Periodontal Regenerative Therapy in Patient with Chronic Periodontitis and Type 2 Diabetes Mellitus: A Case Report

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Bull Tokyo Dent Coll (2016) 57(2): 97 104 Case Report doi:10.2209/tdcpublication.2015-0041 Periodontal Regenerative Therapy in Patient with Chronic Periodontitis and Type 2 Diabetes Mellitus: A Case Report Fumi Seshima 1), Makiko Nishina 2), Takashi Namba 3) and Atsushi Saito 1) 1) Department of Periodontology, Tokyo Dental College, 2-9-18 Misaki-cho, Chiyoda-ku, Tokyo 101-0061, Japan 2) Department of Internal Medicine, Tokyo Dental College Ichikawa General Hospital, 5-11-13 Sugano, Ichikawa, Chiba 272-8513, Japan 3) Namba Dental Clinic, 3-11-1 Akasaka, Minato-ku, Tokyo 107-0052, Japan Received 21 December, 2015/Accepted for publication 12 January, 2016 Abstract We report a case of generalized chronic periodontitis and type 2 diabetes mellitus requiring periodontal treatment including regenerative therapy. The patient was a 66-year-old man who presented with the chief complaint of gingival inflammation and mobile teeth in the molar region. He had been being treated for type 2 diabetes mellitus since 1999. His glycated hemoglobin (HbA1c) level was 7.8%. An initial examination revealed sites with a probing depth of 7 mm in the molar region, and radiography revealed angular bone defects in this area. Based on a clinical diagnosis of generalized chronic periodontitis, the patient underwent initial periodontal therapy. An improvement was observed in periodontal conditions on reevaluation, and his HbA1c level showed a reduction to 6.9%. Periodontal regenerative therapy with enamel matrix derivative was then performed on #16, 26, and 27. Following another reevaluation, a removable partial denture was fabricated for #47 and the patient placed on supportive periodontal therapy (SPT). To date, periodontal conditions have remained stable and the patient s HbA1c level has increased to 7.5% during SPT. The results show the importance of collaboration between dentist and physician in managing periodontal and diabetic conditions in such patients. Key words: Chronic periodontitis Diabetes mellitus Periodontal regeneration Enamel matrix derivative Introduction The signs and symptoms of periodontal disease are recognized as the sixth complication of diabetes mellitus (DM) 6). Increasing prevalence of type 2 (T2) DM is a major health concern in Japan 5). In one study, the rate of periodontal disease in individuals with T2DM was found to be 2.6 times that observed in those without 7). Diabetes mellitus has an adverse effect on periodontal health, and periodontal disease in turn affects glycemic 97

98 Seshima F et al. Fig. 1 Oral view at first visit control and the incidence of complications from diabetes 13). Periodontal medicine is defined as a rapidly emerging branch of periodontology focusing on the wealth of new data establishing a strong relationship between periodontal health or disease and systemic health or disease 14). Therefore, the two-way relationship between DM and periodontitis 10) is a prime issue in the field of periodontal medicine, with effective periodontal treatment important in diabetic care and vice versa. Here we report a case of chronic periodontitis and T2DM requiring periodontal treatment including regenerative therapy. Case Report Written informed consent was obtained from the patient for inclusion in this report. 1. Examination at first visit In February 2014, a 66-year-old man was referred to the Clinic of Conservative Dentistry at Tokyo Dental College Suidobashi Hospital with the chief complaint of gingival inflammation and mobile teeth in the molar region. The patient had been receiving treatment for T2DM since 1999. Treatment had included educational hospitalization (twice) and medication for glycemic control. At the time of his first visit to our clinic, the patient had been visiting his physician regularly, and had been prescribed glimepiride, metformin hydrochloride, sitagliptin, and pioglitazone hydrochloride. His glycated hemoglobin (HbA1c) level was 7.8% and fasting plasma glucose level 183 mg/dl. The patient also had hepatitis B, which had been treated with antiviral entecavir. The virus was below detection level, however, at the first visit to our clinic. The patient had been receiving regular dental check-ups since his early 40 s. In 2013, however, he experienced pain in the molar area. His dentist referred him to our clinic for the treatment of periodontitis. Figure 1 shows an oral view obtained at his first visit.

