| Biomarker ID | 958 |
| PMID | 22792137 |
| Year | 2012 |
| Biomarker | Mutation Status of LEPR (LEPR Gln223Arg) |
| Biomarker Basis | Mutation Based |
| Biomolecule | Mutation |
| Source | NA |
| Subjects | Humans |
| Regulation | Increased Risk of High Grade PCa for Metastasis |
| Odds Ratio/Hazard Ratio/Relative Risk | OR: Multivariate Model (Stepwise Regression): 1.50 (95% CI: 0.91–2.45) Bootstrap: [1.55 (95% CI: 0.93–2.58)] |
| Effect on Pathways | Adipokine Pathway |
| Experiment | LEPR Gln223Arg ( A Vs G mutation) in Patients with High Grade PCa With Metastasis |
| Type of Biomarker | Prognostic |
| Cohort | A total of 449 histologically confirmed prostate cancer and 557 non-prostate cancer patients were included in the analyses. |
| Senstivity | NA |
| Specificity | NA |
| AUC | NA |
| Accuracy | NA |
| Level Of Significance | NA |
| Method Used | NA |
| Clinical | No |
| Remarks | For each SNP, the risk genotypes were coded as 1 and the non-risk alleles as 0. The model was determined by multiplying the b coefficient by the SNPs, plus the c coefficient by the PSA value and the a coefficient by the patient’s age (Inclusive Risk Score = S bi x Xi+c x PSA+a x Age; where Xi = SNPs scaled for risk, bi = coefficient for SNPs, c = coefficient for PSA, a = coefficient for Age). |
| Clinical Trial Number | NA |
| Degree Of Validity | Not validated on independent patient dataset |
| Technical Name | LEPR |