|Corresponding Author: Dr. Rishi Bhimani, Private Practitioner and Proprietor, Freelance Consultant Periodontist, Dr. Rishi’s Dental Clinic, Shop 9 & 10, Sai Palace, Plot 36, sector 14, Vashi, Navi Mumbai-400703, Maharashtra, India|
|Received: July 17, 2019; Accepted: August 19, 2019; Published: October 14, 2019;|
|Citation: Bhimani R. (2019) Low Dose Amlodipine Induced Ginigival Overgrowth - A Case Report. J Oral Health Dent, 2(3): 159-162.|
|Copyrights: ©2019 Bhimani R. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.|
Gingival enlargement is a common manifestation of gingival and periodontal disease having a multifactorial etiology. Anticonvulsants, immunosuppressants and calcium channel blockers have been associated with gingival enlargement in susceptible patients. Amlodipine is a new generation calcium channel blocker used to manage hypertension and angina. Reports of amlodipine associated gingival enlargement are uncommon.
The current case reports gingival enlargement in a 45 years old female, associated with the use of a small dosage (5 mg) of Amlodipine for hypertension. The treatment protocol included non-surgical periodontal therapy, drug substitution, surgical excision of minor fibrotic enlargement as well as extraction and rehabilitation of the offending teeth to improve esthetics and function resulting in an excellent clinical outcome.
Keywords: Amlodipine, Gingival enlargement, Amlodipine-induced gingival overgrowth, Gingival inflammation
Drug-induced gingival enlargement could be an unwanted side-effect of certain group of drugs given for non-dental conditions. Currently, more than 20 prescription medications are associated with gingival enlargement . Drugs associated with gingival overgrowth are broadly categorized into three major groups according to their therapeutic actions, namely, anticonvulsants, immunosuppressants and calcium channel blockers [3,4]. Patients medicated with these drugs may be implicated in this unwanted side effect, which may interfere with esthetics, mastication or speech as well as decrease access for oral hygiene resulting in an increased susceptibility to oral infection, caries and periodontal disease.
Amlodipine is a newer dihydropyridine calcium channel blocker that used in the management of both hypertension and angina. Ellis et al.  first reported gingival sequestration of amlodipine and amlodipine-induced gingival overgrowth. Since then, very few isolated cases of AIGO have appeared in the dental literature, although there are numerous reports of nifedipine (another member of calcium channel blocker-induced gingival overgrowth till date). There is less data on reports of overgrowth with amlodipine at a dose of 5 mg, even after taking it for more than 6 months.
But, in the present case, the gingival overgrowth occurred at a dose of 5 mg within 6 months of use. AIGO was treated in the following phases: (1) thorough Phase-1 therapy, (2) substitution of the drug, (3) surgical excision of the residual gingival overgrowth and (4) Restoration and replacement of teeth.
A 45 year old female patient from a poor socio-economic background, reported to Dr. Rishi’s Dental Clinic, Navi Mumbai with a chief complaint of swollen and bleeding gums for 6-8 months along with bad breath. Patient was not aware of such a type of gum growth previously until she saw diffused, nodular bright-red gum growth in the lower front region and upper and lower right side of the jaws. Her past medical history revealed that she was hypertensive since the past 1.5 years and she was on a combination medication- Telmisartan 40 mg with Amlodipine 5 mg, since then.
Her personal history revealed that she used to brush her teeth once daily with brush and paste, but she avoided brushing the teeth which had enlarged gums, as they bled on brushing. Her general physical examination revealed a moderate built with vital signs within the normal range.
Intraoral examination revealed enlarged marginal and interdental gingiva starting from maxillary right canine (13) up to 2nd molar (17) and from mandibular left lateral incisor (32) up to right 2nd molar (47) (Figure 1).
The enlarged gingiva was nodular in certain areas with bright red color. The contour was rolled-out with soft and edematous consistency. There were visible bands of supra and sub-gingival calculus. Pus exudation presented with mandibular right 2nd premolar (45). Spacing was present between lower incisors along with labial version (Figure 2).
Patient was subjected to complete hemogram and all the parameters were found to be within normal range. Radiographic evaluation of the affected sites revealed extensive bone loss with mandibular left (31) and right central incisor (41) along with pathologic migration. The mandibular lateral incisors (32,42) had greater than 50% alveolar bone support remaining. Her treatment started with non-surgical approach. Scaling and root planing were performed in 2-3 sessions along with 5% Povidone-iodine irrigation for periodontal pockets (Figure 3).
Simultaneously, the patient's physician was consulted regarding drug substitution or withdrawal of the drug. The physician changed the drug from the previous combination of Telmisartan 40 mg + Amlodipine 5 mg to plain Telmisartan 40 mg, eliminating Amlodipine. The patient was prescribed Folic acid supplements, once daily for 15 days. Patient was instructed to maintain good oral hygiene with the use of chlorhexidine oral rinses. A dramatic response was noticed after four weeks of drug substitution and maintenance of regular oral hygiene. There was regression in the size of gingival enlargement with minimal fibrotic component left (Figure 4). In the meanwhile, during the 4 weeks healing period, endodontic therapy was performed for mandibular lateral incisors and canines (32,42,33,43) as they were severely attrited. 31, 41 were extracted due to poor prognosis. Once the extraction site was healed, the minor nodular enlargement was excised along with minor frenotomy was done with RF electrocautery (Figure 5).
After about 2
weeks of healing, the lateral incisors and canines were prepared to receive
fixed partial denture prosthesis, replacing the extracted teeth as well as
restoring function and esthetics (Figure
The patient has been kept on a recall every 6 months.
