\r\n\tBy definition, risk is the value obtained from the assessment of possible consequences (human losses, direct and indirect damages and costs) caused by incidents or accidents, together with the probability of occurrence of hazardous processes due to the conjunction of the factors involved. Risk is a combination of the probability of unfavorable scenarios and their consequences.
\r\n\tIn this context, it is possible, and advisable, to evaluate the expected value of these consequences, in order to establish, based on scenarios, procedures for forecasting, preventing, controlling and mitigating the effects of these hazardous processes to people and assets, associated with both natural and technological risks.
\r\n\tRisk analysis, risk evaluation and risk management are the main pieces of the process known as ‘Risk Assessment’. Risk assessment can be understood as the joint effort of identifying and analysing potential – future - events, i.e., risk analysis, and evaluating the acceptability of risk based on the risk analysis, while considering influencing factors, i.e., risk evaluation. In short, risk assessment analyses what can go wrong, how likely it is to happen and, if it happens, what are the potential consequences.
\r\n\tSince this is a multi-disciplinary domain involving various scientific areas, among which geography, Earth and environmental sciences, ecology, engineering, law, economics, sociology and political sciences, this book aims to gather contributions with a wide spectrum of topics with regard to their theoretical background and field of application. As part of this process, the resulting assessment of risk may be expressed in both quantitative and qualitative approaches.
\r\n\tVulnerability to risks varies widely, primarily depending on the capacity of societies to integrate them in the management of their activities, to mitigate their effects and to recover from the disaster. Two major parameters are decisive for ensuring the development of these capacities and the consequent reduction in vulnerability - expert knowledge and planning.
\r\n\tIt is within the first parameter that one seeks to discern the magnitude of risks and to test new technologies to support the monitoring, evaluation and communication of threats. The concept of risk has, of course, evolved over time, and is now a basic principle in decision-making by politicians, managers, entrepreneurs, builders and civil protection services, in the definition of safety and security systems, completed in safety and emergency plans, and is integrated in crisis management programs associated with accident situations.
\r\n\tRisk assessment is an inherent part of an overall risk management strategy, which attempts to introduce, after a risk assessment, control measures to eliminate or reduce any potential risk-related consequences. This concept is linked today to a new paradigm, in which the technological, social and communicational aspects gain even more relevance.
Chronic total occlusions (CTO) of coronary arteries are defined as a complete coronary arterial occlusion (thrombolysis in myocardial infarction, TIMI grade 0) being present for more than 3 months. About 20% of patients undergoing percutaneous coronary interventions (PCI) reveal a CTO, whereas in patients with prior coronary artery bypass grafting (CABG), CTOs are even more common in more than 50% [1]. Although registry data demonstrate an improvement of the patients’ symptoms such as angina pectoris or dyspnea [2] and a reduction of adverse cardiac events [3, 4] after successful revascularization of a CTO, the overall clinical benefit is still under controversial debate, since prospective randomized controlled studies are still lacking [5, 6]. This is due partly to the greater complexity of catheter-based interventional techniques and the higher demand for materials compared to PCIs of nonchronically occlusive coronary lesions. In contrast, over the last decade, modern and novel developments of special techniques and materials increased the success rates of CTO revascularization in specialized centers toward more than 85% alongside acceptable low complication rates. This technical advance and the growing scientific evidence envisaging potential complete coronary revascularization in patients suffering from coronary multivessel disease [7, 8] have pushed CTO-PCIs into the spotlight of modern interventional cardiology.
\nIn more than 50% left ventricular (LV) function is still preserved in the territory of supply of the CTO artery [9], whereas the maintaining supply by collateral connections (CCs) is sufficient for only 20% of CTO patients while preventing exercise-induced myocardial ischemia [10, 11]. The fractional flow reserve (FFR) distally of the CTO lesion is usually less than 0.5 reflecting an insufficient collateral circulation [12]. Accordingly, exercise-testing oftentimes reveals an exercise-induced myocardial ischemia in the territory of supply of the chronically occluded coronary artery.
