A New Landscape of Human Dental Aging: Causes, Consequences, and Intervention Avenues

Abstract

Aging is accompanied by physical dysfunction and physiologic degeneration that occurs over an individual’s lifetime. Human teeth, like many other organs, inevitably undergo chronological aging and age-related changes throughout the lifespan, resulting in a substantial need for preventive, restorative as well as periodontal dental care. This is particularly the case for seniors at 65 years of age and those older but economically disadvantaged. Dental aging not only interferes with normal chewing and digestion, but also affects daily appearance and interpersonal communications. Further dental aging can incur the case of multiple disorders such as oral cancer, encephalitis, and other systemic diseases. In the next decades or even hundreds of years, the proportion of the elderly in the global population will continue to rise, a tendency that attracts increasing attention across multiple scientific and medical disciplines. Dental aging will bring a variety of problems to the elderly themselves and poses serious challenges to the medical profession and social system. A reduced, but functional dentition comprising 20 teeth in occlusion has been proposed as a measurement index of successful dental aging. Healthy dental aging is critical to healthy aging, from both medical and social perspectives. To date, biomedical research on the causes, processes and regulatory mechanisms of dental aging is still in its infancy. In this article, updated insights into typical manifestations, associated pathologies, preventive strategies and molecular changes of dental aging are provided, with future research directions largely projected.

1. Introduction

Aging is characterized by a progressive decline of the homeostasis and physiological function of multiple organs [1]. In the course of organismal aging, tissue degeneration and alternatively, inadequate tissue regeneration, are intimately linked to weakened immune responses and inefficient wound healing [2]. As a stable arrest of cell cycle progression, senescence was originally reported in human primary fibroblasts, which experienced consecutive passaging under culture conditions with a terminated proliferation [3]. Indeed, cellular senescence takes place comprehensively across almost all types of tissues in vivo [4, 5]. Although senescence represents a self-protective and active mechanism by preventing proliferation of aberrant or damaged cells after exposure to harmful stimuli, either inherent or exogenous, accumulation of senescent cells in aged tissues and organs can form a pathologically favorable niche, allowing organismal aging and the onset and development of various age-related diseases, a typical feature of organismal aging [6-8] (Fig. 1).

Figure 1.

Schematic representation of typical hallmarks of human aging, accompanying chronic diseases and potential interventions. Aging is characterized by a set of typical hallmarks, including genomic instability, epigenetic alterations, mitochondrial dysfunction, loss of proteostasis, telomere attrition, deregulated nutrient sensing, stem cell exhaustion and cellular senescence. During chronological aging, the incidence of age-related pathologies augments in a progressive manner, most of which implicate cellular senescence. Treatment avenues involving genetic, dietary, or pharmacologic approaches represent promising intervention strategies to prevent or ameliorate aging symptoms. Part of the figure (mainly the circle) is adapted with permission from the reference [8]. Copyright year 2020, CellPress.

The activation of persistent or irreparable DNA damage response (DDR), telomere attrition, appearance of lipofuscin, and upregulation of p16 and p21 are considered as major features of senescent cells [9, 10]. Particularly, an enhanced activity of the lysosome enzyme, senescence-associated beta-galactosidase (SA-β-Gal), is widely accepted as a marker of increased lysosomal content during cellular senescence [11]. On the other hand, aging is related to the decrease of autophagy activity [12]. Autophagy represents a highly conserved mechanism to promote cellular homeostasis, which functionally removes defective, disabled, or redundant organelles and protein congeries. Decreased autophagy in older individuals is often associated with several age-related conditions, such as cardiovascular diseases, neurodegenerative disorders and metabolic symptoms [13].

Senescent cells frequently alter their surrounding microenvironments, mainly by producing and secreting a large number of pro-inflammatory molecules, a process widely known as senescence-associated secretory phenotype (SASP) and occurs in a non-cell-autonomous manner [14, 15]. The SASP is usually composed of multiple soluble factors, including but not limited to interleukins, chemokines, growth factors, metallo-proteases, and insoluble extracellular matrix components [16]. These molecules can markedly affect neighboring cells by activating transmembrane receptors and engaging their downstream signal transduction pathways [17].

In the course of aging the immune competency gradually declines, a process that is now termed as immunosenescence and causes increased susceptibility of older individuals to various microbial infections to tooth tissues [1]. Simultaneously, chronic pain, a condition defined as continued pain symptoms lasting more than 3 months regardless of the specific cause or site, has been reported among 38.5% of a cohort composed of 1141 older adults, and is more common among females and among adults over 85 years of age [18]. In dentistry, chronic pain in the elderly is largely attributed to several factors, such as neuropathy and immune system deficiency [19]. However, regenerative dentistry remains yet underdeveloped, although various dental pathologies and disorders affect virtually all the world’s population, particularly those aged [20] (www.euro.who.int/en/health-topics/disease-prevention/oral-health/data-and-statistics).

It has been well documented that dental pulp has a prominent regenerative capacity. In the case of tooth injury, odontoblasts, which are the pulp-derived cells responsible for dentine production, tend to degenerate and are subsequently replaced by undifferentiated mesenchymal cells that migrate to the affected site from the deeper pulp regions [21]. These cells differentiate into new odontoblast-like cells and produce reparative dentine [21, 22]. Dental pulp stem cells (DPSCs) exhibit high proliferative activity and can differentiate into either adipogenic, chondrogenic, myogenic, neurogenic, odontogenic, osteogenic, or vascular lineages [21, 23]. In this article, we aim to deliver an updated outline of dental aging-associated degenerative changes occurring in response to an array of pathophysiological events, and to analyze the relevant causes and major consequences. As experimental therapeutic approaches intimately related to age-dependent senescence constitute a novel and promising field of translational research, we chose to briefly propose future directions by summarizing the advantages and disadvantages of potential therapeutic approaches including those stem-cell-based for the global elderly.

2. Dental aging-related diseases

With the aging of the human body, various oral diseases began to arise gradually, in a manner similar to that of the vast majority of other organs. Many oral health problems are often overlooked, leading to delays of medication. During the aging process of various organs, immune function declines, resulting in a variety of oral pathologies, while systemic disorders such as hypertension and diabetes can co-exist and affect each other, gradually worsening the health status and life quality of the elderly.

