participants with positive cultures were of both genders, primarily in their 40’s, and most commonly presented for spinal surgery due to lumbar disc herniation. This clinical profile may be explained by the reduction in water content of the disc during the fifth decade and the greater susceptibility of the disc to injury, allowing influx of bacteria into the damaged disc and subsequent colonisation and chronic infection.

There was moderate evidence for a relationship between the presence of bacteria and Modic Type 1 changes with disc herniation. This evidence was based on the cohort study [2] and RCT [1] by Albert et al. that recruited low back pain participants with disc herniation and Type 1 Modic changes [2]. In contrast, the cross-sectional studies by Arndt [10] and Wedderkopp [15] found no association between bacteria and Type 1 and 2 Modic changes in people with disc degeneration and Type 1 Modic changes in those with ‘persistent’ low back pain, respectively. It is important to note that Modic Type 1 change and disc herniation are prevalent in 14 to 16% [19,20] and 30% (at the L5/S1 level) of individuals with low back pain, respectively [21]. Moreover, while the prevalence of disc pathology occurring concurrently with Modic Type 1 change has been reported to range from 11.5 to 17.5% [21], these data are not specific to disc herniation, and include other disc pathologies such as disc bulge and disc degeneration. However, overall, these results suggest that the concurrent prevalence of Modic Type 1 change and disc herniation is low and thus individuals with these pathologies, who may respond to treatments such as antibiotics, only represent a select subgroup of the low back pain population. Moreover, although we have focussed on the relationship between bacteria and Modic change, it has been hypothesised that Modic changes may also result from mechanical forces acting on the vertebral endplate. It is clear that further study is required to determine which clinical characteristics clearly identify the presence of bacteria in lumbar discs and the pathological processes involved with the development of Modic change.

The mechanism by which bacteria may enter the lumbar spinal tissue is unclear. There are several hypotheses presented in the literature. It has been suggested that injury to the disc which breaches the disc’s integrity allows low virulent organisms that are commonly present on human skin to travel via the blood stream to the disc [1,2]. The presence of the bacteria in the disc subsequently sets up an inflammatory response in the adjacent bone due to the release of cytokines and propionic acid, which enter the vertebrae through normal disc nutrition. It has also been suggested that the presence of bacteria may be the result of primary disc degeneration which allows pathogenic organisms to enter the disc and/or hinders their elimination [12]. Moreover, Arndt et al. [9] postulated that bacteria may be the result of haematogenous spread from a distant septic location, contiguous spread from an adjacent infection, or transvenous retrograde pathway from the pelvis. It is clear that further investigation is needed to understand the mechanisms underlying the presence of bacteria in spinal disc and bone material.

There is considerable debate in the literature about whether the presence of the bacteria in spinal discs is actually due to infection or a result of contamination during study procedures. While a number of studies in this review reported that the presence of bacteria might be due to low grade infection in the disc [2,11,12,14,16,17], several studies also suggested that contamination may play a role [10,13,15]. The inclusion of control cultures and control groups in future studies may assist in determining whether the low virulent bacteria identified are due to true infection or contamination.

There are several limitations and strengths to this study. There were a small number of studies identified and these were mainly cross-sectional and of modest quality. Only one RCT and one longitudinal study were identified. Studies varied considerably in their methodology, particularly in methods used to identify bacteria and minimize contamination and only three studies included a control group. A meta-analysis was not able to be performed due to the heterogeneity of the studies identified. However, the key strength of this study is that it is the first systematic review on this topic. We have performed a systematic search of the literature, tabulated the key features of the identified studies, performed a best evidence synthesis to summarise the data, and examined causation using the Bradford Hill criteria.

Conclusions

This systematic review found moderate evidence to indicate low virulent bacteria have a role in low back pain with disc herniation and moderate evidence for a relationship between bacteria and Modic Type 1 change associated with disc herniation. While there was also modest evidence for causation, further work is needed to determine whether these low virulent organisms are a result of contamination or represent low grade infection of the lumbar spine which contributes to chronic low back pain associated with type 1 Modic changes in people with disc herniation.

Abbreviations

LBP:

Low back pain

P. acnes :

Propionibacterium acnes

RCT:

Randomized controlled trial

References

  1. Albert H, Sorensen J, Christensen B, Manniche C. Antibiotic treatment in patients with chronic low back pain and vertebral bone edema (Modic type 1 changes): a double-blind randomized clinical controlled trial of efficacy. Eur Spine J. 2013;22:697–707.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Albert H, Lambert P, Rollason J, Sorensen JS, Worthington T, Pedersen MB, et al. Does nuclear tissue infected with bacteria following disc herniations lead to Modic changes in the adjacent vertebrae? Eur Spine J. 2013;22:690–6.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Liberati A, Altman D, Tetzlaff J, Mulrow C, Gøtzsche P, Ioannidis J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ. 2009;339:b2700.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Moher D, Liberati A, Tetzlaff J, Altman D, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151:264–9.

