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 Table of Contents  
REVIEW
Year : 2019  |  Volume : 4  |  Issue : 2  |  Page : 30-36

Role of trace mineral in periodontal health: a review


Department of Periodontics, Nair Hospital Dental College, Mumbai, India

Date of Submission15-Apr-2019
Date of Acceptance07-May-2019
Date of Web Publication9-Jul-2019

Correspondence Address:
Adiya Apon
Department of Periodontics, Nair Hospital Dental College, Mumbai
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2542-3975.260960

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  Abstract 

Periodontal diseases are microbial induced chronic inflammatory conditions characterized by infiltration of leukocytes, loss of connective tissue, alveolar bone resorption, and formation of periodontal pockets. In response to periodontal pathogens, leukocytes elaborate destructive oxidants, proteinases and other factors. Periodontal disease is a chronic inflammatory disease, which leads to alteration of the micronutrient levels such as zinc, selenium, iron and copper. The imbalance of the micronutrient levels leads to increased susceptibility to oxidative damage of tissues. These micronutrients play a role in both health and disease. The vitality of the periodontal tissues in both health and disease depends on the adequate source of essential nutrients being available to the host. Micronutrients are imperative for optimum host response. Populations worldwide are prone to their insufficiency due to lifestyle changes or poor nutritional intake. Balanced levels of these trace minerals such as iron, zinc, selenium and copper are essential to prevent progression of chronic conditions like periodontitis. Their excess as well as deficiency is detrimental to periodontal health. Selenium, zinc and copper are integral components of antioxidant enzymes and prevent reactive oxygen species induced destruction of tissues. Their deficiency can worsen periodontitis associated with systemic conditions like diabetes mellitus. This review focused on the role of micronutrients, namely, iron, zinc, selenium and copper in periodontal health and their association with chronic periodontitis.

Keywords: nutrition; periodontitis; micronutrients; iron; zinc; selenium; copper; diabetes mellitus; anaemia; antioxidant; reference value


How to cite this article:
Apon A, Kamble P. Role of trace mineral in periodontal health: a review. Clin Trials Degener Dis 2019;4:30-6

How to cite this URL:
Apon A, Kamble P. Role of trace mineral in periodontal health: a review. Clin Trials Degener Dis [serial online] 2019 [cited 2019 Aug 24];4:30-6. Available from: http://www.clinicaltdd.com/text.asp?2019/4/2/30/260960




  Introduction Top


Periodontitis is defined as “an inflammatory disease of the supporting tissues of the teeth caused by specific microorganisms or groups of specific microorganisms, resulting in progressive destruction of the periodontal ligament and alveolar bone with pocket formation, recession or both.”[1] Regarding the onset/progression of periodontal breakdown, a number of risk indicators/factors have been identified. These are characterised by genetic, environmental (e.g., stress, bacterial challenge) and lifestyle/behavioral (e.g., exercise, nutrition, smoking).[2] Risk factors are important in the development and propagation of periodontal disease and act predominantly via modification of the host response to bacterial challenge, resulting in less effective clearing of pathogenic species and inflammation resolution, which in turn increases host mediated tissue damage. The onset and progression of disease depend upon a delicate equilibrium between the microbial challenge and the host response.[3]

Nutrition has significant effects on the inflammatory processes as well on the cellular and humoral immune mechanism. The interaction between nutritional status and the immune response to the bacterial challenge can be an underlying factor in the progression of periodontal disease.[4] Nutrients can be divided into six major classes, i.e., fats, carbohydrates, proteins, minerals, vitamins and water; these can be further subdivided into two broad categories, ‘macronutrients’ (fats, carbohydrates and proteins), which are required in large quantities from the diet providing a vital energy source and ‘micronutrients’ (minerals, vitamins, trace elements, and amino-acids), which are essential co-factors required for functioning of many enzyme systems, such as DNA polymerase, RNA polymerase, superoxide dismutase, catalases, and alkaline phosphatase.[4],[5]

Micronutrients are dietary compounds that do not provide energy but are required by living organisms and are essential for optimal health, proper growth, and metabolism.[4],[5]

Micronutrients are required in milligram (mg) to microgram (μg) quantity and include vitamins and minerals. The major minerals are sodium (Na), potassium (K), calcium (Ca), magnesium (Mg), phosphorus (P) and sulfur (S). The trace minerals are: iron (Fe), zinc (Zn), iodine (I), selenium (Se), fluoride (F), copper (Cu), cobalt (Co), chromium (Cr), manganese (Mn) and molybdenum (Mo). Recommended daily allowance of micronutrient such as iron, copper, and zinc is less than 100 μg.[4] Depletion or lack of availability of these nutrients gives rise to malnutrition at either the macro or micronutrient level. Both are detrimental to periodontal health as well as to general health.

