Scientific Article Review:
Reducing Dentine Hypersensitivity with Nano-Hydroxyapatite Toothpaste
Published In: Clinical Oral Investigations
Publication Year: 2018
Study Design
This study was a double-blind randomized controlled trial conducted at a single site, designed to compare the efficacy of nano-hydroxyapatite (n-HAp) toothpaste with fluoride and placebo groups for reducing dentine hypersensitivity.
Funding Sources
The study does not mention specific funding sources.
PICO Framework - what was studied and how?
Population:
Adults aged 20–70 years with hypersensitive teeth (minimum of two hypersensitive teeth confirmed via tactile and airblast sensitivity tests).
Intervention:
Application of nano-hydroxyapatite (2%) gel toothpaste twice daily for four weeks.
Comparison:
Fluoride toothpaste (positive control group) and placebo toothpaste.
Outcomes:
Reduction in dentine hypersensitivity measured using:
- Tactile sensitivity scores.
- Airblast sensitivity scores.
- Subjective Visual Analogue Scale (VAS) pain ratings.
Paragraph Form:
This study examined adults aged 20–70 with hypersensitive teeth to evaluate the efficacy of a nano-hydroxyapatite (2%) gel toothpaste in reducing dentine hypersensitivity. Outcomes were compared to those using a fluoride toothpaste and a placebo toothpaste, measuring improvements in tactile and airblast sensitivity, as well as subjective pain ratings on a Visual Analogue Scale.
Inclusion and Exclusion Criteria
Inclusion Criteria:
- Adults aged 20–70 years with hypersensitive teeth (at least two teeth scoring ≥2 on tactile and airblast sensitivity tests).
- Good periodontal health (no probing depth >4 mm).
- Good overall physical health.
Exclusion Criteria:
- Chipped teeth, defective restorations, or orthodontic appliances.
- Periodontal surgery in the last six months.
- Use of analgesic or anti-inflammatory drugs.
- Pregnancy, lactation, smoking, or substance abuse.
Demographics and Study Design
- Subjects: 105 adults (65 females, 40 males).
-
Cohorts:
- Nano-hydroxyapatite group: 35 participants.
- Fluoride group: 35 participants.
- Placebo group: 35 participants.
Subjects used the assigned toothpaste twice daily for four weeks. All groups were balanced with no significant differences in baseline values.
Primary Outcome Variables and Results
Results Summary:
- Tactile Sensitivity: Reduced from a baseline of 3.17 to 1.98 and 1.83 at 2 and 4 weeks in the experimental group (p < 0.05).
- Airblast Sensitivity: Decreased from a baseline of 2.97 to 1.72 and 1.64 at 2 and 4 weeks in the experimental group (p < 0.05).
- VAS Scores: Showed significant reductions in the experimental group at 2 and 4 weeks compared to baseline (p < 0.05).
Group | Tactile Sensitivity (Baseline) | Tactile Sensitivity (4 Weeks) | Airblast Sensitivity (Baseline) | Airblast Sensitivity (4 Weeks) |
---|---|---|---|---|
Nano-hydroxyapatite | 3.17 | 1.83 | 2.97 | 1.64 |
Fluoride | 2.94 | 2.72 | 3.05 | 2.57 |
Placebo | 2.50 | 2.92 | 2.87 | 2.73 |
Conclusions
The study concluded that nano-hydroxyapatite toothpaste significantly reduced dentine hypersensitivity compared to fluoride and placebo toothpaste. Reductions were seen as early as two weeks and maintained through four weeks.
Discussion
Strengths:
- Use of validated clinical measures (e.g., tactile and airblast tests, VAS).
- Double-blind design minimized bias.
Limitations:
- Study duration limited to four weeks; long-term effects remain unstudied.
- Single-site design may limit generalizability.
Citation
Milia E, et al. Reducing dentine hypersensitivity with nano-hydroxyapatite toothpaste: A double-blind randomized controlled trial. Clin Oral Invest. 2018;22:313–320. PubMed