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Table of Contents   
REVIEW ARTICLE
Year : 2022  |  Volume : 12  |  Issue : 3  |  Page : 309-322
Calcium channel blockers induced gingival overgrowth: A comprehensive review from a dental perspective


1 Department of Periodontics, University of Buffalo, New York, USA
2 Department of Clinical Sciences, College of Dentistry, Ajman University, Ajman, UAE; Centre of Medical and Biomedical Allied Health Sciences Research, Ajman University, Ajman, UAE; Saveetha Dental College and Hospitals, Chennai, Tamil Nadu, India
3 Department of Periodontics, Sr Rajiv Gandhi College of Dental Sciences and Hospital, Bengaluru, Karnataka, India
4 Saveetha Dental College and Hospitals, Chennai, Tamil Nadu, India; University of Puthisastra, Phnom Penh, Cambodia

Date of Submission25-Feb-2022
Date of Decision20-Apr-2022
Date of Acceptance03-May-2022
Date of Web Publication29-Jun-2022

Correspondence Address:
Dr. Sudhir R Varma
Department of Clinical Sciences, College of Dentistry, Ajman University, Ajman
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jispcd.JISPCD_57_22

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   Abstract 

Background: Gingival overgrowth (GO) as a manifestation of calcium channel blockers (CCBs) was first introduced in the literature by Ramon et al. in 1984. Since then, the use of CCBs as a treatment modality for hypertension has been recorded extensively in the literature for its association with GO. Aim: The aim of our study is to evaluate histopathology, treatment, and follow-up for the cases detailed in various studies and also to highlight the protocol mentioned to identify these presentations. Materials and Methods: A broad search was conducted from the period 1980 to 2021 using electronic databases PubMed Central, Scopus, Cochrane, and SciELO databases. About 293 articles were initially chosen. The articles further excluded did not fit the criteria for the study and eventually 50 articles which met the inclusion criteria were chosen as part of this literature review. Results: A comparative analysis was carried out regarding histopathology, treatment modalities, drug dosage, and duration to evaluate the differences in cases between 1980 and 2021. From the available studies, it was found that the histopathological and clinical findings were varied. Treatment strategies employed were different, though follow-ups in most cases were uniform. Conclusion: CCBs and their relationship with GO have been widely reported in the literature. Dentists should approach this condition by taking appropriate medical and dental history and follow evidence-based treatment guidelines to provide more relevant and judicious management of this condition. Inter-disciplinary treatment approaches would provide better outcomes.


Keywords: Amlodipine, calcium channel blockers, drug-induced, gingival overgrowth, nifedipine


How to cite this article:
Damdoum M, Varma SR, Nambiar M, Venugopal A. Calcium channel blockers induced gingival overgrowth: A comprehensive review from a dental perspective. J Int Soc Prevent Communit Dent 2022;12:309-22

How to cite this URL:
Damdoum M, Varma SR, Nambiar M, Venugopal A. Calcium channel blockers induced gingival overgrowth: A comprehensive review from a dental perspective. J Int Soc Prevent Communit Dent [serial online] 2022 [cited 2022 Aug 20];12:309-22. Available from: https://www.jispcd.org/text.asp?2022/12/3/309/348783





   Introduction Top


Gingival overgrowth (GO) is a manifestation of calcium channel blockers (CCBs), and it was first introduced in the literature by Ramon et al. in 1984.[1] Since then, numerous studies have been published in the literature on the association of drugs with GO [Table 1][Table 2][Table 3][Table 4], more specifically, cyclosporin, CCBs, and antiepileptics.[2],[3] The use of CCBs for the treatment of hypertension has been recorded extensively in the literature. Drugs including nifedipine, amlodipine, diltiazem, and verapamil are all subclasses of CCBs and effectively control hypertensive patients.[4],[5],[6],[7],[8] Seymour et al.[9] identified sex, periodontal status, age, genetic predisposition, medications, and drug variables, increasing the risk for developing GO.
Table 1: Study characteristics of selected articles between 1980 and 1999

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Table 2: Site, nature, histopathology, treatment, and follow-up [continuation of Table 1]

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Table 3: Study characteristics of selected articles between 2000-2021

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Table 4: Site, nature, histopathology, treatment, and follow-up [continuation of Table 2A]

