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Prospective observational study assesses microbial diversity related to implant tunnel depth, indicating potential biological implications.
Purpose to assess whether implant mucosal tunnel depth is associated with differences in cultivable microbial diversity in clinically healthy peri-implant tissues. Methods fifty-two patients with single molar implants were included after a standardized 3-month healing period and stratified into three groups according to implant mucosal tunnel depth: <3 mm, 3–5 mm, and > 5 mm. Microbial samples from the inner lining of the implant mucosal tunnel were cultured under aerobic and anaerobic conditions and identified using MALDI-TOF mass spectrometry. As a secondary exploratory outcome, TNF-α expression in peri-implant mucosa was quantified using real-time PCR. Results a total of 262 cultivable isolates representing 46 species were identified, with facultative anaerobic species predominating (81.68%). The highest Shannon diversity index was observed in the 3–5 mm group, whereas tunnels > 5 mm demonstrated reduced cultivable diversity, with clinically significant growth predominantly represented by streptococci. TNF-α expression showed a progressive increase with increasing implant mucosal tunnel depth, reaching approximately 38-fold higher levels in the > 5 mm group compared with < 3 mm ( p < 0.017). Conclusions within the limitations of this exploratory cross-sectional study, implant mucosal tunnel depth was associated with differences in cultivable microbial composition and local TNF-α expression in clinically stable peri-implant tissues. Deeper mucosal tunnels (> 5 mm) demonstrated reduced cultivable species diversity without a consistent predominance of cultivable periodontal pathogens under the applied culture conditions. The observed increase in TNF-α expression should be interpreted as a biologic association rather than evidence of active inflammation or disease. Due to the culture-based methodology and the absence of longitudinal clinical data, no conclusions regarding disease risk or progression can be drawn. Trial registration ClinicalTrials.gov, NCT05870774. Registered on 20,230,425.
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Ashurko et al. (2026) studied this question.
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