Micronutrient deficiencies can be provoked by[6]:

  • Drugs (e.g., antacids, antibiotics, antihypertensives, chelating agents, corticosteroids, diuretics, laxatives, lipid-lowering drugs, non-steroidal anti-inflammatory drugs, and cancer chemotherapeutics);
  • Malabsorption or diarrhea;
  • Lifestyle factors (e.g., diet, malnutrition, chronic alcohol or nicotine abuse, and consumption of fast foods or processed foods);
  • Systemic disorders (e.g., diabetes mellitus, thyroid and parathyroid disorders, liver and kidney diseases, psoriasis, and atopic dermatitis);
  • An increased requirement (e.g., during pregnancy, breastfeeding, growth, physical/mental stress, convalescence, exposure to heavy metals, and heavy sweating);
  • Loss (e.g., following hemodialysis, nephrosis, surgery, or burns).


Micronutrients play a role in both health and disease. The vitality of the periodontal tissues in both health and disease depends on the adequate source of essential nutrients being available to the host.

This review aims to discuss the role of some important trace mineral micronutrients essential for periodontal health.


  Search Strategy and Selection Criteria Top


The PubMed database was searched. Common keywords relating to periodontitis and micronutrients were derived from the literature. We restricted our search studies in English, relating to humans, published after January 1, 1980. Searches were run from January 1, 1980 to March 1, 2019. The full electronic searches are shown in [Table 1].
Table 1: Search strategy and selection criteria

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  Essential Trace Mineral Micronutrients for Periodontal Health Top


Iron

Fe is the most abundant essential trace element in the human body. The total content of Fe in the body is 3–5 g with most of it in the blood. About 4 g of Fe is present in the typical person: 2.5 g in hemoglobin; 0.3 g in myoglobin and cytochromes; and about 1 g in Fe stores (ferritin).[7] The Recommended Daily Allowance for Fe varies with age. Its requirement is highest in women of reproductive age group which is 18 mg/d, while in middle-aged adults, it is about 8 mg/d.[8] Typical intake of Fe is about 10 mg/d, but only about 10% is absorbed. Fe is absorbed in the gut from diet in case of depletion and transported in the form of ferritin. Its reduced absorption results in Fe deficiency anaemia where the hemoglobin levels are < 12 g/dL for adult non-pregnant women and < 13 g/dL for adult men.[9] Furthermore, in Fe deficiency anemia, decreased serum Fe and ferritin levels and increased total Fe binding capacity are seen. This should be distinguished from anemia of chronic disease which is a cytokine-mediated anemia more prevalent in individuals with chronic inflammatory, infectious, or neoplastic disorders and characterized by hypoferremia with adequate reticuloendothelial Fe stores.[10],[11]

Optimal levels of Fe are essential prerequisite for periodontal health and shift in either direction may be detrimental. The role of Fe in periodontal ligament and alveolar bone homeostasis and function was recently verified in an animal model.[12] The PDL cells have the ability to regulate Fe uptake by expressing the light and heavy chain subunits of heteromeric ferritin.[12],[13] This further controls the cyto-differentiation of these cells into osteoblasts and mineralization, thereby affecting the bone density.[12],[13] Fe is essential for both innate and adaptive immune responses.[14] Its deficiency weakens the cell-mediated immunity by reducing lymphocyte count, interferon-γ and interleukin-2 levels and functions of natural killer cells. The delayed type of hypersensitivity response mediated through CD4+ lymphocytes is also disrupted.[15],[16] It also results in reduced immunoglobulin E (IgE) production, high CD4+ to CD8+ T cell ratios, low numbers of CD28+ cells and impaired CD8+ T-cell function.[17] Furthermore, Fe plays an important role in oxidative burst, i.e., the release of reactive oxygen species (ROS) from macrophages and neutrophils. A shift in the levels of Fe may cause oxidative stress leading to periodontal destruction. This is mainly related to the conversion of hydrogen peroxide to ROS through Fenton reactions catalysed by free Fe. Subsequently, there is activation of matrix metalloproteinases, which degrade the extracellular matrix components. This further activates the nuclear factor-kappa B pathway stimulating the release of pro-inflammatory cytokines such as interleukin-1β, interleukin-6, interleukin-8 and tumor necrosis factor-α, which destroy the periodontal tissues and alveolar bone.

