Effect of serum ferritin levels in gingivitis and periodontitis patients before and after nonsurgical periodontal therapeutic intervention

Periodontitis is an inflammatory disease that takes hold of the supporting structures of teeth. The diagnosis is based on traditional approaches, such as clinical attachment loss and periodontal pocket depths. However, recent advances in dentistry have harnessed biomarkers as an alternative diagnostic aid. Serum ferritin is a biomarker whose blood levels can be exploited to differentiate periodontium in health and disease. This article helps justify the importance of serum ferritin as a potential biomarker for investigating periodontitis after performing nonsurgical periodontal therapy in healthy and chronic periodontitis patients. Venous blood was obtained from individuals with dental biofilm-induced gingivitis and Stage 3 Grade A Periodontitis, and serum ferritin levels and hemoglobin (Hb) levels were measured. Non-surgical periodontal therapy was performed on Stage 3 Grade A Periodontitis. After 3 months, blood was collected again, and serum ferritin levels and Hb levels were assessed. High serum ferritin proportions were observed in an individual suffering from Stage 3 Grade A Periodontitis. However, they declined considerably after 3 months after treatment with non-surgical periodontal therapy. Analysis by the generalized estimating equation method exhibited a significant decrease in Oral Hygiene Simplified Index (β = 2.02, p < 0.001), gingival index (β = 1.11, p < 0.001), probing pocket depth (β = 1.03, p < 0.001), clinical attachment level (β = 3.01, p < 0.001), and serum ferritin (β = 76.9, p < 0.001) in the test group compared to the control group. However, no significant difference was noted in Hb. Nevertheless, no significant changes were noticed in healthy subjects. Serum ferritin is a salient biomarker for the pathogenesis of persistent gum affliction.

that smoking, obesity, triglycerides, diabetes, and periodontal disease have an association with serum ferritin levels.It is suggested that patients with periodontitis show changes in cellular and molecular components of peripheral blood due to inflammatory changes in the periodontal tissues.
The purpose of this study was to measure the concentrations of serum ferritin from dental biofilm-induced gingivitis and Stage 3 Grade A Periodontitis patients before and after non-surgical periodontal therapy and test whether these concentrations correlate with clinical parameters associated with periodontal disease.

OBJECTIVES OF THE STUDY
The objectives of this research are to measure the serum ferritin level among dental biofilm-induced gingivitis and Stage 3 Grade A Periodontitis patients and also to evaluate the effect of non-surgical periodontal therapy on serum ferritin levels in Stage 3 Grade A Periodontitis patients.Also, along with serum ferritin level, the Hb level was evaluated in dental biofilminduced gingivitis and Stage 3 Grade A Periodontitis patients and also to evaluate the effect of non-surgical periodontal therapy on Hb level in chronic periodontitis patients.