\nNo prospective randomized controlled studies have been published yet evaluating clinical endpoints in patients with CTO-PCI compared to patients being treated conservatively by optimal medical therapy. However, there are numerous observational studies comparing a successful with unsuccessful CTO-PCI. A meta-analysis of these retrospective registry data show an improvement of angina pectoris and a decrease of consecutive need for CABG surgery after successful CTO-PCI [2].
\nAlthough symptoms’ relief instead of prognostic benefit represents the primary indication for an elective CTO-PCI, the prognostic aspect is debated increasingly as a potential indication. Accordingly, there are still only retrospective cohort studies available suggesting a potential prognostic benefit after successful CTO-PCI [13]. The largest CTO registry from the UK database demonstrated a 30% improvement of long-term survival both for patients with successful PCI of at least one CTO as well as for those with complete coronary revascularization in 13,433 CTO patients [14].
\nSub-analyses of the New York State Registry including more than 21,000 patients with elective coronary stent implantation showed that a complete revascularization was associated with an improved adjusted long-term survival compared to incomplete revascularization including CTOs [8]. These data support the concept targeting the complete revascularization including the revascularization of coronary CTOs.
\nFigure 1 shows own data from a recent monocentric analysis including 1,642 CTO-patients. The prognostic benefit of a CTO-PCI depends on the extend of coronary artery disease and is most prominent in patients with a coronary three-vessel disease [15].
\nAdjusted 3-year mortality of 1,642 CTO patients presenting at the University Heart Centre Bad Krozingen, Germany. A clear prognostic benefit is shown for complete coronary revascularization, especially in patients with a coronary three-vessel disease including a CTO (HR, hazard ratio; CI, confidence interval) a CTO (HR, hazard ratio; CI, confidence interval) [15].
A main mechanism for a beneficial prognostic influence of a successful CTO-PCI may consist in an improved tolerance for future acute coronary syndromes. A sub-analysis from the HORIZONS-AMI-study showed that patients with an ST segment elevation myocardial infarction (STEMI) and a concomitant CTO revealed a significantly increased mortality both in the acute phase and within long-term follow-up, especially in the presence of a coronary three-vessel disease [16]. Another registry database demonstrated that the presence of a CTO was associated with the future development of malignant ventricular arrhythmias in patients with an ischemia-related LV dysfunction [17].
\nThe so-called EURO-CTO-study has just finished the recruiting phase. It represents the first prospective and randomized CTO-study comparing CTO-PCIs with optimal medical treatment focusing on the improvement of predefined clinical endpoints (i.e., quality of live at 1 year, death or myocardial infarction at 3 years). Furthermore, the prospective DECISION-PCI-study from Korea randomizes CTO patients either to PCI or optimal medical treatment in order to evaluate the influence of CTO-PCI on cardiovascular mortality and future myocardial infarction at 5 years.
\nWhether LV function being assessed by cardiovascular magnetic resonance imaging (cMRI) might be improved is currently being evaluated within the REVASC-study, in which 200 patients with CTOs are randomized to PCI or optimal medical treatment. Within a prior smaller cMRI study, regional LV function depended on the extend of transmural scarring after myocardial infarction [18], whereas a further meta-analysis of registry data demonstrated an improvement of global LV ejection fraction (LVEF) of 4.7% [19].
\nAs shown in Figure 2, the principal factors on which the indication for revascularization of a CTO depends on comprise the following:
\nIndications for CTO-revascularization.
Extend of patient’s symptoms under optimal medical therapy.
Exercise testing.
Global and regional ventricular function and viability.
Severity of coronary artery disease.
Localization and morphology of the CTO.
Considering these factors before CTO-PCI allows the estimation of the potential benefit for the patient, as well as the technical severity and risk being associated with the intervention. Using the so-called J-CTO-score reveals optimal graduation of the complexity of the CTO-lesion itself and is more commonly being applied by experienced CTO operators [20].
\nThe latest European guidelines for myocardial revascularization from the year 2014 [21] recommended a class IIa, with a level of evidence B (“Percutaneous recanalization of CTOs may be considered in patients with suspected ischemia reduction in a corresponding myocardial territory and/or angina relief.”), and retrograde recanalization techniques are recommended only by a class IIB, level of evidence C (“Retrograde recanalization of CTOs may be considered after a failed antegrade approach or as the primary approach for selected patients.”).