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Epidemiology

In a 2017 systematic review, it was reported that the most common drug classes prescribed to hypertensive patients were CCBs; from the available CCBs, amlodipine was the most commonly prescribed CCB (37%).[10] CCBs have been extensively reported in the literature as being associated with GO [Tables 1-4]. The first report of CCBs associated with GOs was in 1984 by Ramon et al. A case series was published reporting five similar cases of patients taking nifedipine regularly and who developed GO [Table 1]. Ramon et al. reported the presence of an inflammatory reaction in the nifedipine-induced hyperplasia, which suggests that rigorous hygienic measures might retard its progress and diminish its extent.[1] Since then, many cases have been reported and published in the literature confirming Ramon’s hypothesis on the association of nifedipine-induced gingival overgrowth (NIGO). Amlodipine-induced gingival overgrowth (AIGO) is less commonly reported and commonly present clinically several years after administering the drug. The first time it was reported in the literature was in 1994 by Seymour et al.[11] who published a case series on three patients receiving 5–10 mg of amlodipine daily [Table 2]. They report that in the three patients described, gingival changes can be observed as early as 3 months after dosage.

Prevalence

According to a randomized controlled trial in 1990, GO occurred in 20–83% of patients taking nifedipine.[8] In 1997, a study by Carty et al.[6] reported a 3.3% incidence rate of AIGO, which is significantly less than NIGO. Diltiazem, another CCB, was reported to be associated with GO and reported to have a 74% incidence rate.[12],[13] A hospital-based study carried out in 2015 measured the prevalence of CCBs in association with DIGO, in which it was found that the frequency of GO was 75% for nifedipine, 31.4% for amlodipine, and 25% for amlodipine + metoprolol.[14],[15] In a 2017 prospective clinical study assessing the prevalence of AIGO, they reported that 76% of the patients were found to have GO.[10] In a 2018 clinical study by Tejnani et al., it was reported that the prevalence rate of amlodipine-induced gingival hyperplasia was 3.4%. These numbers show that the prevalence of DIGO is poorly defined, and more extensive clinical trials are needed. Like Seymour et al.[9] reported in 1993, Tejnani et al.[16] reported that the GOs were seen in patients taking amlodipine for a minimum of 3 months.

Histopathology

The histopathology for drug-induced GO (DIGO) is consistent, in which the epithelial layers showed elongated rete pegs, proliferation, acanthosis, and parakeratosis. The underlying connective tissue showed an abundance of ground substance, reduced myxomatous changes, pronounced inflammatory cells, and dense collagen bundles with active fibroblasts[5],[6],[7] [Table 1]. In an isolated case report on NIGO, they found marked epithelial hyperplasia, acanthosis, and moderate inflammatory reactions in the lamina propria.[1] In a study involving a 53-year-old hypertensive female on 20 mg of nifedipine daily, the patient presented with generalized GO covering almost all of the clinical crowns. The histopathological report presented stratified squamous epithelium with hyperplasia and acantholysis; the underlying fibrocollagenous connective tissue showed dense mixed inflammatory infiltrate with congested blood vessels. Histopathological observations were similar when comparing the first report of DIGO and the most recent report[10] [Tables 2] and [4].

Pathophysiology

The exact mechanism behind DIGO has not yet been determined. However, there have been several theories and experimental hypotheses.[13],[14],[15],[16],[17] Two main pathways have been proposed in the literature: an inflammatory and non-inflammatory mechanism[13],[18] [Table 5]. According to the literature, the mechanism for GO caused by CCBs was first proposed by Nyska and co-workers in 1994. Nyska proposed that when CCBs are administered orally, their pharmacotherapeutic effect lowers the blood pressure and, in turn, signals the release of renin and angiotensin-converting enzyme. The angiotensin, which generally would produce aldosterone, is blocked by the calcium ions of the drug, which causes a diversion into another unblocked metabolic pathway. This pathway leads to the overproduction of androgens and adrenocorticotropic hormone (ACTH), which induces hypertrophy of the kidneys. This overproduction in androgens is suggested to act on the gingival tissue and stimulate fibroblast proliferation and collagen production, resulting in GO.[19],[20],[21],[22],[23]
Table 5: Proposed mechanisms for the pathogenesis of DIGO