Study design
The biochemical analysis was carried out in the Department of Periodontics at Karnavati School of Dentistry, Uvarsad, Gandhinagar, Gujarat 382422, India.After dividing the patients into their respective groups (Fig. 1), baseline clinical parameters were recorded, and blood samples were obtained to measure serum ferritin levels.Only oral hygiene instructions were given to those in the control group.At the same time, thorough scaling and root planning were carried out for those in the experimental group, and oral hygiene instructions were given.After 3 months, the patients were called back for reevaluation of clinical parameters and serum ferritin levels.All patients than a few decades ago (Committee on Diagnostic Error in Health Care et al., 2015;Highfield, 2009;Ko et al., 2021;Listgarten, 1986).They contain radiographs that measure alveolar bone levels and probing pocket depths (PPDs), bleeding on probing, clinical attachment levels (CALs), plaque index, and degrees of clinical attachment (Khashaba et al., 2020;Kim et al., 2023;Lang and Bartold, 2018;Preshaw, 2015).The procedure is simple to handle, cost-efficient, and comparably non-intrusive.The periodontal probe's clinical attachment loss appraisal also estimates the injury from prior ruin events.Moreover, the procedure is able to estimate up to 2-3 mm substantial difference (Giannobile et al., 2009;Ko et al., 2021;Taba et al., 2005).
Research on diagnosing oral and periodontal diseases advances toward techniques that identify and measure periodontal risk using biomarkers (Taba et al., 2005).In 1998, the National Institutes of Health Biomarkers Definitions Working Group (2001) defined a biomarker as "a characteristic that is objectively measured and evaluated as an indicator of normal biological processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention." Antibodies to several pathogenic microbes have been found in the local area in the periodontal tissue and systemically in the bloodstream (Martínez-García and Hernández-Lemus, 2021).Periodontal infections that cause periodontitis also cause an inborn or inherent humoral immune response (Stathopoulou et al., 2015).According to studies, the preponderance of the main periodontopathogens has hemolytic activity, which dissolves erythrocytes and results in elevated iron levels (Chu et al., 1991).Such periodontal bacteria may produce excessive amounts of iron, raising local iron concentrations, and eventually producing iron disorders (Guo et al., 2018).
Iron is a fundamental element for virtually all life forms as it takes part in oxidation-reduction reactions necessary for several fundamental biologic processes (Abbaspour et al., 2014;Dev and Babitt, 2017).Among human beings, iron is incorporated into proteins (Ems et al., 2022).These ironcontaining proteins are required for cellular and organismic purposes, including O 2 transportation, xenobiotic metabolism, nucleic acid replication or duplication, and host protection (Dev and Babitt, 2017;Ward and Cloonan, 2019).
Several types of dietary iron are absorbed, including ferritin, heme, and inorganic forms (Abbaspour et al., 2014;Ems et al., 2022).Ferritin performs a variety of specialized tasks, including reprocessing iron in macrophages, momentary and long-standing iron repositories in hepatocytes, and typical intracellular tasks, which conserve iron for cytochromes, nitrogenase, hemoglobin (Hb), myoglobin, and other anabolic enzymes as well as potential detoxification if too much iron enters the cells (Kotla et al., 2022;Sukhbaatar and Weichhart, 2018).As a result, ferritin is typically thought of as a protein that stores iron inside cells (Chiou and Connor, 2018).Commonly people's extracellular fluids include ferritins as well.Clinical conditions, such as cancer, chronic infection, hepatocellular injury, and acute inflammation, result in high serum ferritin levels (Sandnes et al., 2021).
Ferritins are high in infection without signaling body iron overload.As ferritin is an amyloid precursor protein, it is frequently higher in the course of disease.Evidence suggests

RESULTS
The study comprised 40 patients aged 18-45 years: 20 in the control group and 20 in the test group.In the control group, out of 20 patients, 10 were male and 10 were female, with a mean age of 38.7.In the test group, out of 20 patients, 12 were male, and 8 were female, with a mean age of 40.64.

Clinical and laboratory parameters in test group patients
In the control group, significant changes were observed.Except for the Hb level, all other clinical and laboratory parameters declined to exceptional values, as shown below (Table 1 and Fig. 3A and B).met the inclusion criteria: for the control group, no evidence of interproximal attachment loss and probing depth ≤3 mm in all the teeth; for the test group (Eke et al., 2012), two or more interproximal sites with attachment loss ≥4 mm and two or more interproximal sites with probing depth ≥5 mm, not on the same tooth those without a history of any systemic disease or condition, those who were not on anti-inflammatory or antibiotic drugs, mouthwash, or vitamin supplements within a previous 3-month period.After confirming the Hb level (≥12 g/dl), patients were included in the study.The exclusion criteria included pregnant and lactating women and patients who smoked or consumed tobacco products.The patients explained the procedure well, and informed consent was taken before enrollment into the study.

Clinical parameters
The Oral Hygiene Simplified Index (OHI-S) suggested by Greene andVermillion (1964) (Sosiawan et al., 2022) was recorded in the patients of both groups.After that, the gingival index (GI), first coined by Löe-Silness (Gehlot et al., 2022;Löe, 1967;Marçal et al., 2022;McClanahan, 2001), was recorded.PPDs and CAL were measured using a UNC-15 probe in all teeth.The control group had PPDs ≤3 mm with no attachment loss, whereas PPDs defined the test group ≥5 mm and/or attachment loss ≥4 mm at a minimum of two interproximal sites.