Regenerative Therapy for DM Patient 99 Fig. 2 Periodontal examination at first visit Fig. 3 Radiographic view at first visit Gingival inflammation was mostly evident in the molar region. Extrusion of #17 due to the loss of #47 and premature occlusal contact of #27 and 37 were observed. The results of the periodontal examination are shown in Fig. 2. Thirty-one percent of sites had a probing depth (PD) of 4 mm and 4.9% a PD of 7 mm. Bleeding on probing was observed in 15% of sites. The level of plaque control as assessed by the O Leary plaque control record (PCR) 8) was 32%. Radiographic examination (Fig. 3) revealed generalized horizontal and angular bone loss in #16, 26, 27, and 37. As a measure of patientreported outcome, oral health-related quality of life (QoL) was assessed using an oral health-related QoL instrument (OHRQL) 11). The total OHRQL score in this patient was 10. A clinical diagnosis of generalized chronic periodontitis was made according to the classification of the American Academy of Periodontology 1). 2. Treatment plan 1) Initial periodontal therapy This comprised instruction on maintaining oral hygiene, quadrant scaling and root planing (SRP), extraction of an impacted third molar (#38), and occlusal adjustment for #27 and 37. 2) Reevaluation 3) Periodontal surgery for sites with a PD of 4 mm 4) Treatment for recovery of oral function This comprised prosthetic treatment for loss of #47. 5) Supportive periodontal therapy (SPT) or maintenance

100 Seshima F et al. Table 1 Treatment process Periodontitis Diabetes (by physician) February 2014 Initial periodontal therapy Medical diet Oral hygiene instruction Exercise therapy Quadrant SRP Medication ( May 2015) glimepiride (1 mg/d) June 2014 (Reevaluation) metformin hydrochloride (500 mg/d) re-srp (#11 14, 37, 41) sitagliptin (50 mg/d) Extraction (#38) pioglitazone hydrochloride (30 mg/d) July 2014 Surgical periodontal therapy Regenerative therapy with EMD and autogenous graft (#16) Regenerative therapy with EMD alone (#26, 27) (Reevaluation) Treatment for recovery of oral function Removable partial denture (#47) April 2015 present (Reevaluation) SPT Oral hygiene instruction Medication ( June 2015 present) Professional tooth cleaning repaglinide (0.75 mg/d) metformin hydrochloride (500 mg/d) sitagliptin (50 mg/d) pioglitazone hydrochloride (30 mg/d) SRP: scaling and root planing; EMD: enamel matrix derivative; SPT: supportive periodontal therapy 3. Treatment process An outline of the treatment process is shown in Table 1. 1) Initial periodontal therapy After obtaining informed consent for the proposed treatment plan, instruction was given on maintaining oral hygiene and quadrant SRP performed. Occlusal adjustment was implemented for #27 and 37. Subsequent reevaluation revealed a reduction in the PCR score to 18% and a decrease to 12 and 4% for sites with a PD of 4 mm and 7 mm, respectively. The OHRQL total score was 4. The patient s HbA1c level showed a reduction to 6.9%. Therefore, it was decided to extract #38 for prophylactic reasons. The extraction was performed at the Department of Oral Surgery of our hospital. Re-SRP was implemented for #11 14, 37, and 41. 2) Periodontal surgery Tooth #16 contained a deep intrabony defect 8 mm in depth and 3 mm in width. Therefore, regenerative therapy with enamel matrix derivative (EMD; Emdogain Gel, Straumann Japan, Tokyo) was implemented in combination with a autogenous bone graft (Fig. 4). The autogenous bone was harvested from the adjacent area using a bone scraper. Regenerative therapy with application of EMD alone was performed in #26 and 27. 3) Treatment for recovery of oral function The mandibular right molar area was treated with a removal partial denture, as the patient chose not to have dental implant treatment. 4) Supportive periodontal therapy An improvement was observed in gingival inflammation and PD at reevaluation. Various