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Classifications

The classification of GO has been defined in the literature several times over the last century. The most commonly known classifications are Angelopoulos and Goaz Index (1972), hyperplastic index (1985), Bokenkamp classification (1994), and Ingle classification (1999). These classifications vary in their definitions, whether in the nature of the GO or in the direction of overgrowth. Angelopoulos and Goaz[24] described an index that measured the vertical relationship of gingival tissue on the clinical crown: Grade 0: no GO, Grade 1: overgrowth covering cervical third of clinical crown, Grade 2: overgrowth extending to the middle of the clinical crown, Grade 3: overgrowth covering two-thirds of the clinical crown. As defined by Seymour et al.[11] in 1994, the hyperplastic index assesses GOs based on their vertical and horizontal relationship with the clinical crown: Grade 0: absent gingival hyperplasia, Grade 1: blunting of margin, Grade 2: hyperplasia less than two-thirds of the clinical crown, Grade 3: hyperplasia more than two-thirds of the clinical crown. The disadvantage with this index is that it is non-specific and vague. Classifying GOs in this index may be confusing. Bokenkamp’s 1994 classification is similar to Seymour’s hyperplastic index; however, it is more specific and defined: Grade 0: no sign of gingival enlargement, Grade 1: enlargement confined to the interdental papilla, Grade 2: enlargement involving marginal and papillary gingiva, and Grade 3: enlargement diffused and covering almost the entire crown.[25] The most updated and commonly used index in 2021 is Ingle’s 1999 classification, which defined GO in a cohesive and precise manner: Grade 0: no overgrowth, slight stippling, and knife-edge papilla; Grade 1: increase in the density with marked stippling, papilla is rounded, and probing depth is equal to or less than 3 mm; Grade 2: moderate overgrowth, size of the papilla is increased and/or rolled margins, gingival enlargement has a buccolingual dimension of up to 2 mm, probing depth is equal to or less than 6 mm; Grade 3: marked overgrowth, the contour of the margin is convex, enlargement has a buccolingual dimension of approximately 3 mm or more, probing depth is greater than 6 mm, the papilla is retractable; Grade 4: severe overgrowth, thickening of the gingiva, large percentage of the crown is covered, the papilla is retractable, probing depth is greater than 6 mm, and buccolingual dimensions are approximately 3 mm.[26]


   Materials and Methods Top


A broad search of literature published between the years 1980 and 2021 from electronic databases through PubMed Central, Scopus, Cochrane, and SciELO databases was conducted using keywords: Calcium Channel Blockers, Gingival overgrowth, Gingival enlargement, Gingival Hyperplasia. This literature review includes case reports and case series. Fifty articles were chosen to be screened further for drug dosage, duration, site, and nature of overgrowth, treatment, and follow-up [Tables 1-4]. The age group of the patients seen in the studies was from 20 to 65 years and comprised both genders.

The search was carried out using the following keywords: Calcium Channel Blockers, Gingival overgrowth, Gingival enlargement, Gingival Hyperplasia. Advanced search incorporating Boolean operators Calcium Channel Blockers AND Gingival overgrowth AND Gingival enlargement AND Gingival Hyperplasia was performed. The data generated were reviewed and any disagreement was resolved through discussion. A flowchart for this review which emphasized the article selection is shown in [Figure 1].
Figure 1: Flowchart for article selection

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Inclusion criteria

Case reports and case series which highlighted overgrowth/enlargement and hyperplasia were selected for the study. Studies in which patients had taken any other medications but did not contribute to the overgrowth of the tissue were also considered.

Exclusion criteria

Reviews, systematic reviews, animal studies, ex-vivo studies, and other laboratory-based studies were excluded. Studies in which patients were taking immunosuppressants, antihypertensives, and anticonvulsants were discarded.


   Results Top


Approximately 293 publications were found to be related. Further screening identified 46 articles that fulfilled the inclusion criteria. Full texts were evaluated for these articles, and their references were screened for any relevant article. This led to identifying another four articles. Thus, 50 articles met the final inclusion criteria and were considered for this review. [Tables 1-4] summarize the study characteristics of case reports and case series of GO caused by CCBs published between 1984 and 2021. A comparative analysis was done regarding histopathology, treatment modalities, drug dosage, and duration to evaluate the differences between cases in 1984–2000 and 2000–2021. The selected studies detailed the clinical presentation and drug history and also performed elaborate follow-ups, but the proposed mechanism for the pathogenesis of drug-induced gingival growth was not adequately proposed.


   Discussion Top


In 1984, Ramon published a series of five cases of NIGO. This was the first reported case of NIGO in the literature. It included five patients between the ages of 51 and 69 with systemic vascular hypertension. The dosage prescribed varied between 30 and 60 mg of nifedipine daily for a duration of 2–5 years. Ramon reported the nature of the gingival tissues to be firm and relatively hard to touch but bled rather easily on probing and brushing. The histopathological findings of all five cases revealed marked epithelial hyperplasia, acanthosis, and moderate inflammatory reaction in the lamina propria.[1] Since then, there have been many reported cases of NIGO in the literature. It is essential to note the duration of drug consumption and how that affects the outcome of GO. In 1986, Shaftic et al.[27] published a case report of a 61-year-old male patient with hypertension who had been using nifedipine 30 mg/day for only 2 months and developed NIGO. Drug discontinuation was the proposed treatment plan, and 9 days later, the bleeding and pain were eliminated. A 3-month recall visit showed no signs of recurrence as well. In 1993, Seymour et al.[11] published a case series of three hypertensive patients ranging between 35 and 65 years who took 5–10 mg of amlodipine daily for 4–8 months. They reported that it takes an average minimum of 3 months of drug consumption before gingival changes can be noted.

