Genes (23)
Species: human : 23 | |
Human | IL23R | 149233 | interleukin 23 receptor | IL23R polymorphisms may play an important role in the development of osteonecrosis of femoral head | Human | KL | 9365 | klotho | several single nucleotide polymorphisms in bone morphogenic protein 6, annexin A2, and klotho were associated with sickle cell osteonecrosis | Human | VDR | 7421 | vitamin D (1,25- dihydroxyvitamin D3) receptor | Title:Pharmacogenetic risk factors for osteonecrosis of the hip among children with leukemia.|Association:Y|Conclusion:Because folate-related and vitamin D-receptor genetic variants have been associated with bone and vasculature morbidity, these pharmacogenetic associations likely reflect the interaction of antileukemic medications with germline sensitivity to drug actions, and might identify ALL patients at highest risk to develop osteonecrosis. | Human | TYMS | 7298 | thymidylate synthetase | Title:Pharmacogenetic risk factors for osteonecrosis of the hip among children with leukemia.|Association:Not Found|Conclusion:Because folate-related and vitamin D-receptor genetic variants have been associated with bone and vasculature morbidity, these pharmacogenetic associations likely reflect the interaction of antileukemic medications with germline sensitivity to drug actions, and might identify ALL patients at highest risk to develop osteonecrosis. | Human | TP53 | 7157 | tumor protein p53 | Results describe the possible involvement of p53 in the osteocyte apoptosis observed in Idiopathic osteonecrosis of the femoral head | Human | SREBF1 | 6720 | sterol regulatory element binding transcription factor 1 | Polymorphism of the SREBF1 gene is associated with the risk of osteonecrosis of the femoral head in the Korean population | Human | PPARG | 5468 | peroxisome proliferator-activated receptor gamma | the examined polymorphisms and haplotypes of the PPARgamma gene are unlikely to be associated with susceptibility to osteonecrosis of the femoral head | Human | PON1 | 5444 | paraoxonase 1 | We conclude that individuals with PON1 192QQ genotype may have increased risk for osteonecrosis of the femoral head and cerebral white matter lesions | Human | ABCB1 | 5243 | ATP-binding cassette, sub-family B (MDR/TAP), member 1 | The ABCB1 variant type showed a lower incidence of osteonecrosis of the femoral head in patients with femoral head osteonecrosis, The synergistic index between the ABCB1 and CBP genes was >1.00 (1.99), revealing the presence of an interaction | Human | SERPINE1 | 5054 | serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 | Title:Relationship between postrenal transplant osteonecrosis of the femoral head and gene polymorphisms related to the coagulation and fibrinolytic systems in Japanese subjects.|Association:Not Found|Conclusion:Genotypes of PAI-1 4G/5G and MTHFR C677T or plasma concentrations of PAI-1 Ag and tHcy had no effect on the incidence of ONFH in Japanese subjects, unlike the results of studies performed in white subjects. The effect of genetic background on the pathologic conditions that developed in patients with postrenal transplant ONFH may differ according to race. Title:Association of plasminogen activator inhibitor-1 genotype with avascular osteonecrosis in steroid-treated renal allograft recipients|Association:Not Found|Conclusion:Hypofibrinolysis conferred by the 4G/4G PAI-1 gene variant is a major predisposing factor for AVN in renal transplant patients. The risk is particularly high in obese subjects or patients with persistent hyperparathyroidism. A prospective intervention study of early anticoagulation after renal transplantation is needed to assess whether glucocorticoid-associated AVN can be prevented. a genetic variant of the plasminogen activator inhibitor-1 (PAI-1) determines the risk of avascular osteonecrosis in glucocorticoid-treated patients PAI-1 polymorphism (rs6092) was associated with risk of osteonecrosis complicating acute lymphoblastic leukemia | Human | NOS3 | 4846 | nitric oxide synthase 3 (endothelial cell) | The T-786C eNOS polymorphism and resultant reduction of nitric oxide production is associated with, and may contribute to, the pathogenesis of idiopathic osteonecrosis of the femoral head Multifocal and unifocal osteonecrosis are similarly associated with thrombophilia, hypofibrinolysis, and the eNOS T-786C polymorphism carrier state of 4a allele in intron 4 might be a genetic risk factor of nontraumatic femoral head osteonecrosis | Human | MTHFR | 4524 | methylenetetrahydrofolate reductase (NAD(P)H) | Title:Relationship between postrenal transplant osteonecrosis of the femoral head and gene polymorphisms related to the coagulation and fibrinolytic systems in Japanese subjects.