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Genetic determinants of drug-induced gingival overgrowth
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  • Open access
  • Published: 20 May 2026

Genetic determinants of drug-induced gingival overgrowth

  • Thunchanok Kiattiubolwong1,2 na1,
  • Vorthunju Nakhonsri3 na1,
  • Kamornwan Katanyuwong4,
  • Thippawan Jaihan4,
  • Chamaiporn Klinhom5,
  • Chumpol Ngamphiw3,
  • Rujipat Wasitthankasem3,
  • Mark C. Herzberg6,
  • Sissades Tongsima3 &
  • …
  • Piranit Nik Kantaputra1,2 

Scientific Reports (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Computational biology and bioinformatics
  • Diseases
  • Genetics
  • Medical research

Abstract

Drug-induced gingival overgrowth (DIGO) is a multifactorial adverse effect associated with calcium channel blockers and antiepileptic drugs, yet genetic susceptibility-particularly in Asian populations-remains poorly defined. We performed whole-genome sequencing in 74 Thai individuals, including 36 DIGO cases and 38 drug-exposed nonresponder controls. A genome-wide association study was conducted with adjustment for amlodipine exposure, which showed a significant association with DIGO. Complementary analyses included gene-based testing using Multi-marker Analysis of GenoMic Annotation, fine-mapping with Sum of Single Effects, haplotype analysis, and receiver operating characteristic-based risk modeling. Although no single nucleotide polymorphisms (SNPs) reached genome-wide significance, we identified 350 lead SNPs across 34 genes showing strong associations with DIGO (p < 0.001). After multiple-testing correction, six genes/SNPs remained statistically significant (p < 0.05), representing the most robust findings. Haplotype analysis implicated TTC7B, RWDD1, TOM1L1, C1QL2, and BBS1 as DIGO risk genes. These genes, not previously linked to DIGO, are involved in cellular trafficking, phosphoinositide signaling, ciliary function, and protein regulation. Our findings indicate that DIGO susceptibility is driven by genetically determined cellular response pathways in the presence of amlodipine rather than by pharmacokinetic mechanisms. The absence of associations with CYP2C9 and HLA variants previously reported in other populations highlights the importance of ethnically diverse pharmacogenomic studies.

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Acknowledgements

AcknowledgementsWe thank our patients and their families for their kind cooperation and for giving us the consent to use the medical and dental information for the benefit of other patients. This work was supported by Chiang Mai University, The Dental Association of Thailand, and the Genomics Thailand Research Grant of Health Systems Research Institute (P.K.).

Funding

This work was supported by the Genomics Thailand initiative, under the pharmacogenomics focus, funded by the Health Systems Research Institute (P.K.), The Dental Association of Thailand (P.K.), and Chiang Mai University (P.K.).

Author information

Author notes
  1. Thunchanok Kiattiubolwong and Vorthunju Nakhonsri contributed equally to this work.

Authors and Affiliations

  1. Center of Excellence in Medical Genetics Research, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand

    Thunchanok Kiattiubolwong & Piranit Nik Kantaputra

  2. Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai, 50200, Thailand

    Thunchanok Kiattiubolwong & Piranit Nik Kantaputra

  3. National Center for Genetic Engineering and Biotechnology (BIOTEC), Thailand Science Park, Pathum Thani, 12120, Thailand

    Vorthunju Nakhonsri, Chumpol Ngamphiw, Rujipat Wasitthankasem & Sissades Tongsima

  4. Division of Neurology, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand

    Kamornwan Katanyuwong & Thippawan Jaihan

  5. Hang Dong Hospital, Hang Dong, Chiang Mai, 50230, Thailand

    Chamaiporn Klinhom

  6. Department of Diagnostic and Biological Sciences, School of Dentistry, University of Minnesota, Minneapolis, MN, 55455, USA

    Mark C. Herzberg

Authors
  1. Thunchanok Kiattiubolwong
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  2. Vorthunju Nakhonsri
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  3. Kamornwan Katanyuwong
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  4. Thippawan Jaihan
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  5. Chamaiporn Klinhom
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  6. Chumpol Ngamphiw
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  7. Rujipat Wasitthankasem
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  8. Mark C. Herzberg
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  9. Sissades Tongsima
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  10. Piranit Nik Kantaputra
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Corresponding authors

Correspondence to Sissades Tongsima or Piranit Nik Kantaputra.

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Competing interests

The authors declare no competing interests.

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Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Cite this article

Kiattiubolwong, T., Nakhonsri, V., Katanyuwong, K. et al. Genetic determinants of drug-induced gingival overgrowth. Sci Rep (2026). https://doi.org/10.1038/s41598-026-52779-y

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  • Received: 24 December 2025

  • Accepted: 07 May 2026

  • Published: 20 May 2026

  • DOI: https://doi.org/10.1038/s41598-026-52779-y

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Keywords

  • Gingival overgrowth
  • Genetic susceptibility
  • Calcium channel blocker
  • Gingival hyperplasia
  • Gingival hypertrophy
  • Risk factors for gingival enlargement
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