Several studies attempted drug discontinuation and/or non-surgical periodontal therapy and reported successful results in terms of management.[28] A case series published by Routray et al.[29] in 2003 reported a 15-year-old male taking 5 mg of amlodipine daily for hypertension induced by aortoarteritis. The patient reported GOs in the upper and lower arch. It was reported that 4 months after periodontal therapy, there were no signs of inflammation, and 2 months after drug discontinuation, the GOs completely subsided. In 1998, Madi et al.[30] reported that the ideal treatment for DIGO is the discontinuation of the drug. However, since then, numerous studies have been reported which took different approaches to regressing GO. A study by Sam and Sebastian[31] reported AIGO in a 42-year-old patient who was taking amlodipine 10 mg daily for hypertension for the past 8–9 years. This patient presented with massive generalized GO, of which the interdental papilla was lobulated, and erythematous. The gingiva was firm and resilient to the touch. Their treatment strategy included periodontal therapy and drug discontinuation, which ultimately led to the subside of the GO. It was reported that surgical intervention would have been necessary if there was a delay in the periodontal management. Another treatment modality introduced in 1973 included the use of an extraoral appliance to regress GO. Srivastava et al.[32] created articulated models of silicone and polyethylene, which were placed on the gingiva and teeth at night only. They believed the positive pressure exerted by the appliance could shrink and regress the gingival tissue. Although the model was successful in some patients, there lacks evidence regarding the acceptability of this treatment modality.

Among the reviewed articles, several studies reported drug discontinuation and periodontal therapy as an acceptable method of treatment for DIGO.[3],[32] A study reports a 75-year-old male with hypertension and a history of ischemic stroke taking 40 mg of nifedipine daily. In this case report, a conservative treatment plan was made, including oral hygiene instructions, scaling and root surface debridement, and suspension of nifedipine. They reported that at 11 weeks, the GO completely subsided.[3] It is unclear which mode of treatment is considered the gold standard since some articles claim the non-surgical conservative approach to be effective, and others claim that surgical intervention is a necessity in the treatment method. A 2007 case report by Taib et al.[33] reported a 55-year-old hypertensive female taking 5 mg of amlodipine daily who presented with massive GO and inflamed/lobulated interdental papillae. Their study reports that periodontal therapy alone without drug intervention can yield satisfactory results. Surgical and CO2 laser gingivectomies were done to the upper and lower arches without substituting or discontinuing amlodipine. At a 2-year recall visit, the periodontal status was deemed satisfactory, and the patient was sent to a prosthodontist to fabricate an upper and lower removable partial denture. The first time CO2 laser was introduced in the literature as a DIGO treatment in 1988 by Barak and Kaplan.[34] They reported that with CO2 laser gingivectomy, post-operative pain and discomfort are significantly reduced, and bleeding is controlled more efficiently. This is especially important with cardiac patients taking CCBs.

According to the literature, DIGO can occur in patients taking any amount of CCBs. No significant difference in GO severity was noted with different doses of CCBs, although a decrease in GO can appear after dose reduction.[34] It is important to note that DIGO cases reported between 1900 and 1999 mainly consisted of patients taking a higher dose of CCBs when compared with the reported cases between 2000 and 2021 [Tables 1-4]. Santi and Bral[35] reported a case of a 34-year-old male patient who had recently undergone a kidney transplant. The patient was on 120 mg of nifedipine and 100 mg of cyclosporin daily. Both these drugs are known to cause GO, so it was very likely that the patient would suffer from DIGO. However, the dosage of both drugs is relatively high, and it is unclear whether the dosage may have contributed to the amount of GO that the patient presented with. In other studies, a dosage of 5 mg of CCBs daily was enough to cause massive GOs. A 1994 case series by Seymour et al.[11] reported three cases taking 5–10 mg of amlodipine daily who presented with significant probing depth and exhibited a gingival hyperplasia index of 46.60%. In all three cases, amlodipine was substituted, and no recurrence was reported in a 3-month recall visit. It can be observed that most of the studies between 2000 and 2021 report massive GOs in patients taking 5–10 mg of CCBs daily [Tables 3 and 4]. In a 2015 case report by Madi et al.,[30] a 48-year-old hypertensive male who developed GOs after taking amlodipine 5 mg daily for only 3 months was reported.

