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Oral health outcomes in children with tuberous sclerosis complex: a matched case–control study evaluating antiseizure medication and mTOR inhibitor exposure
1Department of Pedodontics, Institute of Graduate Studies in Health Sciences, Istanbul University, 34000 Istanbul, Turkey
2Division of Pediatric Neurology, Department of Pediatrics, Istanbul Faculty of Medicine, Istanbul University, 34000 Istanbul, Turkey
3Department of Pedodontics, Faculty of Dentistry, Istanbul University, 34000 Istanbul, Turkey
4Department of Health Management, Faculty of Health Sciences, Marmara University, 34000 Istanbul, Turkey
DOI: 10.22514/jocpd.2026.133 Vol.50,Issue 5,September 2026 pp.249-255
Submitted: 02 April 2026 Accepted: 08 June 2026
Published: 03 September 2026
*Corresponding Author(s): Büşra Moğul Bağcı E-mail: busramogul@ogr.iu.edu.tr
Background: Tuberous sclerosis complex (TSC) is a rare genetic disorder with neurological and systemic involvement. The relationship of TSC and the anti-seizure medications (ASM) and mammalian target of rapamycin (mTOR) inhibitors used in its treatment with oral and dental health is not fully understood. This study compared oral and dental health parameters in children with TSC and healthy controls and investigated the association between pharmacological treatment exposure and these parameters. Methods: A case-control study was conducted between January and November 2025 at the Istanbul University Faculty of Medicine Pediatric Neurology Clinic on 19 children aged 3–18 years with TSC and 19 age and sex matched healthy controls. Gingival index, gingival overgrowth index, fibroma, enamel pits, decayed/filled/missing teeth (dmft/DMFT) scores, toothbrushing frequency, dental visit frequency, and Wong-Baker pain scores were evaluated. In the TSC group, disease duration, comorbid conditions, and duration of ASM and mTOR inhibitor use were also recorded. Matched between-group comparisons were performed using paired statistical tests, and associations were assessed using Spearman correlation analysis. Results: Gingival index, gingival overgrowth, and enamel pits were significantly higher in the TSC group than in controls (p < 0.05). No significant differences were found between in toothbrushing frequency, dental visits, or fibroma group. Within the TSC group, longer ASM exposure was positively correlated with gingival index and gingival overgrowth, whereas mTOR inhibitor exposure showed a moderate positive correlation with gingival overgrowth but no significant correlation with gingival index. Conclusions: Compared with age and sex matched controls, children with TSC showed higher gingival index scores (2.0 vs. 1.0), greater gingival overgrowth (1.0 vs. 0.0), and a higher prevalence of enamel pits (57.9% vs. 15.8%). Longer ASM exposure was strongly correlated with gingival index (ρ = 0.735) and gingival overgrowth (ρ = 0.801), whereas mTOR inhibitor exposure was moderately correlated only with gingival overgrowth (ρ = 0.488).
Tuberous sclerosis complex; Pediatric dentistry; Gingival overgrowth; Anti-seizure medication; mTOR inhibitors
Büşra Moğul Bağcı,Ceyda Öney Yılmaz,Mine Koruyucu,Edibe Pembegül Yıldız,Meral Timurtaş,Koray Gençay,Hülya Maraş Genç. Oral health outcomes in children with tuberous sclerosis complex: a matched case–control study evaluating antiseizure medication and mTOR inhibitor exposure. Journal of Clinical Pediatric Dentistry. 2026. 50(5);249-255.
[1] Arredondo KH, Jülich K, Roach ES. Tuberous sclerosis complex: diagnostic features, surveillance, and therapeutic strategies. Seminars in Pediatric Neurology. 2024; 51: 101155.
[2] Sparling JD, Hong CH, Brahim JS, Moss J, Darling TN. Oral findings in 58 adults with tuberous sclerosis complex. Journal of the American Academy of Dermatology. 2007; 56: 786–790.
[3] Panwar A, Malik S, Kamarthi N, Gupta S, Goel S, Sharma A, et al. Oral manifestations of tuberous sclerosis complex: a systematic review. Pediatric Dental Journal. 2024; 34: 164–181.
[4] Northrup H, Aronow ME, Bebin EM, Bissler J, Darling TN, de Vries PJ, et al. Updated international tuberous sclerosis complex diagnostic criteria and surveillance and management recommendations. Pediatric Neurology. 2021; 123: 50–66.
[5] Banthia R, Gupta S, Banthia P, Singh P, Raje S, Kaur N. Is periodontal health a predictor of drug-induced gingival overgrowth? A cross-sectional study. Dental Research Journal. 2014; 11: 579–584.
[6] Droździk A, Droździk M. Drug-induced gingival overgrowth—molecular aspects of drug actions. International Journal of Molecular Sciences. 2023; 24: 5448.
[7] Sonis ST, Villa A. A new hypothesis describing the pathogenesis of oral mucosal injury associated with the mammalian target of rapamycin (mTOR) inhibitors. Cancers. 2023; 16: 68.
[8] Garra G, Singer AJ, Taira BR, Chohan J, Cardoz H, Chisena E, et al. Validation of the Wong‐Baker FACES pain rating scale in pediatric emergency department patients. Academic Emergency Medicine. 2010; 17: 50–54.
[9] Moradi G, Mohamadi Bolbanabad A, Moinafshar A, Adabi H, Sharafi M, Zareie B. Evaluation of oral health status based on the decayed, missing and filled teeth (DMFT) index. Iranian Journal of Public Health. 2019; 48: 2050–2057.
[10] Doufexi A, Mina M, Ioannidou E. Gingival overgrowth in children: epidemiology, pathogenesis, and complications. A literature review. Journal of Periodontology. 2005; 76: 3–10.
[11] Ciancio SG. Current status of indices of gingivitis. Journal of Clinical Periodontology. 1986; 13: 375–378, 381–382.
[12] Korporowicz E, Olczak-Kowalczyk D, Lipiec M, Słowińska M, Gozdowski D, Jóźwiak S. Oral findings in children, adolescents and adults with tuberous sclerosis complex. Journal of Clinical Pediatric Dentistry. 2020; 44: 190–195.
[13] Gosnell ES, Krueger D, Ruck P, Buff-Lindner AH, Horn PS, Griffith M. Oral manifestations and quality of life in children with tuberous sclerosis complex: a descriptive study. Pediatric Dentistry. 2021; 43: 140–144.
[14] Suneja B, Chopra S, Thomas AM, Pandian J. A clinical evaluation of gingival overgrowth in children on antiepileptic drug therapy. Journal of Clinical and Diagnostic Research. 2016; 10: ZC32–ZC36.
[15] Joshi VM, Gururaj SB, Thumbigere-Math V, Kugaji MS, Kandaswamy E. Rapamycin’s role in periodontal health and therapeutics: a scoping review. JDR Clinical & Translational Research. 2026; 11: 357–367.
[16] Lygidakis N, Lindenbaum R. Oral fibromatosis in tuberous sclerosis. Oral Surgery, Oral Medicine, Oral Pathology. 1989; 68: 725–728.
[17] Lygidakis N, Lindenbaum R. Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relatives. Clinical Genetics. 1987; 32: 216–221.
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