Medication associated gingival enlargement has been known for a long time. The widespread use of calcium channel blockers began in 1980. The prevalence of Amlodipine associated gingival enlargement has been reported to be 3.3%, which is significantly lower as compared to Nifedipine . Nifedipine is a second generation dihydropyridine whereas amlodipine is a third generation dihydropyridine. Amlodipine has a pharmacological action comparable to nifedipine, but it is preferred over nifedipine due to its higher bio-availability, slow hepatic degradation, near complete absorption and slow elimination making its duration of action longer, thus it needs to be administered once daily, improving patient compliance with minimal side effects as compared to Nifedipine [6-8].
Although the exact role of dental plaque in the pathogenesis of drug associated gingival enlargement is unclear, there is evidence that elimination of local factors and maintenance of good oral hygiene, decreases the severity of gingival enlargement and improves gingival health. In the present case, there were abundant deposits of calculus and plaque retentive factors, at the sites with gingival enlargement. Scaling and root planing removed the local factors along with substitution of Amlodipine by the Physician was done.
Various possible mechanisms have been proposed to explain drug associated gingival enlargement in the past. CCBs affect calcium metabolism by reducing the Ca2+ cell influx, leading to a reduction in the uptake of folic acid, thus limiting the production of active collagenase . As a result of the reduction in collagen degradation, increased collagen accumulation occurs.
Proinflammatory cytokines, such as interleukin-1b and interleukin-6 seem to have a synergistic effect in the enhancement of collagen synthesis by human gingival fibroblasts . Interleukin-6 has been shown to target connective tissue cells, such as fibroblasts, both by enhancing their proliferation and by increasing collagen production and glycosaminoglycan synthesis . This mechanism explains the role of the bacterial biofilm in inducing gingival inflammation, production of cytokines and gingival enlargement. In the present case, immediately after drug substitution, folic acid supplements were prescribed to the patient to replenish the folic acid depletion.
The treatment options for drug-induced gingival enlargement should be based on the medication being used and the clinical presentation of the individual case. The presence of local factors adds to the inflammatory component of the drug induced gingival enlargement. Timely removal of local factors by non-surgical periodontal therapy partially resolves the gingival enlargement. The need for, and timing of, any surgical intervention must be carefully assessed. Surgery is normally performed for cosmetic/aesthetic needs, most commonly being external bevel gingivectomy. In the present case, the persistent fibrotic enlargement was excised by electrocautery as it was minor and nodular in nature.
Prosthetic rehabilitation was carried out to replace the extracted mandibular central incisors, obtaining support from and using the adjacent incisors and canines as abutments. The prosthesis completely changed the smile as well as entailed immense confidence into the patient.
In this case, drug substitution had an additional advantage for the patient. Amlodipine frequently resulted in pedal as well as facial edema. This side effect of Amlodipine was also resolved post drug substitution. The post-treatment results were found to be extremely satisfactory, esthetically as well as functionally. The patient was also extremely delighted with the results and has been maintaining her oral hygiene satisfactorily.
In this case, a combination of drug substitution and periodontal therapy, resolved the gingival overgrowth.
1. Bhatia V, Mittal A, Parida AK, Talwar R, Kaul U (2007) Amlodipine induced gingival hyperplasia: A rare entity. Int J Cardiol 122: 23-24.
2. Rees TD, Levine RA (1995) Systemic drugs as a risk factor periodontal disease initiation and progression. Compendium of Continuing Education in Dentistry, pp: 20-42.
3. (2004) Drug associated gingival enlargement. J Periodontol, pp: 1424-1431.
4. Garzino-Demo P, Carbone M, Carrozzo M, Broccoletti R, Gandolfo S (1998) An increase in gingival volume induced by drugs (phenytoin, cyclosporine and calcium antagonists). A review of the literature. Minerva Stomatologica, pp: 387-398.
5. Ellis JS, Seymour RA, Steele JG, Robertson P, Butler TJ, et al. (1999) Prevalence of gingival overgrowth induced by calcium channel blockers: A community-based study. J Periodontol, pp: 63-67.
6. Jorgensen MG (1997) Prevalence of amlodipine-related gingival hyperplasia. J Periodontol, pp: 676-678.
7. Triveni MG, Rudrakshi C, Mehta DS (2009) Amlodipine-induced gingival overgrowth. J Indian Soc Periodontol, pp: 160-163.
8. Seymour RA, Ellis JS, Thomason JM, Monkman S, Idle JR (1994) Amlodipine-induced gingival overgrowth. J Clin Periodontol 21: 281-283.
9. Barclay S, Thomason JM, Idle JR, Seymour RA (1992) The incidence and severity of nifedipine-induced gingival overgrowth. J Clin Periodontol 19: 311-314.
10. Johnson RB, Zebrowski EJ, Dai X (2000) Synergistic enhancement of collagenous protein synthesis by human gingival fibroblasts exposed to nifedipine and interleukin-1-beta in vitro. J Oral Pathol Med 29: 8-12.
11. Duncan MR, Berman B (1991) Stimulation of collagen and glycosaminoglycan production in cultured human adult dermal fibroblasts by recombinant human interleukin-6. J Invest Dermatol 97: 686-689.
- Chemotherapy Research Journal(ISSN:2642-0236)
- International Journal of Medical and Clinical Imaging(ISSN:2573-1084)
- Journal of Psychiatry and Psychology Research(ISSN:2640-6136)
- Journal of Nursing and Occupational Health
- Journal of Pathology and Toxicology Research
- Journal of Infectious Diseases and Research (ISSN: 2688-6537)
- Journal of Cancer Science and Treatment(ISSN:2641-7472)