\nThis lower recommendation class compared to the PCI of nonchronically occluded coronary lesions is in conflict to the nowadays very high success rates and low complication rates of CTO-PCIs being performed by experienced interventionalists. For instance, patients with prior CABG and a complex morphology of occluded native coronary arteries as well as consecutively occluded bypasses years after CABG surgery may benefit most from a technically demanding and long-lasting antegrade-retrograde but finally successful recanalization of native coronary arteries, as these patients may become free from limiting symptoms in daily life [22].
\nThe close cooperation of members of national and international CTO-expert groups such as the EuroCTO-club in collaboration with Japanese CTO-specialists refined and improved specific CTO techniques for more than 10 years. As a result, their experiences consolidated and were summarized including numerous publications about technical approaches and interventional steps in the so-called expert consensus statements [9, 23, 24].
\nThe primary aim is to advance a coronary guide wire through the CTO lesion into the distal true lumen of the coronary artery. Most interventionalists at first apply a soft, polymer-jacked recanalization wire with a reduced tip diameter, which passes the CTO lesion in about 40% into the right direction usually through microchannels or soft tissue at the site of the occlusion. In the case of hard and severely calcified parts of the occlusion, a so-called “wire escalation strategy” is required using recanalization wires with increasing tip loads. Within a next step, a medium-heavy, very well guidable recanalization wire is used, when the course of the CTO lesion is unclear. In contrast, when the course of the CTO-lesion is recognizable again, a harder recanalization wire with a reduce tip diameter is used, which in turn reveals an increasing force to penetrate the CTO-tissue and is targeted actively into the true distal coronary arterial lumen. The correct distal position of the wire has to be confirmed in two different angulations by contralateral contrast injections through the contralateral coronary artery (i.e., from LCA in the case of RCA-CTO and from RCA in the case of LCA-CTO). This makes a double arterial access necessary for most CTO-PCIs. When the recanalization wire does not pass the distal end of the CTO into the true vessel lumen, the so-called “parallel-wire technique” may be applied. Here, the first wire marks the false pathway, whereas a second mostly harder wire is used additionally and usually enters then the distal lumen. A crucial technical device are microcatheters—catheters of very narrow diameters—which will be advanced over and to the tip of the recanalization wires. They secure the achieved recanalization pathway and thereby exchanging to other recanalization wires becomes possible.
\nAfter successful wire passage through the CTO-lesion, predilation with increasing balloon sizes will be performed with final implantation of drug-eluting coronary stents, which ensure valuable long-term results [25].
\nThe success rates of the above-described antegrade recanalization techniques reach 55–80% depending of characteristics of patients and CTO lesions [26–29].
\nIn about 50% of CTOs, very complex occlusions are present being characterized by a straight nontapered proximal cap, long length or torturous course of the lesion, diffuse alterations of the distal vessel, or prior failures of recanalization attempts [20]. Retrograde recanalization techniques were introduced by Japanese CTO experts and have increased significantly the success rates of these complex CTOs without increasing peri-interventional complication rates [30–32]. The main goal of all retrograde techniques is to advance successfully a coronary wire to the distal end of the CTO lesion using collateral connections originating from the contra-lateral coronary artery. Additionally, ipsilateral retrograde techniques without using contra-lateral collaterals can be applied [33, 34]. Figure 3 shows schematically an occlusion of the right coronary artery (RCA) and wire positioning using epi-myocardial collateral connections to the distal end of the CTO (Figure 3A, B). This retrograde wire marks exactly the distal end of the occlusion and can afterwards be targeted precisely by an antegrade wire, which will be able to be advanced antegradely and parallel to the retrograde “marker” wire into the distal vessel lumen (so-called “marker wire” technique, Figure 3C, D).
\n“Marker-wire” technique (CTO, chronic total occlusion) [34].
Occasionally, more complex retrograde techniques may be performed, such as the “reverse-CART” (“controlled antegrade and retrograde tracking”)-technique [35, 36]. Here, balloon inflation over the antegrade wire creates space within the CTO lesion, which alleviates the entry of the retrograde wire, which may then advance parallel to the antegrade wire into the antegrade guiding catheter (Figure 4A, B). A consecutively introduced microcatheter protects coronary circulation, and within the microcatheter, a 330-cm long special externalization wire can be advanced from retrogradely and outside of the body (so-called “externalization”). After wire externalization, balloon dilation and stent implantation will then be performed antegradely using the externalization wire.