Fe is required for the activation of enzymes such as inducible nitric oxide synthase, myeloperoxidase and NADPH oxidoreductase during bacterial phagocytosis.[14],[18],[19] Its deficiency may inhibit the activity of protective enzymes like myeloperoxidase, which are essential for the bactericidal activity of macrophages.[20] Additionally, it may reduce the levels of oxygen in the gingival tissues which further activates the inflammatory cascade.

Although the evidence for Fe deficiency directly causing chronic periodontitis is weak, the reverse association is comparatively strong.[20],[21],[22],[23] It has been suggested that inflammation due to chronic periodontitis results in increased levels of pro-inflammatory cytokines which suppresses erythropoiesis in bone marrow.[23],[24],[25] Patients with chronic periodontitis have a lower number of erythrocytes and a lower hemoglobin level than healthy controls.[25] A prospective study on a rural Japanese population[26] confirmed that, after adjusting for age, the progression of periodontal disease is associated with a decrease in erythrocyte counts. It was proposed that chronic periodontitis can lead to anemia of chronic disease, which may be explained by a depressed erythropoiesis resulting from the systemic effect of the pro-inflammatory cytokines in response to periodontal pathogens and their products.[21],[23],[27] In addition, improvement in hematological parameters up to 6 months following nonsurgical periodontal therapy of patients with chronic periodontitis was reported.[21],[23],[27]

Chakraborty et al.[20] reported that chronic periodontitis as well as Fe deficiency anemia in patients with and without periodontitis are associated with decreased salivary and serum superoxide dismutase levels compared to healthy controls. There was a significant, negative correlation between serum superoxide dismutase levels and all periodontal parameters. Patients with Fe deficiency anemia and comorbid chronic periodontitis exhibited a higher incidence of bleeding on probing, a higher percentage of sites with clinical attachment loss of ≥ 6 mm, as well as deeper periodontal pocket depths, compared with patients with chronic periodontitis only in this study.

It is documented that Fe affects glucose metabolism and it has been shown that free Fe concentrations in the patients with type 2 diabetes mellitus are higher than those of normal subjects, which could contribute to tissue damage that may potentially elevate the risk of type 2 diabetes mellitus.[28],[29]

Thus, Fe is essential for immunological homeostasis. The general consensus is that both elevated and reduced levels are detrimental to the host immune responses, as well as susceptibility to infections. So, it is necessary to control its levels and needs tight regulation in order to guarantee the protective responses to the health.

Zinc

Zn is an essential trace element which is involved in a multitude of intracellular processes of more than 300 different enzymes, acting as an essential requirement for the successful growth of many internal organs, stabilizing cell membranes, and modulating membrane-bound enzymes and insulin action.[29],[30] It plays an important role in immune function, wound healing, protein synthesis, DNA synthesis, and cell division. In addition, zinc is essential for intracellular binding of tyrosine kinase to the T-cell receptors, CD4 and CD8α, which are required for T-lymphocyte development and activation. In biological systems, zinc exists as Zn2+ and is present in all tissues and fluids of the body. There is 2–4 g of Zn distributed throughout the human body.[31] Zn is stored in prostate, parts of the eye, brain, muscle, bones, kidney, and liver. The recommended dietary allowance of zinc is 8 mg for adult women and 11 mg for adult men.[32]

Zn is stored in liver cells by binding to the cytosolic proteins and accumulates in mitochondria and markedly increases succinate dehydrogenase activity in the organelle. Zn taken up by the liver binds to the subcellular organelles and affects the cellular metabolic system. This micronutrient participates both in the synthesis and actions of the hormones, which are intimately linked to bone metabolism.[33] In blood plasma, Zn is bounded and transported by albumin (60%) and transferrin (10%).[34] Since transferrin also transports Fe, excessive Fe can reduce zinc absorption, and vice versa.[35]