Within the literature, histopathology is consistent and similar. A 2015 case report by Vekaria et al.[36] reported a 55-year-old hypertensive male patient who had been on 40 mg of nifedipine daily. The histopathology report presented stratified squamous epithelium with hyperplasia and acantholysis, and the underlying fibrocollagenous connective tissue showed congested blood vessels. Similarly, in a 2018 case report of AIGO by Asif et al.,[23] they report hyperplastic and acantholytic stratified squamous epithelium with elongated rete peg ridges extending into connective tissue, which was fibrocollagenous and showed focal areas of fibrosis. Infiltration of chronic inflammatory cells and acanthosis was seen, suggesting gingival hyperplasia. Dysplastic changes were not reported in any of the studies. A case series by Srivastava et al.[32] reported three cases of AIGO, and in all three cases, they report hyperplastic stratified squamous epithelium without dysplasia. The underlying connective tissue contained scanty inflammatory cells.

Similarly, a 2018 case report by Quenel et al.[37] presents a case of AIGO in which their histopathological reports presented epithelial hyperplasia with hyperkeratosis without dysplasia. Several studies reported acanthosis in the epithelial layer with epithelial hyperplasia/parakeratosis. A case series by Santi and Bral[35] reported epithelial parakeratosis with irregular acanthosis, dense collagen, pronounced inflammatory cell infiltrate, reduction in myxomatous changes, and vascularity. Inflammatory cells were present in both their patients. A 2015 case report by Mathur et al.[38] reported similar findings of the presence of parakeratinized epithelium with elongated rete pegs and acanthosis and scattered giant cells indicating a superimposed inflammation. The majority of studies also reported the proliferation of fibroblasts and capillaries [Tables 1-4]. Missouris et al.[39] reported gingival acanthosis, parakeratosis, rete pegs, proliferation, varying densities of fibroblastic and capillary proliferation, and mononuclear cell aggregations.

Regarding gingival fibroblasts, they reported strongly sulfated mucopolysaccharides in the fibroblasts and numerous secretory granules. Lymphocytic infiltration is also a common feature in the literature. Smitha[40] reported the inflammatory component observed more toward the epithelium, with lymphocytes being the predominant cells.[41] Similarly, Quenel et al.[37] also reported fibrosis and lymphocytic infiltration predominant around blood vessels. An abundance of dense collagen fibers interspersed between the blood vessels is also a common feature among DIGO. Taib et al.[33] reported irregular fibrous overgrowth composed of collagenous connective tissues with a diffuse chronic inflammatory cell infiltrate and covered by an intact hyperparakeratotic and acanthotic stratified squamous epithelium. Smitha[40] also reported the underlying connective tissue as dense with numerous collagen bundles arranged in a haphazard manner interspersed with fibroblasts. Sharma and Sharma reported that the underlying connective tissue presented bundles of collagen fibers with an admixture of mild chronic inflammatory infiltrate and a small number of blood vessels.[41] Gittaboyina et al.[42] also noted thick collagenized bundles with a few blood vessels and a few areas of focal chronic inflammatory cell aggregations in the connective tissue.

There have been a few cases of secondary reactions that were formed after DIGO. A 2014 case report by Vishnudas et al.[43] presented a 54-year-old hypertensive female who was on 10 mg of amlodipine daily. She presented with non-tender and firm GOs. All teeth were mobile. The histopathology reports presented parakeratinized stratified squamous epithelium, connective tissue with sheets of plasma cells. The plasma cells were reasonably uniform in appearance, with scattered nucleoli. Occasional Dutcher bodies were seen overlying the plasma cell nuclei. The inflammatory infiltrates also contained varying numbers of neutrophils, lymphocytes, and macrophages. The diagnosis of amlodipine-induced plasma cell granuloma was made, and the gingiva was excised surgically. No recurrence was reported 5 months after treatment. In a similar case, Gulati et al.[44] reported a 60-year-old hypertensive female who was on 20 mg of amlodipine daily. She presented with GO as nodular, polypoid masses with a smooth surface. GO was non-tender and non-fluctuant. The histopathological report presented proliferative stratified squamous epithelium. Areas of ulceration were seen. The underlying stroma was fibrocellular with bundles of collagen intersecting, a patchy distribution of chronic inflammatory cells characterized predominantly by mature plasma cells, suggesting a plasma cell lesion. A diagnosis of AIGO with a secondary reaction of plasma cell granuloma was made, and the lesions were excised surgically, and drug substitution was done. The patient was also put on antibiotics coverage. Fifteen months after treatment, the patient presented with no signs of recurrence. In another case report by Yolcu and Aydogdu,[45] they reported a secondary reaction of myeloid sarcoma with concurrent AIGO. They report a 63-year-old hypertensive male on amlodipine for 6 years. Diffuse, erythematous, and firm lesions were noted on the maxillary and mandibular arches. Histopathological reports presented benign-appearing stratified squamous epithelium, with rete pegs elongated. There were dense aggregates of atypical medium-sized cells combined with smaller numbers of inflammatory cells in the underlying fibrous tissue, including plasma cells and lymphocytes. In a 2017 case report by Ramesh and Sadasivan, they reported a case of oral squamous cell carcinoma masquerading as GO. They reported a 49-year-old male patient who had been on nifedipine for the past 5 years. Palpable, firm, mobile, and nodular submandibular lymph nodes on the left side were observed on extraoral examination. The patient was initially advised to take an intraoral periapical radiograph. Radiographic evaluation showed an extensive bone loss. Histopathological reports showed hyperplastic hyper-parakeratinized stratified squamous epithelium with features of dysplasia. A breach in the continuity of the basement membrane was observed. The underlying connective tissue was densely collagenous and showed abundant keratin pearl formation and neoplastic epithelial cells. Chronic inflammatory infiltrate composed of lymphocytes, plasma cells, and neutrophils was also seen. A well-differentiated squamous cell carcinoma diagnosis was made based on these histopathological findings.[46] Biopsies must be taken to rule out secondary reactions or lesions that mimic other lesions.[47],[48],[49],[50]

