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The causal role of circulating inflammatory markers in osteoporosis: a bidirectional Mendelian randomized study.
Dong, Qiu; Wu, Jiayang; Zhang, Huaguo; Luo, Liangping; Wu, Wenrui.
Affiliation
  • Dong Q; Department of Bone and Joint Surgery, First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Wu J; Medical Imaging Centre, First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Zhang H; Department of Ultrasonography, First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Luo L; Medical Imaging Centre, First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Wu W; Medical Imaging Center, The Fifth Affiliated Hospital of Jinan University, Heyuan, Guangdong, China.
Front Immunol ; 15: 1412298, 2024.
Article in En | MEDLINE | ID: mdl-39091505
ABSTRACT

Background:

Osteoporosis (OP) associated with aging exerts substantial clinical and fiscal strains on societal structures. An increasing number of research studies have suggested a bidirectional relationship between circulating inflammatory markers (CIMs) and OP. However, observational studies are susceptible to perturbations in confounding variables. In contrast, Mendelian randomization (MR) offers a robust methodological framework to circumvent such confounders, facilitating a more accurate assessment of causality. Our study aimed to evaluate the causal relationships between CIMs and OP, identifying new approaches and strategies for the prevention, diagnosis and treatment of OP.

Methods:

We analyzed publicly available GWAS summary statistics to investigate the causal relationships between CIMs and OP. Causal estimates were calculated via a systematic analytical framework, including bidirectional MR analysis and Bayesian colocalization analysis.

Results:

Genetically determined levels of CXCL11 (OR = 0.91, 95% CI = 0.85-0.98, P = 0.008, PFDR = 0.119), IL-18 (OR = 0.88, 95% CI = 0.83-0.94, P = 8.66×10-5, PFDR = 0.008), and LIF (OR = 0.86, 95% CI = 0.76-0.96, P = 0.008, PFDR = 0.119) were linked to a reduced risk of OP. Conversely, higher levels of ARTN (OR = 1.11, 95% CI = 1.02-1.20, P = 0.012, PFDR = 0.119) and IFNG (OR = 1.16, 95% CI = 1.03-1.30, P = 0.013, PFDR = 0.119) were associated with an increased risk of OP. Bayesian colocalization analysis revealed no evidence of shared causal variants.

Conclusion:

Despite finding no overall association between CIMs and OP, five CIMs demonstrated a potentially significant association with OP. These findings could pave the way for future mechanistic studies aimed at discovering new treatments for this disease. Additionally, we are the first to suggest a unidirectional causal relationship between ARTN and OP. This novel insight introduces new avenues for research into diagnostic and therapeutic strategies for OP.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoporosis / Biomarkers / Genome-Wide Association Study / Mendelian Randomization Analysis Limits: Female / Humans Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: China Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoporosis / Biomarkers / Genome-Wide Association Study / Mendelian Randomization Analysis Limits: Female / Humans Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: China Country of publication: Suiza