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Association between metabolic syndrome and salivary MMP-8, myeloperoxidase in periodontitis.
Thomas, Julie Toby; Joseph, Betsy; Varghese, Sajit; Thomas, Nebu George; Kamalasanan Vijayakumary, Baiju; Sorsa, Timo; Anil, Sukumaran; Waltimo, Tuomas.
Afiliación
  • Thomas JT; Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Joseph B; Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Varghese S; Department of Periodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Chennai, Tamilnadu, India.
  • Thomas NG; Department of General Medicine, Pushpagiri Institute of Medical Sciences and Research Centre, Thiruvalla, Kerala, India.
  • Kamalasanan Vijayakumary B; Department of Periodontics, Pushpagiri College of Dental Sciences, Thiruvalla, Kerala, India.
  • Sorsa T; Department of Statistics, Women's College, Trivandrum, Kerala, India.
  • Anil S; Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Waltimo T; Division of Periodontology, Department of Dental Medicine, Karolinska Institutet, Stockholm, Sweden.
Oral Dis ; 2024 Jun 09.
Article en En | MEDLINE | ID: mdl-38852177
ABSTRACT

OBJECTIVE:

This study investigated the effect of metabolic syndrome (MetS) on periodontal clinical parameters and salivary biomarkers' matrix metalloproteinase-8 (MMP-8) and myeloperoxidase (MPO) in patients with periodontitis.

METHODS:

A total of 120 participants aged 25-55 were categorized into three groups MetS with periodontitis (n = 40); systemically healthy with periodontitis (n = 40); and systemically and periodontally healthy controls (n = 40). Data collected included systemic parameters like waist circumference (WC), blood pressure (BP), high- and low-density lipoproteins, triglycerides (TG), fasting blood sugar (FBS), and glycated hemoglobin (HbA1c). Periodontal parameters estimated included bleeding on probing score (BoP), full-mouth plaque score (FMPS), periodontal probing depth (PPD), clinical attachment loss (CAL), and the number of missing teeth. Unstimulated whole saliva was analyzed via ELISA for active MMP-8 (aMMP-8), total MMP-8 (tMMP-8), and MPO.

RESULTS:

Participants with MetS and periodontitis exhibited significantly higher periodontal parameters, salivary aMMP-8, and MPO (26.26 vs. 24.1 ng/mL and 13.53 vs. 11.55 ng/mL compared to systemically healthy periodontitis patients) (all p < 0.01). Positive correlations occurred between aMMP-8 and WC, TG, and FBS (p < 0.01), and between MPO and WC, BP, and TG (p < 0.01).

CONCLUSIONS:

The positive associations between these biomarkers and metabolic parameters indicate their potential utility for monitoring cardiovascular and glycemic risk in patients with periodontal disease.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Oral Dis / Oral dis / Oral diseases Asunto de la revista: ODONTOLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Oral Dis / Oral dis / Oral diseases Asunto de la revista: ODONTOLOGIA Año: 2024 Tipo del documento: Article