\n“Reverse-CART” (“controlled antegrade and retrograde tracking”) technique [36].
Most CTO lesions can be recanalized by antegrade techniques. In about 30%, a retrograde technique is necessary due to the complex morphology of the CTO (Figure 5). An escalation of the recanalization strategy is valuable, because an antegrade attempt may be successful in the case of a complex morphology of the CTO. Retrograde methods reveal a high technical expertise and should only be performed independently by interventional cardiologists with sufficient training in antegrade techniques (i.e., >300 antegrade CTO-interventions, >50/year) and additional training in retrograde techniques (25 retrograde cases as second and primary operator each), as stated in a consensus document of the EuroCTO-club [9]. In the presence of high expertise in all recanalization techniques, availability of necessary specific materials and a possible widened indication up to 90% of CTOs can be recanalized. However, the high technical demand and effort in time with longer radiation exposure are justified only in recognition of a presumed clinical benefit for the individual patient.
\nEscalating strategies for recanalization (CART, controlled antegrade and retrograde tracking).
The concept of biomarkers has existed from the time of the inception of ayurvedic medicine, just around the seventh century when the sweetness of urine was linked to diabetes even though the terminology had not been developed then [1]. The perspective of what constitutes the definition of a biomarker is somewhat diverse. Biomarkers (biological markers) are generally biomolecules whose qualitative and quantitative presence provides an indication of the state of a biological system. A more exhaustive definition as provided by the World Health Organization (WHO) led joint venture on chemical safety that describes a biomarker as any substance, structure, or process that can be measured in the body or its products that can influence or predict the incidence of outcome or disease [2]. The application of biomarkers has attained a vital and grounded position in clinical research, usually as predictors of the clinical outcomes for a varied number of disease conditions and their management [3].
\nExtensive scientific investigation into the mechanism of wound healing has revealed that the traditional guides in the determination of the wound healing potential, i.e., erythrocyte sedimentation rate (ESR) and C-reactive protein, do not yield enough positive and negative predictive values [4]. In lieu of the scientific evidence available, the focus has shifted to cytokines, chemokines, and proteases which hold the greatest potential as biomarkers [4].
\nCytokines are proteins of relatively low molecular weight that are secreted to influence or modulate the behavior of immune cells and also other cells [5]. Crucial among them include interleukins, lymphokines, and other signaling molecules such as interferons and tissue necrosis factor (TNF-α). It has been long considered and corroborated by scientific evidence that pro-inflammatory cytokines such as interleukins 1α (IL-1α), 1β (IL-1β), and 6 (IL-6) and TNF-α play essential roles in wound healing process such as the stimulation of keratinocyte and fibroblast proliferation, modulation of immune response, synthesis and breakdown of extracellular matrix proteins, and the chemotaxis of fibroblast to the wound site [6].
\nGrellner et al. [7, 8] in their work to quantitatively analyze pro-inflammatory cytokines in human skin wounds realized an upregulation of the expression of IL-1α, IL-1β, IL-6, and TNF-α in the inflammatory phase of the wound healing process. The levels of these pro-inflammatory cytokines (TNF-α, IL-1, and IL-6) were higher in nonhealing wounds than healing wounds owing to the fact that nonhealing wounds stay in the inflammatory phase of wound healing process [4]. Bilder et al. [9] also report an increase in the levels of IL-8 in chronic nonhealing wounds as opposed to those with a healing potential. Ligi et al. [10] upon the assessment of several studies which evaluated the level expression of cytokines and chemokines in the microenvironment of a chronic ulcer alluded to a heightened pro-inflammatory condition in a nonhealing wound, thus corroborating other studies. It was however noted that the level of cytokines detectable does not necessarily correlate to its bioactivity due to anti-inflammatory cytokines whose presence counteracts the activity of these pro-inflammatory cytokines [10]. There are also specific cytokine inhibitors and proteolytic enzymes that also act on these cytokines to mask their bioavailability [10]. Patel et al. [4] also report the inconsistency in wound and serum levels of cytokines which poses a challenge in its use as reliable biomarkers of nonhealing wounds.
