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Effects of Periodontitis on Heart Rate Variability

Study of Autonomic Modulation - Sympathetic and Parasympathetic - in Periodontitis Through Heart Rate Variability

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07735312
Enrollment
50
Registered
2026-07-29
Start date
2023-07-01
Completion date
2027-04-01
Last updated
2026-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Electrophysiology, Periodontitis

Keywords

Periodontitis, Heart rate variability, Systemic Inflammation

Brief summary

Periodontitis is a chronic inflammatory disease associated with systemic inflammatory burden and possible alterations in autonomic nervous system regulation. Heart rate variability (HRV) has been used as a noninvasive method to assess autonomic modulation and may reflect sympathovagal imbalance associated with inflammatory conditions. This case-control study aims to investigate the association between periodontitis and autonomic modulation assessed by HRV parameters. In addition, the study will evaluate the association between periodontal clinical parameters, HRV indices, and plasma levels of pro- and anti-inflammatory cytokines and biomarkers. Participants with and without periodontitis will undergo periodontal examination, HRV assessment, and blood sample collection for inflammatory marker analyses.

Detailed description

Periodontitis is a chronic multifactorial inflammatory disease associated with dysbiotic dental biofilm and host immune-inflammatory response, leading to progressive destruction of tooth-supporting tissues. In addition to local periodontal inflammation, increasing evidence suggests that periodontitis contributes to systemic inflammatory burden and may be associated with cardiovascular and autonomic dysfunction. The autonomic nervous system plays a central role in cardiovascular regulation and immune-inflammatory modulation. Sympathetic and parasympathetic pathways participate in inflammatory reflex mechanisms capable of modulating cytokine production and systemic inflammatory responses. Alterations in autonomic modulation have been associated with several chronic inflammatory conditions, including rheumatoid arthritis, systemic lupus erythematosus, sepsis, and cardiovascular diseases. Heart rate variability (HRV) is a noninvasive and validated method for evaluating autonomic nervous system modulation and sympathovagal balance. Reduced HRV and increased sympathetic activity have been associated with systemic inflammation, cardiovascular morbidity, and increased mortality risk. However, the relationship between periodontitis and autonomic dysfunction remains incompletely understood, particularly regarding nonlinear HRV dynamics and their association with inflammatory biomarkers. This longitudinal case-control study aims to investigate whether individuals with generalized periodontitis present alterations in autonomic modulation compared with periodontally healthy individuals. The study will evaluate HRV parameters, blood pressure, inflammatory biomarkers, cardiac function, and sympathetic neural activity. In addition, the effects of periodontal treatment on these parameters will be investigated over time. Participants aged between 35 and 50 years will be recruited at the Periodontics Clinic of the School of Dentistry of Ribeirão Preto, University of São Paulo (FORP-USP). Individuals diagnosed with generalized stage III or IV, grade B or C periodontitis according to the 2017 Classification of Periodontal and Peri-Implant Diseases and Conditions will compose the test group. Periodontally healthy individuals or those not meeting periodontitis diagnostic criteria will compose the control group. Groups will be matched according to age and sex. All participants will undergo complete periodontal examination, including probing depth, clinical attachment level, bleeding on probing, plaque index, and tooth loss assessment. Electrocardiographic recordings will be obtained for HRV analysis using time-domain, frequency-domain, symbolic, and nonlinear analyses, including entropy-based methods. Blood pressure measurements and anthropometric evaluations will also be performed. Peripheral blood samples will be collected for analysis of pro-inflammatory cytokines, including IL-1α, IL-1β, TNF-α, IL-6, and IL-17, as well as anti-inflammatory cytokines such as IL-10. C-reactive protein and calcitonin levels will also be evaluated. Gingival crevicular fluid samples will be collected for local inflammatory marker analysis. Supragingival biofilm and fecal samples will be collected for microbiological analysis using 16S rRNA sequencing in order to investigate oral and intestinal microbiome profiles and their association with autonomic and inflammatory parameters. Cardiac structure and function will be evaluated through echocardiography, including conventional and speckle tracking echocardiographic analyses. Sympathetic neural activity will also be assessed by direct muscle sympathetic nerve activity recording through microneurography. Participants diagnosed with periodontitis will receive non-surgical periodontal therapy, including scaling and root planing, oral hygiene instruction, and periodontal maintenance therapy throughout the study. Clinical and laboratory evaluations will be repeated at baseline, 3 months, 6 months, and 12 months after treatment. The primary objective of this study is to determine whether periodontitis is associated with autonomic imbalance characterized by alterations in sympathetic and parasympathetic modulation. Secondary objectives include investigating associations among periodontal parameters, HRV indices, inflammatory biomarkers, blood pressure, cardiac function, and sympathetic activity, as well as evaluating the effects of periodontal treatment on these outcomes. The findings of this study may contribute to a better understanding of the interactions among periodontal inflammation, systemic immune response, autonomic nervous system regulation, and cardiovascular function, potentially supporting new therapeutic and preventive approaches targeting neuroimmune mechanisms associated with chronic inflammatory diseases.

