1.Causal relationship between autoimmune diseases and aplastic anemia: A Mendelian randomization study.
Wenjie LI ; Yaonan HONG ; Rui HUANG ; Yuchen LI ; Ying ZHANG ; Yun ZHANG ; Dijiong WU
Journal of Southern Medical University 2025;45(4):871-879
OBJECTIVES:
To investigate the causal associations between autoimmune diseases and aplastic anemia (AA) using Mendelian randomization analysis.
METHODS:
Publicly available genome-wide association study (GWAS) data were utilized to obtain single nucleotide polymorphisms (SNPs) associated with autoimmune diseases and AA for analysis. The inverse variance weighted (IVW) method was employed as the primary analytical approach, with MR Egger, Weighted Mode, Weighted Median, and Simple Mode methods serving as complementary analyses. Heterogeneity and pleiotropy analyses were conducted using designated functions, and the robustness of Mendelian randomization results was assessed using leave-one-out analysis.
RESULTS:
The two-sample Mendelian randomization analysis using the IVW method revealed significant positive causal associations of rheumatoid arthritis (OR=1.094, 95% CI: 1.023-1.170, P=0.009, adjusted P=0.042), systemic lupus erythematosus (OR=1.111, 95% CI: 1.021-1.208, P=0.015, adjusted P=0.036), Hashimoto thyroiditis (OR=1.206, 95% CI: 1.049-1.387, P=0.009, adjusted P=0.029), and Sicca syndrome (OR=1.173, 95% CI: 1.054-1.306, P=0.004, adjusted P=0.035) with AA, which was supported by the results from the Weighted Median method. Sensitivity analyses indicated no evidence of pleiotropy or heterogeneity, and leave-one-out analysis confirmed the robustness of the causal relationships. No direct evidence was found linking Graves' disease, ulcerative colitis, Crohn's disease, autoimmune hepatitis, primary biliary cholangitis, or primary sclerosing cholangitis with AA (P>0.05, adjusted P>0.05), indicating a lack of causal association. Reverse Mendelian randomization results and multiple corrections indicated that AA was not an influencing factor for autoimmune diseases (adjusted P>0.05).
CONCLUSIONS
Our findings support at the genetic level that rheumatoid arthritis, systemic lupus erythematosus, Hashimoto thyroiditis, and Sicca syndrome are risk factors for AA, and confirm a causal association of the these 4 autoimmune diseases with an increased risk of AA.
Humans
;
Mendelian Randomization Analysis
;
Anemia, Aplastic/genetics*
;
Autoimmune Diseases/complications*
;
Polymorphism, Single Nucleotide
;
Genome-Wide Association Study
;
Arthritis, Rheumatoid/genetics*
;
Lupus Erythematosus, Systemic/genetics*
;
Genetic Predisposition to Disease
2.Observation of low-dose HA/HAA regimen as induction chemotherapy on elderly patients with acute myeloid leukemia.
Dijiong WU ; Baodong YE ; Jianping SHEN ; Yiping SHEN ; Shengyun LIN ; Zhiping HU ; Qinghong YU ; Zhiyin ZHENG ; Laijun PENG ; Shan LIU ; Conghua JI ; Yunfei LUO ; Xiaowen WEN ; Keding SHAO ; Yu ZHANG ; Yanting GAO ; Dan CHEN ; Yuhong ZHOU
Chinese Journal of Hematology 2014;35(3):256-259
3.Overview the Treatment of Chronic Idiopathic Thrombocytopenic Purpura Based on Qi and Yin
Yuhong ZHOU ; Dijiong WU ; Yiping SHEN
Journal of Zhejiang Chinese Medical University 2006;0(05):-
The understanding and treatment of Traditional Chinese Medicine(TCM) on chronic idiopathic thrombocytopenic purpura(CITP) is prosperous,while no conclusion is yielded.By digging out documentation and summarizing clinical experience,"Qi and Yin Discrimination","Viscera Discrimination"and "Meridians Discrimination"are concluded to formulate the idea that the treatment of CIPT should bebased on Qi and Yin in this article,which aims at identifying the understanding of TCM on CITP,and then guiding clinical practice to improve therapeutic effect.

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