The dental status of elderly patients is an important factor affecting the quality of their lives [24]. As one of the major organs of the human body, teeth also have their own age and aging process. Aging teeth are found to have the capacity to lead to a variety of diseases. Caries, periodontitis, incomplete fracture of teeth in the elderly and trigeminal neuralgia are common dental aging-related disorders (Table 1), among which caries (especially root caries) and periodontal disease are the main issues of the elderly. A systematic review showed that the average incidence of root caries in the elderly was about half of the total population [25]. According to a survey of hospitalized elderly people in Chennai, India, the prevalence of caries is 67.3%, and the prevalence of periodontal disease is 51.3% [26].

Table 1.

Human dental aging-related diseases.

Diseases	Pathogenesis	Clinical manifestations	Clinical treatments
Attrition	There is a slow progressive loss of dental hard tissue during mastication. Due to poor occlusal relationship, heavy tooth burden and other reasons, some elderly people are more prone to wear.	Enamel uniformity thinning, or pit-like performance, often towering cusps, sharp edges.	Eliminate pathogenic factors; desensitization treatment; occlusal reconstruction; repair missing teeth and restore occlusal balance.
Dentin hypersensitivity	Caused by gingival retraction, wear, tooth fracture, dental caries and so on.	Irritation pain, mechanical stimulation caused by the most significant symptoms, followed by chemical and temperature stimulation.	Etiological treatment, drug desensitization treatment, repair treatment, laser therapy, root canal therapy in severe cases [150-152].
Periodontitis	Periodontitis is an inflammatory reaction caused by plaque microorganisms and their products acting on periodontal tissue for a long time.	Gingival inflammation and enlargement; periodontal pocket formation; alveolar bone destruction and resorption; tooth loosening and displacement	Non operative periodontal treatment; periodontal tissue engineering [153-160]
Quiescent caries	The cariogenic environment disappeared, and the caries no longer progressed.	Dark brown, as hard as normal enamel, with a shiny surface	Quiescent caries need no treatment [161]
Root caries	Root exposure and plaque accumulation are caused by aging changes, which lead to demineralization, dissolution, and destruction of root hard tissue.	It often occurs on the cheek and tongue of the root of the tooth, showing a "shallow disc", sometimes forming circular damage around the whole root of the tooth; mostly without conscious symptoms	Non-traumatic dental caries filling; drug therapy; filling repair [162-165]
Senile cracked tooth	Due to the uneven wear and tear of the teeth for a long time, the traumatic bite force is formed, which can deepen and widen the enamel plate at the bottom of the tooth pit and fissure in the direction of dentin.	Prolonged masticatory discomfort or occlusal pain can be accompanied by tooth hypersensitivity and pulp congestion; it is common in the first molars.	The severity of apical clefts ranges from mild, requiring no treatment to severe root canal therapy or even removal is necessary [166].
Senile vertical root fracture	Longitudinal root fracture often occurs in middle-aged and elderly molars, in which the mesial root of the lower collar first molar is the most common. The causes are mainly related to traumatic bite force, root development defects and so on.	Long term bite discomfort. The crown is complete, the maxillofacial surface may be severely worn, or the tip may be high and steep, and different degrees of widening images of longitudinal root fissure can be seen on the X-ray.	In most cases, it is often necessary to cut roots or pull out the affected teeth for multiple teeth.
Trigeminal neuralgia	Trigeminal neuralgia is usually distributed along the cephalic nerve, and the cause of the pain is uncertain.	Intermittent severe pain in the distribution area of trigeminal nerve in unilateral or bilateral face	Drug treatment: carbamazepine, phenytoin sodium, etc.; surgical treatment [167-169].

Consistent with the case of cancer, the incidence of which in the United States was 11 times higher for people older than 65 years of age than those younger than 65, it was estimated that among 42, 400 new cases of oral and pharynx cancer, nearly 50% of cases were in those aged 65 years and older [27]. As the population becomes older, the prevalence of head and neck cancer in people aged 65 and above in the Western world will increase by 27% from 2020-2030 [28]. It was shown by the statistics of inpatients in oral and maxillofacial surgery that the leading disease over 65 years old was oral and maxillofacial tumors, followed by salivary gland diseases, and malignant tumors were significantly more than benign tumors [29]. Oral and maxillofacial malignant tumors mainly occur in the mouth, followed by salivary glands and neck, the main tumor sites of oral cancer were tongue and palate, accounting for about 40.2% [30]. The pathological type is mainly squamous cell carcinoma, and its incidence is 53.5%-75.8% [31]. The most frequent primary origins for oral cancer metastasis do not correspond to the relative frequency of the primary tumors in the elderly population, suggesting that metastatic spread is not random. Despite the involvement of gingiva and jawbones in the majority of metastasis events, some other oral mucosal locations may be involved. Among elderly patients with oral and maxillofacial tumors, hemangiomas accounted for the highest proportion (28.05%), followed by papillomas (12.28%), for which the moon tongue and lips, respectively, are prone to [32].

As research continuously progresses, oral microbiota is found to play a key role in age-related systemic disorders (Table 2). Disorders of oral microbiome can cause pathologies of cardiovascular system, respiratory system, nervous system, endocrine system and reproductive system, respectively [33-38]. In the time course, generally, risks of developing dental aging-related diseases continue to increase until the end of an individual’s lifespan (Fig. 2). For example, a study uncovered 23 oral commensal bacteria within atherosclerotic plaques in patients that experienced carotid endarterectomy, catheter-based atherectomy or similar procedures, while 5 of them, namely Campylobacter rectus, Porphyromonas endodontalis, Porphyromonas gingivalis, Prevotella intermedia and Prevotella nigrescens are unique to coronary plaques [39]. Gingival tissues have multiple microbiota, which often causes inflammatory reactions and plays a critical role in assessing the susceptibility of patients to periodontal disorders [40]. The correlation between chronic periodontitis and the risk of malignancy via inflammation of the affected epithelium has been studied widely, with chronic periodontitis exerting systemic influence on development of multiple cancer types that involve consumption of alcohol and smoking, as well as diet, age and gender [40]. Specifically, risk factors for oral squamous cell carcinoma (OSCC) apart from alcohol and tobacco use, encompass poor oral hygiene, inadequately fitting denture-associated inflammation, insufficient nutrition and chronic infections caused by bacteria, fungi or viruses [41]. However, most cases of OSCC are detected at advanced stages, resulting in poor prognosis. A study focusing on microbiota differences between normal individuals, epithelial precursor lesion patients and cancer patients with distinct lifestyles including betel chewing and smoking, unmasked that the oral microbiome compositions of five genera, Bacillus, Enterococcus, Parvimonas, Peptostreptococcus, and Slackia of these individuals are markedly different [42].

