Matthias Tröltzsch

Dr. Matthias Tröltzsch

1. Department of Oral, Maxillofacial Surgery and Facial Plastic Surgery, University Hospital, LMU Munich, Munich, Germany
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Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 May 2021 in Medicina
Verified
Journal Article
Open access
PDF file
SOSven Otto
Sven Otto
SASuad Aljohani
Suad Aljohani
RFRiham M Fliefel
Riham M Fliefel
SESara Ecke
Sara Ecke
OROliver Ristow
Oliver Ristow
MEMichael Ehrenfeld
Michael Ehrenfeld
Medication-related osteonecrosis of the jaw (MRONJ) has become a well-known side effect of antiresorptive, and antiangiogenic drugs commonly used in cancer management. Despite a considerable amount of literature addressing MRONJ, it is still widely accepted that the underlying pathomechanism of MRONJ is unclear. However, several clinical and preclinical studies indicate that infection seems to have a major role in the pathogenesis of MRONJ. Although there is no conclusive evidence for the infection hypothesis yet, available data have shown a robust association between local infection and MRONJ development. This observation is very critical in order to implement policies to reduce the risk of MRONJ in patients under antiresorptive drugs. This critical review was conducted to collect the most reliable evidence regarding the link between local infection and MRONJ pathogenesis.

1 April 2017 in Journal of Cranio-Maxillofacial Surgery
Verified
Journal Article
Closed access
CNChristopher-Philipp Nobis
Christopher-Philipp Nobis
SOSven Otto
Sven Otto
TGTamara Grigorieva
Tamara Grigorieva
MAMohamed Alnaqbi
Mohamed Alnaqbi
MTMatthias Tröltzsch
Matthias Tröltzsch
MKMarco Kesting
Marco Kesting

18 February 2025 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
MPMonika Probst
Monika Probst
FPFlorian Probst
Florian Probst
MTMatthias Tröltzsch
Matthias Tröltzsch
MBMatthias Bruckbauer
Matthias Bruckbauer
AMAlexander W. Marka
Alexander W. Marka
Egon BurianEgon Burian
Egon Burian
Background/Objectives: The aim of this study is to examine the relationship between cervical spine and jaw bone mineral density (BMD) and assess how cortical thickness and BMD influence primary implant stability (PIS) across different bone health conditions. Methods: The study included 29 patients (mean age: 63.7 ± 13.7 years; 13 women) and 15 healthy controls (mean age: 25.3 ± 3.0 years; seven women). Cervical spine (C2–C4) and mandibular BMD were evaluated using asynchronous calibration and manual segmentation. Cortical thickness was measured, and primary implant stability was assessed via insertion torque in Newton centimeters (Ncm). Results: Cervical spine BMD was significantly lower in the patient group compared to controls (203.0 ± 51.0 vs. 252.0 ± 21.7 mg/dL, p < 0.0001). No significant correlation was found between mandibular BMD and cervical spine BMD in both groups (patients: ρ = 0.1287; p = 0.506, controls r = −0.1214; p = 0.667). Linear regression analysis revealed that cortical thickness alone, not implant site BMD, significantly influenced PIS (F(2.74) = 5.597, p = 0.005). Conclusions: Asynchronous calibration accurately quantifies cervical and mandibular BMD. Cortical thickness rather than overall bone density emerges as a critical factor in determining implant stability. These findings suggest that clinicians should prioritize cortical thickness assessment when planning dental implant procedures, potentially improving outcomes across diverse patient bone health profiles.