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Exploring the causal relationship between interleukin-6 or C reactive protein and malignant melanoma using a two-sample Mendelian randomization approach.
Wang, Quan Jun; Zheng, Wei; Pan, Sun Feng.
Afiliação
  • Wang QJ; Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
  • Zheng W; Department of Burns and Plastic Surgery, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
  • Pan SF; Department of Burns and Plastic Surgery, Jiaxing Hospital of Traditional Chinese Medicine, Zhenjiang, Jiaxing, China.
Front Oncol ; 14: 1375362, 2024.
Article em En | MEDLINE | ID: mdl-38952546
ABSTRACT
The goal was to explore the effect of interleukin-6 (IL6) and C reactive protein (CRP) on malignant melanoma (MM) using two-sample Mendelian randomization.

Methods:

Data for this study were obtained from the IEU Open GWAS project website for genome-wide association study data (GWAS) on interleukin-6, C reactive protein levels and malignant melanoma. Inverse variance weighted (IVW) method was mainly used and supplemented with MR-Egger regression and weighted median. Finally, horizontal multivariate validity and heterogeneity tests were performed to assess the stability and reliability of the results.

Results:

The results of univariate two-sample MR analyses showed no significant effect of CRP on MM inverse variance weighting method (OR=0.999, 95% CI 0.998-1.001, P=0.343), MR-Egger regression (OR= 1.000, 95% CI 0.998-1.001, P= 0.180), and weighted median method (OR= 0.999, 95% CI 0.997 to 1.000, P= 0.583), and weighted model (OR= 0.999, 95% CI 0.998 to 1.001, P= 0.328). Also,IL-6 had no significant effect on MM inverse variance weighting method (OR= 1.001, 95% CI 0.999 to 1.002, P=0.461), MR-Egger regression (OR= 1.000, 95% CI 0.997 to 1.004, P= 0.910), weighted median method (OR= 1.000, 95% CI 0.998 to 1.002, P= 0.749), and weighted mode (OR= 1.000, 95% CI 0.998 to 1.002, P= 0.820).

Conclusion:

There was no causal relationship between C-reactive protein and IL-6 on the risk of malignant melanoma.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article