Table 2.

Oral microorganism-related systemic disorders.

Diseases	Pathogenesis
Adverse pregnancy outcomes, APOS	Adverse pregnancy outcomes including preterm birth (PTB), low birth weight (LBW) and pretermlow birth weight (PLBW) have been found to be correlated with changes in oral microflora [170]
Alzheimer's disease, AD	A large number of studies reported that people with periodontitis have an increased risk of developing AD [171], and those with AD or dementia have impaired oral health, as a result of cognitive decline, and are more prone to develop chronic oral diseases, such as periodontitis, tooth loss, and mucosal lesions [172-175].
Atherosclerosis	The pathological mechanism of atherosclerosis caused by oral microbiome is its colonization of atherosclerotic plaques and systemic inflammation caused by oral infection. The oral microbiome colonized on atherosclerotic plaque includes Streptococcus, Veronicus, Porphyromonas gingivalis, Actinobacillus actinomycetes, Treponema denticola, Fusobacterium nucleatum, Forsystenella and Neisseria [176].
Breast cancer	A meta -analysis of available epidemiological studies provided evidence of a modest 19% higher risk of developing breast cancer for individuals with periodontal disease compared to those without periodontal disease [177].
Chronic obstructive pulmonary disease (COPD)	Poor oral hygiene and periodontal conditions significantly increase the risk of COPD and are associated with frequent episodes of COPD. Of note, the dental plaque may lead to further aggravation of COPD [178].
Colorectal cancer	There are significant differences in the abundance of Clostridium nucleatum and Clostridium labile in oral cavity between normal people and patients with colorectal cancer. Periodontal pathogens such as Clostridium nucleatum may promote the progression of colorectal cancer through an inflammatory microenvironment [179].
Diabetes mellitus	The biodiversity and phylogenetic diversity of oral flora in diabetes and prediabetes were significantly lower than those in normal controls and related to the increase of pathogenicity of hyperglycemic flora. Periodontitis increases the risk of diabetes caused by infection or inflammation. To the contrary, diabetes also affects the progression of periodontitis [180].
Esophageal carcinoma	The detection rate of Porphyromonas gingivalis in the lesion area of esophageal squamous cell carcinoma was as high as 61%, while the detection rate in the adjacent area was only 12%, with the normal area not detected [181].
Gastric cancer	Poor oral health is associated with an increased risk of precancerous lesions of gastric cancer. The proportion of Neisseria and Haemophilus in the oral cavity of gastric cancer patients was significantly lower than that of healthy people [182].
Human immunodeficiency virus	HIV infection is associated with a series of oral diseases. Viremia in untreated patients is associated significantly with an increase in the proportion of potentially pathogenic viremia, Proteus, megaclobacter and campylobacter, as compared with healthy controls [183].
Infective endocarditis	Infective endocarditis is a serious infectious condition caused by bacteria and occurs on the inner membrane of the heart wall or the heart valve, often caused by bacteremia. More studies showed that periodontitis is a risk factor for infective endocarditis [184-186].
Inflammatory Bowel disease	Inflammatory bowel disease (IBD) is one of the earliest diseases related to oral microbiome. The intestinal vegetation of oral bacteria is considered to be widely involved in the occurrence and development of inflammatory diseases [187])
Liver cancer	Liver cancer is a common malignant tumor worldwide with high morbidity and mortality. Multiple tooth loss caused by periodontitis increases the risk of primary liver cancer [188].
Liver cirrhosis	Liver cirrhosis is caused by many chronic liver diseases. Compared the changes of intestinal flora in 98 patients with liver cirrhosis and 83 healthy individuals by macrogenomics, approximately 54% of the colonies with different abundance expression were oral microorganisms, indicating origination of part of the abnormal intestinal flora in patients with liver cirrhosis from the oral cavity [189].
Lung cancer	Among people without smoking habits, the incidence of lung cancer in patients with severe periodontitis has increased by 2.5 times. The saliva samples of patients with lung cancer were significantly higher than those of normal controls, suggesting that they may be biomarkers for early detection of lung cancer [190]
Miocardial infarction	Oral bacterial DNA could be detected in coronary artery thrombus aspiration in patients with myocardial infarction, in which the DNA of root canal infection typical bacteria (oral streptococcus) accounted for 78.2% of thrombus aspiration, with periodontal pathogens accounting for 34.7% [191].
Obesity	Obesity is associated with oral microbiome. The changes of salivary microbiota may be a systemic response caused by obesity, and the changes of some bacteria in saliva may be involved in the immune inflammatory process of obesity [192]. Thus, the species of oral bacteria may be used as a biological index of overweight.
Obstructive sleep apnea hypopnea syndrome, (OSAHS)	Changes in the gut microbiota have a pathophysiological role in OSAHS and may be associated with the pathophysiology of metabolic comorbidities in patients diagnosed with OSAHS [193].
Pancreatic cancer	Gastrointestinal cancer is closely related to oral microbiome. Periodontal history and the presence of circulating antibodies against some oral pathogens are linked to the occurrence of pancreatic cancer. Porphyromonas gingivalis and Actinomyces could increase the risk of pancreatic cancer in a large-scale case-control study [194]. The risk of pancreatic cancer in patients with seropositive Helicobacter pylori would increase by 38% (OR=1.38, 95% CI: 1.08~1.75), which suggests that Helicobacter pylori may play a role in the occurrence and development of pancreatic cancer [195].
Poly cystic ovary syndrome, (PCOS)	PCOS is a common female endocrine disease with unknown etiology. The composition of microbial components in PCOS saliva was reported, and the number of actinomycetes in the saliva of PCOS patients declined [196]. In addition, the difference was more significant in PCOS patients with gingivitis.
Rheumatoid arthritis (RA)	RA autoimmunity can be triggered or enhanced by specific oral bacteria that cause periodontal disease, in which Gram-negative bacteria Porphyromonas gingivalis may play important roles [197, 198]. In addition, increased prevalence of periodontitis is observed in patients with RA [199].

Figure 2.

Schematic illustration of pathophysiological risks of an individual in developing dental aging-related disorders. In the time course of chronological aging, teeth are subject to a series of anatomical and/or cytological changes, factors that together contribute to human dental aging and related diseases. Dental aging-related changes typically observed in enamel and dentin, as well as representative dental aging-related disorders are exemplified.

