Osteonecrosis of the Jaws in Patients with Hereditary Thrombophilia/Hypofibrinolysis-From Pathophysiology to Therapeutic Implications.
Minerva Codruţa BădescuElena RezusManuela CiocoiuOana Viola BadulescuLacramioara Ionela ButnariuDiana PopescuIoana BratoiuCiprian RezusPublished in: International journal of molecular sciences (2022)
Osteonecrosis of the jaws (ONJ) usually has a clear etiology. Local infection or trauma, radiotherapy and drugs that disrupt the vascular supply or bone turnover in the jaws are its major contributors. The thrombotic occlusion of the bone's venous outflow that occurs in individuals with hereditary thrombophilia and/or hypofibrinolysis has a less known impact on jaw health and healing capability. Our research provides the most comprehensive, up-to-date and systematized information on the prevalence and significance of hereditary thrombophilia and/or hypofibrinolysis states in ONJ. We found that hereditary prothrombotic abnormalities are common in patients with ONJ refractory to conventional medical and dental treatments. Thrombophilia traits usually coexist with hypofibrinolysis traits. We also found that frequently acquired prothrombotic abnormalities coexist with hereditary ones and enhance their negative effect on the bone. Therefore, we recommend a personalized therapeutic approach that addresses, in particular, the modifiable risk factors of ONJ. Patients will have clear benefits, as they will be relieved of persistent pain and repeated dental procedures.
Keyphrases
- bone mineral density
- risk factors
- healthcare
- ejection fraction
- soft tissue
- chronic pain
- end stage renal disease
- newly diagnosed
- bone loss
- genome wide
- bone regeneration
- oral health
- early stage
- prognostic factors
- radiation therapy
- squamous cell carcinoma
- risk assessment
- gene expression
- locally advanced
- pain management
- radiation induced
- body composition
- climate change
- rectal cancer
- human health
- patient reported