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- W2335408903 abstract "Future Science OAVol. 2, No. 2 EditorialOpen Access10 years of research: from ignoring Modic changes to considerations regarding treatment and prevention of low-grade disc infectionsClaus Manniche & Alan JordanClaus Manniche*Author for correspondence: E-mail Address: claus.manniche@rsyd.dk Spine Center of Southern Denmark & University of Southern Denmark, Oestre Hougvej 55, 5500 Middelfart, DenmarkSearch for more papers by this author & Alan Jordan Broadgate Spine & Joint Clinic, 65 London Wall, London, EC2M 5TU, UKSearch for more papers by this authorPublished Online:5 Apr 2016https://doi.org/10.4155/fsoa-2016-0017AboutSectionsPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack Citations ShareShare onFacebookTwitterLinkedInReddit Keywords: disc infectionlow back painModic changesFigure 1. An MRI T2-weighted image.Typical Modic changes type 1 (high signal intensity) in a lumbar segment. Reproduced with permission from [4].Figure 2. The development of Modic changes.Two associated pathways. Mechanical pathway: (0) normal disc; (1) age-related disc degeneration and the development of spondylosis; (2) end plate damage with development of Modic changes type 1. Infectious pathway: (3) disc degeneration with the development of a disc herniation; (4) invasion of bacteria, causing a disc infection; (5) end plate damage and bacteria with the development of Modic changes type 1.Reproduced with permission from [8].First draft submitted: 24 February 2016; Accepted for publication: 25 February 2016; Published online: 5 April 2016After many years of essentially ignoring or considering Modic changes (MC) as seen on MRI scans as incidental findings, a new era began with the publication of Kjær et al. 10 years ago, who were the first research group in the world to demonstrate a clear correlation between MC and the 1-year prevalence of back pain [1]. This important discovery ‘upset’ the prevailing consensus among back specialists that back pain was predominantly a biopsychosocial phenomenon with an emphasis on the psychosocial dimension [2]. Since Kjær et al.'s publication, the biological dimension of back pain has become a hot topic among back pain researchers throughout the world. Currently, new publications dealing with Modic-related topics are published almost weekly in scientific journals.We will introduce the reader to the concept of MC and present the current status of our knowledge from the very latest scientific literature including the presence of Propionibacterium acnes inside the disc. Many of the bricks involved in this puzzle are beginning to form a biologically sound ‘picture’.Definitions, pathoanatomy/genesis, symptoms & treatmentIn the literature [3,4], three types of MC are defined; MC type 1, type 2 and type 3. Type 1 is characterized by high signal intensity on T2-weighted images (Figure 1) and low signal intensity on T1-weighted images. The extent of each MC can vary from a narrow fringe that simply involves the end plate of the vertebra to spreading into large parts of the adjacent vertebra. MC type 2 is characterized by high signal intensity on both T1- and T2-weighted images. MC type 1 contains vascular tissue and active inflammatory agents; type 2 contains granulation tissue infiltrated by significant amounts of fat cells. This has been demonstrated in biopsy studies. MC Type 3 are rare and do not appear to have any clinical relevance. They represent subchondral bony sclerosis with low T1 and T2 signal intensity. In patients with prolonged back pain, the prevalence of MC is 40%. In individuals with MC, more than 90% will have back pain within 1 year. MC often causes localized pain 24/7 and nocturnal pain is the rule rather than the exception [5]. A direct correlation between the size of the MCs as seen over time and pain intensity variations has been demonstrated [6]. MC type 1 are an important prognostic marker of a poor prognosis regarding relentless pain and reduced daily function [6]. We refer to references [4] and [7] for additional detail.The most common cause of MC may well be that the ordinary disc degenerative processes involving damage and microfractures to the vertebral end plates (Figure 2; nr. 0-1-2). In some patients, the degenerative process results in the development of edema and inflammation of the adjacent vertebrae. Several factors may be involved: end plate damage following disc herniation, ingrowth of capillaries and inflammatory agents related to the end plate structure may be important ingredients in the development of pain and MC in the involved spinal segment [9]. As the bony end plates normally have a rich supply of small free nerve endings, degenerative developments and inflammation likely trigger localized inflammatory pain [9].Following disc herniations or annular tears, bacteria may enter the disc and initiate a discitis (Figure 2: nr. 