Dysbiosis of the oral microbiome plays a critical role in the onset and development of periodontitis, displaying a shift to overgrowth of pathobionts in the normal microflora with elevated local inflammation [43]. As a common pathogen, Fusobacterium nucleatum (F. nucleatum) significantly overgrows in the case of periodontitis and has also been linked to various systemic disorders. Earlier studies reported the detection of antibodies against F. nucleatum in the circulating blood of patients with Alzheimer's disease (AD) or cognitive impairment (CI), but there is a lack of causal relationship and a plausible mechanism connecting these two conditions. A recent study revealed that F. nucleatum activates microglial cells, causing morphological changes, accelerated proliferation and enhanced TNF-α and IL-1β expression in microglial cells [43]. Importantly, F. nucleatum-caused periodontitis promotes exacerbation of the Alzheimer's symptoms in 5 X FAD mice, suggesting a likely link between a periodontal pathogen and the AD. Further, community individuals with AD often experience oral diseases and neuropsychiatric symptoms (NPS) in the course of disease progression. A study disclosed that decayed, missing and filled teeth, loss of attachment, plaque index, oral health behavior, pro-inflammatory cytokines, and salivary bacterial composition significantly differ among individuals diagnosed with AD, mild cognitive impairment (MCI) or subjective cognitive decline (SCD), three groups recruited in parallel [44]. The authors noticed that these parameters were generally poorer in the AD group rather than MCI and SCD groups and proposed targeted dental care and oral-related stress control as a valuable solution for NPS management in future clinics.

A number of epidemiological studies and intervention trials have attempted to demonstrate the relationships between maternal periodontal disorders and adverse pregnancy outcomes (APO), for which periodontal diseases are considered an important risk factor, including fetal growth restriction, gestational diabetes, low birthweight, preterm birth and pre-eclampsia [45]. For instance, a new study exploring the levels of periodontal red-complex bacteria (RCB) in pregnant pre-eclamptic women with periodontal diseases, potentiating the pathophysiology of a bacterial association in both periodontitis and pre-eclampsia [46]. However, restraining the periodontal bacterial load in pregnant women via good oral hygiene can significantly reduce the putative risk of adverse pregnancy outcomes including pre-eclampsia [46]. Thus, orisbacteria in saliva could be exploited as a non-invasive diagnostic indicator for early detection of oral and systemic disorders, while other therapeutic solutions including antimicrobial photodynamic therapy, antimicrobial peptides probiotics, green tea polyphenol and cold atmospheric plasma therapy are used to inhibit the growth of biofilm formation by oral bacteria [47].

3. Dental aging-related anatomical changes

The anatomical changes resulting from aging teeth in humans (Table 3) are basically similar to those of the skeletal system (Figure 3A, 3B). Aging teeth can cause symptoms such as yellow or black teeth, brittle, sensitive, loose teeth, and receding gums. The hard tissues of tooth body include dentin, enamel, and cementum, among which dentin and enamel are the main components that bear chewing pressure. Enamel is the hardest and toughest mineralized tooth tissue, maintaining its functions throughout a lifetime, despite a few millimeters thick with minimal regenerative capacity [48]. With the increase of age, the thickness of enamel becomes thinner, the organic composition and water content further decrease, the weak parts such as pericardium become calcified, and the structure becomes denser [49, 50]. Furthermore, the permeability of enamel is lost, the brittleness is increased [51], while the levels of nitrogen content and neck fluoride are elevated [52, 53]. Enamel hardness showed a decreasing trend from the enamel surface to the dentin-enamel junction (DEJ) [54, 55], and the teeth of elderly patients (55 years or older) had higher elastic modulus and surface hardness than those of younger patients (18 to 30 years old) [56]. Although enamel properties can vary with tooth origin, tooth type and tooth surfaces, different teeth and enamel depths exhibit differential susceptibility to age-related erosions, making it necessary to standardize enamel-related experiments involving the measurement by surface microhardness loss and calcium release [54]. A recent study applying unsupervised machine learning tools to pursue further understanding of relationships between the composition and mechanical behavior of aging enamel suggest that unsupervised learning approaches can reveal complicated structure-property relationships of dental tissues and help gain insights into the materials science of aging and its consequences [57].

Table 3.

Dental aging-related phenotypic changes.

Different parts of teeth	Dental aging phenotypes
Enamel	Loss of permeability, increase of brittleness and the obvious calcification of organic matter between enamel prisms, can result in brittleness and fracture; elevation of nitrogen content in enamel leads to the blackening of teeth; there are changes in enamel structure and refraction, which may be related to changes in enamel structure; aspartic acid in enamel shows more and more racemization, which may become an aging biomarker; fluoride levels in enamel are increased; however, wear rate of enamel is not an accurate age measurement method.
Cementum	The width of cementum increases, mainly at the top. In advanced stages, the deposition of dentin and cementum may be increasingly complete. The rhythmic accumulation of cementum (annular) has been used to determine the age of animals.
Dental arch width	In the process of aging, the mandibular molars tend to move closer to the middle, the first premolars and canines tend to move lingually, and the dental arch narrows left and right.
Dental pulp and cytological changes	Dental pulp fibrosis, reticular atrophy, mucinous degeneration, dental pulp cyst; fat droplet deposition and replacement; calcification of medullary cavity and root canal; hyaline degeneration is usually the intermediate stage of pulp calcification; the circulation and innervation is damaged, and the number of nerve axons in dental pulp decreases; reduction of capillaries and lymphatic vessels; elderly dental pulp stem cells have few cytoplasmic fibers and organelles; the remaining odontoblasts become smaller, flattened and shrunk; mitochondrial molecules gather around a large amount of autofluorescence lipofuscin deposition.
Dentin	The pulp cavdentinscomes smaller due to the continuous deposition of secondary dentin; The secondary dentin becomes irregular, the dentin tubules gradually disappear, and the formation of transparent dentin begins at the root tip. With increased age, the dentin gradually develops to the crown.
Periodontal tissue	Periodontal tissue atrophy is the main feature of aging-related dental changes. It can make the whole tooth have extensive gingival margin and alveolar bone, shrinked back at the same time, and exposed root. Under normal circumstances, this physiological change is called senile periodontal atrophy, which can shrink by about 1 mm at 60-70 years of age. Severe periodontal atrophy is mainly caused by secondary pathological factors. The thickness of periodontal ligament in normal young individuals is 0.21 mm, which can be reduced by 1/3 after the age of 60, a change that is mainly related with the reduction of masticatory function.

Figure 3.