Regenerative Therapy for DM Patient 101 showed a tendency to increase (Table 3), and his physician placed him on repaglinide instead of glimepiride (Table 1). Professional tooth cleaning including subgingival plaque control has been being performed on teeth with a PD of 4 mm at each visit for SPT. Discussion (a) (b) Fig. 4 During regenerative therapy for #16 (a) after debridement, (b) filling of defects with Emdogain Gel and autogenous bone graft levels of improvement were observed radiographically at those sites selected for regenerative therapy. There was resolution of tooth mobility in #37. The periodontal conditions were judged to be stable, and the patient was placed in a recall system for SPT. The total OHRQL score was 4, indicating an improvement in QoL from at first visit. During the first 3 months, the patient was recalled monthly. At 7 months from the start of SPT, periodontal conditions were still stable (Figs. 5 7). In terms of clinical outcome of regenerative therapy, PD showed a reduction of 4 mm from the values at first visit at all sites treated (Table 2). The level of gain in clinical attachment at the treated sites varied from 1 to 4 mm. During SPT, the patient s HbA1c level The present case was one of generalized chronic periodontitis accompanied by T2DM. Periodontal treatment including regenerative therapy was implemented to reduce inflammation and periodontal pockets. The patient had a history of educational hospitalization due to poor glycemic control. On the patient s first visit to our hospital, it was surmised that a combination of DM and less than optimal oral hygiene had contributed to the periodontal destruction observed. One meta-analysis investigating the effect of periodontal therapy on glycemic control in T2DM patients revealed a mean decrease of 0.36% in HbA1c compared to with no treatment 3). The present patient showed an improvement of 0.9% in his HbA1c following initial periodontal therapy, which is consistent with this earlier finding. As we reported previously 9), such an improvement could be attributed to a combination of non-surgical periodontal therapy and diabetic treatment by a physician. The status of glycemic control is an important factor in selecting options for periodontal treatment. According to the guidelines of the Japanese Society of Periodontology 4), an HbA1c level of 6.9% is suggested to be the adequate threshold level of glycemic control for periodontal surgery. In the present case, we implemented periodontal surgery after confirmation of an improvement in HbA1c following non-surgical periodontal therapy. On the other hand, the guidelines recommend that regenerative therapy be avoided in patients with DM if glycemic control is poor. Indeed, they state that evidence is still lacking on the long-term clinical outcome of regenerative therapy in individuals with

102 Seshima F et al. Fig. 5 Oral view after 7 months of supportive periodontal therapy (SPT) Fig. 6 Periodontal examination after 7 months of SPT DM. In a recent study employing an in vivo diabetic model, Bizenjima et al. reported that regenerative therapy using fibroblast growth factor (FGF)-2 had a beneficial effect on new bone formation in surgical periodontal defects, increasing cell proliferation and regulating angiogenesis 2). On the other hand, no beneficial effect was observed on new bone and cementum formation during short-term healing with application of EMD in a similar in vivo diabetic model 12). More pre-clinical and clinical studies are necessary to optimize periodontal regeneration in patients with various levels of glycemic control. It is important to assess the patient s systemic condition at each phase of periodontal treatment. In this regard, it has been reported that sharing of information between

Regenerative Therapy for DM Patient 103 Fig. 7 Radiographic view after 7 months of SPT Table 2 Clinical outcome of regenerative therapy with EMD: change in PD and CAL Treated tooth PD (mm) CAL (mm) First visit 7M SPT Change First visit 7M SPT Change #16 10 5 5 10 6 4 #26 7 3 4 7 4 3 #27 9 5 4 9 8 1 Measured at target (deepest) site EMD: enamel matrix derivative; PD: probing depth; CAL: clinical attachment level; SPT: supportive periodontal therapy Table 3 Change in HbA1c and FPG levels during periodontal treatment First visit (Feb 2014) Post-IP ( June 2014) Post-surgical (Feb 2015) SPT: start (April 2015) SPT: 7M (Nov 2015) HbA1c (%) 7.8 6.9 7.0 7.3 7.5 FPG (mg/dl) 183 118 118 127 147 IP: initial periodontal therapy; SPT: supportive periodontal therapy; HbA1c: glycated hemoglobin; FPG: fasting plasma glucose the periodontist and physician is critical in effectively treating periodontitis and DM 9). In the present case, such cooperation resulted in an improvement in both periodontal and diabetic conditions. An increase was observed, however, in the patient s HbA1c level during SPT, the exact cause of which is unclear. One of the goals in providing periodontal treatment is to reduce PD to 3 mm at all sites requiring surgery. This was not possible, however, in the present patient as periodontal breakdown was too advanced at such sites at his first visit, and even included furcation involvement. The present case supplies further evidence that careful SPT and continuous close collaboration between dental and medical professionals are essential in providing optimal periodontal and diabetic care.