Zn is an integral component of antioxidant enzymes and its altered levels cause oxidative stress. Zn deficiency may cause oxidative damage to membranes, structural strains, altered function of specific receptors and nutrient absorption sites, altered activity of membrane-bound enzymes, altered function of permeability channels, altered function of carrier and transport proteins in the membrane.[36] Zn deficiency also affects the functioning of immune cells such as monocytes (all cells), natural killer cells (reduced cytotoxicity), neutrophils (reduced phagocytosis), T cells and lymphocytes (decreased apoptosis). Furthermore, it increases the secretion of pro-inflammatory cytokines.[37]

Optimal levels of Zn are imperative for growth and development of periodontal tissues. While the deficiency leads to reduced protection of sulpha-hydryl groups and increased production of ROS, excessive levels may act as pro-oxidant by eliciting decline in erythrocyte Cu-Zn superoxide dismutase.[37] This enzyme has been localized in the human periodontal ligament where it prevents free radical induced damage.[38],[39] Therefore, its optimum levels are a prerequisite to maintain the tissues in a healthy state. Animal studies have revealed that dietary deficiency of Zn leads to poorer periodontal health. It alters the thickness and keratinization of oral mucosa which becomes more susceptible to infections. Furthermore, deeper periodontal pockets and thicker palatal tissues have been reported in Zn deficient rats.[40],[41] Zn deficiency has also been shown to reduce osteoblastic activity, collagen and proteoglycan synthesis as well as alkaline phosphatase activity. Serum zinc levels and the severity of periodontal disease were evaluated in patients undergoing periodontal treatment, or in untreated patients, in Sweden by Frithiof et al.[42] Patients with decreased Zn levels showed increased alveolar bone resorption. This could be related to altered bone collagen metabolism with a significant reduction in collagen synthesis and turnover as well as reduced alkaline phosphatase activity.

Thomas et al.[43] compared serum Zn levels in a group of patients with diabetes and periodontitis, with those in a group of patients with periodontitis but without diabetes, and with group of systemically and periodontally healthy control subjects, all from South-West India. The Zn levels were significantly lower in periodontitis patients, with and without diabetes, than in healthy individuals. Zn absorption decreases in diabetic patients, which causes intercellular depletion. Hyperglycemia causes the increased urinary losses of Zn and decreased Zn levels in the body. The decreased levels of Zn affect adversely the ability of the islet cell to produce and secrete insulin.[44] This altered metabolism of Zn leads to some diabetic complications.[45]

Thus, adequate levels of Zn are imperative for both protective immune and bone regenerative processes, which would further prevent the progression of periodontitis.

Selenium

Se is a mineral antioxidant essential for the proper functioning of various organ systems. Its biological functions are mainly exerted through selenoproteins, which are a group of antioxidants involved in activation, proliferation and differentiation of cells of innate and adaptive immunity.[46] They prevent exacerbation of immune responses in chronic inflammation. Various selenoproteins are glutathione peroxidase, thioredoxin reductases, deiodinases and selenoproteins P, K and S.[46] Among them, the glutathione peroxidase system is most widely investigated. Se is present in the glutathione peroxidase system and helps to minimize oxidative damage to lipid membranes. The recommended daily allowance for Se is 55 μg for adult men and adult women.[47]

The glutathione peroxidase enzymes utilize Se at their active sites to detoxify ROS including hydrogen peroxide and phospholipid hydroperoxide. The redox balance at the cellular level regulates the selenoproteins, which indirectly modulate immune cell signalling and function.[46] Likewise, Se regulates the activity of transcription factors (i.e., nuclear factor-κB and activator protein-1) and associated gene expression. It even reduces the levels of tumor necrosis factor-α and cyclooxygenase-2 produced by macrophages in response to lipopolysaccharides and downregulates the expression of adhesion molecules (i.e., intercellular adhesion molecule-1 and vascular cell adhesion molecule-1). Besides, it helps in metabolism of arachidonic acid and eicosanoids. It reduces monocyte adhesion and migration through endothelial cells. This is mainly related to Se induced shedding of L-selectin. At cellular level, dietary Se influences the leukocytic functions such as adherence, migration, phagocytosis and cytokine secretion.[46]