Graphic profiling of human tooth aging and related pathophysiological changes. (A) appearance of aging teeth. (B) anatomic changes in aging teeth. (C) histological changes in aged tooth tissues; (D) major diseases associated with human dental aging and associated phenotypic alterations; E, molecular biological changes in human dental aging.

A "dissolution and precipitation" mechanism were proposed, which may interpret tubule occlusion and sclerotic dentin formation based on the chemical composition and crystal size changes of the minerals deposited in the lumen [58, 59]. With age, once the lumen is filled with minerals, transparency will appear, which is called transparent dentin or hardened dentin. Transparent dentin starts from the top of the root and usually extends to the crown dentin [58], which is different from the pathological transparency of caries and belongs to natural aging, with its flexibility, viscoelasticity, bending strength and cyclic mechanical properties significantly declined [58, 60]. Compared with young dentin, the stress generated by fatigue cracks in old dentin is lower, while the growth rate becomes significantly higher [60, 61]. In the young dentin, elastic resistance of the tissue can prevent the crack from extending to the long axis of the dentin tubule and the vertical direction of the pulp cavity [62]. In the aged dentin, however, due to the decrease of elastic limit, the cracks are more likely to extend along the tooth long axis and dentin tubule long axis [63]. Therefore, aging leads to an increase in the elastic modulus and hardness of teeth, a greater change in the mechanical properties of the inner dentin, a decrease in fracture toughness and strength, an increase in brittleness, a decrease in the ability to resist cracks under stress and elevated susceptibility to fatigue fracture [64]. Despite significant drawbacks includ tooth discoloration, intracanal use of the triple antibiotic paste (TAP) may provide advantages. A recent study demonstrated the association of this practice with scaffolds containing minocycline or doxycycline, and the production of color changes similar to those of dentin when compared with their respective TAP systems, although doxycycline-related discoloration was less dramatic [65].

As a biomarker of aging, aspartic acid in enamel shows more and more racemic activity [66], resulting in irregular continuous deposition of dentin, hardening of dentin tubules and gradually smaller pulp cavity [67-71]. Some studies have reported a high prevalence of dental pulp stone (DPC) in the elderly [72, 73]. However, the association between DPC and age remains controversial [74-76]. Odontoblasts undergo degenerative changes, atrophy and disappearance in most areas of the dental pulp [77]. Of note, dentin features and mechanical properties tend to change with age, with alterations occurring spatially within teeth depending on tubule orientation. Age-related mineral deposition within tubules and collagen maturation in intertubular dentin can markedly compound the spatial effects on mechanical properties of dentin [78]. The dentin tubules are enriched with minerals, the lumen disappear gradually (‘occlusion’) and the dentin around the tubules increases with age. The formation of transparent dentin (‘sclerosis’) begins from the root tip and gradually develops towards the crown [77, 79]. In the course of aging, dentin tends to lack facility to remodel or repair, except at the pulp periphery, where odontoblasts secrete matrix, predentin, especially at the mineralization growth front [80]. More importantly, the post-mitotic odontoblasts succumb to age-related autophagic activity to decline in function, while they continue to secrete dentin matrix until injury or death [80, 81].

Affected by genetic, epigenetic, and environmental factors, the hard tissue of teeth will be abnormally developed or mineralized. Aberrant enamel structure, such as dental fluorosis, usually involves permanent tooth changes, ranging from white spots on light enamel to heavy loss of normal tooth morphology (Fig. 3A). The ultrastructure showed poor enamel mineralization, but the enamel surface was over mineralized, the direction of enamel column was irregular, and the arc structure of enamel dentin boundary was more obvious [82]. Atomic force microscopy showed that there was a positive correlation between the degree, roughness and absolute depth of fluoride damage to dental enamel crystals, and it was also related to histological grading and clinical manifestations of dental fluorosis according to the Thylstrup-Fejerskov classification [83]. Dental fluorosis has clinical and histological manifestations similar to those of other types of enamel mineralization and hypoplasia. The United States Public Health Service recommends a fluoride concentration of 0.7 mg/L of water to prevent caries, one of the most prevalent chronic diseases, while reducing the risk of dental fluorosis, which mainly correlates with systemic consumption of fluorides especially in the early life [84].

Human dentin can be considered as a hierarchical material with multilevel micro-/nano-structures, comprising tubule, perti-tubular dentin (PTD) and intertubular dentin (ITD) as the principal constituents at microscale, while the PTD and ITD are further composed of collagen and hydroxyapatite crystals with different volume fractions at nanoscale [85]. Abnormal dentin structure, such as hereditary opalescent dentin, usually has color changes such as blue, yellow and amber light transmittance of teeth [86]. The ultrastructure showed that the dentin structure of a thin layer of near enamel was largely normal with aging, while other dentin structures markedly changed. For example, the number of dentin tubules was abnormal, the direction was disordered, the shape of tubules was irregular, the diameter of tubules became larger, and there were dentin areas without tubules [87, 88]. Although some studies show roughly normal scallop-like structure [89], other investigations have found that the enamel dentin boundary is linear, loses scallop-like structure, and even has large cracks between enamel and dentin [87].

Current research generally lags for anatomical changes of aging teeth, with related aging mechanisms largely unclear yet. Prior to interventions to teeth themselves to delay the aging process of teeth, only treatment with simple symptomatic alterations can be practiced. For caries, traditional filling and repair methods not only fail to completely restore the original function of the defective teeth, but cause secondary caries and micro-leakage, which is currently an unsolvable problem. Most dental tissue has little or no capacity of self-regeneration [90, 91]. With age, there is less organic substrate or water, and enamel displays a reduced capacity of regenerating itself after significant mineral loss [92]. Therefore, it is technically urgent to develop effective strategies to repair the teeth upon aging-related loss of dental functions. In recent years, tooth regeneration has attracted extensive attention based on the understanding of tooth growth mechanisms, natural tooth morphology regulation in human body and critical signaling pathways associated with tooth regeneration. Despite advances in dental tissue repair and techniques replacing missing teeth with prostheses, clinical treatments cannot regenerate tissues with natural teeth properties. In contrast, tooth tissue engineering (TTE), a promising method for dental tissue regeneration, holds the potential to form durable biological substitutes for soft and mineralized dental tissues [93]. To date, however, partial or complete tooth reconstruction remains a major challenge for future studies of dentistry and oral medicine [17-19].