Collection of blood from the subjects
The skin disinfection at the venous puncture site was conducted with surgical spirit before each sample collection.Strapping with the strip of cloth or a band of rubber 3-4 inches above the antecubital fossa, a blood sample of 5 ml was gathered from the antecubital vein of the forearm using a 25-gauge needle and 5 ml syringe.The collected blood was divided into two parts.The first part was transferred to an aseptic vacuum tube containing an anticoagulant to estimate Hb.The second part was transferred to a sterile vacuum tube with no supplemental anticoagulant to assess the serum ferritin level.The collected blood was kept at room temperature to allow clot formation.Then, serum was segregated from blood by centrifuging at 2,700-3,300 rpm for 15 minutes, and extracted serum was immediately transported to the vial for serum ferritin level measurement (Fig. 2).

Statistical analysis
Clinical and laboratory parameters were recorded for both groups at baseline and 3 months intervals.The mean and standard deviation of the collected data were calculated for both the groups and between.The within-group comparison was made using repeated measured analysis of variance (ANOVA) by adjusting the model with age and sex.The biological parameters of each of the 20 patients were followed at two time points, during enrollment and 3 months later.Therefore, an autocorrelation was created between the responses of each patient.To assess the group effects on changes in biomarkers over time by considering the patient's autocorrelation, a generalized estimating equation (GEE) model was performed, considering an exchangeable correlation matrix.The treatment effects were adjusted by covariates, such as age, sex, and time.Statistical analysis was performed using STATA-15, and charts were prepared using GraphPad Prism 8.3.2 (Fig. 4).Oral Hygiene Simplified Index (mm) = OHI-S; Gingival index (mm) = GI; Probing pocket depths (mm) = PPDs; Clinical attachment level (mm) = CAL; Hemoglobin (g/ dl) = Hb, serum ferritin level (ng/ml).ferritin (β = 76.9, p < 0.001) in the test group compared to the control group.However, no significant difference was noted in Hb (Table 4 and Fig. 3).

DISCUSSION
Periodontitis is a long-standing inflammatory illness caused by infection of the facilitating tissues around the teeth (Hoare et al., 2019;Könönen et al., 2019).A limited group of primarily Gram-negative anaerobic bacteria and spirochetes, including Treponema denticola, Tannerella forsythia, and Porphyromonas gingivalis, colonize and increase to start the infection (Hiranmayi et al., 2017;Zhu et al., 2013).These bacteria expand apically along the surface of the tooth roots, embedded with various other species in biofilms, to encourage the development of periodontal pockets and the obliteration of the alveolar bone and collagenous attachment fibers of the periodontal ligament (Lasserre et al., 2018).
It is reported that ferritin is an acute-phase reactant; it is increased in conditions, such as liver disease, persistent infection, autoimmune disorders, and inflammation (Kell and Pretorius, 2014;Mahroum et al., 2022).Fever, leukocytosis, thrombocytosis, metabolic abnormalities, changes in the concentration of some plasma proteins, and changes in metabolism are among the clinical and metabolic characteristics of the acute phase response (Chakraborty and Burns, 2023).Several plasma proteins, including ferritin, alter because of infection (Kernan and Carcillo, 2017).
Ferritin is essential in iron storage and recycling, apart from its aspect as an acute-phase protein (Kotla et al., 2022).Ferritin plays a critical role in the host immune response (Ganz and Nemeth, 2015), as is conspicuous from its raised level at the same time as infection to hindering infective agents that attempt to bind iron from the host tissue (Gehrer et al., 2023).
The factors which control ferritin expression are iron and proinflammatory cytokines (Moreira et al., 2020).

Clinical and laboratory parameters in control group patients
In the control group, a significant decline was noted in OHI-S (p < 0.001) and GI (p < 0.001).However, no other changes were found in clinical and laboratory parameters (Table 2 and Fig. 3C and D).