\nThe IL-1 family of cytokines is made up of two pro-inflammatory cytokines, namely, IL-α and IL-β. Interleukin 1 is primarily sourced from macrophages in the event of injury, infection, and antigenic challenge although the epidermal, epithelial, lymphoid, and vascular tissues also serve as reservoirs for the polypeptide [11]. The actions of IL-1 span from systemic changes in the neurological, hematologic, endocrinologic, and metabolic systems to some local effects that are particularly relevant in wound healing [12]. By influencing both destructive and repair processes, it contributes the mesenchymal tissue remodeling, and it does so by influencing quite a number of cells. First of all, it stimulates capillary endothelial cells to produce chemokines such as MCP-1 and also cause an upregulation of the synthesis of vascular adhesion molecules such as ICAM-1, VCAM-1, and E-selectin [13, 14]. The combined effect of these two actions is to cause the infiltration of the injury site with mononuclear cells, thus setting the stage for inflammatory response. The expression of matrix metalloproteases (MMPs) from resident fibroblasts is also under the control of IL-1. The call of MMPs to play results in the degradation of the extracellular matrix to allow for enhanced monocyte migration. It also leads to a down-modulation of the inflammatory response as MMPs degrade IL-1. Inhibiting the IL-1 pathway through the use of recombinant antibodies and macrophages from IL-1 receptor knockout mice appeared to turn the tables around as far as the wound microenvironment is concerned by inducing a switch from pro-inflammatory to healing-associated macrophage phenotypes and growth factors [14]. Therefore, there is a negative implication for wound healing in the absence of high expression of IL-1.
\nInterleukin 6 is described as the chief contributor to the stimulation of a majority of the acute-phase proteins during inflammation. IL-6-deficient transgenic mice (IL-6 KO) therefore showed a substantial delayed cutaneous wound healing relative to the wild-type control animals by about threefold, the time required for healing [15].
\nBased on similar animal model studies on IL-6 knockout mice and the administration of recombinant murine IL-6 protein, IL-6 was found to be essential in stimulating the mitogenic activity of keratinocytes, an action that has been linked to scar formation as well as exerting a chemo-attractive action on neutrophils [6]. These effects seek to kick-start the wound healing process. However, a study conducted to determine the indicators of inflammation in the pathogenesis of diabetic foot ulcers identified a positive correlation between high serum IL-6 levels in diabetic patients with foot ulcers and low serum IL-6 levels in those without foot ulcers. This implicates its effect on poor wound healing [16].
\nThis is not surprising as IL-6 has a reputation for dictating the transition from acute to chronic inflammation systemically by its stimulatory effects on T and B cells.
\nTumor necrosis factor alpha (TNF-α) is a key pro-inflammatory cytokine involved in the early phase of most inflammatory events in the body. Employing mouse models, the expression of TNF-α at detectable levels was discovered to happen just after wound creation and sees an increase in the first several hours until it reaches a peak within 24 hours after which it returns to the basal level [17]. Vascular endothelial cells, keratinocytes, and fibroblasts are the major sources of TNF-α which cause an initiation of the inflammatory phase of the wound healing by promoting the recruitment of inflammatory leukocytes. TNF-α is also involved in the regulation of the activity of fibroblasts, keratinocytes, and vascular endothelial cells as well as in modulating synthesis of extracellular matrix proteins and matrix metalloproteinase [17, 18]. Based on diabetic models, an increase in TNF-α level coupled with decrease in IL-10 that has anti-inflammatory properties results in sustained expression of chemokines CXCL2 and CCL2 and leads to continuous infiltration of leucocytes to the injury site. This ultimately prolongs the inflammation and reduces the wound healing potential [19].