4. Dental aging-related cytological changes

Dental pulp is a soft connective tissue, comprising fibroblasts, mesenchymal stem cells (MSCs), nerve fibers, odontoblasts and vessels, while this tissue is originally derived from dental papilla, an ectomesenchymal cell condensation in the developing tooth [94]. The dental papilla cells underlying the enamel epithelium can differentiate into odontoblasts, a process controlled by epithelial-mesenchymal interactions [95]. The cell density of dental pulp in 70-year-old individuals is largely half that of 20-year-old individuals, indicating a reduction in pulp restoration capacity [96]. Specifically, there is a decrease of 15.6% in crown odontoblast cells and 40.6% in root odontoblast cells, with reduced secretion activity and vacuolation of cells, further supporting that the repair ability of dental pulp tends to decline with age [52, 97] (Fig. 3C). In addition, dystrophic calcification in the central pulp of the coronal region and root canal is evident in older individuals, which might be due to their reduced pulpal blood flow [52, 98].

The volume of dental pulp decreases with age, mainly due to secondary dentin deposition throughout lifespan [99]. One of the most obvious characteristics of pulp aging is indeed the continuous secretion of dentin matrix by odontoblast cells, resulting in the reduction of pulp chamber [100]. With age, there are difficulties in endodontic treatment, because of the constriction of pulp chamber space by hyperplasia of secondary and tertiary dentin, as well as pulp stones and diffuse calcification in the radicular pulp [101]. In aged individuals, the pulp appears to be fibrosis-like, the number of pulp cells decreases, the pulp shrinks and becomes smaller and flatter [52, 66, 77, 102]. Fat deposition and substitution occurs [103, 104], arteriosclerosis changes take place in blood vessels, lymphatic vessels and nerves decrease, with supply impaired and mineralization increased [102, 105, 106]. Golgi complexes are shrinked in senescent pulp fibroblasts, while mitochondrial molecules cluster around abundant deposits of spontaneous fluorescence lipofuscin [107].

DPSCs represent a vital subgroup of the adult stem cell family and are considered as a critical source for dental pulp tissue regeneration. Although considerable efforts have been made to identify the DPSC origin, so far, the real origin remains obscure. It was proposed that DPSCs originate from pericytes, cells that reside in the perivascular niche of postnatal dental pulp [108, 109]. Over the past several years studies have indicated that neural crest cell (NCC)-derived MSCs contributing to tissue repair and regeneration are also derived from nerves [110]. Clonal DPSCs from neonatal murine tooth pulp can show multi-differentiation in neural crest lineage for adipocytes, chondrocytes, odontoblasts, neurons and smooth muscles, supporting the existence of neural crest-derived DPSCs with differentiation capacity into cranial mesenchymal tissues and other neural crest-derived tissues [111]. Another study indicated a substantial population of MSCs in the course of dental development, while the self-renewal and repair capacity of a tooth are conferred by peripheral nerve-associated glia. The authors demonstrated that glial cells generate multipotent MSCs producing pulp cells and odontoblasts, providing advanced insights into the dynamics of tooth organogenesis and growth [112].

Compared with other stem cells, DPSCs also have unparalleled advantages, including less ethical problems, simple acquisition, strong activity, aging slowly, low risk of tumorigenesis, small trauma and life-long access for most people. Moreover, origin and neural crest cells have brought therapeutic hope to patients with highly disabling conditions such as spinal cord injury, stroke or neurodegenerative diseases [113], and have become seed cells with considerable potential in tissue engineering. However, in the current actual clinical treatments, such as in the case of repair of an injured tooth, their therapeutic efficacy remains low, particularly for the elderly.

At present, functional pulp regeneration is one of the research hotspots, which requires not only the ability to form dentin (dentinogenesis) but also the capacity to restore dental pulp vasculature (blood vessels) and nerves to ensure proper cell nutrition and maintain viability, as well as to restore and sustain proper defence against potential pathogens encountered in pathophysiologic states such as pulpitis, periodontal disease, and trauma [114] (Fig. 3D). Vital pulp therapies to repair partially damaged dental pulp have been applied with some success in dental clinics [115]. So far, the gold standard material for vital pulp capping is mineral trioxide aggregate (MTA) [116]. More recently, Biodentine has shown great promise for applications in pulp capping [117]. In the past, regenerative endodontics therapies (RETs) have focused on partial regeneration of the dentin-pulp complex, with the goal of protecting the continuous growth of immature tooth roots, and to reduce the risk of fracture associated with traditional apexification procedures in thin and weak roots [118]. More recently, RETs have focused on whole pulp regeneration in an attempt to replace currently used synthetic material-based endodontic treatments that devitalize the tooth by filling the pulp chamber with gutta-percha (GP) or another synthetic material that blocks vital tissue formation [119]. In contrast to partial vital pulp therapy, whole pulp regeneration is focused on total pulp regeneration and revascularization of fully developed teeth by facilitating DPSC-derived odontoblast differentiation and pulp regeneration [120]. DSPC has been successfully isolated from inflamed dental pulp tissue, supporting the feasibility of whole pulp regeneration using autologous cell sources from infected dental pulp [121].

At present, the treatment methods used to repair tooth injury and loss largely depend on the application of synthetic materials to solve structural deficiency, without promoting biological activities such as blood transportation and nerve supply.

5. The landscape of molecular and cellular changes associated with dental aging

Senescent cell accumulation in aging tissues allows formation of favorable microenvironments for both the onset and progression of age-related pathologies. The response to gradual loss of genomic, epigenomic, proteomic and metabolic integrity in aging tissues can be triggered and controlled by two major tumor suppressor pathways: the p53-p21(CDKN1A)-retinoblastoma (RB) axis and the p16(CDKN2A)-RB branch [16]. Although these two pathways can independently arrest cell cycle progression, they can also mutually crosstalk in certain situations, particularly upon cellular senescence [122]. Although being arrested in an essentially irreversible status, senescent cells hold the potential to markedly change their surrounding microenvironments, as they secrete pro-inflammatory and matrix-degrading molecules, a process now known as the SASP [14]. In the local microenvironment, a full spectrum SASP expresses various soluble factors, including interleukins, chemokines, growth factors, metalloproteases, and insoluble extracellular matrix components, which together affect neighboring cells by activation of cell-surface receptors to engage intracellular signal pathways [8]. Recent studies suggest that these cell-non-autonomous processes are associated with many age-related oral conditions, including caries and periodontitis [1, 123].