|Association:Not Found|Conclusion:Genotypes of PAI-1 4G/5G and MTHFR C677T or plasma concentrations of PAI-1 Ag and tHcy had no effect on the incidence of ONFH in Japanese subjects, unlike the results of studies performed in white subjects. The effect of genetic background on the pathologic conditions that developed in patients with postrenal transplant ONFH may differ according to race. The 677C-->T mutation of MTHFR was present in 26.1% of adults with idiopathic osteonecrosis of the femur head and appears to have a role in the complex pathophysiology of the disease No correlation was determined between factor V Leiden, prothrombin G20210A, and Methylenetetrahydrofolate reductase C677T mutations and osteonecrosis in kidney allograft recipients | Human | IL17A | 3605 | interleukin 17A | multiple myeloma patients without osteonecrosis of the jaw and control subjects presented similar values of IL-17 serum levels | Human | HIF1A | 3091 | hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) | variations in HIF1alpha may play an important role in the pathogenesis and risk factor for osteonecrosis of the femoral head | Human | GBA | 2629 | glucosidase, beta, acid | | Human | F5 | 2153 | coagulation factor V (proaccelerin, labile factor) | No correlation was determined between factor V Leiden, prothrombin G20210A, and Methylenetetrahydrofolate reductase C677T mutations and osteonecrosis in renal allograft recipients The purpose of this study was to examine the association between osteonecrosis of the knee and abnormalities in the thrombotic pathway in the form of factor V Leiden and the prothrombin 20210A gene mutation | Human | CYP2C8 | 1558 | cytochrome P450, family 2, subfamily C, polypeptide 8 | Individuals homozygous for the T allele had an increased likelihood of developing osteonecrosis of the jaw (odds ratio 12.75, 95% confidence interval 3.7-43.5) | Human | CTNNB1 | 1499 | catenin (cadherin-associated protein), beta 1, 88kDa | Data suggest the Wnt/beta-catenin signaling pathway may be associated with ethanol-induced osteonecrosis | Human | CREBBP | 1387 | CREB binding protein | in patients with femoral head osteonecrosis, The synergistic index between the ABCB1 and CBP genes was >1.00 (1.99), revealing the presence of an interaction results indicate that the genetic polymorphism of the CBP, which is one of the essential factors exerting the biological effects of glucocorticoids, may affect susceptibility to steroid-induced osteonecrosis in patients after renal transplantation | Human | BMP6 | 654 | bone morphogenetic protein 6 | several single nucleotide polymorphisms in bone morphogenic protein 6, annexin A2, and klotho were associated with sickle cell osteonecrosis | Human | ANXA2 | 302 | annexin A2 | Title:Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.|Association:Not Found|Conclusion:These genes are important in bone morphology, metabolism and vascular disease. Our results may provide insight into the pathogenesis of osteonecrosis in sickle cell disease, help identify individuals who are at high risk for osteonecrosis, and thus allow earlier and more effective therapeutic intervention. several single nucleotide polymorphisms in bone morphogenic protein 6, annexin A2, and klotho were associated with sickle cell osteonecrosis | Human | ALDH2 | 217 | aldehyde dehydrogenase 2 family (mitochondrial) | Title:A case-control study of association between life-style, alcohol dehydrogenase 2 and aldehyde dehydrogenase 2 genotype and idiopathic osteonecrosis of the femoral head.|Association:Not Found|Conclusion:The reason for the insignificant multivariate OR of ALDH2(1/1) may be due to the strong confounding of alcohol consumption on the association between ALDH2 genotype and ION. For females, the small sample size made it impossible to produce any meaningful univariate analysis. | Human | ADH1B | 125 | alcohol dehydrogenase 1B (class I), beta polypeptide | Title:A case-control study of association between life-style, alcohol dehydrogenase 2 and aldehyde dehydrogenase 2 genotype and idiopathic osteonecrosis of the femoral head.|Association:Not Found|Conclusion:The reason for the insignificant multivariate OR of ALDH2(1/1) may be due to the strong confounding of alcohol consumption on the association between ALDH2 genotype and ION. For females, the small sample size made it impossible to produce any meaningful univariate analysis. |
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