    Article  PubMed  Google Scholar 

  5. Lievense A, Bierma-Zeinstra S, Vergahen A, van Baar M, Verhaar J, Koes B. Influence of obesity on the development of osteoarthritis of the hip: a systematic review. Rheumatol. 2002;41:1155–62.

    Article  CAS  Google Scholar 

  6. Lievense A, Bierma-Zeinstra S, Verhagen A, Verhaar J, Koes B. Influence of work on the development of osteoarthritis of the hip: a systematic review. J Rheumatol. 2001;28:2520–8.

    CAS  PubMed  Google Scholar 

  7. de Morton N. The PEDro scale is a valid measure of the methodological quality of clinical trials: a demographic study. Aust J Physiother. 2009;55:129–33.

    Article  PubMed  Google Scholar 

  8. Hill A. The environment and disease: association or causation? Proc R Soc Med. 1965;58:295–300.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Arndt J, Charles Y, Koebel C, Bogorin I, Steib JP. Bacteriology of degenerated lumbar intervertebral disks. J Spinal Disord Tech. 2012;25:E211–6.

    Article  PubMed  Google Scholar 

  10. Ben-Galim P, Rand N, Giladi M, Schwartz D, Ashkenazi E, Millgram M, et al. Association between sciatica and microbial infection: true infection or culture contamination? Spine (Phila Pa 1976). 2006;31:2507–9.

    Article  Google Scholar 

  11. Coscia M, Wack M, Denys G. Low vitulence bacterial infections of intervertebral discs and the resultant spinal disease processes. Los Angeles: Scoliosis Research Society (SRS) Annual Meeting; 2003.

    Google Scholar 

  12. Fritzell P, Bergström T, Welinder-Olsson C. Detection of bacterial DNA in painful degenerated spinal discs in patients without signs of clinical infection. Eur Spine J. 2004;13:702–6.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Carricajo A, Nuti C, Aubert E, Hatem O, Fonsale N, Mallaval F, et al. Propionibacterium acnes contamination in lumbar disc surgery. J Hosp Infect. 2007;66:275–7.

    Article  CAS  PubMed  Google Scholar 

  14. Stirling A, Worthington T, Rafiq M, Lambert P, Elliott T. Association between sciatica and Propionibacterium acnes. Lancet. 2001;357:2024–5.

    Article  CAS  PubMed  Google Scholar 

  15. Wedderkopp N, Thomsen K, Manniche C, Kolmos H, Secher Jensen T, Leboeuf YC. No evidence for presence of bacteria in modic type I changes. Acta Radiol. 2009;50:65–70.

    Article  CAS  PubMed  Google Scholar 

  16. Agarwal V, Golish S, Alamin T. Bacteriologic culture of excised intervertebral disc from immunocompetent patients undergoing single level primary lumbar microdiscectomy. J Spinal Disord Tech. 2011;24:397–400.

    Article  PubMed  Google Scholar 

  17. Stirling A, Rafiq M, Mathur K, Elliott T, Worthington T, Lambert P. Association between sciatica and skin commensals. J Bone Joint Surg (Br). 2002;84B:147.

    Google Scholar 

  18. McDowell A, Patrick S, Eishi Y, Lambert P, Eady A. Propionibacterium acnes in human health and disease. Biomed Res Int. 2013;2013:493564.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Jensen RK, Leboeuf YC. Is the presence of modic changes associated with the outcomes of different treatments? A systematic critical review. BMC Musculoskelet Disord. 2011;12:183.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Keller A, Boyle E, Skog T, Cassidy J, Bautz-Holter E. Are modic changes prognostic for recovery in a cohort of patients with non-specific low back pain? Eur Spine J. 2012;21:418–24.

    Article  PubMed  Google Scholar 

  21. Albert H, Briggs A, Kent P, Byrhagen A, Hansen C, Kjaergaard K. The prevalence of MRI-defined spinal pathoanatomies and their association with modic changes in individuals seeking care for low back pain. Eur Spine J. 2011;20:1355–62.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

Donna M Urquhart is the recipient of an NHMRC Career Development Fellowship (1011975). This work was funded by the Monash University Strategic Grant Scheme (SPG-L 070).

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Correspondence to Donna M Urquhart.

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The authors declare that they have no competing interests.

Authors’ contributions

DU and FC: Study concept, acquisition of data/studies, analysis and interpretation of data, drafting and critical revision of the manuscript, gave final approval for manuscript publication, and agreed to be accountable for all aspects of the work. YZ: Acquisition of data/studies, drafting and critical revision of the manuscript, gave final approval for manuscript publication, and agreed to be accountable for all aspects of the work. AC, JR, PC, SL, and SH: Analysis and interpretation of data, critical revision of the manuscript, gave final approval for manuscript publication, and agreed to be accountable for all aspects of the work.

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Donna M Urquhart and Yiliang Zheng are joint first authors.

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Urquhart, D.M., Zheng, Y., Cheng, A.C. et al. Could low grade bacterial infection contribute to low back pain? A systematic review. BMC Med 13, 13 (2015). https://0-doi-org.brum.beds.ac.uk/10.1186/s12916-015-0267-x

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