DPSCs are considered as a critical source for dental pulp tissue regeneration, such as in the case of repairing an injured tooth, but their therapeutic efficacy remains limited, particularly in the aged individuals. A recent study investigated the differences in DPSC protein expression profiles using proteomics and bioinformatics approaches and identified 75 upregulated proteins and 69 downregulated proteins in DPSCs from elderly donors [124]. Specifically, high mobility group N1 (HMGN1), HMGN2, UCHL1 and the family with sequence similarity 96 member B homeobox gene (FAM96B) were associated with DPSC senescence, while FAM96B plays an important role in suppressing DPSC senescence and promoting osteogenic differentiation and proliferation [124]. Through RNA-seq and qPCR approaches, another study identified the homeobox protein Barx1 as a novel marker for DPSCs [125]. Further analyses with high throughput transcriptomic and proteomic analysis uncovered a set of markers for DPSC populations with accelerated replicative senescence, including CDKN2A, CDKN1A, ACTN2, MYH11 and CNN1 [125] (Fig. 3E). Specifically, expression of the transforming growth factor beta (TGF-β) pathway and the cytoskeletal proteins are increased in rapidly senescent DPSCs, suggesting a decline of stem cell properties and onset of terminal differentiation. Using metabolic flux strategy, the researchers further established a metabolic signature for these senescent DPSCs, which do show up before appearance of typical senescence-associated phenotypes [125].

The process of aging can also affect the ability of DPSCs to promote mineralization. A decreased osteogenic potential was recently observed in senescent human DPSCs, with the decline of differentiation potential towards mineralized tissues including bone and dentine associated with changes in expression of bone-related genes, such as BMP2, β-catenin, RUNX2 and BGLAP [126, 127]. Furthermore, the expression of DMP1 and DSPP, key odontogenic differentiation markers, is markedly decreased in DPSCs cultured in odontogenic medium derived from aged patients [127]. DMP1, a protein that regulates mineralization, translocates from nucleus to cytoplasm during cell differentiation, is eventually secreted to the extracellular space, where it regulates the nucleation of hydroxyapatite [128, 129]. Senescent DPSCs have relatively lower amounts of cytoplasmic DMP1 as compared to their proliferating counterparts during odontogenic differentiation, a tendency that indeed correlates with the diffusing calcific degeneration of the pulp and occurs as a response to aging [127, 130]. However, age-correlated features of DPSCs may be reversed upon exposure to appropriate stimuli and extracellular substrates. For example, DPSCs from aged individuals exhibit regenerative properties similar to those of DPSCs isolated from young patients, when cultured on nanostructured hydroxyapatite scaffolds and used in vivo to eliminate calvaria defects in rats [131].

In the course of aging, secretion of a handful of senescence-associated factors, including matrix metalloproteinases (MMPs) may be changed [17]. The concentration of specific MMPs can increase significantly in inflamed pulp, particularly when compared with the normal pulp [132]. In pulp tissues from patients suffering from acute pulpitis, protein expression of MMP2 and MMP3 was considerably higher than those in the pulp from healthy donors, implying a possible role of MMPs in the case of pulp inflammation and/or tissue damage. Specifically, MMP3 may activate the expression of other MMP molecules, such as MMP1, 7 and 9, which are able to trigger the collagen degradation and eventually cause changes in the extracellular matrix, events that have been observed in tooth tissue pathologies including acute and chronic pulpitis as well as periapical lesions [133, 134]. The development of dental caries into the dental tissues is able to promote inflammatory cell accumulation within dental pulp. These cells secrete inflammatory cytokines such as tumor necrosis factor alpha (TNF-α), a molecule that enhances mineralization [135, 136], partially explaining the emergence of nucleation points, which potently drive the formation of pulp stones in teeth of the aged [137]. Together, these findings indicate that the aging process can substantially affect the DPSC secretome (Table 4) (Fig. 4).

Table 4.

Dental aging-related genes and their changes.

Genes	Functions in aged dental pulp stem cells (DPSCs)
BMI-1	An already known inhibitor of cellular senescence. The expression of BMI-1 (B lymphoma Mo-MLV insertion region 1 homolog) is decreased in senescent DPSCs [200].
BMP2, BGLAP, β-catenin, RUNX2	The osteogenic potential was decreased in senescent human DPSCs, with the decline of differentiation potential towards mineralized tissues including bone and dentine. There are aging-associated changes in expression of bone-related genes [127, 201].
COX7A2, CyB5R3, HMOX2, Keap1, NDUFA2,	The downregulated oxidation promotion-related proteins, including Keap1, COX7A2 and their regulated antioxidative molecules, NDUFA2, HMOX2 and CYB5R3 in aging DPSCs [202-206].
DMP1, DSPP	Senescent DPSCs have relatively lower amounts of cytoplasmic DMP1 as compared to their proliferating counterparts during odontogenic differentiation, a tendency that indeed correlates with the diffusing calcific degeneration of the pulp and occurs as a response to aging [127, 130].
FAM96B	FAM96B plays an important role in suppressing DPSC senescence and promoting osteogenic differentiation and proliferation [124].
GTF2B, NFYB, NR3C	As senescence-specific markers, β-galactosidase activity is increased in aging DPSCs, with the odontogenic differentiation potential disturbed [200, 207].
NFYB, GTF2b, NR3C1	NFYB, GTF2b and NR3C1 are the core transcription factors that affect the aging of DPSCs [126].
HSP60, p16	Expression of p16 is increased with age, whereas heat shock protein 60 (HSP60) is decreased in senescent DPSCs [208, 209].
Rock1	The abnormally high expression of Rock1 is related to the aging of HDPSCs [210].
TGF-β	Upregulated in rapidly senescent DPSCs, indicating a loss of stem cell properties and initiation of terminal differentiation [201].
TNF-α	TNF-α is a molecule that enhances mineralization [135, 211], partially explains the emergence of nucleation points, which potently drive the formation of pulp stones in aged teeth [207].

Figure 4.

Development of DPSC senescence, accumulation of senescent DPSCs in human tooth tissues and their pathological influences. As a critical source for the regeneration of dental pulp tissues, DPSCs exhibit high proliferative activity and can differentiate into adipogenic, chondrogenic, myogenic, neurogenic, odontogenic, osteogenic, or vascular lineages, thus involved in a wide variety of essential activities to maintain tooth homeostasis. However, senescent DPSCs can generate diverse adverse effects that compromise tissue integrity and accelerate pathological progression. DPSC, dental pulp stem cells.