Intergroup comparison of clinical and laboratory parameters
When intergroup comparison was made at intervals of 3 months, the mean values of oral hygiene, GI, CAL, and serum ferritin level showed a better reduction in the test group compared to the control group, while no statistically significant values were noted for PPD and Hb level (Table 3).
In the present study, the intergroup comparison of the mean value of the oral hygiene index at 3 months showed a better reduction in the test group than in the control group.These results agree with those of Chakraborty et al. (2014).
In the present study, the intergroup comparison of the mean value of the GI at 3 months showed a better reduction in the test group than in the control group.The GI score was low throughout the 3 months of the study period.This may be because of proper oral hygiene guidance.However, the better reduction in the GI score in the test group suggests that the intervention provided to this group effectively improved gingival health beyond what can be achieved through good oral hygiene practices alone.These results follow the study conducted by Latha et al. (2015).
In the current research, the intergroup comparison of PPD at 3 months between two groups showed a mean difference of −1.57, which was statistically nonsignificant because in the test group, the mean value after phase-1 therapy reduced and reached up to the 3-month mean value of the control group.Ali and Ahmed (2018) conducted a similar observational study and found statistically significant results in GI, PPD, and CAL.
The mean clinical attachment loss at 3 months between the two groups showed a mean difference of −14.51, which was statistically significant.Thounaojam (2019) did a 1-month intervention study on the effects of chronic periodontitis on serum ferritin levels.He found a mean reduction in serum ferritin levels from the reference point and 1 month after nonsurgical periodontal therapeutic intervention in CP patients and a substantial decline in clinical attachment loss.
No marked difference in Hb level was observed in both, and the groups and mean differences between both groups were statistically not significant.Several studies have examined the correlation between Hb levels and chronic periodontitis.A study conducted by Kolte et al. (2014) revealed no considerable correlation linking Hb level and the severity of inflammation.In lieu, several researchers (Anumolu et al., 2015;Gokhale et al., 2010;Naik et al., 2010;Patel et al., 2013;Parihar et al., 2019;Pradeep and Anuj, 2011;Shetty et al., 2014) showed a significant correlation between Hb level and severity of inflammation, i.e., reduction in Hb level as the severity of inflammation gets higher.
The current research shows a substantial association linking serum ferritin and chronic periodontitis with multiple earlier studies (Bhavya et al., 2017;Chakraborty et al., 2014;Thounaojam, 2019).In all this research and the present study, the result shows a significant depletion in serum ferritin levels and, subsequently, medical periodontal treatment as the level of inflammation gets reduced.Latha et al. (2015), and Ali and Ahmed (2018) did an observational study on the interrelationship uniting serum ferritin levels and chronic periodontitis.They found a significant correlation between serum ferritin and chronic periodontitis.Contrary to all these studies, Prakash et al. (2012) stated that no correlation between Proinflammatory cytokines like that of tumor necrosis factor (TNF), interleukin (IL)-1, and IL-6 play a significant role in periodontitis (Gomes et al., 2016;Ramadan et al., 2020).Clinical studies have shown that TNF-α and IL-1a stimulate ferritin expression by including transcription of the heavy chain ferritin (H-ferritin) gene in mouse adipocytes and human muscle cells, which suggests that ferritin is involved in the immune response to inflammation (Moreira et al., 2020).Lipopolysaccharide of the extracellular membrane of Gramnegative bacteria provokes various reactions involving ferritin (Farhana and Khan, 2022;Maldonado et al., 2016), thereby resulting in upraised serum ferritin in circulation, suggesting that ferritin is possibly embroiled in the host's immune response to bacterial infections (Kernan and Carcillo, 2017).In gingival tissue disruption, local inflammatory arbitrators derived from the host activate and are overexpressed when exposed to pathogenic microbes and their outgrowth (Cekici et al., 2014;Silva et al., 2015).The above mode of action is involved in the correlation between serum ferritin and chronic periodontitis (Thounaojam, 2019).
Periodontitis is a multifactorial disease, and periodontal therapy depends on several factors that can modify host response in patients with generalized infections, those with diabetes, those on immunosuppressive therapy, and other debilitating diseases (Preshaw, 2015;Simpson et al., 2015).Among people with diabetes, individuals' pathogenic microbial deterrent mechanisms are often impaired.The vulnerability toward pathogens is realized and potentiated through high blood glucose levels associated with DM and the level of control of DM (Nagendra et al., 2022).Diabetic patients have an exceptional likelihood of infective disorders (Abu-Ashour et al., 2017).
One of the censorious difficulties pregnant and lactating ladies often face is inadequate iron intake, leading to anemia.However, it is also important to note that pregnant and lactating women may have different nutritional needs and may require additional interventions to address iron deficiency anemia compared to non-pregnant and non-lactating individuals.Therefore, it is possible that excluding this population was necessary to achieve the research objectives and avoid confounding factors.That is why we have excluded pregnant and lactating women (including criteria Hb ≥ 12 g/dl) in this study (Kadry et al., 2018).
Various types of mouthwash are regularly used in the current lifestyle (Joshipura et al., 2017;Macfarlane et al., 2011).Every mouthwash acts as a bacteriostatic or bactericidal on the oral mucosa and gingival tissue (Radzki et al., 2022;Rajendiran et al., 2021).These properties of mouthwashes can alter the result of this study's parameters (Kumar and Varghese, 2020;Rajendiran et al., 2021).Considering this, we have excluded patients who use mouthwashes within 3 months.
Smoking is the most potent behavioral hazardous feature for the incidence and advancement of periodontitis (Silva, 2021).It deleteriously affects all aspects of the periodontium (Jiang et al., 2020;Leite et al., 2018).Tobacco users have been shown to retort to non-surgical therapeutic intervention for periodontitis less than non-smokers (Kanmaz et al., 2021).Smoking can compromise the immune response, serum ferritin level and long-standing periodontitis was found in all these studies.
Based on the results achieved in the present research, it must be emphasized that the present study shows a significant association betwixt serum ferritin levels and the ferocity of inflammation.
However, it is important to note that the study's sample size, demographic characteristics, and other factors may have influenced the results.Additionally, the duration of the study period may not be long enough to fully capture the effects of the intervention over a more extended period.Overall, the findings of this study highlight the potential for effective interventions to improve periodontal health.However, additional studies are required to fully understand the impact of the intervention on clinical attachment loss and its potential for widespread application.

