| Literature DB >> 28604257 |
Efstathios Kastritis1, Pelagia Melea1, Tina Bagratuni1, Ioannis Melakopoulos1, Maria Gavriatopoulou1, Maria Roussou1, Magdalini Migkou1, Evangelos Eleutherakis-Papaiakovou1, Evangelos Terpos1, Meletios A Dimopoulos1.
Abstract
Specific genetic polymorphisms (SNPs) have been correlated with the development of bisphosphonate-related osteonecrosis of the jaw (BRONJ) in small series. We screened 140 myeloma patients (36 patients with and 104 without BRONJ) for the presence of previously identified SNPs in PPARG and CYP2C8 genes. All the patients received exclusively zolendronic acid (ZA) therapy and were followed prospectively for BRONJ. SNPs in both genes were associated with a higher risk of development of early BRONJ, occurring within less than 2 years of ZA therapy (59% vs. 16%, p = .022 for PPARG and 29% vs. 7%, p = .07 for CYP2C8) and a shorter time to develop BRONJ (59% versus 12%, p = .011 for PPARG and 29% versus 0% at 2 years, p = .037 for CYP2C8), independently of indices of poor oral hygiene. Thus, although preliminary, our data indicate that the presence of SNPs in PPARG and CYP2C8 genes may be associated with increased risk of early BRONJ.Entities:
Keywords: CYP2C8; PPARG; Zolendronic acid; osteonecrosis
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Year: 2017 PMID: 28604257 DOI: 10.1080/10428194.2017.1300889
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022