Associations of genetically predicted iron status with 24 gastrointestinal diseases and gut microbiota: a Mendelian randomization study

被引:0
|
作者
Su, Tao [1 ,2 ]
Peng, Xiang [1 ,2 ]
Gan, Ying [3 ]
Wu, Hongzhen [1 ,2 ]
Ma, Shulin [3 ]
Zhi, Min [1 ,2 ]
Lu, Yi [3 ]
Dai, Shixue [4 ]
Yao, Jiayin [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Gastroenterol, Guangdong Prov Key Lab Colorectal & Pelv Floor Dis, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 6, Biomed Innovat Ctr, Guangzhou, Peoples R China
[3] Guangzhou Med Univ, Affiliated TCM Hosp, Dept Anesthesiol, Guangzhou, Peoples R China
[4] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Natl Key Clin Specialty, Dept Gastroenterol,Guangdong Prov Geriatr Inst, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
iron status; gastrointestinal diseases; gut microbiota; Mendelian randomization; liver cancer; DIETARY IRON; CELL-PROLIFERATION; OXIDATIVE STRESS; LIVER FIBROSIS; SUPPLEMENTATION; INFLAMMATION; INCREASES; OVERLOAD; CANCER; RISK;
D O I
10.3389/fgene.2024.1406230
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Iron status has been implicated in gastrointestinal diseases and gut microbiota, however, confounding factors may influence these associations.Objective We performed Mendelian randomization (MR) to investigate the associations of iron status, including blood iron content, visceral iron content, and iron deficiency anemia with the incidence of 24 gastrointestinal diseases and alterations in gut microbiota.Methods Independent genetic instruments linked with iron status were selected using a genome-wide threshold of p = 5 x 10-6 from corresponding genome-wide association studies. Genetic associations related to gastrointestinal diseases and gut microbiota were derived from the UK Biobank, the FinnGen study, and other consortia.Results Genetically predicted higher levels of iron and ferritin were associated with a higher risk of liver cancer. Higher levels of transferrin saturation were linked to a decreased risk of celiac disease, but a higher risk of non-alcoholic fatty liver disease (NAFLD) and liver cancer. Higher spleen iron content was linked to a lower risk of pancreatic cancer. Additionally, higher levels of liver iron content were linked to a higher risk of NAFLD and liver cancer. However, certain associations lost their statistical significance upon accounting for the genetically predicted usage of cigarettes and alcohol. Then, higher levels of iron and ferritin were associated with 11 gut microbiota abundance, respectively. In a secondary analysis, higher iron levels were associated with lower diverticular disease risk and higher ferritin levels with increased liver cancer risk. Higher levels of transferrin saturation were proven to increase the risk of NAFLD, alcoholic liver disease, and liver cancer, but decrease the risk of esophageal cancer. MR analysis showed no mediating relationship among iron status, gut microbiota, and gastrointestinal diseases.Conclusion This study provides evidence suggesting potential causal associations of iron status with gastrointestinal diseases and gut microbiota, especially liver disease.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Causal Effects of Genetically Predicted Iron Status on Sepsis: A Two-Sample Bidirectional Mendelian Randomization Study
    Hu, Yuanlong
    Cheng, Xiaomeng
    Mao, Huaiyu
    Chen, Xianhai
    Cui, Yue
    Qiu, Zhanjun
    FRONTIERS IN NUTRITION, 2021, 8
  • [32] Causal associations between human gut microbiota and osteomyelitis: a Mendelian randomization study
    Zeng, Wenxing
    Wu, Yuheng
    Liang, Xiaoye
    Cun, Dejun
    Ma, Luyao
    Zhang, Jingtao
    Huang, Feng
    Jiang, Ziwei
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2024, 14
  • [33] Causal associations between human gut microbiota and cholelithiasis: a mendelian randomization study
    Li, Wei
    Ren, Ao
    Qin, Qiong
    Zhao, Ling
    Peng, Qiufeng
    Ma, Ruidong
    Luo, Shiqiao
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2023, 13
  • [34] Causal associations between gut microbiota and cutaneous melanoma: a Mendelian randomization study
    Bao, Yan-Qiu
    Zhang, Ying
    Li, Zhou-Na
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [35] Associations between gut microbiota and chronic sinusitis: A bidirectional Mendelian randomization study
    Pu, Kunlin
    Zhang, Zhipeng
    Li, Li
    IMMUNITY INFLAMMATION AND DISEASE, 2024, 12 (07)
  • [36] Genetically predicted glucosamine and longevity: A Mendelian randomization study
    Yoon, So Young
    Narayan, Vikram P.
    CLINICAL NUTRITION ESPEN, 2022, 49 : 556 - 559
  • [37] Gut microbiota and acne: A Mendelian randomization study
    Cao, Qiurui
    Guo, Jinyan
    Chang, Shuangqing
    Huang, Zhifang
    Luo, Qinghua
    SKIN RESEARCH AND TECHNOLOGY, 2023, 29 (09)
  • [38] Gut microbiota and osteonecrosis: A Mendelian randomization study
    Cai, Yong
    Zhou, Chaoqing
    Guan, Junjie
    Dai, Bo
    Zhang, Xingshi
    Jiang, Jizhao
    Zhao, Jun
    MEDICINE, 2025, 104 (10)
  • [39] Associations between gut microbiota and three prostate diseases: a bidirectional two-sample Mendelian randomization study
    Liu, Xiaoyang
    Dong, Qiang
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [40] Genetically determined gut microbiota associates with pulmonary arterial hypertension: a Mendelian randomization study
    Yuan, Ye
    Li, Shan
    Yan, Manrong
    Yang, Yan
    Zhong, Changming
    Hu, Yijie
    BMC PULMONARY MEDICINE, 2024, 24 (01):