LIMITATIONS OF THE STUDY
1.The sample size is small.Thereby, we planned another randomized control multicenter clinical trial with larger sample sizes over a longer duration so that study results can be generalized for India.
2. A single investigator in the current investigation carried out clinical parameters and treatment techniques.This experiment was not double-blinded, so the data gathering may have been biased.Therefore, it could be advantageous for future research to be double-blinded to avoid an opinionated introduction.
3. Ferritin sample was collected from serum; saliva can also be used to evaluate the ferritin level.The advantage of a salivary collection of ferritin would be its non-invasive collection technique.
4. IL 6, plasminogen activator inhibitor type 1, and the TNF-α are the additional inflammatory mediators, which can be measured using enzyme-linked immunosorbent assay kits and can be used to evaluate periodontal inflammation.

CONCLUSION
The findings from this comparative, clinical, and biochemical trial revealed that serum ferritin level is an essential factor in the pathogenesis of periodontal disease.It can be used as a diagnostic marker for periodontal disease or a prognostic marker for disease progression.

RECOMMENDATION
More real-life clinical research studies must be carried out to recognize and realize the beneficial aspect of LAB on human health.Also, governments and academic institutions need to play an active role in incorporating LAB use for human health.Further refinement of delivery means to ensure LAB cells' survival needs to be done.Researchers should further investigate and use probiotics as therapeutics for various illnesses in the best possible ways.

Figure 1 .
Figure 1.A flowchart illustrating the study group.This figure has been drawn utilizing the premium version of BioRender with the Licence number (RJ25DQU2R5).Image Credit: Susmita Sinha.

Figure 2 .
Figure 2. Illustrating the blood collection method.This figure has been drawn utilizing the premium version of BioRender with the Licence number (OQ255QGN01).Image Credit: Susmita Sinha.

Figure 3 .
Figure 3. Within-group difference in case (A and B) and control (C and D) between baseline and follow-up after 3 months.Repeated measured ANOVA was used to estimate the p-value.

Figure 4 .
Figure 4. Longitudinal changes in biological parameters in the test group compared to the control group.Data are presented as a β coefficient with 95% confidence intervals in parentheses and adjusted for age, sex, and duration.Statistical analysis was performed using the GEE model.The p-value of <0.05 is significant.

Table 1 .
Within-group difference in the test group between baseline and follow-up after 3 months.
Repeated measured ANOVA was used to estimate the p-value, and the model was adjusted by age and sex.

Table 2 .
Within-group difference in the control group between baseline and follow-up after 3 months.
Repeated measured ANOVA was used to estimate the p-value, and the model was adjusted by age and sex.

Table 3 .
Biological parameters differ between control and test groups at baseline and follow-up.The multivariate regression model was used to estimate the p-value, and the model was adjusted by age and sex.

Table 4 .
Longitudinal changes in biological parameters in the test group compared to the control group.