Causal relationship between immune cells and post-viral fatigue syndrome: a Mendelian randomization study

被引:0
作者
Wang, Zheyi [1 ]
Bai, Zetai [1 ]
Sun, Yize [2 ]
机构
[1] Shandong Univ, Qilu Hosp, Cheeloo Coll Med, Dept Neurol, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Qilu Hosp Qingdao, Cheeloo Coll Med, Dept Tradit Chinese Med, Qingdao 266035, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Post-viral fatigue syndrome; Immune cells; Mendelian randomization; B cell;
D O I
10.1186/s12985-025-02809-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundAccumulating evidence has hinted at a correlation between immune cells and post-viral fatigue syndrome (PVFS). However, it is still ambiguous whether these associations indicate a causal connection.ObjectiveTo elucidate the potential causal link between immune cells and PVFS, we performed a two-sample Mendelian randomization (MR) study.MethodsWe obtained summary data on PVFS cases (Ncase = 195) and controls (Ncontrol = 382,198) from the FinnGen consortium. Additionally, we retrieved comprehensive statistical information on 731 immune cell features. Our analysis encompassed both forward and reverse MR approaches. To ensure the reliability and validity of our findings, we conducted rigorous sensitivity analyses, addressing issues of robustness and heterogeneity.ResultOur study presents compelling evidence of a probable causal link between immune cells and PVFS. Notably, we have pinpointed 28 distinct types of immune cell traits that potentially exhibit a causal association with PVFS. Among a pool of 7 31 immune cell traits, we identified 28 immune cell types that exhibited a potential causal association with PVFS. These included 9 B cells, 1 conventional dendritic cell (cDC), 1 maturation stage of T cell, 3 myeloid cells, 9 T, B, NK, and monocyte cells (TBNK), and 5 regulatory T cells (Treg).ConclusionThrough genetic analyses, our study has unveiled profound causal connections between specific types of immune cells and PVFS, offering valuable guidance for forthcoming clinical investigations.
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页数:9
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共 24 条
[1]   In vitro B cell experiments explore the role of CD24, CD38, and energy metabolism in ME/CFS [J].
Armstrong, Christopher W. ;
Mensah, Fane F. K. ;
Leandro, Maria J. ;
Reddy, Venkat ;
Gooley, Paul R. ;
Berkovitz, Saul ;
Cambridge, Geraldine .
FRONTIERS IN IMMUNOLOGY, 2024, 14
[2]   Role of adaptive and innate immune cells in chronic fatigue syndrome/myalgic encephalomyelitis [J].
Brenu, Ekua Weba ;
Huth, Teilah K. ;
Hardcastle, Sharni L. ;
Fuller, Kirsty ;
Kaur, Manprit ;
Johnston, Samantha ;
Ramos, Sandra B. ;
Staines, Don R. ;
Marshall-Gradisnik, Sonya M. .
INTERNATIONAL IMMUNOLOGY, 2014, 26 (04) :233-+
[3]  
Burgess S, 2017, EUR J EPIDEMIOL, V32, P377, DOI 10.1007/s10654-017-0255-x
[4]   Post-viral fatigue in COVID-19: A review of symptom assessment methods, mental, cognitive, and physical impairment [J].
Campos, Maria Cristine ;
Nery, Tatyana ;
Starke, Ana Carolina ;
Alves, Ana Cristina de Bem ;
Speck, Ana Elisa ;
Aguiar, Aderbal .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2022, 142
[5]   Fatigue and cognitive impairment in Post-COVID-19 Syndrome: A systematic review and meta-analysis [J].
Ceban, Felicia ;
Ling, Susan ;
Lui, Leanna M. W. ;
Lee, Yena ;
Gill, Hartej ;
Teopiz, Kayla M. ;
Rodrigues, Nelson B. ;
Subramaniapillai, Mehala ;
Di Vincenzo, Joshua D. ;
Cao, Bing ;
Lin, Kangguang ;
Mansur, Rodrigo B. ;
Ho, Roger C. ;
Rosenblat, Joshua D. ;
Miskowiak, Kamilla W. ;
Vinberg, Maj ;
Maletic, Vladimir ;
McIntyre, Roger S. .
BRAIN BEHAVIOR AND IMMUNITY, 2022, 101 :93-135
[6]   Detecting pleiotropy in Mendelian randomisation studies with summary data and a continuous outcome [J].
Del Greco, Fabiola M. ;
Minelli, Cosetta ;
Sheehanc, Nuala A. ;
Thompsonc, John R. .
STATISTICS IN MEDICINE, 2015, 34 (21) :2926-2940
[7]   Mendelian Randomization [J].
Emdin, Connor A. ;
Khera, Amit V. ;
Kathiresan, Sekar .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2017, 318 (19) :1925-1926
[8]   Distinct plasma immune signatures in ME/CFS are present early in the course of illness [J].
Hornig, Mady ;
Montoya, Jose G. ;
Klimas, Nancy G. ;
Levine, Susan ;
Felsenstein, Donna ;
Bateman, Lucinda ;
Peterson, Daniel L. ;
Gottschalk, C. Gunnar ;
Schultz, Andrew F. ;
Che, Xiaoyu ;
Eddy, Meredith L. ;
Komaroff, Anthony L. ;
Lipkin, W. Ian .
SCIENCE ADVANCES, 2015, 1 (01)
[9]  
Huang CL, 2023, LANCET, V401, pE21, DOI [10.1016/S0140-6736(20)32656-8, 10.1016/S0140-6736(23)00810-3]
[10]   FinnGen provides genetic insights from a well-phenotyped isolated population [J].
Kurki, Mitja, I ;
Karjalainen, Juha ;
Palta, Priit ;
Sipila, Timo P. ;
Kristiansson, Kati ;
Donner, Kati M. ;
Reeve, Mary P. ;
Laivuori, Hannele ;
Aavikko, Mervi ;
Kaunisto, Mari A. ;
Loukola, Anu ;
Lahtela, Elisa ;
Mattsson, Hannele ;
Laiho, Paivi ;
Parolo, Pietro Della Briotta ;
Lehisto, Arto A. ;
Kanai, Masahiro ;
Mars, Nina ;
Ramo, Joel ;
Kiiskinen, Tuomo ;
Heyne, Henrike O. ;
Veerapen, Kumar ;
Rueger, Sina ;
Lemmela, Susanna ;
Zhou, Wei ;
Ruotsalainen, Sanni ;
Parn, Kalle ;
Hiekkalinna, Tero ;
Koskelainen, Sami ;
Paajanen, Teemu ;
Llorens, Vincent ;
Gracia-Tabuenca, Javier ;
Siirtola, Harri ;
Reis, Kadri ;
Elnahas, Abdelrahman G. ;
Sun, Benjamin ;
Foley, Christopher N. ;
Aalto-Setala, Katriina ;
Alasoo, Kaur ;
Arvas, Mikko ;
Auro, Kirsi ;
Biswas, Shameek ;
Bizaki-Vallaskangas, Argyro ;
Carpen, Olli ;
Chen, Chia-Yen ;
Dada, Oluwaseun A. ;
Ding, Zhihao ;
Ehm, Margaret G. ;
Eklund, Kari ;
Farkkila, Martti .
NATURE, 2023, 613 (7944) :508-+