Massimo Del Fabbro, MSc, PhD/Sourav Panda, MDS, PhD/Margherita Tumedei, DDS, PhD/Renzo Guarnieri, DDS/Tejas Pande,MDS/Gianluca Colapinto, MD, OMFS, DDS/Massimo Albanese, MD, OMFS/Tiziano Testori, MD, DDS, MSc
Purpose:
To assess the diagnostic accuracy and clinical usefulness of active matrix metalloproteinase-8 (aMMP-8) for the diagnosis of peri-implantitis in patients with dental implants.
Materials and Methods:
The review protocol was registered in PROSPERO. A comprehensive search was conducted in PubMed, Embase, and Scopus up to October 31, 2025, supplemented by manual and gray literature searches. Studies assessing aMMP-8, a collagenase released during active inflammation, in peri-implant sulcular fluid (PISF) for the diagnosis of peri-implantitis were included. Data on biomarker detection methods, diagnostic performance—in terms of sensitivity, specificity, accuracy, and the Area Under the Receiver Operating Characteristic Curve (ROC-AUC)—and correlations with clinical indices were extracted. Eight studies that were published between 2016 and 2025, with a total of 506 patients (293 with healthy peri-implant tissues or mucositis and 213 diagnosed with peri-implantitis), met the inclusion criteria. Study quality was assessed using the Newcastle-Ottawa Scale (NOS). A qualitative analysis was conducted by compiling a summary of findings for all included studies.
Results:
Study quality was generally high (mean NOS score: 7.1 ± 0.6). Seven studies assessed aMMP-8 using pointof- care lateral flow immunoassay and one used immunoassay after PISF freezing and thawing. The aMMP-8 levels were consistently higher in sites with peri-implantitis compared to sites with mucositis and healthy sites. Reported diagnostic sensitivity for peri-implantitis ranged 70% to 100%, specificity from 74.1% to 100.0%, and ROC-AUC from 0.80 to 0.88. Due to heterogeneity across included studies, no meta-analysis was performed.
Conclusions:
aMMP-8 in PISF represents a noninvasive biomarker with a high diagnostic accuracy for early detection of peri-implantitis. Standardization of cutoff thresholds and longitudinal validation are required before routine clinical integration. Int J Oral Maxillofac Implants 2026;41:487–499. doi: 10.11607/jomi.11327