The deficiency of Se may be related to poor dietary intake, presence of chronic diseases and ingestion of drugs that reduce its absorption and proper utilization. Some studies even suggest that alcohol intake may result in poor concentrations of Se.[48]

The beneficial effects of Se on periodontium are mainly due to its antioxidant effects. In vitro and animal studies showed that addition of Se to α-tocopherol accelerated the proliferation rate and wound healing process. This was related to the increased synthesis of basic fibroblastic growth factor and type I collagen from both gingival and periodontal ligament fibroblasts in the presence of Se.[49],[50] Thomas et al.[51] evaluated the concentrations of glutathione, catalase, and Se in the serum of middle-aged patients with type 2 diabetes mellitus and healthy individuals, with and without periodontal disease. The levels of glutathione, catalase, and Se were found to be significantly lower in patients with diabetes and periodontitis compared with healthy controls. Se levels in healthy individuals with periodontitis were also decreased; however, this did not reach significance. A co-morbid impact of periodontitis with diabetes upon systemic micronutrient status was seen, probably because of oxidative stress.[52]

Thus, Se is a protective trace mineral micronutrient for the periodontium and its inclusion in the diet may be vital in “dietary regulation of inflammatory cascade.”[53] Se in the diet would further prevent the progression of destructive periodontal disease.

Copper

Cu is the third most abundant trace element with only 75–100 mg of total amount in the human body.[54] Cu is present in almost every tissue of the body and is stored chiefly in the liver along with the brain, heart, kidney, and muscles.[55] Cu is essential for immunity and combating the oxidative stress induced by reactive oxygen and nitrogen species. It acts as a co-enzyme for cytochrome-C and superoxide dismutase and is involved in electron transport of proteins. It is also required in association with Fe for the formation of hemoglobin and is stored bound to ceruloplasmin, a Cu dependent ferroxidase. Ceruloplasmin helps in oxidising Fe so that ferritin is utilized. Therefore, its deficiency may cause anemia.[56] The Recommended daily allowance for Cu is 900 μg.[57]

Cu plays an important role in cytochrome oxidase functions at the terminal end of the mitochondrial electron transport chain. The loss of this activity can contribute to the characteristic swelling and distortion of mitochondria, which can be observed in Cu deficiency, particularly in metabolically active pancreatic acinar cells, enterocytes, and hepatocytes.[58] Abnormal metabolism of Cu can affect the function of superoxide dismutase and results in decreased protection of cells from superoxide radical.[59] Hyperglycemia and hyperinsulinemia increase the production of free radicals and decrease the efficiency of antioxidant defense systems, which may lead to the complications of diabetes.[60]

Cu deficiency also has a negative influence on neutrophils, macrophages, T cells and natural killer cells. There is impaired production of interleukin-2 and excessive production of pro-inflammatory cytokines, such as tumor necrosis factor-α, matrix metalloproteinase-2 and -9 which degrade the collagen and extracellular matrix components in periodontal ligament.[43] Thomas et al.[51] conducted a study in which elevation of serum Cu level is observed in periodontitis patients causing certain alterations in collagen metabolism. Cu is essential for proper connective tissue development and the elevation in serum Cu may reflect the changes in periodontal collagen metabolism. Sundaram et al.[61] demonstrated the levels of Cu in diabetes and non-diabetes patients with chronic periodontitis; Cu were elevated at baseline and were improved significantly 3 months following nonsurgical periodontal therapy, even in those participants with uncontrolled type 2 diabetes mellitus. A study by Manea and Nechifor[62] has shown that there exists a connection between salivary copper levels and periodontitis.

