Drug-Induced Gingival Enlargement: A Comparative Study on the Effect of Phenytoin, Gabapentin, and Cyclosporin on Gingival Fibroblast Cells

Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers, immunosuppressants, or anticonvulsants are taken. The prevalence of DIGE was shown to be 70% for phenytoin (30% for other anticonvulsant medicines) and 5...

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Published inMolecular biotechnology
Main Authors Veena, K. M., Mohammed Hasil, V., Shenoy, Prashanth, Abhijna Ballal, R., Shetty, Sanath Kumar
Format Journal Article
LanguageEnglish
Published Switzerland 14.03.2025
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ISSN1073-6085
1559-0305
1559-0305
DOI10.1007/s12033-025-01397-6

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Abstract Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers, immunosuppressants, or anticonvulsants are taken. The prevalence of DIGE was shown to be 70% for phenytoin (30% for other anticonvulsant medicines) and 50-80% for cyclosporine. The usage of these medications is increasing as new indications emerge. These drugs act through a common mechanism of action at the cellular level by inhibiting intracellular calcium influx. DIGE is characterized by the presence of varied quantities of inflammatory infiltrates, primarily plasma cells, and an excessive build-up of extracellular matrix like-collagen. Fibroblasts, the cells responsible for collagen synthesis, may become hyperactive, leading to the excessive production of collagen fibers. This increased collagen content can result in the enlargement of gingival tissues. As collagen deposits increase, it hinders normal oral care routines, masticatory processes, and esthetics. In this study, we compared the cytotoxicity of phenytoin, gabapentin, and cyclosporine on gingival fibroblast cells using the methyl thiazolyl-tetrazolium assay to understand their effect on gingival fibroblast cells. Phenytoin had the greatest half-maximal inhibitory concentration (IC50) with a value of 305.78 µg/ml, followed by gabapentin with a value of 260.44 µg/ml and cyclosporin with a value of 243.79 µg/ml. Understanding the cytotoxic thresholds of these medications is essential for improving patient outcomes and minimizing the incidence of gingival enlargement in those requiring long-term therapy. According to the study, cytotoxicity increases along with medication concentration. These findings will assist medical professionals in selecting the drug that poses the least risk of adverse effects on gingival health, ultimately guiding more informed prescribing practices.
AbstractList Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers, immunosuppressants, or anticonvulsants are taken. The prevalence of DIGE was shown to be 70% for phenytoin (30% for other anticonvulsant medicines) and 50-80% for cyclosporine. The usage of these medications is increasing as new indications emerge. These drugs act through a common mechanism of action at the cellular level by inhibiting intracellular calcium influx. DIGE is characterized by the presence of varied quantities of inflammatory infiltrates, primarily plasma cells, and an excessive build-up of extracellular matrix like-collagen. Fibroblasts, the cells responsible for collagen synthesis, may become hyperactive, leading to the excessive production of collagen fibers. This increased collagen content can result in the enlargement of gingival tissues. As collagen deposits increase, it hinders normal oral care routines, masticatory processes, and esthetics. In this study, we compared the cytotoxicity of phenytoin, gabapentin, and cyclosporine on gingival fibroblast cells using the methyl thiazolyl-tetrazolium assay to understand their effect on gingival fibroblast cells. Phenytoin had the greatest half-maximal inhibitory concentration (IC50) with a value of 305.78 µg/ml, followed by gabapentin with a value of 260.44 µg/ml and cyclosporin with a value of 243.79 µg/ml. Understanding the cytotoxic thresholds of these medications is essential for improving patient outcomes and minimizing the incidence of gingival enlargement in those requiring long-term therapy. According to the study, cytotoxicity increases along with medication concentration. These findings will assist medical professionals in selecting the drug that poses the least risk of adverse effects on gingival health, ultimately guiding more informed prescribing practices.
Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers, immunosuppressants, or anticonvulsants are taken. The prevalence of DIGE was shown to be 70% for phenytoin (30% for other anticonvulsant medicines) and 50-80% for cyclosporine. The usage of these medications is increasing as new indications emerge. These drugs act through a common mechanism of action at the cellular level by inhibiting intracellular calcium influx. DIGE is characterized by the presence of varied quantities of inflammatory infiltrates, primarily plasma cells, and an excessive build-up of extracellular matrix like-collagen. Fibroblasts, the cells responsible for collagen synthesis, may become hyperactive, leading to the excessive production of collagen fibers. This increased collagen content can result in the enlargement of gingival tissues. As collagen deposits increase, it hinders normal oral care routines, masticatory processes, and esthetics. In this study, we compared the cytotoxicity of phenytoin, gabapentin, and cyclosporine on gingival fibroblast cells using the methyl thiazolyl-tetrazolium assay to understand their effect on gingival fibroblast cells. Phenytoin had the greatest half-maximal inhibitory concentration (IC50) with a value of 305.78 µg/ml, followed by gabapentin with a value of 260.44 µg/ml and cyclosporin with a value of 243.79 µg/ml. Understanding the cytotoxic thresholds of these medications is essential for improving patient outcomes and minimizing the incidence of gingival enlargement in those requiring long-term therapy. According to the study, cytotoxicity increases along with medication concentration. These findings will assist medical professionals in selecting the drug that poses the least risk of adverse effects on gingival health, ultimately guiding more informed prescribing practices.Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers, immunosuppressants, or anticonvulsants are taken. The prevalence of DIGE was shown to be 70% for phenytoin (30% for other anticonvulsant medicines) and 50-80% for cyclosporine. The usage of these medications is increasing as new indications emerge. These drugs act through a common mechanism of action at the cellular level by inhibiting intracellular calcium influx. DIGE is characterized by the presence of varied quantities of inflammatory infiltrates, primarily plasma cells, and an excessive build-up of extracellular matrix like-collagen. Fibroblasts, the cells responsible for collagen synthesis, may become hyperactive, leading to the excessive production of collagen fibers. This increased collagen content can result in the enlargement of gingival tissues. As collagen deposits increase, it hinders normal oral care routines, masticatory processes, and esthetics. In this study, we compared the cytotoxicity of phenytoin, gabapentin, and cyclosporine on gingival fibroblast cells using the methyl thiazolyl-tetrazolium assay to understand their effect on gingival fibroblast cells. Phenytoin had the greatest half-maximal inhibitory concentration (IC50) with a value of 305.78 µg/ml, followed by gabapentin with a value of 260.44 µg/ml and cyclosporin with a value of 243.79 µg/ml. Understanding the cytotoxic thresholds of these medications is essential for improving patient outcomes and minimizing the incidence of gingival enlargement in those requiring long-term therapy. According to the study, cytotoxicity increases along with medication concentration. These findings will assist medical professionals in selecting the drug that poses the least risk of adverse effects on gingival health, ultimately guiding more informed prescribing practices.
Author Shenoy, Prashanth
Mohammed Hasil, V.
Shetty, Sanath Kumar
Abhijna Ballal, R.
Veena, K. M.
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Cites_doi 10.1007/s12033-023-00861-5
10.1016/j.ajem.2014.03.036
10.7759/cureus.25009
10.1007/s12033-023-00813-z
10.4236/ojst.2014.44025
10.1177/2058738419827765
10.17159/sadj.v78i03.16273
10.4103/0976-237X.132365
10.1177/0022034509350566
10.1093/jscr/rjae304
10.1186/s40780-017-0088-5
10.12998/wjcc.v3.i9.779
10.1111/j.1600-0404.2011.01535.x
10.2174/1874210601711010420
10.2174/1874210601913010430
10.3390/ijerph17218229
10.1902/jop.2005.76.6.941
10.1034/j.1600-0609.2001.t01-1-00440.x
10.4103/0972-124X.113066
10.3390/ijms24065448
10.1111/crj.12178
10.1007/s00018-003-2108-x
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Keywords Drug side effects
Anticonvulsants
Immunosuppressants
Cyclosporin
Gabapentin
Cellular culture
Cytotoxicity
MTT
Fibroblast
Drug-induced gingival enlargement
Gingival enlargement
Phenytoin
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License 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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References EK Sher (1397_CR12) 2023
SH Imam (1397_CR3) 2014; 32
