Seneff Stephanie, Swanson Nancy L, Koenig Gerald, Li Chen
Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA 02139, USA.
Abacus Enterprises, Lummi Island, WA, USA.
Dis Markers. 2016;2016:8376979. doi: 10.1155/2016/8376979. Epub 2016 Sep 28.
Osteonecrosis of the jaw (ONJ), a rare side effect of bisphosphonate therapy, is a debilitating disorder with a poorly understood etiology. FDA's Adverse Event Reporting System (FAERS) provides the opportunity to investigate this disease. Our goals were to analyze FAERS data to discover possible relationships between ONJ and specific conditions and drugs and then to consult the scientific literature to deduce biological explanations. Our methodology revealed a very strong association between gastroesophageal reflux and bisphosphonate-induced ONJ, suggesting acidosis as a key factor. Overgrowth of acidophilic species, particularly , in the oral microbiome in the context of insufficient acid buffering due to impaired salivary glands maintains the low pH that sustains damage to the mucosa. Significant associations between ONJ and adrenal insufficiency, vitamin C deficiency, and Sjögren's syndrome were found. Glucose 6 phosphate dehydrogenase (G6PD) deficiency can explain much of the pathology. An inability to maintain vitamin C and other antioxidants in the reduced form leads to vascular oxidative damage and impaired adrenal function. Thus, pathogen-induced acidosis, hypoxia, and insufficient antioxidant defenses together induce ONJ. G6PD deficiency and adrenal insufficiency are underlying factors. Impaired supply of adrenal-derived sulfated sterols such as DHEA sulfate may drive the disease process.
颌骨坏死(ONJ)是双膦酸盐治疗罕见的副作用,是一种病因不明的使人衰弱的病症。美国食品药品监督管理局(FDA)的不良事件报告系统(FAERS)为研究这种疾病提供了机会。我们的目标是分析FAERS数据,以发现ONJ与特定病症和药物之间可能存在的关系,然后查阅科学文献以推断生物学解释。我们的方法揭示了胃食管反流与双膦酸盐诱导的ONJ之间存在非常强的关联,表明酸中毒是一个关键因素。在唾液腺受损导致酸缓冲不足的情况下,口腔微生物群中嗜酸菌过度生长,维持低pH值,持续损害黏膜。发现ONJ与肾上腺功能不全、维生素C缺乏和干燥综合征之间存在显著关联。葡萄糖6磷酸脱氢酶(G6PD)缺乏可以解释大部分病理情况。无法维持还原形式的维生素C和其他抗氧化剂会导致血管氧化损伤和肾上腺功能受损。因此,病原体诱导的酸中毒、缺氧和抗氧化防御不足共同诱发ONJ。G6PD缺乏和肾上腺功能不全是潜在因素。肾上腺衍生的硫酸化固醇(如硫酸脱氢表雄酮)供应受损可能推动疾病进程。