\nTransforming growth factor describes the superfamily for pluripotent cytokines which have very important functions to perform during disease, homeostasis, development, and repair. These sets of proteins are structurally related, but functionally distinguishable and relevant among them for wound healing are the isoforms TGF-β 1–3 [20]. The roles of these isoforms in the wound healing process can be both distinct and overlapping. However, the overall nature of their contribution to the wound healing has generated some controversy and thus is among the most studied molecules involved in the process [6]. Transforming growth factor β1 (TNF-β1) however has the widest spectrum of actions, affecting all manners of cell types that are involved in all stages of wound healing. These effects have been reported to be both positive and negative [21]. Historically, the synthesis of TNF-β1 from keratinocytes, platelets, and macrophages is upregulated right after injury, and this is crucial for initiating inflammation and granulation tissue formation. In addition, TNF-β1 contributes to the chemotactic migration of cells during wound repair. Some proteases such as MMP-1, MMP-2, MMP-3, and MMP-9 are also under the control of TNF-β1 [6, 22]. Based on human studies, TNF-β1 was found to stimulate the production of extracellular matrix molecules, including collagens and fibronectin, which strengthen the repaired wound. In spite of this knowledge, available evidence goes to raise questions about the true effects of TNF-β1 levels on wound healing [23]. Wound healing in Smad knockout mice, which have the signaling pathway of TNF-β1 blocked, was rather accelerated to the surprise of the investigators. In similar fashion, TNF-β1 knockout mice showed demonstrated reepithelialization during incisional wound repair, in comparison with wild-type mice. The consensus in the face of current evidence is that the selective inhibition of TNF-β1 in some cells may prove beneficial [24].
\nThe growth factors are essentially responsible for the initiation of the proliferation stage of the wound healing process. The platelet-derived growth factor (PDGF), transforming growth factors (TGF-𝛼, TGF-𝛽), insulin growth factor (IGF-1), fibroblast growth factor (FGF), and granulocyte-macrophage colony-stimulating factors (GM-CSF) are examples of growth factors whose roles in wound healing as well as their possible use as biomarkers have been studied extensively based on their expressed levels [25]. In spite of the fact that insight about ideal levels and the spatiotemporal distribution of growth factors is far from complete, available data points to no local growth factor deficiency in chronic leg ulcers with the possible exception of TGF [6]. Trengove et al. [26] after studying wound fluids from both healing and nonhealing wounds arrive at similar conclusion that poor wound healing may be due to inflammatory mediators rather than a deficiency of growth factors.
\nPlatelet-derived growth factors (PDGFs) are made up of a family of homodimeric or heterodimeric growth factors, including PDGF-AA, PDGF-AB, PDGF-BB, PDGF-CC, and PDGF-DD [27]. PDGF has been established to have chemotactic role for cells that migrate to the healing wound site such as fibroblasts, neutrophils, and monocytes. It was actually the very first growth factor shown to have this function [28]. It additionally stimulates the proliferation of fibroblast and the deposition of extracellular matrix. In vitro studies have also revealed that it stimulates insulin growth factor (IGF) release in fibroblasts which is vital to the initiation of the repair process [28]. Lastly, it stimulates fibroblasts to contract collagen matrices and induces the myofibroblast phenotype in the implicated cells. It has thus been established to be a major player in the wound healing and has formed the basis for studies into its clinical application in the treatment of wound healing disorders.
\nOwing to the close proximity of the expression sites of the PDGF, which is predominantly in the epidermis, and its receptors which are also in the dermis and granulating tissue, a paracrine mechanism has been suggested for its action [6, 29]. However, unlike other growth factors like fibroblast growth factor (FGF) and vascular epithelial growth factor (VEGF) that see an overexpression in the microenvironment or at the site of a healing wound or one in a granulation phase, the increase in the expression of PDGF-BB is without this spatial limitation as its levels in plasma also increases. It does make it potentially useful as the biomarker in wound healing [10].
\nThe action of proteases and their inhibitors goes a long way to influence the equilibrium between extracellular matrix (ECM) degradation and deposition which is responsible for the coordinated and timely healing of wounds [30]. There is an overwhelming wealth of evidence to suggest that nonhealing wounds are characterized by an increase in the levels of proteases and an imbalance in the protease/protease inhibitor levels [30, 31]. This manifests as a persistence of proteolysis and degradation of the extracellular matrix causing wound healing to delay. Significant among these proteases are the matrix metalloproteases (MMPs) [32]. MMPs are part of a family of zinc endopeptidase which essentially help in the degradation of provisional extracellular matrix, facilitate the migration of inflammatory cells to the wound site, remodel the granulation tissue, and modulate angiogenesis [28]. MMP activity as measured using Azocoll assay was found to be significantly elevated in chronic wounds as compared to acute wounds, thus implicating it poor wound healing [26].