SP Mpungose (1397_CR10) 2023; 78
A Ramírez-Rámiz (1397_CR8) 2017; 11
D Lauritano (1397_CR22) 2020; 17
MA Sabarudin (1397_CR9) 2022
N Dhalla (1397_CR17) 2024; 2024
F Trullemans (1397_CR5) 2001; 67
AMM Suzuki (1397_CR15) 2009; 88
V Priyadharshini (1397_CR16) 2014; 5
K Emina (1397_CR23) 2022; 1
YP Maneuf (1397_CR6) 2003; 60
FF Farook (1397_CR4) 2019; 13
B Palić (1397_CR14) 2023
V Candotto (1397_CR7) 2019; 33
V Bharti (1397_CR1) 2013; 17
T Kato (1397_CR21) 2005; 76
W Andrew (1397_CR11) 2014
H Hatahira (1397_CR19) 2017; 3
B Suneja (1397_CR13) 2016; 10
I Karimzadeh (1397_CR20) 2015; 1
A Droździk (1397_CR18) 2023; 24
A Matić (1397_CR24) 2023; 22
R Arya (1397_CR25) 2012; 125
AA Agrawal (1397_CR2) 2015; 3
References_xml – year: 2023
  ident: 1397_CR14
  publication-title: Molecular Biotechnology
  doi: 10.1007/s12033-023-00861-5
– volume: 32
  start-page: 1301
  issue: 10
  year: 2014
  ident: 1397_CR3
  publication-title: The American Journal of Emergency Medicine
  doi: 10.1016/j.ajem.2014.03.036
– year: 2022
  ident: 1397_CR9
  publication-title: Cureus
  doi: 10.7759/cureus.25009
– year: 2023
  ident: 1397_CR12
  publication-title: Molecular Biotechnology
  doi: 10.1007/s12033-023-00813-z
– year: 2014
  ident: 1397_CR11
  publication-title: Open Journal of Stomatology
  doi: 10.4236/ojst.2014.44025
– volume: 33
  start-page: 205873841982776
  year: 2019
  ident: 1397_CR7
  publication-title: International Journal of Immunopathology and Pharmacology
  doi: 10.1177/2058738419827765
– volume: 78
  start-page: 145
  issue: 3
  year: 2023
  ident: 1397_CR10
  publication-title: South African Dental Journal
  doi: 10.17159/sadj.v78i03.16273
– volume: 5
  start-page: 268
  issue: 2
  year: 2014
  ident: 1397_CR16
  publication-title: Contemporary Clinical Dentistry
  doi: 10.4103/0976-237X.132365
– volume: 88
  start-page: 1131
  issue: 12
  year: 2009
  ident: 1397_CR15
  publication-title: Journal of Dental Research
  doi: 10.1177/0022034509350566
– volume: 2024
  start-page: rjae304
  issue: 5
  year: 2024
  ident: 1397_CR17
  publication-title: Journal of Surgical Case Reports
  doi: 10.1093/jscr/rjae304
– volume: 3
  start-page: 1
  year: 2017
  ident: 1397_CR19
  publication-title: Journal of Pharmaceutical Health Care and Sciences.
  doi: 10.1186/s40780-017-0088-5
– volume: 3
  start-page: 779
  issue: 9
  year: 2015
  ident: 1397_CR2
  publication-title: World Journal of Clinical Cases
  doi: 10.12998/wjcc.v3.i9.779
– volume: 125
  start-page: 149
  issue: 3
  year: 2012
  ident: 1397_CR25
  publication-title: Acta Neurologica Scandinavica.
  doi: 10.1111/j.1600-0404.2011.01535.x
– volume: 11
  start-page: 420
  year: 2017
  ident: 1397_CR8
  publication-title: The Open Dentistry Journal.
  doi: 10.2174/1874210601711010420
– volume: 1
  start-page: 186
  year: 2022
  ident: 1397_CR23
  publication-title: Diabetes Research and Clinical Practice.
– volume: 13
  start-page: 430
  issue: 1
  year: 2019
  ident: 1397_CR4
  publication-title: The Open Dentistry Journal
  doi: 10.2174/1874210601913010430
– volume: 17
  start-page: 8229
  issue: 21
  year: 2020
  ident: 1397_CR22
  publication-title: International Journal of Environmental Research and Public Health
  doi: 10.3390/ijerph17218229
– volume: 76
  start-page: 941
  issue: 6
  year: 2005
  ident: 1397_CR21
  publication-title: Journal of Periodontology
  doi: 10.1902/jop.2005.76.6.941
– volume: 67
  start-page: 94
  issue: 2
  year: 2001
  ident: 1397_CR5
  publication-title: European Journal of Haematology
  doi: 10.1034/j.1600-0609.2001.t01-1-00440.x
– volume: 17
  start-page: 182
  issue: 2
  year: 2013
  ident: 1397_CR1
  publication-title: Journal of Indian Society of Periodontology
  doi: 10.4103/0972-124X.113066
– volume: 1
  start-page: 1
  issue: 1
  year: 2015
  ident: 1397_CR20
  publication-title: Soc Pharm Journal.
– volume: 24
  start-page: 5448
  issue: 6
  year: 2023
  ident: 1397_CR18
  publication-title: International Journal of Molecular Sciences.
  doi: 10.3390/ijms24065448
– volume: 10
  start-page: ZC32
  issue: 1
  year: 2016
  ident: 1397_CR13
  publication-title: Journal of Clinical and Diagnostic Research
  doi: 10.1111/crj.12178
– volume: 60
  start-page: 742
  year: 2003
  ident: 1397_CR6
  publication-title: Cellular and Molecular Life Sciences CMLS
  doi: 10.1007/s00018-003-2108-x
– volume: 22
  start-page: 1
  year: 2023
  ident: 1397_CR24
  publication-title: Molecular Biotechnology.
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Snippet Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers,...
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Title Drug-Induced Gingival Enlargement: A Comparative Study on the Effect of Phenytoin, Gabapentin, and Cyclosporin on Gingival Fibroblast Cells
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