6. Prevention of human dental aging

In the past 70 years, our global population and its age structure have been changing rapidly, a problem that is increasingly prominent and will continue to exist for the rest of the 21st century. The World Health Organization (WHO) estimates that the global population aged 65 or over is growing at a rate of 2.5%, and the number will reach approximately 1.5 billion by 2050 (www.nia.nih.gov/research/dbsr/global-aging) and 2.37 billion by 2100 [138]. This will clearly pose a major challenge to the healthcare system to ensure a healthy and long life in an aging society.

In 2016, the World Dental Federation adapted its definition of oral health from a narrow focus solely on disease, to a broader, multidimensional view that includes the ability to speak, smile, smell, taste, touch, chew, swallow, and convey a range of emotions through facial expressions with confidence and without pain or discomfort [139]. However, oral health used to be a neglected aspect of global health. With the inversion of population age structure and the expansion of the elderly relative to other age subgroups, the prevalence of oral diseases in the elderly will further increase. In addition, it is evident that the future dental healthcare system will be costly and largely insufficient to meet the mounting challenges.

Dental diseases and functional problems of the elderly mainly include dental caries, periodontal disease and edentulousness [140]. Untreated dental caries in permanent teeth affect approximately 2.5 billion of global populations [141] with the highest incidence at age 70 years. The prevalence of periodontal diseases is highest in those aged 60 years and higher, while advanced periodontitis, the sixth most common health concern worldwide, has profound implications on systemic health [142]. Worldwide, approximately 30% of adults aged 65-74 years are edentulous, whereby periodontal diseases are the primary cause, followed by caries, poor oral hygiene and multimorbidity, a condition commonly defined as the co-existence of multiple chronic disorders that are likely associated with severe tooth loss (Edentulism) by mis-nutrition or inflammatory activities [143, 144]. In addition, dental traumatic injuries caused by falls substantially affect older adults, and more than one in four older adults have a fall each year [145-147].

Most dental diseases are preventable. The most important prevention is to follow up every three months to evaluate emerging caries and soft tissue alterations. Fluoride varnishes need to be scheduled at least twice per year for patients with a high risk of caries and 1.1% sodium fluoride is recommended daily to further promote remineralization. The prevention of periodontitis is plaque control strictly, with chlorhexidine and lishdelin gargle widely accepted for periodontal care and plaque therapeutics of the elderly. In addition, a larger and easier to grasp toothbrush handle has been developed for the elderly with poor hand flexibility, which is convenient to guide brushing [148, 149]. We believe that these preventive measures will maximize the retention time of healthy teeth in the mouth and reduce the rate of edentulous patients. In recent years, with the continued advancement of new technologies, novel materials, and the proposal of the concept of minimally invasive dental treatment, dentists can carry out comprehensive treatment for common oral diseases of the elderly, promote oral and systemic health of the elderly and reduce the disease burden. Establishment and improvement of the prevention and therapeutic system, as well as treatment strategy of oral diseases in the elderly is one of the major goals for years to come.

At present, there is no specific strategy to reverse tooth aging, according to advances of scientific research. However, in daily life, the following methods may be followed to delay aging, prolong the service life of teeth as much as possible, and ensure the quality of lifespan and social dignity (in the order of significance in dentistry and oral healthcare).

1. To develop appropriate eating habits, including but not limited to choosing healthy food and eating less hard food.

2. To keep good oral hygiene habits, such as rinsing mouth after each diet and using household protective articles including dental flushing device, dental floss, mouthwash.

3. To perform regular oral examination to evaluate new caries and oral soft tissue problems.

4. To intervene in irreversible diseases such as nocturnal molars and traumatic occlusion as early as conditions allow.

5. To timely repair the missing teeth to ensure the integrity of dentition and protect the remaining healthy teeth within the mouth.

6. To screen oral and maxillofacial tumors regardless of benign and malignant ones in the elderly, with an effective control of the development of dental neoplasia.

7. Doctors and patients of dental clinics need to establish goals and outline a good prognosis.

8. To store oral healthcare guidebooks in community service center or set up an oral lecture hall to invite doctors to publicize oral healthcare knowledge and serve residents.

7. Concluding remarks and prospects

Due to the distinctive process of tooth development, the formation of hard tooth tissue is transient. Both the dentin-forming odontoblasts and the enamel-forming ameloblasts belong to highly differentiated cell populations, which are difficult to separate and culture. Although studies focusing on tooth aging tends to increase in recent years, current biotechnologies remain unable to successfully achieve functional regeneration of tooth hard tissue, necessitating continued search for materials to aid in hard tissue replacement and tooth implant. At present, the research of tooth aging is far behind that of the vast majority of other organs, such as bone, muscle, skin, liver, lung and blood.

The future prospects in human dental aging intervention can be largely summarized as follows (in the order of technical priority and scientific significance).

1. Dental pulp regeneration: at present, we mainly focus on pulp regeneration of young permanent teeth with partial pulp necrosis. Although advances have been made in regenerating materials, cells and cell-derived factors, there is still a long way to go before functional pulp tissue is regenerated, with regeneration of the pulp of the elderly still challenging.

2. Enamel regeneration and repair: the elderly are often confronted with problems of enamel structure change and repair, but enamel regeneration has not been made possible to date, whereas major progress is basically limited to selection and improvement of materials.

3. Systematic study of the difference between the internal nervous system of teeth, the peripheral nervous system, and the central nervous system (CNS) of other organs may help block and rebuild the link between the dental nerve and the CNS.

4. Aged pulp is always accompanied by an increased accumulation of fat and fibrous cells. The systematic comparison between the fat cells in the pulp and the fat in the abdomen of the human body may provide a solution to achieve a scientific weight loss of the pulp tissue.

5. Tooth aging related model: conventional aging models of DPSCs, or those extracted from elderly teeth, have proved feasible for screening drugs or related molecular mechanisms study, but the real in vivo model has not yet been developed. In vivo models of non-human primates may represent an optimal alternative, in spite of high costs.

6. Non-invasive diagnosis of teeth: with the advancement of modern optics and microdetection technology, related detection equipment is likely to achieve a breakthrough in the next decade. It is imaginable to determine tooth aging quickly, accurately, and noninvasively at home in future.

7. Small molecule compounds: can not only promote dentin regeneration, but even reverse the aging of pulp stem cells or odontoblasts in the near future, making tooth damage repair more efficient and straightforward.

Anyway, we firmly believe that the future antiaging research of human teeth will make significant and continued progress, according to the advance rate of aging-related studies performed for the vast majority of other organs, eventually benefiting the whole mankind.