\nProteases as biomarkers for wound healing hold the key to transform clinical approach to the management of wounds. For example, the appropriateness of using protease-modulating dressing and tissue-engineered products, scaffolds, and skin grafts for the treatment can be made by the determination of the levels of proteases [33].
\nMatrix metalloproteinases (MMPs) are a group of endopeptidase that are zinc and calcium dependent and are usually divided into six groups depending on the substrate they act on. These MMPs consist of collagenases (MMP-1, MMP-3, MMP-8); gelatinases (MMP-2, MMP-9); stromelysins (MMP-3, MMP-10); matrilysins (MMP-7, MMP-26); membrane-type MMPs (MT-MMP) like MMP-14, MMP-15, MMP-16, and MMP-24; and other MMPs (MMP-11, MMP-12, MMP-19, MMP-20, MMP-22, MMP-23, MMP-28) [34].
\nVarious MMPs are relevant to the wound healing process at varied points, and the tight control of their proteolytic activity is also essential to conduct the different events of wound healing [36]. MMPs are however generally involved in the inflammatory, proliferative, and remodeling phases of the wound healing process by modulating cytokine/chemokine activity by activating them enzymatically or influencing their availability by cleaving them from cell surface. Additionally, the actions of MMPs involve the breakdown of proteins part of the cell-cell and cell-extracellular matrix interaction [35, 36].
\nIn terms of the predictive roles of MMPs’ level for the wound healing process, some studies have focused on the MMP-1 to tissue inhibitor of metalloproteinase (TIMP-1) ratio. In one study, for instance, a significant correlation was found between a high ratio of MMP-1/TIMP-1 and good healing (r = 0.65, p = 0.008) with receiver operator curve (ROC) analysis showing an MMP-1/TIMP-1 ratio of 0.39 being the best predictive value for wound healing. High levels of MMP-8 and MMP-9 also appear to have negative predictive value for the process of wound healing [32].
\nWith the growing research into the therapeutic benefits of biomarkers comes the challenge of identifying biomarkers that satisfy the required characteristics for use clinically. It is prudent to validate new biomarkers affecting the wound healing process by employing innovative, simple, and cost-effective molecular approaches to determine the type, level, and activity of all potential biomarkers. With the advent of trendsetting technical knowhow in defining diseases and other biological processes, it has become increasingly possible to identify and characterize novel biomarkers of the wound healing process. Continuing the research into identification of new biomarkers affecting the wound healing process is imperative since it will eventually have weighty health benefits on patients and offer a relevant guide to wound management. This will significantly lower the risks of microbial colonization and invasion of wounds and loss of structural function as a result of chronic wounds.
\nEdited by Jan Oxholm Gordeladze, ISBN 978-953-51-3020-8, Print ISBN 978-953-51-3019-2, 336 pages,
\nPublisher: IntechOpen
\nChapters published March 22, 2017 under CC BY 3.0 license
\nDOI: 10.5772/61430
\nEdited Volume
This book serves as a comprehensive survey of the impact of vitamin K2 on cellular functions and organ systems, indicating that vitamin K2 plays an important role in the differentiation/preservation of various cell phenotypes and as a stimulator and/or mediator of interorgan cross talk. Vitamin K2 binds to the transcription factor SXR/PXR, thus acting like a hormone (very much in the same manner as vitamin A and vitamin D). Therefore, vitamin K2 affects a multitude of organ systems, and it is reckoned to be one positive factor in bringing about "longevity" to the human body, e.g., supporting the functions/health of different organ systems, as well as correcting the functioning or even "curing" ailments striking several organs in our body.
