Immune-mediated pathways between red blood cell traits and prostate cancer: a causal relationship network based on Mendelian randomization evaluation.
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OpenAlex 토픽 ·
Inflammatory Biomarkers in Disease Prognosis
Blood groups and transfusion
Adipokines, Inflammation, and Metabolic Diseases
[BACKGROUND] Although both the immune and hematopoietic systems play important roles in prostate cancer (PCa), few studies have comprehensively investigated the combined influence of these systems on
APA
Ting Yang, Jinyu Zhang, et al. (2026). Immune-mediated pathways between red blood cell traits and prostate cancer: a causal relationship network based on Mendelian randomization evaluation.. The aging male : the official journal of the International Society for the Study of the Aging Male, 29(1), 2641901. https://doi.org/10.1080/13685538.2026.2641901
MLA
Ting Yang, et al.. "Immune-mediated pathways between red blood cell traits and prostate cancer: a causal relationship network based on Mendelian randomization evaluation.." The aging male : the official journal of the International Society for the Study of the Aging Male, vol. 29, no. 1, 2026, pp. 2641901.
PMID
41839839 ↗
Abstract 한글 요약
[BACKGROUND] Although both the immune and hematopoietic systems play important roles in prostate cancer (PCa), few studies have comprehensively investigated the combined influence of these systems on PCa risk.
[METHOD] The datasets used to construct causal networks for evaluation via Mendelian randomization and mediation Mendelian randomization (MMR). Nine analytical approaches were applied to evaluate the causal associations.
[RESULT] The findings revealed that red blood cell count (RBC) and red cell distribution width (RDW) were related to a modest increased risk of PCa, while mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) were related to a modest reduced risk. Further, MMR analyses identified that HLA-DR on dendritic cells mediated the causal effect of RBC on PCa, with a mediated proportion of 12.09%, and that IgD CD38 B cell % B cell mediated the effects of RDW and MCHC on PCa, with mediating proportions of 15.07% and 25.96%, respectively. Moreover, the IgD CD38 B cell % lymphocytes mediated the causal effect of MCHC on PCa, with a mediated proportion of 29.03%.
[CONCLUSION] RBC, RDW, MCH, and MCHC were related to the risk of PCa. Immune cells act as major mediators in this relationship.
[METHOD] The datasets used to construct causal networks for evaluation via Mendelian randomization and mediation Mendelian randomization (MMR). Nine analytical approaches were applied to evaluate the causal associations.
[RESULT] The findings revealed that red blood cell count (RBC) and red cell distribution width (RDW) were related to a modest increased risk of PCa, while mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) were related to a modest reduced risk. Further, MMR analyses identified that HLA-DR on dendritic cells mediated the causal effect of RBC on PCa, with a mediated proportion of 12.09%, and that IgD CD38 B cell % B cell mediated the effects of RDW and MCHC on PCa, with mediating proportions of 15.07% and 25.96%, respectively. Moreover, the IgD CD38 B cell % lymphocytes mediated the causal effect of MCHC on PCa, with a mediated proportion of 29.03%.
[CONCLUSION] RBC, RDW, MCH, and MCHC were related to the risk of PCa. Immune cells act as major mediators in this relationship.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
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