Regenerative endodontic procedures is defined as biologically based procedures designed to replace damaged structures such as dentin, root structures, and cells of the pulp-dentin complex. This new treatment modality aims to promote normal function of the pulp. It has become an alternative to heal apical periodontitis. Regenerative endodontics is the extension of root canal therapy. Conventional root canal therapy cleans and fills the pulp chamber with biologically inert material after destruction of the pulp due to dental caries, congenital deformity or trauma. Regenerative endodontics instead seeks to replace live tissue in the pulp chamber. The ultimate goal of regenerative endodontic procedures is to regenerate the tissues and the normal function of the dentin-pulp complex.
Before this treatment modality is introduced, apexification procedures using either immediate placement of mineral trioxide aggregate apical plug or long term-calcium hydroxide treatment were traditionally used to treat immature permanent tooth. Although these treatments often resolve the signs and symptoms of pathosis, they provide little to no benefit for continued root development. Further root growth, normal pulpal nociception and immune defense are impeded in the procedure of apexification. To replace live tissue, either the existing cells of the body are stimulated to regrow the tissue native to the area or bioactive substances inserted in the pulp chamber. These include stem cell therapy, growth factors, morphogens, tissue scaffolds and biologically active delivery systems.
Closely related to the field of regenerative endodontics, are the clinical procedures apexification and apexogenesis. When the dental pulp of a developing adult tooth dies, root formation is halted leaving an open tooth apex. Attempting to complete root canal on a tooth with an open apex is technically difficult and the long-term prognosis for the tooth is poor.
Apexogenesis, (which can be used when the pulp is injured but not necrotic) leaves the apical one-third of the dental pulp in the tooth which allows the root to complete formation. Apexification, stimulates cells in the periapical area of the tooth to form a dentin-like substance over the apex. Both improve the long-term prognosis for a forming tooth over root canal alone.
Necrotic pulp and open apex can be revitalized with platelet rich fibrin.
History Regenerative endodontics is founded by the seminal work by Dr. Ostby in the early 1960s. He hypothesized that the presence of blood clot within the root canal promotes healing of the pulp, hence maintaining the vitality of the pulp. This can be quite similar to the role of blood clot in other injury site in the healing process. To prove this hypothesis, mature teeth diagnosed with pulpal disease received pulp space debridement followed by enlargement of the apical foramen. Medicament dressing was placed and intracanal bleeding was evoked. Kloroperka obturation placed coronal to the formed blood clot. This study aimed to evaluate the role of the apical blood clot in the healing of apical periodontitis and pulp repair.
Patients were followed from a time period of 17 days to 3.5 years and the treated teeth were then extracted. The newly formed tissue were histologically examined. Resolution of symptoms of inflammation related to enlargement of foramen and overinstrumentation were observed in as early as 17 days. Resolution of apical periodontitis and signs and symptoms of inflammation and radiographic evidence of continued root development and apical narrowing were demonstrated in all teeth.
Histology wise, ingrowth of connective tissue into the canal space was observed. Different levels of mineralised tissue was identified along the canal walls. Mineralised tissue was found embedded in the newly formed tissue. Dental pulp is fibroblast-rich and this result was promising. Odontoblasts were required to aid in pulpal healing but these cells were lacking in this pioneer study. On the other hand, undesired cell types like cementoblasts were found in the tissue. In spite of the shortcomings, this study has established a strong foundation in the field of regenerative endodontics.
The expansion of the field of regenerative endodontics was also dependent on the contributions from important studies in dental trauma. It has been proven that the vitality of dental pulp in immature teeth is preserved and it is free of signs and symptoms of disease even though it has sustained traumatic injuries such as avulsion and intrusion. Clinical success is resultant from the reestablishment of blood supply to the ischemic but uninfected dental pulp tissue. Reinnervation from sensory axons should then followed and the axons is likely to be recruited from the apical region.
In 2011, an important demonstration in the field of regenerative endodontics was found. The investigators found out that the influx of blood in the apical area into the disinfected canals was coincided with a clinically significant mesenchymal stem cells transfer into the root canal system. It is established that these procedures were actually stem cell-based procedures.
Etiology of pulpal necrosis Trauma has been recognised as the most common cause of pulpal necrosis in immature permanent teeth. Up to 35 percent of children between the ages of 7 and 15 years experience traumatic dental injuries when the root development of the permanent teeth are still incomplete. Half of the teeth are then likely to be diagnosed with pulpal necrosis with greater incidence in teeth which suffer from severe injuries like avulsions and combination injuries. Hertwig epithelial root sheath (HERS) could be potentially damaged when the young developing dentition is traumatised. HERS is proven to be essential for root formation and maturation by directing the proliferation and differentiation of multipotent stem cells.
