2018
DOI: 10.5037/jomr.2018.9405
|View full text |Cite
|
Sign up to set email alerts
|

Denosumab Related Osteonecrosis of Jaw: a Case Report

Abstract: BackgroundThis case report shows an affected postmenopausal patient with medicaments related osteonecrosis of the jaw injury associated with increased use of bisphosphonates and Prolia® (denosumab) for the treatment of osteoporosis. The mechanism of action of the receptor activates the denosumab of the nuclear-kB factor binding and makes nuclear-kB Factor, reducing bone volume and reabsorption in the trabecular and cortical bones and, consequently, decreasing an incidence of fractures and maintaining a bone fo… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
6
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 10 publications
(6 citation statements)
references
References 24 publications
0
6
0
Order By: Relevance
“…Long-term administration of denosumab has been shown to have positive effects not only on the prevention of fragility fracture, but also on the amelioration of joint damage in osteoporotic patients [ 15 ]. However, treatment with denosumab is linked to an increased risk of hypocalcaemia and osteonecrosis of the jaw [ 16 ].…”
Section: Current Therapeutic Options and Their Limitationsmentioning
confidence: 99%
“…Long-term administration of denosumab has been shown to have positive effects not only on the prevention of fragility fracture, but also on the amelioration of joint damage in osteoporotic patients [ 15 ]. However, treatment with denosumab is linked to an increased risk of hypocalcaemia and osteonecrosis of the jaw [ 16 ].…”
Section: Current Therapeutic Options and Their Limitationsmentioning
confidence: 99%
“…Denosumab inhibits the receptor activator of nuclear factor-κB binding (RANKL) and the receptor activator of nuclear factor-κB (RANK). This RANKL-RANK complex is essential in osteoclast-mediated bone resorption, and its inhibition decreases the bone turnover, promoting the risk to induce MRONJ [ 6 ]. Its half-life is 25 to 32 days [ 7 ].…”
Section: Introductionmentioning
confidence: 99%
“…Several authors have established the trauma caused by poorly adapted prosthetic rehabilitation as a triggering factor for MRONJ. 12,18,[32][33][34][35][36][37] It is important to note that the removal of the traumatic agent, represented by the dental prosthesis in the case described in this study, may have corresponded to an essential step in the remission of the MRONJ. Also, the use of 0.12% chlorhexidine, a cationic biguanide of broad bacterial spectrum, active against gram-positive, gram-negative and fungus bacteria, 38 associated with the use of clindamycin, an antibiotic with good coverage for gram-positive and anaerobic bacteria, 39 played a key role in the resolution of the case.…”
Section: Discussionmentioning
confidence: 78%