0-3-4-5) [4]. Low or high virulent infections may take place depending upon the bacterial species or subtype [10]. Anaerobic P. acnes bacteria are often present in the herniated mass following an acute disc herniation [4].The degenerative and the infectious pathways may work concurrently and together accelerate the destruction of the spinal segment structures [9,11].In most cases, treatment is similar to that recommended for other cases of disc degeneration/spondylosis that are not spontaneously improving. In most cases, no relief is seen following back exercises or general training [4]. If there is a suspicion of a disc infection, prolonged antibiotic therapy may be an effective treatment. In 2013, a randomized clinical trial (RCT) with 1-year follow-up RCT investigated the efficacy of amoxicillin/clavulanic acid for a 3-month period in patients with disc herniations and MC type 1 as seen on MRI [12]. In more than 50–60% of these patients clinically relevant and statistically significant improvements were seen at the end of treatment with further improvement in the actively treated group up to 1-year follow-up. Another smaller RCT with no follow-up period also demonstrated a positive clinical effect of antibiotic treatment in patients with MC type 1 [13]. Several large RCTs are underway or in the planning stages in Norway, Australia and the UK.The infectious pathway: the scientific caseIt has been acknowledged for many years that disc degeneration – typically initiated by trauma or local mechanical forces – involved the vertebral end plates during the progressive destructive phase, in some patients. The resulting end plate damage is associated with the MRI finding, MC [9–11].In 2008, a Danish research group proposed the theory that in addition to the degenerative/mechanical pathway toward developing MC, an alternative infectious pathway likely took place concurrently [4]. The infectious pathway takes place as a result of a series of occurrences in and around the disc and end plates as is the case for the degenerative/mechanical pathway. The latest research in this field appears to confirm the existence of an infectious pathway: Low virulent bacteria enter the disc following a herniation or small trauma related annular tears [11,14]. This process may well be facilitated by the tearing of end plate fragments often seen in biopsies of herniated material that render the end plate damaged, which also delays herniated disc material resorption and results in neovascularization [15–18];The bacteria are randomly transported through the circulatory system to the discs or may enter from contamination in spinal-related surgical procedures [4,11,18];When the skin barrier is broken, there is a risk of bacterial spreading from the folds of the skin and sebaceous glands to spine despite sterilization procedures [19]. In some cases, the invading bacteria may have a nonskin origination, for example, from the oral cavity, as shown by Rollason et al. in a phylogenetic study [20];The most commonly found bacteria in the disc and herniated discal tissue are different subtypes of P. acnes [20–22];Bacteria with sufficiently virulent characteristics are able to colonize intradiscally [10];This is followed by inflammation and accelerated degeneration that in turn leads to end plate damage and MC changes as seen on MRI scans [10,23,24];Disc-related inflammation will lead to back pain and the injection of anti-inflammatory agents has demonstrated short-term pain reduction in several studies [23,25];A long-term antibiotic regimen results in a 50% reduction of pain in 50% of patients with low back pain following a disc herniation and Modic changes type 1 [12,13].Conclusion & future perspectiveAs the infectious pathway is shown to exist as an alternative to the degenerative/mechanical pathway, it is relevant to ask how we can differentiate the diagnoses ‘low virulent bacterial discitis/MC’ from ‘mechanical disc degeneration/MC?’ In which cases is antibiotic treatment relevant to consider? Which antibiotic regimes are most effective and provide the patients and the environment with the highest degree of protection? Are there other treatment alternatives? Can one imagine preventative steps which may prevent a bacterial infection through contamination?There are currently no conclusive answers to these questions.We must acknowledge that differing analytical methods used to identify which bacteria are found in discs are by no means effective. When the spread of findings ranges from 3 to 53% regarding the presence of bacteria in discal tissue [11], this is likely due to poor and difficult analytical methods. More readily available and reliable analytical methods are required. Perhaps it may be possible to develop blood tests that are sensitive for intradiscal bacterial infection?The MRI-based diagnostics are not completed yet. End plate damage has not been standardized [4,26] and the interpretation of MC