The presence of dens evaginatus or dens invaginatus were the second most common etiology of pulp necrosis in immature teeth. Dens evaginatus is more common between these 2 dental anomalies. It is seen on clinical and radiographic examination as an additional cusp, typically projecting into the occlusal table of a mandibular premolar. The incidence of dens evaginatus has been reported to affect up to 6% of the population, with greater incidence in certain ethnic groups. Dens invaginatus is a rare dental anomaly where there is an infolding of enamel into the dentine.
The presence of dens evaginatus can lead to rapid pulpal necrosis when there is continuous trauma from occlusion. In both dens evaginatus and dens invaginatus, direct exposure of pulp to the oral environment will eventually lead to inflammation and infection of the pulp.
Clinical problem Odontogenesis is a multiplex and long process of postnatal organogenesis. A tooth needs a supplemental 3 years after eruption to complete the root formation and mark the end of tooth development.
Early loss of young immature permanent teeth can be detrimental, leading to loss of function and interference of phonetics. Maxillary and mandibular bone development may be altered, especially when the patient is still growing. Psychosocial health of young patient can be severely impacted. Implants can interfere with the normal orofacial growth and hence this is contraindicated in patients who are still undergoing cranio skeletal development.
Apexification procedures were traditionally used to treat teeth with pulpal pathology to resolve the signs and symptoms of pulp pathosis. Long term calcium hydroxide treatment or placement of mineral trioxide aggregate apical plug was performed. However, these treatments provide little to no benefit for continuous root development, leaving a thin fragile dentinal wall. This can increase the susceptibility of the tooth to fractures and decrease the survival rate of the tooth.
Therefore, it is important that dentists should make effort by all means to retain the natural dentition hopefully beyond the maturation stage. Both vital and non vital pulp therapies should be taken into consideration to keep the natural teeth as long as possible.
Biological basis of regenerative endodontics A successful tissue regeneration relies on an appropriate source of stem progenitor cells, growth factors and scaffolds to control the development of the specific tissue.
The first component for tissue engineering is an appropriate source of progenitor/stem cells by using cells which are able to differentiate into the desired tissue component. The use of postnatal autologous stem cells, especially the mesenchymal stem cells is optimal in regenerative endodontic applications. These mesenchymal stem cells are found in dental pulp (DPSCs), the apical papilla (SCAP) and even in the inflamed periapical tissue (iPAPCs) collected during endodontic surgical procedures. Some other potential sources of postnatal stem cells in the oral environment are the tooth germ progenitor cells (TGPCs), dental follicle stem cells (DFSCs), salivary gland stem cells (SGSCs), stem cells from human exfoliated deciduous teeth (SHED), periodontal ligament stem cells (BMSCs), oral epithelial stem cells (OESCs), gingival-derived mesenchymal stem cells (GMSCs) and periosteal stem cells (PSCs).
The second component of tissue engineering focuses on growth factors or other tissue-inducing mediators. By definition, stem cells are capable to differentiate into various cell phenotypes based on their lineage and exposure to the environmental stimuli, for instance, growth factors, extracellular matrix, hypoxia, or other conditions. Therefore, the environment is an important factor in regulating tissue differentiation. The clinical procedure of lacerating the apical papilla and subsequently delivering a high local concentration of stem cells into the root canal space may not be adequate to direct their differentiation into cells of the pulp-dentin complex. Growth factors should be considered as important adjuncts instead. It is important to remember this key concept while interpreting the histological studies after regenerative procedures, where the lack of control of endogenous growth factors may result in histologic signs of tissue repair rather than regeneration. This issue is significant for regenerative procedures, since the non-collagenous proteins contained within dentin include several crucial growth factors such as TGF-β.
The third component of tissue engineering is a scaffold. Scaffolds play a major role in regulating stem cell differentiation by local release of growth factors, or by the signaling cascade that is triggered when stem cells bind to the extracellular matrix and to each other. Scaffolds may be endogenous, such as collagen, dentin, etc., or synthetic substances, such as hydrogels, mineral trioxide aggregate or other compounds. This is an essential principle in the interpretation of clinical regenerative studies. For instance, instrumentation of dentin cylinders followed by irrigation with 5.25% NaOCl and extensive washing results in a dentin surface that promotes differentiation of cells into clastic-like cells which resorb dentin. On the contrary, if the dentin cylinders are irrigated with 17% EDTA either alone, or following NaOCl treatment, a dentin surface that promotes cell differentiation into cells expressing an appropriate marker for a mineralizing phenotype, such as the dentin sialoprotein is produced. Therefore, the selection of irrigants as well as their sequence may play essential roles in conditioning dentin into a surface capable of supporting differentiation of a desired cell phenotype.
Cell homing