Some of the limitations in our review was providing treatment guidelines, and associating the required treatment along with histopathological and clinical interpretation seen from most case reports has been a challenge. Secondly, oral hygiene status could not be considered as a variable in our review, due to an element of bias. Clinical studies could have provided more detailed interpretation but again, requirement of a large sample size is needed, which was not seen from the available repositories.


   Conclusion Top


GO caused by the consumption of CCBs has been widely reported in the literature. The management of DIGO varies. However, most studies support drug substitution as the primary form of treatment. The exact pathogenesis of DIGO remains poorly defined by the literature, and more research is required to understand the specific correlation of drugs to GO. Dentists need to take a detailed medical and dental history. This circumvents the possibility of any unwanted outcomes and allows the dentist to provide judicious and evidence-based treatment to the patient.

Acknowledgement

Not applicable.

Financial support and sponsorship

Nil.

Conflicts of interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Authors contributions

SRV, MD, MN, AV—Conceptualization, methodology, study design; analysis—interpretation of data and critical revision, manuscript editing, reviewing and final draft, methodology, study design.

Ethical policy and institutional review board statement

Not applicable.

Patient declaration of consent

Not applicable.

Data availability statement

Data of literature are available on appropriate request.

 
   References Top

1.
Ramon Y, Behar S, Kishon Y, Engelberg IS Gingival hyperplasia caused by nifedipine—A preliminary report. Int J Cardiol 1984;5:195-206.  Back to cited text no. 1
    
2.
Aral CA, Dilber E, Aral K, Sarica Y, Sivrikoz ON Management of cyclosporine and nifedipine-induced gingival hyperplasia. J Clin Diagn Res 2015;9:ZD12-5.  Back to cited text no. 2
    
3.
Fornaini C, Rocca JP CO2 laser treatment of drug-induced gingival overgrowth—Case report. Laser Ther 2012;21:39-42.  Back to cited text no. 3
    
4.
Morikawa S, Nasu M, Miyashita Y, Nakagawa T Treatment of calcium channel blocker-induced gingival overgrowth without modifying medication. BMJ Case Reports CP 2021;14:e238872.  Back to cited text no. 4
    
5.
Marshall RI, Bartold PM Medication induced gingival overgrowth. Oral Dis 1998;4:130-51.  Back to cited text no. 5
    
6.
Carty O, Walsh E, Abdelsalem A, MaCarthy D Case report: Drug-induced gingival overgrowth associated with the use of a calcium channel blocker (amlodipine). J Ir Dent Assoc 2015;61:248-51.  Back to cited text no. 6
    
7.
Newman MG, Takei H, Klokkevold PR, Carranza FA Gingival Enlargement. 13th ed. Elsevier Health Sciences, Saunders; 2019. p. 1532-6.  Back to cited text no. 7
    
8.
Shibukawa Y, Fujinami K, Yamashita S Clinical case report of long-term follow-up in type-2 diabetes patient with severe chronic periodontitis and nifedipine-induced gingival overgrowth. Bull Tokyo Dent Coll 2012;53:91-9.  Back to cited text no. 8
    