Interventions

PROCEDURENon-surgical periodontal therapy

Non-surgical periodontal treatment including oral hygiene instruction, supragingival scaling, scaling and root planing, and periodontal maintenance therapy.

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged between 35 and 50 years; * Presence of at least 15 teeth, excluding third molars and teeth indicated for extraction; * Individuals diagnosed with generalized stage III or IV, grade B or C periodontitis according to the 2017 Classification of Periodontal and Peri-Implant Diseases and Conditions; * At least 30% of teeth presenting probing depth and clinical attachment loss ≥ 5 mm with bleeding on probing; * Ability and willingness to provide written informed consent.

Exclusion criteria

* Completely edentulous individuals; * Individuals presenting fewer than 15 teeth; * Pregnant women; * Smokers; * Individuals diagnosed with type 1 or type 2 diabetes mellitus; * Individuals with chronic systemic diseases, including chronic arterial hypertension, class III or IV heart failure, or Parkinson's disease; * Individuals with pacemakers or atrial fibrillation/flutter; * Individuals who received periodontal treatment within the previous 12 months; * Individuals who used systemic antibiotics within the previous 6 months; * Individuals with contraindications to periodontal procedures; * Individuals requiring antibiotic prophylaxis before periodontal treatment; * Individuals with blood dyscrasias or anticoagulant conditions associated with increased bleeding risk.

Design outcomes

Primary

MeasureTime frameDescription
Autonomic modulation (frequency-domain analysis)Baseline, 3 months, 6 months, and 12 monthsAssessment of autonomic modulation using absolute low-frequency (LF) and high-frequency (HF) power derived from heart rate variability analysis of electrocardiographic recordings. Results will be reported as milliseconds squared (ms²).
Autonomic modulation (normalized units)Baseline, 3 months, 6 months, and 12 months.Assessment of autonomic modulation using normalized low-frequency (LFnu) and high-frequency (HFnu) components derived from heart rate variability analysis of electrocardiographic recordings. Results will be reported as normalized units (nu).
Autonomic modulation (symbolic analysis)Baseline, 3 months, 6 months, and 12 months.Assessment of autonomic modulation using symbolic analysis of heart rate variability, including the percentage of 0V and 2UV patterns. Results will be reported as percentages (%).
Autonomic modulation (nonlinear analysis)Baseline, 3 months, 6 months, and 12 months.Assessment of autonomic modulation using entropy derived from nonlinear heart rate variability analysis of electrocardiographic recordings.

Secondary

MeasureTime frameDescription
Periodontal clinical parameters (millimeters)Baseline, 3 months, 6 months, and 12 monthsAssessment of periodontal clinical status using probing depth (PD) and clinical attachment level (CAL) measured in millimeters (mm).
Periodontal inflammatory parameters (percentage)Baseline, 3 months, 6 months, and 12 months.Assessment of periodontal inflammatory status using bleeding on probing (BOP), reported as the percentage of sites exhibiting bleeding on probing (%).
Dental plaque accumulation (percentage)Baseline, 3 months, 6 months, and 12 months.Assessment of oral hygiene status using the plaque index, reported as the percentage of sites with visible dental plaque (%).

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 30, 2026