Genetically predicted metabolites mediate the causal associations between autoimmune thyroiditis and immune cells

被引:2
作者
Chen, Yongzhao [1 ]
Jiang, Bo [2 ]
Qu, Cheng [2 ]
Jiang, Chaoyu [2 ]
Zhang, Chen [2 ]
Wang, Yanxue [2 ]
Chen, Fei [3 ]
Sun, Xitai [4 ]
Su, Lei [2 ]
Luo, Yuqian [5 ]
机构
[1] Nanjing Univ Chinese Med, Nanjing Drum Tower Hosp, Dept Gen Surg, Affiliated Hosp, Nanjing, Peoples R China
[2] Nanjing Univ, Nanjing Drum Tower Hosp, Dept Gen Surg, Affiliated Hosp,Med Sch, Nanjing, Peoples R China
[3] Southern Med Univ, Zhujiang Hosp, Gen Surg Ctr, Dept Thyroid Surg, Guangzhou, Peoples R China
[4] Nanjing Univ Chinese Med, Nanjing Drum Tower Hosp, Dept Gen Surg, Div Pancreas & Metab Surg,Affiliated Hosp, Nanjing, Peoples R China
[5] Nanjing Univ, Nanjing Drum Tower Hosp, Clin Med Res Ctr, Affiliated Hosp,Med Sch, Nanjing, Peoples R China
来源
FRONTIERS IN ENDOCRINOLOGY | 2024年 / 15卷
基金
中国国家自然科学基金;
关键词
autoimmune thyroiditis; immune cells; metabolites; Mendelian randomization; mediation effects; MENDELIAN RANDOMIZATION; T-CELLS; INSTRUMENTS; LEPTIN; EPIDEMIOLOGY; DISEASES; COMPLEX; CHOLINE; BIAS;
D O I
10.3389/fendo.2024.1424957
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction We aimed to comprehensively investigate the causal relationship between 731 immune cell traits and autoimmune thyroiditis (AIT) and to identify and quantify the role of 1400 metabolic traits as potential mediators in between.Methods Using summary-level data from genome-wide association studies (GWAS) we performed a two-sample bidirectional Mendelian randomization (MR) analysis of genetically predicted AIT and 731 immune cell traits. Furthermore, we used a two-step MR analysis to quantify the proportion of the total effects (that the immune cells exerted on the risk of AIT) mediated by potential metabolites.Results We identified 24 immune cell traits (with odds ratio (OR) ranging from 1.3166 6 to 0.6323) and 10 metabolic traits (with OR ranging from 1.7954 to 0.6158) to be causally associated with AIT, respectively. Five immune cell traits (including CD38 on IgD+ CD24-, CD28 on CD28+ CD45RA+ CD8br, HLA DR+ CD4+ AC, TD CD4+ %CD4+, and CD8 on EM CD8br) were found to be associated with the risk of AIT, which were partially mediated by metabolites (including glycolithocholate sulfate, 5alpha-androstan-3alpha,17beta-diol disulfate, arachidonoylcholine, X-15486, and kynurenine). The proportion of genetically predicted AIT mediated by the identified metabolites could range from 5.58% to 17.7%.Discussion Our study identified causal associations between AIT and immune cells which were partially mediated by metabolites, thus providing guidance for future clinical and basic research.
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页数:13
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共 70 条
  • [41] Clinical differences between IgG4 Hashimoto's thyroiditis and primary thyroid lymphoma
    Liu, Liyuan
    Yu, Yang
    Chen, Lei
    Zhang, Yang
    Lu, Guizhi
    Gao, Ying
    Zhang, Junqing
    [J]. EUROPEAN THYROID JOURNAL, 2022, 11 (03)
  • [42] Immunological aspects of autoimmune thyroid disease - Complex interplay between cells and cytokines
    Luty, Justyna
    Ruckemann-Dziurdzinska, Katarzyna
    Witkowski, Jacek M.
    Bryl, Ewa
    [J]. CYTOKINE, 2019, 116 : 128 - 133
  • [43] Sphingomyelin is a prospective metabolic immune checkpoint for natural killer cells
    Ma, Hongdi
    Wang, Xuben
    Zheng, Xiaohu
    Wei, Haiming
    [J]. CLINICAL AND TRANSLATIONAL MEDICINE, 2023, 13 (09):
  • [44] Defining Memory CD8 T Cell
    Martin, Matthew D.
    Badovinac, Vladimir P.
    [J]. FRONTIERS IN IMMUNOLOGY, 2018, 9
  • [45] Cutting Edge: Distinct Glycolytic and Lipid Oxidative Metabolic Programs Are Essential for Effector and Regulatory CD4+ T Cell Subsets
    Michalek, Ryan D.
    Gerriets, Valerie A.
    Jacobs, Sarah R.
    Macintyre, Andrew N.
    MacIver, Nancie J.
    Mason, Emily F.
    Sullivan, Sarah A.
    Nichols, Amanda G.
    Rathmell, Jeffrey C.
    [J]. JOURNAL OF IMMUNOLOGY, 2011, 186 (06) : 3299 - 3303
  • [46] Quinolinate as a Marker for Kynurenine Metabolite Formation and the Unresolved Question of NAD+ Synthesis During Inflammation and Infection
    Moffett, John R.
    Arun, Peethambaran
    Puthillathu, Narayanan
    Vengilote, Ranjini
    Ives, John A.
    Badawy, Abdulla A-B
    Namboodiri, Aryan M.
    [J]. FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [47] Expression of CCR7 and CD45RA in CD4+ and CD8+ subsets in cerebrospinal fluid of 134 patients with inflammatory and non-inflammatory neurological diseases
    Mullen, Katherine M.
    Gocke, Anne R.
    Allie, Rameeza
    Ntranos, Achilles
    Grishkan, Inna V.
    Pardo, Carlos
    Calabresi, Peter A.
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 2012, 249 (1-2) : 86 - 92
  • [48] The generation of antibody-secreting plasma cells
    Nutt, Stephen L.
    Hodgkin, Philip D.
    Tarlinton, David M.
    Corcoran, Lynn M.
    [J]. NATURE REVIEWS IMMUNOLOGY, 2015, 15 (03) : 160 - 171
  • [49] Complex genetic signatures in immune cells underlie autoimmunity and inform therapy
    Orru, Valeria
    Steri, Maristella
    Sidore, Carlo
    Marongiu, Michele
    Serra, Valentina
    Olla, Stefania
    Sole, Gabriella
    Lai, Sandra
    Dei, Mariano
    Mulas, Antonella
    Virdis, Francesca
    Piras, Maria Grazia
    Lobina, Monia
    Marongiu, Mara
    Pitzalis, Maristella
    Deidda, Francesca
    Loizedda, Annalisa
    Onano, Stefano
    Zoledziewska, Magdalena
    Sawcer, Stephen
    Devoto, Marcella
    Gorospe, Myriam
    Abecasis, Goncalo R.
    Floris, Matteo
    Pala, Mauro
    Schlessinger, David
    Fiorillo, Edoardo
    Cucca, Francesco
    [J]. NATURE GENETICS, 2020, 52 (10) : 1036 - +
  • [50] Changes in plasma levels of fat-derived hormones adiponectin, leptin, resistin and visfatin in patients with rheumatoid arthritis
    Otero, M.
    Lago, R.
    Gomez, R.
    Lago, F.
    Dieguez, C.
    Gomez-Reino, J. J.
    Gualillo, O.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (09) : 1198 - 1201