104 Seshima F et al. References 1) Armitage GC (1999) Development of a classification system for periodontal diseases and conditions. Ann Periodontol 4:1 6. 2) Bizenjima T, Seshima F, Ishizuka Y, Takeuchi T, Kinumatsu T, Saito A (2015) Fibroblast growth factor-2 promotes healing of surgically created periodontal defects in rats with early, streptozotocin-induced diabetes via increasing cell proliferation and regulating angiogenesis. J Clin Periodontol 42:62 71. 3) Engebretson S, Kocher T (2013) Evidence that periodontal treatment improves diabetes outcomes: a systematic review and meta-analysis. J Clin Periodontol 40:S153 S163. 4) Japanese Society of Periodontology (2015) Guideline for periodontal treatment of patients with diabetes mellitus, 2nd ed., Japanese Society of Periodontology, Tokyo. (in Japanese) 5) Kawamori R, Tajima N, Iwamoto Y, Kashiwagi A, Shimamoto K, Kaku K (2009) Voglibose for prevention of type 2 diabetes mellitus: a randomised, double-blind trial in Japanese individuals with impaired glucose tolerance. Lancet 373:1607 1614. 6) Löe H (1993) Periodontal disease. The sixth complication of diabetes mellitus. Diabetes Care 16:329 334. 7) Nelson RG, Shlossman M, Budding LM, Pettitt DJ, Saad MF, Genco RJ, Knowler WC (1990) Periodontal disease and NIDDM in Pima Indians. Diabetes Care 13:836 840. 8) O Leary TJ, Drake RB, Naylor JE (1972) The plaque control record. J Periodontol 43:38. 9) Ota M, Seshima F, Okubo N, Kinumatsu T, Tomita S, Okubo T, Saito A (2013) A collaborative approach to care for patients with periodontitis and diabetes. Bull Tokyo Dent Coll 54:51 57. 10) Preshaw PM, Alba AL, Herrera D, Jepsen S, Konstantinidis A, Makrilakis K, Taylor R (2012) Periodontitis and diabetes: a two-way relationship. Diabetologia 55:21 31. 11) Saito A, Hosaka Y, Kikuchi M, Akamatsu M, Fukaya C, Matsumoto S, Ueshima F, Hayakawa H, Fujinami K, Nakagawa T (2010) Effect of initial periodontal therapy on oral healthrelated quality of life in patients with periodontitis in Japan. J Periodontol 81:1001 1009. 12) Shirakata Y, Eliezer M, Nemcovsky CE, Weinreb M, Dard M, Sculean A, Bosshardt DD, Moses O (2014) Periodontal healing after application of enamel matrix derivative in surgical supra/ infrabony periodontal defects in rats with streptozotocin-induced diabetes. J Periodontal Res 49:93 101. 13) Taylor GW, Borgnakke WS (2008) Periodontal disease: associations with diabetes, glycemic control and complications. Oral Dis 14:191 203. 14) Williams RC, Offenbacher S (2000) Periodontal medicine: the emergence of a new branch of periodontology. Periodontol 2000 23:9 12. Correspondence: Dr. Atsushi Saito Department of Periodontology, Tokyo Dental College, 2-9-18 Misaki-cho, Chiyoda-ku, Tokyo 101-0061, Japan E-mail: atsaito@tdc.ac.jp