types 1 and 2 are often based upon the radiologists’ subjective evaluation.It seems appropriate to treat patients with MC type 1. It is, therefore, imperative to continue researching the utilization of antibiotic treatment for this condition. Which treatment regimen is most effective? Is perioperative preventative antibiotic treatment relevant in the prevention of low virulent discitis?P. acnes beyond the skin may result in many different serious opportunistic infections: in bone, implants, glands, lungs and vascular tissues, and there are still many unanswered questions before puzzle has been completed [27].The current increased documentation of an infectious pathway in disc disease has increased our need to address the related questions not least due to the fact that appropriate treatment forms for this condition already seems to be visible in the horizon.DisclaimerThe opinions expressed in this editorial are those of the authors and do not necessarily reflect the views of Future Science Ltd.Financial & competing interests disclosureC Manniche and A Jordan are two of the owners of MASTMedical.com and Persica Ltd; companies related to educational and research developing activities regarding the new spine disease ‘Modic changes’. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.No writing assistance was utilized in the production of this manuscript.Open accessThis work is licensed under the Creative Commons Attribution 4.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/References1 Kjaer P, Korsholm L, Bendix T, Sorensen JS, Leboeuf-Yde C. Modic changes and their associations with clinical findings. Eur. Spine J. 15, 1312–1319 (2006).Crossref, Medline, Google Scholar2 Pincus T, Kent P, Bronfort G, Loisel P, Pransky G, Hartvigsen J. Twenty-five years with the biopsychosocial model of low back pain – Is it time to celebrate? A report from the twelfth international forum for primary care research on low back pain. 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Ther. 9(12), 1149–1156 (2011).Crossref, Medline, CAS, Google ScholarFiguresReferencesRelatedDetailsCited ByLow‐field magnetic resonance imaging characteristics of multifocal vertebral lesions in dogs28 January 2021 | Veterinary Record, Vol. 189, No. 5Chronic low back pain, Modic changes and low-grade virulent infection: efficacy of antibiotic treatmentClaus Manniche & Gerard M Hall7 April 2021 | Future Science OA, Vol. 7, No. 6Classification of certain vertebral degenerations using MRI image features28 May 2021 | Biomedical Physics & Engineering Express, Vol. 7, No. 4Chronic low back pain, bacterial infection and treatment with antibioticsThe Spine Journal, Vol. 21, No. 6Mechanisms and Origins of Spinal Pain: from Molecules to Anatomy, with Diagnostic Clues and Imaging FindingsRadioGraphics, Vol. 40, No. 4 Are Opioids Needed to Treat Chronic Low Back Pain? A Review of Treatment Options and Analgesics in Development 1 May 2020 | Journal of Pain Research, Vol. Volume 13New insights link low-virulent disc infections to the etiology of severe disc degeneration and Modic changesClaus Manniche & Søren O'Neill5 June 2019 | Future Science OA, Vol. 5, No. 5New insights link low-virulent disc infections to the etiology of severe disc degeneration and Modic changes18 March 2019 | Future Science OA, Vol. 2016Bacteria—Human Interactions: Leads for Personalized Medicine3 August 2019Transforaminal Epiduroscopic Basivertebral Nerve Laser Ablation for Chronic Low Back Pain Associated with Modic Changes: A Preliminary Open-Label StudyPain Research and Management, Vol. 2018¿Supone la presencia de cambios Modic en pacientes con dolor lumbar crónico una peor evolución clínica y una mayor posibilidad de precisar cirugía? Evolución a 10 añosRevista Española de Cirugía Ortopédica y Traumatología, Vol. 62, No. 4Are Modic changes in patients with chronic low back pain indicative of a worse clinical course? 10 years of follow-upRevista Española de Cirugía Ortopédica y Traumatología (English Edition), Vol. 62, No. 4 Vol. 2, No. 2 Follow us on social media for the latest updates Metrics History Published online 5 April 2016 Published in print June 2016 Information© Claus MannicheKeywordsdisc infectionlow back painModic changesDisclaimerThe opinions expressed in this editorial are those of the authors and do not necessarily reflect the views of Future Science Ltd.Financial & competing interests disclosureC Manniche and A Jordan are two of the owners of MASTMedical.com and Persica Ltd; companies related to educational and research developing activities regarding the new spine disease ‘Modic changes’. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.No writing assistance was utilized in the production of this manuscript.Open accessThis work is licensed under the Creative Commons Attribution 4.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/PDF download" @default.
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