9.
Seymour RA, Ellis JS, Thomason JM Risk factors for drug-induced gingival overgrowth. J Clin Periodontol 2000;27:217-23.  Back to cited text no. 9
    
10.
Wang AL, Iadecola C, Wang G New generations of dihydropyridines for treatment of hypertension. J Geriatr Cardiol 2017;14:67-72.  Back to cited text no. 10
    
11.
Seymour RA, Ellis JS, Thomason JM, Monkman S, Idle JR Amlodipine-induced gingival overgrowth. J Clin Periodontol 1994;21:281-3.  Back to cited text no. 11
    
12.
Brown RS, Sein P, Corio R, Bottomley WK Nitrendipine-induced gingival hyperplasia. First case report. Oral Surg Oral Med Oral Pathol 1990;70:593-6.  Back to cited text no. 12
    
13.
Klar LA Gingival hyperplasia during Dilantin therapy: A survey of 312 patients. J Publ Health Dent 1973;33:180-5.  Back to cited text no. 13
    
14.
Gopal S, Joseph R, Santhosh VC, Kumar VV, Joseph S, Shete AR Prevalence of gingival overgrowth induced by antihypertensive drugs: A hospital-based study. J Indian Soc Periodontol 2015;19:308-11.  Back to cited text no. 14
    
15.
Jayanthi R, Kalifa AM, Archana BM, Jayachandran S, Varghesse F Prevalence and severity of amlodipine induced gingival overgrowth. Int J Contemp Med Res 2017;4:377-9.  Back to cited text no. 15
    
16.
Tejnani A, Gandevivala A, Bhanushali D, Gourkhede S Combined treatment for a combined enlargement. J Indian Soc Periodontol 2014;18:516-9.  Back to cited text no. 16
    
17.
Conlin PR, Williams GH Use of calcium channel blockers in hypertension. Adv Intern Med 1998;43:533-62.  Back to cited text no. 17
    
18.
Brown RS, Beaver WT, Bottomley WK On the mechanism of drug-induced gingival hyperplasia. J Oral Pathol Med 1991;20:201-9.  Back to cited text no. 18
    
19.
Nyska A, Shemesh M, Tal H, Dayan D Gingival hyperplasia induced by calcium channel blockers: Mode of action. Med Hypotheses 1994;43:115-8.  Back to cited text no. 19
    
20.
Border WA, Noble NA Transforming growth factor beta in tissue fibrosis. N Engl J Med 1994;331:1286-92.  Back to cited text no. 20
    
21.
van der Vleuten CJ, Trijbels-Smeulders MA, van de Kerkhof PC Telangiectasia and gingival hyperplasia as side-effects of amlodipine (Norvasc) in a 3-year-old girl. Acta Derm Venereol 1999;79:323-4.  Back to cited text no. 21
    
22.
Das SJ, Olsen I Keratinocyte growth factor is upregulated by the hyperplasia-inducing drug nifedipine. Cytokine 2000;12:1566-9.  Back to cited text no. 22
    
23.
Asif SM, Shaik N, Barthunia B, Kaleem SM, Zakirulla M, Kota MZ, et al. Nifedipine induced gingival enlargement in an edentulous patient: A case report with one year follow up. BMC Oral Health 2018;18:227.  Back to cited text no. 23
    
24.
Angelopoulos AP, Goaz PW Incidence of diphenylhydantoin gingival hyperplasia. Oral Surg Oral Med Oral Pathol 1972;34:898-906.  Back to cited text no. 24
    
25.
Bökenkamp A, Bohnhorst B, Beier C, Albers N, Offner G, Brodehl J Nifedipine aggravates cyclosporine A-induced gingival hyperplasia. Pediatr Nephrol 1994;8:181-5.  Back to cited text no. 25
    
26.
Inglés E, Rossmann JA, Caffesse RG New clinical index for drug-induced gingival overgrowth. Quintessence Int 1999;30:467-73.  Back to cited text no. 26
    
27.
Shaftic AA, Widdup LL, Abate MA, Jacknowitz AI Nifedipine-induced gingival hyperplasia. Drug Intell Clin Pharm 1986;20:602-5.  Back to cited text no. 27
    
28.
Sun L, Wang C, Xi S, Zhou T, Wang G, Gang X Felodipine-associated gingival overgrowth in a type 2 diabetic patient: A case report and literature review. Exp Ther Med 2019;17:3399-402.  Back to cited text no. 28
    
29.
Routray SN, Mishra TK, Pattnaik UK, Satapathy C, Mishra CK, Behera M Amlodipine-induced gingival hyperplasia. J Assoc Physicians India 2003;51:818-9.  Back to cited text no. 29
    