\\n\\nChapter 1 Introductory Chapter: Vitamin K2 by Jan Oxholm Gordeladze
\\n\\nChapter 2 Vitamin K, SXR, and GGCX by Kotaro Azuma and Satoshi Inoue
\\n\\nChapter 3 Vitamin K2 Rich Food Products by Muhammad Yasin, Masood Sadiq Butt and Aurang Zeb
\\n\\nChapter 4 Menaquinones, Bacteria, and Foods: Vitamin K2 in the Diet by Barbara Walther and Magali Chollet
\\n\\nChapter 5 The Impact of Vitamin K2 on Energy Metabolism by Mona Møller, Serena Tonstad, Tone Bathen and Jan Oxholm Gordeladze
\\n\\nChapter 6 Vitamin K2 and Bone Health by Niels Erik Frandsen and Jan Oxholm Gordeladze
\\n\\nChapter 7 Vitamin K2 and its Impact on Tooth Epigenetics by Jan Oxholm Gordeladze, Maria A. Landin, Gaute Floer Johnsen, Håvard Jostein Haugen and Harald Osmundsen
\\n\\nChapter 8 Anti-Inflammatory Actions of Vitamin K by Stephen J. Hodges, Andrew A. Pitsillides, Lars M. Ytrebø and Robin Soper
\\n\\nChapter 9 Vitamin K2: Implications for Cardiovascular Health in the Context of Plant-Based Diets, with Applications for Prostate Health by Michael S. Donaldson
\\n\\nChapter 11 Vitamin K2 Facilitating Inter-Organ Cross-Talk by Jan O. Gordeladze, Håvard J. Haugen, Gaute Floer Johnsen and Mona Møller
\\n\\nChapter 13 Medicinal Chemistry of Vitamin K Derivatives and Metabolites by Shinya Fujii and Hiroyuki Kagechika
\\n"}]'},components:[{type:"htmlEditorComponent",content:'This book serves as a comprehensive survey of the impact of vitamin K2 on cellular functions and organ systems, indicating that vitamin K2 plays an important role in the differentiation/preservation of various cell phenotypes and as a stimulator and/or mediator of interorgan cross talk. Vitamin K2 binds to the transcription factor SXR/PXR, thus acting like a hormone (very much in the same manner as vitamin A and vitamin D). Therefore, vitamin K2 affects a multitude of organ systems, and it is reckoned to be one positive factor in bringing about "longevity" to the human body, e.g., supporting the functions/health of different organ systems, as well as correcting the functioning or even "curing" ailments striking several organs in our body.
\n\nChapter 1 Introductory Chapter: Vitamin K2 by Jan Oxholm Gordeladze
\n\nChapter 2 Vitamin K, SXR, and GGCX by Kotaro Azuma and Satoshi Inoue
\n\nChapter 3 Vitamin K2 Rich Food Products by Muhammad Yasin, Masood Sadiq Butt and Aurang Zeb
\n\nChapter 4 Menaquinones, Bacteria, and Foods: Vitamin K2 in the Diet by Barbara Walther and Magali Chollet
\n\nChapter 5 The Impact of Vitamin K2 on Energy Metabolism by Mona Møller, Serena Tonstad, Tone Bathen and Jan Oxholm Gordeladze
\n\nChapter 6 Vitamin K2 and Bone Health by Niels Erik Frandsen and Jan Oxholm Gordeladze
\n\nChapter 7 Vitamin K2 and its Impact on Tooth Epigenetics by Jan Oxholm Gordeladze, Maria A. Landin, Gaute Floer Johnsen, Håvard Jostein Haugen and Harald Osmundsen
\n\nChapter 8 Anti-Inflammatory Actions of Vitamin K by Stephen J. Hodges, Andrew A. Pitsillides, Lars M. Ytrebø and Robin Soper
\n\nChapter 9 Vitamin K2: Implications for Cardiovascular Health in the Context of Plant-Based Diets, with Applications for Prostate Health by Michael S. Donaldson
\n\nChapter 11 Vitamin K2 Facilitating Inter-Organ Cross-Talk by Jan O. Gordeladze, Håvard J. Haugen, Gaute Floer Johnsen and Mona Møller
\n\nChapter 13 Medicinal Chemistry of Vitamin K Derivatives and Metabolites by Shinya Fujii and Hiroyuki Kagechika
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