As Cu serves as a cofactor for metalloenzyme like superoxide dismutase, an essential antioxidant for chronic periodontitis, optimal levels of Cu are essential for preventing exacerbation of inflammatory pathways.[43]


  Recommendations of Micronutritional Therapy For a Healthy Periodontium Top


Nutrition is the mainstay of good health and immune system, and micronutrient administration to overcome their deficiencies is justified. There are two options to achieve this objective: Firstly, dietary modification; and secondly, administration of supplements. It has been suggested that where dietary manipulation is difficult, fortified foods and supplements may be a more practical choice. However, the argument regarding the cost-benefit effects and use of multi-micronutrient additives still prevails.[63] Even though numerous studies have evaluated the relationship between micronutrients and periodontal disease, intervention studies utilizing trace minerals in humans are scarce.[20],[43],[51] A randomized, parallel clinical trial evaluated the influence of multivitamin tablets as an adjunct to periodontal therapy over a 60-day period and significant improvement in probing depths of subjects with chronic periodontitis was seen in subjects who received the experimental treatment.[64]

The trace mineral micronutrients, Zn, Fe, Se and Cu, have been deeply investigated for their role in immune function and resistance to infection. Evidence from preclinical and clinical trials suggests that although Fe is essential for immune function, its supplementation does not necessarily decrease morbidity and mortality.[53] This could be related to the complexity of mechanisms of Fe homeostasis. Alternatively, strong evidence exists for the use of Se and Zn as dietary modulators due to their antioxidant and anti-inflammatory actions.[65] They prevent periodontal destruction by reducing the levels of plasma oxidative stress markers and pro-inflammatory cytokines. Furthermore, their administration in conjunction with periodontal therapy accelerated wound healing and improved the clinical periodontal parameters. A study investigated the effect of antioxidant therapy on the progression of periodontal disease when used as a monotherapy and/or as an adjunct to non-surgical debridement.[66] About 6 mg of antioxidants was administered in three divided doses for 2 weeks in the form of soft gel containing lycopene 2000 μg, Zn 7.5 mg and Se 35 μg. The results showed significant improvement in the salivary antioxidant levels and its response to periodontal therapy.[66]

Even though some reliable evidence exists, caution should be practised when advising supplements, as risk for toxicity cannot be ruled out. Following guidelines may be helpful in determining the micronutrient requirements for oral and general health.[67]

  1. Dietary assessment of nutritional intake should be done by a dietician. This involves use of a questionnaire to explore the dietary intake over a period of time;
  2. Clinical assessment of nutritional status through changes in skin, nails, eyes, hair, mouth, neck, abdomen and extremities should be done;
  3. Screening tools like, the Malnutrition Universal Screening Tool, a five-step screening method, may be utilized to identify individuals who are malnourished or at risk of malnutrition. This tool scores the malnutrition risk as low, medium or high, which helps the workers to develop a strategic plan for improving the dietary intake of the subjects[68];
  4. Anthropometric assessment, including weight, body mass index and arm circumference, may be used to calculate muscular circumference of the arm, which indicates the lean body mass.[67] Additionally, biometric impedance analysis to estimate total body water, extracellular water, fat-free mass and body cell mass helps in identification of malnourished individuals. These parameters may be utilized in building a formal diet plan for the subjects[69];
  5. Biochemical tests should be done to confirm the levels of specific micronutrients; however, they should be correlated with clinical parameters.[70] The nutrients may be supplemented with the presence of specific indications;
  6. Administration of supplements should be further verified through the results of randomized controlled clinical trials in periodontitis subjects.



  Conclusion Top


Trace elements are indispensable for the functioning of many physiologic and biochemical reactions. Many of them are metals and their exact role, i.e., patho-physiology of periodontal disease is less evident and debatable. It is one of the most difficult tasks to diagnose trace element deficiencies nutritionally as well as clinically. So, the need of the hour is to consider the dietary intake of the patients and also the host inflammatory response for the better treatment outcome and for the general health of patients suffering from periodontal diseases. A formal assessment combined with minor dietary shifts may be sufficient to achieve optimal levels for periodontal health. Future controlled clinical trials are warranted to elucidate their exact role in chronic periodontitis.

Author contributions

Concept, design, definition of intellectual content, literature search, manuscript preparation, editing and review: AA, PK. Both authors approved the final mamuscript.

Conflicts of interest

None declared.

Financial support

None.

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The Copyright License Agreement has been signed by both authors before publication.

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Checked twice by iThenticate.

Peer review

Externally peer reviewed.

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This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

C-Editor: Zhao M; S-Editors: Li JY, Li CH; L-Editors: Qiu Y, Wang L; T-Editor: Jia Y



 
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