30.
Madi M, Shetty SR, Babu SG, Achalli S Amlodipine-induced gingival hyperplasia—A case report and review. West Indian Med J 2015;64:279-82.  Back to cited text no. 30
    
31.
Sam G, Sebastian SC Nonsurgical management of nifedipine induced gingival overgrowth. Case Rep Dent 2014;2014:741402.  Back to cited text no. 31
    
32.
Srivastava AK, Kundu D, Bandyopadhyay P, Pal AK Management of amlodipine-induced gingival enlargement: Series of three cases. J Indian Soc Periodontol 2010;14:279-81.  Back to cited text no. 32
    
33.
Taib H, Ali TBT, Kamin S Amlodipine-induced gingival overgrowth: A case report. Arch Orofac Sci 2007;2:61-4.  Back to cited text no. 33
    
34.
Barak S, Kaplan I The CO2 laser in the excision of gingival hyperplasia caused by nifedipine. J Clin Periodontol 1988;15:633-5.  Back to cited text no. 34
    
35.
Santi E, Bral M Effect of treatment on cyclosporine- and nifedipine-induced gingival enlargement: Clinical and histologic results. Int J Periodont Restorative Dent 1998;18:1424-31.  Back to cited text no. 35
    
36.
Vekaria A, Sheth T, Shah S, Shah M Nifedipine-induced gingival enlargement—A systematic treatment approach: A case report. J Adv Oral Res 2015;6:49-52.  Back to cited text no. 36
    
37.
Quenel L, Keribin P, Giran G, Tessier MH, Lesclous P Amlodipine-induced gingival enlargement: A case report. J Stomatol Oral Maxillofac Surg 2020;121:308-11.  Back to cited text no. 37
    
38.
Mathur S, Khatri RK, Mathur R, Srivastav, R Nag BP Drug-induced gingival overgrowth: A rare case report. J Clin Diagn Res 2015;9:ZD31.  Back to cited text no. 38
    
39.
Missouris GG, Kalaitzidis RG, Cappuccio FP, MacGregor GA Gingival hyperplasia caused by calcium channel blockers. J Hum Hypertens 2000;14:155-6.  Back to cited text no. 39
    
40.
Smitha K Amlodipine-induced gingival overgrowth in a patient with uncontrolled type 2 diabetes mellitus with hypercholesterolemia: A case report. Clin Adv Periodont 2012;2:115-22.  Back to cited text no. 40
    
41.
Sharma S, Sharma A Amlodipine-induced gingival enlargement—A clinical report. Compend Contin Educ Dent 2012;33:e78-82.  Back to cited text no. 41
    
42.
Gittaboyina S, Mana TK, Koduganti RR, Reddy PVN Amlodipine induced gingival enlargement. J Oral Res Rev 2016;8:23.  Back to cited text no. 42
    
43.
Vishnudas B, Sameer Z, Shriram B, Rekha K Amlodipine induced plasma cell granuloma of the gingiva: A novel case report. J Nat Sci Biol Med 2014;5:472-6.  Back to cited text no. 43
    
44.
Gulati R, Ratre MS, Khetarpal S, Varma M A case report of a gingival plasma cell granuloma in a patient on antihypertensive therapy: Diagnostic enigma. Front Dent 2019;16:144-8.  Back to cited text no. 44
    
45.
Yolcu A, Aydogdu I Amlodipine-induced gingival hypertrophy. Eur J Intern Med 2020;78:127-8.  Back to cited text no. 45
    
46.
Ramesh R, Sadasivan A Oral squamous cell carcinoma masquerading as gingival overgrowth. Eur J Dent 2017;11:390-4.  Back to cited text no. 46
    
47.
Sunil PM, Nalluswami JS, Sanghar SJ, Joseph I Nifedipine-induced gingival enlargement: Correlation with dose and oral hygiene. J Pharm Bioallied Sci 2012;4:S191-3.  Back to cited text no. 47
    
48.
Uppal J, Trivedi H, Gupta ND, Bey A Periodontal management of severe periodontitis and generalized gingival enlargement in a patient with chronic renal failure. J Indian Soc Periodontol 2020;24:284-8.  Back to cited text no. 48
    
49.
El Hawari M, Alameddine S, Gill T, Hussain M Medication-induced gingival overgrowth. Kansas J Med 2013;6:80-1.  Back to cited text no. 49
    
50.
Jose J, Santhosh YL, Naveen MR, Kumar V Case report of amlodipine induced gingival hyperplasia—Late onset at a low dose. Asian J Pharm Clin Res 2011;4:65-6.  Back to cited text no. 50
    


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  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5]



 

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