4.3 Article

Multifactorial Landscape Parses to Reveal a Predictive Model for Knee Osteoarthritis

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MDPI
DOI: 10.3390/ijerph18115933

关键词

multifactorial; knee osteoarthritis; genetic models; haplotypes; ROC curve analysis; predictive marker

资金

  1. women scientist scheme of the Department of Science and Technology, New Delhi [SR/WOS-A/LS-532/2016]

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This study aimed to investigate whether a combination of significant risk variables, pro-inflammatory markers, and candidate genes could serve as a predictive marker for knee osteoarthritis (KOA). The study identified higher BMI, triglycerides, poor sleep, IL-6, IL-1 beta, and hsCRP as independent predictors for KOA. Additionally, specific haplotypes within CRP, IL-6, VDR, and eNOS genes were found to impact KOA risk, further enhancing the predictive ability of the model.
The present study attempted to investigate whether concerted contributions of significant risk variables, pro-inflammatory markers, and candidate genes translate into a predictive marker for knee osteoarthritis (KOA). The present study comprised 279 confirmed osteoarthritis patients (Kellgren and Lawrence scale >= 2) and 287 controls. Twenty SNPs within five genes (CRP, COL1A1, IL-6, VDR, and eNOS), four pro-inflammatory markers (interleukin-6 (IL-6), interleuin-1 beta (IL-1 beta), tumor necrosis factor alpha (TNF-alpha), and high sensitivity C-reactive protein (hsCRP)), along with significant risk variables were investigated. A receiver operating characteristic (ROC) curve was used to observe the predictive ability of the model for distinguishing patients with KOA. Multivariable logistic regression analysis revealed that higher body mass index (BMI), triglycerides (TG), poor sleep, IL-6, IL-1 beta, and hsCRP were independent predictors for KOA after adjusting for the confounding from other risk variables. Four susceptibility haplotypes for the risk of KOA, AGT, GGGGCT, AGC, and CTAAAT, were observed within CRP, IL-6, VDR, and eNOS genes, which showed their impact in recessive beta(SE): 2.11 (0.76), recessive beta(SE): 2.75 (0.59), dominant beta(SE): 1.89 (0.52), and multiplicative modes beta(SE): 1.89 (0.52), respectively. ROC curve analysis revealed the model comprising higher values of BMI, poor sleep, IL-6, and IL-1 beta was predictive of KOA (AUC: 0.80, 95%CI: 0.74-0.86, p < 0.001), and the strength of the predictive ability increased when susceptibility haplotypes AGC and GGGGCT were involved (AUC: 0.90, 95%CI: 0.87-0.95, p < 0.001).This study offers a predictive marker for KOA based on the risk scores of some pertinent genes and their genetic variants along with some pro-inflammatory markers and traditional risk variables.

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